FIELD OF INVENTION

The present invention relates to a promoter identified from Nicotiana tabacum (tobacco). This invention further relates to the use of said promoter to control the expression of exogenous DNAs of interest in transgenic plants of diverse plant species.

BACKGROUND OF THE INVENTION

Bacteria from the genus Agrobacteπum have the ability to transfer specific segments of DNA (T-DNA) to plant cells, where they stably integrate into the nuclear chromosomes. Analyses of plants harbouring the T-DNA have revealed that this genetic element may be integrated at numerous locations, and can occasionally be found within genes. One strategy which has been exploited to identify integration events within genes is to transform plant cells with specially designed T-DNA vectors which contain a reporter gene, devoid of c s-acting transcriptional and translational expression signals (i.e. promoterless), located at the end of the T-DNA. Upon integration, the initiation codon of the promoterless gene (reporter gene) will be juxtaposed to plant sequences. The consequence of T-DNA insertion adjacent to, and downstream of, gene promoter elements may be the activation of reporter gene expression. The resulting hybrid genes, referred to as T-DNA-mediated gene fusions, consist of unknown and thus un-characterized plant promoters residing at their natural location within the chromosome, and the coding sequence of a marker gene located on the inserted T-DNA (Fobert et al., 1991, Plant Mol. Biol. 17, 837-851).

It has generally been assumed that activation of promoterless or eπhanceriess marker genes result from T-DNA insertions within or immediately adjacent to genes. The recent isolation of several T-DNA insertional mutants

(Koncz ef al., 1992, Plant Mol. Biol. 20, 963-976; reviewed in Feldmann, 1991 , Plant J. 1, 71-82; Van Lijsebettens et al., 1991 , Plant Sci. 80, 27-37; Walden et al., 1991 , Plant J. 1: 281-288; Yanofsky et al., 1990, Nature 346, 35-39), shows that this is the case for at least some insertions. However, other possibilities exist. One of these possibilities is that integration of the T-DNA activates silent regulatory sequences that are not associated with genes. Lindsey et al. (1993, Transgenic Res. 2, 33-47) referred to such sequences as "pseudo-promoters" and suggested that they may be responsible for activating marker genes in some transgenic lines. Fobert et al. (1994, Plant J. 6, 567-577) have cloned such sequences and have referred to these as "cryptic promoters".

SUMMARY OF THE INVENTION

The present invention is directed to a promoter identified from Nicotiana tabacum (tobacco).

The transgenic tobacco plant, T1275, contained a 4.38 kb EcoR\IXba\ fragment containing the 2.15 kb promoterless GUS-nos gene and 2.23 kb of 5 ^* flanking tobacco DNA (2225 bp). This 5' flanking DNA showed no homology to known sequences.

Thus, this invention embraces a promoter characterized in that it comprises at least an 18 bp contiguous sequence of SEQ ID NO:1.

The promoter could not be detected in soybean, potato, sunflower, Arabidopsis, B. napus, B. oleracea, corn, wheat or black spruce by Southern blot analysis. Expression of the cloned fragment in transgenic tobacco, N. tabacum c.v. Petit Havana, SRI and transgenic B. napus c.v. Westar was observed in leaf, ste , root, developing seed and flower. By transient expression analysis, GUS activity was also observed in leaf tissue of soybean, alfalfa, Arabidopsis,

tobacco, β. napus, pea and suspension cultured cells of oat, corn, wheat and barley.

Thus this invention also provides for a promoter that is a constitutive promoter. Furthermore, this promoter functions in diverse plant species when introduced on a cloning vector.

The present invention also embraces a constitutive promoter having a DNA sequence, substantially homologous to SEQ ID NO: 1.

The transcription start site for the introduced GUS gene in transgenic tobacco was located in the plant DNA upstream of the insertion site. It was the same in leaf, stem, root, seeds and flower. Furthermore, the native site was silent in both untransformed and transgenic tobacco.

Thus according to the present invention there is provided a constitutive promoter from tobacco that is cryptic, and that functions in diverse plant species when introduced in a cloning vector.

This invention also relates to a chimeric gene construct comprising a DNA of interest for which constitutive expression is desired, and a constitutive promoter, comprising at least an 18 bp contiguous sequence of SEQ ID NO: 1.

