Sunflower disease resistance genes

Abstract

Compositions and methods for enhancing disease resistance in plants are provided. Compositions comprise sunflower resistance gene analogs. The methods involve transforming a plant with a resistance nucleotide sequence. The methods find use in enhancing broad-based resistance in plants to pathogens. Also provided are transformed plants, plant cells, tissues, and seeds having enhanced disease resistance. The R gene analogs can be used as molecular markers for disease resistance.

Description

FIELD OF THE INVENTION

The invention relates to the genetic manipulation of plants, particularly to transforming plants with genes that enhance disease resistance, and breeding program for screening tolerance/resistance lines.

BACKGROUND OF THE INVENTION

Disease in plants is caused by biotic and abiotic causes. Biotic causes include fungi, viruses, bacteria, and nematodes. Of these, fungi are the most frequent causative agent of disease on plants. Abiotic causes of disease in plants include extremes of temperature, water, oxygen, soil pH, plus nutrient-element deficiencies and imbalances, excess heavy metals, and air pollution.

A host of cellular processes enables plants to defend themselves from disease caused by pathogenic agents. These processes apparently form an integrated set of resistance mechanisms that is activated by initial infection and then limits further spread of the invading pathogenic microorganism.

Subsequent to recognition of a potentially pathogenic microbe, plants can activate an array of biochemical responses. Generally, the plant responds by inducing several local responses in the cells immediately surrounding the infection site. The most common resistance response observed in both non-host and race-specific interactions is termed the “hypersensitive response” (HR). In the hypersensitive response, cells contacted by the pathogen, and often neighboring cells, rapidly collapse and dry in a necrotic fleck. Other responses include the deposition of callose, the physical thickening of cell walls by lignification, and the synthesis of various antibiotic small molecules and proteins. Genetic factors in both the host and the pathogen determine the specificity of these local responses, which can be very effective in limiting the spread of infection.

The hypersensitive response in many plant-pathogen interactions results from the expression of a resistance (R) gene in the plant and a corresponding avirulence (avr) gene in the pathogen. (Flor (1971) Ann. Rev. Phytopath . 9:274). This interaction is associated with the rapid, localized cell death of the hypersensitive response. R genes that respond to specific bacterial, fungal, or viral pathogens, have been isolated from a variety of plant species and several appear to encode cytoplasmic proteins.

The resistance gene in the plant and the avirulence gene in the pathogen often conform to a gene-for-gene relationship. That is, resistance to a pathogen is only observed when the pathogen carries a specific avirulence gene and the plant carries a corresponding or complementing resistance gene. The theory has been developed by genetic studies of plant/pathogen interactions in a variety of plant systems (Keen (1990) Ann. Rev. Genet . 24:447-463). Because avrR gene-for-gene relationships are observed in many plant-pathogen systems and are accompanied by a characteristic set of defense responses, a common molecular mechanism underlying avrR gene mediated resistance has been postulated. A simple model which has been proposed is that pathogen avr genes directly or indirectly generate a specific molecular signal (ligand) that is recognized by cognate receptors encoded by plant R genes.

Both plant resistance genes and corresponding pathogen avirulence genes have been cloned. The plant kingdom contains thousands of R genes with specific specificities for viral, bacterial, fungal, or nematode pathogens. Although there are differences in the defense responses induced during different plant-pathogen interactions, some common themes are apparent among R gene-mediated defenses. The function of a given R gene is dependent on the genotype of the pathogen. Plant pathogens produce a diversity of potential signals, and in a fashion analogous to the production of antigens by mammalian pathogens, some of these signals are detectable by some plants.

Recently a number of R genes have been isolated from various plant species that interact with different pathogens (avr) genes (Bent (1996) Plant Cell 8:1757-1771; Hammond-Kosack et al. (1997) Ann. Rev. Plant Physiol. Plant Mol. Biol . 48:575-607; Ellis etal. (1988) Cur. Opin. in Plant Path . 1:288-293). The recent development of new methods for gene isolation in plants has permitted isolation of many R genes from other plant species (Yu et al. (1996) Proc. Natl. Acad. Sci. USA 93:11751-11756; Leister et al. (1998) Proc. Natl. Acad. Sci. USA . 95:370-375). Although the products of most avirulence genes show very little homology with each other, the reported R genes have conserved functional domains such as the protein kinase (PK) domain, leucine-rich regions (LRR), nucleotide-binding sites (NBS) Bent (1996) Plant Cell 8:1757-1771; Ellis et al. (1988) Cur. Opin. in Plant Path . 1:288-293).

The R genes can be classified into four main classes based on the structure of R gene products (Bent (1996) Plant Cell 8:1757-1771; Ellis et al. (1988) Cur. Opin. in Plant Path . 1:288-293; Hammond-Kosack et al. (1997) Ann. Rev. Plant Physiol. Plant Mol. Biol . 48:575-607; NBS-LRR (nucleotide-binding site-Leucine-rich repeat), LRR-TM-PK (Leucine-rich repeat-transmembrane domain-protein kinase), LRR-TM (Leucine-rich repeat-transmembrane domain), and PK (protein kinase). The largest number of characterized R proteins is the NBS-LRR type. These group genes can be recognized into two subgroups by the presence or absence of an amino-terminal region (TIR domain). TIR domain has sequence and structural similarity to the cytoplasmic signaling domains of Toll and interleukin-1 receptor (Baker et al. (1997) Science 276:726-733; Parker et al. (1997) Plant Cell 9:879-894).

The first subgroup includes tobacco TMV N gene, Hammond-Kosack et al. (1997) Ann. Rev. Plant Physiol. Plant Mol. Biol . 48:575-607, L6 (flax rust resistance), Hammond-Kosack et al. (1997) Ann. Rev. Plant Physiol. Plant Mol. Biol . 48:575-607, and RPP5 (downy mildew resistance), Parker et al. (1997) Plant Cell 9:879-894. The second subgroup without TIR domain includes RPS2, RPM1 Hammond-Kosack et al. (1997) Ann. Rev. Plant Physiol. Plant Mol. Biol . 48:575-607, and Prf Salmeron et al. (1996) Cell 86:123-133. These three R genes contain an amino-terminal leucine zipper (LZ) domain. The LZ domain may involve in protein-protein interaction in the signaling pathways. The proteins in these two subclasses signal through different pathways. Proteins in the TIR class signal via a pathway that includes EDS1 (Parker et al. (1996) Plant Cell 8:2033-2046) whereas the other class signals through a pathway that includes NDR1 gene (Centry et al. (1997) Science 278:1963-1965). The function of NBS may relate to HR and evidence has shown that NBS of RPS2 binds nucleotide (Ellis et al. (1988) Curr. Opin. in Plant Path . 1:288-293). Many NBS-LRR plant genes have been identified through plant genome sequencing projects (Botella et al. (1997) Plant J . 12:1197-1121), and by PCR using degenerate primers based on the NBS motifs. Yu et al. (1996) Proc. Natl. Acad Sci. USA 93:11751-11756; Leister et al. (1998) Proc. Natl. Acad. Sci. USA . 95:370-375.

Both LRR-TM-PK and PK classes of R genes contain kinase domain. Ligand binding activates the protein kinase domain. The first receptor-like protein kinase (RLK) gene is maize ZmPK1 that was isolated using degenerate primers to the kinase domain (Walker et al. (1990) Nature 345:743-746). Since then, a number of RLKs have been isolated from plants. The plant RLKs belongs to serine/threonine kinase family except ZmPK1. All of the plant RLKs can be classified according to the features of the predicted extracellular domain and transmambrane domain, such as LRR and TM. The function of kinase in defense signaling pathways has been dissected in the Pto/AvrPto interactions (Oldroyd et al. (1988) Proc. Natl. Acad. Sci. USA 95:10300-10305; Martin et al. (1996) Molecular Aspects of Pathogenicity and Resistance: Requirement for Signal Transduction , (pages 163-186). In the signal transduction, Pto, together with Prf, is required for the hypersensitive response induction after AvrPto perception. Pto also interacts with a family of transcriptional factors-Pti4, Pti5, and Pti6- that binds to a conserved cis-element present in promoter region of many genes encoding PR proteins (Zhou et al. (1997) EMBO J . 16:3207-3218). Expression of PR proteins is specifically enhanced upon Pto-Avrpto recognition in transgenic tobacco proteins (Zhou et al. (1997) EMBO J . 16:3207-3218).

In general, an R gene provides resistance against only some strains of a particular pathogen species. However, it has been demonstrated that R genes can be functional in heterologous systems (Thilmony et al. (1995) Plant Cell 7:1529-1536; Parker et al. (1996) Plant Cell 8:2033-2046). Furthermore, overexpression of R gene Prf activates pathways in a pathogen-independent manner and leads to the activation of systemic acquired resistance (SAR). The transgene-induced SAR has implications for the generation of broad-spectrum disease resistance in agricultural crop plants (Oldroyd et al. (1988) Proc. Natl. Acad. Sci. USA 95:10300-10305). One example of a strain-nonspecific resistance gene, mlo, has been cloned (Buschges et al. (1997) Cell 88:695-705).

As noted, among the causative agents of infectious disease of crop plants, the phytopathogenic fungi play the dominant role. Phytopathogenic fungi cause devastating epidemics, as well as causing significant annual crop yield losses. All of the approximately 300,000 species of flowering plants are attacked by pathogenic fungi. However, a single plant species can be host to only a few fungal species, and similarly, most fungi usually have a limited host range.

Plant disease outbreaks have resulted in catastrophic crop failures that have triggered famines and caused major social change. Generally, the best strategy for plant disease control is to use resistant cultivars selected or developed by plant breeders for this purpose. However, the potential for serious crop disease epidemics persists today, as evidenced by outbreaks of the Victoria blight of oats and southern corn leaf blight. Accordingly, molecular methods are needed to supplement traditional breeding methods to protect plants from pathogen attack.

SUMMARY OF THE INVENTION

Compositions and methods for creating or enhancing resistance to plant pests in a plant are provided. Compositions of the invention comprise novel disease resistance analogs from sunflower and variants of such resistance genes. The methods involve stably transforming a plant with nucleotide sequences of the invention operably linked with a promoter capable of driving expression of a gene in a plant cell. The sunflower R gene analogs and variants thereof may be used to modulate expression of the resistance gene analogs in plants and to engineer plants with broad-spectrum disease resistance. The methods of the invention find use in controlling plant pests, including fungal pathogens, viruses, nematodes, insects, and the like.

The compositions of the invention are additionally useful as genetic markers. Such genes can be used to facilitate the sunflower breeding programs for disease resistance.

Transformed plants and seeds, as well as methods for making such plants and seeds are additionally provided.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 : Multiple Alignment of PK1A (SEQ ID NO: 2) and PK1B (SEQ ID NO: 4) amino acid sequence with other protein kinases. Other PK proteins included: A protein kinase, NAK_ARATH from Arabidopsis (S38326) (SEQ ID NO: 57); APK1A is another protein kinase from Arabidopsis (D12522) (SEQ ID NO: 58); PK_ARATH is a protein kinase from Arabidopsis (D88207) (SEQ ID NO: 59); PTO-KINASE is a pto like protein kinase from tomato (U28007) (SEQ ID NO: 60).

FIG. 2 : Protein Distance Analysis (PHYLIP) of sunflower PK1A, PK1B and other known protein kinases using Neighbor-Joining/UPGMA method (version 3.572c).

FIG. 3 : Alignment of the deduced amino acid sequences of two sunflower NBS-LRR contigs (SEQ ID NO: 8, amino acids 1 through 157 and SEQ ID NO: 13, amino acids 285 through 456) with that of the disease-resistance genes of tobacco N (SEQ ID NO: 61), flax M (rust) (SEQ ID NO: 62), and arabidopsis RPP5 (SEQ ID NO: 63) and RPS2 (SEQ ID NO: 64) using the CLUSTAL W method.

FIG. 4 : Sequence comparison between RS6-8 contig (SEQ ID NO: 8) and TMV tobacco resistance protein N (SEQ ID NO: 61).

FIG. 5 : Example of an expression vector containing R gene operably linked to a UBI promoter.

DETAILED DESCRIPTION OF THE INVENTION

The invention is drawn to methods for creating or enhancing resistance in a plant to plant pests. Accordingly, the methods are also useful in protecting plants against fungal pathogens, viruses, nematodes, insects and the like.

The R genes of the invention can be used as markers in genetic mapping as well as in assessing disease resistance in a plant of interest. Thus, the sequences can be used in breeding programs. See, for example, Gentzbittel et al. (1998) Theor. Appl. Genet . 96:519-523.

Additional uses for the sequences of the invention include using the sequences as bait to isolate other signaling components on defense/resistance pathways and to isolate the corresponding promoter sequences. The sequences may also be used to modulate plant development processes, such as pollen development, regulation of organ shape, differentiation of aleurone and shoot epidermis, embryogenic competence, and cell/cell interactions. See, generally, Sambrook et al. (1989) Molecular Cloning: A Laboratory Manual (2nd ed., Cold Spring Harbor Laboratory Press, Plainview, N.Y.).

Methods for creating or enhancing disease resistance in a plant are provided. The methods involve stably transforming a plant with a DNA construct comprising an sunflower R nucleotide sequence of the invention operably linked to promoter that drives expression in a plant. Such methods find use in agriculture particularly in limiting the impact of plant pathogens on crop plants. The sunflower R nucleotide sequences are selected from nucleotide sequences encoding sunflower R proteins. Preferably, such sunflower R proteins encode protein kinases (PK) and nucleotide binding site-leucine rich repeat-type proteins (NBS-LRR). More preferably, such sunflower R proteins are selected from the proteins whose amino acid sequences are set forth in SEQ ID NOs: 2, 4, and 8 and the proteins encoded by the nucleotide sequences set forth in SEQ ID NOs: 1, 3, 5, 6, 7, 10-13, and 14. While the choice of promoter will depend on the desired timing and location of expression of the antipathogenic nucleotides sequences, specific promoters include pathogen-inducible promoters.

By “disease resistance” is intended that the plants avoid or suppress the disease symptoms that are the outcome of plant-pathogen interaction. That is, pathogens are prevented from causing plant diseases and the associated disease symptoms. The methods of the invention can be utilized to protect plants from disease, particularly those diseases that are caused by plant pathogens, such as broomrape, sclerotina, downey mildew, etc.

The resistance gene (R) analogs of the invention share homology to disease resistance genes from other plants, including TMV resistance gene N, rust resistance Gene M, downy mildew resistance gene, receptor-like protein kinase, and protein kinase. The R genes of the invention have conserved functional domains such as the protein kinase (PK) domain, leucine-rich regions (LRR), nucleotide-binding sites (NBS). Thus, the genes find use in engineering plants for broad-spectrum disease resistance.

Compositions of the invention comprise sunflower R nucleotides. By “sunflower R nucleotides,” is intended coding and antisense sequences for sunflower resistance genes as well as fragments and variants thereof. Nucleotide sequences encoding sunflower resistance proteins are provided in SEQ ID NOs: 1, 3, 5, 6, 7, 10-13, and 14. Alignment of the sequences with other protein kinases are provided in FIGS. 1 and 2 . Four sequences having a protein kinase domain are provided; PK1A (SEQ ID NO: 1), PK1B (SEQ ID NO: 3), PK4 (SEQ ID NO: 5) and PK5 (SEQ ID NO: 6). Amino acid sequences for PK1A and PK1B are also provided (SEQ ID NOs: 2 and 4). Six NBS-LRR type analog sequences RS6-8, RAS4-5, RS7-4, RAS5-1, RS6-8 and RS7-4 are provided in SEQ ID NOs: 7, 9-12, and 14, respectively.

Protein kinases play critical roles in regulating of biochemical changes associated with cellular growth. Thus, the sequences of the invention may find use in modulating (decreasing or increasing cellular growth and/or metabolism. The proteins of the invention may be useful for modulating phosphorylation states of molecules.

Compositions of the invention include isolated nucleic acid molecules comprising nucleotide sequences encoding the DNA sequence shown in the sequence listings, or the nucleotide sequence encoding the DNA sequence deposited in a bacteria host, that are involved in modulating cellular growth and/or metabolism. In particular, the present invention provides for isolated nucleic acid molecules comprising nucleotide sequences encoding the amino acid sequences shown in the sequence listing, or the nucleotide sequences encoding the DNA sequences deposited in a bacterial host as Patent Deposit Nos. PTA-139, PTA-140, PTA-141, PTA-142, PTA-135, PTA-137, PTA-136, and PTA-138, and fragments and variants thereof. Further provided are polypeptides having an amino acid sequence encoded by a nucleic acid molecule described herein, for example those set forth in the sequence listings, or those deposited in a bacterial host as Patent Deposit Nos. PTA-139, PTA-140, PTA-141, PTA-142, PTA-135, PTA-137, PTA-136, and PTA-138, and fragments and variants thereof.

Plasmids containing the nucleotide sequences of the invention were deposited with the Patent Depository of the American Type Culture Collection (ATCC), Manassas, Va., on May 26, 2000. The following plasmids were deposited: pHp 15541 containing PK1A, pHp 15542 containing PK1B, pHp 15543 containing PK4, pHp15544 containing PK5, pHp 15537 containing RS6-8, pHp 15539 containing RAS4-5, pHp 15538 containing 7-4, pHp 15540 containing RAS5-1, and assigned Patent Deposit Nos. PTA-139, PTA-140, PTA-141, PTA-142, PTA-135, PTA-137, PTA-136, and PTA-138, respectively. These deposits will be maintained under the terms of the Budapest Treaty on the International Recognition of the Deposit of Microorganisms for the Purposes of Patent Procedure. These deposits were made merely as a convenience for those of skill in the art and are not an admission that a deposit is required under 35 U.S.C. §112.

Thus, the invention encompasses isolated or substantially purified nucleic acid or protein compositions. An “isolated” or “purified” nucleic acid molecule or protein, or biologically active portion thereof, is substantially or essentially free from components that normally accompany or interact with the nucleic acid molecule or protein as found in its naturally occurring environment. Thus, an isolated or purified nucleic acid molecule or protein is substantially free of other cellular material, or culture medium when produced by recombinant techniques, or substantially free of chemical precursors or other chemicals when chemically synthesized. Preferably, an “isolated” nucleic acid is free of sequences (preferably protein encoding sequences) that naturally flank the nucleic acid (i.e., sequences located at the 5′ and 3′ ends of the nucleic acid) in the genomic DNA of the organism from which the nucleic acid is derived. For example, in various embodiments, the isolated nucleic acid molecule can contain less than about 5 kb, 4 kb, 3 kb, 2 kb, 1 kb, 0.5 kb, or 0.1 kb of nucleotide sequences that naturally flank the nucleic acid molecule in genomic DNA of the cell from which the nucleic acid is derived. A protein that is substantially free of cellular material includes preparations of protein having less than about 30%, 20%, 10%, 5%, (by dry weight) of contaminating protein. When the protein of the invention or biologically active portion thereof is recombinantly produced, preferably culture medium represents less than about 30%, 20%, 10%, or 5% (by dry weight) of chemical precursors or non-protein-of-interest chemicals.

Fragments and variants of the disclosed nucleotide sequences and proteins encoded thereby are also encompassed by the present invention. By “fragment” is intended a portion of the nucleotide sequence or a portion of the amino acid sequence and hence protein encoded thereby. Fragments of a nucleotide sequence may encode protein fragments that retain the biological activity of the native protein and hence modulate or regulate gene activity. Alternatively, fragments of a nucleotide sequence that are useful as hybridization probes generally do not encode fragment proteins retaining biological activity. Thus, fragments of a nucleotide sequence may range from at least about 20 nucleotides, about 50 nucleotides, about 100 nucleotides, and up to the full-length nucleotide sequence encoding the proteins of the invention.

A fragment of an R nucleotide sequence that encodes a biologically active portion of an R protein of the invention will encode at least 15, 25, 30, 50, 100, 150, 200, 250, 300, 350, or 400 contiguous amino acids, or up to the total number of amino acids present in a full-length R protein of the invention (for example, 457, 413, 571, or 476 amino acids for SEQ ID NO: 2, 4, 8, or 13, respectively). Fragments of an R nucleotide sequence that are useful as hybridization probes or PCR primers generally need not encode a biologically active portion of an R protein.

