The invention encompasses biotechnology inventions, including biotechnology products and processes.

Background of the Invention Phosphatidic acid phosphatase (PAP) (also referred to in the art as phosphatidate phosphohydrolase) is known to be an important enzyme for glycerolipid biosynthesis.

In particular, PAP catalyzes the conversion of phosphatidic acid (PA) (also referred to in the art as phosphatidate) into diacylglycerol (DAG). DAG is an important branch point intermediate just downstream of PA in the pathways for biosynthesis of glycerophosphate- based phospholipids (Kent, Anal. Rev. Biochem. 64: 315- 343,1995).

In eukaryotic cells, PA, the precursor molecule for all glycerophospholipids, is converted either to CDP- diacylglycerol (CDP-DAG) by CDP-DAG synthase (CDS) or to DAG by phosphatidic acid phosphatase (PAP). In mammalian cells, CDP-DAG is the precursor to phosphatidylinositol (PI), phosphatidylglycerol (PG), and cardiolipin (CL); whereas diacylglycerol is the precursor to triacylglycerol (TG), phosphatidylethanolamine (PE), and phosphatidylcholine (PC) in all eukaryotic cells.

Therefore, the partitioning of phosphatidic acid between

CDP-diacylglycerol and diacylglycerol is an important regulatory point in eukaryotic phospholipid metabolism (Shen et al., J. Biol. Chem. 271: 789-795,1996).

In addition to being an important enzyme for glycerolipid biosynthesis, PAP is also an important enzyme for signal transduction. PAP catalyses the dephosphorylation of PA to DAG. DAG is a well-studied lipid second messenger which is essential for the activation of protein kinase C (Kent, Anal. Rev. Biochem.

64: 315-343,1995); whereas PA itself is also a lipid messenger implicated in various signaling pathways such as NADPH oxidase activation and calcium mobilization (English, Cell Signal. 8: 341-347,1996). The regulation of PAP activity can therefore affect the balance of divergent signaling processes that the cell receives in terms of PA and DAG (Brindley et al., Chem. Phys. Lipids 80: 45-57,1996).

Various forms of PAP have been isolated in porcine (Kai et al., J. Biol. Chem. 271: 18931-18938,1996) and rat species (Brindley et al., Chem. Phys. Lipids 80: 45- 57,1996). Furthermore, the putative amino acid sequence of murine PAP has been identified. Kai et al., supra.

Prior to the instant invention, however, human PAP had not been identified or isolated.

Genes coding for PAP have been identified in E. coli (Dillon et al, J. Biol. Chem. 260: 12078-12083,1985) and in mouse (Kai et al., J. Biol. Chem. 271: 18931-18938, 1996). Furthermore, the following GenBank human cDNA clones are available: accession nos. H17855, N75714, and W70040. No uses were known, however, for these polynucleotide sequences.

Accordingly, there is a need for the identification and isolation of human PAP and for methods of using human

PAP, for example, for the dephosphorylation of a substrate.

Summary of the Invention It is therefore an object of the present invention to provide a polynucleotide sequences encoding three or more variants of human PAP, namely PAP-a (1 and 2), PAP- (3 and PAP-7.

It is a further object to provide the isolated protein of these three variants.

It is yet a further object to provide a biotechnology method for preparing these variants via recombinant methods.

It is a further object to provide a biotechnology method of using these variants or human PA in general to synthesize DAG.

In accomplishing these and other objects there is provided an isolated polynucleotide encoding human phosphatidic acid phosphatase wherein the polynucleotide encodes a protein comprising a polypeptide sequence selected from the group consisting of (i) the sequence at amino acid number 1 to amino acid number 284 (SEQ ID NO : 2) in Figure 1, (ii) the sequence at amino acid number 1 to amino acid number 285 (SEQ ID NO : 4) in Figure 2, and (iii) the sequence at amino acid number 1 to amino acid number 276 (SEQ ID NO : 8) in Figure 4.

There is further provided an isolated human phosphatidic acid phosphatase protein, wherein the protein comprises a polypeptide sequence selected from the group consisting of (i) the sequence at amino acid number 1 to amino acid number 284 (SEQ ID NO : 2) in Figure 1, (ii) the sequence at amino acid number 1 to amino acid number 285 (SEQ ID NO : 4) in Figure 2, and (iii) the sequence at amino acid number 1 to amino acid number 276 (SEQ ID NO : 8) in Figure 4.

There if further provided a method of preparing a human phosphatidic acid phosphatase- protein comprising the steps of (i) transforming a host cell with an expression vector comprising a polynucleotide encoding human phosphatidic acid phosphatase, (ii) culturing the transformed host cells which express the protein and (iii) isolating the protein.

There if further provided a method of dephosphorylating a substrate comprising contacting the substrate with an effective amount of isolated human phosphatidic acid phosphatase protein such that the protein catalyzes the dephosphorylation of the substrate.

It is further provided that the substrate of this method is selected from the group consisting of phosphatidic acid, lysophosphatidic acid, ceramide 1-phosphate, and sphingosine 1-phosphate. It is further provided that this method occurs in vitro, and comprises a step of isolating the dephosphoryled substrate. Additionally, the method can occur in vivo, and is effected by the administration of human phosphatidic acid phosphatase to a mammal in need thereof.

Brief Description of the Drawings Figure 1 shows the DNA sequence of the cDNA insert of the human PAP-al isolated herein and the corresponding amino acid sequence (SEQ ID NOS: 1 and 2).

Figure 2 shows the DNA sequence of the cDNA insert of the human PAP-a2 isolated herein and the corresponding amino acid sequence (SEQ ID NOS: 3 and 4).

Figure 3 shows the DNA sequence of the cDNA insert of the human PAP- isolated herein and the corresponding amino acid sequence (SEQ ID NOS: 5 and 6).

Figure 4 shows the DNA sequence of the cDNA insert of the human PAP-isolated herein and the corresponding amino acid sequence (SEQ ID NOS : 7 and 8).

Figure 5 shows amino acid sequences alignment of the murine PAP coding sequence and the coding sequences for human PAP-a (1 and 2), PAP- and PAP- (SEQ ID NOS: 9-13).

Figure 6 shows the effect of IL-1 (3 on PAP- (3 expression in human endothelial ECV304 cells using Northern blot analysis.

Figure 7 depicts a thin layer chromatography analysis demonstrating the increase in PA dephosphorylation in cells transfected with either the PAP-al or PAP-a2 cDNA expression plasmids.

Figure 8 shows the differential expression of PAP- a MARNA in various tumor versus normal tissues.

Figure 9 is a schematic representation of glycerophospholipid biosynthesis involving the conversion of PA to either DAG or CDP-DAG. The synthesis of PA to DAG involves the PAP enzyme, while the synthesis of PA to CPD-DAG involves the CDS enzyme.

Detailed Description of Preferred Embodiments This invention relates to isolated human phosphatidic acid phosphatase. More particularly, this invention relates to three variants of human phosphatidic acid phosphatase namely PAP-a (1 and 2), PAP- and PAP-y.

Examples of the uses for human PAP include the following. PAP is an important tool for enzymatic catalysis of several biologically significant proteins.

As discussed above, PAP catalyzes the dephosphorylation of PA to DAG. DAG, in turn, is essential for the activation of protein kinase C (Kent, Anal. Rev. Biochem.

64: 315-343,1995).

Moreover, PAP catalyzes the dephosphorylation of lysophosphatidic acid (LPA), ceramide 1-phosphate (C-1- P), and sphingosine 1-phosphate (S-1-P) (Brindley et al., Chem. Phys. Lipids 80: 45-57, 1996). In the case of LPA, S-1-P, and C-1-P, the products of the PAP reaction are monoacylglycerol, sphingosine, and ceramide,

respectively. PAP can control the balance of a wide spectrum of lipid mediators of cell activation and signal transduction by modulating the phosphorylated state of these lipids.

Additionally, the human PAP of the present invention are likely to define a new family of tumor suppressor genes that can be used as candidate genes for gene therapy for the treatment of certain tumors. The relationship of PAP and tumor suppression is evidenced in findings that PAP activity is lower in fibroblast cell lines transformed with either the ras or fps oncogene than in the parental ratl cell line (Brindley et al., Chem. Phys. Lipids 80: 45-57,1996). Decrease in PAP activity in transformed cells correlates with a concomitant increase in PA concentration. Moreover, elevated PAP activity and lower level of PA has been observed in contact-inhibited fibroblasts relative to proliferating and transformed fibroblasts (Brindley et al., Chem. Phys. Lipids 80: 45-57,1996). Therefore, PAP plays a role in decreasing cell division and as such can provide a useful tool in treating cancer.

Additionally, PA, the substrate for the enzyme PAP, has been implicated in cytokine induced inflammatory responses (Bursten et al., Circ. Shock 44: 14-29,1994; Abraham et al., J. Exp. Med. 181: 569-575,1995; Rice et al., Proc. Natl. Acad. Sci. USA 91: 3857-3861 1994; Leung et al., Proc. Natl. Acad. Sci. USA 92: 4813-4817,1995) and the modulation of numerous protein kinases involved in signal transduction (English et al., Chem. Phys.

Lipids 80: 117-132,1996). Because of the possibility that activation of human PAP expression can counter- balance the inflammatory response from cytokine stimulation through degradation of excess amount of PA in cells, the genes encoding human PAP can be used in gene therapy for the treatment of inflammatory diseases.

Human PAP described herein can also be used in gene therapy for the treatment of obesity associated with diabetes. PAP activity is decreased in the livers and hearts of the grossly obese and insulin resistant JCR: LA corpulent rat compared to the control lean phenotype (Brindley et al., Chem. Phys. Lipids 80: 45-57,1996).

Human PAP described herein therefore can provide an important tool for the treatment of obesity associated with diabetes.

1. Human PAP As used herein,"phosphatidic acid phosphatase"or "PAP"refers to a protein capable of catalyzing the dephosphorylation of PA to DAG. PAP also includes proteins capable of catalyzing the dephosphorylation of lysophosphatidic acid (LPA), ceramide 1-phosphate (C-1- P), and sphingosine 1-phosphate (S-1-P).

As used herein,"isolated"PAP denotes a degree of separation of the protein from other materials endogenous to the host organism. As used herein,"purified"denotes a higher degree of separation than isolated. A purified protein is sufficiently free of other materials endogenous to the host organism such that any remaining materials do not adversely affect the biological properties of the protein, for example, a purified protein is one sufficiently pure to be used in a pharmaceutical context.

As used herein,"human"PAP refers to PAP naturally occurring (or"native") in the human species, including natural variations due to allelic differences. The term "human PAP,"however, is not limited to native human proteins, but also includes amino acid sequence variants of native human PAP that demonstrate PAP activity, as defined above.

Variants often exhibit the same qualitative biological activity as the naturally-occurring analogue,

although variants also are selected in order to modify the characteristics of PAP protein. In a preferred embodiment, therefore, human PAP includes the amino acid sequences of Figures 1-4 (SEQ ID NOS: 2,4,6 and 8), being PAP-a1, PAP-a2, PAP-a and PAP-, respectively and variants thereof.

