60/200, 688, filed April 28, 2000. The entire contents of the above-referenced application are incorporated herein by this reference.

Background of the Invention The oxidation and reduction of molecules is of critical importance in many cellular metabolic and catabolic pathways."Redox"reactions play important roles in the production and breakdown of nearly all major metabolic intermediates, including amino acids, vitamins, energy molecules (e. g., glucose, sucrose, and their breakdown products), signal molecules (e. g., transcription factors and neurotransmitters), and nucleic acids. A large class of enzymes which facilitate some of these molecular alterations, termed oxidoreductases, have been identified. In the forward reaction, these enzymes catalyze the transfer of a hydride ion from the target substrate to the enzyme or a cofactor of the enzyme (e. g., NAD+, NADP+, FAD+), thereby oxidizing the substrate. These enzymes may also participate in the reverse reaction, wherein a molecular group of the target molecule is reduced by the transfer of a hydride group from the enzyme. Members of the oxidoreductases family are found in nearly all organisms, from prokaryotes to Drosophila to humans. Both between species and within the same species, oxidoreductases vary widely ; disparate family members are frequently classified by the cofactor used by the enzyme (e. g., NAD+, NADP+, FAD+), or by the particular substrate (s) of the enzyme (see, for example, Cavener, D. R. (1992) J. Mol. Biol. 223 : 811-814).

Different oxidoreductases are specific for a wide array of biological and chemical substrates. For example, there exist oxidoreductases specific for steroids (Kass and Sampson (1998) Biochemistry 37 : 17990-800), neurotransmitters (Lamark et al. (1991) Mol.

Microbiol. 5 : 1049-1064), energy metabolites (Krasney et al. (1990) Mol. Biol. Evol. 7 : 155- 177 ; Frederick), alcohols (Ledeboer et al. (1985) NucleicAcids Res. 13 : 3069-3082 ; Koutz et al. (1989) Yeast 5 : 167-177), lipids (Funk et al. (1992) Proc. Natl. Acad. Sci. USA 89 : 3962- 3966), amino acid precursors and nucleotide precursors (Wright et al. (1993) Proc. Natl.

Acad. Sci. USA 90 : 10690-10694). Accordingly, oxidoreductase activity contributes to the ability of the cell to grow and differentiate, to proliferate, and to communicate and interact with other cells. Therefore, a wide range of metabolic disorders and related pathogenic states relate to the oxidoreductases, both directly and indirectly (see, for example, Salazar et al. (1997) J Biol. Chem. 272 : 26425-26433).

Summary of the Invention The present invention is based, at least in part, on the discovery of a novel family of oxidoreductase related proteins, referred to herein interchangeably as"Oxidoreductase Protein"or"OP"nucleic acid and protein molecules. The OP molecules of the present invention are useful as targets for developing modulating agents to regulate a variety of cellular processes such as cellular proliferation and/or migration, cellular metabolism (e. g., for energy production and energy storage), transduction of intracellular signaling, embryological development, and immune response. The present invention is also based, at least in part, on the discovery that the OP molecules of the present invention are upregulated in tumor cells, e. g., colon tumor cells, and are involved in the regulation of methionine production in these cells, thereby modulating the ability of tumor cells to proliferate.

Accordingly, in one aspect, this invention provides isolated nucleic acid molecules encoding OP proteins or biologically active portions thereof, as well as nucleic acid fragments suitable as primers or hybridization probes for the detection of OP-encoding nucleic acids.

In one embodiment, an OP nucleic acid molecule of the invention is at least 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, 99. 5% or more identical to the nucleotide sequence (e. g., to the entire length of the nucleotide sequence) shown in SEQ ID NO : 1 or 3 or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number , or a complement thereof.

In a preferred embodiment, the isolated nucleic acid molecule includes the nucleotide sequence shown SEQ ID NO : 1 or 3, or a complement thereof. In another embodiment, the nucleic acid molecule includes SEQ ID NO : 3 and nucleotides 1-252 of SEQ ID NO : 1. In another embodiment, the nucleic acid molecule includes SEQ ID NO : 3 and nucleotides 2038-2343 of SEQ ID NO : 1. In another preferred embodiment, the nucleic acid molecule consists of the nucleotide sequence shown in SEQ ID NO : 1 or 3. In another preferred embodiment, the nucleic acid molecule includes a fragment of at least 50, 100, 200, 300, 400, 500, 600, 700, 800, 900, 1000, 1100, 1200, 1300, 1400, 1500, 1600, 1700, 1800, 1900, 2000, 2100, 2200, 2300 or more nucleotides (e. g., contiguous nucleotides) of the nucleotide sequence of SEQ ID NO : 1 or 3, or a complement thereof.

In another embodiment, an OP nucleic acid molecule includes a nucleotide sequence encoding a protein having an amino acid sequence sufficiently identical to the amino acid sequence of SEQ ID NO : 2 or an amino acid sequence encoded by the DNA insert of the plasmid deposited with ATCC as Accession Number. In a preferred embodiment, an OP nucleic acid molecule includes a nucleotide sequence encoding a protein having an amino acid sequence at least 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 86%, 87%, 88%,

89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, 99. 5% or more identical to the entire length of the amino acid sequence of SEQ ID NO : 2, or the amino acid sequence encoded by the DNA insert of the plasmid deposited with ATCC as Accession Number In another preferred embodiment, an isolated nucleic acid molecule encodes the amino acid sequence of human OP. In yet another preferred embodiment, the nucleic acid molecule includes a nucleotide sequence encoding a protein having the amino acid sequence of SEQ ID NO : 2, or the amino acid sequence encoded by the DNA insert of the plasmid deposited with ATCC as Accession Number Another embodiment of the invention features nucleic acid molecules, preferably OP nucleic acid molecules, which specifically detect OP nucleic acid molecules relative to nucleic acid molecules encoding non-OP proteins. For example, in one embodiment, such a nucleic acid molecule is at least 20, 30, 40, 50, 100, 200-300, 300-500, 500-1000, 1000- 1500, 1500-2000, 2000-2300 or more nucleotides in length and hybridizes under stringent conditions to a nucleic acid molecule comprising the nucleotide sequence shown in SEQ ID NO : 1, the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number, or a complement thereof.

In other preferred embodiments, the nucleic acid molecule encodes a naturally occurring allelic variant of a polypeptide comprising the amino acid sequence of SEQ ID NO : 2, or an amino acid sequence encoded by the DNA insert of the plasmid deposited with ATCC as Accession Number, wherein the nucleic acid molecule hybridizes to a complement of a nucleic acid molecule comprising SEQ ID NO : 1 or 3 under stringent conditions.

Another embodiment of the invention provides an isolated nucleic acid molecule which is antisense to an OP nucleic acid molecule, e. g., the coding strand of an OP nucleic acid molecule.

Another aspect of the invention provides a vector comprising an OP nucleic acid molecule. In certain embodiments, the vector is a recombinant expression vector. In another embodiment, the invention provides a host cell containing a vector of the invention.

In yet another embodiment, the invention provides a host cell containing a nucleic acid molecule of the invention. The invention also provides a method for producing a protein, preferably an OP protein family member, by culturing a host cell in a suitable medium, e. g., a mammalian host cell such as a non-human mammalian cell, of the invention containing a recombinant expression vector, such that the protein is produced.

Another aspect of this invention features isolated or recombinant OP proteins and polypeptides. In preferred embodiments, the isolated OP protein family member includes at

least one or more of the following domains : a GMC oxidoreductase signature domain and/or a transmembrane domain.

In a preferred embodiment, the OP protein family member has an amino acid sequence at least about 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, 99. 5% or more identical to the amino acid sequence of SEQ ID NO : 2, or the amino acid sequence encoded by the DNA insert of the plasmid deposited with ATCC as Accession Number, and includes at least one or more of the following domains : a GMC oxidoreductase signature domain, a transmembrane domain.

In another preferred embodiment, the OP protein family member modulates oxidoreductase activity, and includes at least one or more of the following domains : a GMC oxidoreductase signature domain, a transmembrane domain.

In yet another preferred embodiment, the OP protein family member is encoded by a nucleic acid molecule having a nucleotide sequence which hybridizes under stringent hybridization conditions to a complement of a nucleic acid molecule comprising the nucleotide sequence of SEQ ID NO : 1 or 3, and includes at least one or more of the following domains : a GMC oxidoreductase signature domain, a transmembrane domain.

In another embodiment, the invention features fragments of the protein having the amino acid sequence of SEQ ID NO : 2, wherein the fragment comprises at least 15, 20, 30, 40, 50, 60, 70, 80, 90, or 100 amino acids (e. g., contiguous amino acids) of the amino acid sequence of SEQ ID NO : 2, or an amino acid sequence encoded by the DNA insert of the plasmid deposited with the ATCC as Accession Number. In another embodiment, the protein, preferably an OP protein, has the amino acid sequence of SEQ ID NO : 2.

In another embodiment, the invention features an isolated OP protein family member which is encoded by a nucleic acid molecule consisting of a nucleotide sequence at least about 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, 99. 5% or more identical to a nucleotide sequence of SEQ ID NO : 1 or 3, or a complement thereof. This invention further features an isolated protein, preferably an OP protein, which is encoded by a nucleic acid molecule consisting of a nucleotide sequence which hybridizes under stringent hybridization conditions to a nucleic acid molecule comprising a complement of a the nucleotide sequence of SEQ ID NO : 1 or 3.

The proteins of the present invention or portions thereof, e. g., biologically active portions thereof, can be operatively linked to a non-OP polypeptide (e. g., heterologous amino acid sequences) to form fusion proteins. The invention further features antibodies, such as monoclonal or polyclonal antibodies, that specifically bind proteins of the invention, preferably OP proteins. In addition, the OP proteins or biologically active portions thereof

can be incorporated into pharmaceutical compositions, which optionally include pharmaceutically acceptable carriers.

In another aspect, the present invention provides a method for detecting the presence of an OP nucleic acid molecule, protein or polypeptide in a biological sample by contacting the biological sample with an agent capable of detecting an OP nucleic acid molecule, protein or polypeptide such that the presence of an OP nucleic acid molecule, protein or polypeptide is detected in the biological sample.

In another aspect, the present invention provides a method for detecting the presence of OP activity in a biological sample by contacting the biological sample with an agent capable of detecting an indicator of OP activity such that the presence of OP activity is detected in the biological sample.

In another aspect, the invention provides a method for modulating OP activity comprising contacting a cell capable of expressing OP with an agent that modulates OP activity such that OP activity in the cell is modulated. In one embodiment, the agent inhibits OP activity. In another embodiment, the agent stimulates OP activity. In one embodiment, the agent is an antibody that specifically binds to an OP protein. In another embodiment, the agent modulates expression of OP by modulating transcription of an OP gene or translation of an OP mRNA. In yet another embodiment, the agent is a nucleic acid molecule having a nucleotide sequence that is antisense to the coding strand of an OP mRNA or an OP gene.

In one embodiment, the methods of the present invention are used to treat a subject having a disorder characterized by aberrant or unwanted OP protein or nucleic acid expression or activity (e. g., a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder) by administering an agent which is an OP modulator to the subject. In one embodiment, the OP modulator is an OP protein. In another embodiment the OP modulator is an OP nucleic acid molecule. In yet another embodiment, the OP modulator is a peptide, peptidomimetic, or other small molecule. In a preferred embodiment, the disorder characterized by aberrant or unwanted OP protein or nucleic acid expression is a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder.

The present invention also provides diagnostic assays for identifying the presence or absence of a genetic alteration characterized by at least one of (i) aberrant modification or mutation of a gene encoding an OP protein ; (ii) mis-regulation of the OP gene ; and (iii) aberrant post-translational modification of an OP protein, wherein a wild-type form of the gene encodes a protein with an OP activity.

In another aspect the invention provides methods for identifying a compound that binds to or modulates the activity of an OP protein, by providing an indicator composition comprising an OP protein having OP activity, contacting the indicator composition with a

test compound, and determining the effect of the test compound on OP activity in the indicator composition to identify a compound that modulates the activity of an OP protein.

In another embodiment, the invention provides methods for treating a subject having a cellular proliferation disorder.

Other features and advantages of the invention will be apparent from the following detailed description and claims.

Brief Description of the Drawings Figures 1A and 1B depict the cDNA sequence and predicted amino acid sequence of the human OP. The nucleotide sequence corresponds to nucleic acids 1 to 2343 of SEQ ID NO : 1. The amino acid sequence corresponds to amino acids 1 to 594 of SEQ ID NO : 2. The nucleotide coding region of the human OP corresponds to SEQ ID NO : 3.

Figure 2 depicts a structural, hydrophobicity, and antigenicity analysis of the human OP protein.

Figure 3 depicts the results of a search which was performed against the HMM database using the amino acid sequence of human OP. This search resulted in the identification of a GMC oxidoreductase signature domain in the human OP protein.

Figure 4A and 4B depict the results of a search performed against the ProDom database using the amino acid sequence of human OP.

Detailed Description of the Invention The present invention is based, at least in part, on the discovery of novel molecules, referred to herein"Oxidoreductase Protein"or"OP"nucleic acid and protein molecules, which are novel members of a family of enzymes possessing oxidoreductase activity. These novel molecules are capable of oxidizing and/or reducing molecular groups by catalyzing the transfer of a hydride moiety and, thus, play a role in or function in a variety of cellular processes, e. g., proliferation, metabolism, differentiation, hormonal responses, and inter-or intra-cellular communication.

As used herein, the term"oxidoreductase"includes a molecule which is involved in the oxidation or reduction of a biochemical molecule (e. g., a metabolic precursor which contains a molecular group which can be oxidized or reduced) by catalyzing the transfer of a hydride ion to or from the biochemical molecule. Oxidoreductase molecules are involved in the metabolism and catabolism of biochemical molecules necessary for energy production or storage, for intra-or inter-cellular signaling, and for metabolism or catabolism of metabolically important biomolecules. Examples of oxidoreductases include glucose

oxidases, methanol oxidases, choline dehydrogenases, glucose dehydrogenases, cholesterol oxidases, alcohol dehydrogenases, and cellobiose dehydrogenases.

The OP proteins of the present invention show homology to the choline dehydrogenase family of oxidoreductases. Choline dehydrogenase (CDH) is the first enzyme of the glycine betaine synthetic pathway. Betaine, an atypical amino acid that is non-proteinogenic yet important as an osmoprotectant, is synthesized by a two-step oxidation of choline. This reaction takes place in the mitochondrial matrix by the membrane bound CDH and betaine aldehyde dehydrogenase (Landfald and Strom (1986) J Bacteriol.

165 : 849-55 ; Styrvold et al. (1986) J. Bacteriol. 165 : 856-63 ; Grossman and Hebert (1989) Am. J Physiol. 256 (1 Pt. 2) : F107-12 ; Zhang et al. (1992) Biochim. Biophys. Acta.

1117 : 333-9). CDH is also coupled to the respiratory chain. Betaine is further important in mammalian organisms as a major methyl group donor and nitrogen source.

Methyl groups derived from betaine may be used for recycling homocysteine to methionine. It is known that some tumor cells have an increased need for methionine for survival. Methionine dependent tumor cells are unable to proliferate, and they arrest in the G2 phase of the cell cycle. For example, MCF-7 breast cancer cells grown in methyl- deficient media show inhibition of cell proliferation and induction of apoptosis. Fresh patient colon tumors have also been shown to be methionine dependent based on cell cycle analyses. Metastatic colon tumors have a higher methionine dependence than primary tumors. Other examples of methionine dependence in tumors have been seen in small cell lung cancer and gliomas.

Human OP is overexpressed in various tumors, e. g., colon tumors, as compared to normal tissues (see Examples section, infra). Human OP is further elevated in later stage tumors. Elevation of the levels of the OP molecules of the present invention in tumor cells may increase tumor survival by increasing the supply of methionine available to the tumor cells. Accordingly, inhibition of the OP molecules of the present invention may cause tumor cell growth arrest and/or apoptosis, making the OP molecules of the present invention useful for the treatment of cellular proliferation, growth, apoptosis, differentiation, and/or migration disorders.

As used herein,"cellular proliferation, growth, apoptosis, differentiation, and/or migration disorders"include those disorders that affect cellular proliferation, growth, apoptosis, differentiation, and/or migration processes. As used herein, a"cellular proliferation, growth, apoptosis, differentiation, and/or migration process"is a process by which a cell increases in number, size or content, by which a cell undergoes programmed cell death, by which a cell develops a specialized set of characteristics which differ from that of other cells, or by which a cell moves closer to or further from a particular location or stimulus. Examples of cellular proliferation, growth, apoptosis, differentiation, and/or

migration disorders include cancer, e. g., colon cancer, lung cancer, brain cancer, as well as other types of carcinomas, sarcomas, lymphomas, and/or leukemias ; tumor angiogenesis and metastasis ; skeletal dysplasia ; hepatic disorders ; and hematopoietic and/or myeloproliferative disorders. Other examples of disorders characterized by aberrant regulation of apoptosis include stroke-associated cell death and neurodegenerative disorders such as Alzheimer's disease, dementias related to Alzheimer's disease (such as Pick's disease), Parkinson's and other Lewy diffuse body diseases, senile dementia, and Huntington's disease.

The OP molecules of the present invention may also be useful for the treatment of disorders characterized by the aberrant or abnormal regulation of the levels of choline, betaine (e. g., a disorder associated with aberrant regulation of osmolarity by betaine), homocysteine (e. g., homocystinuria), and/or methionine in a subject.

The OP molecules of the present invention may still further be useful for the treatment of disorders affecting tissues in which OP protein is expressed, e. g., primary osteoblasts, pituitary, CaCO cells, keratinocytes, aortic endothelial cells, fetal kidney, fetal lung, mammary epithelium, fetal spleen, fetal liver, umbilical smooth muscle, RAII Burkitt Lymphoma cells, lung, prostate, K53 red blood cells, fetal dorsal spinal cord, insulinoma cells, normal breast and ovarian epithelia, retina, HMC-1 mast cells, ovarian ascites, d8 dendritic cells, megakaryocytes, human mobilized bone morrow, mammary carcinoma, melanoma cells, lymph, vein, U937/A70p B cells, A549con cells, WT LN Cap testosterone cells, esophagus, and other tissues and/or cell types described further in Example 4.

In an alternate embodiment, any and all of the above described disorders may simply be referred to as"OP associated or related disorders".

The term"family"when referring to the protein and nucleic acid molecules of the invention is intended to mean two or more proteins or nucleic acid molecules having a common structural domain or motif and having sufficient amino acid or nucleotide sequence homology as defined herein. Such family members can be naturally or non-naturally occurring and can be from either the same or different species. For example, a family can contain a first protein of human origin, as well as other, distinct proteins of human origin or alternatively, can contain homologues of non-human origin. Members of a family may also have common functional characteristics.

For example, the family of OP proteins comprise at least one, and preferably three or more"transmembrane domains."As used herein, the term"transmembrane domain" includes an amino acid sequence of about 15 amino acid residues in length which spans the plasma membrane. More preferably, a transmembrane domain includes about at least 10, 15, 20, 25, 30, 35, 40, 45 or more amino acid residues and spans the plasma membrane.

Transmembrane domains are rich in hydrophobic residues, and typically have a helical

structure. In one embodiment, at least 50%, 60%, 70%, 80%, 90%, 95% or more of the amino acid residues of a transmembrane domain are hydrophobic, e. g., leucines, isoleucines, tyrosines, or tryptophans. Transmembrane domains are described in, for example, Zagotta W. N. et al. (1996) Annv. Rev. Neurosci. 19 : 235-63, the contents of which are incorporated herein by reference. Amino acid residues 41-57, 292-311, and 545-564 of the human OP polypeptide (SEQ ID NO : 2) comprise transmembrane domains (Figure 2).

In another embodiment, an OP molecule of the present invention is identified based on the presence of an GMC oxidoreductase signature domain in the protein or corresponding nucleic acid molecule. As used herein, the term GMC oxidoreductase signature domain includes a protein domain having an amino acid sequence of about 375-650, more preferably about 450-600 amino acid residues, or most preferably about 500-550 amino acids and has a bit score for the alignment of the sequence to the GMC oxidoreductase signature domain (HMM) of at least about 100, 200, 300, 400, 500, 600, 700, 800, or more.

Preferably, a GMC oxidoreductase signature domain includes at least about 526 amino acid residues and has a bit score for the alignment of the sequence to the GMC oxidoreductase signature domain (HMM) of about 767. 7. The GMC oxidoreductase signature domain has been assigned the PFAM labels"GMCoxredl"and"GMCoxred2"under accession number PS00623 and PS00624, respectively (see the Pfam website, available online through Washington University in Saint Louis). GMC oxidoreductase signature domains are involved in oxidoreductase activity and are described in, for example, Cavener (1992) J.

Mol. Biol. 223 : 811-814, the contents of which are incorporated herein by reference.

To identify the presence of a GMC oxidoreductase signature domain in an OP protein and make the determination that a protein of interest has a particular profile, the amino acid sequence of the protein is searched against a database of HMMs (e. g., the Pfam database, release 2. 1) using the default parameters (see the Pfam website, available online through Washington University in Saint Louis). A search was performed against the HMM database resulting in the identification of a GMC oxidoreductase signature domain in the amino acid sequence of SEQ ID NO : 2 (at about residues 41-567). The results of this search are set forth in Figure 3.

A description of the Pfam database can be found in Sonhammer et al. (1997) Proteins 28 : 405-420, and a detailed description of HMMs can be found, for example, in Gribskov et al. (1990) Meth. Enzymol. 183 : 146-159 ; Gribskov et al. (1987) Proc. Natl. Acad.

Sci. USA 84 : 4355-4358 ; Krogh et al. (1994) J MoL BioL 235 : 1501-1531 ; and Stultz et al. (1993) Protein Sci. 2 : 305-314, the contents of which are incorporated herein by reference.

Isolated OP proteins of the present invention, have an amino acid sequence sufficiently identical to the amino acid sequence of SEQ ID NO : 2, or are encoded by a nucleotide sequence sufficiently identical to SEQ ID NO : 1 or 3. As used herein, the term

"sufficiently identical"refers to a first amino acid or nucleotide sequence which contains a sufficient or minimum number of identical or equivalent (e. g., an amino acid residue which has a similar side chain) amino acid residues or nucleotides to a second amino acid or nucleotide sequence such that the first and second amino acid or nucleotide sequences share common structural domains or motifs and/or a common functional activity. For example, amino acid or nucleotide sequences which share common structural domains have at least 30%, 40%, or 50% homology, preferably 60% homology, more preferably 70%-80%, and even more preferably 90-95% homology across the amino acid sequences of the domains and contain at least one and preferably two structural domains or motifs, are defined herein as sufficiently identical. Furthermore, amino acid or nucleotide sequences which share at least 30%, 40%, or 50%, preferably 60%, more preferably 70-80%, or 90-95% homology and share a common functional activity are defined herein as sufficiently identical.

As used interchangeably herein, a"OP activity","biological activity of OP,"or "functional activity of OP,"includes an activity exerted by an OP protein, polypeptide or nucleic acid molecule on an OP-responsive cell or tissue, or on an OP protein substrate, as determined in vivo, or in vitro, according to standard techniques. In one embodiment, an OP activity is a direct activity, such as an association with an OP-target molecule. As used herein, a"target molecule"or"binding partner"is a molecule with which an OP protein binds or interacts in nature, such that OP-mediated function is achieved. An OP target molecule can be a non-OP molecule or an OP accessory polypeptide or molecule of the present invention (e. g., NAD+, FAD+, or other cofactor). As used herein, an"accessory" peptide or molecule refers to a peptide or molecule whose presence is may be needed for the proper activity of a protein (e. g., a cofactor or a metal ion that is needed by an enzyme). In an exemplary embodiment, an OP target molecule is an OP ligand (e. g., choline and/or an acceptor molecule to be reduced or oxidized choline and/or an acceptor molecule to be reduced or oxidized). Alternatively, an OP activity is an indirect activity, such as a cellular signaling activity mediated by interaction of the OP protein with an OP ligand. The biological activities of OP are described herein. For example, the OP proteins of the present invention can have one or more of the following activities : 1) modulation of metabolism and catabolism of biochemical molecules, e. g., molecules necessary for energy production or storage ; 2) modulation of betaine synthesis from choline ; 3) modulation of methionine synthesis from homocysteine ; 4) modulation of intra-or inter-cellular signaling ; 5) modulation of cellular proliferation and/or migration ; and/or 6) modulation of hormonal responses.

Accordingly, another embodiment of the invention features isolated OP proteins and polypeptides having an OP activity. Other preferred proteins are OP proteins having one or more of the following domains : a transmembrane domain, a GMC oxidoreductase signature

domain, and, preferably, an OP activity. Additional preferred OP proteins have at least one GMC oxidoreductase signature domain, and/or at least one transmembrane domain and are, preferably, encoded by a nucleic acid molecule having a nucleotide sequence which hybridizes under stringent hybridization conditions to a nucleic acid molecule comprising a complement of the nucleotide sequence of SEQ ID NO : 1 or 3.

The nucleotide sequence of the isolated human OP cDNA and the predicted amino acid sequence of the human OP polypeptide are shown in Figure 1 and in SEQ ID NO : 1 and SEQ ID NO : 2, respectively. A plasmid containing the nucleotide sequence encoding human OP was deposited with the American Type Culture Collection (ATCC), 10801 University Boulevard, Manassas, VA 20110-2209, on and assigned Accession Number These deposits will be maintained under the terms of the Budapest Treaty on the International Recognition of the Deposit of Microorganisms for the Purposes of Patent Procedure. These deposits was made merely as a convenience for those of skill in the art and are not an admission that a deposit is required under 35 U. S. C. § 112.

The human OP gene, which is approximately 2343 nucleotides in length, encodes a protein having a molecular weight of approximately 65. 3 kD and which is approximately 594 amino acid residues in length.

Various aspects of the invention are described in further detail in the following subsections : I. Isolated Nucleic Acid Molecules One aspect of the invention pertains to isolated nucleic acid molecules that encode OP proteins or biologically active portions thereof, as well as nucleic acid fragments sufficient for use as hybridization probes to identify OP-encoding nucleic acid molecules (e. g., OP mRNA) and fragments for use as PCR primers for the amplification or mutation of OP nucleic acid molecules. As used herein, the term"nucleic acid molecule"is intended to include DNA molecules (e. g., cDNA or genomic DNA) and RNA molecules (e. g., mRNA) and analogs of the DNA or RNA generated using nucleotide analogs. The nucleic acid molecule can be single-stranded or double-stranded, but preferably is double-stranded DNA.

The term"isolated nucleic acid molecule"includes nucleic acid molecules which are separated from other nucleic acid molecules which are present in the natural source of the nucleic acid. For example, with regards to genomic DNA, the term"isolated"includes nucleic acid molecules which are separated from the chromosome with which the genomic DNA is naturally associated. Preferably, an"isolated"nucleic acid is free of sequences which naturally flank the nucleic acid (i. e., sequences located at the 5'and 3'ends of the nucleic acid) in the genomic DNA of the organism from which the nucleic acid is derived.