This invention further relates to a cloning vector containing said chimeric gene construct.

This invention also includes a plant cell which has been transformed with said chimeric gene, or said cloning vector. Furthermore, this invention embraces transgenic plants containing said chimeric gene, or said cloning vector.

This invention further relates to any transgenic plant containing a constitutive promoter, having a DNA sequence substantially homologous to SEQ ID NO: 1 , operatively linked to a DNA region that is transcribed into RNA.

Also included in the present invention is a method of conferring constitutive expression of a gene in a plant, comprising: operatively linking an exogenous DNA of interest, for which constitutive expression is desired, with a constitutive promoter comprising at least an 18 bp contiguous sequence of SEQ ID NO:1 , to produce a chimeric gene construct and introducing the chimeric gene construct into a plant capable of expressing the chimeric gene construct.

BRIEF DESCRIPTION OF THE DRAWINGS

These and other features of the invention will become more apparent from the following description in which reference is made to the appended drawings wherein:

FIGURE 1 shows the constitutive expression of GUS in all tissues of plant T1275, including leaf segments (a), stem cross-sections (b), roots (c), flower cross-sections (d), ovary cross-sections (e), immature embryos (f), mature embryos (g), and seed cross-sections (h).

FIGURE 2 shows the GUS specific activity, which reveals that the level of GUS expression in T1275 is comparable to levels in plants expressing Ca V 35S - GUS - nos genes in leaf tissues.

FIGURE 3 is the Southern blot analysis of Eco Rl digested T1275 DNA with a GUS gene coding region probe (lane 1) and a nptll gene coding region probe (lane 2) revealing a single T-DNA insertion site in plant T1275.

FIGURE 4 shows the cloned GUS gene fusion from pT1275. The arrow indicates the GUS mRNA start site within the plant DNA sequence.

FIGURE 5 shows the restriction map of the isolated plant DNA sequence. The arrow indicates the GUS mRNA start site within the plant DNA sequence.

FIGURE 6 shows that GUS specific activity varies in leaves of individual, regenerated, greenhouse-grown tobacco plants selected at random

(Figure 6A) and is generally correlated with the level of accumulated GUS mRNA measured by RNase protection assay and densitometry of autoradiograms

(Figure 6B).

FIGURE 7 shows that transcripts corresponding to the native plant sequence in situ do not accumulate (3) in leaves of untransformed (lane U) or transgenic (lane T25) tobacco plants; whereas, transcripts corresponding to the same plant sequence fused to the GUS gene within the T-DNA inserted into transgenic plant T25 (lane T25) are present in the protected fragment indicated (2). The undigested probe (1) is presented in lane P as a control.

DESCRIPTION OF PREFERRED EMBODIMENT

The present invention relates to plant gene regulatory sequences. Specifically this invention relates to a promoter, identified by T-DNA tagging with a promoterless β-glucuronidase gene (GUS) to generate a transgenic N. tabacum plant that expresses GUS activity constitutively.

This invention is also directed to a promoter that comprises a nucleotide sequence of at least 18 contiguous base pairs of SEQ ID NO:1.

Oligonucleotides of 18 bp or more are useful in constructing heterologous promoters that comprise fragments of the promoter as defined in SEQ ID NO: 1.

The use of such heterologous promoters is well established in the literature. For example, fragments of specific elements within the 35S CaMV promoter have been duplicated or combined with other promoter fragments to produce chimeric promoters with desired properties (e.g. U.S. 5,491 ,288, 5,424,200, 5,322,938, 5,196,525, 5,164,316). Furthermore, oligonucleotides of 18 bps or longer are useful as probes or PCR primers in identifying or amplifying related DNA or RNA sequences in other tissues or organisms.

In the context of this disclosure, the term "promoter" or "promoter region" refers to a sequence of DNA, usually upstream (5') to the coding sequence of a structural gene, which controls the expression of the coding region by providing the recognition for RNA polymerase and/or other factors required for transcription to start at a particular site.