Amino acid sequence variants of the protein can be substitutional, insertional or deletion variants.

Deletion variants lack one or more residues of the native protein which are not essential for biological activity.

An example of a common deletion variant is a protein lacking transmembrane sequences. Another example is a protein lacking secretory signal sequences or signal sequences directing the protein to bind to a particular part of a cell.

Substitutional variants typically contain the exchange of one amino acid for another at one or more sites within the protein, and are designed to modulate one or more properties of the protein such as stability against proteolytic cleavage. Substitutions preferably are conservative, that is, one amino acid is replaced with one of similar shape and charge. Conservative substitutions are well known in the art and include, for example, the changes of: alanine to serine; arginine to lysine; asparigine to glutamine or histidine; aspartate to glutamate; cysteine to serine; glutamine to asparigine; glutamate to aspartate; glycine to proline; histidine to asparigine or glutamine; isoleucine to leucine or valine; leucine to valine or isoleucine; lysine to arginine, glutamine, or glutamate; methionine to leucine or isoleucine; phenylalanine to tyrosine, leucine or methionine; serine to threonine; threonine to serine; tryptophan to tyrosine; tyrosine to tryptophan or phenylalanine; and valine to isoleucine or leucine.

Of course, other amino acid substitutions can be undertaken.

Insertional variants contain fusion proteins such as those used to allow rapid purification of the protein and also can include hybrid proteins containing sequences from other proteins and polypeptides which are protein homologues.

Variants of human PAP also include fragments, analogs, derivatives, muteins and mimetics of the natural PAP protein that retain the ability to cause the beneficial results described above. Fragments of the human PAP protein refer to portions of the amino acid sequence of the PAP polypeptide that also retain this ability.

Variants can be generated directly from the human PAP protein itself by chemical modification by proteolytic enzyme digestion, or by combinations thereof.

Additionally, methods of synthesizing polypeptides directly from amino acid residues also exist.

Non-peptide compounds that mimic the binding and function of the human PAP protein ("mimetics") can be produced by the approach outlined in Saragovi et al., Science 253: 792-95 (1991). Mimetics are peptide- containing molecules which mimic elements of protein secondary structure. See, for example, Johnson et al.,"Peptide Turn Mimetics"in BIOTECHNOLOGY AND PHARMACY, Pezzuto et al., Eds., (Chapman and Hall, New York, 1993).

The underlying rationale behind the use of peptide mimetics is that the peptide backbone of proteins exists chiefly to orient amino acid side chains in such a way as to facilitate molecular interactions For the purposes of the present invention, appropriate mimetics can be considered to be the equivalent of the human PAP protein itself.

More typically, at least in the case of gene therapy, variants are created by recombinant techniques employing genomic or cDNA cloning methods. Site-specific

and region-directed mutagenesis techniques can be employed. See CURRENT PROTOCOLS IN MOLECULAR BIOLOGY vol. 1, ch. 8 (Ausubel et al. eds., J. Wiley & Sons 1989 & Supp. 1990-93); PROTEIN ENGINEERING (Oxender & Fox eds., A. Liss, Inc. 1987). In addition, linker-scanning and PCR-mediated techniques can be employed for mutagenesis. See PCR TECHNOLOGY (Erlich ed., Stockton Press 1989); CURRENT PROTOCOLS IN MOLECULAR BIOLOGY, vols. 1 & 2, supra. Protein sequencing, structure and modeling approaches for use with any of the above techniques are disclosed in PROTEIN ENGINEERING, loc. cit. and CURRENT PROTOCOLS IN MOLECULAR BIOLOGY, vols. 1 & 2, supra.

2. Polynucleotides Encoding Human PAP The present invention further includes isolated polynucleotides encoding human phosphatidic acid phosphatase. As used herein, an"isolated" polynucleotide denotes a degree of separation of the polynucleotide from its naturally occurring environment, e. g., from its native intact genome. In a preferred embodiment, the isolated polynucleotides correspond to those shown in Figure 1 at nucleotide number 342 to nucleotide number 1193 of SEQ ID NO : 1 ; Figure 2 at nucleotide number 342 to nucleotide number 1196 of SEQ ID NO : 3; Figure 3 at nucleotide number 294 to nucleotide number 1226 of SEQ ID NO : 5; and Figure 4 at nucleotide number 4 to nucleotide number 833 of SEQ ID NO : 7.

The invention furthermore relates to a polynucleotide whose sequence is degenerate with respect to the sequences mentioned above in accordance with the nature of the genetic code. Degeneracy is often referred to as codon/anticodon wobble, and is discussed in Watson et al., MOLECULAR BIOLOGY OF THE GENE (4th ed. 1987) at 437-43.

The present invention further includes bases, nucleosides, nucleotides, oligonucleotides derived from the isolated polynucleotides of the present invention.

The term"derived"when used in the context of the present invention connotes a degree of similarity that is sufficient to indicate the original polynucleotide from which hybrid forms, or portions thereof, were obtained. Also within the scope of the invention are so- called"polyamide"or"peptide"nucleic acids ("PNAs") derived from the polynucleotides of the present invention. PNAs are constructed by replacing the (deoxy) ribose phosphate backbone of a subject polynucleotide with an achiral polyamide backbone or the like. See Nielsen et al., Science 254: 1497-54 (1991).

The above polynucleotides and derivations thereof can be used as important tools in recombinant DNA and other protocols involving nucleic acid hybridization techniques. More specifically, oligonucleotides and nucleic acids derived from the isolated polynucleotides shown in Figures 1-4 (SEQ ID NOS: 1, 3,5, and 7) can be used as hybridization probes, capable of recognizing and specifically binding to complementary nucleic acid sequences, providing thereby a means of detecting, identifying, locating and measuring complementary nucleic acid sequences in a biological sample.

Biological samples include, among a great many others, blood or blood serum, lymph, ascites fluid, urine, microorganism or tissue culture medium, cell extracts, or the like, derived from a biological source, or a solution containing chemically synthesized protein, or an extract or solution prepared from such fluid from a biological source.

An oligonucleotide containing a modified nucleotide of the invention can be used as a primer to initiate nucleic acid synthesis at locations in a DNA or RNA molecule comprising the sequence complementary to the

oligonucleotide sequence. The synthesized nucleic acid strand would have incorporated, at its 5'terminus, the oligonucleotide primer bearing the invention and would, therefore, be detectable by exploitation of the characteristics of the detectable label. Two such primers, specific for different nucleotide sequences on complementary strands of dsDNA, can be used in the polymerase chain reaction (PCR) to synthesize and amplify the amount of a nucleotide sequence. The detectable label present on the primers will facilitate the identification of desired PCR products. PCR, combined with techniques for preparing complementary DNA (cDNA) can be used to amplify various RNAs, with oligonucleotide primers again serving both to provide points for initiation of synthesis in the cDNA duplex flanking the desired sequence and to identify the desired product.

Primers labeled with the invention may also be utilized for enzymatic nucleic acid sequencing by the dideoxy chain-termination technique.

The invention can be applied to measure or quantitate the amount of DNA present in a sample. For instance, the concentration of nucleic acid can be measured by comparing detectable labels incorporated into the unknown nucleic acid with the concentration of detectable labels incorporated into known amounts of nucleic acid.

Such a comparative assessment can be done using biotin where the respective concentrations are determined by an enzyme-linked assay utilizing the streptavidin- alkaline phosphatase conjugate and a substrate yielding a soluble chromogenic or chemiluminescent signal.

3. Recombinant Production of Human PAP In a further embodiment human PAP is expressed via recombinant methods known to those of skill in the art.

The polynucleotides of the present invention can be

expressed in any number of different recombinant DNA expression systems to generate large amounts of protein, which can then be purified and used for the various applications of human PAP described above. Included within the present invention are proteins having native glycosylation sequences, and deglycosylated or unglycosylated proteins prepared by the methods described below.

Recombinant technology for producing desired proteins is known by ordinarily skilled artisans and includes providing a coding sequence for a desired protein, and operably linking the coding sequence to polynucleotide sequences capable of effecting its expression.

With regard to one aspect of the invention, it often is desirable to produce human PAP as a fusion protein, freed from upstream, downstream or intermediate sequences, or as a protein linked to leader sequences, effecting secretion of human PAP into cell culture medium.

A typical expression system will also contain control sequences necessary for transcription and translation of a message. Known control sequences include constitutive or inducible promoter systems, translational initiation signals (in eucaryotic expression), polyadenylation translation termination sites, and transcription terminating sequences.

Expression vectors containing controls which permit operably linking of desired coding sequences to required control systems are known by the skilled artisan. Such vectors can be found which are operable in a variety of hosts.

Human PAP of the present invention may be produced in procaryotic cells using appropriate controls, such as trp or lac promoters, or in eucaryotic host cells, capable of effecting post-translational processing that

permits proteins to assume desired three-dimensional conformation. Eucaryotic control systems and expression vectors are known; including leu and glycolytic promoters useful in yeast, the viral SV40 and adenovirus and CMV promoters in mammalian cells, and the baculovirus system which is operable in insect cells. Plant vectors with suitable promoters, such as the nos promoter are also available.

Standard laboratory manuals (e. g., Sambrook et al., MOLECULAR CLONING: A LABORATORY MANUAL, Second Edition, (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY 1989) present standard techniques and methodologies for expressing polynucleotides encoding a desired protein, culturing appropriate cells, providing suitable expression conditions, and recovering a resulting protein from culture.

In preparing the inventive human PAP, a suitable polynucleotide encoding human PAP, constructed utilizing any of the foregoing techniques is operable linked to an expression vector which is then transformed into a compatible host. Host cells are cultured using conditions appropriate for growth. Expression of the desired human PAP is preferably induced after some predetermined growth level has occurred. Human PAP production is monitored and the desired protein isolated from culture either from a supernatant, or by first lysing host cells with an appropriate agent, or by other methods known to the skilled artisan.

In another preferred embodiment, a polynucleotide encoding human PAP is ligated into a mammalian expression vector. A preferred mammalian expression vector is the plasmid"pCE2."The plasmid pCE2 is derived from pREP7b (Leung, et al., Proc. Natl. Acad. Sci. USA, 92: 4813- 4817,1995) with the RSV promoter region replaced by the CMV enhancer and the elongation factor-la (EF-la) promoter and intron. The CMV enhancer of the pCE2 vector

is constructed from a 380 bp Xba I-Sph I fragment produced by PCR from pCEP4 (Invitrogen, San Diego, CA) using the primers 5'-GGCTCTAGAT ATTAATAGTA ATCAATTAC-3' (SEQ ID NO : 14) and 5'-CCTCACGCAT GCACCATGGT AATAGC-3' (SEQ ID NO : 15). The EF-la promoter and intron (Uetsuki, et al., J. Biol. Chem., 264: 5791-5798,1989) are constructed from a 1200 bp Sph I-Asp718 I fragment produced by PCR from human genomic DNA using the primers 5'-GGTGCATGCG TGAGGCTCCG GTGC-3' (SEQ ID NO : 16) and 5'- GTAGTTTTCA CGGTACCTGA AATGGAAG-3' (SEQ ID NO : 17). These 2 fragments are ligated into a Xba I/Asp718 I digested vector derived from pREP7b to generate pCE2.