For example, in various embodiments, the isolated OP nucleic acid molecule can contain less than about 5 kb, 4kb, 3kb, 2kb, 1 kb, 0. 5 kb or 0. 1 kb of nucleotide sequences which naturally flank the nucleic acid molecule in genomic DNA of the cell from which the nucleic acid is derived. Moreover, an"isolated"nucleic acid molecule, such as a cDNA molecule, can be substantially free of other cellular material, or culture medium when produced by recombinant techniques, or substantially free of chemical precursors or other chemicals when chemically synthesized.

A nucleic acid molecule of the present invention, e. g., a nucleic acid molecule having the nucleotide sequence of SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number, or a portion thereof, can be isolated using standard molecular biology techniques and the sequence information provided herein. Using all or portion of the nucleic acid sequence of SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number, as a hybridization probe, OP nucleic acid molecules can be isolated using standard hybridization and cloning techniques (e. g., as described in Sambrook, J. et al., Molecular Cloning : A Laboratory Manual. 2"d ed., Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, 1989).

Moreover, a nucleic acid molecule encompassing all or a portion of SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number can be isolated by the polymerase chain reaction (PCR) using synthetic oligonucleotide primers designed based upon the sequence of SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number A nucleic acid of the invention can be amplified using cDNA, mRNA or alternatively, genomic DNA, as a template and appropriate oligonucleotide primers according to standard PCR amplification techniques. The nucleic acid so amplified can be cloned into an appropriate vector and characterized by DNA sequence analysis.

Furthermore, oligonucleotides corresponding to OP nucleotide sequences can be prepared by standard synthetic techniques, e. g., using an automated DNA synthesizer.

In a preferred embodiment, an isolated nucleic acid molecule of the invention comprises the nucleotide sequence shown in SEQ ID NO : 1. The sequence of SEQ ID NO : 1 corresponds to the human OP cDNA. This cDNA comprises sequences encoding the human OP protein (i. e.,"the coding region", from nucleotides 253-2034), as well as 5'untranslated sequences (nucleotides 1-252) and 3'untranslated sequences (nucleotides 2035-2343).

Alternatively, the nucleic acid molecule can comprise only the coding region of SEQ ID NO : 1 (e. g., nucleotides 253-2034, corresponding to SEQ ID NO : 3). In another embodiment, the nucleic acid molecule can comprise the coding region of SEQ ID NO : 1

(e. g., nucleotides 253-2034, corresponding to SEQ ID NO : 3), as well as a stop codon (e. g., nucleotides 2034-2037 of SEQ ID NO : 1).

In another preferred embodiment, an isolated nucleic acid molecule of the invention comprises a nucleic acid molecule which is a complement of the nucleotide sequence shown in SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number, or a portion of any of these nucleotide sequences. A nucleic acid molecule which is complementary to the nucleotide sequence shown in SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number, is one which is sufficiently complementary to the nucleotide sequence shown in SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number , such that it can hybridize to the nucleotide sequence shown in SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number, thereby forming a stable duplex.

In still another preferred embodiment, an isolated nucleic acid molecule of the present invention comprises a nucleotide sequence which is at least about 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, 99. 5% or more identical to the entire length of the nucleotide sequence shown in SEQ ID NO : 1 or 3, or the entire length of the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number, or a portion of any of these nucleotide sequences.

Moreover, the nucleic acid molecule of the invention can comprise only a portion of the nucleic acid sequence of SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number, for example, a fragment which can be used as a probe or primer or a fragment encoding a portion of an OP protein, e. g., a biologically active portion of an OP protein. The nucleotide sequence determined from the cloning of the OP gene allows for the generation of probes and primers designed for use in identifying and/or cloning other OP family members, as well as OP homologues from other species. The probe/primer typically comprises substantially purified oligonucleotide. The oligonucleotide typically comprises a region of nucleotide sequence that hybridizes under stringent conditions to at least about 12 or 15, preferably about 20 or 25, more preferably about 30, 35, 40, 45, 50, 55, 60, 65, or 75 consecutive nucleotides of a sense sequence of SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number, of an anti-sense sequence of SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number, or of a naturally occurring allelic variant or mutant of SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid

deposited with ATCC as Accession Number. In one embodiment, a nucleic acid molecule of the present invention comprises a nucleotide sequence which is greater than 50, 100, 200, 300, 400, 500, 600, 700, 800, 900, 1000, 1100, 1200, 1300, 1400, 1500, 1600, 1700, 1800 or more nucleotides in length and hybridizes under stringent hybridization conditions to a nucleic acid molecule of SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number Probes based on the OP nucleotide sequences can be used to detect transcripts or genomic sequences encoding the same or homologous proteins. In preferred embodiments, the probe further comprises a label group attached thereto, e. g., the label group can be a radioisotope, a fluorescent compound, an enzyme, or an enzyme co-factor. Such probes can be used as a part of a diagnostic test kit for identifying cells or tissue which misexpress an OP protein, such as by measuring a level of an OP-encoding nucleic acid in a sample of cells from a subject, e. g., detecting OP mRNA levels or determining whether a genomic OP gene has been mutated or deleted.

A nucleic acid fragment encoding a"biologically active portion of an OP protein" can be prepared by isolating a portion of the nucleotide sequence of SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number, which encodes a polypeptide having an OP biological activity (the biological activities of the OP proteins are described herein), expressing the encoded portion of the OP protein (e. g., by recombinant expression in vitro) and assessing the activity of the encoded portion of the OP protein.

The invention further encompasses nucleic acid molecules that differ from the nucleotide sequence shown in SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number, due to degeneracy of the genetic code and, thus, encode the same OP proteins as those encoded by the nucleotide sequence shown in SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number. In another embodiment, an isolated nucleic acid molecule of the invention has a nucleotide sequence encoding a protein having an amino acid sequence shown in SEQ ID NO : 2.

In addition to the OP nucleotide sequences shown in SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number, it will be appreciated by those skilled in the art that DNA sequence polymorphisms that lead to changes in the amino acid sequences of the OP proteins may exist within a population (e. g., the human population). Such genetic polymorphism in the OP genes may exist among individuals within a population due to natural allelic variation.

As used herein, the terms"gene"and"recombinant gene"refer to nucleic acid molecules

which include an open reading frame encoding an OP protein, preferably a mammalian OP protein, and can further include non-coding regulatory sequences, and introns.

Allelic variants of human OP include both functional and non-functional OP proteins. Functional allelic variants are naturally occurring amino acid sequence variants of the human OP protein that maintain the ability to bind an OP ligand or substrate (e. g., choline and/or an acceptor molecule to be reduced or oxidized choline and/or an acceptor molecule to be reduced or oxidized) and/or modulate oxidoreductase activity and/or oxidoreductase-associated signaling mechanisms, and/or cellular proliferation, growth, apoptosis, differentiation, and/or migration disorders. Functional allelic variants will typically contain only conservative substitution of one or more amino acids of SEQ ID NO : 2, or substitution, deletion or insertion of non-critical residues in non-critical regions of the protein.

Non-functional allelic variants are naturally-occurring amino acid sequence variants of the human OP proteins that do not have the ability to either bind an OP ligand or substrate (e. g., choline and/or an acceptor molecule to be reduced or oxidized) and/or modulate oxidoreductase activity and/or oxidoreductase-associated signaling mechanisms, and/or cellular proliferation, growth, apoptosis, differentiation, and/or migration disorders.

Non-functional allelic variants will typically contain a non-conservative substitution, a deletion, or insertion or premature truncation of the amino acid sequence of SEQ ID NO : 2, or a substitution, insertion or deletion in critical residues or critical regions.

The present invention further provides non-human orthologues of the human OP protein. Orthologues of the human OP protein are proteins that are isolated from non- human organisms and possess the same ability to bind an OP ligand or substrate (e. g., choline and/or an acceptor molecule to be reduced or oxidized) and/or modulate oxidoreductase activity and/or oxidoreductase-associated signaling mechanisms, and/or cellular proliferation, growth, apoptosis, differentiation, and/or migration disorders.

Orthologues of the human OP protein can readily be identified as comprising an amino acid sequence that is substantially identical to SEQ ID NO : 2.

Moreover, nucleic acid molecules encoding other OP family members and, thus, which have a nucleotide sequence which differs from the OP sequences of SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number are intended to be within the scope of the invention. For example, another OP cDNA can be identified based on the nucleotide sequence of human OP. Moreover, nucleic acid molecules encoding OP proteins from different species, and which, thus, have a nucleotide sequence which differs from the OP sequences of SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number are intended to be within the scope of the invention.

For example, a mouse OP cDNA can be identified based on the nucleotide sequence of a human OP.

Nucleic acid molecules corresponding to natural allelic variants and homologues of the OP cDNAs of the invention can be isolated based on their homology to the OP nucleic acids disclosed herein using the cDNAs disclosed herein, or a portion thereof, as a hybridization probe according to standard hybridization techniques under stringent hybridization conditions. Nucleic acid molecules corresponding to natural allelic variants and homologues of the OP cDNAs of the invention can further be isolated by mapping to the same chromosome or locus as the OP gene.

Accordingly, in another embodiment, an isolated nucleic acid molecule of the invention is at least 15, 20, 25, 30 or more nucleotides in length and hybridizes under stringent conditions to the nucleic acid molecule comprising the nucleotide sequence of SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number. In other embodiment, the nucleic acid is at least 50, 100, 200, 300, 400, 500, 600, 700, 800, 900, 1000, 1100, 1200, 1300, 1400, 1500, 1600, 1700, 1800, 1900, 2000, 2100, 2200, 2300, or more nucleotides in length.

As used herein, the term"hybridizes under stringent conditions"is intended to describe conditions for hybridization and washing under which nucleotide sequences that are significantly identical or homologous to each other remain hybridized to each other.

Preferably, the conditions are such that sequences at least about 70%, more preferably at least about 80%, even more preferably at least about 85% or 90% identical to each other remain hybridized to each other. Such stringent conditions are known to those skilled in the art and can be found in Current Protocols in Molecular Biology, Ausubel et al., eds., John Wiley & Sons, Inc. (1995), sections 2, 4, and 6. Additional stringent conditions can be found in Molecular Cloning : A Laboratory Manual, Sambrook et al., Cold Spring Harbor Press, Cold Spring Harbor, NY (1989), chapters 7, 9, and 11. A preferred, non-limiting example of stringent hybridization conditions includes hybridization in 4X sodium chloride/sodium citrate (SSC), at about 65-70°C (or alternatively hybridization in 4X SSC plus 50% formamide at about 42-50°C) followed by one or more washes in 1X SSC, at about 65-70°C. A preferred, non-limiting example of highly stringent hybridization conditions includes hybridization in 1X SSC, at about 65-70°C (or alternatively hybridization in 1X SSC plus 50% formamide at about 42-50°C) followed by one or more washes in 0. 3X SSC, at about 65-70°C. A preferred, non-limiting example of reduced stringency hybridization conditions includes hybridization in 4X SSC, at about 50-60°C (or alternatively hybridization in 6X SSC plus 50% formamide at about 40-45°C) followed by one or more washes in 2X SSC, at about 50-60°C. Ranges intermediate to the above-recited values, e. g., at 65-70°C or at 42-50°C are also intended to be encompassed by the present

invention. SSPE (lxSSPE is O. 15M NaCI, lOmM NaH2P04, and 1. 25mM EDTA, pH 7. 4) can be substituted for SSC (1X SSC is 0. 15M NaCI and 15mM sodium citrate) in the hybridization and wash buffers ; washes are performed for 15 minutes each after hybridization is complete. The hybridization temperature for hybrids anticipated to be less than 50 base pairs in length should be 5-10°C less than the melting temperature (Tm) of the hybrid, where Tm is determined according to the following equations. For hybrids less than 18 base pairs in length, Tm (°C) = 2 (&num of A + T bases) + 4 (&num of G + C bases). For hybrids between 18 and 49 base pairs in length, Tm (°C) = 81. 5 + 16. 6 (logio [Na+]) + 0. 41 (% G+C)- (600/N), where N is the number of bases in the hybrid, and [Na+] is the concentration of sodium ions in the hybridization buffer ([Na+] for 1X SSC = 0. 165 M). It will also be recognized by the skilled practitioner that additional reagents may be added to hybridization and/or wash buffers to decrease non-specific hybridization of nucleic acid molecules to membranes, for example, nitrocellulose or nylon membranes, including but not limited to blocking agents (e. g., BSA or salmon or herring sperm carrier DNA), detergents (e. g., SDS), chelating agents (e. g., EDTA), Ficoll, PVP and the like. When using nylon membranes, in particular, an additional preferred, non-limiting example of stringent hybridization conditions is hybridization in 0. 25-0. 5M NaH2P04, 7% SDS at about 65°C, followed by one or more washes at 0. 02M NaH2PO4, 1% SDS at 65°C (see e. g., Church and Gilbert (1984) Proc. Natl. Acad. Sci. USA 81 : 1991-1995), or alternatively 0. 2X SSC, 1% SDS.

Preferably, an isolated nucleic acid molecule of the invention that hybridizes under stringent conditions to the sequence of SEQ ID NO : 1 or 3 corresponds to a naturally- occurring nucleic acid molecule. As used herein, a"naturally-occurring"nucleic acid molecule refers to an RNA or DNA molecule having a nucleotide sequence that occurs in nature (e. g., encodes a natural protein).

In addition to naturally-occurring allelic variants of the OP sequences that may exist in the population, the skilled artisan will further appreciate that changes can be introduced by mutation into the nucleotide sequences of SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number thereby leading to changes in the amino acid sequence of the encoded OP proteins, without altering the functional ability of the OP proteins. For example, nucleotide substitutions leading to amino acid substitutions at"non-essential"amino acid residues can be made in the sequence of SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number. A"non-essential"amino acid residue is a residue that can be altered from the wild-type sequence of OP (e. g., the sequence of SEQ ID NO : 2) without altering the biological activity, whereas an"essential"amino acid residue is required for biological activity. For example, amino acid residues that are conserved among the OP proteins of the present invention, e. g., those present in the GMC

oxidoreductase signature domains (s) or the transmembrane domain (s), are predicted to be particularly unamenable to alteration. Furthermore, additional amino acid residues that are conserved between the OP proteins of the present invention and other members of the oxidoreductase family are not likely to be amenable to alteration.

Accordingly, another aspect of the invention pertains to nucleic acid molecules encoding OP proteins that contain changes in amino acid residues that are not essential for activity. Such OP proteins differ in amino acid sequence from SEQ ID NO : 2, yet retain biological activity. In one embodiment, the isolated nucleic acid molecule comprises a nucleotide sequence encoding a protein, wherein the protein comprises an amino acid sequence at least 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, 99. 5% or more identical to SEQ ID NO : 2.

An isolated nucleic acid molecule encoding an OP protein identical to the protein of SEQ ID NO : 2, can be created by introducing one or more nucleotide substitutions, additions or deletions into the nucleotide sequence of SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number, such that one or more amino acid substitutions, additions or deletions are introduced into the encoded protein. Mutations can be introduced into SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number by standard techniques, such as site-directed mutagenesis and PCR-mediated mutagenesis. Preferably, conservative amino acid substitutions are made at one or more predicted non-essential amino acid residues. A"conservative amino acid substitution"is one in which the amino acid residue is replaced with an amino acid residue having a similar side chain. Families of amino acid residues having similar side chains have been defined in the art. These families include amino acids with basic side chains (e. g., lysine, arginine, histidine), acidic side chains (e. g., aspartic acid, glutamic acid), uncharged polar side chains (e. g., glycine, asparagine, glutamin, serine, threonine, tyrosine, cysteine), nonpolar side chains (e. g., alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine, tryptophan), beta-branched side chains (e. g., threonin, valine, isoleucine) and aromatic side chains (e. g., tyrosine, phenylalanine, tryptophan, histidine). Thus, a predicted nonessential amino acid residue in an OP protein is preferably replaced with another amino acid residue from the same side chain family. Alternatively, in another embodiment, mutations can be introduced randomly along all or part of an OP coding sequence, such as by saturation mutagenesis, and the resultant mutants can be screened for OP biological activity to identify mutants that retain activity. Following mutagenesis of SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number

, the encoded protein can be expressed recombinantly and the activity of the protein can be determined.

In another preferred embodiment, a mutant OP protein can be assayed for the ability to modulate metabolism and catabolism of biochemical molecules, e. g., molecules necessary for energy production or storage ; modulate betaine synthesis from choline ; modulate methionine synthesis from homocysteine ; modulate intra-or inter-cellular signaling ; modulate cellular proliferation and/or migration, and/or modulate hormonal responses.

In addition to the nucleic acid molecules encoding OP proteins described above, another aspect of the invention pertains to isolated nucleic acid molecules which are antisense thereto. An"antisense"nucleic acid comprises a nucleotide sequence which is complementary to a"sense"nucleic acid encoding a protein, e. g., complementary to the coding strand of a double-stranded cDNA molecule or complementary to an mRNA sequence. Accordingly, an antisense nucleic acid can hydrogen bond to a sense nucleic acid. The antisense nucleic acid can be complementary to an entire OP coding strand, or to only a portion thereof. In one embodiment, an antisense nucleic acid molecule is antisense to a"coding region"of the coding strand of a nucleotide sequence encoding OP. The term "coding region"refers to the region of the nucleotide sequence comprising codons which are translated into amino acid residues (e. g., the coding region of human OP corresponds to SEQ ID NO : 3). In another embodiment, the antisense nucleic acid molecule is antisense to a"noncoding region"of the coding strand of a nucleotide sequence encoding OP. The term "noncoding region"refers to 5'and 3'sequences which flank the coding region that are not translated into amino acids (i. e., also referred to as 5'and 3'untranslated regions).

Given the coding strand sequences encoding OP disclosed herein (e. g., SEQ ID NO : 3), antisense nucleic acids of the invention can be designed according to the rules of Watson and Crick base pairing. The antisense nucleic acid molecule can be complementary to the entire coding region of OP mRNA, but more preferably is an oligonucleotide which is antisense to only a portion of the coding or noncoding region of OP mRNA. For example, the antisense oligonucleotide can be complementary to the region surrounding the translation start site of OP mRNA. An antisense oligonucleotide can be, for example, about 5, 10, 15, 20, 25, 30, 35, 40, 45 or 50 nucleotides in length. An antisense nucleic acid of the invention can be constructed using chemical synthesis and enzymatic ligation reactions using procedures known in the art. For example, an antisense nucleic acid (e. g., an antisense oligonucleotide) can be chemically synthesized using naturally occurring nucleotides or variously modified nucleotides designed to increase the biological stability of the molecules or to increase the physical stability of the duplex formed between the antisense and sense nucleic acids, e. g., phosphorothioate derivatives and acridine substituted nucleotides can be used. Examples of modified nucleotides which can be used to generate

the antisense nucleic acid include 5-fluorouracil, 5-bromouracil, 5-chlorouracil, 5- iodouracil, hypoxanthine, xantine, 4-acetylcytosine, 5- (carboxyhydroxylmethyl) uracil, 5- carboxymethylaminomethyl-2-thiouridine, 5-carboxymethylaminomethyluracil, dihydrouracil, beta-D-galactosylqueosine, inosine, N6-isopentenyladenine, 1- methylguanine, 1-methylinosine, 2, 2-dimethylguanine, 2-methyladenine, 2-methylguanine, 3-methylcytosine, 5-methylcytosine, N6-adenine, 7-methylguanine, 5- methylaminomethyluracil, 5-methoxyaminomethyl-2-thiouracil, beta-D-mannosylqueosine, 5'-methoxycarboxymethyluracil, 5-methoxyuracil, 2-methylthio-N6-isopentenyladenine, uracil-5-oxyacetic acid (v), wybutoxosine, pseudouracil, queosine, 2-thiocytosine, 5-methyl- 2-thiouracil, 2-thiouracil, 4-thiouracil, 5-methyluracil, uracil-5-oxyacetic acid methylester, uracil-5-oxyacetic acid (v), 5-methyl-2-thiouracil, 3- (3-amino-3-N-2-carboxypropyl) uracil, (acp3) w, and 2, 6-diaminopurine. Alternatively, the antisense nucleic acid can be produced biologically using an expression vector into which a nucleic acid has been subcloned in an antisense orientation (i. e., RNA transcribed from the inserted nucleic acid will be of an antisense orientation to a target nucleic acid of interest, described further in the following subsection).

The antisense nucleic acid molecules of the invention are typically administered to a subject or generated in situ such that they hybridize with or bind to cellular mRNA and/or genomic DNA encoding an OP protein to thereby inhibit expression of the protein, e. g., by inhibiting transcription and/or translation. The hybridization can be by conventional nucleotide complementarity to form a stable duplex, or, for example, in the case of an antisense nucleic acid molecule which binds to DNA duplexes, through specific interactions in the major groove of the double helix. An example of a route of administration of antisense nucleic acid molecules of the invention include direct injection at a tissue site.

Alternatively, antisense nucleic acid molecules can be modified to target selected cells and then administered systemically. For example, for systemic administration, antisense molecules can be modified such that they specifically bind to receptors or antigens expressed on a selected cell surface, e. g., by linking the antisense nucleic acid molecules to peptides or antibodies which bind to cell surface receptors or antigens. The antisense nucleic acid molecules can also be delivered to cells using the vectors described herein. To achieve sufficient concentrations of the antisense molecules, vector constructs in which the antisense nucleic acid molecule is placed under the control of a strong pol II or pol III promoter are preferred.

In yet another embodiment, the antisense nucleic acid molecule of the invention is an a-anomeric nucleic acid molecule. An a-anomeric nucleic acid molecule forms specific double-stranded hybrids with complementary RNA in which, contrary to the usual p-units, the strands run parallel to each other (Gaultier et al. (1987) Nucleic Acids Res. 15 : 6625-

6641). The antisense nucleic acid molecule can also comprise a 2'-o-methylribonucleotide (Inoue et al. (1987) Nucleic Acids Res. 15 : 6131-6148) or a chimeric RNA-DNA analogue (Inoueetal. (1987) FEBSLett. 215 : 327-330).

In still another embodiment, an antisense nucleic acid of the invention is a ribozyme.

Ribozymes are catalytic RNA molecules with ribonuclease activity which are capable of cleaving a single-stranded nucleic acid, such as an mRNA, to which they have a complementary region. Thus, ribozymes (e. g., hammerhead ribozymes (described in Haseloff and Gerlach (1988) Nature 334 : 585-591)) can be used to catalytically cleave OP mRNA transcripts to thereby inhibit translation of OP mRNA. A ribozyme having specificity for an OP-encoding nucleic acid can be designed based upon the nucleotide sequence of an OP cDNA disclosed herein (i. e., SEQ ID NO : 1 or 3, or the nucleotide sequence of the DNA insert of the plasmid deposited with ATCC as Accession Number ). For example, a derivative of a Tetrahymena L-19 IVS RNA can be constructed in which the nucleotide sequence of the active site is complementary to the nucleotide sequence to be cleaved in an OP-encoding mRNA. See, e. g., Cech et al. U. S. Patent No.

4, 987, 071 ; and Cech et al. U. S. Patent No. 5, 116, 742. Alternatively, OP mRNA can be used to select a catalytic RNA having a specific ribonuclease activity from a pool of RNA molecules. See, e. g., Bartel, D. and Szostak, J. W. (1993) Science 261 : 1411-1418.

Alternatively, OP gene expression can be inhibited by targeting nucleotide sequences complementary to the regulatory and/or 5'untranslated region of the OP nucleotides (e. g., the OP promoter and/or enhancers ; e. g., nucleotides 1-252 of SEQ ID NO : 1) to form triple helical structures that prevent transcription of the OP gene in target cells. See generally, Helene, C. (1991) AnticancerDrugDes. 6 (6) : 569-84 ; Helene, C. et al. (1992) Ann. N. Y Acad. Sci. 660 : 27-36 ; and Maher, L. J. (1992) Bioessays 14 (12) : 807-15.

In yet another embodiment, the OP nucleic acid molecules of the present invention can be modified at the base moiety, sugar moiety or phosphate backbone to improve, e. g., the stability, hybridization, or solubility of the molecule. For example, the deoxyribose phosphate backbone of the nucleic acid molecules can be modified to generate peptide nucleic acids (see Hyrup, B. and Nielsen, P. E. (1996) Bioorg Med. Chem. 4 (1) : 5-23). As used herein, the terms"peptide nucleic acids"or"PNAs"refer to nucleic acid mimics, e. g., DNA mimics, in which the deoxyribose phosphate backbone is replaced by a pseudopeptide backbone and only the four natural nucleobases are retained. The neutral backbone of PNAs has been shown to allow for specific hybridization to DNA and RNA under conditions of low ionic strength. The synthesis of PNA oligomers can be performed using standard solid phase peptide synthesis protocols as described in Hyrup and Nielsen (1996) supra and Perry-O'Keefe et al. (1996) Proc. Natl. Acad. Sci. USA 93 : 14670-675.

PNAs of OP nucleic acid molecules can be used in therapeutic and diagnostic applications. For example, PNAs can be used as antisense or antigene agents for sequence- specific modulation of gene expression by, for example, inducing transcription or translation arrest or inhibiting replication. PNAs of OP nucleic acid molecules can also be used in the analysis of single base pair mutations in a gene (e. g., by PNA-directed PCR clamping) ; as 'artificial restriction enzymes'when used in combination with other enzymes (e. g., S1 nucleases (Hyrup and Nielsen (1996) supra)) ; or as probes or primers for DNA sequencing or hybridization (Hyrup and Nielsen (1996) supra ; Perry-O'Keefe et al. (1996) supra).

In another embodiment, PNAs of OP can be modified (e. g., to enhance their stability or cellular uptake), by attaching lipophilic or other helper groups to PNA, by the formation of PNA-DNA chimeras, or by the use of liposomes or other techniques of drug delivery known in the art. For example, PNA-DNA chimeras of OP nucleic acid molecules can be generated which may combine the advantageous properties of PNA and DNA. Such chimeras allow DNA recognition enzymes (e. g., RNAse H and DNA polymerases), to interact with the DNA portion while the PNA portion would provide high binding affinity and specificity. PNA-DNA chimeras can be linked using linkers of appropriate lengths selected in terms of base stacking, number of bonds between the nucleobases, and orientation (Hyrup and Nielsen (1996) supra). The synthesis of PNA-DNA chimeras can be performed as described in Hyrup and Nielsen (1996) supra and Finn, P. J. et al. (1996) Nucleic Acids Res. 24 (17) : 3357-63. For example, a DNA chain can be synthesized on a solid support using standard phosphoramidite coupling chemistry and modified nucleoside analogs, e. g., 5'- (4-methoxytrityl) amino-5'-deoxy-thymidine phosphoramidite, can be used as a between the PNA and the 5'end of DNA (Mag, M. et al. (1989) Nucleic Acids Res.

17 : 5973-88). PNA monomers are then coupled in a stepwise manner to produce a chimeric molecule with a 5'PNA segment and a 3'DNA segment (Finn P. J. et al. (1996) supra).

Alternatively, chimeric molecules can be synthesized with a 5'DNA segment and a 3'PNA segment (Peterser, K. H. et al. (1975) Bioorganic Med. Chem. Lett. 5 : 1119-11124).