Thus, a fragment of an R nucleotide sequence may encode a biologically active portion of an R protein, or it may be a fragment that can be used as a hybridization probe or PCR primer using methods disclosed below. A biologically active portion of an R protein can be prepared by isolating a portion of one of the R nucleotide sequences of the invention, expressing the encoded portion of the R protein (e.g., by recombinant expression in vitro), and assessing the activity of the encoded portion of the R protein. Nucleic acid molecules that are fragments of an R nucleotide sequence comprise at least 16, 20, 50, 75, 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, 600, or 650 nucleotides, or up to the number of nucleotides present in a full-length R nucleotide sequence disclosed herein (for example, 1593, 1559, 2114, 850, 2594, 2793, 670, 1200, 3450, or 1360 nucleotides for SEQ ID NO[s]: 1, 3, 4, 5, 6, 7, 9, 10, 11, 12, or 14, respectively).

By “variants” is intended substantially similar sequences. For nucleotide sequences, conservative variants include those sequences that, because of the degeneracy of the genetic code, encode the amino acid sequence of one of the R polypeptides of the invention. Naturally occurring allelic variants such as these can be identified with the use of well-known molecular biology techniques, as, for example, with polymerase chain reaction (PCR) and hybridization techniques as outlined below. Variant nucleotide sequences also include synthetically derived nucleotide sequences, such as those generated, for example, by using site-directed mutagenesis but which still encode an R protein of the invention. Generally, variants of a particular nucleotide sequence of the invention will have at least 50%, 55%, 60%, 65%, 70%, generally at least 75%, 80%, 85%, preferably about 90% to 95% or more, and more preferably about 98% or more sequence identity to that particular nucleotide sequence as determined by sequence alignment programs described elsewhere herein using default parameters.

By “variant” protein is intended a protein derived from the native protein by deletion (so-called truncation) or addition of one or more amino acids to the N-terminal and/or C-terminal end of the native protein; deletion or addition of one or more amino acids at one or more sites in the native protein; or substitution of one or more amino acids at one or more sites in the native protein. Variant proteins encompassed by the present invention are biologically active, that is they continue to possess the desired biological activity of the native protein, that is, modulating or regulatory activity as described herein. Such variants may result from, for example, genetic polymorphism or from human manipulation. Biologically active variants of a native R protein of the invention will have at least 40%, 50%, 60%, 70%, generally at least 75%, 80%, 85%, preferably about 90% to 95% or more, and more preferably about 98% or more sequence identity to the amino acid sequence for the native protein as determined by sequence alignment programs described elsewhere herein using default parameters. A biologically active variant of a protein of the invention may differ from that protein by as few as 1-15 amino acid residues, as few as 1-10, such as 6-10, as few as 5, as few as 4, 3, 2, or even 1 amino acid residue.

The proteins of the invention may be altered in various ways including amino acid substitutions, deletions, truncations, and insertions. Methods for such manipulations are generally known in the art. For example, amino acid sequence variants of the R proteins can be prepared by mutations in the DNA. Methods for mutagenesis and nucleotide sequence alterations are well known in the art. See, for example, Kunkel (1985) Proc. Natl. Acad. Sci. USA 82:488-492; Kunkel et al. (1987) Methods in Enzymol . 154:367-382; U.S. Pat. No. 4,873,192; Walker and Gaastra, eds. (1983) Techniques in Molecular Biology (MacMillan Publishing Company, New York) and the references cited therein. Guidance as to appropriate amino acid substitutions that do not affect biological activity of the protein of interest may be found in the model of Dayhoff et al. (1978) Atlas of Protein Sequence and Structure (Natl. Biomed. Res. Found., Washington, D.C.), herein incorporated by reference. Conservative substitutions, such as exchanging one amino acid with another having similar properties, may be preferable.

Thus, the genes and nucleotide sequences of the invention include both the naturally occurring sequences as well as mutant forms. Likewise, the proteins of the invention encompass both naturally occurring proteins as well as variations and modified forms thereof. Such variants will continue to possess the desired modulating or regulatory activity. Obviously, the mutations that will be made in the DNA encoding the variant must not place the sequence out of reading frame and preferably will not create complementary regions that could produce secondary mRNA structure. See, EP Patent Application Publication No. 75,444.

The deletions, insertions, and substitutions of the protein sequence encompassed herein are not expected to produce radical changes in the characteristics of the protein. However, when it is difficult to predict the exact effect of the substitution, deletion, or insertion in advance of doing so, one skilled in the art will appreciate that the effect will be evaluated by routine screening assays. That is, the activity can be evaluated by its effect on the plant defense system. See, for example U.S. Pat. No. 5,614,395, herein incorporated by reference.

Variant nucleotide sequences and proteins also encompass sequences and proteins derived from a mutagenic and recombinogenic procedure such as DNA shuffling. With such a procedure, one or more different R coding sequences can be manipulated to create a new R sequence possessing the desired properties. In this manner, libraries of recombinant polynucleotides are generated from a population of related sequence polynucleotides comprising sequence regions that have substantial sequence identity and can be homologously recombined in vitro or in vivo. For example, using this approach, sequence motifs encoding a domain of interest may be shuffled between the R gene of the invention and other known R genes to obtain a new gene coding for a protein with an improved property of interest, such as an increased K m in the case of an enzyme. Strategies for such DNA shuffling are known in the art. See, for example, Stemmer (1994) Proc. Natl. Acad. Sci. USA 91:10747-10751; Stemmer (1994) Nature 370:389-391; Crameri et al. (1997) Nature Biotech . 15:436-438; Moore et al. (1997) J. Mol. Biol . 272:336-347; Zhang et al. (1997) Proc. Natl. Acad. Sci. USA 94:4504-4509; Crameri et al. (1998) Nature 391:288-291; and U.S. Pat. Nos. 5,605,793 and 5,837,458. Alternatively, variants may have been manipulated to lose biological activity. Such variants can be made by site directed mutagenesis and the like.

In this manner, the present invention encompasses the R genes and proteins as well as components and fragments thereof. That is, it is recognized that component polypeptides or fragments of the proteins may be produced which retain activity. These fragments include truncated sequences, as well as N-terminal, C-terminal, internal and internally deleted amino acid sequences of the proteins.

It is recognized that with these nucleotide sequences, antisense constructions, complementary to at least a portion of the messenger RNA (mRNA) for the R genes or a regulatory flanking sequences can be constructed. Antisense nucleotides are constructed to hybridize with the corresponding mRNA. Therefore, modifications of the sequences may be made as long as the sequences hybridize to and interfere with expression of the corresponding mRNA. In this manner, antisense constructions having 70%, preferably 80%, more preferably 85% sequence identity to the corresponding antisense sequences may be used. Furthermore, portions of the antisense nucleotides may be used to disrupt the expression of the target gene. Generally, sequences of at least 50 nucleotides, 100 nucleotides, 200 nucleotides, or greater may be used.

The nucleotide sequences of the invention can be used to isolate corresponding sequences from other organisms, particularly other plants. Methods are readily available in the art for the hybridization of nucleic acid sequences. Coding sequences from other plants may be isolated according to well known techniques based on their sequence homology to the coding sequences set forth herein. In these techniques all or part of the known coding sequence is used as a probe which selectively hybridizes to other R coding sequences present in a population of cloned genomic DNA fragments or cDNA fragments (i.e. genomic or cDNA libraries) from a chosen organism.

In this manner, methods such as PCR, hybridization, and the like can be used to identify such sequences based on their sequence homology to the sequences set forth herein. Sequences isolated based on their sequence identity to the entire R sequence set forth herein or to fragments thereof are encompassed by the present invention. Such sequences include sequences that are orthologs of the disclosed sequences. By “orthologs” is intended genes derived from a common ancestral gene and which are found in different species as a result of speciation. Genes found in different species are considered orthologs when their nucleotide sequences and/or their encoded protein sequences have a high percentage of sequence identity and/or similarity. Functions of orthologs are often highly conserved among species.

In a PCR approach, oligonucleotide primers can be designed for use in PCR reactions to amplify corresponding DNA sequences from cDNA or genomic DNA extracted from any plant of interest. Methods for designing PCR primers and PCR cloning are generally known in the art and are disclosed in Sambrook et al. (1989) Molecular Cloning: A Laboratory Manual (2d ed., Cold Spring Harbor Laboratory Press, Plainview, N.Y.). See also Innis et al., eds. (1990) PCR Protocols: A Guide to Methods and Applications (Academic Press, New York); Innis and Gelfand, eds. (1995) PCR Strategies (Academic Press, New York); and Innis and Gelfand, eds. (1999) PCR Methods Manual (Academic Press, New York). Known methods of PCR include, but are not limited to, methods using paired primers, nested primers, single specific primers, degenerate primers, gene-specific primers, vector-specific primers, partially-mismatched primers, and the like.

In hybridization techniques, all or part of a known nucleotide sequence is used as a probe that selectively hybridizes to other corresponding nucleotide sequences present in a population of cloned genomic DNA fragments or cDNA fragments (i.e., genomic or cDNA libraries) from a chosen organism. The hybridization probes may be genomic DNA fragments, cDNA fragments, RNA fragments, or other oligonucleotides, and may be labeled with a detectable group such as 32 P, or any other detectable marker. Thus, for example, probes for hybridization can be made by labeling synthetic oligonucleotides based on the R sequence of the invention. Methods for preparation of probes for hybridization and for construction of cDNA and genomic libraries are generally known in the art and are disclosed in Sambrook et al. ( 1989) Molecular Cloning: A Laboratory Manual (2d ed., Cold Spring Harbor Laboratory Press, Plainview, N.Y.).

For example, the entire R sequence disclosed herein, or one or more portions thereof, may be used as a probe capable of specifically hybridizing to corresponding R sequences and messenger RNAs. To achieve specific hybridization under a variety of conditions, such probes include sequences that are unique among R sequences and are preferably at least about 10 nucleotides in length, and most preferably at least about 20 nucleotides in length. Such probes may be used to amplify corresponding R sequences from a chosen plant by PCR. This technique may be used to isolate additional coding sequences from a desired plant or as a diagnostic assay to determine the presence of coding sequences in a plant. Hybridization techniques include hybridization screening of plated DNA libraries (either plaques or colonies; see, for example, Sambrook et al. (1989) Molecular Cloning: A Laboratory Manual (2d ed., Cold Spring Harbor Laboratory Press, Plainview, N.Y.).

Hybridization of such sequences may be carried out under stringent conditions. By “stringent conditions” or “stringent hybridization conditions” is intended conditions under which a probe will hybridize to its target sequence to a detectably greater degree than to other sequences (e.g., at least 2-fold over background). Stringent conditions are sequence-dependent and will be different in different circumstances. By controlling the stringency of the hybridization and/or washing conditions, target sequences that are 100% complementary to the probe can be identified (homologous probing). Alternatively, stringency conditions can be adjusted to allow some mismatching in sequences so that lower degrees of similarity are detected (heterologous probing). Generally, a probe is less than about 1000 nucleotides in length, preferably less than 500 nucleotides in length.

Typically, stringent conditions will be those in which the salt concentration is less than about 1.5 M Na ion, typically about 0.01 to 1.0 M Na ion concentration (or other salts) at pH 7.0 to 8.3 and the temperature is at least about 30° C. for short probes (e.g., 10 to 50 nucleotides) and at least about 60° C. for long probes (e.g., greater than 50 nucleotides). Stringent conditions may also be achieved with the addition of destabilizing agents such as formamide. Exemplary low stringency conditions include hybridization with a buffer solution of 30 to 35% formamide, 1 M NaCl, 1% SDS (sodium dodecyl sulphate) at 37° C., and a wash in 1× to 2×SSC (20×SSC=3.0 M NaCl/0.3 M trisodium citrate) at 50 to 55° C. Exemplary moderate stringency conditions include hybridization in 40 to 45% formamide, 1.0 M NaCl, 1% SDS at 37° C., and a wash in 0.5× to 1×SSC at 55 to 60° C. Exemplary high stringency conditions include hybridization in 50% formamide, 1 M NaCl, 1% SDS at 37° C., and a wash in 0.1×SSC at 60 to 65° C. Duration of hybridization is generally less than about 24 hours, usually about 4 to about 12 hours.

Specificity is typically the function of post-hybridization washes, the critical factors being the ionic strength and temperature of the final wash solution. For DNA-DNA hybrids, the T m can be approximated from the equation of Meinkoth and Wahl (1984) Anal. Biochem . 138:267-284: T m =81.5° C.+16.6 (log M)+0.41 (%GC)−0.61 (% form)−500/L; where M is the molarity of monovalent cations, %GC is the percentage of guanosine and cytosine nucleotides in the DNA, % form is the percentage of formamide in the hybridization solution, and L is the length of the hybrid in base pairs. The T m is the temperature (under defined ionic strength and pH) at which 50% of a complementary target sequence hybridizes to a perfectly matched probe. T m is reduced by about 1° C. for each 1% of mismatching; thus, T m , hybridization, and/or wash conditions can be adjusted to hybridize to sequences of the desired identity. For example, if sequences with ≧90% identity are sought, the T m can be decreased 10° C. Generally, stringent conditions are selected to be about 5° C. lower than the thermal melting point (T m ) for the specific sequence and its complement at a defined ionic strength and pH. However, severely stringent conditions can utilize a hybridization and/or wash at 1, 2, 3, or 4° C. lower than the thermal melting point (T m ); moderately stringent conditions can utilize a hybridization and/or wash at 6, 7, 8, 9, or 10° C. lower than the thermal melting point (T m ); low stringency conditions can utilize a hybridization and/or wash at 11, 12, 13, 14, 15, or 20° C. lower than the thermal melting point (T m ). Using the equation, hybridization and wash compositions, and desired T m , those of ordinary skill will understand that variations in the stringency of hybridization and/or wash solutions are inherently described. If the desired degree of mismatching results in a T m of less than 45° C. (aqueous solution) or 32° C. (formamide solution), it is preferred to increase the SSC concentration so that a higher temperature can be used. An extensive guide to the hybridization of nucleic acids is found in Tijssen (1993) Laboratory Techniques in Biochemistry and Molecular Biology—Hybridization with Nucleic Acid Probes , Part I, Chapter 2 (Elsevier, N.Y.); and Ausubel et al., eds. (1995) Current Protocols in Molecular Biology , Chapter 2 (Greene Publishing and Wiley-Interscience, New York). See Sambrook et al. (1989) Molecular Cloning: A Laboratory Manual (2d ed., Cold Spring Harbor Laboratory Press, Plainview, N.Y.).

Thus, isolated sequences that encode for an R protein and which hybridize under stringent conditions to the R sequence disclosed herein, or to fragments thereof, are encompassed by the present invention. Such sequences will be at least 50% to 55% homologous, about 60%, 65%, to 70% homologous, and even about 75%, 80%, 85%, 90%, 95% to 98% homologous or more with the disclosed sequence. That is, the sequence identity of sequences may range, sharing at least 50 % to 55%, about 60%, 65% to 70%, and even about 75%, 80%, 85%, 90%, 95% to 98% or more sequence identity.

The following terms are used to describe the sequence relationships between two or more nucleic acids or polynucleotides: (a) “reference sequence”, (b) “comparison window”, (c) “sequence identity”, (d) “percentage of sequence identity”, and (e) “substantial identity”.

(a) As used herein, “reference sequence” is a defined sequence used as a basis for sequence comparison. A reference sequence may be a subset or the entirety of a specified sequence; for example, as a segment of a full-length cDNA or gene sequence, or the complete cDNA or gene sequence.

(b) As used herein, “comparison window” makes reference to a contiguous and specified segment of a polynucleotide sequence, wherein the polynucleotide sequence in the comparison window may comprise additions or deletions (i.e., gaps) compared to the reference sequence (which does not comprise additions or deletions) for optimal alignment of the two sequences. Generally, the comparison window is at least 20 contiguous nucleotides in length, and optionally can be 30, 40, 50, 100, or longer. Those of skill in the art understand that to avoid a high similarity to a reference sequence due to inclusion of gaps in the polynucleotide sequence a gap penalty is typically introduced and is subtracted from the number of matches.

Methods of alignment of sequences for comparison are well known in the art. Thus, the determination of percent sequence identity between any two sequences can be accomplished using a mathematical algorithm. Non-limiting examples of such mathematical algorithms are the algorithm of Myers and Miller (1988) CABIOS 4:11-17; the local homology algorithm of Smith et al. (1981) Adv. Appl. Math . 2:482; the homology alignment algorithm of Needleman and Wunsch (1970) J. Mol. Biol . 48:443-453; the search-for-similarity-method of Pearson and Lipman (1988) Proc. Natl. Acad. Sci . 85:2444-2448; the algorithm of Karlin and Altschul (1990) Proc. Natl. Acad. Sci. USA 872264, modified as in Karlin and Altschul (1993) Proc. Natl. Acad. Sci. USA 90:5873-5877.

Computer implementations of these mathematical algorithms can be utilized for comparison of sequences to determine sequence identity. Such implementations include, but are not limited to: CLUSTAL in the PC/Gene program (available from Intelligenetics, Mountain View, Calif.); the ALIGN program (Version 2.0) and GAP, BESTFIT, BLAST, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Version 8 (available from Genetics Computer Group (GCG), 575 Science Drive, Madison, Wis., USA). Alignments using these programs can be performed using the default parameters. The CLUSTAL program is well described by Higgins et al. (1988) Gene 73:237-244 (1988); Higgins et al. (1989) CABIOS 5:151-153; Corpet et al. (1988) Nucleic Acids Res . 16:10881-90; Huang et al. (1992) CABIOS 8:155-65; and Pearson et al. (1994) Meth. Mol. Biol . 24:307-331. The ALIGN program is based on the algorithm of Myers and Miller (1988) supra. A PAM120 weight residue table, a gap length penalty of 12, and a gap penalty of 4 can be used with the ALIGN program when comparing amino acid sequences. The BLAST programs of Altschul et al (1990) J. Mol. Biol . 215:403 are based on the algorithm of Karlin and Altschul (1990) supra. BLAST nucleotide searches can be performed with the BLASTN program, score=100, wordlength=12, to obtain nucleotide sequences homologous to a nucleotide sequence encoding a protein of the invention. BLAST protein searches can be performed with the BLASTX program, score=50, wordlength=3, to obtain amino acid sequences homologous to a protein or polypeptide of the invention. To obtain gapped alignments for comparison purposes, Gapped BLAST (in BLAST 2.0) can be utilized as described in Altschul et al. (1997) Nucleic Acids Res . 25:3389. Alternatively, PSI-BLAST (in BLAST 2.0) can be used to perform an iterated search that detects distant relationships between molecules. See Altschul et al. (1997) supra. When utilizing BLAST, Gapped BLAST, PSI-BLAST, the default parameters of the respective programs (e.g., BLASTN for nucleotide sequences, BLASTX for proteins) can be used. See http://www.ncbi.nlm.nih.gov. Alignment may also be performed manually by inspection.

Unless otherwise stated, sequence identity/similarity values provided herein refer to the value obtained using GAP version 10 using the following parameters: % identity using GAP Weight of 50 and Length Weight of 3; % similarity using Gap Weight of 12 and Length Weight of 4, or any equivalent program. By “equivalent program” is intended any sequence comparison program that, for any two sequences in question, generates an alignment having identical nucleotide or amino acid residue matches and an identical percent sequence identity when compared to the corresponding alignment generated by GAP Version 10.

GAP uses the algorithm of Needleman and Wunsch (1970) J. Mol. Biol . 48: 443-453, to find the alignment of two complete sequences that maximizes the number of matches and minimizes the number of gaps. GAP considers all possible alignments and gap positions and creates the alignment with the largest number of matched bases and the fewest gaps. It allows for the provision of a gap creation penalty and a gap extension penalty in units of matched bases. GAP must make a profit of gap creation penalty number of matches for each gap it inserts. If a gap extension penalty greater than zero is chosen, GAP must, in addition, make a profit for each gap inserted of the length of the gap times the gap extension penalty. Default gap creation penalty values and gap extension penalty values in Version 10 of the Wisconsin Genetics Software Package for protein sequences are 8 and 2, respectively. For nucleotide sequences the default gap creation penalty is 50 while the default gap extension penalty is 3. The gap creation and gap extension penalties can be expressed as an integer selected from the group of integers consisting of from 0 to 200. Thus, for example, the gap creation and gap extension penalties can be 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65 or greater.