In another preferred embodiment of the present invention, pCE2 containing a polynucleotide expressing human PAP is used to transform a host cell which then expresses the protein. Preferred host cells include the human embryonic kidney cell line 293-EBNA (Invitrogen, San Diego, CA), endothelial ECV304 cells, and epithelial A549 cells.

4. Dephosphorvlation of Substrate In another embodiment, the present invention includes a method of dephosphorylating a substrate by contacting the substrate with an effective amount of isolated human PAP. An'effective amount"of human PAP is an amount which will dephosphorylate a detectable amount of substrate. Such an amount can be determined empirically based on variables well known to those of skill in the art, such as reaction time and temperature.

In one embodiment, the substrate includes phosphatidic acid, lysophosphatidic acid, ceramide 1- phosphate, and sphingosine 1-phosphate. In another embodiment, the isolated human PAP includes PAP-a (1 and 2), PAP-0 and PAP-and variants thereof.

In a further embodiment, the dephosphorylation of substrate occurs in vitro, by contacting a substrate with

recombinantly produced human PAP expressed by the methods described above. The dephosphorylated substrate is then isolated by standard isolation and purification methods, including for example, thin layer chromatography or high pressure liquid chromatography.

In another embodiment, the dephosphorylation of substrate occurs in vivo via the administration of human PAP to a mammal, preferably a human."Administration" means delivery of human PAP protein to a mammal by methods known to those of skill in the art including, but not limited to: orally, for example in the form of pills, tablets, lacquer tablets, coated tablets, granules, hard gelatin capsules, soft gelatin capsules, solutions, syrups, emulsions, suspensions or aerosol mixtures; rectally, for example in the form of suppositories; parenterally, for example in the form of injection solutions or infusion solutions, microcapsules or rods; percutaneously, for example in the form of ointments or tinctures; transdermally; intravascularly, intracavitarily; intramuscularly; subcutaneously; and nasally, for example in the form of nasal sprays or inhalants.

The administration of human PAP protein includes the administration of the protein combined in a mixture with a pharmaceutically acceptable carrier vehicle. Suitable vehicles and their formulation, inclusive of other human proteins, e. g. human serum albumin, are described for example in Remington's Pharmaceutical Sciences by E. W.

Martin, which is hereby incorporated by reference. Such compositions will contain an effective amount of protein hereof together with a suitable amount of vehicle in order to prepare pharmaceutically acceptable compositions suitable for effective administration to the host.

Such compositions should be stable for appropriate periods of time, preferably are acceptable for administration to humans and preferably are readily

manufacturable. Although pharmaceutical solution formulations are provided in liquid form appropriate for immediate use, formulations may also be provided in frozen or in lyophilized form. In the former case, the composition must be thawed prior to use. The latter form is often used to enhance the stability of the medicinal agent contained in the composition under a wide variety of storage conditions. Such lyophilized preparations are reconstituted prior to use by the addition of suitable pharmaceutically acceptable diluents, such as sterile water or sterile physiological saline solution.

Additionally, administration is meant to include delivery of human PAP protein to a mammal by means of gene therapy techniques, i. e., by the delivery of polynucleotides encoding human PAP to PAP-deficient cells, whereby human PAP is then expressed in the cell.

Gene therapy techniques are known to those of skill in the art. For example, listing of present-day vectors suitable for use in gene therapy of the present invention is set forth in Hodgson, Bio/Technology 13: 222 (1995).

See also, Culver et al., Science, 256: 1550-62 (1992).

Additionally, liposome-mediated gene transfer is another suitable method for the introduction of a recombinant vector containing a polynucleotide encoding human PAP into a PAP-deficient cell. See Caplen et al., Nature Med. 1: 39-46 (1995) and Zhu et al., Science 261: 209-211 (1993).

Additionally, viral vector-mediated gene transfer is also a suitable method for the introduction of a recombinant vector containing the gene encoding human PAP into a PAP-deficient cell. Examples of appropriate viral vectors are adenovirus vectors. Detailed discussions of the use of adenoviral vectors for gene therapy can be found in Berkner, Biotechniques 6: 616-629 (1988), Trapnell, Advanced Drug Delivery Rev. 12: 185-199 (1993).

The following examples merely illustrate the invention and, as such, are not to be considered as limiting the invention set forth in the claims.

Example 1 Clonina and Expression of Human PAP-a, PAP- and PAP- Homology search of the Genbank database (Boguski, et al., Science 265: 1993-1994,1994) of expressed sequence tag (dbEST) using the murine PAP protein sequence (Kai et al., J. Biol. Chem. 271: 18931-18938, 1996) as probe identified several short stretches of human cDNA sequences with homology to the murine PAP protein sequence. These cDNA sequences of interest were derived from single-run partial sequencing of random human cDNA cloning projects carried out mainly by I. M. A. G. E. Consortium [LLNL] cDNA clones program. Based on the partial DNA sequences available in the GenBank database, the human cDNA clones that are homologous to the murine PAP protein sequence can be grouped into three classes, suggesting the presence of at least three different human PAP variants, designated as PAP-a, PAP- ß, and PAP-here. For instance, a potential human PAP-a clone (GenBank #H17855) identified contains sequence homologous to aa 272-283 and the 3'-untranslated region of murine PAP; a potential human PAP- clone (GenBank #W70040) identified contains sequence similarities corresponding to aa 175-251 of murine PAP; and a potential human PAP-clone (GenBank #N75714) identified contains sequences similarities corresponding to aa 18- 142 of murine PAP. These cDNA clones were purchased (Genome Systems, St. Louis, MO) for further analysis.

DNA sequence determination of the entire cDNA inserts of these clones showed clone H17855 contained sequences that are homologous to the N-and C-terminal sequences of murine PAP with a gap of about 150 bp that led to a frame shift in reading frame. This clone is most likely a

spuriously spliced form of PAP-a clone. Clone W70040 was found to be a full-length PAP- clone, and clone N75714 was found to be a partial PAP-clone with an open reading frame homologous to the region from aal8 to the C-terminus of murine PAP.

To assemble a full-length functional PAP-a clone, synthetic oligonucleotides o_papalF, 5'-ggcatggtAC CATGTTTGAC AAGACGCGGC-3' (SEQ ID NO : 18), based on the N- terminal region of PAP-a and o_papalR, 5'-CATATGTAGT ATTCAATGTA ACC-3' (SEQ ID NO : 19), based on a region downstream of a Pst I site complementary to the coding strand of PAP-a were used to amplify the N-terminal coding region of PAP-a from a human lung cDNA library (Life Technologies, Inc., Gaithersburg, MD). The 450 bp Acc65 I-Pst I fragment generated was inserted into a Acc65 I/Pst I vector from pBluescript (II) SK (-) (Stratagene, San Diego, CA) for further analysis. DNA sequence analysis of the subclones obtained revealed at least two different classes of clones with sequences that diverged at the putative exon of interest, suggesting the presence of two alternatively spliced forms of PAP-a.

These two alternatively spliced forms of PAP-a are designated as PAP-al and PAP-a2 here. Each of the individual 450 bp Acc65 I-Pst I fragment generated by PCR was combined with the 810 bp Pst I-Not I fragment derived from clone H17855 for ligation into a Acc65 I/ Not I mammalian expression vector derived from pCE2 for the generation of expression plasmids for PAP-al and PAP- a2. The plasmid pCE2 was derived from pREP7b (Leung, et al., Proc. Natl. Acad. Sci. USA, 92: 4813-4817,1995) with the RSV promoter region replaced by the CMV enhancer and the elongation factor-la (EF-1a) promoter and intron.

The CMV enhancer of the pCE2 vector was constructed from a 380 bp Xba I-Sph I fragment produced by PCR from pCEP4 (Invitrogen, San Diego, CA) using the primers 5'- GGCTCTAGAT ATTAATAGTA ATCAATTAC-3' (SEQ ID NO: 14) and 5'-

CCTCACGCAT GCACCATGGT AATAGC-3' (SEQ ID NO : 15). The EF- 1a promoter and intron (Uetsuki, et al., J. Biol. Chem., 264: 5791-5798,1989) was constructed from a 1200 bp Sph I-Asp718 I fragment produced by PCR from human genomic DNA using the primers 5'-GGTGCATGCG TGAGGCTCCG GTGC-3' (SEQ ID NO : 16) and 5'-GTAGTTTTCA CGGTACCTGA AATGGAAG-3' (SEQ ID NO : 17). These 2 fragments were ligated into a Xba I/Asp718 I digested vector derived from pREP7b to generate pCE2.

The DNA sequence determined from clone N75714 was used as a probe to search for clones with overlapping sequences in the GenBank database. Clone Z43618 was found to contain an additional 5'-sequence with a potential ATG initiation codon. To assemble a full- length PAP-7 clone, synthetic oligonucleotides opapglF, 5'-tgatggctagcATGCAGAGA AGATGGGTCT TCGTGCTGCT CGACGTG-3' (SEQ ID NO : 20), based on the N-terminal region of PAP- and o_papglR, 5'-AGTGCGGGAT CCCATAAGTG GTTG-3', (SEQ ID NO : 21) based on a region complementary to the coding strand of PAP-just downstream of its stop codon were used to generate the full-length coding region of PAP- by PCR using the clone N75714 as template. The 820 bp Nhe I-BamH I fragment obtained was then ligated into a Nhe I/BamH I mammalian expression vector derived from pCE2.

Figures 1,2,3 and 4 show the translated DNA sequences of the putative human cDNA clones for PAP-al, a2, ß and, (SEQ ID NOS: 1, 3,5 and 7) respectively.

The designated ATG initiation site for translation of each cDNA clone fulfills the requirement for an adequate initiation site according to Kozak (Kozak, Critical Rev.

Biochem. Mol. Biol. 27: 385-402,1992).

The amino acid sequence of each open reading frame (Figures 1,2,3 and 4 (SEQ ID NOS: 2,4,6 and 8)) was used as the query sequence to search for homologous sequences in protein databases. Search of the Genbank

database from the National Center for Biotechnology Information (NCBI) using the blastp program showed that these proteins are most homologous to the murine PAP sequence (Kai et al., J. Biol. Chem. 271: 18931-18938, 1996), and a rat endoplasmic reticulum resident transmembrane protein of unknown function, Dri 42, whose expression is up-regulated during epithelial differentiation (Barila et al., J. Biol. Chem. 271: 29928-29936,1996).

Example 2 Activation of PAP-/ Transcription by ILl- It is possible that activation of PAP-0 expression can counter-balance the inflammatory response from IL-1/3 stimulation through degradation of the excess amount of PA in cells. To determine whether ILl-0, an inflammatory cytokine, would activate the transcription of PAP mRNAs, Northern analysis of PAP-ß mRNA levels (Fig. 6) was performed in human endothelial ECV304 cells at various times after IL-10 stimulation. Figure 6 shows that PAP-0 mRNA expression was induced after incubation of ECV304 cells with IL-lß after at least 6 hours, suggesting that PAP-0 is a late-response gene to IL-10 stimulation. This indicates that human PAP may act to reduce IL-10 induced inflammation by degrading excess PA in cells.