There are generally two types of promoters, inducible and constitutive promoters. An inducible promoter is a promoter that is capable of directly or indirectly activating transcription of one or more DNA sequences or genes in response to an inducer. In the absence of an inducer the DNA sequences or genes will not be transcribed. Typically the protein factor, that binds specifically to an inducible promoter to activate transcription, is present in an inactive form which is then directly or indirectly converted to the active form by the inducer. The inducer can be a chemical agent such as a protein, metabolite, growth regulator, herbicide or phenolic compound or a physiological stress imposed directly by heat, cold, salt, or toxic elements or indirectly through the action of a pathogen or disease agent such as a virus. A plant cell containing an inducible promoter may be exposed to an inducer by externally applying the inducer to the cell or plant such as by spraying, watering, heating or similar methods.

A constitutive promoter directs the expression of a gene throughout the various parts of a plant and continuously throughout plant development.

Examples of known constitutive promoters include those associated with the CaMV 35S transcript. (Odell et al., 1985, Nature, 313: 810-812), the rice actin 1 (Zhang et al, 1991, Plant Cell, 3: 1155-1165) and triosephosphate isomerase 1 (Xu et al, 1994, Plant Physiol. 106: 459-467) genes, the maize ubiquitin 1 gene (Cornejo et al, 1993, Plant Mol. Biol. 29: 637-646), the Arabidopsis ubiquitin 1 and 6 genes (Holtorf et al, 1995, Plant Mol. Biol. 29: 637-646), and the tobacco translational initiation factor 4A gene (Mandel et al, 1995 Plant Mol. Biol. 29: 995-1004). The present invention is directed to a DNA sequence which contains a promoter capable of directing the expression of a gene. Preferably the promoter is a constitutive promoter isolated from N. tabacum.

The term "constitutive" as used herein does not necessarily indicate that a gene is expressed at the same level in all cell types, but that the gene is expressed in a wide range of cell types, although some variation in abundance is often observed.

The present invention is further directed to a chimeric gene construct containing a DNA of interest operatively linked to the promoter of the present invention. Any exogenous gene can be used and manipulated according to the present invention to result in the expression of said exogenous gene. A DNA of interest may include, but is not limited to, a gene encoding a protein, a DNA that is transcribed to produce antisense RNA, or a transcript product that functions in some manner that mediates the expression of other DNAs, for example that results in the co-suppression of other DNAs or the like.

The chimeric gene construct of the present invention can further comprise a 3' untranslated region. A 3' untranslated region refers to that portion of a gene comprising a DNA segment that contains a polyadenylation signal and any other regulatory signals capable of effecting mRNA processing or gene expression. The polyadenylation signal is usually characterized by effecting the addition of polyadenylic acid tracks to the 3' end of the mRNA precursor.

Polyadenylation signals are commonly recognized by the presence of homology to the canonical form 5' AATAAA-3' although variations are not uncommon.

Examples of suitable 3' regions are the 3' transcribed non- translated regions containing a polyadenylation signal of Agrobacterium tumor inducing (Ti) plasmid genes, such as the nopaline synthase (Nos gene) and plant genes such as the soybean storage protein genes and the small subunit of the ribulose-1 , 5-bisphosphate carboxylase (ssRUBISCO) gene. The 3' untranslated region from the structural gene of the present construct can therefore be used to construct chimeric genes for expression in plants.

The chimeric gene construct of the present invention can also include further enhancers, either translation or transcription enhancers, as may be required. These enhancer regions are well known to persons skilled in the art, and can include the ATG initiation codon and adjacent sequences. The initiation codon must be in phase with the reading frame of the coding sequence to ensure translation of the entire sequence. The translation control signals and initiation codons can be from a variety of origins, both natural and synthetic. Translational initiation regions may be provided from the source of the transcriptional initiation region, or from the structural gene. The sequence can also be derived from the promoter selected to express the gene, and can be specifically modified so as to increase translation of the mRNA.

To aid in identification of transformed plant cells, the constructs of this invention may be further manipulated to include plant selectable markers. Useful selectable markers include enzymes which provide for resistance to an antibiotic such as gentamycin, hygromycin, kanamycin, and the like. Similarly, enzymes providing for production of a compound identifiable by colour change such as GUS (β-glucuronidase), or luminescence, such as luciferase are useful.