In other embodiments, the oligonucleotide may include other appended groups such as peptides (e. g., for targeting host cell receptors in vivo), or agents facilitating transport across the cell membrane (see, e. g., Letsinger et al. (1989) Proc. Natl. Acad. Sci. USA 86 : 6553-6556 ; Lemaitre et al. (1987) Proc. Natl. Acad. Sci. USA 84 : 648-652 ; PCT Publication No. W088/09810) or the blood-brain barrier (see, e. g., PCT Publication No.

W089/10134). In addition, oligonucleotides can be modified with hybridization-triggered cleavage agents (See, e. g., Krol et al. (1988) Biotechniques 6 : 958-976) or intercalating agents (See, e. g., Zon (1988) Pharm. Res. 5 : 539-549). To this end, the oligonucleotide may be conjugated to another molecule (e. g., a peptide, hybridization triggered cross-linking agent, transport agent, or hybridization-triggered cleavage agent).

II. Isolated OP Proteins and Anti-OP Antibodies One aspect of the invention pertains to isolated OP proteins, and biologically active portions thereof, as well as polypeptide fragments suitable for use as immunogens to raise anti-OP antibodies. In one embodiment, native OP proteins can be isolated from cells or tissue sources by an appropriate purification scheme using standard protein purification techniques. In another embodiment, OP proteins are produced by recombinant DNA techniques. Alternative to recombinant expression, an OP protein or polypeptide can be synthesized chemically using standard peptide synthesis techniques.

An"isolated"or"purified"protein or biologically active portion thereof is substantially free of cellular material or other contaminating proteins from the cell or tissue source from which the OP protein is derived, or substantially free from chemical precursors or other chemicals when chemically synthesized. The language"substantially free of cellular material"includes preparations of OP protein in which the protein is separated from cellular components of the cells from which it is isolated or recombinantly produced. In one embodiment, the language"substantially free of cellular material"includes preparations of OP protein having less than about 30% (by dry weight) of non-OP protein (also referred to herein as a"contaminating protein"), more preferably less than about 20% of non-OP protein, still more preferably less than about 10% of non-OP protein, and most preferably less than about 5% non-OP protein. When the OP protein or biologically active portion thereof is recombinantly produced, it is also preferably substantially free of culture medium, i. e., culture medium represents less than about 20%, more preferably less than about 10%, and most preferably less than about 5% of the volume of the protein preparation.

The language"substantially free of chemical precursors or other chemicals"includes preparations of OP protein in which the protein is separated from chemical precursors or other chemicals which are involved in the synthesis of the protein. In one embodiment, the language"substantially free of chemical precursors or other chemicals"includes preparations of OP protein having less than about 30% (by dry weight) of chemical precursors or non-OP chemicals, more preferably less than about 20% chemical precursors or non-OP chemicals, still more preferably less than about 10% chemical precursors or non- OP chemicals, and most preferably less than about 5% chemical precursors or non-OP chemicals.

As used herein, a"biologically active portion"of an OP protein includes a fragment of an OP protein which participates in an interaction between an OP molecule and a non-OP molecule (e. g., choline and/or an acceptor molecule to be reduced or oxidized). Biologically active portions of an OP protein include peptides comprising amino acid sequences sufficiently identical to or derived from the amino acid sequence of the OP protein, e. g., the

amino acid sequence shown in SEQ ID NO : 2, which include fewer amino acids than the full length OP proteins, and exhibit at least one activity of an OP protein. Typically, biologically active portions comprise a domain or motif with at least one activity of the OP protein, e. g., the ability to bind an OP ligand or substrate (e. g., choline and/or an acceptor molecule to be reduced or oxidized), the ability to metabolize an OP ligand or substrate (e. g., choline and/or an acceptor molecule to be reduced or oxidized), the ability to modulate oxidoreductase activity, or the ability to modulate cellular proliferation, growth, apoptosis, differentiation, and/or migration disorders. A biologically active portion of an OP protein can be a polypeptide which is, for example, 10, 25, 50, 100, 200, 300, or more amino acids in length. Biologically active portions of an OP protein can be used as targets for developing agents which modulate an OP mediated activity, e. g., the ability to bind an OP ligand or substrate (e. g., choline and/or an acceptor molecule to be reduced or oxidized) ; the ability to metabolize an OP ligand or substrate (e. g., choline and/or an acceptor molecule to be reduced or oxidized), the ability to modulate oxidoreductase activity, or the ability to modulate cellular proliferation, growth, apoptosis, differentiation, and/or migration disorders.

In one embodiment, a biologically active portion of an OP protein comprises at least one GMC oxidoreductase signature domain and/or at least one transmembrane domain. It is to be understood that a preferred biologically active portion of an OP protein of the present invention may contain at least one GMC oxidoreductase signature domain. Yet another preferred biologically active portion of an OP protein may contain at least one transmembrane domain. Moreover, other biologically active portions, in which other regions of the protein are deleted, can be prepared by recombinant techniques and evaluated for one or more of the functional activities of a native OP protein.

In a preferred embodiment, the OP protein has an amino acid sequence shown in SEQ ID NO : 2. In other embodiments, the OP protein is substantially identical to SEQ ID NO : 2, and retains the functional activity of the protein of SEQ ID NO : 2, yet differs in amino acid sequence due to natural allelic variation or mutagenesis, as described in detail in subsection I above. Accordingly, in another embodiment, the OP protein is a protein which comprises an amino acid sequence at least about 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, 99. 5% or more identical to SEQ ID NO : 2.

To determine the percent identity of two amino acid sequences or of two nucleic acid sequences, the sequences are aligned for optimal comparison purposes (e. g., gaps can be introduced in one or both of a first and a second amino acid or nucleic acid sequence for optimal alignment and non-identical sequences can be disregarded for comparison purposes). In a preferred embodiment, the length of a reference sequence aligned for

comparison purposes is at least 30%, preferably at least 40%, more preferably at least 50%, even more preferably at least 60%, and even more preferably at least 70%, 80%, or 90% of the length of the reference sequence (e. g., when aligning a second sequence to the OP amino acid sequence of SEQ ID NO : 2 having 594 amino acid residues, at least 178, preferably at least 238, more preferably at least 297, even more preferably at least 356, and even more preferably at least 416, 475 or 534 amino acid residues are aligned). The amino acid residues or nucleotides at corresponding amino acid positions or nucleotide positions are then compared. When a position in the first sequence is occupied by the same amino acid residue or nucleotide as the corresponding position in the second sequence, then the molecules are identical at that position (as used herein amino acid or nucleic acid"identity" is equivalent to amino acid or nucleic acid"homology"). The percent identity between the two sequences is a function of the number of identical positions shared by the sequences, taking into account the number of gaps, and the length of each gap, which need to be introduced for optimal alignment of the two sequences.

The comparison of sequences and determination of percent identity between two sequences can be accomplished using a mathematical algorithm. In a preferred embodiment, the percent identity between two amino acid sequences is determined using the Needleman and Wunsch (J : Mol. Biol. (48) : 444-453 (1970)) algorithm which has been incorporated into the GAP program in the GCG software package (available online through the website of the Genetics Computer Group), using either a Blosum 62 matrix or a PAM250 matrix, and a gap weight of 16, 14, 12, 10, 8, 6, or 4 and a length weight of 1, 2, 3, 4, 5, or 6. In yet another preferred embodiment, the percent identity between two nucleotide sequences is determined using the GAP program in the GCG software package (available online through the website of the Genetics Computer Group), using a NWSgapdna. CMP matrix and a gap weight of 40, 50, 60, 70, or 80 and a length weight of 1, 2, 3, 4, 5, or 6. In another embodiment, the percent identity between two amino acid or nucleotide sequences is determined using the algorithm of Meyers, E. and Miller, W. ( (1988) Comput. Appl.

Biosci. 4 : 11-17) which has been incorporated into the ALIGN program (version 2. 0 or 2. 0U), using a PAM120 weight residue table, a gap length penalty of 12 and a gap penalty of 4.

The nucleic acid and protein sequences of the present invention can further be used as a"query sequence"to perform a search against public databases to, for example, identify other family members or related sequences. Such searches can be performed using the NBLAST and XBLAST programs (version 2. 0) of Altschul et al. (1990) J : Mol. Biol.

215 : 403-10. BLAST nucleotide searches can be performed with the NBLAST program, score = 100, wordlength = 12 to obtain nucleotide sequences homologous to OP nucleic acid molecules of the invention. BLAST protein searches can be performed with the XBLAST

program, score = 100, wordlength = 3 to obtain amino acid sequences homologous to OP protein molecules of the invention. To obtain gapped alignments for comparison purposes, Gapped BLAST can be utilized as described in Altschul et al. (1997) Nucleic Acids Res.

25 (17) : 3389-3402. When utilizing BLAST and Gapped BLAST programs, the default parameters of the respective programs (e. g., XBLAST and NBLAST) can be used. See the website of the National Center for Biotechnology Information.

The invention also provides OP chimeric or fusion proteins. As used herein, an OP "chimeric protein"or"fusion protein"comprises an OP polypeptide operatively linked to a non-OP polypeptide. A"OP polypeptide"includes a polypeptide having an amino acid sequence corresponding to OP, whereas a"non-OP peptide"includes a polypeptide having an amino acid sequence corresponding to a protein which is not substantially homologous to an OP protein, e. g., a protein which is different from the OP protein and which is derived from the same or a different organism. Within an OP fusion protein the OP polypeptide can correspond to all or a portion of an OP protein. In a preferred embodiment, an OP fusion protein comprises at least one biologically active portion of an OP protein. In another preferred embodiment, an OP fusion protein comprises at least two biologically active portions of an OP protein. Within the fusion protein, the term"operatively linked"is intended to indicate that the OP polypeptide and the non-OP polypeptide are fused in-frame to each other. The non-OP polypeptide can be fused to the N-terminus or C-terminus of the OP polypeptide.

For example, in one embodiment, the fusion protein is a GST-OP fusion protein in which the OP sequences are fused to the C-terminus of the GST sequences. Such fusion proteins can facilitate the purification of recombinant OP.

In another embodiment, the fusion protein is an OP protein containing a heterologous signal sequence at its N-terminus. In certain host cells (e. g., mammalian host cells), expression and/or secretion of OP can be increased through use of a heterologous signal sequence.

The OP fusion proteins of the invention can be incorporated into pharmaceutical compositions and administered to a subject in vivo. The OP fusion proteins can be used to affect the bioavailability of an OP ligand or substrate. Use of OP fusion proteins may be useful therapeutically for the treatment of disorders caused by, for example, (i) aberrant modification or mutation of a gene encoding an OP protein ; (ii) mis-regulation of the OP gene ; and (iii) aberrant post-translational modification of an OP protein.

Moreover, the OP-fusion proteins of the invention can be used as immunogens to produce anti-OP antibodies in a subject, to purify OP ligands and in screening assays to identify molecules which inhibit the interaction of OP with an OP ligand or substrate.

Preferably, an OP chimeric or fusion protein of the invention is produced by standard recombinant DNA techniques. For example, DNA fragments coding for the different polypeptide sequences are ligated together in-frame in accordance with conventional techniques, for example by employing blunt-ended or stagger-ended termini for ligation, restriction enzyme digestion to provide for appropriate termini, filling-in of cohesive ends as appropriate, alkaline phosphatase treatment to avoid undesirable joining, and enzymatic ligation. In another embodiment, the fusion gene can be synthesized by conventional techniques including automated DNA synthesizers. Alternatively, PCR amplification of gene fragments can be carried out using anchor primers which give rise to complementary overhangs between two consecutive gene fragments which can subsequently be annealed and reamplified to generate a chimeric gene sequence (see, for example, Current Protocols in Molecular Biology, eds. Ausubel et al. John Wiley & Sons : 1992).

Moreover, many expression vectors are commercially available that already encode a fusion moiety (e. g., a GST polypeptide). An OP-encoding nucleic acid can be cloned into such an expression vector such that the fusion moiety is linked in-frame to the OP protein.

The present invention also pertains to variants of the OP proteins which function as either OP agonists (mimetics) or as OP antagonists. Variants of the OP proteins can be generated by mutagenesis, e. g., discrete point mutation or truncation of an OP protein. An agonist of the OP proteins can retain substantially the same, or a subset, of the biological activities of the naturally occurring form of an OP protein. An antagonist of an OP protein can inhibit one or more of the activities of the naturally occurring form of the OP protein by, for example, competitively modulating an OP-mediated activity of an OP protein. Thus, specific biological effects can be elicited by treatment with a variant of limited function. In one embodiment, treatment of a subject with a variant having a subset of the biological activities of the naturally occurring form of the protein has. fewer side effects in a subject relative to treatment with the naturally occurring form of the OP protein.

In one embodiment, variants of an OP protein which function as either OP agonists (mimics) or as OP antagonists can be identified by screening combinatorial libraries of mutants, e. g., truncation mutants, of an OP protein for OP protein agonist or antagonist activity. In one embodiment, a variegated library of OP variants is generated by combinatorial mutagenesis at the nucleic acid level and is encoded by a variegated gene library. A variegated library of OP variants can be produced by, for example, enzymatically ligating a mixture of synthetic oligonucleotides into gene sequences such that a degenerate set of potential OP sequences is expressible as individual polypeptides, or alternatively, as a set of larger fusion proteins (e. g., for phage display) containing the set of OP sequences therein. There are a variety of methods which can be used to produce libraries of potential OP variants from a degenerate oligonucleotide sequence. Chemical synthesis of a

degenerate gene sequence can be performed in an automatic DNA synthesizer, and the synthetic gene then ligated into an appropriate expression vector. Use of a degenerate set of genes allows for the provision, in one mixture, of all of the sequences encoding the desired set of potential OP sequences. Methods for synthesizing degenerate oligonucleotides are known in the art (see, e. g., Narang, S. A. (1983) Tetrahedron 39 : 3 ; Itakura et al. (1984) Annu. Rev. Biochem. 53 : 323 ; Itakura et al. (1984) Science 198 : 1056 ; Ike et al. (1983) Nucleic Acid Res. 11 : 477.

In addition, libraries of fragments of an OP protein coding sequence can be used to generate a variegated population of OP fragments for screening and subsequent selection of variants of an OP protein. In one embodiment, a library of coding sequence fragments can be generated by treating a double stranded PCR fragment of an OP coding sequence with a nuclease under conditions wherein nicking occurs only about once per molecule, denaturing the double stranded DNA, renaturing the DNA to form double stranded DNA which can include sense/antisense pairs from different nicked products, removing single stranded portions from reformed duplexes by treatment with S 1 nuclease, and ligating the resulting fragment library into an expression vector. By this method, an expression library can be derived which encodes N-terminal, C-terminal and internal fragments of various sizes of the OP protein.

Several techniques are known in the art for screening gene products of combinatorial libraries made by point mutations or truncation, and for screening cDNA libraries for gene products having a selected property. Such techniques are adaptable for rapid screening of the gene libraries generated by the combinatorial mutagenesis of OP proteins. The most widely used techniques, which are amenable to high through-put analysis, for screening large gene libraries typically include cloning the gene library into replicable expression vectors, transforming appropriate cells with the resulting library of vectors, and expressing the combinatorial genes under conditions in which detection of a desired activity facilitates isolation of the vector encoding the gene whose product was detected. Recursive ensemble mutagenesis (REM), a new technique which enhances the frequency of functional mutants in the libraries, can be used in combination with the screening assays to identify OP variants (Arkin and Youvan (1992) Proc. Natl. Acad. Sci. USA 89 : 7811-7815 ; Delagrave et al.

(1993) Protein Eng 6 (3) : 327-331).

In one embodiment, cell based assays can be exploited to analyze a variegated OP library. For example, a library of expression vectors can be transfected into a cell line, e. g., a neuronal cell line, which ordinarily responds to OP in a particular OP ligand-dependent manner. The transfected cells are then contacted with an OP ligand and the effect of expression of the mutant on signaling by the OP ligand can be detected, e. g., by monitoring OP activity, changes in concentration of metabolites of OP (e. g., betaine or methionine),

signaling mechanisms which rely on the activity of OP, or the activity of an OP-regulated transcription factor. Plasmid DNA can then be recovered from the cells which score for inhibition, or alternatively, potentiation of signaling by the OP ligand, and the individual clones further characterized. In related cell-based assays, changes in ligands or target proteins of OP (e. g., choline and/or an acceptor molecule to be reduced or oxidized) can be measured in live cells which express OP molecules of the invention. For example, the OP proteins of the present invention are choline dehydrogenases. Accordingly, the levels of choline and/or betaine can be measured. In another embodiment, the levels of homocysteine and/or methionine can be measured.

Such an assay can be used for screening compound libraries for useful ligands which interact'with OP, or can be used to identify variants of OP which have useful properties.

Other cell-based assays include those which can monitor fluxes in intracellular metabolite levels which result from OP activity, e. g., cellular staining or flow cytometry (Valet and Raffael (1985) Naturwiss. 72 : 600-602). Also within the scope of the invention are assays and models which utilize OP nucleic acids to create transgenic organisms for identifying useful pharmaceutical compounds or variants of the OP molecules.

An isolated OP protein, or a portion or fragment thereof, can be used as an immunogen to generate antibodies that bind OP using standard techniques for polyclonal and monoclonal antibody preparation. A full-length OP protein can be used or, alternatively, the invention provides antigenic peptide fragments of OP for use as immunogens. The antigenic peptide of OP comprises at least 8 amino acid residues of the amino acid sequence shown in SEQ ID NO : 2 and encompasses an epitope of OP such that an antibody raised against the peptide forms a specific immune complex with OP.

Preferably, the antigenic peptide comprises at least 10 amino acid residues, more preferably at least 15 amino acid residues, even more preferably at least 20 amino acid residues, and most preferably at least 30 amino acid residues.

Preferred epitopes encompassed by the antigenic peptide are regions of OP that are located on the surface of the protein, e. g., hydrophilic regions, as well as regions with high antigenicity (see, for example, Figure 2).

An OP immunogen typically is used to prepare antibodies by immunizing a suitable subject (e. g., rabbit, goat, mouse or other mammal) with the immunogen. An appropriate immunogenic preparation can contain, for example, recombinantly expressed OP protein or a chemically synthesized OP polypeptide. The preparation can further include an adjuvant, such as Freund's complete or incomplete adjuvant, or similar immunostimulatory agent.

Immunization of a suitable subject with an immunogenic OP preparation induces a polyclonal anti-OP antibody response.

Accordingly, another aspect of the invention pertains to anti-OP antibodies. The term"antibody"as used herein refers to immunoglobulin molecules and immunologically active portions of immunoglobulin molecules, i. e., molecules that contain an antigen binding site which specifically binds (immunoreacts with) an antigen, such as OP. Examples of immunologically active portions of immunoglobulin molecules include F (ab) and F (ab') 2 fragments which can be generated by treating the antibody with an enzyme such as pepsin.

The invention provides polyclonal and monoclonal antibodies that bind OP. The term "monoclonal antibody"or"monoclonal antibody composition", as used herein, refers to a population of antibody molecules that contain only one species of an antigen binding site capable of immunoreacting with a particular epitope of OP. A monoclonal antibody composition thus typically displays a single binding affinity for a particular OP protein with which it immunoreacts.

Polyclonal anti-OP antibodies can be prepared as described above by immunizing a suitable subject with an immunogen. The anti-OP antibody titer in the immunized subject can be monitored over time by standard techniques, such as with an enzyme linked immunosorbent assay (ELISA) using immobilized OP. If desired, the antibody molecules directed against OP can be isolated from the mammal (e. g., from the blood) and further purified by well known techniques, such as protein A chromatography to obtain the IgG fraction. At an appropriate time after immunization, e. g., when the anti-OP antibody titers are highest, antibody-producing cells can be obtained from the subject and used to prepare monoclonal antibodies by standard techniques, such as the hybridoma technique originally described by Kohler and Milstein (1975) Nature 256 : 495-497) (see also, Brown et al. (1981).

J Immunol. 127 : 539-46 ; Brown et al. (1980) J : Biol. Chem. 255 : 4980-83 ; Yeh et al. (1976) Proc. Natl. Acad. Sci. USA 76 : 2927-31 ; and Yeh et al. (1982) Int. J : Cancer 29 : 269-75), the more recent human B cell hybridoma technique (Kozbor et al. (1983) Immunol. Today 4 : 72), the EBV-hybridoma technique (Cole et al. (1985) Monoclonal Antibodies and Cancer Therapy, Alan R. Liss, Inc., pp. 77-96) or trioma techniques. The technology for producing monoclonal antibody hybridomas is well known (see generally, Kenneth, R. H. in Monoclonal Antibodies : A New Dimension In Biological Analyses, Plenum Publishing Corp., New York, New York (1980) ; Lerner, E. A. (1981) Yale J. Biol. Med. 54 : 387-402 ; Gefter, M. L. et al. (1977) Somatic Cell Genet. 3 : 231-36). Briefly, an immortal cell line (typically a myeloma) is fused to lymphocytes (typically splenocytes) from a mammal immunized with an OP immunogen as described above, and the culture supernatants of the resulting hybridoma cells are screened to identify a hybridoma producing a monoclonal antibody that binds OP.

Any of the many well known protocols used for fusing lymphocytes and immortalized cell lines can be applied for the purpose of generating an anti-OP monoclonal

antibody (see, e. g., Galfre, G. et al. (1977) Nature 266 : 55052 ; Gefter et aL (1977) supra ; Lerner (1981) supra ; Kenneth, Monoclonal Antibodies, cited supra). Moreover, the ordinarily skilled worker will appreciate that there are many variations of such methods which also would be useful. Typically, the immortal cell line (e. g., a myeloma cell line) is derived from the same mammalian species as the lymphocytes. For example, murine hybridomas can be made by fusing lymphocytes from a mouse immunized with an immunogenic preparation of the present invention with an immortalized mouse cell line.

Preferred immortal cell lines are mouse myeloma cell lines that are sensitive to culture medium containing hypoxanthine, aminopterin and thymidine ("HAT medium"). Any of a number of myeloma cell lines can be used as a fusion partner according to standard techniques, e. g., the P3-NSl/1-Ag4-1, P3-x63-Ag8. 653 or Sp2/0-Agl4 myeloma lines.

These myeloma lines are available from ATCC. Typically, HAT-sensitive mouse myeloma cells are fused to mouse splenocytes using polyethylene glycol ("PEG"). Hybridoma cells resulting from the fusion are then selected using HAT medium, which kills unfused and unproductively fused myeloma cells (unfused splenocytes die after several days because they are not transformed). Hybridoma cells producing a monoclonal antibody of the invention are detected by screening the hybridoma culture supernatants for antibodies that bind OP, e. g., using a standard ELISA assay.

Alternative to preparing monoclonal antibody-secreting hybridomas, a monoclonal anti-OP antibody can be identified and isolated by screening a recombinant combinatorial immunoglobulin library (e. g., an antibody phage display library) with OP to thereby isolate immunoglobulin library members that bind OP. Kits for generating and screening phage display libraries are commercially available (e. g., the Pharmacia Recombinant Phage Antibody System, Catalog No. 27-9400-01 ; and the Stratagene SurfZ4pTMPhage Display Kit, Catalog No. 240612). Additionally, examples of methods and reagents particularly amenable for use in generating and screening antibody display library can be found in, for example, Ladner et al. U. S. Patent No. 5, 223, 409 ; Kang et al. PCT International Publication No. WO 92/18619 ; Dower et al. PCT International Publication No. WO 91/17271 ; Winter et al. PCT International Publication WO 92/20791 ; Markland et al. PCT International Publication No. WO 92/15679 ; Breitling et al. PCT International Publication WO 93/01288 ; McCafferty et al. PCT International Publication No. WO 92/01047 ; Garrard et al. PCT International Publication No. WO 92/09690 ; Ladner et al. PCT International Publication No. WO 90/02809 ; Fuchs et al. (1991) Biotechnology (NI) 9 : 1369-1372 ; Hay et al. (1992) Hum. Antibod. Hybridomas 3 : 81-85 ; Huse et al. (1989) Science 246 : 1275-1281 ; Griffiths et al. (1993) EMBO J 12 : 725-734 ; Hawkins et al. (1992) J. Mol. Biol. 226 : 889-896 ; Clackson et al. (1991) Nature 352 : 624-628 ; Gram et al. (1992) Proc. Natl. Acad. Sci. USA 89 : 3576- 3580 ; Garrard et al. (1991) Biotechnology (N 9 : 1373-1377 ; Hoogenboom et al. (1991)

Nucleic Acids Res. 19 : 4133-4137 ; Barbas et al. (1991) Proc. Natl. Acad. Sci. USA 88 : 7978- 7982 ; and McCafferty et al. (1990) Nature 348 : 552-554.

Additionally, recombinant anti-OP antibodies, such as chimeric and humanized monoclonal antibodies, comprising both human and non-human portions, which can be made using standard recombinant DNA techniques, are within the scope of the invention.

Such chimeric and humanized monoclonal antibodies can be produced by recombinant DNA techniques known in the art, for example using methods described in Robinson et al.

International Application No. PCT/US86/02269 ; Akira et al. European Patent Application 184, 187 ; Taniguchi, M., European Patent Application 171, 496 ; Morrison et al. European Patent Application 173, 494 ; Neuberger et al. PCT International Publication No. WO 86/01533 ; Cabilly et al. U. S. Patent No. 4, 816, 567 ; Cabilly et al. European Patent Application 125, 023 ; Better et al. (1988) Science 240 : 1041-1043 ; Liu et al. (1987) Proc.

Natl. Acad. Sci. USA 84 : 3439-3443 ; Liu et al. (1987) J. Immunol. 139 : 3521-3526 ; Sun et al.

(1987) Proc. Natl. Acad. Sci. USA 84 : 214-218 ; Nishimura et al. (1987) Cancer Res. 47 : 999- 1005 ; Wood et al. (1985) Nature 314 : 446-449 ; and Shaw et al. (1988) J. Natl. Cancer Inst.

80 : 1553-1559) ; Morrison, S. L. (1985) Science 229 : 1202-1207 ; Oi et al. (1986) Biotechniques 4 : 214 ; Winter U. S. Patent 5, 225, 539 ; Jones et al. (1986) Nature 321 : 552-525 ; Verhoeyen et al. (1988) Science 239 : 1534 ; and Beidler et al. (1988) J : Immunol. 141 : 4053- 4060.

An anti-OP antibody (e. g., monoclonal antibody) can be used to isolate OP by standard techniques, such as affinity chromatography or immunoprecipitation. An anti-OP antibody can facilitate the purification of natural OP from cells and of recombinantly produced OP expressed in host cells. Moreover, an anti-OP antibody can be used to detect OP protein (e. g., in a cellular lysate or cell supernatant) in order to evaluate the abundance and pattern of expression of the OP protein. Anti-OP antibodies can be used diagnostically to monitor protein levels in tissue as part of a clinical testing procedure, e. g., to, for example, determine the efficacy of a given treatment regimen. Detection can be facilitated by coupling (i. e., physically linking) the antibody to a detectable substance. Examples of detectable substances include various enzymes, prosthetic groups, fluorescent materials, luminescent materials, bioluminescent materials, and radioactive materials. Examples of suitable enzymes include horseradish peroxidase, alkaline phosphatase, p-galactosidase, or acetylcholinesterase ; examples of suitable prosthetic group complexes include streptavidin/biotin and avidin/biotin ; examples of suitable fluorescent materials include umbelliferone, fluorescein, fluorescein isothiocyanate, rhodamine, dichlorotriazinylamine fluorescein, dansyl chloride or phycoerythrin ; an example of a luminescent material includes luminol; examples of bioluminescent materials include luciferase, luciferin, and aequorin, and examples of suitable radioactive material include 125I, 131I, 35S or 3H.