Example 3 PAP-al and PAP-a2 Dephosphorylation of PA to DAG The expression of PAP-al and PAP-a2 cDNA was found to increase PA dephosphorylation in mammalian cells.

The expression plasmids for PAP-al, PAP-a2 and the control vector were transiently transfected into 293-EBNA (EB293) cells (Invitrogen, San Diego, CA) using the lipofectant DOTAP (Boehringer Mannheim, Indianapolis, IN). PAP activities were followed by TLC analysis based on the conversion of [C14] PA (DuPont NEN, Boston, MA) to

[Cl4] DAG using membrane fractions isolated from the various cell extracts. Figure 7 shows membrane fractions derived from cells transfected with either the PAP-al (lanes 6 and 7) or PAP-a2 (lanes 8 and 9) produced more [Cl4] DAG those from untransfected cells (lanes 2 and 3) or from cells transfected with the control pCE2 vector (lanes 4 and 5). In this particular chromatography system, DAG can be resolved into two bands, possibly due to heterogeneity in the acyl-chains. It appears that PAP-al and PAP-a2 preferentially dephosphorylate different species of PA as evidenced by the change in relative intensity of the two DAG bands (lanes 6 to 9).

Example 4 Differential Expression of PAP-a MARNA in Selected Tumor Versus Normal Tissues The possibility that PAP-a expression can degrade the excess amount of PA in cells suggests that PAP-a may be down-regulated in tumor cells when compared to normal cells, as tumor cells tend to be more inflammatory due to a possibly higher level of PA when compared to normal or resting cells. To test this hypothesis, Northern analysis using PAP-a (1 and 2) cDNA probe was performed on RNA blots derived from various matching pairs of tumor and normal tissues (Invitrogen, Carlsbad, CA). Figure 8 shows the expression levels of PAP-a mRNA are substantially higher in five out of eight of the normal tissues examined; namely, colon, rectal, breast, fallopian tube, and ovarian tissues when compared to the corresponding tumor tissues.

SEQUENCE LISTING (1) GENERAL INFORMATION: (i) APPLICANT: LEUNG, David W.

TOMPKINS, Christopher K.

(ii) TITLE OF INVENTION : HUMAN PHOSPHATIDIC ACID PHOSPHATASE (iii) NUMBER OF SEQUENCES : 21 (iv) CORRESPONDENCE ADDRESS: (A) ADDRESSEE: Foley & Lardner (B) STREET: 3000 K Street, N. W., Suite 500 (C) CITY: Washington (D) STATE: D. C.

(E) COUNTRY : USA (F) ZIP: 20007-5109 (v) COMPUTER READABLE FORM: (A) MEDIUM TYPE: Floppy disk (B) COMPUTER: IBM PC compatible (C) OPERATING SYSTEM: PC-DOS/MS-DOS (D) SOFTWARE: PatentIn Release #1. 0, Version #1. 30 (vi) CURRENT APPLICATION DATA: (A) APPLICATION NUMBER : US 08/842,827 (B) FILING DATE: 17-APR-1997 (C) CLASSIFICATION: (viii) ATTORNEY/AGENT INFORMATION: (A) NAME: BENT, Stephen A.