GAP presents one member of the family of best alignments. There may be many members of this family, but no other member has a better quality. GAP displays four figures of merit for alignments: Quality, Ratio, Identity, and Similarity. The Quality is the metric maximized in order to align the sequences. Ratio is the quality divided by the number of bases in the shorter segment. Percent Identity is the percent of the symbols that actually match. Percent similarity is the percent of the symbols that are similar. Symbols that are across from gaps are ignored. A similarity is scored when the scoring matrix value for a pair of symbols is greater than or equal to 0.50, the similarity threshold. The scoring matrix used in Version 10 of the Wisconsin Genetics Software Package is BLOSUM62 (see Henikoff and Henikoff (1989) Proc. Natl. Acad. Sci. USA 89:10915).

(c) As used herein, “sequence identity” or “identity” in the context of two nucleic acid or polypeptide sequences makes reference to the residues in the two sequences that are the same when aligned for maximum correspondence over a specified comparison window. When percentage of sequence identity is used in reference to proteins it is recognized that residue positions which are not identical often differ by conservative amino acid substitutions, where amino acid residues are substituted for other amino acid residues with similar chemical properties (e.g., charge or hydrophobicity) and therefore do not change the functional properties of the molecule. When sequences differ in conservative substitutions, the percent sequence identity may be adjusted upwards to correct for the conservative nature of the substitution. Sequences that differ by such conservative substitutions are said to have “sequence similarity” or “similarity”. Means for making this adjustment are well known to those of skill in the art. Typically this involves scoring a conservative substitution as a partial rather than a full mismatch, thereby increasing the percentage sequence identity. Thus, for example, where an identical amino acid is given a score of 1 and a non-conservative substitution is given a score of zero, a conservative substitution is given a score between zero and 1. The scoring of conservative substitutions is calculated, e.g., as implemented in the program PC/GENE (Intelligenetics, Mountain View, Calif.).

(d) As used herein, “percentage of sequence identity” means the value determined by comparing two optimally aligned sequences over a comparison window, wherein the portion of the polynucleotide sequence in the comparison window may comprise additions or deletions (i.e., gaps) as compared to the reference sequence (which does not comprise additions or deletions) for optimal alignment of the two sequences. The percentage is calculated by determining the number of positions at which the identical nucleic acid base or amino acid residue occurs in both sequences to yield the number of matched positions, dividing the number of matched positions by the total number of positions in the window of comparison, and multiplying the result by 100 to yield the percentage of sequence identity.

(e)(i) The term “substantial identity” of polynucleotide sequences means that a polynucleotide comprises a sequence that has at least 70% sequence identity, preferably at least 80%, more preferably at least 90%, and most preferably at least 95%, compared to a reference sequence using one of the alignment programs described using standard parameters. One of skill in the art will recognize that these values can be appropriately adjusted to determine corresponding identity of proteins encoded by two nucleotide sequences by taking into account codon degeneracy, amino acid similarity, reading frame positioning, and the like. Substantial identity of amino acid sequences for these purposes normally means sequence identity of at least 60%, more preferably at least 70%, 80%, 90%, and most preferably at least 95%.

Another indication that nucleotide sequences are substantially identical is if two molecules hybridize to each other under stringent conditions. Generally, stringent conditions are selected to be about 5° C. lower than the thermal melting point (T m ) for the specific sequence at a defined ionic strength and pH. However, stringent conditions encompass temperatures in the range of about 1° C. to about 20° C. lower than the T m , depending upon the desired degree of stringency as otherwise qualified herein. Nucleic acids that do not hybridize to each other under stringent conditions are still substantially identical if the polypeptides they encode are substantially identical. This may occur, e.g., when a copy of a nucleic acid is created using the maximum codon degeneracy permitted by the genetic code. One indication that two nucleic acid sequences are substantially identical is when the polypeptide encoded by the first nucleic acid is immunologically cross reactive with the polypeptide encoded by the second nucleic acid.

(e)(ii) The term “substantial identity” in the context of a peptide indicates that a peptide comprises a sequence with at least 70% sequence identity to a reference sequence, preferably 80%, more preferably 85%, most preferably at least 90% or 95% sequence identity to the reference sequence over a specified comparison window. Preferably, optimal alignment is conducted using the homology alignment algorithm of Needleman and Wunsch (1970) J. Mol. Biol . 48:443-453. An indication that two peptide sequences are substantially identical is that one peptide is immunologically reactive with antibodies raised against the second peptide. Thus, a peptide is substantially identical to a second peptide, for example, where the two peptides differ only by a conservative substitution. Peptides that are “substantially similar” share sequences as noted above except that residue positions that are not identical may differ by conservative amino acid changes.

The invention is drawn to compositions and methods for inducing resistance in a plant to plant pests. Accordingly, the compositions and methods are also useful in protecting plants against fungal pathogens, viruses, nematodes, insects and the like.

By “disease resistance” is intended that the plants avoid the disease symptoms that are the outcome of plant-pathogen interactions. That is, pathogens are prevented from causing plant diseases and the associated disease symptoms, or alternatively, the disease symptoms caused by the pathogen is minimized or lessened. The methods of the invention can be utilized to protect plants from disease, particularly those diseases that are caused by plant pathogens.

Pathogens of the invention include, but are not limited to, viruses or viroids, bacteria, insects, nematodes, fungi, and the like. Viruses include any plant virus, for example, tobacco or cucumber mosaic virus, ringspot virus, necrosis virus, maize dwarf mosaic virus, etc. Specific fungal and viral pathogens for the major crops include: Soybeans: Phytophthora megasperma fsp. glycinea, Macrophomina phaseolina, Rhizoctonia solani, Sclerotinia sclerotiorum, Fusarium oxysporum, Diaporthe phaseolorum var. sojae ( Phomopsis sojae ), Diaporthe phaseolorum var. caulivora, Sclerotium roltsii, Cercospora kikuchii, Cercospora sojina, Peronospora manshurica, Colletotrichum dematium ( Colletotichum truncatum ), Corynespora cassiicola, Septoria glycines, Phyllosticta sojicola, Alternaria alternata, Pseudomonas syringae p.v. glycinea, Xanthomonas campestris p.v. phaseoli, Microsphaera diffusa, Fusarium semitectum, Phialophora gregata , Soybean mosaic virus, Glomerella glycines , Tobacco Ring spot virus, Tobacco Streak virus, Phakopsora pachyrhizi, Pythium aphanidermatum, Pythium ultimum, Pythium debaryanum , Tomato spotted wilt virus, Heterodera glycines Fusarium solani ; Canola: Albugo candida, Alternaria brassicae, Leptosphaeria maculans, Rhizoctonia solani, Sclerotinia sclerotiorum, Mycosphaerella brassiccola, Pythium ultimum, Peronospora parasitica, Fusarium roseum, Alternaria alternata ; Alfalfa: Clavibater michiganese subsp. insidiosum, Pythium ultimum, Pythium irregulare, Pythium splendens, Pythium debaryanum, Pythium aphanidermatum, Phytophthora megasperma, Peronospora trifoliorum, Phoma medicaginis var. medicaginis, Cercospora medicaginis, Pseudopeziza medicaginis, Leptotrochila medicaginis, Fusarium, Xanthomonas campestris p.v. alfalfae, Aphanomyces euteiches, Stemphylium herbarum, Stemphylium alfalfae ; Wheat: Pseudomonas syringae p.v. atrofaciens, Urocystis agropyri, Xanthomonas campestris p.v. translucens, Pseudomonas syringae p.v. syringae, Alternaria alternata, Cladosporium herbarum, Fusarium graminearum, Fusarium avenaceum, Fusarium culmorum, Ustilago tritici, Ascochyta tritici, Cephalosporium gramineum, Collotetrichum graminicola, Erysiphe graminis f.sp. tritici, Puccinia graminis f.sp. tritici, Puccinia recondita f.sp. tritici, Puccinia striiformis, Pyrenophora tritici - repentis, Septoria nodorum, Septoria tritici, Septoria avenae, Pseudocercosporella herpotrichoides, Rhizoctonia solani, Rhizoctonia cerealis, Gaeumannomyces graminis var. tritici, Pythium aphanidermatum, Pythium arrhenomanes, Pythium ultimum, Bipolaris sorokiniana , Barley Yellow Dwarf Virus, Brome Mosaic Virus, Soil Borne Wheat Mosaic Virus, Wheat Streak Mosaic Virus, Wheat Spindle Streak Virus, American Wheat Striate Virus, Claviceps purpurea, Tilletia tritici, Tilletia laevis, Ustilago tritici, Tilletia indica, Rhizoctonia solani, Pythium arrhenomannes, Pythium gramicola, Pythium aphanidermatum , High Plains Virus, European wheat striate virus; Sunflower: Plasmophora halstedii, Sclerotinia sclerotiorum , Aster Yellows, Septoria helianthi, Phomopsis helianthi, Alternaria helianthi, Alternaria zinniae, Botrytis cinerea, Phoma macdonaldii, Macrophominaphaseolina, Erysiphe cichoracearum, Rhizopus oryzae, Rhizopus arrhizus, Rhizopus stolonifer, Puccinia helianthi, Verticillium dahliae, Erwinia carotovorum pv. carotovora, Cephalosporium acremonium, Phytophthora cryptogea, Albugo tragopogonis ; Corn: Fusarium moniliforme var. subglutinans, Erwinia stewartii, Fusarium moniliforme, Gibberella zeae ( Fusarium graminearum ), Stenocarpella maydi ( Diplodia maydis ), Pythium irregulare, Pythium debaryanum, Pythium graminicola, Pythium splendens, Pythium ultimum, Pythium aphanidermatum, Aspergillus flavus, Bipolaris maydis O, T ( Cochliobolus heterostrophus ), Helminthosporium carbonum I, II & III ( Cochliobolus carbonum ), Exserohilum turcicum I, II & III, Helminthosporium pedicellatum, Physoderma maydis, Phyllosticta maydis, Kabatiella maydis, Cercospora sorghi, Ustilago maydis, Puccinia sorghi, Puccinia polysora, Macrophomina phaseolina, Penicillium oxalicum, Nigrospora oryzae, Cladosporium herbarum, Curvularia lunata, Curvularia inaequalis, Curvularia pallescens, Clavibacter michiganense subsp. nebraskense, Trichoderma viride , Maize Dwarf Mosaic Virus A & B, Wheat Streak Mosaic Virus, Maize Chlorotic Dwarf Virus, Claviceps sorghi, Pseudonomas avenae, Erwinia chrysanthemi pv. zea, Erwinia carotovora, Corn stunt spiroplasma, Diplodia macrospora, Sclerophthora macrospora, Peronosclerospora sorghi, Peronosclerospora philippinensis, Peronosclerospora maydis, Peronosclerospora sacchari, Sphacelotheca reiliana, Physopella zeae, Cephalosporium maydis, Cephalosporium acremonium , Maize Chlorotic Mottle Virus, High Plains Virus, Maize Mosaic Virus, Maize Rayado Fino Virus, Maize Streak Virus, Maize Stripe Virus, Maize Rough Dwarf Virus; Sorghum: Exserohilum turcicum, Colletotrichum graminicola ( Glomerella graminicola ), Cercospora sorghi, Gloeocercospora sorghi, Ascochyta sorghina, Pseudomonas syringae p.v. syringae, Xanthomonas campestris p.v. holcicola, Pseudomonas andropogonis, Puccinia purpurea, Macrophomina phaseolina, Perconia circinata, Fusarium moniliforme, Alternaria alternata, Bipolaris sorghicola, Helminthosporium sorghicola, Curvularia lunata, Phoma insidiosa, Pseudomonas avenae ( Pseudomonas alboprecipitans ), Ramulispora sorghi, Ramulispora sorghicola, Phyllachara sacchari, Sporisorium reilianum ( Sphacelotheca reiliana ), Sphacelotheca cruenta, Sporisorium sorghi , Sugarcane mosaic H, Maize Dwarf Mosaic Virus A & B, Claviceps sorghi, Rhizoctonia solani, Acremonium strictum, Sclerophthona macrospora, Peronosclerospora sorghi, Peronosclerospora philippinensis, Sclerospora graminicola, Fusarium graminearum, Fusarium oxysporum, Pythium arrhenomanes, Pythium graminicola , etc.

Nematodes include parasitic nematodes such as root-knot, cyst, and lesion nematodes, including Heterodera and Globodera spp; particularly Globodera rostochiensis and globodera pailida (potato cyst nematodes); Heterodera glycines (soybean cyst nematode); Heterodera schachtii (beet cyst nematode); and Heterodera avenae (cereal cyst nematode).

Insect pests include insects selected from the orders Coleoptera, Diptera, Hymenoptera, Lepidoptera, Mallophaga, Homoptera, Hemiptera, Orthoptera, Thysanoptera, Dermaptera, Isoptera, Anoplura, Siphonaptera, Trichoptera, etc., particularly Coleoptera and Lepidoptera. Insect pests of the invention for the major crops include: Maize: Ostrinia nubilalis , European corn borer; Agrotis ipsilon , black cutworm; Helicoverpa zea , corn earworm; Spodoptera frugiperda , fall armyworm; Diatraea grandiosella , southwestern corn borer; Elasmopalpus lignosellus , lesser cornstalk borer; Diatraea saccharalis , surgarcane borer; Diabrotica virgifera , western corn rootworm; Diabrotica longicornis barberi , northern corn rootworm; Diabrotica undecimpunctata howardi , southern corn rootworm; Melanotus spp., wireworms; Cyclocephala borealis , northern masked chafer (white grub); Cyclocephala immaculata , southern masked chafer (white grub); Popillia japonica , Japanese beetle; Chaetocnema pulicaria , corn flea beetle; Sphenophorus maidis , maize billbug; Rhopalosiphum maidis , corn leaf aphid; Anuraphis maidiradicis , corn root aphid; Blissus leucopterus leucopterus , chinch bug; Melanoplus femurrubrum , redlegged grasshopper; Melanoplus sanguinipes , migratory grasshopper; Hylemya platura , seedcorn maggot; Agromyza parvicornis , corn blot leafminer; Anaphothrips obscrurus , grass thrips; Solenopsis milesta , thief ant; Tetranychus urticae , twospotted spider mite; Sorghum: Chilo partellus , sorghum borer; Spodoptera frugiperda , fall armyworm; Helicoverpa zea , corn earworm; Elasmopalpus lignosellus , lesser cornstalk borer; Feltia subterranea , granulate cutworm; Phyllophaga crinita , white grub; Eleodes, Conoderus, and Aeolus spp., wireworms; Oulema melanopus , cereal leaf beetle; Chaetocnema pulicaria , corn flea beetle; Sphenophorus maidis , maize billbug; Rhopalosiphum maidis ; corn leaf aphid; Sipha flava , yellow sugarcane aphid; Blissus leucopterus leucopterus , chinch bug; Contarinia sorghicola , sorghum midge; Tetranychus cinnabarinus , carmine spider mite; Tetranychus urticae , twospotted spider mite; Wheat: Pseudaletia unipunctata , army worm; Spodoptera frugiperda , fall armyworm; Elasmopalpus lignosellus , lesser cornstalk borer; Agrotis orthogonia , western cutworm; Elasmopalpus lignosellus , lesser cornstalk borer; Oulema melanopus , cereal leaf beetle; Hypera punctata , clover leaf weevil; Diabrotica undecimpunctata howardi , southern corn rootworm; Russian wheat aphid; Schizaphis graminum , greenbug; Macrosiphum avenae , English grain aphid; Melanoplus femurrubrum , redlegged grasshopper; Melanoplus differentialis , differential grasshopper; Melanoplus sanguinipes , migratory grasshopper; Mayetiola destructor , Hessian fly; Sitodiplosis mosellana , wheat midge; Meromyza americana , wheat stem maggot; Hylemya coarctata , wheat bulb fly; Frankliniella fusca , tobacco thrips; Cephus cinctus , wheat stem sawfly; Aceria tulipae , wheat curl mite; Sunflower: Suleima helianthana , sunflower bud moth; Homoeosoma electellum , sunflower moth; zygogramma exclamationis , sunflower beetle; Bothyrus gibbosus , carrot beetle; Neolasioptera murtfeldtiana , sunflower seed midge; Cotton: Heliothis virescens , cotton budworm; Helicoverpa zea , cotton bollworm; Spodoptera exigua , beet armyworm; Pectinophora gossypiella , pink bollworm; Anthonomus grandis grandis , boll weevil; Aphis gossypii , cotton aphid; Pseudatomoscelis seriatus , cotton fleahopper; Trialeurodes abutilonea , bandedwinged whitefly; Lygus lineolaris , tarnished plant bug; Melanoplus femurrubrum , redlegged grasshopper; Melanoplus differentialis , differential grasshopper; Thrips tabaci , onion thrips; Franklinkiella fusca , tobacco thrips; Tetranychus cinnabarinus , carmine spider mite; Tetranychus urticae , twospotted spider mite; Rice: Diatraea saccharalis , sugarcane borer; Spodoptera frugiperda , fall armyworm; Helicoverpa zea , corn earworm; Colaspis brunnea , grape colaspis; Lissorhoptrus oryzophilus , rice water weevil; Sitophilus oryzae , rice weevil; Nephotettix nigropictus , rice leafhopper; Blissus leucopterus leucopterus , chinch bug; Acrosternum hilare , green stink bug; Soybean: Pseudoplusia includens , soybean looper; Anticarsia gemmatalis , velvetbean caterpillar; Plathypena scabra , green cloverworm; Ostrinia nubilalis , European corn borer; Agrotis ipsilon , black cutworm; Spodoptera exigua , beet armyworm; Heliothis virescens , cotton budworm; Helicoverpa zea , cotton bollworm; Epilachna varivestis , Mexican bean beetle; Myzus persicae , green peach aphid; Empoasca fabae , potato leafhopper; Acrosternum hilare , green stink bug; Melanoplus femurrubrum , redlegged grasshopper; Melanoplus differentialis , differential grasshopper; Hylemya platura , seedcorn maggot; Sericothrips variabilis , soybean thrips; Thrips tabaci , onion thrips; Tetranychus turkestani , strawberry spider mite; Tetranychus urticae , twospotted spider mite; Barley: Ostrinia nubilalis , European corn borer; Agrotis ipsilon , black cutworm; Schizaphis graminum , greenbug; Blissus leucopterus leucopterus , chinch bug; Acrosternum hilare , green stink bug; Euschistus servus , brown stink bug; Delia platura , seedcorn maggot; Mayetiola destructor , Hessian fly; Petrobia latens , brown wheat mite; Oil Seed Rape: Brevicoryne brassicae , cabbage aphid; Phyllotreta cruciferae , Flea beetle; Mamestra configurata , Bertha armyworm; Plutella xylostella , Diamond-back moth; Delia ssp., Root maggots.

The R sequences or antisense R sequences of the invention can be introduced into any plant in accordance with the methods disclosed herein to enhance or create resistance to plant pests. The sequences to be introduced may be used in expression cassettes for expression in any plant of interest where expression in the plant cell is necessary for description. In other instances, such as for description or recombination, oligonucleotides are synthesized, purified and introduced into the plant cell.

The R sequences of the invention are provided in expression cassettes for expression in the plant of interest. The cassette will include 5′ and 3′ regulatory sequences operably linked to an R sequence of the invention. By “operably linked” is intended a functional linkage between a promoter and a second sequence, wherein the promoter sequence initiates and mediates transcription of the DNA sequence corresponding to the second sequence. Generally, operably linked means that the nucleic acid sequences being linked are contiguous and, where necessary to join two protein coding regions, contiguous and in the same reading frame. The cassette may additionally contain at least one additional gene to be co-transformed into the organism. Alternatively, the additional gene(s) can be provided on multiple expression cassettes.