III. Recombinant Expression Vectors and Host Cells Another aspect of the invention pertains to vectors, preferably expression vectors, containing a nucleic acid encoding an OP protein (or a portion thereof). As used herein, the term"vector"refers to a nucleic acid molecule capable of transporting another nucleic acid to which it has been linked. One type of vector is a"plasmid", which refers to a circular double stranded DNA loop into which additional DNA segments can be ligated. Another type of vector is a viral vector, wherein additional DNA segments can be ligated into the viral genome. Certain vectors are capable of autonomous replication in a host cell into which they are introduced (e. g., bacterial vectors having a bacterial origin of replication and episomal mammalian vectors). Other vectors (e. g., non-episomal mammalian vectors) are integrated into the genome of a host cell upon introduction into the host cell, and thereby are replicated along with the host genome. Moreover, certain vectors are capable of directing the expression of genes to which they are operatively linked. Such vectors are referred to herein as"expression vectors". In general, expression vectors of utility in recombinant DNA techniques are often in the form of plasmids. In the present specification,"plasmid" and'4vector"can be used interchangeably as the plasmid is the most commonly used form of vector. However, the invention is intended to include such other forms of expression vectors, such as viral vectors (e. g., replication defective retroviruses, adenoviruses and adeno-associated viruses), which serve equivalent functions.

The recombinant expression vectors of the invention comprise a nucleic acid of the invention in a form suitable for expression of the nucleic acid in a host cell, which means that the recombinant expression vectors include one or more regulatory sequences, selected on the basis of the host cells to be used for expression, which is operatively linked to the nucleic acid sequence to be expressed. Within a recombinant expression vector,"operably linked"is intended to mean that the nucleotide sequence of interest is linked to the regulatory sequence (s) in a manner which allows for expression of the nucleotide sequence (e. g., in an in vitro transcription/translation system or in a host cell when the vector is introduced into the host cell). The term"regulatory sequence"is intended to include promoters, enhancers and other expression control elements (e. g., polyadenylation signals).

Such regulatory sequences are described, for example, in Goeddel (1990) Methods Enzymol.

185 : 3-7. Regulatory sequences include those which direct constitutive expression of a nucleotide sequence in many types of host cells and those which direct expression of the nucleotide sequence only in certain host cells (e. g., tissue-specific regulatory sequences). It will be appreciated by those skilled in the art that the design of the expression vector can depend on such factors as the choice of the host cell to be transformed, the level of expression of protein desired, and the like. The expression vectors of the invention can be

introduced into host cells to thereby produce proteins or peptides, including fusion proteins or peptides, encoded by nucleic acids as described herein (e. g., OP proteins, mutant forms of OP proteins, fusion proteins, and the like).

The recombinant expression vectors of the invention can be designed for expression of OP proteins in prokaryotic or eukaryotic cells. For example, OP proteins can be expressed in bacterial cells such as E. coli, insect cells (using baculovirus expression vectors) yeast cells or mammalian cells. Suitable host cells are discussed further in Goeddel (1990) supra. Alternatively, the recombinant expression vector can be transcribed and translated in vitro, for example using T7 promoter regulatory sequences and T7 polymerase.

Expression of proteins in prokaryotes is most often carried out in E. coli with vectors containing constitutive or inducible promoters directing the expression of either fusion or non-fusion proteins. Fusion vectors add a number of amino acids to a protein encoded therein, usually to the amino terminus of the recombinant protein. Such fusion vectors typically serve three purposes : 1) to increase expression of recombinant protein ; 2) to increase the solubility of the recombinant protein ; and 3) to aid in the purification of the recombinant protein by acting as a ligand in affinity purification. Often, in fusion expression vectors, a proteolytic cleavage site is introduced at the junction of the fusion moiety and the recombinant protein to enable separation of the recombinant protein from the fusion moiety subsequent to purification of the fusion protein. Such enzymes, and their cognate recognition sequences, include Factor Xa, thrombin and enterokinase. Typical fusion expression vectors include pGEX (Pharmacia Biotech Inc ; Smith, D. B. and Johnson, K. S. (1988) Gene 67 : 31-40), pMAL (New England Biolabs, Beverly, MA) and pRIT5 (Pharmacia, Piscataway, NJ) which fuse glutathione S-transferase (GST), maltose E binding protein, or protein A, respectively, to the target recombinant protein.

Purified fusion proteins can be utilized in OP activity assays (e. g., direct assays or competitive assays described in detail below), or to generate antibodies specific for OP proteins, for example. In a preferred embodiment, an OP fusion protein expressed in a retroviral expression vector of the present invention can be utilized to infect bone marrow cells which are subsequently transplanted into irradiated recipients. The pathology of the subject recipient is then examined after sufficient time has passed (e. g., six (6) weeks).

Examples of suitable inducible non-fusion E. coli expression vectors include pTrc (Amannetal. (1988) Gene 69 : 301-315) and pET 1 ld (Studier et al. (1990) Methods Enzymol. 185 : 60-89). Target gene expression from the pTrc vector relies on host RNA polymerase transcription from a hybrid trp-lac fusion promoter. Target gene expression from the pET lid vector relies on transcription from a T7 gnl 0-lac fusion promoter mediated by a coexpressed viral RNA polymerase (T7 gnl). This viral polymerase is

supplied by host strains BL21 (DE3) or HMS174 (DE3) from a resident prophage harboring a T7 gnl gene under the transcriptional control of the lacUV 5 promoter.

One strategy to maximize recombinant protein expression in E. coli is to express the protein in a host bacteria with an impaired capacity to proteolytically cleave the recombinant protein (Gottesman, S. (1990) Methods Enzymol. 185 : 119-128). Another strategy is to alter the nucleic acid sequence of the nucleic acid to be inserted into an expression vector so that the individual codons for each amino acid are those preferentially utilized in E. coli (Wada et al. (1992) Nucleic Acids Res. 20 : 2111-2118). Such alteration of nucleic acid sequences of the invention can be carried out by standard DNA synthesis techniques.

In another embodiment, the OP expression vector is a yeast expression vector.

Examples of vectors for expression in yeast S cerivisae include pYepSecl (Baldari et al.

(1987) EMBO J. 6 : 229-234), pMFa (Kurjan and Herskowitz (1982) Cell 30 : 933-943), pJRY88 (Schultz et al. (1987) Gene 54 : 113-123), pYES2 (Invitrogen Corporation, San Diego, CA), and picZ (Invitrogen Corp, San Diego, CA).

Alternatively, OP proteins can be expressed in insect cells using baculovirus expression vectors. Baculovirus vectors available for expression of proteins in cultured insect cells (e. g., Sf 9 cells) include the pAc series (Smith et al. (1983) Mol. Cell Biol.

3 : 2156-2165) and the pVL series (Lucklow and Summers (1989) Virology 170 : 31-39).

In yet another embodiment, a nucleic acid of the invention is expressed in mammalian cells using a mammalian expression vector. Examples of mammalian expression vectors include pCDM8 (Seed, B. (1987) Nature 329 : 840) and pMT2PC (Kaufman et al. (1987) EMBU J. 6 : 187-195). When used in mammalian cells, the expression vector's control functions are often provided by viral regulatory elements. For example, commonly used promoters are derived from polyoma, Adenovirus 2, cytomegalovirus and Simian Virus 40. For other suitable expression systems for both prokaryotic and eukaryotic cells see chapters 16 and 17 of Sambrook, J. et al., Molecular Cloning : A Laboratory Manual. 2nd ed., Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, 1989.

In another embodiment, the recombinant mammalian expression vector is capable of directing expression of the nucleic acid preferentially in a particular cell type (e. g., tissue- specific regulatory elements are used to express the nucleic acid). Tissue-specific regulatory elements are known in the art. Non-limiting examples of suitable tissue-specific promoters include the albumin promoter (liver-specific ; Pinkert et al. (1987) Genes Dev. 1 : 268-277), lymphoid-specific promoters (Calame and Eaton (1988) Adv. Immunol. 43 : 235-275), in particular promoters of T cell receptors (Winoto and Baltimore (1989) EMBO J. 8 : 729-733) and immunoglobulins (Banerji et al. (1983) Cell 33 : 729-740 ; Queen and Baltimore (1983) Cell 33 : 741-748), neuron-specific promoters (e. g., the neurofilament promoter ; Byrne and

Ruddle (1989) Proc. Natl. Acad. Sci. USA 86 : 5473-5477), pancreas-specific promoters (Edlund et al. (1985) Science 230 : 912-916), and mammary gland-specific promoters (e. g., milk whey promoter ; U. S. Patent No. 4, 873, 316 and European Application Publication No.

264, 166). Developmentally-regulated promoters are also encompassed, for example the murine hox promoters (Kessel and Gruss (1990) Science 249 : 374-379) and the a-fetoprotein promoter (Campes and Tilghman (1989) Genes Dev. 3 : 537-546).

The expression characteristics of an endogenous OP gene within a cell line or microorganism may be modified by inserting a heterologous DNA regulatory element into the genome of a stable cell line or cloned microorganism such that the inserted regulatory element is operatively linked with the endogenous OP gene. For example, an endogenous OP gene which is normally"transcriptionally silent", i. e., an OP gene which. is normally not expressed, or is expressed only at very low levels in a cell line or microorganism, may be activated by inserting a regulatory element which is capable of promoting the expression of a normally expressed gene product in that cell line or microorganism. Alternatively, a transcriptionally silent, endogenous OP gene may be activated by insertion of a promiscuous regulatory element that works across cell types.

A heterologous regulatory element may be inserted into a stable cell line or cloned microorganism, such that it is operatively linked with an endogenous OP gene, using techniques, such as targeted homologous recombination, which are well known to those of skill in the art, and described, e. g., in Chappel, U. S. Patent No. 5, 272, 071 ; PCT publication No. WO 91/06667, published May 16, 1991.

The invention further provides a recombinant expression vector comprising a DNA molecule of the invention cloned into the expression vector in an antisense orientation. That is, the DNA molecule is operatively linked to a regulatory sequence in a manner which allows for expression (by transcription of the DNA molecule) of an RNA molecule which is antisense to OP mRNA. Regulatory sequences operatively linked to a nucleic acid cloned in the antisense orientation can be chosen which direct the continuous expression of the antisense RNA molecule in a variety of cell types, for instance viral promoters and/or enhancers, or regulatory sequences can be chosen which direct constitutive, tissue specific or cell type specific expression of antisense RNA. The antisense expression vector can be in the form of a recombinant plasmid, phagemid or attenuated virus in which antisense nucleic acids are produced under the control of a high efficiency regulatory region, the activity of which can be determined by the cell type into which the vector is introduced. For a discussion of the regulation of gene expression using antisense genes see Weintraub, H. et al. Antisense RNA as a molecular tool for genetic analysis, Reviews-Trends in Genetics, Vol. 1 (1) 1986.

Another aspect of the invention pertains to host cells into which an OP nucleic acid molecule of the invention is introduced, e. g., an OP nucleic acid molecule within a recombinant expression vector or an OP nucleic acid molecule containing sequences which allow it to homologously recombine into a specific site of the host cell's genome. The terms "host cell"and"recombinant host cell"are used interchangeably herein. It is understood that such terms refer not only to the particular subject cell but to the progeny or potential progeny of such a cell. Because certain modifications may occur in succeeding generations due to either mutation or environmental influences, such progeny may not, in fact, be identical to the parent cell, but are still included within the scope of the term as used herein.

A host cell can be any prokaryotic or eukaryotic cell. For example, an OP protein can be expressed in bacterial cells such as E. coli, insect cells, yeast or mammalian cells (such as Chinese hamster ovary cells (CHO) or COS cells). Other suitable host cells are known to those skilled in-the art.

Vector DNA can be introduced into prokaryotic or eukaryotic cells via conventional transformation or transfection techniques. As used herein, the terms"transformation"and "transfection"are intended to refer to a variety of art-recognized techniques for introducing foreign nucleic acid (e. g., DNA) into a host cell, including calcium phosphate or calcium chloride co-precipitation, DEAE-dextran-mediated transfection, lipofection, or electroporation. Suitable methods for transforming or transfecting host cells can be found in Sambrook et al. (Molecular Cloning A Laborafory Manual., 2nd ed., Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, 1989), and other laboratory manuals.

For stable transfection of mammalian cells, it is known that, depending upon the expression vector and transfection technique used, only a small fraction of cells may integrate the foreign DNA into their genome. In order to identify. and select these integrants, a gene that encodes a selectable marker (e. g., resistance to antibiotics) is generally introduced into the host cells along with the gene of interest. Preferred selectable markers include those which confer resistance to drugs, such as G418, hygromycin and methotrexate.

Nucleic acid encoding a selectable marker can be introduced into a host cell on the same vector as that encoding an OP protein or can be introduced on a separate vector. Cells stably transfected with the introduced nucleic acid can be identified by drug selection (e. g., cells that have incorporated the selectable marker gene will survive, while the other cells die).

A host cell of the invention, such as a prokaryotic or eukaryotic host cell in culture, can be used to produce (i. e., express) an OP protein. Accordingly, the invention further provides methods for producing an OP protein using the host cells of the invention. In one embodiment, the method comprises culturing the host cell of the invention (into which a

recombinant expression vector encoding an OP protein has been introduced) in a suitable medium such that an OP protein is produced. In another embodiment, the method further comprises isolating an OP protein from the medium or the host cell.

The host cells of the invention can also be used to produce non-human transgenic animals. For example, in one embodiment, a host cell of the invention is a fertilized oocyte or an embryonic stem cell into which OP-coding sequences have been introduced. Such host cells can then be used to create non-human transgenic animals in which exogenous OP sequences have been introduced into their genome or homologous recombinant animals in which endogenous OP sequences have been altered. Such animals are useful for studying the function and/or activity of an OP and for identifying and/or evaluating modulators of OP activity. As used herein, a"transgenic animal"is a non-human animal, preferably a mammal, more preferably a rodent such as a rat or mouse, in which one or more of the cells -of the animal includes a transgene. Other examples of transgenic animals include non- human primates, sheep, dogs, cows, goats, chickens, amphibians, and the like. A transgene is exogenous DNA which is integrated into the genome of a cell from which a transgenic animal develops and which remains in the genome of the mature animal, thereby directing the expression of an encoded gene product in one or more cell types or tissues of the transgenic animal. As used herein, a"homologous recombinant animal"is a non-human animal, preferably a mammal, more preferably a mouse, in which an endogenous OP gene has been altered by homologous recombination between the endogenous gene and an exogenous DNA molecule introduced into a cell of the animal, e. g., an embryonic cell of the animal, prior to development of the animal.

A transgenic animal of the invention can be created by introducing an OP-encoding nucleic acid into the male pronuclei of a fertilized oocyte, e. g., by microinjection, retroviral infection, and allowing the oocyte to develop in a pseudopregnant female foster animal.

The OP cDNA sequence of SEQ ID NO : 1 or 3 can be introduced as a transgene into the genome of a non-human animal. Alternatively, a nonhuman homologue of a human OP gene, such as a mouse or rat OP gene, can be used as a transgene. Alternatively, an OP gene homologue, such as another OP family member, can be isolated based on hybridization to the OP cDNA sequences of SEQ ID NO : 1 or 3, or the DNA insert of the plasmid deposited with ATCC as Accession Number (described further in subsection I above) and used as a transgene. Intronic sequences and polyadenylation signals can also be included in the transgene to increase the efficiency of expression of the transgene. A tissue-specific regulatory sequence (s) can be operably linked to an OP transgene to direct expression of an OP protein to particular cells. Methods for generating transgenic animals via embryo manipulation and microinjection, particularly animals such as mice, have become conventional in the art and are described, for example, in U. S. Patent Nos. 4, 736, 866 and

4, 870, 009, both by Leder et al. U. S. Patent No. 4, 873, 191 by Wagner et al. and in Hogan, B., Manipulating the Mouse Embryo (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N. Y., 1986). Similar methods are used for production of other transgenic animals.

A transgenic founder animal can be identified based upon the presence of an OP transgene in its genome and/or expression of OP mRNA in tissues or cells of the animals. A transgenic founder animal can then be used to breed additional animals carrying the transgene. Moreover, transgenic animals carrying a transgene encoding an OP protein can further be bred to other transgenic animals carrying other transgenes.

To create a homologous recombinant animal, a vector is prepared which contains at least a portion of an OP gene into which a deletion, addition or substitution has been introduced to thereby alter, e. g., functionally disrupt, the OP gene. The OP gene can be a human gene (e. g., the cDNA of SEQ ID NO : 1, 3, 4, or 6), but more preferably, is a non- human homologue of a human OP gene (e. g., a cDNA isolated by stringent hybridization with the nucleotide sequence of SEQ ID NO : 1, 3, 4, or 6). For example, a mouse OP gene can be used to construct a homologous recombination nucleic acid molecule, e. g., a vector, suitable for altering an endogenous OP gene in the mouse genome.

In a preferred embodiment, the homologous recombination nucleic acid molecule is designed such that, upon homologous recombination, the endogenous OP gene is functionally disrupted (i. e., no longer encodes a functional protein ; also referred to as a "knock out"vector). Alternatively, the homologous recombination nucleic acid molecule can be designed such that, upon homologous recombination, the endogenous OP gene is mutated or otherwise altered but still encodes functional protein (e. g., the upstream regulatory region can be altered to thereby alter the expression of the endogenous OP protein). In the homologous recombination nucleic acid molecule, the altered portion of the OP gene is flanked at its 5'and 3'ends by additional nucleic acid sequence of the OP gene to allow for homologous recombination to occur between the exogenous OP gene carried by the homologous recombination nucleic acid molecule and an : endogenous OP gene in a cell, e. g., an embryonic stem cell. The additional flanking OP nucleic acid sequence is of sufficient length for successful homologous recombination with the endogenous gene.

Typically, several kilobases of flanking DNA (both at the 5'and 3'ends) are included in the homologous recombination nucleic acid molecule (see, e. g., Thomas, K. R. and Capecchi, M. R. (1987) Cell 51 : 503 for a description of homologous recombination vectors). The homologous recombination nucleic acid molecule is introduced into a cell, e. g., an embryonic stem cell line (e. g., by electroporation) and cells in which the introduced OP gene has homologously recombined with the endogenous OP gene are selected (see e. g., Li, E. et al. (1992) Cell 69 : 915). The selected cells can then injected into a blastocyst of an animal (e. g., a mouse) to form aggregation chimeras (see e. g., Bradley, A. in

Teratocarcinomas and Embryonic Stem Cells : A Practical Approach, Robertson, E. J., ed.

(IRL, Oxford, 1987) pp. 113-152). A chimeric embryo can then be implanted into a suitable pseudopregnant female foster animal and the embryo brought to term. Progeny harboring the homologously recombined DNA in their germ cells can be used to breed animals in which all cells of the animal contain the homologously recombined DNA by germline transmission of the transgene. Methods for constructing homologous recombination nucleic acid molecules, e. g., vectors, or homologous recombinant animals are described further in Bradley, A. (1991) Curr. Opin. Biotechnol. 2 : 823-829 and in PCT International Publication Nos. : WO 90/11354 by Le Mouellec et al. ; WO 91/01140 by Smithies et al. ; WO 92/0968 by Zijlstra et al. ; and WO 93/04169 by Berns et al.

In another embodiment, transgenic non-human animals can be produced which contain selected systems which allow for regulated expression of the transgene. One example of such a system is the cre/loxP recombinase system of bacteriophage P I. For a description of the crelloxP recombinase system, see, e. g., Lakso et al. (1992) Proc. Natl.

Acad. Sci. USA 89 : 6232-6236. Another example of a recombinase system is the FLP recombinase system of Saccharomyces cerevisiae (O'Gorman et al. (1991) Science 251 : 1351-1355. If a cre/loxP recombinase system is used to regulate expression of the transgene, animals containing transgenes encoding both the Cre recombinase and a selected protein are required. Such animals can be provided through the construction of"double" transgenic animals, e. g., by mating two transgenic animals, one containing a transgene encoding a selected protein and the other containing a transgene encoding a recombinase.

Clones of the non-human transgenic animals described herein can also be produced according to the methods described in Wilmut, I. et al. (1997) Nature 385 : 810-813 and PCT International Publication Nos. WO 97/07668 and WO 97/07669. In brief, a cell, e. g., a somatic cell, from the transgenic animal can be isolated and induced to exit the growth cycle and enter Go phase. The quiescent cell can then be fused, e. g., through the use of electrical pulses, to an enucleated oocyte from an animal of the same species from which the quiescent cell is isolated. The reconstructed oocyte is then cultured such that it develops to morula or blastocyte and then transferred to pseudopregnant female foster animal. The offspring borne of this female foster animal will be a clone of the animal from which the cell, e. g., the somatic cell, is isolated.

IV. Pharmaceutical Compositions The OP nucleic acid molecules, fragments of OP proteins, and anti-OP antibodies (also referred to herein as"active compounds") of the invention can be incorporated into pharmaceutical compositions suitable for administration. Such compositions typically comprise the nucleic acid molecule, protein, or antibody and a pharmaceutically acceptable

carrier. As used herein the language"pharmaceutically acceptable carrier"is intended to include any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like, compatible with pharmaceutical administration. The use of such media and agents for pharmaceutically active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active compound, use thereof in the compositions is contemplated. Supplementary active compounds can also be incorporated into the compositions.

A pharmaceutical composition of the invention is formulated to be compatible with its intended route of administration. Examples of routes of administration include parenteral, e. g., intravenous, intradermal, subcutaneous, oral (e. g., inhalation), transdermal (topical), transmucosal, and rectal administration. Solutions or suspensions used for parenteral, intradermal, or subcutaneous application can include the following components : a sterile diluent such as water for injection, saline solution, fixed oils, polyethylene glycols, glycerine, propylene glycol or other synthetic solvents ; antibacterial agents such as benzyl alcohol or methyl parabens ; antioxidants such as ascorbic acid or sodium bisulfite ; chelating agents such as ethylenediaminetetraacetic acid ; buffers such as acetates, citrates or phosphates and agents for the adjustment of tonicity such as sodium chloride or dextrose. pH can be adjusted with acids or bases, such as hydrochloric acid or sodium hydroxide. The parenteral preparation can be enclosed in ampoules, disposable syringes or multiple dose vials made of glass or plastic.

Pharmaceutical compositions suitable for injectable use include sterile aqueous solutions (where water soluble) or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersion. For intravenous administration, suitable carriers include physiological saline, bacteriostatic water, Cremophor ELTM (BASF, Parsippany, NJ) or phosphate buffered saline (PBS). In all cases, the composition must be sterile and should be fluid to the extent that easy syringeability exists. It must be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms such as bacteria and fungi. The carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (for example, glycerol, propylene glycol, and liquid polyetheylene glycol, and the like), and suitable mixtures thereof. The proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants. Prevention of the action of microorganisms can be achieved by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, ascorbic acid, thimerosal, and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars, polyalcohols such as manitol, sorbitol, sodium chloride in the composition. Prolonged absorption of the injectable

compositions can be brought about by including in the composition an agent which delays absorption, for example, aluminum monostearate and gelatin.

Sterile injectable solutions can be prepared by incorporating the active compound (e. g., a fragment of an OP protein or an anti-OP antibody) in the required amount in an appropriate solvent with one or a combination of ingredients enumerated above, as required, followed by filtered sterilization. Generally, dispersions are prepared by incorporating the active compound into a sterile vehicle which contains a basic dispersion medium and the required other ingredients from those enumerated above. In the case of sterile powders for the preparation of sterile injectable solutions, the preferred methods of preparation are vacuum drying and freeze-drying which yields a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof.

Oral compositions generally include an inert diluent or an edible carrier. They can be enclosed in gelatin capsules or compressed into tablets. For the purpose of oral therapeutic administration, the active compound can be incorporated with excipients and used in the form of tablets, troches, or capsules. Oral compositions can also be prepared using a fluid carrier for use as a mouthwash, wherein the compound in the fluid carrier is applied orally and swished and expectorated or swallowed. Pharmaceutically compatible binding agents, and/or adjuvant materials can be included as part of the composition. The tablets, pills, capsules, troches and the like can contain any of the following ingredients, or compounds of a similar nature : a binder such as microcrystalline cellulose, gum tragacanth or gelatin ; an excipient such as starch or lactose, a disintegrating agent such as alginic acid, Primogel, or corn starch ; a lubricant such as magnesium stearate or Sterotes ; a glidant such as colloidal silicon dioxide ; a sweetening agent such as sucrose or saccharin ; or a flavoring agent such as peppermint, methyl salicylate, or orange flavoring.

For administration by inhalation, the compounds are delivered in the form of an aerosol spray from pressured container or dispenser which contains a suitable propellant, e. g., a gas such as carbon dioxide, or a nebulizer.

Systemic administration can also be by transmucosal or transdermal means. For transmucosal or transdermal administration, penetrants appropriate to the barrier to be permeated are used in the formulation. Such penetrants are generally known in the art, and include, for example, for transmucosal administration, detergents, bile salts, and fusidic acid derivatives. Transmucosal administration can be accomplished through the use of nasal sprays or suppositories. For transdermal administration, the active compounds are formulated into ointments, salves, gels, or creams as generally known in the art.

The compounds can also be prepared in the form of suppositories (e. g., with conventional suppository bases such as cocoa butter and other glycerides) or retention enemas for rectal delivery.

In one embodiment, the active compounds are prepared with carriers that will protect the compound against rapid elimination from the body, such as a controlled release formulation, including implants and microencapsulated delivery systems. Biodegradable, biocompatible polymers can be used, such as ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoesters, and polylactic acid. Methods for preparation of such formulations will be apparent to those skilled in the art. The materials can also be obtained commercially from Alza Corporation and Nova Pharmaceuticals, Inc. Liposomal suspensions (including liposomes targeted to infected cells with monoclonal antibodies to viral antigens) can also be used as pharmaceutically acceptable carriers. These can be prepared according to methods known to those skilled in the art, for example, as described in U. S. Patent No. 4, 522, 811.

It is especially advantageous to formulate oral or parenteral compositions in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used herein refers to physically discrete units suited as unitary dosages for the subject to be treated ; each unit containing a predetermined quantity of active compound calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier. The specification for the dosage unit forms of the invention are dictated by and directly dependent on the unique characteristics of the active compound and the particular therapeutic effect to be achieved, and the limitations inherent in the art of compounding such an active compound for the treatment of individuals.

Toxicity and therapeutic efficacy of such compounds can be determined by standard pharmaceutical procedures in cell cultures or experimental animals, e. g., for determining the LD50 (the dose lethal to 50% of the population) and the ED50 (the dose therapeutically effective in 50% of the population). The dose ratio between toxic and therapeutic effects is the therapeutic index and it can be expressed as the ratio LD50/ED50. Compounds which exhibit large therapeutic indices are preferred. While compounds that exhibit toxic side effects may be used, care should be taken to design a delivery system that targets such compounds to the site of affected tissue in order to minimize potential damage to uninfected cells and, thereby, reduce side effects.