(B) REGISTRATION NUMBER: 29,768 (C) REFERENCE/DOCKET NUMBER: 77319/125 (ix) TELECOMMUNICATION INFORMATION: (A) TELEPHONE: (202) 672-5300 (B) TELEFAX: (202) 672-5399 (C) TELEX: 904136 (2) INFORMATION FOR SEQ ID NO : 1 : (i) SEQUENCE CHARACTERISTICS : (A) LENGTH: 1563 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ix) FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 342.. 1193 (ix) FEATURE: (A) NAME/KEY: mat_peptide (B) LOCATION: 342.. 1193 (xi) SEQUENCE DESCRIPTION: SEQ ID NO : 1 : CCTGTGGGAG AGAGCGCCGG GATCCGGACG GGGTAGCAAC CGGGGCAGGC CGTGCCGGCT 60 GAGGAGGTCC TGAGGCTACA GAGCTGCCGC GGCTGGCACA CGAGCGCCTC GGCACTAACC 120 GAGTGTTCGC GGGGGCTGTG AGGGGAGGGC CCCGGGCGCC ATTGCTGGCG GTGGGAGCGC 180 CGCCCGGTCT CAGCCCGCCC TCGGCTGCTC TCCTCCTCCG GCTGGGAGGG GCCGTATCTC 240 GGGGCCGTCG CCAGCCCCGG CCCGGGCTCG ATAATCAAGG GCCTCGGCCG TCGTCCCGCA 300 CCTCATTCCA TCGCCCTTGC CGGGCAGCCC GGGCAGAGAC C ATG TTT GAC AAG 353 Met Phe Asp Lys 1 ACG CGG CTG CCG TAC GTG GCC CTC GAT GTG CTC TGC GTG TTG CTG GCT 401 Thr Arg Leu Pro Tyr Val Ala Leu Asp Val Leu Cys Val Leu Leu Ala 5 10 15 20 GGA TTG CCT TTT GCA ATT CTT ACT TCA AGG CAT ACC CCC TTC CAA CGA 449 Gly Leu Pro Phe Ala Ile Leu Thr Ser Arg His Thr Pro Phe Gln Arg 25 30 35 GGA GTA TTC TGT AAT GAT GAG TCC ATC AAG TAC CCT TAC AAA GAA GAC 497 Gly Val Phe Cys Asn Asp Glu Ser Ile Lys Tyr Pro Tyr Lys Glu Asp 40 45 50 ACC ATA CCT TAT GCG TTA TTA GGT GGA ATA ATC ATT CCA TTC AGT ATT 545 Thr Ile Pro Tyr Ala Leu Leu Gly Gly Ile Ile Ile Pro Phe Ser Ile 55 60 65 ATC GTT ATT ATT CTT GGA GAA ACC CTG TCT GTT TAC TGT AAC CTT TTG 593 Ile Val Ile Ile Leu Gly Glu Thr Leu Ser Val Tyr Cys Asn Leu Leu 70 75 80 CAC TCA AAT TCC TTT ATC AGG AAT AAC TAC ATA GCC ACT ATT TAC AAA 641 His Ser Asn Ser Phe Ile Arg Asn Asn Tyr Ile Ala Thr Ile Tyr Lys 85 90 95 100 GCC ATT GGA ACC TTT TTA TTT GGT GCA GCT GCT AGT CAG TCC CTG ACT 689 Ala Ile Gly Thr Phe Leu Phe Gly Ala Ala Ala Ser Gln Ser Leu Thr 105 110 115 GAC ATT GCC AAG TAT TCA ATA GGC AGA CTG CGG CCT CAC TTC TTG GAT 737 Asp Ile Ala Lys Tyr Ser Ile Gly Arg Leu Arg Pro His Phe Leu Asp 120 125 130 GTT TGT GAT CCA GAT TGG TCA AAA ATC AAC TGC AGC GAT GGT TAC ATT 785 Val Cys Asp Pro Asp Trp Ser Lys Ile Asn Cys Ser Asp Gly Tyr Ile 135 140 145 GAA TAC TAC ATA TGT CGA GGG AAT GCA GAA AGA GTT AAG GAA GGC AGG 833 Glu Tyr Tyr Ile Cys Arg Gly Asn Ala Glu Arg Val Lys Glu Gly Arg 150 155 160 TTG TCC TTC TAT TCA GGC CAC TCT TCG TTT TCC ATG TAC TGC ATG CTG 881 Leu Ser Phe Tyr Ser Gly His Ser Ser Phe Ser Met Tyr Cys Met Leu 165 170 175 180 TTT GTG GCA CTT TAT CTT CAA GCC AGG ATG AAG GGA GAC TGG GCA AGA 929 Phe Val Ala Leu Tyr Leu Gln Ala Arg Met Lys Gly Asp Trp Ala Arg 185 190 195 CTC TTA CGC CCC ACA CTG CAA TTT GGT CTT GTT GCC GTA TCC ATT TAT 977 Leu Leu Arg Pro Thr Leu Gln Phe Gly Leu Val Ala Val Ser Ile Tyr 200 205 210 GTG GGC CTT TCT CGA GTT TCT GAT TAT AAA CAC CAC TGG AGC GAT GTG 1025 Val Gly Leu Ser Arg Val Ser Asp Tyr Lys His His Trp Ser Asp Val 215 220 225 TTG ACT GGA CTC ATT CAG GGA GCT CTG GTT GCA ATA TTA GTT GCT GTA 1073 Leu Thr Gly Leu Ile Gln Gly Ala Leu Val Ala Ile Leu Val Ala Val 230 235 240 TAT GTA TCG GAT TTC TTC AAA GAA AGA ACT TCT TTT AAA GAA AGA AAA 1121 Tyr Val Ser Asp Phe Phe Lys Glu Arg Thr Ser Phe Lys Glu Arg Lys 245 250 255 260 GAG GAG GAC TCT CAT ACA ACT CTG CAT GAA ACA CCA ACA ACT GGG AAT 1169 Glu Glu Asp Ser His Thr Thr Leu His Glu Thr Pro Thr Thr Gly Asn 265 270 275 CAC TAT CCG AGC AAT CAC CAG CCT TGAAAGGCAG CAGGGTGCCC AGGTGAAGCT 1223 His Tyr Pro Ser Asn His Gln Pro 280 GGCCTGTTTT CTAAAGGAAA ATGATTGCCA CAAGGCAAGA GGATGCATCT TTCTTCCTGG 1283 TGTACAAGCC TTTAAAGACT TCTGCTGCTG ATATGCCTCT TGGATGCACA CTTTGTGTGT 1343 ACATAGTTAC CTTTAACTCA GTGGTTATCT AATAGCTCTA AACTCATTAA AAAAACTCCA 1403 AGCCTTCCAC CAAAACAGTG CCCCACCTGT ATACATTTTT ATTAAAAAAA TGTAATGCTT 1463 ATGTATAAAC ATGTATGTAA TATGCTTTCT ATGAATGATG TTTGATTTAA ATATAATACA 1523 TATTAAAATG TATGGGAGAA CCAAAAAAAA AAAAAAAAAA 1563 (2) INFORMATION FOR SEQ ID NO : 2: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 284 amino acids (B) TYPE: amino acid (D) TOPOLOGY: linear (ii) MOLECULE TYPE: protein (xi) SEQUENCE DESCRIPTION: SEQ ID NO : 2: Met Phe Asp Lys Thr Arg Leu Pro Tyr Val Ala Leu Asp Val Leu Cys 1 5 10 15 Val Leu Leu Ala Gly Leu Pro Phe Ala Ile Leu Thr Ser Arg His Thr 20 25 30 Pro Phe Gln Arg Gly Val Phe Cys Asn Asp Glu Ser Ile Lys Tyr Pro 35 40 45 Tyr Lys Glu Asp Thr Ile Pro Tyr Ala Leu Leu Gly Gly Ile Ile Ile 50 55 60 Pro Phe Ser Ile Ile Val Ile Ile Leu Gly Glu Thr Leu Ser Val Tyr 65 70 75 80 Cys Asn Leu Leu His Ser Asn Ser Phe Ile Arg Asn Asn Tyr Ile Ala 85 90 95 Thr Ile Tyr Lys Ala Ile Gly Thr Phe Leu Phe Gly Ala Ala Ala Ser 100 105 110 Gln Ser Leu Thr Asp Ile Ala Lys Tyr Ser Ile Gly Arg Leu Arg Pro 115 120 125 His Phe Leu Asp Val Cys Asp Pro Asp Trp Ser Lys Ile Asn Cys Ser 130 135 140 Asp Gly Tyr Ile Glu Tyr Tyr Ile Cys Arg Gly Asn Ala Glu Arg Val 145 150 155 160 Lys Glu Gly Arg Leu Ser Phe Tyr Ser Gly His Ser Ser Phe Ser Met 165 170 175 Tyr Cys Met Leu Phe Val Ala Leu Tyr Leu Gln Ala Arg Met Lys Gly 180 185 190 Asp Trp Ala Arg Leu Leu Arg Pro Thr Leu Gln Phe Gly Leu Val Ala 195 200 205 Val Ser Ile Tyr Val Gly Leu Ser Arg Val Ser Asp Tyr Lys His His 210 215 220 Trp Ser Asp Val Leu Thr Gly Leu Ile Gln Gly Ala Leu Val Ala Ile 225 230 235 240 Leu Val Ala Val Tyr Val Ser Asp Phe Phe Lys Glu Arg Thr Ser Phe 245 250 255 Lys Glu Arg Lys Glu Glu Asp Ser His Thr Thr Leu His Glu Thr Pro 260 265 270 Thr Thr Gly Asn His Tyr Pro Ser Asn His Gln Pro 275 280 (2) INFORMATION FOR SEQ ID NO : 3: (i) SEQUENCE CHARACTERISTICS : (A) LENGTH : 1566 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ix)FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 342.. 1196 (ix)FEATURE: (A) NAME/KEY: mat peptide (B) LOCATION: 342.. 1196 (xi) SEQUENCE DESCRIPTION: SEQ ID NO : 3: CCTGTGGGAG AGAGCGCCGG GATCCGGACG GGGTAGCAAC CGGGGCAGGC CGTGCCGGCT 60 GAGGAGGTCC TGAGGCTACA GAGCTGCCGC GGCTGGCACA CGAGCGCCTC GGCACTAACC 120 GAGTGTTCGC GGGGGCTGTG AGGGGAGGGC CCCGGGCGCC ATTGCTGGCG GTGGGAGCGC 180 CGCCCGGTCT CAGCCCGCCC TCGGCTGCTC TCCTCCTCCG GCTGGGAGGG GCCGTATCTC 240 GGGGCCGTCG CCAGCCCCGG CCCGGGCTCG ATAATCAAGG GCCTCGGCCG TCGTCCCGCA 300 CCTCATTCCA TCGCCCTTGC CGGGCAGCCC GGGCAGAGAC C ATG TTT GAC AAG 353 Met Phe Asp Lys 1 ACG CGG CTG CCG TAC GTG GCC CTC GAT GTG CTC TGC GTG TTG CTG GCT 401 Thr Arg Leu Pro Tyr Val Ala Leu Asp Val Leu Cys Val Leu Leu Ala 5 10 15 20 TCC ATG CCT ATG GCT GTT CTA AAA TTG GGC CAA ATA TAT CCA TTT CAG 449 Ser Met Pro Met Ala Val Leu Lys Leu Gly Gln Ile Tyr Pro Phe Gln 25 30 35 AGA GGC TTT TTC TGT AAA GAC AAC AGC ATC AAC TAT CCG TAC CAT GAC 497 Arg Gly Phe Phe Cys Lys Asp Asn Ser Ile Asn Tyr Pro Tyr His Asp 40 45 50 AGT ACC GCC GCA TCC ACT GTC CTC ATC CTA GTG GGG GTT GGC TTG CCC 545 Ser Thr Ala Ala Ser Thr Val Leu Ile Leu Val Gly Val Gly Leu Pro 55 60 65 GTT TCC TCT ATT ATT CTT GGA GAA ACC CTG TCT GTT TAC TGT AAC CTT 593 Val Ser Ser Ile Ile Leu Gly Glu Thr Leu Ser Val Tyr Cys Asn Leu 70 75 80 TTG CAC TCA AAT TCC TTT ATC AGT AAT AAC TAC ATA GCC ACT ATT TAC 641 Leu His Ser Asn Ser Phe Ile Ser Asn Asn Tyr Ile Ala Thr Ile Tyr 85 90 95 100 AAA GCC ATT GGA ACC TTT TTA TTT GGT GCA GCT GCT AGT CAG TCC CTG 689 Lys Ala Ile Gly Thr Phe Leu Phe Gly Ala Ala Ala Ser Gln Ser Leu 105 110 115 ACT GAC ATT GCC AAG TAT TCA ATA GGC AGA CTG CGG CCT CAC TTC TTG 737 Thr Asp Ile Ala Lys Tyr Ser Ile Gly Arg Leu Arg Pro His Phe Leu 120 125 130 GAT GTT TGT GAT CCA GAT TGG TCA AAA ATC AAC TGC AGC GAT GGT TAC 785 Asp Val Cys Asp Pro Asp Trp Ser Lys Ile Asn Cys Ser Asp Gly Tyr 135 140 145 ATT GAA TAC TAC ATA TGT CGA GGG AAT GCA GAA AGA GTT AAG GAA GGC 833 Ile Glu Tyr Tyr Ile Cys Arg Gly Asn Ala Glu Arg Val Lys Glu Gly 150 155 160 AGG TTG TCC