Such an expression cassette is provided with a plurality of restriction sites for insertion of the R sequence to be under the transcriptional regulation of the regulatory regions. The expression cassette may additionally contain selectable marker genes.

The expression cassette will include in the 5′-3′ direction of transcription, a transcriptional and translational initiation region, an R sequence of the invention, and a transcriptional and translational termination region functional in plants. The transcriptional initiation region, the promoter, may be native or analogous or foreign or heterologous to the plant host. Additionally, the promoter may be the natural sequence or alternatively a synthetic sequence. By “foreign” is intended that the transcriptional initiation region is not found in the native plant into which the transcriptional initiation region is introduced. As used herein, a chimeric gene comprises a coding sequence operably linked to a transcription initiation region that is heterologous to the coding sequence.

A number of promoters can be used in the practice of the invention. The promoters can be selected based on the desired outcome. For example, constitutive, inducible, particularly pathogen-inducible, or tissue specific promoters may be used. Such promoters include those from pathogenesis-related proteins (PR proteins), which are induced following infection by a pathogen; e.g., PR proteins, SAR proteins, beta-1,3-glucanase, chitinase, etc. See, for example, Redolfi et al. (1983) Neth. J. Plant Pathol . 89:245-254; Uknes et al. (1992) The Plant Cell 4:645-656; and Van Loon (1985) Plant Mol. Virol . 4:111-116.

Of interest are promoters that are expressed locally at or near the site of pathogen infection. See, for example, Marineau et al. (1987) Plant Mol. Biol . 9:335-342; Matton et al. (1989) Molecular Plant - Microbe Interactions 2:325-331; Somsisch et al. (1986) Proc. Natl. Acad. Sci. USA 83:2427-2430; Somsisch et al. (1988) Molecular and General Genetics 2:93-98; and Yang, Y (1996) Proc. Natl. Acad. Sci. USA 93:14972-14977. See also, Chen et al. (1996) Plant J . 10:955-966; Zhang and Sing (1994) Proc. Natl. Acad. Sci. USA 91:2507-2511; Warner et al. (1993) Plant J . 3:191-201; Siebertz et al. (1989) Plant Cell 1:961-968; and the references cited therein. Of particular interest is the inducible promoter for the maize PRms gene, whose expression is induced by the pathogen Fusarium moniliforme (see, for example, Cordero et al. (1992) Physiological and Molecular Plant Pathology 41:189-200).

Constitutive promoters include, for example, the core promoter of the Rsyn7 promoter and other constitutive promoters disclosed in WO 99/43838, the 35S promoter, the core 35S promoter, and the like. Other constitutive promoters include, for example, U.S. Pat. Nos. 5,608,149; 5,608,144; 5,604,121; 5,569,597; 5,466,785; 5,399,680; 5,268,463; 5,608,142. see also, co-pending application entitled “Constitutive Maize Promoters, application Ser. No. 09/257,584 filed Feb. 25, 1999, and herein incorporated by reference.

Tissue specific promoters include those described in Yamamoto et al. (1997) Plant J . 12(2):255-265; Kawamata et al. (1997) Plant Cell Physiol . 38(7):792-803; Hansen et al. (1997) Mol. Gen Genet . 254(3):337-343; Russell et al. (1997) Transgenic Res . 6(2):157-168; Rinehart et al. (1996) Plant Physiol . 112(3):1331-1341; Van Camp et al. (1996) Plant Physiol . 112(2):525-535; Canevascini et al. (1996) Plant Physiol . 112(2):513-524; Yamamoto et al. (1994) Plant Cell Physiol . 35(5):773-778; Lam (1994) Results Probl. Cell. Differ . 20:181-196; Orozco et al. (1993) Plant Mol. Biol . 23(6):1129-1138; Matsuoka et al. (1993) Proc. Natl. Acad. Sci. U.S.A . 90(20):9586-9590; and Guevara-Garcia et al. (1993) Plant J . 4(3):495-505.

While it may be preferable to express the sequences using heterologous promoters, the native promoter sequences may be used. Such constructs would change expression levels of R protein in the plant or plant cell. Thus, the phenotype of the plant or plant cell is altered.

The termination region may be native with the transcriptional initiation region, may be native with the operably linked DNA sequence of interest, or may be derived from another source. Convenient termination regions are available from the Ti-plasmid of A. tumefaciens , such as the octopine synthase and nopaline synthase termination regions. See also Guerineau et al. (1991) Mol. Gen. Genet . 262:141-144; Proudfoot (1991) Cell 64:671-674; Sanfacon et al. (1991) Genes Dev . 5:141-149; Mogen et al. (1990) Plant Cell 2:1261-1272; Munroe et al. (1990) Gene 91:151-158; Ballas et al. (1989) Nucleic Acids Res . 17:7891-7903; and Joshi et al. (1987) Nucleic Acid Res . 15:9627-9639.

Where appropriate, the gene(s) may be optimized for increased expression in the transformed plant. That is, the genes can be synthesized using plant-preferred codons for improved expression. See, for example, Campbell and Gowri (1990) Plant Physiol . 92:1-11 for a discussion of host-preferred codon usage. Methods are available in the art for synthesizing plant-preferred genes. See, for example, U.S. Pat. Nos. 5,380,831, and 5,436,391, and Murray et al. (1989) Nucleic Acids Res . 17:477-498, herein incorporated by reference.

Additional sequence modifications are known to enhance gene expression in a cellular host. These include elimination of sequences encoding spurious polyadenylation signals, exon-intron splice site signals, transposon-like repeats, and other such well-characterized sequences that may be deleterious to gene expression. The G-C content of the sequence may be adjusted to levels average for a given cellular host, as calculated by reference to known genes expressed in the host cell. When possible, the sequence is modified to avoid predicted hairpin secondary mRNA structures.

The expression cassettes may additionally contain 5′ leader sequences in the expression cassette construct. Such leader sequences can act to enhance translation. Translation leaders are known in the art and include: picornavirus leaders, for example, EMCV leader (Encephalomyocarditis 5′ noncoding region) (Elroy-Stein et al. (1989) Proc. Natl. Acad. Sci. USA 86:6126-6130); potyvirus leaders, for example, TEV leader (Tobacco Etch Virus) (Gallie et al. (1995) Gene 165(2):233-238), MDMV leader (Maize Dwarf Mosaic Virus) ( Virology 154:9-20), and human immunoglobulin heavy-chain binding protein (BiP) (Macejak et al. (1991) Nature 353:90-94); untranslated leader from the coat protein mRNA of alfalfa mosaic virus (AMV RNA 4) (Jobling et al. (1987) Nature 325:622-625); tobacco mosaic virus leader (TMV) (Gallie et al. (1989) in Molecular Biology of RNA , ed. Cech (Liss, N.Y.), pp. 237-256); and maize chlorotic mottle virus leader (MCMV) (Lommel et al. (1991) Virology 81:382-385). See also, Della-Cioppa et al. (1987) Plant Physiol . 84:965-968. Other methods known to enhance translation can also be utilized, for example, introns, and the like.

Generally, the expression cassette will comprise a selectable marker gene for the selection of transformed cells. Selectable marker genes are utilized for the selection of transformed cells or tissues. Marker genes include genes encoding antibiotic resistance, such as those encoding neomycin phosphotransferase II (NEO) and hygromycin phosphotransferase (HPT), as well as genes conferring resistance to herbicidal compounds, such as glufosinate ammonium, bromoxynil, imidazolinones, and 2,4-dichlorophenoxyacetate (2,4-D). See generally, Yarranton (1992) Curr. Opin. Biotech . 3:506-511; Christopherson et al. (1992) Proc. Natl. Acad. Sci. USA 89:6314-6318; Yao et al. (1992) Cell 71:63-72; Reznikoff (1992) Mol. Microbiol . 6:2419-2422; Barkley et al. (1980) in The Operon , pp. 177-220; Hu et al. (1987) Cell 48:555-566; Brown et al. (1987) Cell 49:603-612; Figge et al. (1988) Cell 52:713-722; Deuschle et al. (1989) Proc. Natl. Acad. Aci. USA 86:5400-5404; Fuerst et al. (1989) Proc. Natl. Acad. Sci. USA 86:2549-2553; Deuschle et al. (1990) Science 248:480483; Gossen (1993) Ph.D. Thesis, University of Heidelberg; Reines et al. (1993) Proc. Natl. Acad. Sci. USA 90:1917-1921; Labow et al. (1990) Mol. Cell. Biol . 10:3343-3356; Zambretti et al. (1992) Proc. Natl. Acad. Sci. USA 89:3952-3956; Baim et al. (1991) Proc. Natl. Acad. Sci. USA 88:5072-5076; Wyborski et al. (1991) Nucleic Acids Res . 19:4647-4653; Hillenand-Wissman (1989) Topics Mol. Struc. Biol . 10:143-162; Degenkolb et al. (1991) Antimicrob. Agents Chemother . 35:1591-1595; Kleinschnidt et al. (1988) Biochemistry 27:1094-1104; Bonin (1993) Ph.D. Thesis, University of Heidelberg; Gossen et al. (1992) Proc. Natl. Acad. Sci. USA 89:5547-5551; Oliva et al. (1992) Antimicrob. Agents Chemother . 36:913-919; Hlavka et al. (1985) Handbook of Experimental Pharmacology , Vol. 78 (Springer-Verlag, Berlin); Gill et al. (1988) Nature 334:721-724. Such disclosures are herein incorporated by reference.

The above list of selectable marker genes is not meant to be limiting. Any selectable marker gene can be used in the present invention.

In preparing the expression cassette, the various DNA fragments may be manipulated, so as to provide for the DNA sequences in the proper orientation and, as appropriate, in the proper reading frame. Toward this end, adapters or linkers may be employed to join the DNA fragments or other manipulations may be involved to provide for convenient restriction sites, removal of superfluous DNA, removal of restriction sites, or the like. For this purpose, in vitro mutagenesis, primer repair, restriction, annealing, resubstitutions, e.g., transitions and transversions, may be involved.

The sequences of the present invention can be used to transform or transfect any plant. In this manner, genetically modified plants, plant cells, plant tissue, seed, and the like can be obtained. Transformation protocols as well as protocols for introducing nucleotide sequences into plans may vary depending on the type of plant or plant cell, i.e. monocot or dicot, targeted for transformation. It is recognized that the transformation protocols may be used for transfection or introduction of the oligonucleotide sequences to disrupt R gene function. Suitable methods of introducing nucleotide sequences into plant cells and subsequent insertion into the plant genome include microinjection (Crossway et al. (1986) Biotechniques 4:320-334), electroporation (Riggs et al. (1986) Proc. Natl. Acad Sci. USA 83:5602-5606, Agrobacterium-mediated transformation (Townsend et al., U.S. Pat. No. 5,563,055; Zhao et al., U.S. Pat. No. 5,981,840), direct gene transfer (Paszkowski et al. (1984) EMBO J . 3:2717-2722), and ballistic particle acceleration (see, for example, Sanford et al., U.S. Pat. No. 4,945,050; Tomes et al., U.S. Pat. No. 5,879,918; Tomes et al., U.S. Pat. No. 5,886,244; Bidney et al., U.S. Pat. No. 5,932,782; Tomes et al. (1995) “Direct DNA Transfer into Intact Plant Cells via Microprojectile Bombardment,” in Plant Cell, Tissue, and Organ Culture: Fundamental Methods , ed. Gamborg and Phillips (Springer-Verlag, Berlin); and McCabe et al. (1988) Biotechnology 6:923-926). Also see Weissinger et al. (1988) Ann. Rev. Genet . 22:421-477; Sanford et al. (1987) Particulate Science and Technology 5:27-37 (onion); Christou et al. (1988) Plant Physiol . 87:671-674 (soybean); McCabe et al. (1988) Bio/Technology 6:923-926 (soybean); Finer and McMullen (1991) In Vitro Cell Dev. Biol . 27P:175-182 (soybean); Singh et al. (1998) Theor. Appl. Genet . 96:319-324 (soybean); Datta et al. (1990) Biotechnology 8:736-740 (rice); Klein et al. (1988) Proc. Natl. Acad. Sci. USA 85:4305-4309 (maize); Klein et al. (1988) Biotechnology 6:559-563 (maize); Tomes, U.S. Pat. No. 5,240,855; Buising et al., U.S. Pat. Nos. 5,322,783 and 5,324,646; Tomes et al. (1995) “Direct DNA Transfer into Intact Plant Cells via Microprojectile Bombardment,” in Plant Cell, Tissue, and Organ Culture: Fundamental Methods , ed. Gamborg (Springer-Verlag, Berlin) (maize); Klein et al. (1988) Plant Physiol . 91:440-444 (maize); Fromm et al. (1990) Biotechnology 8:833-839 (maize); Hooykaas-Van Slogteren et al. (1984) Nature ( London ) 311:763-764; Bowen et al., U.S. Pat. No. 5,736,369 (cereals); Bytebier et al. (1987) Proc. Natl. Acad. Sci. USA 84:5345-5349 (Liliaceae); De Wet et al. (1985) in The Experimental Manipulation of Ovule Tissues , ed. Chapman et al. (Longman, N.Y.), pp. 197-209 (pollen); Kaeppler et al. (1990) Plant Cell Reports 9:415-418 and Kaeppler et al. (1992) Theor. Appl. Genet . 84:560-566 (whisker-mediated transformation); D'Halluin et al. (1992) Plant Cell 4:1495-1505 (electroporation); Li et al. (1993) Plant Cell Reports 12:250-255 and Christou and Ford (1995) Annals of Botany 75:407-413 (rice); Osjoda et al. (1996) Nature Biotechnology 14:745-750 (maize via Agrobacterium tumefaciens ); all of which are herein incorporated by reference.

The cells that have been transformed may be grown into plants in accordance with conventional ways. See, for example, McCormick et al. (1986) Plant Cell Reports 5:81-84. These plants may then be grown, and either pollinated with the same transformed strain or different strains, and the resulting hybrid having constitutive expression of the desired phenotypic characteristic identified. Two or more generations may be grown to ensure that expression of the desired phenotypic characteristic is stably maintained and inherited and then seeds harvested to ensure expression of the desired phenotypic characteristic has been achieved.

The present invention may be used for transformation of any plant species, including, but not limited to, monocots and dicots. Examples of plant species of interest include, but are not limited to, corn ( Zea mays ), Brassica sp. (e.g., B. napus, B. rapa, B. juncea ), particularly those Brassica species useful as sources of seed oil, alfalfa ( Medicago sativa ), rice ( Oryza sativa ), rye ( Secale cereale ), sorghum ( Sorghum bicolor, Sorghum vulgare ), millet (e.g., pearl millet ( Pennisetum glaucum ), proso millet ( Panicum miliaceum ), foxtail millet ( Setaria italica ), finger millet ( Eleusine coracana )), sunflower ( Helianthus annuus ), safflower ( Carthamus tinctorius ), wheat ( Triticum aestivum ), soybean ( Glycine max ), tobacco ( Nicotiana tabacum ), potato ( Solanum tuberosum ), peanuts ( Arachis hypogaea ), cotton ( Gossypium barbadense, Gossypium hirsutum ), sweet potato ( Ipomoea batatus ), cassava ( Manihot esculenta ), coffee (Coffea spp.), coconut ( Cocos nucifera ), pineapple ( Ananas comosus ), citrus trees (Citrus spp.), cocoa ( Theobroma cacao ), tea ( Camellia sinensis ), banana (Musa spp.), avocado ( Persea americana ), fig ( Ficus casica ), guava ( Psidium guajava ), mango ( Mangifera indica ), olive ( Olea europaea ), papaya ( Carica papaya ), cashew ( Anacardium occidentale ), macadamia ( Macadamia integrifolia ), almond ( Prunus amygdalus ), sugar beets ( Beta vulgaris ), sugarcane (Saccharum spp.), oats, barley, vegetables, ornamentals, and conifers.

Vegetables include tomatoes ( Lycopersicon esculentum ), lettuce (e.g., Lactuca sativa ), green beans ( Phaseolus vulgaris ), lima beans ( Phaseolus limensis ), peas (Lathyrus spp.), and members of the genus Cucumis such as cucumber ( C. sativus ), cantaloupe ( C. cantalupensis ), and musk melon ( C. melo ). Ornamentals include azalea (Rhododendron spp.), hydrangea ( Macrophylla hydrangea ), hibiscus ( Hibiscus rosasanensis ), roses (Rosa spp.), tulips (Tulipa spp.), daffodils (Narcissus spp.), petunias ( Petunia hybrida ), carnation ( Dianthus caryophyllus ), poinsettia ( Euphorbia pulcherrima ), and chrysanthemum.

Conifers that may be employed in practicing the present invention include, for example, pines such as loblolly pine ( Pinus taeda ), slash pine ( Pinus elliotii ), ponderosa pine ( Pinus ponderosa ), lodgepole pine ( Pinus contorta ), and Monterey pine ( Pinus radiata ); Douglas-fir ( Pseudotsuga menziesii ); Western hemlock ( Tsuga canadensis ); Sitka spruce ( Picea glauca ); redwood ( Sequoia sempervirens ); true firs such as silver fir ( Abies amabilis ) and balsam fir ( Abies balsamea ); and cedars such as Western red cedar ( Thuja plicata ) and Alaska yellow-cedar ( Chamaecyparis nootkatensis ). Preferably, plants of the present invention are crop plants (for example, corn, alfalfa, sunflower, Brassica, soybean, cotton, safflower, peanut, sorghum, wheat, millet, tobacco, etc.), more preferably corn and soybean plants, yet more preferably corn plants.

Plants of particular interest include grain plants that provide seeds of interest, oil-seed plants, and leguminous plants. Seeds of interest include grain seeds, such as corn, wheat, barley, rice, sorghum, rye, etc. Oil-seed plants include cotton, soybean, safflower, sunflower, Brassica, maize, alfalfa, palm, coconut, etc. Leguminous plants include beans and peas. Beans include guar, locust bean, fenugreek, soybean, garden beans, cowpea, mungbean, lima bean, fava bean, lentils, chickpea, etc.

The methods of the invention can be used with other methods for increasing pathogen resistance in plants. See, for example, Cai et al. (1997) Science 275:832-834; Roberts and Gallum (1984) J. Heredity 75:147-148; Ryerson and Heath (1996) Plant Cell 8:393-402 and Dangl et al. (1996) Plant Cell 8:1793-1807.

The R sequences of the invention are also useful as molecular markers. Such markers are useful in breeding programs, particularly those aimed at improving disease resistance. The sunflower R sequences have been mapped to chromosome locations and these positions related to known disease resistance loci.

The present invention provides a method of genotyping a plant comprising a polynucleotide of the present invention. Genotyping provides a means of distinguishing homologs of a chromosome pair and can be used to differentiate segregants in a plant population. Molecular marker methods can be used for phylogenetic studies, characterizing genetic relationships among crop varieties, identifying crosses or somatic hybrids, localizing chromosomal segments affecting monogenic traits, map based cloning, and the study of quantitative inheritance. See, e.g., Plant Molecular Biology: A Laboratory Manual , Chapter 7, Clark, Ed., Springer-Verlag, Berlin (1997). For molecular marker methods, see generally, The DNA Revolution by Andrew H. Paterson (1996) (Chapter 2) in: Genome Mapping in Plants (ed. Andrew H. Paterson) by Academic Press/R. G. Landis Company, Austin, Tex., pp. 7-21.

The particular method of genotyping in the present invention may employ any number of molecular marker analytic techniques such as, but not limited to, restriction fragment length polymorphisms (RFLPs). RFLPs are the product of allelic differences between DNA restriction fragments caused by nucleotide sequence variability. As is well known to those of skill in the art, RFLPs are typically detected by extraction of genomic DNA and digestion with a restriction enzyme. Generally, the resulting fragments are separated according to size and hybridized with a probe; single copy probes are preferred. Restriction fragments from homologous chromosomes are revealed. Differences in fragment size among alleles represent an RFLP. Thus, the present invention further provides a means to follow segregation of a gene or nucleic acid of the present invention as well as chromosomal sequences genetically linked to these genes or nucleic acids using such techniques as RFLP analysis. Linked chromosomal sequences are within 50 centiMorgans (cM), often within 40 or 30 cM, preferably within 20 or 10 cM, more preferably within 5, 3, 2, or 1 cM of a gene.