The data obtained from the cell culture assays and animal studies can be used in formulating a range of dosage for use in humans. The dosage of such compounds lies preferably within a range of circulating concentrations that include the ED50 with little or no toxicity. The dosage may vary within this range depending upon the dosage form employed and the route of administration utilized. For any compound used in the method of the invention, the therapeutically effective dose can be estimated initially from cell culture assays. A dose may be formulated in animal models to achieve a circulating plasma concentration range that includes the IC50 (i. e., the concentration of the test compound

which achieves a half-maximal inhibition of symptoms) as determined in cell culture. Such information can be used to more accurately determine useful doses in humans. Levels in plasma may be measured, for example, by high performance liquid chromatography.

As defined herein, a therapeutically effective amount of protein or polypeptide (i. e., an effective dosage) ranges from about 0. 001 to 30 mg/kg body weight, preferably about 0. 01 to 25 mg/kg body weight, more preferably about 0. 1 to 20 mg/kg body weight, and even more preferably about 1 to 10 mg/kg, 2 to 9 mg/kg, 3 to 8 mg/kg, 4 to 7 mg/kg, or 5 to 6 mg/kg body weight. The skilled artisan will appreciate that certain factors may influence the dosage required to effectively treat a subject, including but not limited to the severity of the disease or disorder, previous treatments, the general health and/or age of the subject, and other diseases present. Moreover, treatment of a subject with a therapeutically effective amount of a protein, polypeptide, or antibody can include a single treatment or, preferably, can include a series of treatments.

In a preferred example, a subject is treated with antibody, protein, or polypeptide in the range of between about 0. 1 to 20 mg/kg body weight, one time per week for between about 1 to 10 weeks, preferably between 2 to 8 weeks, more preferably between about 3 to 7 weeks, and even more preferably for about 4, 5, or 6 weeks. It will also be appreciated that the effective dosage of antibody, protein, or polypeptide used for treatment may increase or decrease over the course of a particular treatment. Changes in dosage may result and become apparent from the results of diagnostic assays as described herein.

The present invention encompasses agents which modulate expression or activity.

An agent may, for example, be a small molecule. For example, such small molecules include, but are not limited to, peptides, peptidomimetics, amino acids, amino acid analogs, polynucleotides, polynucleotide analogs, nucleotides, nucleotide analogs, organic or inorganic compounds (i. e., including heteroorganic and organometallic compounds) having a molecular weight less than about 10, 000 grams per mole, organic or inorganic compounds having a molecular weight less than about 5, 000 grams per mole, organic or inorganic compounds having a molecular weight less than about 1, 000 grams per mole, organic or inorganic compounds having a molecular weight less than about 500 grams per mole, and salts, esters, and other pharmaceutically acceptable forms of such compounds. It is understood that appropriate doses of small molecule agents depends upon a number of factors within the ken of the ordinarily skilled physician, veterinarian, or researcher. The dose (s) of the small molecule will vary, for example, depending upon the identity, size, and condition of the subject or sample being treated, further depending upon the route by which the composition is to be administered, if applicable, and the effect which the practitioner desires the small molecule to have upon the nucleic acid or polypeptide of the invention.

Exemplary doses include milligram or microgram amounts of the small molecule per kilogram of subject or sample weight (e. g., about 1 microgram per kilogram to about 500 milligrams per kilogram, about 100 micrograms per kilogram to about 5 milligrams per kilogram, or about 1 microgram per kilogram to about 50 micrograms per kilogram. It is furthermore understood that appropriate doses of a small molecule depend upon the potency of the small molecule with respect to the expression or activity to be modulated. Such appropriate doses may be determined using the assays described herein. When one or more of these small molecules is to be administered to an animal (e. g., a human) in order to modulate expression or activity of a polypeptide or nucleic acid of the invention, a physician, veterinarian, or researcher may, for example, prescribe a relatively low dose at first, subsequently increasing the dose until an appropriate response is obtained. In addition, it is understood that the specific dose level for any particular animal subject will depend upon a variety of factors including the activity of the specific compound employed, the age, body weight, general health, gender, and diet of the subject, the time of administration, the route of administration, the rate of excretion, any drug combination, and the degree of expression or activity to be modulated.

In certain embodiments of the invention, a modulator of OP activity is administered in combination with other agents (e. g., a small molecule), or in conjunction with another, complementary treatment regime. For example, in one embodiment, a modulator of OP activity is used to treat a cellular proliferation ; growth, apoptosis, differentiation, and/or migration disorder. Accordingly, modulation of OP activity may be used in conjunction with, for example, another agent used to treat the disorder, e. g., a chemotherapeutic agent such as 5-FU.

Further, an antibody (or fragment thereof) may be conjugated to a therapeutic moiety such as a cytotoxin, a therapeutic agent or a radioactive metal ion. A cytotoxin or cytotoxic agent includes any agent that is detrimental to cells. Examples include taxol, cytochalasin B, gramicidin D, ethidium bromide, emetin, mitomycin, etoposide, tenoposide, vincristine, vinblastine, colchicin, doxorubicin, daunorubicin, dihydroxy anthracin dione, mitoxantrone, mithramycin, actinomycin D, 1-dehydrotestosterone, glucocorticoids, procaine, tetracaine, lidocaine, propranolol, and puromycin and analogs or homologs thereof. Therapeutic agents include, but are not limited to, antimetabolites (e. g., methotrexate, 6-mercaptopurine, 6- thioguanine, cytarabine, 5-fluorouracil decarbazine), alkylating agents (e. g., mechlorethamine, thioepa chlorambucil, melphalan, carmustine (BSNU) and lomustine (CCNU), cyclothosphamide, busulfan, dibromomannitol, streptozotocin, mitomycin C, and cis-dichlorodiamine platinum (II) (DDP) cisplatin), anthracyclines (e. g., daunorubicin (formerly daunomycin) and doxorubicin), antibiotics (e. g., dactinomycin (formerly

actinomycin), bleomycin, mithramycin, and anthramycin (AMC)), and anti-mitotic agents (e. g., vincristine and vinblastine).

The conjugates of the invention can be used for modifying a given biological response, the drug moiety is not to be construed as limited to classical chemical therapeutic agents. For example, the drug moiety may be a protein or polypeptide possessing a desired biological activity. Such proteins may include, for example, a toxin such as abrin, ricin A, pseudomonas exotoxin, or diphtheria toxin ; a protein such as tumor necrosis factor, alpha- interferon, beta-interferon, nerve growth factor, platelet derived growth factor, tissue plasminogen activator ; or, biological response modifiers such as, for example, lymphokines, interleukin-1 ("IL-1"), interleukin-2 ("IL-2"), interleukin-6 ("IL-6"), granulocyte macrophage colony stimulating factor ("GM-CSF"), granulocyte colony stimulating factor ("G-CSF"), or other growth factors.

Techniques for conjugating such therapeutic moiety to antibodies are well known, see, e. g., Arnon et al."Monoclonal Antibodies for Immunotargeting of Drugs in Cancer Therapy", in Monoclonal Antibodies and Cancer Therapy, Reisfeld et al. (eds.), pp. 243-56 (Alan R. Liss, Inc. 1985) ; Hellstrom et al."Antibodies For Drug Delivery", in Controlled Drug Delivery (2 dEd.), Robinson et al. (eds.), pp. 623-53 (Marcel Dekker, Inc. 1987) ; Thorpe,"Antibody Carriers Of Cytotoxic Agents In Cancer Therapy : A Review", in Monoclonal Antibodies'84 : Biological and Clinical Applications, Pinchera et al. (eds.), pp.

475-506 (1985) ;"Analysis, Results, and Future Prospective of the Therapeutic Use of Radiolabeled Antibody in Cancer Therapy", in Monoclonal Antibodies for Cancer Detection and Therapy, Baldwin et al. (eds.), pp. 303-16 (Academic Press 1985), and Thorpe et al.

"The Preparation and Cytotoxic Properties of Antibody-Toxin Conjugates", Immunol. Rev.

62 : 119-58 (1982). Alternatively, an antibody can be conjugated to a second antibody to form an antibody heteroconjugate as described by Segal in U. S. Patent No. 4, 676, 980.

The nucleic acid molecules of the invention can be inserted into vectors and used as gene therapy vectors. Gene therapy vectors can be delivered to a subject by, for example, intravenous injection, local administration (see U. S. Patent 5, 328, 470) or by stereotactic injection (see e. g., Chen et al. (1994) Proc. Natl. Acad. Sci USA 91 : 3054-3057). The pharmaceutical preparation of the gene therapy vector can include the gene therapy vector in an acceptable diluent, or can comprise a slow release matrix in which the gene delivery vehicle is imbedded. Alternatively, where the complete gene delivery vector can be produced intact from recombinant cells, e. g., retroviral vectors, the pharmaceutical preparation can include one or more cells which produce the gene delivery system.

The pharmaceutical compositions can be included in a container, pack, or dispenser together with instructions for administration.

V. Uses and Methods of the Invention The nucleic acid molecules, proteins, protein homologues, and antibodies described herein can be used in one or more of the following methods : a) screening assays ; b) predictive medicine (e. g., diagnostic assays, prognostic assays, monitoring clinical trials, and pharmacogenetics) ; and c) methods of treatment (e. g., therapeutic and prophylactic). As described herein, an OP protein of the invention has one or more of the following activities : the ability to bind an OP ligand or substrate (e. g., choline and/or an acceptor molecule to be reduced or oxidized) ; the ability to modulate metabolism of an OP ligand or substrate (e. g., metabolism of choline into betaine or homocysteine into methionine, and/or metabolism of other metabolites to be reduced or metabolites to be oxidized) ; the ability to modulate an oxidoreductase-associated signaling mechanism ; the ability to modulate cellular proliferation, apoptosis, or migration ; and/or the ability to modulate cellular proliferation, growth, apoptosis, differentiation, and/or migration disorders. Thus, an OP protein of the invention can be used to, for example, modulate the ability to bind an OP ligand or substrate (e. g., choline and/or an acceptor molecule to be reduced or oxidized) ; the ability to modulate metabolism of an OP ligand or substrate (e. g., metabolism of choline into betaine or homocysteine into methionine, and/or metabolism of other metabolites to be reduced or metabolites to be oxidized) ; the ability to modulate an oxidoreductase-associated signaling mechanism ; the ability to modulate cellular proliferation, apoptosis, or migration ; and/or the ability to modulate cellular proliferation, growth, apoptosis, differentiation, and/or migration disorders.

The isolated nucleic acid molecules of the invention can be used, for example, to express OP protein (e. g., via a recombinant expression vector in a host cell in gene therapy applications), to detect OP mRNA (e. g., in a biological sample) or a genetic alteration in an OP gene, and to modulate OP activity, as described further below. The OP proteins can be used to treat disorders characterized by insufficient or excessive production of an OP ligand or substrate or production of OP inhibitors. In addition, the OP proteins can be used to screen for naturally occurring OP ligands or substrates to screen for drugs or compounds which modulate OP activity, as well as to treat disorders characterized by insufficient or excessive production of OP protein or production of OP protein forms which have decreased, aberrant or unwanted activity compared to OP wild type protein (e. g., cellular proliferation, growth, apoptosis, differentiation, and/or migration disorders). Moreover, the anti-OP antibodies of the invention can be used to detect and isolate OP proteins, regulate the bioavailability of OP proteins, and modulate OP activity.

A. Screening Assays : The invention provides a method (also referred to herein as a"screening assay") for identifying modulators, ie., candidate or test compounds or agents (e. g., peptides, peptidomimetics, small molecules or other drugs) which bind to OP proteins, have a stimulatory or inhibitory effect on, for example, OP expression or OP activity, or have a stimulatory or inhibitory effect on, for example, the expression or activity of an OP ligand or substrate.

In one embodiment, the invention provides assays for screening candidate or test compounds which are substrates or ligands of an OP protein or polypeptide or biologically active portion thereof. In another embodiment, the invention provides assays for screening candidate or test compounds which bind to or modulate the activity of an OP protein or polypeptide or biologically active portion thereof. The test compounds of the present invention can be obtained using any of the numerous approaches in combinatorial library methods known in the art, including : biological libraries ; spatially addressable parallel solid phase or solution phase libraries ; synthetic library methods requiring deconvolution ; the 'one-bead one-compound'library method ; and synthetic library methods using affinity chromatography selection. The biological library approach is limited to peptide libraries, while the other four approaches are applicable to peptide, non-peptide oligomer or small molecule libraries of compounds (Lam, K. S. (1997) Anticancer Drug Des. 12 : 145).

Examples of methods for the synthesis of molecular libraries can be found in the art, for example in : DeWitt et al. (1993) Proc. Natl. Acad. Sci. USA 90 : 6909 ; Erb et al. (1994) Proc. natal. Acad. Sci. USA 91 : 11422 ; Zuckermannetal. (1994) R Med. Chem. 37 : 2678 ; Cho et al. (1993) Science 261 : 1303 ; Carrell et al. (1994) Angew. Chem. Int. Ed. Engl.

33 : 2059 ; Carell et al. (1994) Angew. Chem. Int. Ed. Engl. 33 : 2061 ; and in Gallop et al.

(1994) J Med Chem. 37 : 1233.

Libraries of compounds may be presented in solution (e. g., Houghten (1992) Biotechniques 13 : 412-421), or on beads (Lam (1991) Nature 354 : 82-84), chips (Fodor (1993) Nature 364 : 555-556), bacteria (Ladner USP 5, 223, 409), spores (Ladner US'409), plasmids (Cull et al. (1992) Proc. Natl. Acad. Sci. USA 89 : 1865-1869) or on phage (Scott and Smith (1990) Science 249 : 386-390) ; (Devlin (1990) Science 249 : 404-406) ; (Cwirla et al. (1990) Proc. Natl. Acad. Sci. 87 : 6378-6382) ; (Felici (1991) J. Mol. Biol. 222 : 301-310) ; (Ladner supra).

In one embodiment, an assay is a cell-based assay in which a cell which expresses an OP protein or biologically active portion thereof is contacted with a test compound and the ability of the test compound to modulate OP activity is determined. Determining the ability of the test compound to modulate OP activity can be accomplished by monitoring, for example, changes in intracellular betaine or methionine concentration by, e. g., flow

cytometry, or by the activity of an OP-regulated transcription factor. The cell, for example, can be of mammalian origin, e. g., a colon cell or a tumor cell.

The ability of the test compound to modulate OP binding to a ligand or substrate (e. g., choline and/or an acceptor molecule to be reduced or oxidized) or to bind to OP can also be determined. Determining the ability of the test compound to modulate OP binding to a ligand or substrate can be accomplished, for example, by coupling the OP ligand or substrate with a radioisotope or enzymatic label such that binding of the OP ligand or substrate to OP can be determined by detecting the labeled OP ligand or substrate in a complex. Determining the ability of the test compound to bind OP can be accomplished, for example, by coupling the compound with a radioisotope or enzymatic label such that binding of the compound to OP can be determined by detecting the labeled OP compound in a complex. For example, compounds (e. g., OP ligands or substrates) can be. labeled with 1251, 35S, 14C, or 3H, either directly or indirectly, and the radioisotope detected by direct counting of radioemission or by scintillation counting. Alternatively, compounds can be enzymatically labeled with, for example, horseradish peroxidase, alkaline phosphatase, or luciferase, and the enzymatic label detected by determination of conversion of an appropriate substrate to product.

It is also within the scope of this invention to determine the ability of a compound (e. g., an OP ligand or substrate such as choline and/or an acceptor molecule to be reduced or oxidized) to interact with OP without the labeling of any of the interactants. For example, a microphysiometer can be used to detect the interaction of a compound with OP without the labeling of either the compound or the OP. McConnell, H. M. et al. (1992) Science 257 : 1906-1912. As used herein, a"microphysiometer" (e. g., Cytosensor) is an analytical instrument that measures the rate at which a cell acidifies its environment using a light- addressable potentiometric sensor (LAPS). Changes in. this acidification rate can be used as an indicator of the interaction between a compound and OP.

In another embodiment, an assay is a cell-based assay comprising contacting a cell expressing an OP target molecule (e. g., an OP ligand or substrate such as choline and/or an acceptor molecule to be reduced or oxidized) with a test compound and determining the ability of the test compound to modulate (e. g., stimulate or inhibit) the activity of the OP target molecule. Determining the ability of the test compound to modulate the activity of an OP target molecule can be accomplished, for example, by determining the ability of the OP protein to bind to or interact with the OP target molecule.

Determining the ability of the OP protein or a biologically active fragment thereof, to bind to or interact with an OP target molecule or ligand (e. g., choline and/or an acceptor molecule to be reduced or oxidized) can be accomplished by one of the methods described above for determining direct binding. In a preferred embodiment, determining the ability of

the OP protein to bind to or interact with an OP target molecule or ligand can be accomplished by determining the activity of the target molecule. For example, the activity of the target molecule (e. g., catalytic/enzymatic activity) can be determined by monitoring the effect of the target on an appropriate substrate (e. g., choline and/or an acceptor molecule to be reduced or oxidized choline and/or an acceptor molecule to be reduced or oxidized), detecting the induction of a reporter gene (comprising a target-responsive regulatory element operatively linked to a nucleic acid encoding a detectable marker, e. g., luciferase), or detecting a target-regulated cellular response such as changes in betaine or methionine levels or changes in cellular proliferation responses. Methionine levels in cells (e. g., tumor cells) may be measured as described in, for example, Example 5 (infra), and in Tan et al.

(1999) Clin. Cancer Res. 5 : 2157-2163. Further methods related to methionine levels and tumor proliferation can be found in, for example, Guo et al. (1993) Cancer Res. 53 : 2479- 2483 ; Wu et al. (1998) Nutr. Cancer 32 : 13-19 ; Poirson-Bichat et al. (2000) Clin. Cancer Res. 6 : 643-653 ; and Mikol and Lipkin (1984) J. Natl. Cancer Inst. 72 : 19-22. Betaine levels may be measured as described in, for example, Zhang et al. (1992) Biochim. Biophys. Acta 1117 (3) : 333-9.

Determining the ability of the OP protein or a biologically active fragment thereof, to bind to or interact with an OP target molecule or ligand (e. g., choline and/or an acceptor molecule to be reduced or oxidized) can further be accomplished by measuring OP choline dehydrogenase activity (as described in, for example, Example 6 (infra), and in Zhang et al.

(1992) supra or Grossman and Hebert (1989) Am. J. Physiol. 256 (1 Pt. 2) : F107-12), or by measuring cellular proliferation using any one of the numerous methods known to those skilled in the art.

In yet another embodiment, an assay of the present invention is a cell-free assay in which an OP protein or biologically active portion thereof is contacted with a test compound and the ability of the test compound to bind to the OP protein or biologically active portion thereof is determined. Preferred biologically active portions of the OP proteins to be used in assays of the present invention include fragments which participate in interactions with non- OP molecules, e. g., fragments with high surface probability scores (see, for example, Figure 2). Binding of the test compound to the OP protein can be determined either directly or indirectly as described above. In a preferred embodiment, the assay includes contacting the OP protein or biologically active portion thereof with a known compound which binds OP to form an assay mixture, contacting the assay mixture with a test compound, and determining the ability of the test compound to interact with an OP protein, wherein determining the ability of the test compound to interact with an OP protein comprises determining the ability of the test compound to preferentially bind to OP or biologically active portion thereof as compared to the known compound.

In another embodiment, the assay is a cell-free assay in which an OP protein or biologically active portion thereof is contacted with a test compound and the ability of the test compound to modulate (e. g., stimulate or inhibit) the activity of the OP protein or biologically active portion thereof is determined. Determining the ability of the test compound to modulate the activity of an OP protein can be accomplished, for example, by determining the ability of the OP protein to bind to an OP target molecule by one of the methods described above for determining direct binding. Determining the ability of the OP protein to bind to an OP target molecule can also be accomplished using a technology such as real-time Biomolecular Interaction Analysis (BIA). Sjolander, S. and Urbaniczky, C.

(1991) Anal. Chem. 63 : 2338-2345 and Szabo et al. (1995) Curr. Opin. Struct. Biol. 5 : 699- 705. As used herein,"BIA"is a technology for studying biospecific interactions in real time, without labeling any of the interactants (e. g., BIAcore). Changes in the optical phenomenon of surface plasmon resonance (SPR) can be used as an indication of real-time reactions between biological molecules.

In an alternative embodiment, determining the ability of the test compound to modulate the activity of an OP protein can be accomplished by determining the ability of the OP protein to further modulate the activity of a downstream effector of an OP target molecule. For example, the activity of the effector molecule on an appropriate target can be determined or the binding of the effector to an appropriate target can be determined as previously described.

In yet another embodiment, the cell-free assay involves contacting an OP protein or biologically active portion thereof with a known compound which binds the OP protein (e. g., choline) to form an assay mixture, contacting the assay mixture with a test compound, and determining the ability of the test compound to interact with the OP protein, wherein determining the ability of the test compound to interact with the OP protein comprises determining the ability of the OP protein to preferentially bind to or modulate the activity of an OP target molecule.

In more than one embodiment of the above assay methods of the present invention, it may be desirable to immobilize either OP or its target molecule to facilitate separation of complexed from uncomplexed forms of one or both of the proteins, as well as to accommodate automation of the assay. Binding of a test compound to an OP protein, or interaction of an OP protein with a target molecule in the presence and absence of a candidate compound, can be accomplished in any vessel suitable for containing the reactants. Examples of such vessels include microtitre plates, test tubes, and micro- centrifuge tubes. In one embodiment, a fusion protein can be provided which adds a domain that allows one or both of the proteins to be bound to a matrix. For example, glutathione-S- transferase/OP fusion proteins or glutathione-S-transferase/target fusion proteins can be

adsorbed onto glutathione sepharose beads (Sigma Chemical, St. Louis, MO) or glutathione derivatized microtitre plates, which are then combined with the test compound or the test compound and either the non-adsorbed target protein or OP protein, and the mixture incubated under conditions conducive to complex formation (e. g., at physiological conditions for salt and pH). Following incubation, the beads or microtitre plate wells are washed to remove any unbound components, the matrix immobilized in the case of beads, complex determined either directly or indirectly, for example, as described above.

Alternatively, the complexes can be dissociated from the matrix, and the level of OP binding or activity determined using standard techniques.

Other techniques for immobilizing proteins on matrices can also be used in the screening assays of the invention. For example, either an OP protein or an OP target molecule can be immobilized utilizing conjugation of biotin and streptavidin. Biotinylated OP protein or target molecules can be prepared from biotin-NHS (N-hydroxy-succinimide) using techniques known in the art (e. g., biotinylation kit, Pierce Chemicals, Rockford, IL), and immobilized in the wells of streptavidin-coated 96 well plates (Pierce Chemical).

Alternatively, antibodies reactive with OP protein or target molecules but which do not interfere with binding of the OP protein to its target molecule can be derivatized to the wells of the plate, and unbound target or OP protein trapped in the wells by antibody conjugation.

Methods for detecting such complexes, in addition to those described above : for the GST- immobilized complexes, include immunodetection of complexes using antibodies reactive with the OP protein or target molecule, as well as enzyme-linked assays which rely on detecting an enzymatic activity associated with the OP protein or target molecule.

In another embodiment, modulators of OP expression are identified in a method wherein a cell is contacted with a candidate compound and the expression of OP mRNA or protein in the cell is determined. The level of expression of OP mRNA or protein in the presence of the candidate compound is compared to the level of expression of OP mRNA or protein in the absence of the candidate compound. The candidate compound can then be identified as a modulator of OP expression based on this comparison. For example, when expression of OP mRNA or protein is greater (statistically significantly greater) in the presence of the candidate compound than in its absence, the candidate compound is identified as a stimulator of OP mRNA or protein expression. Alternatively, when expression of OP mRNA or protein is less (statistically significantly less) in the presence of the candidate compound than in its absence, the candidate compound is identified as an inhibitor of OP mRNA or protein expression. The level of OP mRNA or protein expression in the cells can be determined by methods described herein for detecting OP mRNA or protein.

In yet another aspect of the invention, the OP proteins can be used as"bait proteins" in a two-hybrid assay or three-hybrid assay (see, e. g., U. S. Patent No. 5, 283, 317 ; Zervos et al. (1993) Cell 72 : 223-232 ; Madura et al. (1993) J : Biol. Chem. 268 : 12046-12054 ; Bartel et al. (1993) Biotechniques 14 : 920-924 ; Iwabuchi et al. (1993) Oncogene 8 : 1693-1696 ; and Brent W094/10300), to identify other proteins, which bind to or interact with OP ("OP- binding proteins"or"OP-bp") and are involved in OP activity. Such OP-binding proteins are also likely to be involved in the propagation of signals by the OP proteins or OP targets as, for example, downstream elements of an OP-mediated signaling pathway. Alternatively, such OP-binding proteins are likely to be OP inhibitors.

The two-hybrid system is based on the modular nature of most transcription factors, which consist of separable DNA-binding and activation domains. Briefly, the assay utilizes two different DNA constructs. In one construct, the gene that codes for an OP protein is fused to a gene encoding the DNA binding domain of a known transcription factor (e. g., GAL-4). In the other construct, a DNA sequence, from a library of DNA sequences, that encodes an unidentified protein ("prey"or"sample") is fused to a gene that codes for the activation domain of the known transcription factor. If the"bait"and the"prey"proteins are able to interact, in vivo, forming an OP-dependent complex, the DNA-binding and activation domains of the transcription factor are brought into close proximity. This proximity allows transcription of a reporter gene (e. g., LacZ) which is operably linked to a transcriptional regulatory site responsive to the transcription factor. Expression of the reporter gene can be detected and cell colonies containing the functional transcription factor can be isolated and used to obtain the cloned gene which encodes the protein which interacts with the OP protein.

In another aspect, the invention pertains to a combination of two or more of the assays described herein. For example, a modulating agent can be identified using a cell- based or a cell free assay, and the ability of the agent to modulate the activity of an OP protein can be confirmed in vivo, e. g., in an animal such as ; an animal model for tumorigenesis.

For example, the ability of the agent to modulate the activity of an OP protein can be tested in an animal such as an animal model for a cellular proliferation disorder, e. g., tumorigenesis. Animal based models for studying tumorigenesis in vivo are well known in the art (reviewed in Animal Models of Cancer Predisposition Syndromes, Hiai, H. and Hino, O. (eds.) 1999, Progress in Experimental Tumor Research, Vol. 35 ; Clarke, A. R. (2000) Carcinogenesis 21 : 435-41) and include, for example, carcinogen-induced tumors (Rithidech, K. et al. (1999) Mutat. Res. 428 : 33-39 ; Miller, M. L. et al. (2000) Environ. Mol.

Mutagen. 35 : 319-327), injection and/or transplantation of tumor cells into an animal, as well as animals bearing mutations in growth regulatory genes, for example, oncogenes (e. g., ras)

(Arbeit, J. M. et al. (1993) Am. J. Pathol. 142 : 1187-1197 ; Sinn, E. et al. (1987) Cell, 49 : 465- 475 ; Thorgeirsson, SS et al. Toxicol Lett (2000) 112-113 : 553-555) and tumor suppressor genes (e. g., p53) (Vooijs, M. et al. (1999) Oncogene 18 : 5293-5303 ; Clark A. R. (1995) Cancer Metast. Rev. 14 : 125-148 ; Kumar, T. R. et al. (1995) J. Intern. Med. 238 : 233-238 ; Donehower, L. A. et al. (1992) Nature 356215-221). Furthermore, experimental model systems are available for the study of, for example, ovarian cancer (Hamilton, T. C. et al.