TTC TAT TCA GGC CAC TCT TCG TTT TCC ATG TAC TGC ATG 881 Arg Leu Ser Phe Tyr Ser Gly His Ser Ser Phe Ser Met Tyr Cys Met 165 170 175 180 CTG TTT GTG GCA CTT TAT CTT CAA GCC AGG ATG AAG GGA GAC TGG GCA 929 Leu Phe Val Ala Leu Tyr Leu Gln Ala Arg Met Lys Gly Asp Trp Ala 185 190 195 AGA CTC TTA CGC CCC ACA CTG CAA TTT GGT CTT GTT GCC GTA TCC ATT 977 Arg Leu Leu Arg Pro Thr Leu Gln Phe Gly Leu Val Ala Val Ser Ile 200 205 210 TAT GTG GGC CTT TCT CGA GTT TCT GAT TAT AAA CAC CAC TGG AGC GAT 1025 Tyr Val Gly Leu Ser Arg Val Ser Asp Tyr Lys His His Trp Ser Asp 215 220 225 GTG TTG ACT GGA CTC ATT CAG GGA GCT CTG GTT GCA ATA TTA GTT GCT 1073 Val Leu Thr Gly Leu Ile Gln Gly Ala Leu Val Ala Ile Leu Val Ala 230 235 240 GTA TAT GTA TCG GAT TTC TTC AAA GAA AGA ACT TCT TTT AAA GAA AGA 1121 Val Tyr Val Ser Asp Phe Phe Lys Glu Arg Thr Ser Phe Lys Glu Arg 245 250 255 260 AAA GAG GAG GAC TCT CAT ACA ACT CTG CAT GAA ACA CCA ACA ACT GGG 1169 Lys Glu Glu Asp Ser His Thr Thr Leu His Glu Thr Pro Thr Thr Gly 265 270 275 AAT CAC TAT CCG AGC AAT CAC CAG CCT TGAAAGGCAG CAGGGTGCCC 1216 Asn His Tyr Pro Ser Asn His Gln Pro 280 285 AGGTGAAGCT GGCCTGTTTT CTAAAGGAAA ATGATTGCCA CAAGGCAAGA GGATGCATCT 1276 TTCTTCCTGG TGTACAAGCC TTTAAAGACT TCTGCTGCTG ATATGCCTCT TGGATGCACA 1336 CTTTGTGTGT ACATAGTTAC CTTTAACTCA GTGGTTATCT AATAGCTCTA AACTCATTAA 1396 AAAAACTCCA AGCCTTCCAC CAAAACAGTG CCCCACCTGT ATACATTTTT ATTAAAAAAA 1456 TGTAATGCTT ATGTATAAAC. XTGTATGTAA TATGCTTTCT ATGAATGATG TTTGATTTAA 1516 ATATAATACA TATTAAAATG TATGGGAGAA CCAAAAAAAA AAAAAAAAAA 1566 (2) INFORMATION FOR SEQ ID NO : 4: (i) SEQUENCECHARACTERISTICS: (A) LENGTH: 285 amino acids (B) TYPE: amino acid (D) TOPOLOGY: linear (ii) MOLECULE TYPE: protein (xi) SEQUENCE DESCRIPTION: SEQ ID NO : 4: Met Phe Asp Lys Thr Arg Leu Pro Tyr Val Ala Leu Asp Val Leu Cys 1 5 10 15 Val Leu Leu Ala Ser Met Pro Met Ala Val Leu Lys Leu Gly Gln Ile 20 25 30 Tyr Pro Phe Gln Arg Gly Phe Phe Cys Lys Asp Asn Ser Ile Asn Tyr 35 40 45 Pro Tyr His Asp Ser Thr Ala Ala Ser Thr Val Leu Ile Leu Val Gly 50 55 60 Val Gly Leu Pro Val Ser Ser Ile Ile Leu Gly Glu Thr Leu Ser Val 65 70 75 80 Tyr Cys Asn Leu Leu His Ser Asn Ser Phe Ile Ser Asn Asn Tyr Ile 85 90 95 Ala Thr Ile Tyr Lys Ala Ile Gly Thr Phe Leu Phe Gly Ala Ala Ala 100 105 110 Ser Gln Ser Leu Thr Asp Ile Ala Lys Tyr Ser Ile Gly Arg Leu Arg 115 120 125 Pro His Phe Leu Asp Val Cys Asp Pro Asp Trp Ser Lys Ile Asn Cys 130 135 140 Ser Asp Gly Tyr Ile Glu Tyr Tyr Ile Cys Arg Gly Asn Ala Glu Arg 145 150 155 160 Val Lys Glu Gly Arg Leu Ser Phe Tyr Ser Gly His Ser Ser Phe Ser 165 170 175 Met Tyr Cys Met Leu Phe Val Ala Leu Tyr Leu Gln Ala Arg Met Lys 180 185 190 Gly Asp Trp Ala Arg Leu Leu Arg Pro Thr Leu Gln Phe Gly Leu Val 195 200 205 Ala Val Ser Ile Tyr Val Gly Leu Ser Arg Val Ser Asp Tyr Lys His 210 215 220 His Trp Ser Asp Val Leu Thr G1. t Leu Ile Gln Gly Ala Leu Val Ala 225 230 235 240 Ile Leu Val Ala Val Tyr Val Ser Asp Phe Phe Lys Glu Arg Thr Ser 245 250 255 Phe Lys Glu Arg Lys Glu Glu Asp Ser His Thr Thr Leu His Glu Thr 260 265 270 Pro Thr Thr Gly Asn His Tyr Pro Ser Asn His Gln Pro 275 28G 285 (2) INFORMATION FOR SEQ ID NO : 2 : (i) SEQUENCE CHARACTERISTICS : (A) LENGTH: 1362 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS : single (D) TOPOLOGY: linear (ix)FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 294.. 1226 (ix)FEATURE: (A) NAME/KEY: mat peptide (B) LOCATION: 294.. 1226 (xi) SEQUENCE DESCRIPTION: SEQ ID NO : 5: GGCGCAGCTC TGCAAAAGTT TCTGCTCGGG ATCTGGCTCT CTTCCCCTTG GACTTTAGAA 60 CGATTTAGGG TTGACAGAGG AAAGCAGAGG CGCGCAGGAG GAGCAGAAAA CACCACCTTC 120 TGCAGTTGGA GGCAGGCAGC CCCGGCTGCA CTCTAGCCGC CGCGCCCGGA GCCGGGGCCG 180 ACCCGCCACT ATCCGCAGCA GCCTCGGCC GGAGGCGACC CGGGCGCCTG GGTGTGTGGC 240 TGCTGTTGCG GGACGTCTTC GCGGGGCGGG AGGCTCGCGC CGCAGCCAGC GCC ATG 296 Met 1 CAA AAC TAC AAG TAC GAC AAA GCG ATC GTe CCG GAG AGC AAG AAC GGC 344 Gln Asn Tyr Lys Tyr Asp Lys Ala Ile Val Pro Glu Ser Lys Asn Gly 5 10 15 GGC AGC CCG GCG CTC AAC AAC AAC CCG AGG AGG AGC GGC AGC AAG CGG 392 Gly Ser Pro Ala Leu Asn Asn Asn Pro Arg Arg Ser Gly Ser Lys Arg 20 25 30 GTG CTG CTC ATC TGC CTC GAC CTC TTC TGC CTC TTC ATG GCG GGC CTC 440 Val Leu Leu Ile Cys Leu Asp Leu Phe Cys Leu Phe Met Ala Gly Leu 35 40 45 CCC TTC CTC ATC ATC GAG ACA AGC ACC ATC AAG CCT TAC CAC CGA GGG 488 Pro Phe Leu Ile Ile Glu Thr Ser Thr Ile Lys Pro Tyr His Arg Gly 50 55 60 65 TTT TAC TGC AAT GAT GAG AGC ATC AAG TAC CCA CTG AAA ACT GGT GAG 536 Phe Tyr Cys Asn Asp Glu Ser Ile Lys Tyr Pro'Leu Lys Thr Gly Glu 70 75 80 ACA ATA AAT GAC GCT GTG CTC TGT GCC GTG GGG ATC GTC ATT GCC ATC 584 Thr He Asn Asp Ala Val Leu Cys Ala Val Gly Ile Val Ile Ala Ile 85 90 95 CTC GCC ATC ATC ACG GGG GAA TTC TAC CGG ATC TAT TAC CTG AAG AAG 632 Leu Ala Ile Ile Thr Gly Glu Phe Tyr Arg Ile Tyr Tyr Leu Lys Lys 100 105 110 TCG CGG TCG ACG ATT CAG AAC CCC TAC GTG GCA GCA CTC TAT AAG CAA 680 Ser Arg Ser Thr Ile Gln Asn Pro Tyr Val Ala Ala Leu Tyr Lys Gln 115 120 125 GTG GGC TGC TTC CTC TTT GGC TGT GCC ATC AGC CAG TCT TTC ACA GAC 728 Val Gly Cys Phe Leu Phe Gly Cys Ala Ile Ser Gln Ser Phe Thr Asp 130 135 140 145 ATT GCC AAA GTG TCC ATA GGG CGC CTG CGT CCT CAC TTC TTG AGT GTC 776 Ile Ala Lys Val Ser Ile Gly Arg Leu Arg Pro His Phe Leu Ser Val 150 155 160 TGC AAC CCT GAT TTC AGC CAG ATC AAC TGC TCT GAA GGC TAC ATT CAG 824 Cys Asn Pro Asp Phe Ser Gln Ile Asn Cys Ser Glu Gly Tyr Ile Gln 165 170 175 AAC TAC AGA TGC AGA GGT GAT GAC AGC AAA GTC CAG GAA GCC AGG AAG 872 Asn Tyr Arg Cys Arg Gly Asp Asp Ser Lys Val Gln Glu Ala Arg Lys 180 185 190 TCC TTC TTC TCT GGC CAT GCC TCC TTC TCC ATG TAC ACT ATG CTG TAT 920 Ser Phe Phe Ser Gly His Ala Ser Phe Ser Met Tyr Thr Met Leu Tyr 195 200 205 TTG GTG CTA TAC CTG CAG GCC CGC TTC ACT TGG CGA GGA GCC CGC CTG 968 Leu Val Leu Tyr Leu Gln Ala Arg Phe Thr Trp Arg Gly Ala Arg Leu 210 215 220 225 CTC CGG CCC CTC CTG CAG TTC ACC TTG ATC ATG ATG GCC TTC TAC ACG 1016 Leu Arg Pro Leu Leu Gln Phe Thr Leu Ile Met Met Ala Phe Tyr Thr 230 235 240 GGA CTG TCT CGC GTA TCA GAC CAC AAG CAC CAT CCC AGT GAT GTT CTG 1064 Gly Lé Ser Arg Val Ser Asp His Lys His His Pro Ser Asp Val Leu 245 250 255 GCA GGA TTT GCT CAA GGA GCC CTG GTG GCC TGC TGC ATA GTT TTC TTC 1112 Ala Giv Phe Ala Gln Gly Ala Leu Val Ala Cys Cys Ile Val Phe Phe 260 265 270 GTG TCT GAC CTC TTC AAG ACT AAG ACG ACG CTC TCC CTG CCT GCC CCT 1160 Val Ser Asp Leu Phe Lys Thr Lys Thr Thr Leu Ser Leu Pro Ala Pro 275 280 285 GCT ATC CGG AAG GAA ATC CTT TCA CCT GTG GAC ATT ATT GAC AGG AAC 1208 Ala Ile Arg Lys Glu Ile Leu Ser Pro Val Asp Ile Ile Asp Arg Asn 290 295 300 305 AAT CAC CAC AAC ATG ATG TAGGTGCCAC CCACCTCCTG AGCTGTTTTT 1256 Asn His His Asn Met Met 310 GTAAAATGAC TGCTGACAGC AAGTTCTTGC TGCTCTCCAA TCTCATCAGA CAGTAGAATG 1316 TAGGGAAAAA CTTTTGCCCG ACTGATTTTT AAAAAAAAAA AAAAAA 1362 (2) INFORMATION FOR SEQ ID NO : 6: (i) SEQUENCE CHARACTERISTICS : (A) LENGTH: 311 amino acids (B) TYPE: amino acid (D) TOPOLOGY : linear (ii) MOLECULE TYPE: protein (xi) SEQUENCE DESCRIPTION: SEQ ID NO : 6: Met Gln Asn Tyr Lys Tyr Asp Lys Ala Ile Val Pro Glu Ser Lys Asn 1 5 10 15 Gly Gly Ser Pro Ala Leu Asn Asn Asn Pro Arg Arg Ser Gly Ser Lys 20 25 30 Arg Val Leu Leu Ile Cys Leu Asp Leu Phe Cys Leu Phe Met Ala Gly 35 40 45 Leu Pro Phe Leu Ile Ile Glu Thr Ser Thr Ile Lys Pro Tyr His Arg 50 55 60 Gly Phe Tyr Cys Asn Asp Glu Ser Ile Lys Tyr Pro Leu Lys Thr Gly 65 70 75 80 Glu Thr Ile Asn Asp Ala Val Leu Cys Ala Val Gly Ile Val Ile Ala 85 90 95 Ile Leu Ala Ile Ile Thr Gly Glu Phe Tyr Arg Ile Tyr Tyr Leu Lys 100 105 110 Lys Ser Arg Ser Thr Ile Gln Asn Pro Tyr Val Ala Ala Leu Tyr Lys 115 120 125 Gln Val Gly Cys Phe Leu Phe Gly Cys Ala Ile Ser Gln Ser Phe Thr 130 135 140 Asp Ile Ala Lys Val Ser Ile Gly Arg Leu Arg Pro His Phe Leu Ser 145 150 155 160 Val Cys Asn Pro Asp Phe Ser Gln Ile Asn Cys Ser Glu Gly Tyr Ile 165 170 175 Gln Asn Tyr Arg Cys Arg Gly Asp Asp Ser Lys Val Gln Glu Ala Arg 180 185 190 Lys Ser Phe Phe Ser Gly His Ala Ser Phe Ser Met Tyr Thr Met Leu 195200 205 Tyr Leu Val Leu Tyr Leu Gln Ala Arg Phe Thr Trp Arg Gly Ala Arg 210 215 220 Leu Leu Arg Pro Leu Leu Gln Phe Thr Leu Ile Met Met Ala Phe Tyr 225 230 235 240 Thr Gly Leu Ser Arg Val Ser Asp His Lys His His Pro Ser Asp Val 245 250 255 Leu Ala Gly Phe Ala Gln Gly Ala Leu Val Ala Cys Cys Ile Val Phe 260 265 270 Phe Val Ser Asp Leu Phe Lys Thr Lys Thr Thr Leu Ser Leu Pro Ala 275 280 285 Pro Ala Ile Arg Lys Glu Ile Leu Ser Pro Val Asp Ile Ile Asp Arg 290 295 300 Asn Asn His His Asn Met Met 305 310 (2) INFORMATION FOR SEQ ID NO : 7: (i) SEQUENCE CHARACTERISTICS : (A) LENGTH : 1232 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS : single (D) TOPOLOGY: linear (ix)FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 4.. 