In the present invention, the nucleic acid probes employed for molecular marker mapping of plant nuclear genomes selectively hybridize, under selective hybridization conditions, to a gene encoding a polynucleotide of the present invention. In one embodiment, the probes are selected from polynucleotides of the present invention. Typically, these probes are cDNA probes or PstI genomic clones. The length of the probes is discussed in greater detail, supra, but are typically at least 15 bases in length, more preferably at least 20, 25, 30, 35, 40, or 50 bases in length. Generally, however, the probes are less than about 1 kilobase in length. Preferably, the probes are single copy probes that hybridize to a unique locus in a haploid chromosome complement. Some exemplary restriction enzymes employed in RFLP mapping are EcoRI, EcoRv, and SstI. As used herein the term “restriction enzyme” includes reference to a composition that recognizes and, alone or in conjunction with another composition, cleaves at a specific nucleotide sequence.

The method of detecting an RFLP comprises the steps of (a) digesting genomic DNA of a plant with a restriction enzyme; (b) hybridizing a nucleic acid probe, under selective hybridization conditions, to a sequence of a polynucleotide of the present of said genomic DNA; (c) detecting therefrom a RFLP. Other methods of differentiating polymorphic (allelic) variants of polynucleotides of the present invention can be had by utilizing molecular marker techniques well known to those of skill in the art including such techniques as: 1) single-stranded conformation analysis (SSCP); 2) denaturing gradient gel electrophoresis (DGGE); 3) RNase protection assays; 4) allele-specific oligonucleotides (ASOs); 5) the use of proteins which recognize nucleotide mismatches, such as the E. coli mutS protein; and 6) allele-specific PCR. Other approaches based on the detection of mismatches between the two complementary DNA strands include clamped denaturing gel electrophoresis (CDGE); heteroduplex analysis (HA); and chemical mismatch cleavage (CMC). Exemplary polymorphic variants are provided in Table I, supra. Thus, the present invention further provides a method of genotyping comprising the steps of contacting, under stringent hybridization conditions, a sample suspected of comprising a polynucleotide of the present invention with a nucleic acid prober. Generally, the sample is a plant sample; preferably, a sample suspected of comprising a sunflower polynucleotide of the present invention (e.g., gene, mRNA). The nucleic acid probe selectively hybridizes, under stringent conditions, to a subsequence of a polynucleotide of the present invention comprising a polymorphic marker. Selective hybridization of the nucleic acid probe to the polymorphic marker nucleic acid sequence yields a hybridization complex. Detection of the hybridization complex indicates the presence of that polymorphic marker in the sample. In one embodiment, the nucleic acid probe comprises a polynucleotide of the present invention.

The following examples are offered by way of illustration and not by way of limitation.

EXPERIMENTAL

EXAMPLE 1

Cloning of Sunflower Disease Resistant Genes

MATERIALS AND METHODS

Plant Material

Sunflower plants and maize plants were grown in the greenhouse. For PCR-based isolation of R gene homologs and pto-like protein kinase genes we used the sunflower line SMF 3. Sunflower pathogen, Scierotinia sclerotiorum was maintained on PDA plate at 20° C. in dark.

PCR Amplification of Sunflower R Gene and Pto Homologs

To isolate R gene homologs, two conserved regions (NBS-LRR) of amino acid identity in the N gene from tobacco, the PRS2 gene from Arabidopsis, and the L6 gene from flax were used to design degenerate oligonucleotide primers as reported previously (Leister et al. (1998) Proct. Natl. Acad. Sci. USA 95:370-375) with the modifications as indicated in Table 1. Degenerate primers were designed based on motifs conserved between pto, fen, and APK1 in order to clone sunflower pto homologs. Table 1 summarizes the degenerate primers used for cloning R homologs and pto-like genes.

PCRs were performed in a total volume of 25 ul in 10 mM Tris-HCL, pH 8.3; 1.5 mM MgCL2; 50 mM KCL; 0.1 mM dNTPs; 0.25 uM of each primer with 0.5 units of advantage cDNA polymerase mix (Clontech) or Pwo DNA ploymerase (Boehringer). Genomic DNA and/or cDNA library mixtures were used as template for PCR amplification.

TABLE 1
Degenerate primers for isolating the R genes.
(A). NBS-LRR type R gene (N, Rps2, and L6 genes (18)):
Sense: 5′ GGN GGN RTN GGN AAN ACN AC 3′ biocode # 26433;
SEQ ID NO: 15
Antisense #1: 5′ AG NGY NAG NGG NAG NCC 3′ biocode # 26924;
SEQ ID NO: 16
Antisense #2: 5′ AG NGY NAG NGG NAA NCC 3′ biocode # 26925;
SEQ ID NO: 17
Antisense #3: 5′ AG NGY NAA NGG NAG NCC 3′ biocode # 26926;
SEQ ID NO: 18
Antisense #4: 5′ AG NGY NAA NGG NAA NCC 3′ biocode # 26927;
SEQ ID NO: 19
Antisense #5: 5′ AA NGY NAG NGG NAG NCC 3′ biocode # 26928;
SEQ ID NO: 20
Antisense #6: 5′ AA NGY NAG NGG NAA NCC 3′ biocode # 26929;
SEQ ID NO: 21
Antisense #7: 5′ AA NGY NAA NGG NAG NCC 3′ biocode # 26930;
SEQ ID NO: 22
Antisense #8: 5′ AA NGY NAA NGG NAA NCC 3′ biocode # 26931;
SEQ ID NO: 23
(B). Primers for pto and fen homologous (16).
GFGDVYK:
pto sense 1:                     biocode # 26967;
5′ GGN TTY GGN RAN GTN TAY AA 3′
SEQ ID NO: 24
pto sense 2:                     biocode # 26968;
5′ GGN TTY GGN RAN GTN TAY AG 3′
SEQ ID NO: 25
GAA(R/K)GL:
anti-sense: 5′ TRN CCN YKN GCN GCN CC 3′ biocode # 26970;
SEQ ID NO: 26
GFSYVD:
anti-sense: 5′ CCR AAN SYR TAN ACR TC 3′ biocode # 26971;
SEQ ID NO: 27
**R = A/G; Y = C/T; D = A/G/T; H = A/C/T; and N = A/G/T/C

Analysis of Amplified PCR Products

Amplified PCR fragments with the expected sizes of 450-550 bp for NBS-LRR primers, 340 bp for NBS primers and 600 bp for pto primers were individually sliced out of gels for a second round of PCR amplification with the same conditions as the initial PCR. Each second-round PCR amplification yielded a single band of the expected size which represented a heterogeneous population of PCR products. The PCR products were cloned into a TA vector (Clontech) according to the suppliers instructions. Fifty clones of each PCR product population were picked randomly and grouped by restriction analysis using 4-bp recognition enzymes (Alu I and Msp I). At least one representative clone of each identified group was selected for DNA sequencing using an Applied Biosystems 373A (ABI) automated sequencer at the Nucleic Acid Analysis Facility of Pioneer Hi-Bred International, Incorporated. DNA sequence analysis was carried out with the Sequencer (3.0). Multiple-sequence alignment (Clustal W) of the DNA sequence and phylogenetic analysis (PHYLIP) were made with the Curatool (CuraGen).

Construction of the Sclerotinia-infected and Resistance-enhanced (oxox-induced) Sunflower cDNA Libraries

Six-week-old SMF3 sunflower plants were infected with Sclerotinia sclerotritim by petiole inoculation with Sclerotinia-infested carrot plugs. Six days after infection, leaf and stem tissues were collected from infected plants for total RNA isolation. Total RNA was also isolated from sunflower transgenic plants (SID 610255) expressing a wheat oxalate oxidase gene (oxox) at the six-week stage. Our previous studies have showed that elevated levels of H 2 O 2 , SA and PR1 protein were detected in oxox-transgenic plants at the six-week stage and the plants showed more resistance to Sclerotinia infection WO99/04013. mRNA was isolated using an mRNA purification kit (BRL) according to the manufacturer's instructions. cDNA libraries were constructed with the ZAP-cDNA synthesis kit into pBluescript phagemid (Stratagene). A cDNA library mixture for PCR cloning was made of oxox transgenic stem and Sclerotinia-infected leaf libraries (1:2 mix).

Isolation of Full-length or Flanking Sequences by PCR Amplification of cDNA Ends

Full-length or flanking sequences of identified sunflower R gene and PK gene homologues were isolated using directly amplified Sclerotinia-infected cDNA libraries or the Marathon cDNA Amplification Kit (Clontech) according to the manufacturer's instructions. To facilitate cloning full-length cDNAs from the initial cloned regions, we designed a pair of 28 bp vector primers flanking the cloned cDNAs on both the 3′ and 5′ ends of the pBS vector. The vector primers were utilized to directionally amplify either a 5′ or 3′ end of a cDNA using one vector primer (pBS-upper or pBS-lower) and a gene-specific primer. Once the anticipated 5′ end of a specific gene with an intact ATG start codon was cloned and sequenced, the full-length cDNA was amplified using a second gene-specific primer containing sequence upstream of the ATG and a vector primer at the 3′ end. The PCR products were cloned and sequenced as described above.

RESULTS

Clone Full-length of cDNAs Related to Disease Resistance

A PCR-based cloning method to efficiently isolate full-length cDNAs of disease resistance-related R genes and protein kinase genes, as well as other plant defense genes, from sunflower cDNA libraries has been developed. A cDNA library mixture containing both oxox-transgenic cDNA library and Sclerotinia-infected cDNA library (1:2 mix) was used as a source of templates for PCR amplification. Using cDNA libraries as a source of DNA templates for PCR amplification had two benefits: (1) the number of unexpected PCR products was reduced as compared with genomic DNA as a source of templates and (2) disease-induced cDNA libraries increased the chance of isolating defense-related genes. To facilitate cloning full-length cDNAs from the initially cloned regions, a pair of 28 bp vector primers (Table 2) the flanking cDNAs on the ends (3′ and 5′) of pBS vector was designed and used to directionally amplify either the 5′ or 3′ end of the cDNA with one of the vector primers paired with a gene-specific primer (Table 2a and 2b). The 5′ end of the gene with the intact ATG start codon was cloned and sequenced. The full-length cDNA was amplified by using a second gene-specific primer containing the upstream ATG region sequence and a vector primer at the 3′ end. The PCR products were cloned and sequenced as described above. This method was used in the full-length clone isolation as indicated below.

TABLE 2
Gene Specific primers for R end RACE and full length cloning
(A): Specific primers for R gene end RACE
RS-1: CGATGTGAAGGTAGGGAATGAG     Biocode: 27101;
SEQ ID NO: 28
RS-2: GGGAGTGAGATAATAGGAAGGAGC   Biocode: 27102;
SEQ ID NO: 29
RS-3: GGTAGGGAGTGAGATAGAAGGAAG   Biocode: 27103;
SEQ ID NO: 30
RS-4: TATGAAGTGAATTTGTTATCACA    Biocode: 27104;
SEQ ID NO: 31
RS-5: TATGAAGTGAGTTTGTTATCACA    Biocode: 27105;
SEQ ID NO: 32
RS-6: AAGACGACTCTCGCATCTGCTGCCTA Biocode: 27166;
SEQ ID NO: 33
RS-7: GAAGACGACTCTCGCATCTGCTGCTT Biocode: 27167;
SEQ ID NO: 34
RAS-1: GCCACCAGCATAAGAAACTACC    Biocode: 27106;
SEQ ID NO: 35
RAS-2: GGCCGTCAGCATAAGAAACTAC    Biocode: 27107;
SEQ ID NO: 36
RAS-3: GGAGGCCACTAGCATAAGAAAC    Biocode: 27108;
SEQ ID NO: 37
RAS-4: GGGGAGGCCACCAGCATAAGAAACTA Biocode: 27168;
SEQ ID NO: 38
RAS-5: CGAAGGGGAGGCCACTAGCATAAGAA Biocode: 27169;
SEQ ID NO: 39
RAS-6: CAATTATTATCCGGCTCCCCTCACCA Biocode: 27170;
SEQ ID NO: 40
RAS-7: TCTTATATCGTGTCTGCATGGCGGGT Biocode: 27171;
SEQ ID NO: 41
RAS-8: CACTTCATAAATCGTTTGCGCCCTGC Biocode: 27172;
SEQ ID NO: 42
(B) PK SPECIFIC PRIMERS FOR RACE:
PKS1 *: GCAGCGGTCAGATTGTAGCTGTCAAA biocode: 27884;
SEQ ID NO: 43
Group 1
PKAS1: GCCAGCCGCTATCTTCATTCTTGTGT biocode: 27885;
SEQ ID NO: 44
PKS2: GGATAGGAACGGGCTGCAGGGTAAC  biocode: 27886;
SEQ ID NO: 45
PKAS2: TTTGGTCACCATCAGCACAGTATCCG biocode: 27887;
SEQ ID NO: 46
PKS3: CTTGGGTTTGGGGAGGTGTACAGAGG biocode: 27888;
SEQ ID NO: 47
PKS4: CTTGGATGCTGCAATTAAGCGACTGG biocode: 27889;
SEQ ID NO: 48
Group 2
PKAS4: GGCGGCGCCTATGCATATTTTGAGT biocode: 27890;
SEQ ID NO: 49
PKS5: CTTCAAAACCGGGGTCTGGAGTCGTT biocode: 27891;
SEQ ID NO: 50
Group 3
PKAS5: CGGAGACTCCATGTTAGCGGTTGAAA biocode: 27892;
SEQ ID NO: 51
(C) PK primers for full length cloning:
PK4-RACE:                        biocode: 29131;
AACTATGTCTTTCCATACCAGTCACCCGG
SEQ ID NO: 52
PK5-RACE:                        biocode: 29132;
TCGGAGACTCCATGTTAGCGGTTGAA
SEQ ID NO: 53
PK1-RACE:                        biocode: 29136;
GACCGTTCCTTCAATTAATGGGTTGC
SEQ ID NO: 54
Vector primers
PBS-upper:                       biocode: 27164;
GCGATTAAGTTGGGTAACGCCAGGGT
SEQ ID NO: 55
PBS-lower: TCCGGCTCGTATGTTGTGTGGAATTG biocode: 27165;
SEQ ID NO: 56
*: RS primers: for cloning 3′ end of cDNA clones and RAS for cloning 5′ end of cDNAs.
*PKS for the 3′ end ofcDNA clones and PKAS for the 5′ end clones
**Group 1 (PK1): clones pto-1,-8,-16,-18
Group 2 (PK4): clone pto-21
Group 3 (PK5): clone pto-6

Protein Kinase cDNAs

Four different full-length PK cDNAs have been cloned from sunflower cDNA libraries. Isolation of full-length PK cDNA clones was performed with three rounds of cloning efforts using PCR-based techniques. The first step of the PK cloning was performed by PCR amplification using degenerate primers based on conserved regions between pto, fen and an Arabidopsis PK (Table 1). The initial PCR amplification resulted in the expected bands (about 350 bp). The anticipated PCR products were isolated from the gel, and then re-amplified. The PCR products were cloned into TA vectors. Restriction digestions of cloned fragments with Alu I and Msp I resulted in several different patterns. Six clones were identified as PK positive. Four of the six PK clones showed differences only at the degenerate primer regions and were considered as one group. PK positive clones were classified into three different groups of PK homologous (PK1, PK4 and PK5) based on sequence similarity. Gene-specific primers (Table 2b) were made for cloning of the 3′ and 5′ end of the three different groups of PK. Finally, PK clones containing 5′ end sequence were used to design new primers (Table 2c) for cloning full-length cDNA clones. The amino acid sequence of PK1A is highly similar to that of PK1B (FIG. 1 ). Both are closely related to PTO kinase from tomato (FIG. 1 ), which is a disease resistance protein against bacterial speck disease. Sequence comparison indicated that PK4 was highly similar to a receptor-like protein kinase and disease resistance protein kinase. Currently, for the PK5 group, only one 5′-end clone has been sequenced. It had 971 bp long and coded a 170 amino acid protein. A BLASTX search showed it had 68% identity with protein kinase APK1A from Arabidopsis.

NBS-LRR Type R Gene Homologs

The PCR products were amplified from sunflower and maize genomic DNAs and sunflower cDNA libraries using degenerate primers. One major expected band of about 500 bp was amplified from a sunflower source using NBS-LRR primers. A similar size band was amplified from maize genomic DNA. These expected bands amplified from the cDNA library mix were isolated and/or re-amplified, and then cloned into TA vectors. Separate PCR amplifications of sunflower genomic DNA and cDNAs using degenerate NBS-LRR primers each produced a large band around 500 bp. Restriction digestion of cloned fragments with Alu I and Msp I resulted in several different patterns. The presence of a heterogeneous PCR product suggested the involvement of a multigene family. At least one representative clone was selected from each different digestion group for sequence analysis. A total of six different R gene homologs from sunflower were identified using the BLAST algorithm to search GenBank. Based on the initial sequence information several gene specific primers were made (Table 1b) to clone both the 5′ and 3′ ends by PCR amplification. Four clones have been isolated. Two 3′-end clones (RS6-8 and RS7-4) and two 5′-end clones (RAS4-5 and RAS5-1) can form two contigs (RS6-8 contig and RS7-4 contig) (SEQ ID NOs: 7, 9-12, and 14). Both contigs showed high homology with the tobacco mosaic virus (TMV) resistance gene N, the downy mildew resistance gene and the rust resistance gene (FIGS. 3 and 4 ). In summary, six NBS-LRR type homologs were isolated using a PCR-based cloning strategy. R homolog clones from sunflower showed the highest homology to the R genes from other dicot plants

EXAMPLE 2

Transformation and Regeneration of Transgenic Maize Plants

Immature maize embryos from greenhouse donor plants are bombarded with a plasmid containing the R gene operably linked to a UBI promoter ( FIG. 5 ) and the selectable marker gene PAT (Wohlleben et al. (1988) Gene 70:25-37), which confers resistance to the herbicide Bialaphos. Alternatively, the selectable marker gene is provided on a separate plasmid. Transformation is performed as follows. Media recipes follow below.

Preparation of Target Tissue

The ears are husked and surface sterilized in 30% Chlorox bleach plus 0.5% Micro detergent for 20 minutes, and rinsed two times with sterile water. The immature embryos are excised and placed embryo axis side down (scutellum side up), 25 embryos per plate, on 560Y medium for 4 hours and then aligned within the 2.5-cm target zone in preparation for bombardment.

Preparation of DNA

A plasmid vector comprising the R gene operably linked to a UBI promoter is made. This plasmid DNA plus plasmid DNA containing a PAT selectable marker is precipitated onto 1.1 μm (average diameter) tungsten pellets using a CaCl 2 precipitation procedure as follows:

100 μl prepared tungsten particles in water

10 μl (1 μg) DNA in Tris EDTA buffer (1 μg total DNA)

100 μl 2.5 M CaCl 2

10 μl 0.1 M spermidine

Each reagent is added sequentially to the tungsten particle suspension, while maintained on the multitube vortexer. The final mixture is sonicated briefly and allowed to incubate under constant vortexing for 10 minutes. After the precipitation period, the tubes are centrifuged briefly, liquid removed, washed with 500 ml 100% ethanol, and centrifuged for 30 seconds. Again the liquid is removed, and 105 μl 100% ethanol is added to the final tungsten particle pellet. For particle gun bombardment, the tungsten/DNA particles are briefly sonicated and 10 μl spotted onto the center of each macrocarrier and allowed to dry about 2 minutes before bombardment.

Particle Gun Treatment

The sample plates are bombarded at level #4 in particle gun #HE34-1 or #HE34-2. All samples receive a single shot at 650 PSI, with a total of ten aliquots taken from each tube of prepared particles/DNA.