(1984) Semin. Oncol. 11 : 285-298 ; Rahman, N. A. et al. (1998) Mol. Cell. Endocrinol.

145 : 167-174 ; Beamer, W. G. et al. (1998) Toxicol. Pathol. 26 : 704-710), gastric cancer (Thompson, J. et al. (2000) Int. J Cancer 86 : 863-869 ; Fodde, R. et al. (1999) Cytogenet.

Cell Genet. 86 : 105-111), breast cancer (Li, M. et al. (2000) Oncogene 19 : 1010-1019 ; Green, J. E. et al. (2000) Oncogene 19 : 1020-1027), melanoma (Satyamoorthy, K. et al.

(1999) Cancer Metast. Rev. 18 : 401-405), and prostate cancer (Shirai, T. et al. (2000) Mutat.

Res. 462 : 219-226 ; Bostwick, D. G. et al. (2000) Prostate 43 : 286-294).

This invention further pertains to novel agents identified by the above-described screening assays. Accordingly, it is within the scope of this invention to further use an agent identified as described herein in an appropriate animal model. For example, an agent identified as described herein (e. g., an OP modulating agent, an antisense OP nucleic acid molecule, an OP-specific antibody, or an OP-binding partner) can be used in an animal model to determine the efficacy, toxicity, or side effects of treatment with such an agent.

Alternatively, an agent identified as described herein can be used in an animal model to determine the mechanism of action of such an agent. Furthermore, this invention pertains to uses of novel agents identified by the above-described screening assays for treatments as described herein.

In another aspect, cell-based systems, as described herein, may be used to identify compounds which may act to ameliorate tumorigenic or apoptotic disease symptoms. For example, such cell systems may be exposed to a compound, suspected of exhibiting an ability to ameliorate tumorigenic or apoptotic disease symptoms, at a sufficient concentration and for a time sufficient to elicit such an amelioration of tumorigenic or apoptotic disease symptoms in the exposed cells. After exposure, the cells are examined to determine whether one or more of the tumorigenic or apoptotic disease cellular phenotypes has been altered to resemble a more normal or more wild type, non-tumorigenic disease or non-apoptotic disease phenotype. Cellular phenotypes that are associated with tumorigenic disease states include aberrant proliferation and migration, angiogenesis, anchorage independent growth, and loss of contact inhibition. Cellular phenotypes that are associated with apoptotic disease states include aberrant DNA fragmentation, membrane blebbing, caspase activity, and cytochrome c release from mitochondria.

In addition, animal-based tumorigenic disease systems, such as those described herein, may be used to identify compounds capable of ameliorating tumorigenic or apoptotic disease symptoms. Such animal models may be used as test substrates for the identification of drugs, pharmaceuticals, therapies, and interventions which may be effective in treating tumorigenic or apoptotic disease. For example, animal models may be exposed to a compound, suspected of exhibiting an ability to ameliorate tumorigenic or apoptotic disease symptoms, at a sufficient concentration and for a time sufficient to elicit such an amelioration of tumorigenic or apoptotic tumorigenic or apoptotic disease symptoms in the exposed animals. The response of the animals to the exposure may be monitored by assessing the reversal of disorders associated with tumorigenic disease, for example, by counting the number of tumors and/or measuring their size before and after treatment. In addition, the animals may be monitored by assessing the reversal of disorders associated with tumorigenic disease, for example, reduction in tumor burden, tumor size, and invasive and/or metastatic potential before and after treatment.

With regard to intervention, any treatments which reverse any aspect of tumorigenic or apoptotic disease symptoms should be considered as candidates for human tumorigenic or apoptotic disease therapeutic intervention. Dosages of test agents may be determined by deriving dose-response curves.

Additionally, gene expression patterns may be utilized to assess the ability of a compound to ameliorate cardiovascular or tumorigenic disease symptoms. For example, the expression pattern of one or more genes may form part of a"gene expression profile"or "transcriptional profile"which may be then be used in such an assessment."Gene expression profile"or"transcriptional profile", as used herein, includes the pattern of mRNA expression obtained for a given tissue or cell type under a given set of conditions.

Such conditions may include, but are not limited to, the presence of a tumor, e. g., a colon or lung tumor, including any of the control or experimental conditions described herein, for example, synchronized cells induced to enter the cell cycle, or RER-or Smad4 models.

Other conditions may include, for example, cell differentiation, transformation, metastasis, and carcinogen exposure. Gene expression profiles may be generated, for example, by utilizing a differential display procedure, Northern analysis and/or RT-PCR. In one embodiment, OP gene sequences may be used as probes and/or PCR primers for the generation and corroboration of such gene expression profiles.

Gene expression profiles may be characterized for known states, either tumorigenic or apoptotic disease or normal, within the cell-and/or animal-based model systems.

Subsequently, these known gene expression profiles may be compared to ascertain the effect a test compound has to modify such gene expression profiles, and to cause the profile to more closely resemble that of a more desirable profile.

For example, administration of a compound may cause the gene expression profile of a tumorigenic or apoptotic disease model system to more closely resemble the control system. Administration of a compound may, alternatively, cause the gene expression profile of a control system to begin to mimic a tumorigenic or apoptotic disease state. Such a compound may, for example, be used in further characterizing the compound of interest, or may be used in the generation of additional animal models.

B. Detection Assays Portions or fragments of the cDNA sequences identified herein (and the corresponding complete gene sequences) can be used in numerous ways as polynucleotide reagents. For example, these sequences can be used to : (i) map their respective genes on a chromosome ; and, thus, locate gene regions associated with genetic disease ; (ii) identify an individual from a minute biological sample (tissue typing) ; and (iii) aid in forensic identification of a biological sample. These applications are described in the subsections below.

1. Chromosome Mapping Once the sequence (or a portion of the sequence) of a gene has been isolated, this sequence can be used to map the location of the gene on a chromosome. This process is called chromosome mapping. Accordingly, portions or fragments of the OP nucleotide sequences, described herein, can be used to map the location of the OP genes on a chromosome. The mapping of the OP sequences to chromosomes is an important first step in correlating these sequences with genes associated with disease.

Briefly, OP genes can be mapped to chromosomes by preparing PCR primers (preferably 15-25 bp in length) from the OP nucleotide sequences. Computer analysis of the OP sequences can be used to predict primers that do not span more than one exon in the genomic DNA, thus complicating the amplification process. These primers can then be used for PCR screening of somatic cell hybrids containing individual human chromosomes. Only those hybrids containing the human gene corresponding to the OP sequences will yield an amplified fragment.

Somatic cell hybrids are prepared by fusing somatic cells from different mammals (e. g., human and mouse cells). As hybrids of human and mouse cells grow and divide, they gradually lose human chromosomes in random order, but retain the mouse chromosomes.

By using media in which mouse cells cannot grow, because they lack a particular enzyme, but human cells can, the one human chromosome that contains the gene encoding the needed enzyme, will be retained. By using various media, panels of hybrid cell lines can be established. Each cell line in a panel contains either a single human chromosome or a small

number of human chromosomes, and a full set of mouse chromosomes, allowing easy mapping of individual genes to specific human chromosomes (D'Eustachio P. et al. (1983) Science 220 : 919-924). Somatic cell hybrids containing only fragments of human chromosomes can also be produced by using human chromosomes with translocations and deletions.

PCR mapping of somatic cell hybrids is a rapid procedure for assigning a particular sequence to a particular chromosome. Three or more sequences can be assigned per day using a single thermal cycler. Using the OP nucleotide sequences to design oligonucleotide primers, sublocalization can be achieved with panels of fragments from specific chromosomes. Other mapping strategies which can similarly be used to map an OP sequence to its chromosome include in situ hybridization (described in Fan, Y. et al. (1990) Proc. Natl. Acad. Sci. USA 87 : 6223-27), pre-screening with labeled flow-sorted chromosomes, and pre-selection by hybridization to chromosome specific cDNA libraries.

Fluorescence in situ hybridization (FISH) of a DNA sequence to a metaphase chromosomal spread can further be used to provide a precise chromosomal location in one step. Chromosome spreads can be made using cells whose division has been blocked in metaphase by a chemical such as colcemid that disrupts the mitotic spindle. The chromosomes can be treated briefly with trypsin, and then stained with Giemsa. A pattern of light and dark bands develops on each chromosome, so that the chromosomes can be identified individually. The FISH technique can be used with a DNA sequence as short as 500 or 600 bases. However, clones larger than 1, 000 bases have a higher likelihood of binding to a unique chromosomal location with sufficient signal intensity for simple detection. Preferably 1, 000 bases, and more preferably 2, 000 bases will suffice to get good results at a reasonable amount of time. For a review of this technique, see Verma et al.

Human Chromosomes : A Manual of Basic Techniques (Pergamon Press, New York 1988).

Reagents for chromosome mapping can be used individually to mark a single chromosome or a single site on that chromosome, or panels of reagents can be used for marking multiple sites and/or multiple chromosomes. Reagents corresponding to noncoding regions of the genes actually are preferred for mapping purposes. Coding sequences are more likely to be conserved within gene families, thus increasing the chance of cross hybridizations during chromosomal mapping.

Once a sequence has been mapped to a precise chromosomal location, the physical position of the sequence on the chromosome can be correlated with genetic map data (such data are found, for example, in McKusick, V., Mendelian Inheritance in Man, available on- line through Johns Hopkins University Welch Medical Library). The relationship between a gene and a disease, mapped to the same chromosomal region, can then be identified through

linkage analysis (co-inheritance of physically adjacent genes), described in, for example, Egeland, J. et al. (1987) Nature 325 : 783-787.

Moreover, differences in the DNA sequences between individuals affected and unaffected with a disease associated with the OP gene, can be determined. If a mutation is observed in some or all of the affected individuals but not in any unaffected individuals, then the mutation is likely to be the causative agent of the particular disease. Comparison of affected and unaffected individuals generally involves first looking for structural alterations in the chromosomes, such as deletions or translocations that are visible from chromosome spreads or detectable using PCR based on that DNA sequence. Ultimately, complete sequencing of genes from several individuals can be performed to confirm the presence of a mutation and to distinguish mutations from polymorphisms.

2. Tissue Typing The OP sequences of the present invention can also be used to identify individuals from minute biological samples. The United States military, for example, is considering the use of restriction fragment length polymorphism (RFLP) for identification of its personnel.

In this technique, an individual's genomic DNA is digested with one or more restriction enzymes, and probed on a Southern blot to yield unique bands for identification. This method does not suffer from the current limitations of"Dog Tags"which can be lost, switched, or stolen, making positive identification difficult. The sequences of the present invention are useful as additional DNA markers for RFLP (described in U. S. Patent 5, 272, 057).

Furthermore, the sequences of the present invention can be used to provide an alternative technique which determines the actual base-by-base DNA sequence of selected portions of an individual's genome. Thus, the OP nucleotide sequences described herein can be used to prepare two PCR primers from the 5'and 3'ends of the sequences. These primers can then be used to amplify an individual's DNA and subsequently sequence it.

Panels of corresponding DNA sequences from individuals, prepared in this manner, can provide unique individual identifications, as each individual will have a unique set of such DNA sequences due to allelic differences. The sequences of the present invention can be used to obtain such identification sequences from individuals and from tissue. The OP nucleotide sequences of the invention uniquely represent portions of the human genome.

Allelic variation occurs to some degree in the coding regions of these sequences, and to a greater degree in the noncoding regions. It is estimated that allelic variation between individual humans occurs with a frequency of about once per each 500 bases. Each of the sequences described herein can, to some degree, be used as a standard against which DNA from an individual can be compared for identification purposes. Because greater numbers

of polymorphisms occur in the noncoding regions, fewer sequences are necessary to differentiate individuals. The noncoding sequences of SEQ ID NO : 1 can comfortably provide positive individual identification with a panel of perhaps 10 to 1, 000 primers which each yield a noncoding amplified sequence of 75-100 bases. If predicted coding sequences, such as those in SEQ ID NO : 3 are used, a more appropriate number of primers for positive individual identification would be 500-2, 000.

If a panel of reagents from OP nucleotide sequences described herein is used to generate a unique identification database for an individual, those same reagents can later be used to identify tissue from that individual. Using the unique identification database, positive identification of the individual, living or dead, can be made from extremely small tissue samples.

3. Use of Partial OP Sequences in Forensic Biology DNA-based identification techniques can also be used in forensic biology. Forensic biology is a scientific field employing genetic typing of biological evidence found at a crime scene as a means for positively identifying, for example, a perpetrator of a crime. To make such an identification, PCR technology can be used to amplify DNA sequences taken from very small biological samples such as tissues, e. g., hair or skin, or body fluids, e. g., blood, saliva, or semen found at a crime scene. The amplified sequence can then be compared to a standard, thereby allowing identification of the origin of the biological sample.

The sequences of the present invention can be used to provide polynucleotide reagents, e. g., PCR primers, targeted to specific loci in the human genome, which can enhance the reliability of DNA-based forensic identifications by, for example, providing another"identification marker" (i. e., another DNA sequence that is unique to a particular individual). As mentioned above, actual base sequence information can be used for identification as an accurate alternative to patterns formed by restriction enzyme generated fragments. Sequences targeted to noncoding regions of SEQ ID NO : 1 are particularly appropriate for this use as greater numbers of polymorphisms occur in the noncoding regions, making it easier to differentiate individuals using this technique. Examples of polynucleotide reagents include the OP nucleotide sequences or portions thereof, e. g., fragments derived from the noncoding regions of SEQ ID NO : 1, having a length of at least 20 bases, preferably at least 30 bases.

The OP nucleotide sequences described herein can further be used to provide polynucleotide reagents, e. g., labeled or labelable probes which can be used in, for example, an in situ hybridization technique, to identify a specific tissue, e. g., brain tissue. This can be very useful in cases where a forensic pathologist is presented with a tissue of unknown

origin. Panels of such OP probes can be used to identify tissue by species and/or by organ type.

In a similar fashion, these reagents, e. g., OP primers or probes can be used to screen tissue culture for contamination (i. e., screen for the presence of a mixture of different types of cells in a culture).

C. Predictive Medicine : The present invention also pertains to the field of predictive medicine in which diagnostic assays, prognostic assays, and monitoring clinical trials are used for prognostic (predictive) purposes to thereby treat an individual prophylactically. Accordingly, one aspect of the present invention relates to diagnostic assays for determining OP protein and/or nucleic acid expression as well as OP activity, in the context of a biological sample (e. g., blood, serum, cells, tissue) to thereby determine whether an individual is afflicted with a disease or disorder, or is at risk of developing a disorder, associated with aberrant or unwanted OP expression or activity, e. g., a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder. The invention also provides for prognostic (or predictive) assays for determining whether an individual is at risk of developing a disorder associated with OP protein, nucleic acid expression or activity. For example, mutations in an OP gene can be assayed in a biological sample. Such assays can be used for prognostic or predictive purpose to thereby prophylactically treat an individual prior to the onset of a disorder characterized by or associated with OP protein, nucleic acid expression or activity.

Another aspect of the invention pertains to monitoring the influence of agents (e. g., drugs, compounds) on the expression or activity of OP in clinical trials.

These and other agents are described in further detail in the following sections.

1. Diagnostic Assays An exemplary method for detecting the presence or absence of OP protein or nucleic acid in a biological sample involves obtaining a biological sample from a test subject and contacting the biological sample with a compound or an agent capable of detecting OP protein or nucleic acid (e. g., mRNA, or genomic DNA) that encodes OP protein such that the presence of OP protein or nucleic acid is detected in the biological sample. A preferred agent for detecting OP mRNA or genomic DNA is a labeled nucleic acid probe capable of hybridizing to OP mRNA or genomic DNA. The nucleic acid probe can be, for example, the OP nucleic acid set forth in SEQ ID NO : 1 or 3, or the DNA insert of the plasmid deposited with ATCC as Accession Number, or a portion thereof, such as an oligonucleotide of at least 15, 30, 50, 100, 250 or 500 nucleotides in length and sufficient to

specifically hybridize under stringent conditions to OP mRNA or genomic DNA. Other suitable probes for use in the diagnostic assays of the invention are described herein.

A preferred agent for detecting OP protein is an antibody capable of binding to OP protein, preferably an antibody with a detectable label. Antibodies can be polyclorial, or more preferably, monoclonal. An intact antibody, or a fragment thereof (e. g., Fab or F (ab') 2) can be used. The term"labeled", with regard to the probe or antibody, is intended to encompass direct labeling of the probe or antibody by coupling (ie., physically linking) a detectable substance to the probe or antibody, as well as indirect labeling of the probe or antibody by reactivity with another reagent that is directly labeled. Examples of indirect labeling include detection of a primary antibody using a fluorescently labeled secondary antibody and end-labeling of a DNA probe with biotin such that it can be detected with fluorescently labeled streptavidin. The term"biological sample"is intended to include tissues, cells and biological fluids isolated from a subject, as well as tissues, cells and fluids present within a subject. That is, the detection method of the invention can be used to detect OP mRNA, protein, or genomic DNA in a biological sample in vitro as well as in vivo. For example, in vitro techniques for detection of OP mRNA include Northern hybridizations and in situ hybridizations. In vitro techniques for detection of OP protein include enzyme linked immunosorbent assays (ELISAs), Western blots, immunoprecipitations and immunofluorescence. In vitro techniques for detection of OP genomic DNA include Southern hybridizations. Furthermore, in vivo techniques for detection of OP protein include introducing into a subject a labeled anti-OP antibody. For example, the antibody can be labeled with a radioactive marker whose presence and location in a subject can be detected by standard imaging techniques.

In one embodiment, the biological sample contains protein molecules from the test subject. Alternatively, the biological sample can contain mRNA molecules. from the test subject or genomic DNA molecules from the test subject. A preferred biological sample is a serum sample isolated by conventional means from a subject.

In another embodiment, the methods further involve obtaining a control biological sample from a control subject, contacting the control sample with a compound or agent capable of detecting OP protein, mRNA, or genomic DNA, such that the presence of OP protein, mRNA or genomic DNA is detected in the biological sample, and comparing the presence of OP protein, mRNA or genomic DNA in the control sample with the presence of OP protein, mRNA or genomic DNA in the test sample.

The invention also encompasses kits for detecting the presence of OP in a biological sample. For example, the kit can comprise a labeled compound or agent capable of detecting OP protein or mRNA in a biological sample ; means for determining the amount of OP in the sample ; and means for comparing the amount of OP in the sample with a standard.

The compound or agent can be packaged in a suitable container. The kit can further comprise instructions for using the kit to detect OP protein or nucleic acid.

2. Prognostic Assays The diagnostic methods described herein can furthermore be utilized to identify subjects having or at risk of developing a disease or disorder associated with aberrant or unwanted OP expression or activity, e. g., a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder. As used herein, the term"aberrant"includes an OP expression or activity which deviates from the wild type OP expression or activity.

Aberrant expression or activity includes increased or decreased expression or activity, as well as expression or activity which does not follow the wild type developmental pattern of expression or the subcellular pattern of expression. For example, aberrant OP expression or activity is intended to include the cases in which a mutation in the OP gene causes the OP gene to be under-expressed or over-expressed and situations in which such mutations result in a non-functional OP protein or a protein which does not function in a wild-type fashion, e. g., a protein which does not interact with an OP ligand (e. g., choline and/or an acceptor molecule to be reduced or oxidized), or one which interacts with a non-OP ligand (e. g., a co- factor, a metabolite to be reduced, a metabolite to be oxidized). As used herein, the term "unwanted"includes an unwanted phenomenon involved in a biological response such as aberrant metabolism of OP substrates (e. g., choline) or aberrant cellular functions and processes in which OP participates. For example, the term unwanted includes an OP expression or activity which is undesirable in a subject, such as aberrant cellular proliferation and/or migration. Examples of cellular proliferation, growth, apoptosis, differentiation, and/or migration disorders include tumors and/or cancers such as colon, lung, and brain tumors ; metastatic tumors, e. g., metastatic colon tumors ; neurodegenerative disorders, including stroke-associated apoptosis ; disorders associated with the production of betaine from choline ; and disorders associated with the recycling of methionine from homocysteine.

The assays described herein, such as the preceding diagnostic assays or the following assays, can be utilized to identify a subject having or at risk of developing a disorder associated with a misregulation in OP protein activity or nucleic acid expression. Such disorders include the disorders listed above.

Alternatively, the prognostic assays can be utilized to identify a subject having or at risk for developing a disorder associated with a misregulation in OP protein activity or nucleic acid expression, such as the disorders listed above Thus, the present invention provides a method for identifying a disease or disorder associated with aberrant or unwanted OP expression or activity in which a test sample is

obtained from a subject and OP protein or nucleic acid (e. g., mRNA or genomic DNA) is detected, wherein the presence of OP protein or nucleic acid is diagnostic for a subject having or at risk of developing a disease or disorder associated with aberrant or unwanted OP expression or activity. As used herein, a"test sample"refers to a biological sample obtained from a subject of interest. For example, a test sample can be a biological fluid (e. g., serum), cell sample (e. g. a tumor sample), or tissue (e. g., colon tissue).

Furthermore, the prognostic assays described herein can be used to determine whether a subject can be administered an agent (e. g., an agonist, antagonist, peptidomimetic, protein, peptide, nucleic acid, small molecule, or other drug candidate) to treat a disease or disorder associated with aberrant or unwanted OP expression or activity. For example, such methods can be used to determine whether a subject can be effectively treated with an agent for a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder.

Thus, the present invention provides methods for determining whether a subject can be effectively treated with an agent for a disorder associated with aberrant or unwanted OP expression or activity in which a test sample is obtained and OP protein or nucleic acid. expression or activity is detected (e. g., wherein the abundance of OP protein or nucleic acid expression or activity is diagnostic for a subject that can be administered the agent to treat a disorder associated with aberrant or unwanted OP expression or activity).

The methods of the invention can also be used to detect genetic alterations in an OP gene, thereby determining if a subject with the altered gene is at risk for a disorder characterized by misregulation in OP protein activity or nucleic acid expression, e. g., a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder. In preferred embodiments, the methods include detecting, in a sample of cells from the subject, the presence or absence of a genetic alteration characterized by at least one of an alteration affecting the integrity of a gene encoding an OP protein, or the mis-expression of the OP gene. For example, such genetic alterations can be detected by ascertaining the existence of at least one of 1) a deletion of one or more nucleotides from an OP gene ; 2) an addition of one or more nucleotides to an OP gene ; 3) a substitution of one or more nucleotides of an OP gene, 4) a chromosomal rearrangement of an OP gene ; 5) an alteration in the level of a messenger RNA transcript of an OP gene, 6) aberrant modification of an OP gene, such as of the methylation pattern of the genomic DNA, 7) the presence of a non-wild type splicing pattern of a messenger RNA transcript of an OP gene, 8) a non-wild type level of an OP protein, 9) allelic loss of an OP gene, and 10) inappropriate post-translational modification of an OP protein. As described herein, there are a large number of assays known in the art which can be used for detecting alterations in an OP gene. A preferred biological sample is a tissue or serum sample isolated by conventional means from a subject.

In certain embodiments, detection of the alteration involves the use of a probe/primer in a polymerase chain reaction (PCR) (see, e. g., U. S. Patent Nos. 4, 683, 195 and 4, 683, 202), such as anchor PCR or RACE PCR, or, alternatively, in a ligation chain reaction (LCR) (see, e. g., Landegran et al. (1988) Science 241 : 1077-1080 ; and Nakazawa et al. (1994) Proc.

Natl. Acad. Sci. USA 91 : 360-364), the latter of which can be particularly useful for detecting point mutations in the OP gene (see Abravaya et al. (1995) Nucleic Acids Res. 23 : 675-682).

This method can include the steps of collecting a sample of cells from a subject, isolating nucleic acid (e. g., genomic, mRNA or both) from the cells of the sample, contacting the nucleic acid sample with one or more primers which specifically hybridize to an OP gene under conditions such that hybridization and amplification of the OP gene (if present) occurs, and detecting the presence or absence of an amplification product, or detecting the size of the amplification product and comparing the length to a control sample. It is anticipated that PCR and/or LCR may be desirable to use as a preliminary amplification step in conjunction with any of the techniques used for detecting mutations described herein.

Alternative amplification methods include : self sustained sequence replication (Guatelli, J. C. et al. (1990) Proc. Natl. Acad. Sci. USA 87 : 1874-1878), transcriptional amplification system (Kwoh, D. Y. et al. (1989) Proc. Natl. Acad. Sci. USA 86 : 1173-1177), Q-Beta Replicase (Lizardi, P. M. et al. (1988) Bio-Technology 6 : 1197), or any other nucleic acid amplification method, followed by the detection of the amplified molecules using techniques well known to those of skill in the art. These detection schemes are especially useful for the detection of nucleic acid molecules if such molecules are present in very low numbers.

In an alternative embodiment, mutations in an OP gene from a sample cell can be identified by alterations in restriction enzyme cleavage patterns. For example, sample and control DNA is isolated, amplified (optionally), digested with one or more restriction endonucleases, and fragment length sizes are determined by gel electrophoresis and compared. Differences in fragment length sizes between sample and control DNA indicates mutations in the sample DNA. Moreover, the use of sequence specific ribozymes (see, for example, U. S. Patent No. 5, 498, 531) can be used to score for the presence of specific mutations by development or loss of a ribozyme cleavage site.

In other embodiments, genetic mutations in OP can be identified by hybridizing a sample and control nucleic acids, e. g., DNA or RNA, to high density arrays containing hundreds or thousands of oligonucleotides probes (Cronin, M. T. et al. (1996) Hum. Mutat.

7 : 244-255 ; Kozal, M. J. et al. (1996) Nat. Med. 2 : 753-759). For example, genetic mutations in OP can be identified in two dimensional arrays containing light-generated DNA probes as described in Cronin et al. (1996) supra. Briefly, a first hybridization array of probes can be used to scan through long stretches of DNA in a sample and control to identify base changes

between the sequences by making linear arrays of sequential overlapping probes. This step allows the identification of point mutations. This step is followed by a second hybridization array that allows the characterization of specific mutations by using smaller, specialized probe arrays complementary to all variants or mutations detected. Each mutation array is composed of parallel probe sets, one complementary to the wild-type gene and the other complementary to the mutant gene.

In yet another embodiment, any of a variety of sequencing reactions known in the art can be used to directly sequence the OP gene and detect mutations by comparing the sequence of the sample OP with the corresponding wild-type (control) sequence. Examples of sequencing reactions include those based on techniques developed by Maxam and Gilbert ( (1977) Proc. Natl. Acad Sci. USA 74 : 560) or Sanger ( (1977) Proc. Natl. Acad Sci. USA 74 : 5463). It is also contemplated that any of a variety of automated sequencing procedures can be utilized when performing the diagnostic assays ( (1995) Biotechniques 19 : 448), including sequencing by mass spectrometry (see, e. g., PCT International Publication No.

WO 94/16101 ; Cohen et al. (1996) Adv. Chromatogr. 36 : 127-162 ; and Griffin et al. (1993) Appl. Biochem. Biotechnol. 38 : 147-159).