833 (ix)FEATURE: (A) NAME/KEY: mat_peptide (B) LOCATION: 4.. 833 (-xi) SEQUENCE DESCRIPTION: SEQ ID NO : 7: ACC ATG CAG CGG AGG TGG GTC TTC GTG CTG CTC GAC GTG CTG TGC TTA 48 Met Gln Arg Arg Trp Val Phe Val Leu Leu Asp Val Leu Cys Leu 1 5 10 15 CTG GTC GCC TCC CTG CCC TTC GCT ATC CTG ACG CTG GTG AAC GCC CCG 96 Leu Val Ala Ser Leu Pro Phe Ala Ile Leu Thr Leu Val Asn Ala Pro 20 25 30 TAC AAG CGA GGA TTT TAC TGC GGG GAT GAC TCC ATC CGG TAC CCC TAC 144 Tyr Lys Arg Gly Phe Tyr Cys Gly Asp Asp Ser Ile Arg Tyr Pro Tyr 35 40 45 CGT CCA GAT ACC ATC ACC CAC GGG CTC ATG GCT GGG GTC ACC ATC ACG 192 Arg Pro Asp Thr Ile Thr His Gly Leu Met Ala Gly Val Thr Ile Thr 50 55 60 GCC ACC GTC ATC CTT GTC TCG GCC GGG GAA GCC TAC CTG GTG TAC ACA 240 Ala Thr Val Ile Leu Val Ser Ala Gly Glu Ala Tyr Leu Val Tyr Thr 65 70 75 GAC CGG CTC TAT TCT CGC TCG GAC TTC AAC AAC TAC GTG GCT GCT GTA 288 Asp Arg Leu Tyr Ser Arg Ser Asp Phe As-a Asn Tyr Val Ala Ala Val 80 85 90 95 TAC AAG GTG CTG GGG ACC TTC CTG TTT GGG GCT GCC GTG AGC CAG TCT 336 Tyr Lys Val Leu Gly Thr Phe Leu Phe Gly Ala Ala Val Ser Gln Ser 100 105 110 CTG ACA GAC CTG GCC AAG TAC ATG ATT GGG CGT CTG AAG CCC AAC TTC 384 Leu Thr Asp Leu Ala Lys Tyr Met Ile Gly Arg Leu Lys Pro Asn Phe 115 120 125 CTA GCC GTC TGC GAC CCC GAC TGG AGC CGG GTC AAC TGC TCG GTC TAT 432 Leu Ala Val Cys Asp Pro Asp Trp Ser Arg Val Asn Cys Ser Val Tyr 130 135 140 GTG CAG CTG GAG AAG GTG TGC AGG GGA AAC CCT GCT GAT GTC ACC GAG 480 Val Gln Leu Glu Lys Val Cys Arg Gly Asn Pro Ala Asp Val Thr Glu 145 150 155 GCC AGG TTG TCT TTC TAC TCG GGA CAC TCT TCC TTT GGG ATG TAC TGC 528 Ala Arg Leu Ser Phe Tyr Ser Gly His Ser Ser Phe Gly Met Tyr Cys 160 165 170 175 ATG GTG TTC TTG GCG CTG TAT GTG CAG GCA CGA CTC TGT TGG AAG TGG 576 Met Val Phe Leu Ala Leu Tyr Val Gln Ala Arg Leu Cys Trp Lys Trp 180 185 190 GCA CGG CTG CTG CGA CCC ACA GTC CAG TTC TTC CTG GTG GCC TTT GCC 624 Ala Arg Leu Leu Arg Pro Thr Val Gln Phe Phe Leu Val Ala Phe Ala 195 200 205 CTC TAC GTG GGC TAC ACC CGC GTG TCT GAT TAC AAA CAC CAC TGG AGC 672 Leu Tyr Val Gly Tyr Thr Arg Val Ser Asp Tyr Lys His His Trp Ser 210 215 220 GAT GTC CTT GTT GGC CTC CTG CAG GGG GCA CTG GTG GCT GCC CTC ACT 720 Asp Val Leu Val Gly Leu Leu Gln Gly Ala Leu Val Ala Ala Leu Thr 225 230 235 GTC TGC TAC ATC TCA GAC TTC TTC AAA GCC CGA CCC CCA CAG CAC TGT 768 Val Cys Tyr Ile Ser Asp Phe Phe Lys Ala Arg Pro Pro Gln His Cys 240 245 250 255 CTG AAG GAG GAG GAG CTG GAA CGG AAG CCC AGC CTG TCA CTG ACG TTG 816 Leu Lys Glu Glu Glu Leu Glu Arg Lys Pro Ser Leu Ser Leu Thr Leu 260 265 270 ACC CTG GGG CGA GGC TG ACCACAACCA CTTATGGGAT ACCCGCACTC 863 Thr Leu Gly Arg Gly 275 TTCTTCCTGA GGCCGGACCC CGCCCAGGCA GGGAGCTGCT GTGAGTCCAG CTGATGCCCA 923 CCCAGGTGGT CCCTCCAGCC TGGTTAGGCA CTGAGGGTTC TGGACGGGCT CCAGGAACCC 983 TGGGCTGATG GGAGCAGTGA GCGGTTCCGC TGCCCC--GC CCTGCACTGG ACCAGGAGTC 1043 TGGAGATGCC TGGGTAGCCC TCAGCATTTG GAGGGGAACC TGTTCCCGTC GGTCCCCAAA 1103 TATCCCCTTC TTTTTATGGG GTTAAGGAAG GGACCGAGAG ATCAGATAGT TGCTGTTTTG 1163 TAAAATGTAA TGTATATGTG GTTTTTAGTA AAATAGGGCA CCTGTTTCAC AAAAAAAAAA 1223 AAAAAAAAA 1232 (2) INFORMATION FOR SEQ ID NO : 8 : (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 276 amino acids (B) TYPE: amino acid (D) TOPOLOGY : linear (ii) MOLECULE TYPE: protein (xi) SEQUENCE DESCRIPTION: SEQ ID N0 : 8 : Met Gln Arg Arg Trp Val Phe Val Leu Leu Asp Val Leu Cys Leu Leu 1 5 10 15 Val Ala Ser Leu Pro Phe Ala Ile Leu Thr Leu Val Asn Ala Pro Tyr 20 25 30 Lys Arg Gly Phe Tyr Cys Gly Asp Asp Ser He Arg Tyr Pro Tyr Arg 35 40 45 Pro Asp Thr Ile Thr His Gly Leu Met Ala slay Val Thr Ile Thr Ala 50 55 60 Thr Val Ile Leu Val Ser Ala Gly Glu Ala Tyr Leu Val Tyr Thr Asp 65 70 75 80 Arg Leu Tyr Ser Arg Ser Asp Phe Asn Asn Tyr Val Ala Ala Val Tyr 85 90 95 Lys Val Leu Gly Thr Phe Leu Phe Gly Ala Ala Val Ser Gln Ser Leu 100 105 110 Thr Asp Leu Ala Lys Tyr Met Ile Gly Arg Leu Lys Pro Asn Phe Leu 115 120 125 Ala Val Cys Asp Pro Asp Trp Ser Arg Val Asn Cys Ser Val Tyr Val 130 135 140 Gln Leu Glu Lys Val Cys Arg Gly Asn Pro Ala Asp Val Thr Glu Ala 145 150 155 160 Arg Leu Ser Phe Tyr Ser Gly His Ser Ser Phe Gly Met Tyr Cys Met 165 170 175 Val Phe Leu Ala Leu Tyr Val Gln Ala Arg Leu Cys Trp Lys Trp Ala 180 185 190 Arg Leu Leu Arg Pro Thr Val Gln Phe Phe Leu Val Ala Phe Ala Leu 195 200 205 Tyr Val Gly Tyr Thr Arg Val Ser Asp Tyr Lys His His Trp Ser Asp 210 215 220 Val Leu Val Gly Leu Leu Gln Gly Ala Leu Val Ala Ala Leu Thr Val 225 230 235 240 Cys Tyr Ile Ser Asp Phe Phe Lys Ala Arg Pro Pro Gin His Cys Leu 245 250 255 Lys Glu Glu Glu Leu Glu Arg Lys Pro Ser Leu Ser Leu Thr Leu Thr 260 265 270 Leu Gly Arg Gly 275 (2) INFORMATION FOR SEQ ID NO : 9: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 283 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (xi) SEQUENCE DESCRIPTION: SEQ ID NO : 9: Met Phe Asp Lys Thr Arg Leu Pro Tyr Val Ala Leu Asp Val Ile Cys 1 5 10 15 Val Leu Leu Ala Gly Leu Pro Phe Ala Ile Leu Thr Ser Arg His Thr 20 25 30 Pro Phe Gln Arg Gly Ile Phe Cys Asn Asp Asp Ser Ile Lys Tyr Pro 35 40 45 Tyr Lys Glu Asp Thr Ile Pro Tyr Ala Leu Leu Gly Gly Ile Val Ile 50 55 au Pro Phe Cys Ile Ile Val Met Ser Ile Gly Glu Ser Leu Ser Val Tyr 65 70 75 80 Phe Asn Val Leu His Ser Asn Ser Phe Val Gly Asn Pro Tyr Ile Ala 85 90 95 Thr Ile Tyr Lys Ala Val Gly Ala Phe Leu Phe Gly Val Ser Ala Ser 100 105 110 Gln Ser Leu Thr Asp Ile Ala Lys Tyr Thr Ile Gly Ser Leu Arg Pro 115 120 125 His Phe Leu Ala Ile Cys Asn Pro Asp Trp Ser Lys Ile Asn Cys Ser 130 135 140 Asp Gly Tyr Ile Glu Asp Tyr Ile Cys Gln Gly Asn Glu Glu Lys Val 145 150 155 160 Lys Glu Gly Arg Leu Ser Phe Tyr Ser Gly His Ser Ser Phe Ser Met 165 170 175 Tyr Cys Met Leu Phe Val Ala Leu Tyr Leu Gln Ala Arg Met Lys Gly 180 185 190 Asp Trp Ala Arg Leu Leu Arg Pro Met Leu Gln Phe Gly Leu He Ala 195 200 205 Phe Ser Ile Tyr Val Gly Leu Ser Arg Val Ser Asp Tyr Lys His His 210 215 220 Trp Ser Asp Val Thr Val Gly Leu Ile Gln Gly Ala Ala Met Ala Ile 225 230 235 240 Leu Val Ala Leu Tyr Val Ser Asp Phe Phe Lys Asp Thr His Ser Tyr 245 250 255 Lys Glu Arg Lys Glu Glu Asp Pro His Thr Thr Leu His Glu Thr Ala 260 265 270 Ser Ser Arg Asn Tyr Ser Thr Asn His Glu Pro 275 280 (2) INFORMATION FOR SEQ ID NO : 10: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 284 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (xi) SEQUENCE DESCRIPTION: SEQ ID NO : 10: Met Phe Asp Lys Thr Arg Leu Pro Tyr Val Ala Leu Asp Val Leu Cys 1 5 10 15 Val Leu Leu Ala Gly Leu Pro Phe Ala Ile Leu Thr Ser Arg His Thr 20 25 30 Pro Phe Gln Arg Gly Val Phe Cys Asn Asp Glu Ser Ile Lys Tyr Pro 35 40 45 Tyr Lys Glu Asp Thr Ile Pro Tyr Ala Leu Leu Gly Gly Ile Ile Ile 50 55 60 Pro Phe Ser Ile Ile