Also considered part of this invention are transgenic plants containing the chimeric gene construct comprising the promoter of the present invention. Methods of regenerating whole plants from plant cells are known in the art, and the method of obtaining transformed and regenerated plants is not critical to this invention. In general, transformed plant cells are cultured in an appropriate medium, which may contain selective agents such as antibiotics, where selectable markers are used to facilitate identification of transformed plant cells. Once callus forms, shoot formation can be encouraged by employing the appropriate plant hormones in accordance with known methods and the shoots transferred to rooting medium for regeneration of plants. The plants may then be used to establish repetitive generations, either from seeds or using vegetative propagation techniques.

The constructs of the present invention can be introduced into plant cells using Ti plasmids, Ri plasmids, plant virus vectors, direct DNA transformation, micro-injection, electroporation, etc. For reviews of such techniques see for example Weissbach and Weissbach, Methods for Plant Molecular Biology, Academy Press, New York VIII, pp. 421-463 (1988); and Geierson and Corey, Plant Molecular Biology, 2d Ed. (1988). The present invention further includes a suitable vector comprising the chimeric gene construct.

When specific sequences are referred to in the present invention, it is understood that these sequences include within their scope sequences that are "substantially homologous" to said specific sequences. Sequences are "substantially homologous" when at least about 70%, preferably at least about 80% and most preferably at least about 90% of the nucleotides match over a defined length of the molecule. Sequences that are "substantially homologous" include any substitution, deletion, or addition within the sequence. DNA sequences that are substantially homologous can be identified in Southern hybridization experiments, for example under stringent hybridization conditions

(see Maniatis et al., in Molecular Cloning (A Laboratory Manual), Cold Spring Harbor Laboratory (1982) p 387 to 389).

The specific sequences, referred to in the present invention, also include sequences which are "functionally equivalent" to said specific sequences. In the present invention functionally equivalent sequences refer to sequences which although not identical to the specific sequences provide the same or substantially the same function. DNA sequences that are functionally equivalent include any substitution, deletion or addition within the sequence. With reference to the present invention functionally equivalent sequences will direct the expression of an exogenous gene constitutively.

While this invention is described in detail with particular reference to preferred embodiments thereof, said embodiments are offered to illustrate but not limit the invention.

EXAMPLES

Characterization of a Constitutive promoter - GUS Fusion

Transfer of binary constructs to Agrobacterium and leaf disc transformation of N. tabacum SR1 were performed as described by Fobert et al. (1991, Plant Mol. Biol. 17, 837-851). Plant tissue was maintained on 100 μg/ml kanamycin sulfate (Sigma) throughout in vitro culture.

From the transgenic plants produced, one of these, T1275, was chosen for detailed study because of its high level and constitutive expression of GUS.

Fluorogenic and histological GUS assays were performed according to Jefferson (Plant Mol. Biol. Rep., 1987, 5, 387-405), as modified by Fobert et al. (Plant Mol. Biol., 1991, 17, 837-851). For initial screening, leaves

11 were harvested from in vitro grown plantlets. Later nine different tissues: leaf (L), stem (S), root (R), anther (A), petal (P), ovary (O), sepal (Se), seeds 10 days post anthesis (S1) and seeds 20 days post-anthesis (S2), were collected from plants grown in the greenhouse and analyzed. For detailed, quantitative analysis of GUS activity, leaf, stem and root tissues were collected from kanamycin resistant F1 progeny grown in vitro. Floral tissues were harvested at developmental stages 8-10 (Koltunow et al., 1990, Plant Cell 2, 1201-1224) from the original transgenic plants. Flowers were also tagged and developing seeds were collected from capsules at 10 and 20 dpa. In all cases, tissue was weighed, immediately frozen in liquid nitrogen, and stored at -80°C.

Tissues analyzed by histological assay were at the same developmental stages as those listed above. Different hand-cut sections were analyzed for each organ. For each plant, histological assays were performed on at least two different occasions to ensure reproducibility. Except for floral organs, all tissues were assayed in phosphate buffer according to Jefferson (1987, Plant Mol. Biol. Rep. 5, 387-405), with 1 mM X-Gluc (Sigma) as substrate. Flowers were assayed in the same buffer containing 20% (v/v) methanol (Kosugi et al., 1990, Plant Sci. 70, 133-140).