Other methods for detecting mutations in the OP gene include methods in which protection from cleavage agents is used to detect mismatched bases in RNA/RNA or RNA/DNA heteroduplexes (Myers et al. (1985) Science 230 : 1242). In general, the art technique of"mismatch cleavage"starts by providing heteroduplexes of formed by hybridizing (labeled) RNA or DNA containing the wild-type OP sequence with potentially mutant RNA or DNA obtained from a tissue sample. The double-stranded duplexes are treated with an agent which cleaves single-stranded regions of the duplex such as which will exist due to basepair mismatches between the control and sample strands. For instance, RNA/DNA duplexes can be treated with RNase and DNA/DNA hybrids treated with S 1 nuclease to enzymatically digesting the mismatched regions. In other embodiments, either DNA/DNA or RNA/DNA duplexes can be treated with hydroxylamine or osmium tetroxide and with piperidine in order to digest mismatched regions. After digestion of the mismatched regions, the resulting material is then separated by size on denaturing polyacrylamide gels to determine the site of mutation. See, for example, Cotton et al.

(1988) Proc. Natl. Acad. Sci. USA 85 : 4397 ; Saleeba et al. (1992) Methods Enzymol.

217 : 286-295. In a preferred embodiment, the control DNA or RNA can be labeled for detection.

In still another embodiment, the mismatch cleavage reaction employs one or more proteins that recognize mismatched base pairs in double-stranded DNA (so called"DNA mismatch repair"enzymes) in defined systems for detecting and mapping point mutations in OP cDNAs obtained from samples of cells. For example, the mutY enzyme of E. coli

cleaves A at G/A mismatches and the thymidine DNA glycosylase from HeLa cells cleaves T at G/T mismatches (Hsu et al. (1994) Carcinogenesis 15 : 1657-1662). According to an exemplary embodiment, a probe based on an OP sequence, e. g., a wild-type OP sequence, is hybridized to a cDNA or other DNA product from a test cell (s). The duplex is treated with a DNA mismatch repair enzyme, and the cleavage products, if any, can be detected from electrophoresis protocols or the like. See, for example, U. S. Patent No. 5, 459, 039.

In other embodiments, alterations in electrophoretic mobility will be used to identify mutations in OP genes. For example, single strand conformation polymorphism (SSCP) may be used to detect differences in electrophoretic mobility between mutant and wild type nucleic acids (Orita et al. (1989) Proc. Natl. Acad. Sci. USA 86 : 2766, see also Cotton (1993) Mutat. Res. 285 : 125-144 ; and Hayashi (1992) Genet. Anal. Tech. Appl. 9 : 73-79). Single- stranded DNA fragments of sample and control OP nucleic acids will be denatured and allowed to renature. The secondary structure of single-stranded nucleic acids varies according to sequence, the resulting alteration in electrophoretic mobility enables the detection of even a single base change. The DNA fragments may be labeled or detected with labeled probes. The sensitivity of the assay may be enhanced by using RNA (rather than DNA), in which the secondary structure is more sensitive to a change in sequence. In a preferred embodiment, the subject method utilizes heteroduplex analysis to separate double stranded heteroduplex molecules on the basis of changes in electrophoretic mobility (Keen etal. (1991) Trends Genet. 7 : 5).

In yet another embodiment the movement of mutant or wild-type fragments in polyacrylamide gels containing a gradient of denaturant is assayed using denaturing gradient gel electrophoresis (DGGE) (Myers et al. (1985) Nature 313 : 495). When DGGE is used as the method of analysis, DNA will be modified to insure that it does not completely denature, for example by adding a GC clamp of approximately 40 bp of high-melting GC-rich DNA by PCR. In a further embodiment, a temperature gradient is used in place of a denaturing gradient to identify differences in the mobility of control and sample DNA (Rosenbaum and Reissner (1987) Biophys. Chem. 265 : 12753).

Examples of other techniques for detecting point mutations include, but are not limited to, selective oligonucleotide hybridization, selective amplification, or selective primer extension. For example, oligonucleotide primers may be prepared in which the known mutation is placed centrally and then hybridized to target DNA under conditions which permit hybridization only if a perfect match is found (Saiki et al. (1986) Nature 324 : 163) ; Saiki et al. (1989) Proc. Natl. Acad. Sci USA 86 : 6230). Such allele specific oligonucleotides are hybridized to PCR amplified target DNA or a number of different mutations when the oligonucleotides are attached to the hybridizing membrane and hybridized with labeled target DNA.

Alternatively, allele specific amplification technology which depends on selective PCR amplification may be used in conjunction with the instant invention. Oligonucleotides used as primers for specific amplification may carry the mutation of interest in the center of the molecule (so that amplification depends on differential hybridization) (Gibbs et al.

(1989) Nucleic Acids Res. 17 : 2437-2448) or at the extreme 3'end of one primer where, under appropriate conditions, mismatch can prevent, or reduce polymerase extension (Prossner (1993) Tibtech 11 : 238). In addition it may be desirable to introduce a novel restriction site in the region of the mutation to create cleavage-based detection (Gasparini et al. (1992) Mol. Cell Probes 6 : 1). It is anticipated that in certain embodiments amplification may also be performed using Taq ligase for amplification (Barany (1991) Proc. Natl. Acad.

Sci. USA 88 : 189). In such cases, ligation will occur, only if there is a perfect match at the 3' end of the 5'sequence making it possible to detect the presence of a known mutation at a specific site by looking for the presence or absence of amplification.

The methods described herein may be performed, for example, by utilizing pre- packaged diagnostic kits comprising at least one probe nucleic acid or antibody reagent described herein, which may be conveniently used, e. g., in clinical settings to diagnose patients exhibiting symptoms or family history of a disease or illness involving an OP gene.

Furthermore, any cell type or tissue in which OP is expressed may be utilized in the prognostic assays described herein.

3. Monitoring of Effects During Clinical Trials Monitoring the influence of agents (e. g., drugs) on the expression or activity of an OP protein (e. g., the modulation of metabolism and catabolism of biochemical molecules, e. g., molecules necessary for energy production or storage ; the modulation of betaine synthesis from choline ; the modulation of methionine synthesis from homocysteine ; the modulation of intra-or inter-cellular signaling ; the modulation of cellular proliferation and/or migration ; and/or the modulation of hormonal responses) can be applied not only in basic drug screening, but also in clinical trials. For example, the effectiveness of an agent determined by a screening assay as described herein to increase OP gene expression, protein levels, or upregulate OP activity, can be monitored in clinical trials of subjects exhibiting decreased OP gene expression, protein levels, or downregulated OP activity. Alternatively, the effectiveness of an agent determined by a screening assay to decrease OP gene expression, protein levels, or suppress OP activity, can be monitored in clinical trials of subjects exhibiting increased OP gene expression, protein levels, or upregulated OP activity.

In such clinical trials, the expression or activity of an OP gene, and preferably, other genes that have been implicated in, for example, cellular proliferation, growth, apoptosis,

differentiation, and/or migration disorders can be used as a"read out"or markers of the phenotype of a particular cell.

For example, and not by way of limitation, genes, including OP, that are modulated in cells by treatment with an agent (e. g., compound, drug or small molecule) which modulates OP activity (e. g., identified in a screening assay as described herein) can be identified. Thus, to study the effect of agents on cellular proliferation, growth, apoptosis, differentiation, and/or migration disorders, for example, in a clinical trial, cells can be isolated and RNA prepared and analyzed for the levels of expression of OP and other genes implicated in the cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder, respectively. The levels of gene expression (e. g., a gene expression pattern) can be quantified by northern blot analysis or RT-PCR, as described herein, or alternatively by measuring the amount of protein produced, by one of the methods as described herein, or by measuring the levels of activity of OP or other genes. In this way, the gene-expression pattern can serve as a marker, indicative of the physiological response of the cells to the agent. Accordingly, this response state may be determined before, and at various points during treatment of the individual with the agent.

In a preferred embodiment, the present invention provides a method for monitoring the effectiveness of treatment of a subject with an agent (e. g., an agonist, antagonist, peptidomimetic, protein, peptide, nucleic acid, small molecule, or other drug candidate identified by the screening assays described herein) including the steps of (i) obtaining a pre-administration sample from a subject prior to administration of the agent ; (ii) detecting the level of expression of an OP protein, mRNA, or genomic DNA in the preadministration sample ; (iii) obtaining one or more post-administration samples from the subject ; (iv) detecting the level of expression or activity of the OP protein, mRNA, or genomic DNA in the post-administration samples ; (v) comparing the level of expression or activity of the OP protein, mRNA, or genomic DNA in the pre-administration sample with the OP protein, mRNA, or genomic DNA in the post administration sample or samples ; and (vi) altering the administration of the agent to the subject accordingly. For example, increased administration of the agent may be desirable to increase the expression or activity of OP to higher levels than detected, i. e., to increase the effectiveness of the agent. Alternatively, decreased administration of the agent may be desirable to decrease expression or activity of OP to lower levels than detected, i. e., to decrease the effectiveness of the agent. According to such an embodiment, OP expression or activity may be used as an indicator of the effectiveness of an agent, even in the absence of an observable phenotypic response.

D. Methods of Treatment : The present invention provides for both prophylactic and therapeutic methods of treating a subject at risk of (or susceptible to) a disorder or having a disorder associated with aberrant or unwanted OP expression or activity, e. g., a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder. As used herein,"treatment"of a subject includes the application or administration of a therapeutic agent to a subject, or application or administration of a therapeutic agent to a cell or tissue from a subject, who has a diseases or disorder, has a symptom of a disease or disorder, or is at risk of (or susceptible to) a disease or disorder, with the purpose to cure, heal, alleviate, relieve, alter, remedy, ameliorate, improve, or affect the disease or disorder, the symptom of the disease or disorder, or the risk of (or susceptibility to) the'disease or disorder. As used herein, a "therapeutic agent"includes, but is not limited to, small molecules, peptides, polypeptides, antibodies, ribozymes, and antisense oligonucleotides.

With regards to both prophylactic and therapeutic methods of treatment, such treatments may be specifically tailored or modified, based on knowledge obtained from the field of pharmacogenomics."Pharmacogenomics", as used herein, refers to the application of genomics technologies such as gene sequencing, statistical genetics, and gene expression analysis to drugs in clinical development and on the market. More specifically, the term refers the study of how a patient's genes determine his or her response to a drug (e. g., a patient's"drug response phenotype", or"drug response genotype"). Thus, another aspect of the invention provides methods for tailoring an individual's prophylactic or therapeutic treatment with either the OP molecules of the present invention or OP modulators according to that individual's drug response genotype. Pharmacogenomics allows a clinician or physician to target prophylactic or therapeutic treatments to patients who will most benefit from the treatment and to avoid treatment of patients who will experience toxic drug-related side effects.

1. Prophylactic Methods In one aspect, the invention provides a method for preventing in a subject, a disease or condition associated with an aberrant or unwanted OP expression or activity, by administering to the subject an OP or an agent which modulates OP expression or at least one OP activity. Subjects at risk for a disease which is caused or contributed to by aberrant or unwanted OP expression or activity can be identified by, for example, any or a combination of diagnostic or prognostic assays as described herein. Administration of a prophylactic agent can occur prior to the manifestation of symptoms characteristic of the OP aberrancy, such that a disease or disorder is prevented or, alternatively, delayed in its progression. Depending on the type of OP aberrancy, for example, an OP, OP agonist or OP

antagonist agent can be used for treating the subject. The appropriate agent can be determined based on screening assays described herein.

2. Therapeutic Methods Another aspect of the invention pertains to methods of modulating OP expression or activity for therapeutic purposes. Accordingly, in an exemplary embodiment, the modulatory method of the invention involves contacting a cell with an OP or agent that modulates one or more of the activities of OP protein activity associated with the cell. An agent that modulates OP protein activity can be an agent as described herein, such as a nucleic acid or a protein, a naturally-occurring target molecule of an OP protein (e. g., an OP ligand or substrate), an OP antibody, an OP agonist or antagonist, a peptidomimetic of an OP agonist or antagonist, or other small molecule. In one embodiment, the agent stimulates one or more OP activities. Examples of such stimulatory agents include active OP protein and a nucleic acid molecule encoding OP that has been introduced into the cell. In another embodiment, the agent inhibits one or more OP activities. Examples of such inhibitory agents include antisense OP nucleic acid molecules, anti-OP antibodies, and OP inhibitors.

These modulatory methods can be performed in vitro (e. g., by culturing the cell with the agent) or, alternatively, in vivo (e. g., by administering the agent to a subject). As such, the present invention provides methods of treating an individual afflicted with a disease or disorder characterized by aberrant or unwanted expression or activity of an OP protein or nucleic acid molecule such as a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder. In one embodiment, the method involves administering an agent (e. g., an agent identified by a screening assay described herein), or combination of agents that modulates (e. g., upregulates or downregulates) OP expression or activity. In another embodiment, the method involves administering an OP protein or nucleic acid molecule as therapy to compensate for reduced, aberrant, or unwanted OP expression or activity.

Stimulation of OP activity is desirable in situations in which OP is abnormally downregulated and/or in which increased OP activity is likely to have a beneficial effect.

Likewise, inhibition of OP activity is desirable in situations in which OP is abnormally upregulated and/or in which decreased OP activity is likely to have a beneficial effect.

3. Pharmacogenomics The OP molecules of the present invention, as well as agents, or modulators which have a stimulatory or inhibitory effect on OP activity (e. g., OP gene expression) as identified by a screening assay described herein can be administered to individuals to treat (prophylactically or therapeutically) disorders associated with aberrant or unwanted OP activity (e. g., cellular proliferation, growth, apoptosis, differentiation, and/or migration

disorders). In conjunction with such treatment, pharmacogenomics (i. e., the study of the relationship between an individual's genotype and that individual's response to a foreign compound or drug) may be considered. Differences in metabolism of therapeutics can lead to severe toxicity or therapeutic failure by altering the relation between dose and blood concentration of the pharmacologically active drug. Thus, a physician or clinician may consider applying knowledge obtained in relevant pharmacogenomics studies in determining whether to administer an OP molecule or OP modulator as well as tailoring the dosage and/or therapeutic regimen of treatment with an OP molecule or OP modulator.

Pharmacogenomics deals with clinically significant hereditary variations in the response to drugs due to altered drug disposition and abnormal action in affected persons.

See, for example, Eichelbaum, M. et al. (1996) Clin. Exp. Pharmacol. Physiol. 23 (10- 11) : 983-985 and Linder, M. W. et al. (1997) Clin. Chen. 43 (2) : 254-266. In general, two types of pharmacogenetic conditions can be differentiated. Genetic conditions transmitted as a single factor altering the way drugs act on the body (altered drug action) or genetic conditions transmitted as single factors altering the way the body acts on drugs (altered drug metabolism). These pharmacogenetic conditions can occur either as rare genetic defects or as naturally-occurring polymorphisms. For example, glucose-6-phosphate dehydrogenase deficiency (G6PD) is a common inherited enzymopathy in which the main clinical complication is haemolysis after ingestion of oxidant drugs (anti-malarials, sulfonamides, analgesics, nitrofurans) and consumption of fava beans.

One pharmacogenomics approach to identifying genes that predict drug response, known as"a genome-wide association", relies primarily on a high-resolution map of the human genome consisting of already known gene-related markers (e. g., a"bi-allelic"gene marker map which consists of 60, 000-100, 000 polymorphic or variable sites on the human genome, each of which has two variants). Such a high-resolution genetic map can be compared to a map of the genome of each of a statistically significant number of patients taking part in a Phase 11/111 drug trial to identify markers associated with a particular observed drug response or side effect. Alternatively, such a high resolution map can be generated from a combination of some ten-million known single nucleotide polymorphisms (SNPs) in the human genome. As used herein, a"SNP"is a common alteration that occurs in a single nucleotide base in a stretch of DNA. For example, a SNP may occur once per every 1000 bases of DNA. A SNP may be involved in a disease process, however, the vast majority may not be disease-associated. Given a genetic map based on the occurrence of such SNPs, individuals can be grouped into genetic categories depending on a particular pattern of SNPs in their individual genome. In such a manner, treatment regimens can be tailored to groups of genetically similar individuals, taking into account traits that may be common among such genetically similar individuals.

Alternatively, a method termed the"candidate gene approach", can be utilized to identify genes that predict drug response. According to this method, if a gene that encodes a drugs target is known (e. g., an OP protein of the present invention), all common variants of that gene can be fairly easily identified in the population and it can be determined if having one version of the gene versus another is associated with a particular drug response.

As an illustrative embodiment, the activity of drug metabolizing enzymes is a major determinant of both the intensity and duration of drug action. The discovery of genetic polymorphisms of drug metabolizing enzymes (e. g., N-acetyltransferase 2 (NAT 2) and cytochrome P450 enzymes CYP2D6 and CYP2C19) has provided an explanation as to why some patients do not obtain the expected drug effects or show exaggerated drug response and serious toxicity after taking the standard and safe dose of a drug. These polymorphisms are expressed in two phenotypes in the population, the extensive metabolizer (EM) and poor metabolizer (PM). The prevalence of PM is different among different populations. For example, the gene coding for CYP2D6 is highly polymorphic and several mutations have been identified in PM, which all lead to the absence of functional CYP2D6. Poor metabolizers of CYP2D6 and CYP2C19 quite frequently experience exaggerated drug response and side effects when they receive standard doses. If a metabolite is the active therapeutic moiety, PM show no therapeutic response, as demonstrated for the analgesic effect of codeine mediated by its CYP2D6-formed metabolite morphine. The other extreme are the so called ultra-rapid metabolizers who do not respond to standard doses. Recently, the molecular basis of ultra-rapid metabolism has been identified to be due to CYP2D6 gene amplification.

Alternatively, a method termed the"gene expression profiling", can be utilized to identify genes that predict drug response. For example, the gene expression of an animal dosed with a drug (e. g., an OP molecule or OP modulator of the present invention) can give an indication whether gene pathways related to toxicity have been turned on.

Information generated from more than one of the above pharmacogenomics approaches can be used to determine appropriate dosage and treatment regimens for prophylactic or therapeutic treatment an individual. This knowledge, when applied to dosing or drug selection, can avoid adverse reactions or therapeutic failure and thus enhance therapeutic or prophylactic efficiency when treating a subject with an OP molecule or OP modulator, such as a modulator identified by one of the exemplary screening assays described herein.

4. Use of OP Molecules as Surrogate Markers The OP molecules of the invention are also useful as markers of disorders or disease states, as markers for precursors of disease states, as markers for predisposition of disease

states, as markers of drug activity, or as markers of the pharmacogenomic profile of a subject. Using the methods described herein, the presence, absence and/or quantity of the OP molecules of the invention may be detected, and may be correlated with one or more biological states in vivo. For example, the OP molecules of the invention may serve as surrogate markers for one or more disorders or disease states or for conditions leading up to disease states.

As used herein, a"surrogate marker"is an objective biochemical marker which correlates with the absence or presence of a disease or disorder, or with the progression of a disease or disorder (e. g :, with the presence or absence of a tumor). The presence or quantity of such markers is independent of the causation of the disease. Therefore, these markers may serve to indicate whether a particular course of treatment is effective in lessening a disease state or disorder. Surrogate markers are of particular use when the presence or extent of a disease state or disorder is difficult to assess through standard methodologies (e. g., early stage tumors), or when an assessment of disease progression is desired before a potentially dangerous clinical endpoint is reached (e. g., an assessment of cardiovascular disease may be made using cholesterol levels as a surrogate marker, and an analysis of HIV infection may be made using HIV RNA levels as a surrogate marker, well in advance of the undesirable clinical outcomes of myocardial infarction or fully-developed AIDS). Examples of the use of surrogate markers in the art include : Koomen et al. (2000) J. Mass. Spectrorn.

35 : 258-264 ; and James (1994) AIDS Treatment News Archive 209.

The OP molecules of the invention are also useful as pharmacodynamic markers. As used herein, a"pharmacodynamic markers an objective biochemical marker which correlates specifically with drug effects. The presence or quantity of a pharmacodynamic marker is not related to the disease state or disorder for which the drug is being administered ; therefore, the presence or quantity of the marker is indicative of the presence or activity of the drug in a subject. For example, a pharmacodynamic marker may be indicative of the concentration of the drug in a biological tissue, in that the marker is either expressed or transcribed or not expressed or transcribed in that tissue in relationship to the level of the drug. In this fashion, the distribution or uptake of the drug may be monitored by the pharmacodynamic marker. Similarly, the presence or quantity of the pharmacodynamic marker may be related to the presence or quantity of the metabolic product of a drug, such that the presence or quantity of the marker is indicative of the relative breakdown rate of the drug in vivo. Pharmacodynamic markers are of particular use in increasing the sensitivity of detection of drug effects, particularly when the drug is administered in low doses. Since even a small amount of a drug may be sufficient to activate multiple rounds of marker (e. g., an OP marker) transcription or expression, the amplified marker may be in a quantity which is more readily detectable than the drug itself. Also, the marker may be more easily

detected due to the nature of the marker itself ; for example, using the methods described herein, anti-OP antibodies may be employed in an immune-based detection system for an OP protein marker, or OP-specific radiolabeled probes may be used to detect an OP mRNA marker. Furthermore, the use of a pharmacodynamic marker may offer mechanism-based prediction of risk due to drug treatment beyond the range of possible direct observations.

Examples of the use of pharmacodynamic markers in the art include : Matsuda et al. US 6, 033, 862 ; Hattis et aL (1991) Env. Health Perspect. 90 : 229-238 ; Schentag (1999) Am. J.

Health-Syst. Pharm. 56 Suppl. 3 : S21-S24 ; and Nicolau (1999) Am. J Health-Syst. Pharm.

56 Suppl. 3 : S16-S20.

The OP molecules of the invention are also useful as pharmacogenomic markers. As used herein, a"pharmacogenomic marker"is an objective biochemical marker which correlates with a specific clinical drug response or susceptibility in a subject (see, e. g., McLeod et al. (1999) Eur. J. Cancer 35 (12) : 1650-1652). The presence or quantity of the pharmacogenomic marker is related to the predicted response of the subject to a specific drug or class of drugs prior to administration of the drug. By assessing the presence or quantity of one or more pharmacogenomic markers in a subject, a drug therapy which is most appropriate for the subject, or which is predicted to have a greater degree of success, may be selected. For example, based on the presence or quantity of RNA, or protein (e. g., OP protein or RNA) for specific tumor markers in a subject, a drug or course of treatment may be selected that is optimized for the treatment of the specific tumor likely to be present in the subject. Similarly, the presence or absence of a specific sequence mutation in OP DNA may correlate OP drug response. The use of pharmacogenomic markers therefore permits the application of the most appropriate treatment for each subject without having to administer the therapy.

E. Electronic Apparatus Readable Media and Arrays Electronic apparatus readable media comprising OP sequence information is also provided. As used herein,"OP sequence information"refers to any nucleotide and/or amino acid sequence information particular to the OP molecules of the present invention, including but not limited to full-length nucleotide and/or amino acid sequences, partial nucleotide and/or amino acid sequences, polymorphic sequences including single nucleotide polymorphisms (SNPs), epitope sequences, and the like. Moreover, information"related to" said OP sequence information includes detection of the presence or absence of a sequence (e. g., detection of expression of a sequence, fragment, polymorphism, etc.), determination of the level of a sequence (e. g., detection of a level of expression, for example, a quantitative detection), detection of a reactivity to a sequence (e. g., detection of protein expression and/or levels, for example, using a sequence-specific antibody), and the like. As used

herein,"electronic apparatus readable media"refers to any suitable medium for storing, holding, or containing data or information that can be read and accessed directly by an electronic apparatus. Such media can include, but are not limited to : magnetic storage media, such as floppy discs, hard disc storage medium, and magnetic tape ; optical storage media such as compact discs ; electronic storage media such as RAM, ROM, EPROM, EEPROM and the like ; and general hard disks and hybrids of these categories such as magnetic/optical storage media. The medium is adapted or configured for having recorded thereon OP sequence information of the present invention.

As used herein, the term"electronic apparatus"is intended to include any suitable computing or processing apparatus or other device configured or adapted for storing data or information. Examples of electronic apparatus suitable for use with the present invention include stand-alone computing apparatuses ; networks, including a local area network (LAN), a wide area network (WAN) Internet, Intranet, and Extranet ; electronic appliances such as a personal digital assistants (PDAs), cellular phone, pager and the like ; and local and distributed processing systems.

As used herein,"recorded"refers to a process for storing or encoding information on the electronic apparatus readable medium. Those skilled in the art can readily adopt any of the presently known methods for recording information on known media to generate manufactures comprising the OP sequence information.

A variety of software programs and formats can be used to store the sequence information on the electronic apparatus readable medium. For example, the sequence information can be represented in a word processing text file, formatted in commercially-available software such as WordPerfect and Microsoft Word, represented in the form of an ASCII file, or stored in a database application, such as DB2, Sybase, Oracle, or the like, as well as in other forms. Any number of dataprocessor structuring formats (e. g., text file or database) may be employed in order to obtain or create a medium having recorded thereon the OP sequence information.

By providing OP sequence information in readable form, one can routinely access the sequence information for a variety of purposes. For example, one skilled in the art can use the sequence information in readable form to compare a target sequence or target structural motif with the sequence information stored within the data storage means. Search means are used to identify fragments or regions of the sequences of the invention which match a particular target sequence or target motif.

The present invention therefore provides a medium for holding instructions for performing a method for determining whether a subject has an OP associated disease or disorder or a pre-disposition to a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder, wherein the method comprises the steps of determining OP

sequence information associated with the subject and based on the OP sequence information, determining whether the subject has a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder or a pre-disposition to a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder, and/or recommending a particular treatment for the disease, disorder, or pre-disease condition.

The present invention further provides in an electronic system and/or in a network, a method for determining whether a subject has a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder or a pre-disposition to a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder wherein the method comprises the steps of determining OP sequence information associated with the subject, and based on the OP sequence information, determining whether the subject has a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder or a pre-disposition to a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder, and/or recommending a particular treatment for the disease, disorder or pre-disease condition. The method may further comprise the step of receiving phenotypic information associated with the subject and/or acquiring from a network phenotypic information associated with the subject.

The present invention also provides in a network, a method for determining whether a subject has a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder or a pre-disposition to a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder associated with OP, said method comprising the steps of receiving OP sequence information from the subject and/or information related thereto, receiving phenotypic information associated with the subject, acquiring information from the network corresponding to OP and/or a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder, and based on one or more of the phenotypic information, the OP information (e. g., sequence information and/or information related thereto), and the acquired information, determining whether the subject has a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder or a pre-disposition to a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder. The method may further comprise the step of recommending a particular treatment for the disease, disorder or pre- disease condition.

The present invention also provides a business method for determining whether a subject has a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder or a pre-disposition to a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder, said method comprising the steps of receiving information related to OP (e. g., sequence information and/or information related thereto), receiving phenotypic information associated with the subject, acquiring information from the network related to

OP and/or related to a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder, and based on one or more of the phenotypic information, the OP information, and the acquired information, determining whether the subject has a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder or a pre- disposition to a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder. The method may further comprise the step of recommending a particular treatment for the disease, disorder or pre-disease condition.