Val Ile He Leu Gly Glu Thr Leu Ser Val Tyr 65 70 75 80 Cys Asn Leu Leu His Ser Asn Ser Phe Ile Arg Asn Asn Tyr Ile Ala 85 90 95 Thr Ile Tyr Lys Ala Ile Gly Thr Phe Leu Phe Gly Ala Ala Ala Ser 100 105 110 Gln Ser Leu Thr Asp Ile Ala Lys Tyr Ser Ile Gly Arg Leu Arg Pro 115 120 125 His Phe Leu Asp Val Cys Asp Pro Asp Trp Ser Lys Ile Asn Cys Ser 130 135 140 Asp Gly Tyr Ile Glu Tyr Tyr Ile Cys Arg Gly Asn Ala Glu Arg Val 145 150 155 160 Lys Glu Gly Arg Leu Ser Phe Tyr Ser Gly His Ser Ser Phe Ser Met 165 170 175 Tyr Cys Met Leu Phe Val Ala Leu Tyr Leu Gln Ala Arg Met Lys Gly 180 185 190 Asp Trp Ala Arg Leu Leu Arg Pro Thr Leu Gln Phe Gly Leu Val Ala 195 200 205 Val Ser Ile Tyr Val Gly Leu Ser Arg Val Ser Asp Tyr Lys His His 210 215 220 Trp Ser Asp Val Leu Thr Gly Leu Ile Gln Gly Ala Leu Val Ala Ile 225 230 235 240 Leu Val Ala Val Tyr Val Ser Asp Phe Phe Lys Glu Arg Thr Ser Phe 245 250 255 Lys Glu Arg Lys Glu Glu Asp Ser His Thr Thr Leu His Glu Thr Pro 260 265 270 Thr Thr Gly Asn His Tyr Pro Ser Asn His Gln Pro 275 280 (2) INFORMATION FOR SEQ ID NO : 11 : (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 285 amino acids (B) TYPE: amino acid (C) STRANDEDNESS : single (D) TOPOLOGY: linear (xi) SEQUENCE DESCRIPTION: SEQ ID NO : 11 : Met Phe Asp Lys Thr Arg Leu Pro Tyr Val Ala Leu Asp Val Leu Cys 1 5 10 15 Val Leu Leu Ala Ser Met Pro Met Ala Val Leu Lys Leu Gly Gln Ile 20 25 30 Tyr Pro Phe Gln Arg Gly Phe Phe Cys Lys Asp Asn Ser Ile Asn Tyr 35 40 45 Pro Tyr His Asp Ser Thr Ala Ala Ser Thr Val Leu Ile Leu Val Gly 50 55 60 Val Gly Leu Pro Val Ser Ser Ile Ile Leu Gl. Glu Thr Leu Ser Val 65 70 75 80 Tyr Cys Asn Leu Leu His Ser Asn Ser Phe Ile Arg Asn Asn Tyr Ile 85 90 95 Ala Thr Ile Tyr Lys Ala Ile Gly Thr Phe Leu Phe Gly Ala Ala Ala 100 105 110 Ser Gln Ser Leu Thr Asp Ile Ala Lys Tyr Ser Ile Gly Arg Leu Arg 115 120 125 Pro His Phe Leu Asp Val Cys Asp Pro Asp Trp Ser Lys Ile Asn Cys 130135 140 Ser Asp Gly Tyr Ile Glu Tyr Tyr Ile Cys Arg Gly Asn Ala Glu Arg 145 150 155 160 Val Lys Glu Gly Arg Leu Ser Phe Tyr Ser Gly His Ser Ser Phe Ser 165 170 175 Met Tyr Cys Met Leu Phe Val Ala Leu Tyr Leu Gln Ala Arg Met Lys 180 185 190 Gly Asp Trp Ala Arg Leu Leu Arg Pro Thr Leu Gln Phe Gly Leu Val 195 200 205 Ala Val Ser Ile Tyr Val Gly Leu Ser Arg Val Ser Asp Tyr Lys His 210 215 220 His Trp Ser Asp Val Leu Thr Gly Leu Ile Gln Gly Ala Leu Val Ala 225 230 235 240 Ile Leu Val Ala Val Tyr Val Ser Asp Phe Phe Lys Glu Arg Thr Ser 245 250 255 Phe Lys Glu Arg Lys Glu Glu Asp Ser His Thr Thr Leu His Glu Thr 260 265 270 Pro Thr Thr Gly Asn His Tyr Pro Ser Asn His Gln Pro 275 280 285 (2) INFORMATION FOR SEQ ID NO : 12: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 311 amino acids (B) TYPE: amino acid (C) STRANDEDNESS : single (D) TOPOLOGY: linear (xi) SEQUENCE DESCRIPTION: SEQ ID NO : 12: Met Gln Asn Tyr Lys Tyr Asp Lys Ala Ile Val Pro Glu Ser Lys Asn 1 5 10 15 Gly Gly Ser Pro Ala Leu Asn Asn Asn Pro Arg Arg Ser Gly Ser Lys 20 25 30 Arg Val Leu Leu Ile Cys Leu Asp Leu Phe Cys Leu Phe Met Ala Gly 35 40 45 Leu Pro Phe Leu Ile Ile Glu Thr Ser Thr Ile Lys Pro Tyr His Arg 50 55 60 Gly Phe Tyr Cys Asn Asp Glu Ser Ile Lys Tyr Pro Leu Lys Thr Gly 65 70 75 80 Glu Thr Ile Asn Asp Ala Val Leu Cys Ala Val Gly Ile Val Ile Ala 85 90 95 Ile Leu Ala Ile Ile Thr Gly Glu Phe Tyr Arg Ile Tyr Tyr Leu Lys 100 105 110 Lys Ser Arg Ser Thr Ile Gln Asn Pro Tyr Val Ala Ala Leu Tyr Lys 115 120 125 Gln Val Gly Cys Phe Leu Phe Gly Cys Ala Ile Ser Gln Ser Phe Thr 130 135 140 Asp Ile Ala Lys Val Ser Ile Gly Arg Leu Arg Pro His Phe Leu Ser 145 150 155 160 Val Cys Asn Pro Asp Phe Ser Gln Ile Asn Cys Ser Glu Gly Tyr Ile 165 170 175 Gln Asn Tyr Arg Cys Arg Gly Asp Asp Ser Lys Val Gln Glu Ala Arg 180 185 190 Lys Ser Phe Phe Ser Gly His Ala Ser Phe Ser Met Tyr Thr Met Leu 195 200 205 Tyr Leu Val Leu Tyr Leu Gln Ala Arg Phe Thr Trp Arg Gly Ala Arg 210 215 220 Leu Leu Arg Pro Leu Leu Gln Phe Thr Leu Ile Met Met Ala Phe Tyr 225 230 235 240 Thr Gly Leu Ser Arg Val Ser Asp His Lys His His Pro Ser Asp Val 245 250 255 Leu Ala Gly Phe Ala Gln Gly Ala Leu Val Ala Cys Cys Ile Val Phe 260 265 270 Phe Val Ser Asp Leu Phe Lys Thr Lys Thr Thr Leu Ser Leu Pro Ala 275 280 285 Pro Ala Ile Arg Lys Glu Ile Leu Ser Pro Val Asp Ile He Asp Arg 290 295 300 Asn Asn His His Asn Met Met 305 310 (2) INFORMATION FOR SEQ ID NO : 13: (i) SEQUENCE CHARACTERISTICS : (A) LENGTH: 276 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (xi) SEQUENCE DESCRIPTION: SEQ ID NO : 13: Met Gln Arg Arg Trp Val Phe Val Leu Leu Asp Val Leu Cys Leu Leu 1 5 10 15 Val Ala Ser Leu Pro Phe Ala Ile Leu Thr Leu Val Asn Ala Pro Tyr 20 25 30 Lys Arg Gly Phe Tyr Cys Glu asp Asp Ser Ile Arg Tyr Pro Tyr Arg 35 40 45 Pro Asp Thr Ile Thr His Gly Leu Met Ala Gly Val Thr Ile Thr Ala 50 55 60 Thr Val Ile Leu Val Ser Ala Gly Glu Ala Tyr Leu Val Tyr Thr Asp 65 70 75 80 Arg Leu Tyr Ser Arg Ser Asp Phe Asn Asn Tyr Val Ala Ala Val Tyr 85 90 95 Lys Val Leu Gly Thr Phe Leu Phe Gly Ala Ala Val Ser Gln Ser Leu 100 105 110 Thr Asp Leu Ala Lys Tyr Met : He Gly Arg Leu Lys Pro Asn Phe Leu 115 120 125 Ala Val Cys Asp Pro Asp Trp Ser Arg Val Asn Cys Ser Val Tyr Val 130 135 140 Gln Leu Glu Lys Val Cys Arg Gly Asn Pro Ala Asp Val Thr Glu Ala 145 150 155 160 Arg Leu Ser Phe Tyr Ser Gly His Ser Ser Phe Gly Met Tyr Cys Met 165 170 175 Val Phe Leu Ala Leu Tyr Val Gin Ala Arg Leu Cys Trp Lys Trp Ala 180 185 190 Arg Leu Leu Arg Pro Thr Val Gin Phe Phe Leu Val Ala Phe Ala Leu 195 200 205 Tyr Val Gly Tyr Thr Arg Val Ser Asp Tyr Lys His His Trp Ser Asp 210 215 220 Val Leu Val Gly Leu Leu Gln Gly Ala Leu Val Ala Ala Leu Thr Val 225 230 235 240 Cys Tyr Ile Ser Asp Phe Phe ys Ala Arg Pro Pro Gln His Cys Leu 245 250 255 Lys Glu Glu Glu Leu Glu Arg L,-. *s Pro Ser Leu Ser Leu Thr Leu Thr 260 265 270 Leu Gly Arg Gly 275 (2) INFORMATION FOR SEQ ID NO : 14: (i) SEQUENCE CHARACTERISTICS : (A) LENGTH: 29 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS : single (D) TOPOLOGY: linear (xi) SEQUENCE DESCRIPTION: SEQ ID NO : 14: GGCTCTAGAT ATTAATAGTA ATCAATTAC 29 (2) INFORMATION FOR SEQ ID NO : 15 : (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 26 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS : single (D) TOPOLOGY: linear (xi) SEQUENCE DESCRIPTION: SEQ ID NO : 15: CCTCACGCAT GCACCATGGT AATAGC 26 (2) INFORMATION FOR SEQ ID NO : 16: (i) SEQUENCE CHARACTERISTICS : (A) LENGTH: 24 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (xi) SEQUENCE DESCRIPTION: SEQ ID NO : 16: GGTGCATGCG TGAGGCTCCG GTGC 24 (2) INFORMATION FOR SEQ ID NO : 17: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 28 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (xi) SEQUENCE DESCRIPTION: SEQ ID NO : 17: GTAGTTTTCA CGGTACCTGA AATGGAAG 28 (2) INFORMATION FOR SEQ ID NO : 18: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 30 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (xi) SEQUENCE DESCRIPTION: SEQ ID NO : 18: GGCATGGTAC CATGTTTGAC AAGACGCGGC 30 (2) INFORMATION FOR SEQ ID NO : 19 : (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 23 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (xi) SEQUENCE DESCRIPTION : SEQ ID NO : 19 : CATATGTAGT ATTCAATGTA ACC 23 (2) INFORMATION FOR SEQ ID NO : 20: (i) SEQUENCE CHARACTERISTICS : (A) LENGTH: 47 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS : single (D) TOPOLOGY: linear (xi) SEQUENCE DESCRIPTION: SEQ ID NO : 20: TGATGGCTAG CATGCAGAGA AGATGGGTCT TCGTGCTGCT CGACGTG 47 (2) INFORMATION FOR SEQ ID NO : 21: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 24 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (xi) SEQUENCE DESCRIPTION: SEQ ID NO : 21: AGTGCGGGAT CCCATAAGTG GTTG 24