GUS activity in plant T1275 was found in all tissues. Figure 1 shows the constitutive expression of GUS by histochemical staining with X-Gluc of T1275, including leaf (a), stem (b), root (c), flower (d), ovary (e), embryos (f and g), and seed (h).

Constitutive GUS expression was confirmed with the more sensitive fluorogenic assay of plant tissue from transformed plant T1275. These results are shown in Figure 2. GUS expression was evident in all tissue types including leaf (L), stem (S), root (R), anther (A), pistil (P), ovary (O), sepal (Se), seeds at 10 dpa (S1) and 20 dpa (S2). Furthermore, the level of GUS expression is comparable to the level of expression in transformed plants

containing the constitutive promoter CaMV 35S in a GUS - nos fusion. As reported by Fobert er al. (1991 , Plant Molecular Biology, 17: 837-851) GUS activity in transformed plants containing pBI121 (Clontech), which contains a CaMV 35S - GUS - nos chimeric gene, was as high as 18,770 ± 2450 (pmole MU per minute per mg protein).

Genetic Analysis of Transgenic Plant T1275

The T-DNA contains a kanamycin resistance gene. Seeds from self-pollinated transgenic plants were surface-sterilized in 70% ethanol for 1 min and in undiluted Javex bleach (6% sodium hypochloride) for 25 min. Seeds were then washed several times with sterile distilled water, dried under laminar flow, and placed in Petri dishes containing MSO medium supplemented with 100 μg/ml kanamycin as described in Miki et al. (1993, Methods in Plant Molecular Biology and Biotechnology, Eds., B.R. Glick and J.E. Tompson, CRC Press, Boca Raton, 67-88). At least 90 plantlets were counted for each transformant. The number of green (kanamycin-resistant) and bleached (kanamycin-sensitive) plantlets were counted after 4-6 weeks, and analyzed using the Chi ² test at a significance level of P<0.05.

The genetic analysis results are shown below in Table 1 , which demonstrates that the T-DNA loci segregated as a single locus of insertion.

TABLE 1 Genetic Analysis of Transgenic Plant T1275

No. of No. of Observed Expected Chi ²

Progeny Progeny Ratio Ratio

Km ^r Km ⁸

262 88 3:1 ^* 3:1 0

^* Consistent with a single dominant gene

Southern Blot Analysis

The T-DNA in the transgenic plant T1275 was analyzed using either a GUS gene coding region probe or a nptll gene coding region probe.

Genomic DNA was isolated from freeze-dried leaves using the protocol of Sanders et al. (1987, Nucleic Acid Res. 15, 1543-1558). Ten micrograms of T1275 DNA was digested for several hours with EcoRI using the appropriate manufacturer-supplied buffer supplemented with 2.5 mM spermidine. After electrophoresis through a 0.8% TAE agarose gel, Southern blot analysis was conducted using standard protocols. As the T-DNA from the construct containing the constitutive promoter - GUS - nos construct contains only a single Eco Rl recognition site the hybridizing fragments are composed of both T-DNA and flanking tobacco DNA sequences. The length of the fragment will vary depending on the location of the nearest Eco Rl site. Using the GUS gene as a probe (Figure 3 - lane 1), the fragment to the nearest Eco Rl site in the plant DNA will be detected. With T1275, one such fragment was located. Using the nptll coding region as a probe (Figure 3 - lane 2), which hybridizes to sequences on the opposite side of the Eco Rl site, again only one hybridization band was evident. As can also be seen in Figure 3, no major rearrangements occurred within the T-DNA.

Cloning and Analysis of the Constitutive Promoter - GUS Fusion

Genomic DNA was isolated from leaves according to Hattori et al. (1987, Anal. Biochem. 165, 70-74). Ten μg of T1275 total DNA was digested with EcoRI and Xbal according to the manufacturer's instructions. The digested DNA was size-fractionated on a 0.7% agarose gel. The DNA fragments of about 4 to 6 kb were isolated from the gel using the Elu-Quick kit (Schleicher and Schuell) and ligated to iambdaGEM-2 arms previously digested with EcoRI and Xoal and phosphatase-treated. About 40,000 plaques were transferred to a nylon membrane (Hybond, Amersham) and screened with the ³² P-labelled 2kb GUS insert isolated form pBI121 , essentially as described in Rutledge et al. (1991 , Mol. Gen Genet. 229, 31-40). The positive clones were isolated. The Xbal-EcoRI fragment (see restriction map of Figure 4 and Figure 5) was isolated from the lambda phage and cloned into pTZ19R previously digested with Xbal and EcoRI and treated with intestinal calf phosphatase.