The invention also includes an array comprising an OP sequence of the present invention. The array can be used to assay expression of one or more genes in the array. In one embodiment, the array can be used to assay gene expression in a tissue to ascertain tissue specificity of genes in the array. In this manner, up to about 7600 genes can be simultaneously assayed for expression, one of which can be OP. This allows a profile to be developed showing a battery of genes specifically expressed in one or more tissues.

In addition to such qualitative determination, the invention allows the quantitation of gene expression. Thus, not only tissue specificity, but also the level of expression of a battery of genes in the tissue is ascertainable. Thus, genes can be grouped on the basis of their tissue expression per se and level of expression in that tissue. This is useful, for example, in ascertaining the relationship of gene expression between or among tissues.

Thus, one tissue can be perturbed and the effect on gene expression in a second tissue can be determined. In this context, the effect of one cell type on another cell type in response to a biological stimulus can be determined. Such a determination is useful, for example, to know the effect of cell-cell interaction at the level of gene expression. If an agent is administered therapeutically to treat one cell type but has an undesirable effect on another cell type, the invention provides an assay to determine the molecular basis of the undesirable effect and thus provides the opportunity to co-administer a counteracting agent or otherwise treat the undesired effect. Similarly, even within a single cell type, undesirable biological effects can be determined at the molecular level. Thus, the effects of an agent on expression of other than the target gene can be ascertained and counteracted.

In another embodiment, the array can be used to monitor the time course of expression of one or more genes in the array. This can occur in various biological contexts, as disclosed herein, for example development of a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder, progression of a cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder, and processes, such a cellular transformation associated with the cellular proliferation, growth, apoptosis, differentiation, and/or migration disorder.

The array is also useful for ascertaining the effect of the expression of a gene on the expression of other genes in the same cell or in different cells (e. g., ascertaining the effect of

OP expression on the expression of other genes). This provides, for example, for a selection of alternate molecular targets for therapeutic intervention if the ultimate or downstream target cannot be regulated.

The array is also useful for ascertaining differential expression patterns of one or more genes in normal and abnormal cells. This provides a battery of genes (e. g., including OP) that could serve as a molecular target for diagnosis or therapeutic intervention.

This invention is further illustrated by the following examples which should not be construed as limiting. The contents of all references, patents and published patent applications cited throughout this application, as well as the Figures and the Sequence Listing, are incorporated herein by reference.

EXAMPLES EXAMPLE 1 : IDENTIFICATION AND CHARACTERIZATION OF HUMAN OP cDNA In this example, the identification and characterization of the gene encoding human OP (clone Fbh26343) is described.

Isolation of the human OP cDNA The invention is based, at least in part, on the discovery of a human gene encoding a novel protein, referred to herein as OP. The entire sequence of the human clone Fbh26343 was determined and found to contain an open reading frame termed"human OP."The nucleotide sequence encoding the human OP protein is shown in Figure 1 and is set forth as SEQ ID NO : 1. The protein encoded by this nucleic acid comprises about 594 amino acids and has the amino acid sequence shown in Figure 1 and set forth as SEQ ID NO : 2. The coding region (open reading frame) of SEQ ID NO : 1 is set forth as SEQ ID NO : 3. Clone Fbh26343, comprising the coding region of human OP, was deposited with the American Type Culture Collection (ATCC), 10801 University Boulevard, Manassas, VA 20110- 2209, on, and assigned Accession No.

Analysis of the Human OP Molecule A search for domain consensus sequences was performed using the amino acid sequence of human OP and a database of HMMs (the Pfam database, release 2. 1) using the default parameters (described above). The search revealed a GMC oxidoreductase signature

domain (Pfam label GMC oxred ; Pfam Accession Numbers PS00623 and PS00624) within SEQ ID NO : 2 at residues 41-567.

A search was performed against the ProDom database resulting in the identification of a portion of the deduced amino acid sequence of human OP (SEQ ID NO : 2) which has a 39% identity to ProDom entry"FAD flavoprotein oxidoreductase precursor dehydrogenase lyase signal protein cellobiose isoform") over residues 41 to 351 and 37% identical over residues 488-568. In addition, human OP is 50% identical to ProDom entry"L-sorbosone dehydrogenase, FAD dependent"over residues 501-573. In addition, human OP is 57% identical to ProDom entry"NADH : N-amido-scyllo-inosamine oxidoreductase"over residues 40-74 and 32% identical over residues 254 to 308. The results of this analysis are set forth in Figure 4.

A search was also performed against the Prosite database, and resulted in the identification of one possible glycosaminoglycan attachment site within the human OP protein at residues 308-311. In addition, protein kinase C phosphorylation sites were identified within the human OP protein at residues 81-83, 85-87, 283-285, 494-496, 515- 517, and 592-594. This search also identified casein kinase II phosphorylation sites at residues 37-40, 231-234, 415-418, 455-458, 494-497 of human OP. A tyrosine phosphorylation site motif was also identified in the human OP protein at residues 503-510.

The search also identified the presence of N-myristoylation site motifs at residues 20-25, 47- 52, 129-134, 296-301, 309-314, 329-334, 374-379, and 429-434. In addition, the search identified an amidation site at residues 234-237, and a GMC oxidoreductase signature sequence at amino acids 297-311 of human OP.

An analysis of the possible cellular localization of the human OP protein based on its amino acid sequence was performed using the methods and algorithms described in Nakai and Kanehisa (1992) Genomics 14 : 897-911, and available online through the PSORT server website. The results from this analysis predict that the human OP protein is found in the mitochondria, in the cytoplasm, in the nucleus, and in peroxisome.

An analysis of putative post-translationally truncated variants indicated that the mature protein may have residue 16 of SEQ ID NO : 2 (arginin) as the N-terminal residue.

EXAMPLE 2 : EXPRESSION OF RECOMBINANT HUMAN OP PROTEIN IN BACTERIAL CELLS In this example, human OP is expressed as a recombinant glutathione-S-transferase (GST) fusion polypeptide in E. coli and the fusion polypeptide is isolated and characterized.

Specifically, human OP is fused to GST and this fusion polypeptide is expressed in E. coli, e. g., strain PEB199. Expression of the GST-human OP fusion protein in PEB199 is induced with IPTG. The recombinant fusion polypeptide is purified from crude bacterial lysates of

the induced PEB 199 strain by affinity chromatography on glutathione beads. Using polyacrylamide gel electrophoretic analysis of the polypeptide purified from the bacterial lysates, the molecular weight of the resultant fusion polypeptide is determined.

EXAMPLE 3 : EXPRESSION OF RECOMBINANT HUMAN OP PROTEIN IN COS CELLS To express the human OP gene in COS cells, the pcDNA/Amp vector by Invitrogen Corporation (San Diego, CA) is used. This vector contains an SV40 origin of replication, an ampicillin resistance gene, an E. coli replication origin, a CMV promoter followed by a polylinker region, and an SV40 intron and polyadenylation site. A DNA fragment encoding the entire human OP protein and an HA tag (Wilson et al. (1984) Cell 37 : 767) or a FLAG tag fused in-frame to its 3'end of the fragment is cloned into the polylinker region of the vector, thereby placing the expression of the recombinant protein under the control of the CMV promoter.

To construct the plasmid, the human OP DNA sequence is amplified by PCR using two primers. The 5'primer contains the restriction site of interest followed by approximately twenty nucleotides of the human OP coding sequence starting from the initiation codon ; the 3'end sequence contains complementary sequences to the other restriction site of interest, a translation stop codon, the HA tag or FLAG tag and the last 20 nucleotides of the human OP coding sequence. The PCR amplified fragment and the pCDNA/Amp vector are digested with the appropriate restriction enzymes and the vector is dephosphorylated using the CIAP enzyme (New England Biolabs, Beverly, MA).

Preferably the two restriction sites chosen are different so that the human OP gene is inserted in the correct orientation. The ligation mixture is transformed into E. coli cells (strains HB101, DH5a, SURE, available from Stratagene Cloning Systems, La Jolla, CA, can be used), the transformed culture is plated on ampicillin media plates, and resistant colonies are selected. Plasmid DNA is isolated from transformants and examined by restriction analysis for the presence of the correct fragment.

COS cells are subsequently transfected with the human OP-pcDNA/Amp plasmid DNA using the calcium phosphate or calcium chloride co-precipitation methods, DEAE- dextran-mediated transfection, lipofection, or electroporation. Other suitable methods for transfecting host cells can be found in Sambrook, J. et al., Molecular Cloning : A Laboratory Manual. 2"d 2G', Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, 1989. The expression of the human OP polypeptide is detected by radiolabeling (35S-methionine or 35S-cysteine available from NEN, Boston, MA, can be used) and immunoprecipitation (Harlow, E. and Lane, D.

Ahtibodies : A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring

Harbor, NY, 1988) using an HA specific monoclonal antibody. Briefly, the cells are labeled for 8 hours with 35S-methionine (or 35S-cysteine). The culture media are then collected and the cells are lysed using detergents (RIPA buffer, 150 mM NaCl, 1% NP-40, 0. 1% SDS, 0. 5% DOC, 50 mM Tris, pH 7. 5). Both the cell lysate and the culture media are precipitated with an HA specific monoclonal antibody. Precipitated polypeptides are then analyzed by SDS-PAGE.

Alternatively, DNA containing the human OP coding sequence is cloned directly into the polylinker of the pCDNA/Amp vector using the appropriate restriction sites. The resulting plasmid is transfected into COS cells in the manner described above, and the expression of the human OP polypeptide is detected by radiolabeling and immunoprecipitation using a human OP specific monoclonal antibody.

EXAMPLE 4 : ANALYSIS OF HUMAN OP EXPRESSION This example describes the expression of human OP mRNA in various tissues, tumors, cell lines, and disease models, as determined using the TaqMan procedure and in situ hybridization analysis.

The Taqman procedure is a quantitative, real-time PCR-based approach to detecting mRNA. The RT-PCR reaction exploits the 5'nuclease activity of AmpliTaq Gold DNA Polymerase to cleave a TaqManTM probe during PCR. Briefly, cDNA was generated from the samples of interest and served as the starting material for PCR amplification. In addition to the 5'and 3'gene-specific primers, a gene-specific oligonucleotide probe (complementary to the region being amplified) was included in the reaction (i. e., the Taqman probe). The TaqManTM probe included an oligonucleotide with a fluorescent reporter dye covalently linked to the 5'end of the probe (such as FAM (6- carboxyfluorescein), TET (6-carboxy-4, 7, 2', 7'-tetrachlorofluorescein), JOE (6-carboxy-4, 5- dichloro-2, 7-dimethoxyfluorescein), or VIC) and a quencher dye (TAMRA (6-carboxy- N, N, N', N'-tetramethylrhodamine) at the 3'end of the probe.

During the PCR reaction, cleavage of the probe separated the reporter dye and the quencher dye, resulting in increased fluorescence of the reporter. Accumulation of PCR products was detected directly by monitoring the increase in fluorescence of the reporter dye. When the probe was intact, the proximity of the reporter dye to the quencher dye resulted in suppression of the reporter fluorescence. During PCR, if the target of interest was present, the probe specifically annealed between the forward and reverse primer sites.

The 5'-3'nucleolytic activity of the AmpliTaq Gold DNA Polymerase cleaved the probe between the reporter and the quencher only if the probe hybridized to the target. The probe fragments were then displaced from the target, and polymerization of the strand continued.

The 3'end of the probe was blocked to prevent extension of the probe during PCR. This

process occurred in every cycle and did not interfere with the exponential accumulation of product. RNA was prepared using the trizol method and treated with DNase to remove contaminating genomic DNA. cDNA was synthesized using standard techniques. Mock cDNA synthesis in the absence of reverse transcriptase resulted in samples with no detectable PCR amplification of the control GAPDH or p-actin gene confirming efficient removal of genomic DNA contamination.

For in situ analysis, various tissues, e. g., tissues obtained from liver or colon, were first frozen on dry ice. Ten-micrometer-thick sections of the tissues were postfixed with 4% formaldehyde in DEPC treated 1X phosphate-buffered saline (PBS) at room temperature for 10 minutes before being rinsed twice in DEPC IX phosphate-buffered saline and once in 0. 1 M triethanolamine-HCl (pH 8. 0). Following incubation in 0. 25% acetic anhydride-0. 1 M triethanolamine-HCl for 10 minutes, sections were rinsed in DEPC 2X SSC (1X SSC is 0. 15M NaCI plus 0. 015M sodium citrate). Tissues were then dehydrated through a series of ethanol washes, incubated in 100% chloroform for 5 minutes, and then rinsed in 100% ethanol for 1 minute and 95% ethanol for 1 minute and allowed to air dry.

Hybridizations were performed with 35 S-radiolabeled (5 x 107 cpm/ml) cRNA probes. Probes were incubated in the presence of a solution containing 600 mM NaCl, 10 mM Tris (pH 7. 5), 1 mM EDTA, 0. 01% sheared salmon sperm DNA, 0. 01% yeast tRNA, 0. 05% yeast total RNA type X1, 1X Denhardt's solutionv 50% formamide, 10% dextran sulfate, 100 mM dithiothreitol, 0. 1% sodium dodecyl sulfate (SDS), and 0. 1% sodium thiosulfate for 18 hours at 55°C.

After hybridization, slides were washed with 2X SSC. Sections were then sequentially incubated at 37°C in TNE (a solution containing 10 mM Tris-HCl (pH 7. 6), 500 mM NaCl, and 1 mM EDTA), for 10 minutes, in TNE with 10 pg of RNase A per ml for 30 minutes, and finally in TNE for 10 minutes. Slides were then rinsed with 2X SSC at room temperature, washed with 2X SSC at 50°C for 1 hour, washed with 0. 2X SSC at 55°C for 1 hour, and 0. 2X SSC at 60°C for 1 hour. Sections were then dehydrated rapidly through serial ethanol-0. 3 M sodium acetate concentrations before being air dried and exposed to Kodak Biomax MR scientific imaging film for 24 hours and subsequently dipped in NB-2 photoemulsion and exposed at 4°C for 7 days before being developed and counter stained.

As indicated by the data obtained from the Taqman analysis, human OP was expressed highly in the following tissues : normal fetal heart, normal brain cortex, brain (hypothalamus), brain (glioblastoma), normal breast, breast tumor (IDC), prostate tumor, colon tumor, normal kidney, normal liver, fibrotic liver, normal fetal liver, and skeletal muscle. Human OP is also expressed in the following tissues : normal heart, heart (congestive heart failure), normal spinal cord, normal prostate, normal ovary, and lung (chronic obstructive pulmonary disease).

Human OP showed increased expression in 100% of the clinical colon tumor samples tested, compared with clinical normal colon tissue samples.

Human OP showed increased expression in 100% of the clinical liver metastasis samples tested, compared with clinical normal liver tissue samples.

Human OP showed increased expression in 57% of the clinical lung tumors tested, compared with clinical normal lung tissue samples.

Human OP showed expression in most Xenograft friendly cell lines, e. g., MCF-7, ZR75, T47D, DLD-1, SW 480, SW 620, HCT 116, Colo 205, NCIH 125, NCIH 322, NCIH 460, and A549. Colon tumor cell lines show increased OP expression in later stages as follows : Cell line Stage Relative Expression SW 480 B 8. 0 HCT 116 B/C 20. 6 DLD-1 C 19. 9 Colo 205 Ascites 62. 5 SW 620 Lymph Metastasis 104. 7 The results from the in situ hybridization analysis indicate that human OP is expressed in 100% of primary colon tumors tested and 100% of metastatic tumors tested, as compared to 0% in normal tissues tested.

The data also indicate that human OP is focally expressed in 20% of lung tumors tested, as compared to 0% of the corresponding normal tissues.

EXAMPLE 5 : CELL CYCLE ANALYSIS This example describes the results from studies designed to determine how the expression of human OP mRNA is regulated during the cell cycle.

Transcriptional profiling analysis showed that human OP expression was increased in aphidocholine synchronized MCFlOa cells within the GO/G1 phase of the cell cycle.

Human OP also showed cell cycle regulated expression in aphidocholine synchronized HCT 116 colon carcinoma cells, with higher expression in the G2/M phase of the cell cycle.

Human OP also showed cell cycle regulated expression in aphidocholine synchronized A549 lung carcinoma cells.

Reintroduction of Smad4, a tumor supressor gene in the TGFß signaling pathway, into SW 480 cells (colon carcinoma cells that are deficient in the expression of Smad4) by transient transfection caused a decrease in the expression of human OP in these cells.

Human OP expression was upregulated in the RER- (replication error) cell lines Caco2 and SW 480, as compared to RER+ cell lines. RER-cell lines have increased difficulty in mismatch repair during DNA replication.

Increased expression of human OP in RER-cells and in Smad4 deficient cells indicates that increased human OP expression is associated with situations known to cause progression to later stage tumors, ie., errors in TGF P signaling and mismatch repair.

EXAMPLE 6 : MEASUREMENT OF METHIONINE LEVELS IN TUMOR CELLS This example describes the measurement of methionine levels in tumor cells, as may be determined using the methods of Tan, Y. et al. (1999) Clin. Cancer Res. 5 : 2157-2163, the contents of which are incorporated herein by reference.

Briefly, tumor methionine levels are determined using an HPLC machine (Hitachi L- 5200A Intelligent pump ; Hitachi, Ltd., Tokyo, Japan) after derivitization of serum amino acids with the fluoraldehyde reagent OPA as described in Tan, Y. et al. (1997) Anticancer Res. l 7 : 3857-3860 and Lishko, V. K. et ale (1993) Anticancer Res. 13 : 1465-1468.

Supernatants are prepared from tumor tissue after sonication for 30 seconds and subsequent centrifugation at 13, 000 rpm for 10 minutes. Tumor supernatant samples (25 ul) are precipitated by acetonitrile (75 lli). Ten, ul of supernatant are mixed with 5 ul of OPA.

After 1 minute, 50 u. of 0. 1 M sodium acetate (pH 7. 0) are added, and a 20 cl sample is loaded on a reversed-phase Supelcosil LC-18-DB column (particle size : 5 urn, 25 cm x 4. 8 mm) at room temperature. The column is eluted with solution A (tetrahydrofuran : methanol : 0. 1 M sodium acetate (pH 7. 2) ; 5 : 95 : 900) and solution B (methanol). A gradient from 20-60% of solution B, run a flow rate of 1. 5 ml/min, resolves the amino acids. The eluate is read with a fluorescence spectrophotometer (Hitachi, F 1000) at a wavelength of 350-450 nm. The limit of detection is-0. 1 uM methionine.

EXAMPLE 7 : MEASUREMENT OF OP CHOLINE DEHYDROGENASE ACTIVITY This example describes the measurement of OP choline dehydrogenase activity in cells, as may be determined using the methods of Zhang, J. et al. (1992) Biochim. Biophys.

Acta 1117 : 333-339, the contents of which are incorporated herein by reference.

The following methods are used to assay the choline dehydrogenase activity of the OP molecules of the invention. The methods are performed with purified OP molecules, or with mitochondrial preparations containing OP molecules, as described below.

Preparation of mitochondria A 12 gram wet weight tissue or cell sample (e. g., a normal tissue or cell sample, or a tumor sample) is homogenized in 108 ml 0. 25 M sucrose at a temperature of not more than 4°C and centrifuged at 700 x g at 4°C for 8 minutes. The supernatant is subsequently centrifuged at 17, 000 x g at 4°C for 10 minutes. The resulting mitochondrial pellet is resuspended in 30 ml of 0. 25 M sucrose and repeatedly treated as above at least three times.

The purity of the mitochondria is confirmed by determining the activities of a mitochondrial marker, fumarase (Stenech, J. (1984) in Experimental Biochemistry (Stenech, J., ed.), pp. 400-401, Allyn and Bacon, Boston) ; a cytosolic marker, lactate dehydrogenase (Worthington Biochemicals, Freehold, NJ) ; and a microsomal marker, glucose-6- phosphatase (Leloir, L. F. and Cardini, C. E. (1975) Methods Enzymol. 3 : 840-844). This preparation is kept frozen at-90°C until used. The protein concentration of the mitochondria is determined by the method of Bradford ( (1976) Anal.. Biochem. 72 : 248-254).

Colorimetric OP choline dehydrogenase assay OP choline dehydrogenase activity may be measured by the PMS-DCIP colorimetric method, as described in Singer, T. P. (1974) in Methods of Biochemical Analysis (Glick, D., ed.), Vol. 22, pp. 133-169, John Wiley, New York ; and Rendina, G. and Singer, [. P. (1959) J Biol. Chem. 234 : 1605-1610.

Radioenzymatic assay of OP choline dehydrogenase activity A mitochondrial preparation containing OP molecules, made using the methods described above, is incubated with [methyl-14G] choline (55 mCi/mmol ; ICN Biomedicals, Irvine, CA) in reaction medium containing 40 mM Tris buffer (pH 7. 6) or 40 mM glycine buffer (pH 8. 5) for varying amounts of time at 37°C. The reaction is inactivated by adding 1/10 of the reaction volume in the form of 1. 2 M HC1. Mixtures are extracted with one reaction volume of methanol and 2 volumes of chloroform. After briefly vortexing at room temperature, the phases are separated by low speed centrifugation and collected.

HPLC purification of choline, betaine aldehyde, and betaine 50 p1 of the methanol-water phase (see above) is mixed with 100 1 of methanol and then analyzed by HPLC (3 x 8C Pecosphere Cartridge, silica column (Perkin Elmer, Norwalk, CT)). The reaction products are eluted (at a flow rate of 1. 5 ml/minute) with

buffer A containing 800 ml acetonitrile, 68 ml ethanol, 5 ml of 3 : 2 (v/v) 1. 0 M ammonium acetate-glacial acetic acid buffer, 127 ml water, and 10 ml 1. 0 M potassium dihydrogen phosphate. The radioactivity of the eluent is determined using an on-line solid scintillant radiometric detector (Model BL 507A, Berthold, Nashua, NH). The efficiency of detection is determined using radiolabeled standards. After each sample is run, the column is washed for 5 minutes with buffer B containing the same components as buffer A in the following volumes (ml) : 400 : 68 : 132 : 400 : 10. In a typical chromatogram, only the three peaks of interest are detected, i. e., the [methyl-14C] choline substrate, and the two oxidation products, betaine aldehyde and betaine (betaine aldehyde is an intermediate in the two-step oxidation process that produces betaine from choline). The combined radioactivity in these three peaks is taken as 100%. In order to determine the amount of each product formed, the following formula is used : DPM in peak moles of product = total DPM x moles choline substrate in incubation medium PartialpuriClcation of OP choline dehydrogenase Mitochondria are centrifuged at 17, 000 x g at 4°C to remove the original buffer. The mitochondrial pellet is resuspended in 1. 2 M sucrose, 0. 05 mM EDTA, and 40 mM ammonium acetate for 45 minutes at 25°C. The resulting preparation is centrifuged at 24, 000 x g at 4°C for 10 minutes (Beckman, Ti 50. 2 rotor). The resulting pellet is referred to interchangeably herein as an"aged mitochondrial pellet"or"aged mitochondria" (Lin, C. S. and Wu, R. D. (1986) J Prot. Chem. 5 : 193-200).

The aged mitochondrial pellet is resuspended by gentle stirring in 60 mM glycine- NaOH buffer (pH 10) at 4°C for 40 minutes. The resulting preparation is centrifuged at 24, 000 x g at 4°C for 10 minutes. The supernatant is discarded after centrifugation.

The pellet is extracted with 0. 2 mg digitonin per mg protein. Digitonin is dissolved in 0. 25 M warm sucrose and sonicated with a probe sonicator for 1-2 minutes and then chilled and gently added drop-wise to the mitochondrial preparation over a 5 minutes period. After incubation for 25 minutes at 4°C, the preparation is centrifuged at 24, 000 x g at 4°C for 10 minutes. The pellet is resuspended in 0. 25 M NaCl (Lin and Wu (1986) supra).

The digitonin-extracted mitochondrial preparation in 0. 25 M NaCl is sonicated at 4°C for 5 minutes and subsequently centrifuged at 100, 000 x g at 4°C for 30 minutes (Beckman, Ti 50. 2 rotor). The pellet is resuspended in a buffer containing 0. 12 M sucrose,

0. 05 mM EDTA, 6. 0 mM choline (Fisher, Springfield, NJ ; recrystallized in methanol), 0. 03 M potassium phosphate, and 1. 0 M NaCl. Lubrol WX (0. 2 mg per mg protein ; Serva, Feinbiochemica, Heidelberg, Germany) is added, the preparation is shaken for 10 minutes at 4°C and subsequently centrifuged at 100, 000 x g for 30 minutes. The solubilized OP molecules are present in the supernatant (Lin and Wu (1986) supra).

Thin layer chromatography separation of choline oxidation product Choline, betaine aldehyde, and betaine are purified by thin layer chromatography on silica gel plates (LK5D ; Whatman Company) developed with a mixture containing chloroform, methanol, and 0. 1 M HC1 (65 : 30 : 4 ; v/v) and visualized by staining in iodine vapor.

Measurement of OY choline dehydrogenase activity In one experiment, 62. 5 u. g OP protein (mitochondrial preparation) is incubated with 0. 572 u. Ci, 0. 15 mM [methyl-14C] choline in Tris buffer (pH 7. 6) at 37°C. The total reaction volume is 150 u. l. In another experiment, 31. 5 u. g OP protein (mitochondrial preparation) is incubated with 0. 27 JlCi, 0. 13 mM [methyl-14C] choline in Tris buffer (pH 8. 5) at 37°C. The total reaction volume is 150 Ill. In still another experiment, varying amounts of OP protein (mitochondrial preparation) are incubated with 0. 92 u. Ci, 0. 2 mM [methyl-l4C] choline in Tris buffer (pH 7. 6) for 10 minutes at 37°C. The total reaction volume is 150 In another experiment, the effect of electron acceptors and cyanide on OP activity is measured. 0. 5 mg of OP protein (mitochondrial preparation) is incubated with 0. 1 mM, 0. 41 pLCi [methyl-14C] choline in Kregs-Hanseleit buffer (pH 7. 75), in the presence of 1 mM potassium cyanide (KCN), phenazine methosulfate (PMS) and dichloroindophenol (DCIP), or PMS, DCIP, and KCN. The total reaction volume is 0. 5 ml. The reaction mixture is incubated at 37°C for 20 minutes. In another experiment, 11 ug OP protein (solubilized preparation) is incubated with 20 nmol, 0. 271lCi [methyl-il4C] choline. at 37°C in 0. 01 M KH2PO4 (pH 7. 7) for 40 minutes in the presence or absence of 0. 1 mM NAD+, or 1. 0 mM PMS, or 0. 1 mM PMS and 0. 1 mM NAD+ together. The total reaction volume is 195 ul.

In another experiment, the effect of changes in pH on OP activity is measured. 63 llg OP protein is incubated in 40 mM phosphate, 40 mM glycine, 40 mM Hepes, 40 mM boric acid, or 40 mM Tris buffer at different pH. The [methyl-14C] choline concentration is 0. 8 u. Ci, 0. 19 mM for Tris-HCl and phosphate buffer, and 0. 25 u. Ci, 0. 13 mM for other buffers. The reactions are carried out at 37°C for 10 minutes.

Equivalents Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments of the invention described herein. Such equivalents are intended to be encompassed by the following claims.