Subsequent Treatment

Following bombardment, the embryos are kept on 560Y medium for 2 days, then transferred to 560R selection medium containing 3 mg/liter Bialaphos, and subcultured every 2 weeks. After approximately 10 weeks of selection, selection-resistant callus clones are transferred to 288J medium to initiate plant regeneration. Following somatic embryo maturation (2-4 weeks), well-developed somatic embryos are transferred to medium for germination and transferred to the lighted culture room. Approximately 7-10 days later, developing plantlets are transferred to 272V hormone-free medium in tubes for 7-10 days until plantlets are well established. Plants are then transferred to inserts in flats (equivalent to 2.5″ pot) containing potting soil and grown for 1 week in a growth chamber, subsequently grown an additional 1-2 weeks in the greenhouse, then transferred to classic 600 pots (1.6 gallon) and grown to maturity. Plants are monitored and scored for disease resistance.

Bombardment and Culture Media

Bombardment medium (560Y) comprises 4.0 g/l N6 basal salts (SIGMA C-1416), 1.0 ml/l Eriksson's Vitamin Mix (1000X SIGMA-1511), 0.5 mg/l thiamine HCl, 120.0 g/l sucrose, 1.0 mg/l 2,4-D, and 2.88 g/l L-proline (brought to volume with D-I H 2 O following adjustment to pH 5.8 with KOH); 2.0 g/l Gelrite (added after bringing to volume with D-I H 2 O); and 8.5 mg/l silver nitrate (added after sterilizing the medium and cooling to room temperature). Selection medium (560R) comprises 4.0 g/l N6 basal salts (SIGMA C-1416), 1.0 ml/l Eriksson's Vitamin Mix (1000X SIGMA-1511), 0.5 mg/l thiamine HCl, 30.0 g/l sucrose, and 2.0 mg/l 2,4-D (brought to volume with D-I H 2 O following adjustment to pH 5.8 with KOH); 3.0 g/l Gelrite (added after bringing to volume with D-I H 2 O); and 0.85 mg/l silver nitrate and 3.0 mg/l bialaphos(both added after sterilizing the medium and cooling to room temperature).

Plant regeneration medium (288J) comprises 4.3 g/l MS salts (GIBCO 11117-074), 5.0 ml/l MS vitamins stock solution (0.100 g nicotinic acid, 0.02 g/l thiamine HCL, 0.10 g/l pyridoxine HCL, and 0.40 g/l glycine brought to volume with polished D-I H 2 O) (Murashige and Skoog (1962) Physiol. Plant . 15:473), 100 mg/l myo-inositol, 0.5 mg/l zeatin, 60 g/l sucrose, and 1.0 ml/l of 0.1 mM abscisic acid (brought to volume with polished D-I H 2 O after adjusting to pH 5.6); 3.0 g/l Gelrite (added after bringing to volume with D-I H 2 O); and 1.0 mg/l indoleacetic acid and 3.0 mg/l bialaphos (added after sterilizing the medium and cooling to 60° C.). Hormone-free medium (272V) comprises 4.3 g/l MS salts (GIBCO 11117-074), 5.0 ml/l MS vitamins stock solution (0.100 g/l nicotinic acid, 0.02 g/l thiamine HCL, 0.10 g/l pyridoxine HCL, and 0.40 g/l glycine brought to volume with polished D-l H 2 O), 0.1 g/l myo-inositol, and 40.0 g/l sucrose (brought to volume with polished D-I H 2 O after adjusting pH to 5.6); and 6 g/l bacto-agar (added after bringing to volume with polished D-I H 2 O), sterilized and cooled to 60° C.

EXAMPLE 3

Virus-mediated Transformation

The methods of the invention involve introducing a nucleotide construct into a plant. By “introducing” is intended presenting to the plant the nucleotide construct in such a manner that the construct gains access to the interior of a cell of the plant. The methods of the invention do not depend on a particular method for introducing a nucleotide construct to a plant, only that the nucleotide construct gains access to the interior of at least one cell of the plant. Methods for introducing nucleotide constructs into plants are known in the art including, but not limited to, stable transformation methods, transient transformation methods, and virus-mediated methods.

By “stable transformation” is intended that the nucleotide construct introduced into a plant integrates into the genome of the plant and is capable of being inherited by progeny thereof. By “transient transformation” is intended that a nucleotide construct introduced into a plant does not integrate into the genome of the plant.

The nucleotide constructs of the invention may be introduced into plants by contacting plants with a virus or viral nucleic acids. Generally, such methods involve incorporating a nucleotide construct of the invention within a viral DNA or RNA molecule. It is recognized that the an R protein of the invention may be initially synthesized as part of a viral polyprotein, which later may be processed by proteolysis in vivo or in vitro to produce the desired recombinant protein. Further, it is recognized that promoters of the invention also encompass promoters utilized for transcription by viral RNA polymerases. Methods for introducing nucleotide constructs into plants and expressing a protein encoded therein, involving viral DNA or RNA molecules, are known in the art. See, for example, U.S. Pat. Nos. 5,889,191, 5,889,190, 5,866,785, 5,589,367 and 5,316,931; herein incorporated by reference.

EXAMPLE 4

Agrobacterium-mediated Transformation

For Agrobacterium-mediated transformation of maize with an R gene, preferably the method of Zhao is employed (U.S. Pat. No. 5,981,840, and PCT patent publication WO98/32326; the contents of which are hereby incorporated by reference). Briefly, immature embryos are isolated from maize and the embryos contacted with a suspension of Agrobacterium, where the bacteria are capable of transferring the R gene to at least one cell of at least one of the immature embryos (step 1: the infection step). In this step the immature embryos are preferably immersed in an Agrobacterium suspension for the initiation of inoculation. The embryos are co-cultured for a time with the Agrobacterium (step 2: the co-cultivation step). Preferably the immature embryos are cultured on solid medium following the infection step. Following this co-cultivation period an optional “resting” step is contemplated. In this resting step, the embryos are incubated in the presence of at least one antibiotic known to inhibit the growth of Agrobacterium without the addition of a selective agent for plant transformants (step 3: resting step). Preferably the immature embryos are cultured on solid medium with antibiotic, but without a selecting agent, for elimination of Agrobacterium and for a resting phase for the infected cells. Next, inoculated embryos are cultured on medium containing a selective agent and growing transformed callus is recovered (step 4: the selection step). Preferably, the immature embryos are cultured on solid medium with a selective agent resulting in the selective growth of transformed cells. The callus is then regenerated into plants (step 5: the regeneration step), and preferably calli grown on selective medium are cultured on solid medium to regenerate the plants.

EXAMPLE 5

Transformation and Regeneration of Transgenic Soybean Embryos

Soybean embryos are bombarded with a plasmid containing the R gene operably linked to a UBI promoter ( FIG. 5 ) as follows. To induce somatic embryos, cotyledons, 3-5 mm in length dissected from surface-sterilized, immature seeds of the soybean cultivar A2872, are cultured in the light or dark at 26° C. on an appropriate agar medium for six to ten weeks. Somatic embryos producing secondary embryos are then excised and placed into a suitable liquid medium. After repeated selection for clusters of somatic embryos that multiplied as early, globular-staged embryos, the suspensions are maintained as described below.

Soybean embryogenic suspension cultures can maintained in 35 ml liquid media on a rotary shaker, 150 rpm, at 26° C. with florescent lights on a 16:8 hour day/night schedule. Cultures are subcultured every two weeks by inoculating approximately 35 mg of tissue into 35 ml of liquid medium.

Soybean embryogenic suspension cultures may then be transformed by the method of particle gun bombardment (Klein et al. (1987) Nature (London) 327:70-73, U.S. Pat. No. 4,945,050). A Du Pont Biolistic PDS 1000/HE instrument (helium retrofit) can be used for these transformations.

A selectable marker gene that can be used to facilitate soybean transformation is a transgene composed of the 35S promoter from Cauliflower Mosaic Virus (Odell et al. (1985) Nature 313:810-812), the hygromycin phosphotransferase gene from plasmid pJR225 (from E. coli ; Gritz et al. (1983) Gene 25:179-188), and the 3′ region of the nopaline synthase gene from the T-DNA of the Ti plasmid of Agrobacterium tumefaciens . The expression cassette comprising the R gene operably linked to the UBI promoter can be isolated as a restriction fragment. This fragment can then be inserted into a unique restriction site of the vector carrying the marker gene.

To 50 μl of a 60 mg/ml 1 μm gold particle suspension is added (in order): 5 μl DNA (1 μg/μl), 20 μl spermidine (0.1 M), and 50 μl CaCl 2 (2.5 M). The particle preparation is then agitated for three minutes, spun in a microfuge for 10 seconds and the supernatant removed. The DNA-coated particles are then washed once in 400 μl 70% ethanol and resuspended in 40 μl of anhydrous ethanol. The DNA/particle suspension can be sonicated three times for one second each. Five microliters of the DNA-coated gold particles are then loaded on each macro carrier disk.

Approximately 300-400 mg of a two-week-old suspension culture is placed in an empty 60×15 mm petri dish and the residual liquid removed from the tissue with a pipette. For each transformation experiment, approximately 5-10 plates of tissue are normally bombarded. Membrane rupture pressure is set at 1100 psi, and the chamber is evacuated to a vacuum of 28 inches mercury. The tissue is placed approximately 3.5 inches away from the retaining screen and bombarded three times. Following bombardment, the tissue can be divided in half and placed back into liquid and cultured as described above.

Five to seven days post bombardment, the liquid media may be exchanged with fresh media, and eleven to twelve days post-bombardment with fresh media containing 50 mg/ml hygromycin. This selective media can be refreshed weekly. Seven to eight weeks post-bombardment, green, transformed tissue may be observed growing from untransformed, necrotic embryogenic clusters. Isolated green tissue is removed and inoculated into individual flasks to generate new, clonally propagated, transformed embryogenic suspension cultures. Each new line may be treated as an independent transformation event. These suspensions can then be subcultured and maintained as clusters of immature embryos or regenerated into whole plants by maturation and germination of individual somatic embryos.

EXAMPLE 6

Transformation and Regeneration of Sunflower Meristem Tissues

Sunflower meristem tissues are transformed with an expression cassette containing the R gene operably linked to a UBI promoter as follows (see also European Patent Number EP 0 486233, herein incorporated by reference, and Malone-Schoneberg et al. (1994) Plant Science 103:199-207). Mature sunflower seed ( Helianthus annuus L.) are dehulled using a single wheat-head thresher. Seeds are surface sterilized for 30 minutes in a 20% Chlorox bleach solution with the addition of two drops of Tween 20 per 50 ml of solution. The seeds are rinsed twice with sterile distilled water.

Split embryonic axis explants are prepared by a modification of procedures described by Schrammeijer et al. (Schrammeijer et al. (1990) Plant Cell Rep . 9: 55-60). Seeds are imbibed in distilled water for 60 minutes following the surface sterilization procedure. The cotyledons of each seed are then broken off, producing a clean fracture at the plane of the embryonic axis. Following excision of the root tip, the explants are bisected longitudinally between the primordial leaves. The two halves are placed, cut surface up, on GBA medium consisting of Murashige and Skoog mineral elements (Murashige et al. (1962) Physiol. Plant ., 15: 473-497), Shepard's vitamin additions (Shepard (1980) in Emergent Techniques for the Genetic Improvement of Crops (University of Minnesota Press, St. Paul, Minn.), 40 mg/l adenine sulfate, 30 g/l sucrose, 0.5 mg/l 6-benzyl-aminopurine (BAP), 0.25 mg/l indole-3-acetic acid (IAA), 0.1 mg/l gibberellic acid (GA 3 ), pH 5.6, and 8 g/l Phytagar.

The explants are subjected to microprojectile bombardment prior to Agrobacterium treatment (Bidney et al. (1992) Plant Mol. Biol . 18: 301-313). Thirty to forty explants are placed in a circle at the center of a 60×20 mm plate for this treatment. Approximately 4.7 mg of 1.8 mm tungsten microprojectiles are resuspended in 25 ml of sterile TE buffer (10 mM Tris HCl, 1 mM EDTA, pH 8.0) and 1.5 ml aliquots are used per bombardment. Each plate is bombarded twice through a 150 mm nytex screen placed 2 cm above the samples in a PDS 1000® particle acceleration device.

Disarmed Agrobacterium tumefaciens strain EHA105 is used in all transformation experiments. A binary plasmid vector comprising the expression cassette that contains the R gene operably linked to the UBI promoter is introduced into Agrobacterium strain EHA105 via freeze-thawing as described by Holsters et al. (1978) Mol. Gen. Genet . 163:181-187. This plasmid further comprises a kanamycin selectable marker gene (i.e, nptII). Bacteria for plant transformation experiments are grown overnight (28° C. and 100 RPM continuous agitation) in liquid YEP medium (10 gm/l yeast extract, 10 gm/l Bactopeptone, and 5 gm/l NaCl, pH 7.0) with the appropriate antibiotics required for bacterial strain and binary plasmid maintenance. The suspension is used when it reaches an OD 600 of about 0.4 to 0.8. The Agrobacterium cells are pelleted and resuspended at a final OD 600 of 0.5 in an inoculation medium comprised of 12.5 mM MES pH 5.7, 1 gm/l NH 4 Cl, and 0.3 gm/l MgSO 4 .

Freshly bombarded explants are placed in an Agrobacterium suspension, mixed, and left undisturbed for 30 minutes. The explants are then transferred to GBA medium and co-cultivated, cut surface down, at 26° C. and 18-hour days. After three days of co-cultivation, the explants are transferred to 374B (GBA medium lacking growth regulators and a reduced sucrose level of 1%) supplemented with 250 mg/l cefotaxime and 50 mg/l kanamycin sulfate. The explants are cultured for two to five weeks on selection and then transferred to fresh 374B medium lacking kanamycin for one to two weeks of continued development. Explants with differentiating, antibiotic-resistant areas of growth that have not produced shoots suitable for excision are transferred to GBA medium containing 250 mg/l cefotaxime for a second 3-day phytohormone treatment. Leaf samples from green, kanamycin-resistant shoots are assayed for the presence of NPTII by ELISA and for the presence of transgene expression by assaying for R protein activity.

NPTII-positive shoots are grafted to Pioneer® hybrid 6440 in vitro-grown sunflower seedling rootstock. Surface sterilized seeds are germinated in 48-0 medium (half-strength Murashige and Skoog salts, 0.5% sucrose, 0.3% gelrite, pH 5.6) and grown under conditions described for explant culture. The upper portion of the seedling is removed, a 1 cm vertical slice is made in the hypocotyl, and the transformed shoot inserted into the cut. The entire area is wrapped with parafilm to secure the shoot. Grafted plants can be transferred to soil following one week of in vitro culture. Grafts in soil are maintained under high humidity conditions followed by a slow acclimatization to the greenhouse environment. Transformed sectors of T 0 plants (parental generation) maturing in the greenhouse are identified by NPTII ELISA and/or by the R protein activity analysis of leaf extracts while transgenic seeds harvested from NPTII-positive T 0 plants are identified by the R protein activity analysis of small portions of dry seed cotyledon.

An alternative sunflower transformation protocol allows the recovery of transgenic progeny without the use of chemical selection pressure. Seeds are dehulled and surface-sterilized for 20 minutes in a 20% Chlorox bleach solution with the addition of two to three drops of Tween 20 per 100 ml of solution, then rinsed three times with distilled water. Sterilized seeds are imbibed in the dark at 26° C. for 20 hours on filter paper moistened with water. The cotyledons and root radical are removed, and the meristem explants are cultured on 374E (GBA medium consisting of MS salts, Shepard vitamins, 40 mg/l adenine sulfate, 3% sucrose, 0.5 mg/l 6-BAP, 0.25 mg/l IAA, 0.1 mg/l GA, and 0.8% Phytagar at pH 5.6) for 24 hours under the dark. The primary leaves are removed to expose the apical meristem, around 40 explants are placed with the apical dome facing upward in a 2 cm circle in the center of 374M (GBA medium with 1.2% Phytagar), and then cultured on the medium for 24 hours in the dark.

Approximately 18.8 mg of 1.8 μm tungsten particles are resuspended in 150 μl absolute ethanol. After sonication, 8 μl of it is dropped on the center of the surface of macrocarrier. Each plate is bombarded twice with 650 psi rupture discs in the first shelf at 26 mm of Hg helium gun vacuum.

The plasmid of interest is introduced into Agrobacterium tumefaciens strain EHA105 via freeze thawing as described previously. The pellet of overnight-grown bacteria at 28 ° C. in a liquid YEP medium (10 g/l yeast extract, 10 g/l Bactopeptone, and 5 g/l NaCl, pH 7.0) in the presence of 50 μg/l kanamycin is resuspended in an inoculation medium (12.5 mM 2-mM 2-(N-morpholino) ethanesulfonic acid, MES, 1 g/l NH 4 Cl and 0.3 g/l MgSO 4 at pH 5.7) to reach a final concentration of 4.0 at OD 600. Particle-bombarded explants are transferred to GBA medium (374E), and a droplet of bacteria suspension is placed directly onto the top of the meristem. The explants are co-cultivated on the medium for 4 days, after which the explants are transferred to 374C medium (GBA with 1% sucrose and no BAP, IAA, GA3 and supplemented with 250 μg/ml cefotaxime). The plantlets are cultured on the medium for about two weeks under 16-hour day and 26° C. incubation conditions.

Explants (around 2 cm long) from two weeks of culture in 374C medium are screened for R protein activity using assays known in the art. After positive (i.e., for R protein expression) explants are identified, those shoots that fail to exhibit R protein activity are discarded, and every positive explant is subdivided into nodal explants. One nodal explant contains at least one potential node. The nodal segments are cultured on GBA medium for three to four days to promote the formation of auxiliary buds from each node. Then they are transferred to 374C medium and allowed to develop for an additional four weeks. Developing buds are separated and cultured for an additional four weeks on 374C medium. Pooled leaf samples from each newly recovered shoot are screened again by the appropriate protein activity assay. At this time, the positive shoots recovered from a single node will generally have been enriched in the transgenic sector detected in the initial assay prior to nodal culture.

Recovered shoots positive for R protein expression are grafted to Pioneer hybrid 6440 in vitro-grown sunflower seedling rootstock. The rootstocks are prepared in the following manner. Seeds are dehulled and surface-sterilized for 20 minutes in a 20% Chlorox bleach solution with the addition of two to three drops of Tween 20 per 100 ml of solution, and are rinsed three times with distilled water. The sterilized seeds are germinated on the filter moistened with water for three days, then they are transferred into 48 medium (half-strength MS salt, 0.5% sucrose, 0.3% gelrite pH 5.0) and grown at 26° C. under the dark for three days, then incubated at 16-hour-day culture conditions. The upper portion of selected seedling is removed, a vertical slice is made in each hypocotyl, and a transformed shoot is inserted into a V-cut. The cut area is wrapped with parafilm. After one week of culture on the medium, grafted plants are transferred to soil. In the first two weeks, they are maintained under high humidity conditions to acclimatize to a greenhouse environment.

All publications and patent applications mentioned in the specification are indicative of the level of those skilled in the art to which this invention pertains. All publications and patent applications are herein incorporated by reference to the same extent as if each individual publication or patent application was specifically and individually indicated to be incorporated by reference.

Although the foregoing invention has been described in some detail by way of illustration and example for purposes of clarity of understanding, it will be obvious that certain changes and modifications may be practiced within the scope of the appended claims.