The plant DNA sequence within the clone has not been previously reported in sequence data bases. It is not observed among diverse species as Southern blots did not reveal bands hybridizing with the fragment in soybean, potato, sunflower, Arabidopsis, B. napus, B. oleracea, corn, wheat or black spruce (data not shown). In tobacco, Southern blots did not reveal evidence for gross rearrangements at or upstream of the T-DNA insertion site (data not shown).

For analysis of transient expression of GUS activity mediated by biolistics (Sandford et al, 1983, Methods Enzymol, 217: 483-509), the Xbal - EcoRI fragment was subcloned in pUC19 and GUS activity was detected by staining with X-Gluc as described above. Leaf tissue of greenhouse-grown plants or cell suspension cultures were examined for the number of blue spots that stained. As shown in Table 2, the T1275 promoter - GUS nos gene was active in each of the diverse species examined.

TABLE 2 Transient Expression of GUS Activity in Tissues of Diverse Plant Species

Tissue Source Species GUS Activity *

Leaf Soybean +++

Alfalfa ++

Arabidopsis +

Leaf disc Tobacco ++ β. napus + Pea +

Cell Cultures Oat + Corn + Wheat + Barley ++

* Numbers of blue spots: 1 - 10 (+), 10 - 100 (++), 100 - 400 (+++)

The 4.2kb fragment containing about 2.2kb of the T1275 promoter fused to the GUS gene and the nos 3' was isolated by digesting pTZ-T1275 with Hind\\\ and EcoRI. The isolated fragment was ligated into the pRD400 vector (Datla et al., 1992, Gene, 211:383-384) previously digested with H/ndlll and EcoRI and treated with calf intestinal phosphatase. Transfer of the binary vector to Agrobacterium tumefaciens and leaf disc transformation of N. tabacum SR1 were perfoimed as described above. GUS activity was examined in several organs of many independent transgenic lines. GUS mRNA was also examined in the same organ by RNase protection assay (Melton et al, 1984, Nucleic Acids Res. 121 : 7035 - 7056) using a probe that mapped the mRNA 5' end in both untransformed and transgenic tissues. RNA was isolated from frozen-ground tissues using the TRIZOL Reagent (Life Technologies) as described by the manufacturer. For each assay 10 - 30 ug of total RNA was hybridized to an antisense RNA probe corresponding to 600 bases of the T1275 plant sequence and 400 bases of the GUS gene. Assays were performed using the RPAII kit (Ambion CA) as described by the manufacturer. The protected fragments were

separated on a 5% Long Ranger acrylamide (J.J. Baker, NJ.) denaturing gel which was dried and exposed to Kodak X-RP film.

Analysis of leaves of randomly-selected, green house-grown plants regenerated from culture revealed a wide range of GUS specific activities (Figure 6A). Plants transformed with pBl 121 (CLONETECH) which contains the 35S- GϋS-nos gene yielded comparable specific activity levels (data not shown). Generally, the level of GUS mRNA in the leaves (Figure 6B) correlated with the GUS specific activities. Furthermore, the presence of a single band of about 600 bases in all samples indicated that the GUS transcription start site was located about 180 bases upstream of the T-DNA insertion site within the plant DNA sequence.

For analysis of GUS expression in different organs, lines derived from progeny of the above lines were examined in detail. Table 3 shows the GUS specific activities in one of these plants. It is expressed in leaf, stem, root, developing seeds and the floral organs, sepals, petals, anthers, pistils and ovaries at varying levels, confirming constitutive expression. Introduction of the same vector into β. napus also revealed expression of GUS activity in these organs (data not shown) indicating that constitutive expression was not specific to tobacco. Examination of GUS mRNA in the tobacco organs showed that the transcription start sites was the same in each and the level of mRNA was similar except in flower buds where it was lower (Table 3).