64 1 1593 DNA Helianthus annuus 1ttccttcaat ta atg ggt tgc ttt tct tgt ttc gat tca aag gaa gat gga 51aaa tct aag cct caa aag act agg gct gat cac aat gaa gtt cac cca 99tct gcc cct tca aat atc tca aga tta cct tct ggt ttg gat aga cag 147aaa tct aga aat aat gtt agt ttg agg aaa gaa tcg tcg ggt tcg aaa 195gac ggg tcg cag ggt cag att gct gct cat aca ttc act ttc cgg gag 243ctt gca gct gca aca aac aat ttt agc cct gat tgt ttg cta gga gaa 291gga ggg ttt ggc cat gtg tat aga gga cgg ctt ccg ggc agc ggt cag 339att gta gct gtc aaa caa ttg gat agg aac ggg ctg cag ggt aac cgt 387gaa ttt ctc gta gaa gtt ctt atg ctc agc ctt tta cat cat ccc aat 435ttg gtg aat tta atc gga tac tgt gct gat ggt gac caa aga ctt ctt 483gtt tat gaa ttc atg cca ttg gga tcg tta gaa gat cat ctt cat gat 531ctc cca cca gaa aaa gaa gcg tta gat tgg aac aca aga atg aag ata 579gcg gct ggt gca gct cga ggt ttg gaa ttt ctt cac gat aag gct aat 627cct cct gtt att tac agg gat ttc aaa tca tca aac att ttg ctc ggt 675gag gga ttt caa cca aag ctt tct gat ttc ggg cta gcg aag ttg ggc 723ccg acg gga gat aag tct cat gta tcc aca cgg gtc atg gga acg tat 771ggt tac tgt gct cct gag tat gcg atg acc ggt caa ctc act gtt aag 819tct gat gtg tat agc ttt ggg gtg gtt ttc tta gag ctt att aca ggc 867cga aaa gcc att gac agc agt gca ccg caa gga cag cag aat ctc gtc 915act tgg gca cga ccc tta ttc aac gac aga agg aaa ttt gca aca ttg 963gca gac ccc agg ctt gaa gga cat tat ccc atg agg ggt ctg tac cag 1011gct cta gcg gtt gca tcg atg tgc atc caa gaa cag gct gcg gct cga 1059ccg ctt ata gga gac gtg gtc act gcc tta tct tat ctt gcg aac cac 1107acc tat gat ccc aat gcg gcc tct ggt caa agc aac cgg tac aac aac 1155ggt gag aga acc agt aga att tca aag aat gaa gaa ggt ggt ggg tcg 1203ggt cgt agc agg tgg ggg gat cta gaa ggt tcc gac aaa gga gat tcg 1251cct cga gaa act caa act cca agg atg ctg aat cga gat ctt gat cga 1299gaa cgg gct gtt gct gag gct aaa atg tgg gta gaa aaa aga cga caa 1347agt gca caa ggc agc ttt gat ggg aat gct aac ggt taagagacga 1393gtgttggtgc gttactgtgg tgttttgaac ttttgaccac cacgatttga tttttttctt 1453ttgttttccc tgtacccgat tcaggagaaa aaattcggat aaacaggcgg gtgtttatgt 1513ataccaaata tgaggtgaat gggaaaactt attatggttt atgggttatt ttgttgttgt 1573aaaaaaaaaa aaaaaaaaaa 1593 2 457 PRT Helianthus annuus 2Met Gly Cys Phe Ser Cys Phe Asp Ser Lys Glu Asp Gly Lys Ser Lys 1 5 10 15Pro Gln Lys Thr Arg Ala Asp His Asn Glu Val His Pro Ser Ala Pro 20 25 30Ser Asn Ile Ser Arg Leu Pro Ser Gly Leu Asp Arg Gln Lys Ser Arg 35 40 45Asn Asn Val Ser Leu Arg Lys Glu Ser Ser Gly Ser Lys Asp Gly Ser 50 55 60Gln Gly Gln Ile Ala Ala His Thr Phe Thr Phe Arg Glu Leu Ala Ala65 70 75 80Ala Thr Asn Asn Phe Ser Pro Asp Cys Leu Leu Gly Glu Gly Gly Phe 85 90 95Gly His Val Tyr Arg Gly Arg Leu Pro Gly Ser Gly Gln Ile Val Ala 100 105 110Val Lys Gln Leu Asp Arg Asn Gly Leu Gln Gly Asn Arg Glu Phe Leu 115 120 125Val Glu Val Leu Met Leu Ser Leu Leu His His Pro Asn Leu Val Asn 130 135 140Leu Ile Gly Tyr Cys Ala Asp Gly Asp Gln Arg Leu Leu Val Tyr Glu145 150 155 160Phe Met Pro Leu Gly Ser Leu Glu Asp His Leu His Asp Leu Pro Pro 165 170 175Glu Lys Glu Ala Leu Asp Trp Asn Thr Arg Met Lys Ile Ala Ala Gly 180 185 190Ala Ala Arg Gly Leu Glu Phe Leu His Asp Lys Ala Asn Pro Pro Val 195 200 205Ile Tyr Arg Asp Phe Lys Ser Ser Asn Ile Leu Leu Gly Glu Gly Phe 210 215 220Gln Pro Lys Leu Ser Asp Phe Gly Leu Ala Lys Leu Gly Pro Thr Gly225 230 235 240Asp Lys Ser His Val Ser Thr Arg Val Met Gly Thr Tyr Gly Tyr Cys 245 250 255Ala Pro Glu Tyr Ala Met Thr Gly Gln Leu Thr Val Lys Ser Asp Val 260 265 270Tyr Ser Phe Gly Val Val Phe Leu Glu Leu Ile Thr Gly Arg Lys Ala 275 280 285Ile Asp Ser Ser Ala Pro Gln Gly Gln Gln Asn Leu Val Thr Trp Ala 290 295 300Arg Pro Leu Phe Asn Asp Arg Arg Lys Phe Ala Thr Leu Ala Asp Pro305 310 315 320Arg Leu Glu Gly His Tyr Pro Met Arg Gly Leu Tyr Gln Ala Leu Ala 325 330 335Val Ala Ser Met Cys Ile Gln Glu Gln Ala Ala Ala Arg Pro Leu Ile 340 345 350Gly Asp Val Val Thr Ala Leu Ser Tyr Leu Ala Asn His Thr Tyr Asp 355 360 365Pro Asn Ala Ala Ser Gly Gln Ser Asn Arg Tyr Asn Asn Gly Glu Arg 370 375 380Thr Ser Arg Ile Ser Lys Asn Glu Glu Gly Gly Gly Ser Gly Arg Ser385 390 395 400Arg Trp Gly Asp Leu Glu Gly Ser Asp Lys Gly Asp Ser Pro Arg Glu 405 410 415Thr Gln Thr Pro Arg Met Leu Asn Arg Asp Leu Asp Arg Glu Arg Ala 420 425 430Val Ala Glu Ala Lys Met Trp Val Glu Lys Arg Arg Gln Ser Ala Gln 435 440 445Gly Ser Phe Asp Gly Asn Ala Asn Gly 450 455 3 1559 DNA Helianthus annuus CDS (81)...(1319) 3tcggcttcgt taccttacct tcttcatcgt cggcatcatt tatccatatc caacttaacg 60gtttcatcta gattacagta atg ggt tgt ttt cct tgc ttt gaa tcc agt caa 113 Met Gly Cys Phe Pro Cys Phe Glu Ser Ser Gln 1 5 10gag gac aac aac ttc aat cac caa aaa gtc ggc cat gaa gtc cac cca 161Glu Asp Asn Asn Phe Asn His Gln Lys Val Gly His Glu Val His Pro 15 20 25tcc gcc cct tcc aat att tcc aga tta tct tcc ggg gtt gat agg atg 209Ser Ala Pro Ser Asn Ile Ser Arg Leu Ser Ser Gly Val Asp Arg Met 30 35 40aaa acg aga aac aat gtt aat aat gct gct agc cta agg agg gag tca 257Lys Thr Arg Asn Asn Val Asn Asn Ala Ala Ser Leu Arg Arg Glu Ser 45 50 55tca ggg ccg ccg gat gct caa atc gcc gca caa acc ttc aca ttc cgc 305Ser Gly Pro Pro Asp Ala Gln Ile Ala Ala Gln Thr Phe Thr Phe Arg 60 65 70 75gag ctt gca gcc gcc acc aat aat ttt cag cct gat tgc ttc tta agg 353Glu Leu Ala Ala Ala Thr Asn Asn Phe Gln Pro Asp Cys Phe Leu Arg 80 85 90gag ggt ggt ttt ggt tgt gta tat aga gga cgt ctt cag agt agt ggt 401Glu Gly Gly Phe Gly Cys Val Tyr Arg Gly Arg Leu Gln Ser Ser Gly 95 100 105caa gtt gta gct gtt aaa cag ctg gat aga aat gga ctc caa ggt aac 449Gln Val Val Ala Val Lys Gln Leu Asp Arg Asn Gly Leu Gln Gly Asn 110 115 120cgt gag ttt ctt gtt gaa gtt ctt atg ctc agc ctt tta cat cat cca 497Arg Glu Phe Leu Val Glu Val Leu Met Leu Ser Leu Leu His His Pro 125 130 135aac ttg gtc aat ttg att ggc tac tgc gct gac ggt gac caa cga ctt 545Asn Leu Val Asn Leu Ile Gly Tyr Cys Ala Asp Gly Asp Gln Arg Leu140 145 150 155ctt gtc tat gag ttt atg gcc ttg ggt tcc ttg gaa gat cac ctt cat 593Leu Val Tyr Glu Phe Met Ala Leu Gly Ser Leu Glu Asp His Leu His 160 165 170gat gtt ccg cct gac aga gaa cca tta gat tgg aca cag gat gaa gat 641Asp Val Pro Pro Asp Arg Glu Pro Leu Asp Trp Thr Gln Asp Glu Asp 175 180 185agc ggc tgt gca gcc aag ggg ttg gag ttt ctt cat gat aaa gct aac 689Ser Gly Cys Ala Ala Lys Gly Leu Glu Phe Leu His Asp Lys Ala Asn 190 195 200cca cca gtt att tat cgg gac ttc aaa tca tca aac att ttg ctg gat 737Pro Pro Val Ile Tyr Arg Asp Phe Lys Ser Ser Asn Ile Leu Leu Asp 205 210 215gag gga ttt caa cca aag ctg tcc gac ttc ggg ctc gcg aaa ctg ggc 785Glu Gly Phe Gln Pro Lys Leu Ser Asp Phe Gly Leu Ala Lys Leu Gly220 225 230 235ccc act gga gac aag tct cat gtt tcc aca cgg gtg atg ggt aca tac 833Pro Thr Gly Asp Lys Ser His Val Ser Thr Arg Val Met Gly Thr Tyr 240 245 250ggt tac tgt gct cct gag tat gcc atg act ggt cag tta acg gtc aaa 881Gly Tyr Cys Ala Pro Glu Tyr Ala Met Thr Gly Gln Leu Thr Val Lys 255 260 265tcc gat gtg tac agc ttt ggt gtc gtc ttt tta gag ctt att acc ggt 929Ser Asp Val Tyr Ser Phe Gly Val Val Phe Leu Glu Leu Ile Thr Gly 270 275 280aga aaa gcc ata gat agc act caa cca cat gga cag cag aac ctg gtg 977Arg Lys Ala Ile Asp Ser Thr Gln Pro His Gly Gln Gln Asn Leu Val 285 290 295aca tgg gca cga cct ttg ttc aac gac aga agg aaa ttc aca tcg ttg 1025Thr Trp Ala Arg Pro Leu Phe Asn Asp Arg Arg Lys Phe Thr Ser Leu300 305 310 315gtg gac cca cgg tta gaa ggt cgg tac cca atg cgg ggg ctg tac cag 1073Val Asp Pro Arg Leu Glu Gly Arg Tyr Pro Met Arg Gly Leu Tyr Gln 320 325 330gcg cta gcg gtg gca tcc atg tgt att caa gaa cag gtt gca gcc cgg 1121Ala Leu Ala Val Ala Ser Met Cys Ile Gln Glu Gln Val Ala Ala Arg 335 340 345cct ttg att gct gac gtg gta act gcg cta tct tat ctt gca aac cag 1169Pro Leu Ile Ala Asp Val Val Thr Ala Leu Ser Tyr Leu Ala Asn Gln 350 355 360ggg tac gat ccg acc aca gct ccc agc ttc ata aca tca tca gca gcg 1217Gly Tyr Asp Pro Thr Thr Ala Pro Ser Phe Ile Thr Ser Ser Ala Ala 365 370 375ccg gcg gca agg aga gac tta aaa ccg caa ggt ttt cga aaa acg atg 1265Pro Ala Ala Arg Arg Asp Leu Lys Pro Gln Gly Phe Arg Lys Thr Met380 385 390 395aag ggg gtt gca gca gat ggg att tgg aag aat cgg att ctc cca aag 1313Lys Gly Val Ala Ala Asp Gly Ile Trp Lys Asn Arg Ile Leu Pro Lys 400 405 410aaa ctg taaagatgct tgagagagaa agggctgttg cagaagcaaa aatgtgggtt 1369Lys Leugaaaaaagaa gacagagtgg gtagtagatg tttgttttac atacattgtt cagatgatga 1429ttcaaagggt gggttgttga caaagtccaa accaattttt ctgcagtaat attgtatgta 1489tatttcttat gggaaaagag gagatcaaac agaacttaaa ggtcggcttg attgaaaaaa 1549aaaaaaaaaa 1559 4 413 PRT Helianthus annuus 4Met Gly Cys Phe Pro Cys Phe Glu Ser Ser Gln Glu Asp Asn Asn Phe 1 5 10 15Asn His Gln Lys Val Gly His Glu Val His Pro Ser Ala Pro Ser Asn 20 25 30Ile Ser Arg Leu Ser Ser Gly Val Asp Arg Met Lys Thr Arg Asn Asn 35 40 45Val Asn Asn Ala Ala Ser Leu Arg Arg Glu Ser Ser Gly Pro Pro Asp 50 55 60Ala Gln Ile Ala Ala Gln Thr Phe Thr Phe Arg Glu Leu Ala Ala Ala65 70 75 80Thr Asn Asn Phe Gln Pro Asp Cys Phe Leu Arg Glu Gly Gly Phe Gly 85 90 95Cys Val Tyr Arg Gly Arg Leu Gln Ser Ser Gly Gln Val Val Ala Val 100 105 110Lys Gln Leu Asp Arg Asn Gly Leu Gln Gly Asn Arg Glu Phe Leu Val 115 120 125Glu Val Leu Met Leu Ser Leu Leu His His Pro Asn Leu Val Asn Leu 130 135 140Ile Gly Tyr Cys Ala Asp Gly Asp Gln Arg Leu Leu Val Tyr Glu Phe145 150 155 160Met Ala Leu Gly Ser Leu Glu Asp His Leu His Asp Val Pro Pro Asp 165 170 175Arg Glu Pro Leu Asp Trp Thr Gln Asp Glu Asp Ser Gly Cys Ala Ala 180 185 190Lys Gly Leu Glu Phe Leu His Asp Lys Ala Asn Pro Pro Val Ile Tyr 195 200 205Arg Asp Phe Lys Ser Ser Asn Ile Leu Leu Asp Glu Gly Phe Gln Pro 210 215 220Lys Leu Ser Asp Phe Gly Leu Ala Lys Leu Gly Pro Thr Gly Asp Lys225 230 235 240Ser His Val Ser Thr Arg Val Met Gly Thr Tyr Gly Tyr Cys Ala Pro 245 250 255Glu Tyr Ala Met Thr Gly Gln Leu Thr Val Lys Ser Asp Val Tyr Ser 260 265 270Phe Gly Val Val Phe Leu Glu Leu Ile Thr Gly Arg Lys Ala Ile Asp 275 280 285Ser Thr Gln Pro His Gly Gln Gln Asn Leu Val Thr Trp Ala Arg Pro 290 295 300Leu Phe Asn Asp Arg Arg Lys Phe Thr Ser Leu Val Asp Pro Arg Leu305 310 315 320Glu Gly Arg Tyr Pro Met Arg Gly Leu Tyr Gln Ala Leu Ala Val Ala 325 330 335Ser Met Cys Ile Gln Glu Gln Val Ala Ala Arg Pro Leu Ile Ala Asp 340 345 350Val Val Thr Ala Leu Ser Tyr Leu Ala Asn Gln Gly Tyr Asp Pro Thr 355 360 365Thr Ala Pro Ser Phe Ile Thr Ser Ser Ala Ala Pro Ala Ala Arg Arg 370 375 380Asp Leu Lys Pro Gln Gly Phe Arg Lys Thr Met Lys Gly Val Ala Ala385 390 395 400Asp Gly Ile Trp Lys Asn Arg Ile Leu Pro Lys Lys Leu 405 410 5 2114 DNA Helianthus annuus misc_feature (1)...(2114) n = A,T,C or G 5ggcacgagcc tagttaaaac tttaactatg tctttccata tcagtcaccc ggctgaatct 60tcctcctcat attcaccaca accgtgccgt caatttacct tttcggagat tcaacttgca 120acccaaaact ttgatgagtc gttggtgata ggacgtgggg ggtttggcaa ggtttacaga 180ggaaccttca cttatgggga aacatacttg gatgctgcaa ttaagcgact ggaatcaggt 240tctagtcaag gagcggtaga gtttagggct gaaattgaga tgctctcaaa tctaaggcac 300tgtcatttgg tgtctttaat tggttactgt agtgatgggc aagagatggt tcttgtatat 360gaacatatgc ccaatggaac tcttgcagat cgtctccaca agcgtcgagc tcctctaact 420tgggtaagaa gactcaaaat atgcataggg gccgctcgtg gtttagatta cttgcacact 480ggtacgggta ttaaccatgg agttatacat cgggatgtta agagcacaaa tatattgtta 540gatgacaatt gggcagctaa ggtttctgac tttggtttgt ccaaaattgg tccaacaaat 600cagccttcaa cttatgttaa cactttggtg agaggcacct ttggatatat ggatccagat 660tactttcaaa caggtaggct gactcgaaag tctgacgtgt atgcctttgg ggtggtcctg 720tttgaagtcc tatgtgggaa acaagtagta ctgatgagga gcactggggt ttggcaacat 780gggctcaaga ctctcttaaa gaaggaaggc taaagcaaat tgttgattct aatttaaggg 840ggagaatatc cccaaaatgt ttgaaggagt ttgcactact agctgaccgg tgtttgcata 900gccgtcccaa gcaacgtcct gcaatggcgg aggttgtgat tggtcttgag tcaatcctag 960ccttacagga gaaaaccgag agtacatggg taccaacatt tctctttcca tccacttggg 1020aaaagacagt tggaggtaca gatttaaaat ccctggaacg atacctctac aatgttggag 1080gtgaagacaa aatagtacac aagtttgatt ttataacgat tcttgatgca actgaaaact 1140tctctgaagc taataagatt tcatcctgct catatgattc cgtgtacaag ggacggctac 1200aaaatggaca agatataaca gtcactcaat attcaaaagc ctccacatat aaactgtgta 1260tgaatgaagc atcaatactt gtaaaggttg aacatcaaaa tttgattcag ttgcttggat 1320attgcattca cggaacagaa gtgtacctca tctatgactt tccacttaat gcaactatgg 1380ctgacatgat ttatgatcct agtgtaatct tttggactgg ataaacggta caaaataatc 1440ctagacatag ccagagcact tgtatatctt cacangcatg ctccattcgg atcatacatc 1500ttgatgtaaa cccgcaacat tctatagatg aagttatacc cagctgtcag gtttggggag 1560cagtgacacc agtgagacag attgcgtttc tcttgataat gtctttggga ctatgggata 1620cattgcacct gaatatcata ggacattacg ttgctcaact aaggcagatg tctatagttt 1680tggtgtgttg atttttgaaa cagtaactgg gaaaaccata cagaatttat tatctctagc 1740tttagacaag caccttggtt ttgcagacta tatccacaaa aattggttgg aagggacatt 1800gtcagatata attgatcccc aaattgatgc tgattcagtt tcgatgacta aattcgtgga 1860gattgggttg ttgtgtgttc aaggattagc agcggatagg ccaacaatgg aggaggttat 1920tggcatgttg cttggcacct cgtctctaac ttttcatgtg tcggaaatgc gagaaaggat 1980gatgtttaat ggcgtgacta catatttata taatatgaaa gtgaaaggtc ggtggtaata 2040agacaaaaca ccgaccaaat tacaaaactg cccctaataa atttatttta ttgtgccaaa 2100aaaaaaaaaa aaaa 2114 6 850 DNA Helianthus annuus 6cttgctactg aacctcgttg tgggtttctg caaattcatc ttttttcacc acaaattgtt 60aaaaaaagat tttttttttt ttttaattta attgtggcat agttaactgt gaaacttggt 120tccagtgcaa aagattgccc catatctttc tttcatgtga taaaacagag ttgcatgtta 180tctcttttca cctttttcac aacacccaga tcagatctgc ttttcttttt ataaaatctt 240gttgtttcaa gaatcttgtt gaagtgaaaa aagacaccca ctttcaagaa taataataat 300catttcaatg ggtatttgtt tgagtgctag aatcaaagct gaaagcccat atcacacagg 360ggtgagttca agaactggaa gtacagaagg aaatgataat ggtaattcaa gtggcagcaa 420ctgcaaccct ccgatccccc ggagcgaagg tgaaatcttg caatcttgta acttgaagag 480ttttaattat tcggatcttc gaatggctac gagaaatttt cggcccgata gcgtgttggg 540cgaaggtggg ttcgggtcgg tttataaagg gtggatcgat gaacaatcgt tcgccgcttc 600aaaaccgggg tctggagtcg ttgttgctgt caaaagactt aatgcagaaa gttttcaagg 660tcacagagaa tggctggcgg aagtgaacta tttagggcag ttttcgcacc cgaatctcgt 720gaatttgatt gggtattgtt tggaagacga acatcggctt ctagtttacg agttcatgcc 780acgaggcagc ttggagaatc acttgttcag gaaaggatct tattttcaac cgctaacatg 840gagtctccga 850 7 2594 DNA Helianthus annuus CDS (21)...