Assays performed with RNA from leaves, stem, root, developing seeds and flowers of untransformed tobacco did not reveal a protected fragment using the same probe as above (Figure 7). It is therefore assumed that the insertion site is transcriptionaly silent in untransformed tobacco and is activated by T-DNA insertion. The region upstream of the insertion site is therefore another example of a plant cryptic promoter (Fobert et al, 1994, Plant J. 6:568- 577).

TABLE 3

GUS Specific Activity and Relative RNA Levels in the Organs of Progeny of Transgenic Line T64

Organ Relative GUS GUS Specific Activity RNA Levels in (picomol/MU/min/mg protein) T64 Progeny (grey scale Transformed Untransformed units) Tobacco T64 Tobacco

Leaf 1774 988.32 3.02

Stem 1820 826.48 7.58

Root 1636 4078.45 22.18

14 day post 1790 253.21 10.03 anthesis

Seeds

Flower - buds 715 2.59 ND*

Petals ND ^* 28.24 1.29

Anthers ND ^* 4.64 0.35

Pistils ND* 9.76 1.72

Sepals ND* 110.02 2.48

Ovary ND* 4.42 2.71

* Not Done

All scientific publications and patent documents are incorporated herein by reference.

The present invention has been described with regard to preferred embodiments. However, it will be obvious to persons skilled in the art that a number of variations and modifications can be made without departing from the scope of the invention as described in the following claims.

SEQUENCE LISTING

(1) GENERAL INFORMATION:

(i) APPLICANT:

(A ⁾ NAME: HER MAJESTY IN RIGHT OF CANADA, AS REPRESENTED BY THE

MINISTER OF AGRICULTURE AND AGRI-FOOD CANADA

(B) STREET: Central Experimental Farm

(C) CITY: Ottawa

(D) STATE: Ontario

(E) COUNTRY: Canada

(F) POSTAL CODE (ZIP) : K1A 0C6

(A) NAME: PIERRE FOBERT

(B) STREET: 707 Tobin Terrace

(C) CITY: Saskatoon

(D) STATE: Saskatchewan

(E) COUNTRY: Canada

(F) POSTAL CODE (ZIP) : S7N 4P4

(A) NAME: VENKATRAN N. IYER

(B) STREET: 2595 Maquinna Road

(C) CITY: Kelowna

(D) STATE: ^' British Columbia

(E) COUNTRY: Canada

(F) POSTAL CODE (ZIP) : V1W 2R9

(ii) TITLE OF INVENTION: Promoter From Tobacco (iii) NUMBER OF SEQUENCES: 1

(iv) 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 (EPO)

(2) INFORMATION FOR SEQ ID NO: 1:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 2224 base pairs

(B) TYPE: nucleic acid

(C) STRANDEDNESS: double

(D) TOPOLOGY: linear

(xi) SEQUENCE DESCRIPTION: SEQ ID NO: 1: TCTAGACTTA CAGAAAGTCT CTAACACGTG AGGGAATGAT CCCTTTCCTT ACCTCCCTGT 60

AGAGATATTG GCTTTTCAAC AACTAGTACA TAAATATGCG ACTTTGACCG TGTATCCCCA 120

GTCAAAAGGG AACTTCACCC TCCTAGTTCT TTATTTCCAA CATACATGGG GAGTAATGCT 180

AAATTTACAT AGAAGAATAA TAAAATGAAC TGTAACTAAT GATGTACTGT TCCAAAGAGA 240

TGAGGACGTC AACATATTTA TTCCTTCAGC CCTTTTCAGA ATAATACCAT AAGTAGAAGA 300

AATGGCACAT AAAATGAAGT CCTCGGCAAG TCAAATGTAA ATCTGAACCC ACCCAGCTAA 350

CCCAGTGAAC TCAACTTTCC TGGATAGATC AGCACTCCTT CATGACATTG CATGCCTTCT 4 0

CTTTAAAGAG CCGCTTGATC TCTGAAAACC AAATGAATCT CCACAGAGAG ATTTCGAGCT 480

CCATGAGACG CCTTTTGGTT CTTGATTTAC TAAACCTATA AAAATGAAAG GAAGTAGGAC 540

AACTGCATTT TGCCGCTTAA GATGCTTCGG CGCTTTGTGA ATTTTAAGTC ATGAGAAAGT S00

ACAATGTTGG AATCTCACAT TAGAACAATG TATTTGTAAT AACCTAGGAA AGCAAAGCTA S60

GAAGGGAGGT GCAGCTAAAT CTTCTTCTAC CTTGTTATCC TTGCATTTCT TGAGGAGGAG 720

GAACTGTCCT CGCAGGTGCA AAATCTGCAG TCGCCCAAAA GGATATTCAG AAGTATATTA 780

CAACATGTTT AATGGTTAAC CAAGTGAAAG ATCAAAATAG TCATTAGAAC AAAATGCGTG 840

CTCAGAGCGT ATCTACTAGT TCATCAACCC AGTACACATC TCTGAATTTC ATCTCTTGCC 900

GTTGAACTAA GTCAATTGGT CAAAGACGCA TAACATGAGA GACACTCATA AAACGGCTGA 960

ATAACATGCA GAAGACGTCA TGCGCCTTAG GTCTCATTAT GCATGAGATT ATTAGTTATA 1020

TGCTCCTTCA GTTTGACTAG AAATGAAAAA TCAGTTAAGC CTGTAACGAA ATGATAACCT 1080

GCTTCAAGAA GATTAGACTA TTTTTCATAA AATATGCAGT GCCGTGAAAT AGATACTTAA 11 0

TCTTAGGCAG GAAAAATCTT CTATTGGGCC ATAATAAGAA CTACCAATTA GAAAGGAGGT 1200

AGAAAGCTCC GATACTGTTA TGAAGGCCAT TCTAAGTGCT GATGTGAATT TCCCAATACA 1260

AAATGACAAC AAAAACAAAA GCCTCAATCC TAAGCTAGTT GGGGTCGCTA TATAAATCCT 1320

CGACATCCAT TTAACTCCAC TTGGACTCCT TTCTTTCCAA TATTTTAATA TTGTTAGATT 1380

AATCATAAAA TTGCTTAGCT TTCTACTGGC ACTTAACCTA CTGCAACCCT CCTCTTCTGG 1440

GATTCCAACA CAAACAACTA AGAGGAATTT GAAAAAAAGA AAGCAAATGT GAGAAGAGAC 1500

AAAATGTACA ATGATACCTC TTCTTGCAGC AAAGGAGGCA GGTTCTCTGC TGAGACAAGG 1560

TTCTCTATTT CCTGCAAGAC CTTCGTATCT TTTATTCGAG ACCATGTATG TGGAGGTAAC 1620

GCCAGCAATA GTGCTGTCAG CACATCGTTG CTTGCAGGGG ATCTTCTGCA AGCATCTCTA 1680

TTTCCTGAAG GTCTAACCTC GAAGATTTAA GATTTAATTA CGTTTATAAT TACAAAATTG 1740

ATTCTAGTAT CTTTAATTTA ATGCTTATAC ATTATTAATT AATTTAGTAC TTTCAATTTG 1800

TTTTCAGAAA TTATTTTACT ATTTTTTATA AAATAAAAGG GAGAAAATGG CTATTTAAAT 1860

ACTAGCCTAT TTTATTTCAA TTTTAGCTTA AAATCAGCCC CAATTAGCCC CAATTTCAAA 1920

TTCAAATGGT CCAGCCCAAT TCCTAAATAA CCCACCCCTA ACCCGCCCGG TTTCCCCTTT 1980

TGATCCAGGC CGTTGATCAT TTTGATCAAC GCCCAGAATT TCCCCTTTTC CTTTTTTAAT 2040

TCCCAAACAC CCCTAACTCT ATCCCATTTC TCACCAACCG CCACATATGA ATCCTCTTAT 2100

CTCTCAAACT CTCTCGAACC TTCCCCTAAC CCTAGCAGCC TCTCATCATC CTCACCTCAA 2160

AACCCACCGG AATACATGGC TTCTCAAGCC GTGGAAACCT TATACTCACC TCCCTTTGCT 2220

CTTA ²²⁴