(1733) 7ctctcgcatc tgctgcctat atg gaa att tct cac cta ttc gaa ggt tgt tgt 53 Met Glu Ile Ser His Leu Phe Glu Gly Cys Cys 1 5 10ctt ctt gaa aat att cgt gag gaa tca agc aaa cag ggt ttg aaa aag 101Leu Leu Glu Asn Ile Arg Glu Glu Ser Ser Lys Gln Gly Leu Lys Lys 15 20 25ttg caa gaa aat ttt ctc tca ctt gtt ttg aaa acc gat gtg aag gta 149Leu Gln Glu Asn Phe Leu Ser Leu Val Leu Lys Thr Asp Val Lys Val 30 35 40ggg aat gag ata ata gga agg agc atg ata aaa agt agg cta tct cac 197Gly Asn Glu Ile Ile Gly Arg Ser Met Ile Lys Ser Arg Leu Ser His 45 50 55aaa agg ttt tta gtt gtt ctc gat gat gtt gat aat ttt gag caa ctt 245Lys Arg Phe Leu Val Val Leu Asp Asp Val Asp Asn Phe Glu Gln Leu 60 65 70 75gag gcg ttg gcg gga tcc cac gat tgg ttt ggt gag ggg agc cgg ata 293Glu Ala Leu Ala Gly Ser His Asp Trp Phe Gly Glu Gly Ser Arg Ile 80 85 90ata att acg act aga gat gtg cat ttg cta tcc agc agg gcg caa acg 341Ile Ile Thr Thr Arg Asp Val His Leu Leu Ser Ser Arg Ala Gln Thr 95 100 105att tat gaa gtg aat ttg tta tca caa gat gaa gca atc aag ctc tta 389Ile Tyr Glu Val Asn Leu Leu Ser Gln Asp Glu Ala Ile Lys Leu Leu 110 115 120aaa aga tat gca tac cat aaa gat aaa cct gtt gaa gag tat gag atg 437Lys Arg Tyr Ala Tyr His Lys Asp Lys Pro Val Glu Glu Tyr Glu Met 125 130 135ctt gca gaa gag gta gtt tct tat gct ggt ggg ctc cca cta gcg ctt 485Leu Ala Glu Glu Val Val Ser Tyr Ala Gly Gly Leu Pro Leu Ala Leu140 145 150 155aaa gtt cta ggt tcg ttt cta tat ggc aaa gac aag gat gag tgg aag 533Lys Val Leu Gly Ser Phe Leu Tyr Gly Lys Asp Lys Asp Glu Trp Lys 160 165 170agt acg ttg gcc aag tta aaa tgc atc ccg gaa gag aag gtc atg gag 581Ser Thr Leu Ala Lys Leu Lys Cys Ile Pro Glu Glu Lys Val Met Glu 175 180 185aga ctc aaa ata agt tat gat gga ctt gaa ccc tac cag aaa gag tta 629Arg Leu Lys Ile Ser Tyr Asp Gly Leu Glu Pro Tyr Gln Lys Glu Leu 190 195 200ttc tta gat att gca tgt ttc atg agg aga tgg tgg tta caa tcg gtt 677Phe Leu Asp Ile Ala Cys Phe Met Arg Arg Trp Trp Leu Gln Ser Val 205 210 215ttg gat cgt gca atg atg gtg ctt gat gct tgt aat ttg cac cct gtt 725Leu Asp Arg Ala Met Met Val Leu Asp Ala Cys Asn Leu His Pro Val220 225 230 235ata ggg tta aag gtg ttg gaa caa aaa tcc ctc ata aaa gtt tca aaa 773Ile Gly Leu Lys Val Leu Glu Gln Lys Ser Leu Ile Lys Val Ser Lys 240 245 250aaa gga aga ttt gag atg cat gac ttg ata gaa gaa atg gcc cac tac 821Lys Gly Arg Phe Glu Met His Asp Leu Ile Glu Glu Met Ala His Tyr 255 260 265att gtt aga ggg gaa cac cct aat aat cct gaa aag cat agc agg att 869Ile Val Arg Gly Glu His Pro Asn Asn Pro Glu Lys His Ser Arg Ile 270 275 280tgg aat agg gaa gat ttg gaa gag ctt tgt gct atg gga gca gct gca 917Trp Asn Arg Glu Asp Leu Glu Glu Leu Cys Ala Met Gly Ala Ala Ala 285 290 295ccc tca atg gaa aat gaa gta tta gct aat ttg cca atg tat ata att 965Pro Ser Met Glu Asn Glu Val Leu Ala Asn Leu Pro Met Tyr Ile Ile300 305 310 315agc cat cca ggt cta cta ctt gat gtt gtt cca aac atg aag aac ctt 1013Ser His Pro Gly Leu Leu Leu Asp Val Val Pro Asn Met Lys Asn Leu 320 325 330cga tgg ata atg ttg att ggt cat ggg gat ccg tca tct tca ttc cca 1061Arg Trp Ile Met Leu Ile Gly His Gly Asp Pro Ser Ser Ser Phe Pro 335 340 345tca aat ttt cag cca aca aag ctt cgt tgt cta atg ttg ata gag agc 1109Ser Asn Phe Gln Pro Thr Lys Leu Arg Cys Leu Met Leu Ile Glu Ser 350 355 360aag caa aaa gaa ctc tgg gaa ggg tgt aag agt cta cca aat ttg aaa 1157Lys Gln Lys Glu Leu Trp Glu Gly Cys Lys Ser Leu Pro Asn Leu Lys 365 370 375att ctt gat ctc tcg ggt tca agt aac cta atc aag aca cca gat ttt 1205Ile Leu Asp Leu Ser Gly Ser Ser Asn Leu Ile Lys Thr Pro Asp Phe380 385 390 395gaa ggc ctt cca tgt ctt gaa aga ttg att tta aaa tat tgt gag aga 1253Glu Gly Leu Pro Cys Leu Glu Arg Leu Ile Leu Lys Tyr Cys Glu Arg 400 405 410tta gaa gag att cat cca tca att gga tat cac aaa agg ctt gtt tac 1301Leu Glu Glu Ile His Pro Ser Ile Gly Tyr His Lys Arg Leu Val Tyr 415 420 425gtg aac atg aaa ggg tgt gca aga ctt aaa agg ttt cca ccc atc ata 1349Val Asn Met Lys Gly Cys Ala Arg Leu Lys Arg Phe Pro Pro Ile Ile 430 435 440cac atg aaa aaa ttg gag act ctt aat ctc agt gat tgc agt aaa ctt 1397His Met Lys Lys Leu Glu Thr Leu Asn Leu Ser Asp Cys Ser Lys Leu 445 450 455caa cag ttt ccg gat atc cag tca aac atg gat agc ttg gta acc att 1445Gln Gln Phe Pro Asp Ile Gln Ser Asn Met Asp Ser Leu Val Thr Ile460 465 470 475gat ctg cat aat act ggt ata gaa ata atc cca ccg tca gtt gga cga 1493Asp Leu His Asn Thr Gly Ile Glu Ile Ile Pro Pro Ser Val Gly Arg 480 485 490ttt tgt acc aac ctt gtt tct tta gat tta agt caa tgt tac aaa ctg 1541Phe Cys Thr Asn Leu Val Ser Leu Asp Leu Ser Gln Cys Tyr Lys Leu 495 500 505aaa agg ata gag gac agc ttt cat ctc tta aaa agt ttg aaa gac ctg 1589Lys Arg Ile Glu Asp Ser Phe His Leu Leu Lys Ser Leu Lys Asp Leu 510 515 520aat ctc agt tgt tgt ttt ggg tta caa tct ttt cgt caa gac cgg ttg 1637Asn Leu Ser Cys Cys Phe Gly Leu Gln Ser Phe Arg Gln Asp Arg Leu 525 530 535gtg agc ctc aag cta cct cag ttt cca cgt ttt cta agg aaa tta aat 1685Val Ser Leu Lys Leu Pro Gln Phe Pro Arg Phe Leu Arg Lys Leu Asn540 545 550 555ctt aga ggc tgc aga ttg gaa gat gga ggc atc cca tct gat ata ttt 1733Leu Arg Gly Cys Arg Leu Glu Asp Gly Gly Ile Pro Ser Asp Ile Phe 560 565 570taattgccag acctcccatc aagcatagct attctcaaag caaaaggttg tgactcactt 1793gaaattgtaa gagatttatc agactataaa tggttgtgga aagtctcact ttggaggaga 1853gcgaataaga gggtactact ttatatgctt gaggaaaatg cagttaaaga agatcgcttt 1913atgagcgtgt taagtcccaa tgttcaacca tcaagcattt ataccaaact tgtcacattg 1973caacttccac acaactggta tagtgacttt agtggatttt tattatcatt aggtgaccgt 2033tatgggacgt accgcatagt aattaagcag gagatgtcca ccgatcactc tgaaaagtct 2093gatgaagatc gggaacaacg taactatgaa agggtgggtt acgtaccctt tagttcattg 2153aggcacatcc catggttcaa tcctacatac cctaaaaata tttcatttca aataatggat 2213aaatatggta atacgaagaa aattggtctt aatgtagaac ttgttcgtag taaaagtaaa 2273atatgtgatt taaacgaaca cccaatcgat tactcagagt gttgggatga agaatataaa 2333gatacaaaga cctttgacat cgtatatgat tcaaagtcct ctgaaattca gatttcatgg 2393gaacatccgt agtcgatctc agtttcaaat ttcaacattt gcccacattt tgttaccatt 2453ctaagtttgc ttttgtttca ccaacatcat tgcgacctga aagaagttgt aataaatgtt 2513cctctattaa ctcttaagac ttcacattct atactttgtt cattaccagg ttaaaaaaaa 2573aaaaaaaaaa aaaaaaaaaa a 2594 8 571 PRT Helianthus annuus 8Met Glu Ile Ser His Leu Phe Glu Gly Cys Cys Leu Leu Glu Asn Ile 1 5 10 15Arg Glu Glu Ser Ser Lys Gln Gly Leu Lys Lys Leu Gln Glu Asn Phe 20 25 30Leu Ser Leu Val Leu Lys Thr Asp Val Lys Val Gly Asn Glu Ile Ile 35 40 45Gly Arg Ser Met Ile Lys Ser Arg Leu Ser His Lys Arg Phe Leu Val 50 55 60Val Leu Asp Asp Val Asp Asn Phe Glu Gln Leu Glu Ala Leu Ala Gly65 70 75 80Ser His Asp Trp Phe Gly Glu Gly Ser Arg Ile Ile Ile Thr Thr Arg 85 90 95Asp Val His Leu Leu Ser Ser Arg Ala Gln Thr Ile Tyr Glu Val Asn 100 105 110Leu Leu Ser Gln Asp Glu Ala Ile Lys Leu Leu Lys Arg Tyr Ala Tyr 115 120 125His Lys Asp Lys Pro Val Glu Glu Tyr Glu Met Leu Ala Glu Glu Val 130 135 140Val Ser Tyr Ala Gly Gly Leu Pro Leu Ala Leu Lys Val Leu Gly Ser145 150 155 160Phe Leu Tyr Gly Lys Asp Lys Asp Glu Trp Lys Ser Thr Leu Ala Lys 165 170 175Leu Lys Cys Ile Pro Glu Glu Lys Val Met Glu Arg Leu Lys Ile Ser 180 185 190Tyr Asp Gly Leu Glu Pro Tyr Gln Lys Glu Leu Phe Leu Asp Ile Ala 195 200 205Cys Phe Met Arg Arg Trp Trp Leu Gln Ser Val Leu Asp Arg Ala Met 210 215 220Met Val Leu Asp Ala Cys Asn Leu His Pro Val Ile Gly Leu Lys Val225 230 235 240Leu Glu Gln Lys Ser Leu Ile Lys Val Ser Lys Lys Gly Arg Phe Glu 245 250 255Met His Asp Leu Ile Glu Glu Met Ala His Tyr Ile Val Arg Gly Glu 260 265 270His Pro Asn Asn Pro Glu Lys His Ser Arg Ile Trp Asn Arg Glu Asp 275 280 285Leu Glu Glu Leu Cys Ala Met Gly Ala Ala Ala Pro Ser Met Glu Asn 290 295 300Glu Val Leu Ala Asn Leu Pro Met Tyr Ile Ile Ser His Pro Gly Leu305 310 315 320Leu Leu Asp Val Val Pro Asn Met Lys Asn Leu Arg Trp Ile Met Leu 325 330 335Ile Gly His Gly Asp Pro Ser Ser Ser Phe Pro Ser Asn Phe Gln Pro 340 345 350Thr Lys Leu Arg Cys Leu Met Leu Ile Glu Ser Lys Gln Lys Glu Leu 355 360 365Trp Glu Gly Cys Lys Ser Leu Pro Asn Leu Lys Ile Leu Asp Leu Ser 370 375 380Gly Ser Ser Asn Leu Ile Lys Thr Pro Asp Phe Glu Gly Leu Pro Cys385 390 395 400Leu Glu Arg Leu Ile Leu Lys Tyr Cys Glu Arg Leu Glu Glu Ile His 405 410 415Pro Ser Ile Gly Tyr His Lys Arg Leu Val Tyr Val Asn Met Lys Gly 420 425 430Cys Ala Arg Leu Lys Arg Phe Pro Pro Ile Ile His Met Lys Lys Leu 435 440 445Glu Thr Leu Asn Leu Ser Asp Cys Ser Lys Leu Gln Gln Phe Pro Asp 450 455 460Ile Gln Ser Asn Met Asp Ser Leu Val Thr Ile Asp Leu His Asn Thr465 470 475 480Gly Ile Glu Ile Ile Pro Pro Ser Val Gly Arg Phe Cys Thr Asn Leu 485 490 495Val Ser Leu Asp Leu Ser Gln Cys Tyr Lys Leu Lys Arg Ile Glu Asp 500 505 510Ser Phe His Leu Leu Lys Ser Leu Lys Asp Leu Asn Leu Ser Cys Cys 515 520 525Phe Gly Leu Gln Ser Phe Arg Gln Asp Arg Leu Val Ser Leu Lys Leu 530 535 540Pro Gln Phe Pro Arg Phe Leu Arg Lys Leu Asn Leu Arg Gly Cys Arg545 550 555 560Leu Glu Asp Gly Gly Ile Pro Ser Asp Ile Phe 565 570 9 2793 DNA Helianthus annuus 9acgagcagcc atgaagcaaa atgcatcagt gacattgttg gtacaatttc ttctaggctt 60tcttcactaa atacaaacga taataaagac ctcatcggaa tagagacccg cttacaagat 120cttatatcaa agttggaaat cgagtcaggt ggtgtgcgca tggttggaat atggggagtt 180gggggtggtg gtaagactac tctcgcatct gctgcctata tggaaatttc tcacctattc 240gaaggttgtt gtcttcttga aaatattcgt gaggaatcaa gcaaacaggg tttgaaaaag 300ttgcaagaaa attttctctc acttgttttg aaaaccgatg tgaaggtagg gaatgagata 360ataggaagga gcatgataaa aagtaggcta tctcacaaaa ggtttttagt tgttctcgat 420gatgttgata attttgagca acttgaggcg ttggcgggat cccacgattg gtttggtgag 480gggagccgga taataattac gactagagat gtgcatttgc tatccagcag ggcgcaaacg 540atttatgaag tgaatttgtt atcacaagat gaagcaatca agctcttaaa aagatatgca 600tatcataaag ataaacctgt tgaagagtat gagatgcttg cagaagaggt agtttcttat 660gctggtgggc tcccactagc gcttaaagtt ctaggttcgt ttctatatgg caaagacaag 720gatgagtgga agagtacgtt ggccaagtta aaatgcatcc cggaagagaa ggtcatggag 780agactcaaaa taagttatga tggacttgaa ccctaccaga aagagttatt cttagatatt 840gcatgtttca tgaggagatg gtggttacaa tcggttttgg atcgtgcaat gatggtgctt 900gatgcttgta atttgcaccc tgttataggg ttaaaggtgt tggaacaaaa atccctcata 960aaagtttcaa aaaaaggaag atttgagatg catgacttga tagaagaaat ggcccactac 1020attgttagag gggaacaccc taataatcct gaaaagcata gcaggatttg gaatagggaa 1080gatttggaag agctttgtgc tatgggagca gctgcaccct caatggaaaa tgaagtatta 1140gctaatttgc caatgtatat aattagccat ccaggtctac tacttgatgt tgttccaaac 1200atgaagaacc ttcgatggat aatgttgatt ggtcatgggg atccgtcatc ttcattccca 1260tcaaattttc agccaacaaa gcttcgttgt ctaatgttga tagagagcaa gcaaaaagaa 1320ctctgggaag ggtgtaagag tctaccaaat ttgaaaattc ttgatctctc gggttcaagt 1380aacctaatca agacaccaga ttttgaaggc cttccatgtc ttgaaagatt gattttaaaa 1440tattgtgaga gattagaaga gattcatcca tcaattggat atcacaaaag gcttgtttac 1500gtgaacatga aagggtgtgc aagacttaaa aggtttccac ccatcataca catgaaaaaa 1560ttggagactc ttaatctcag tgattgcagt aaacttcaac agtttccgga tatccagtca 1620aacatggata gcttggtaac cattgatctg cataatactg gtatagaaat aatcccaccg 1680tcagttggac gattttgtac caaccttgtt tctttagatt taagtcaatg ttacaaactg 1740aaaaggatag aggacagctt tcatctctta aaaagtttga aagacctgaa tctcagttgt 1800tgttttgggt tacaatcttt tcgtcaagac cggttggtga gcctcaagct acctcagttt 1860ccacgttttc taaggaaatt aaatcttaga ggctgcagat tggaagatgg aggcatccca 1920tctgatatat tttaattgcc agacctccca tcaagcatag ctattctcaa agcaaaaggt 1980tgtgactcac ttgaaattgt aagagattta tcagactata aatggttgtg gaaagtctca 2040ctttggagga gagcgaataa gagggtacta ctttatatgc ttgaggaaaa tgcagttaaa 2100gaagatcgct ttatgagcgt gttaagtccc aatgttcaac catcaagcat ttataccaaa 2160cttgtcacat tgcaacttcc acacaactgg tatagtgact ttagtggatt tttattatca 2220ttaggtgacc gttatgggac gtaccgcata gtaattaagc aggagatgtc caccgatcac 2280tctgaaaagt ctgatgaaga tcgggaacaa cgtaactatg aawsrgtggg ttacgtaccc 2340tttagttcat tgaggcacat cccatggttc aatcctacat accctaaaaa tatttcattt 2400caaataatgg ataaatatgg taatacgaag aaaattggtc ttaatgtaga acttgttcgt 2460agtaaaagta aaatatgtga tttaaacgaa cacccaatcg attactcaga gtgttgggat 2520gaagaatata aagatacaaa gacctttgac atcgtatatg attcaaagtc ctctgaaatt 2580cagatttcat gggaacatcc gtagtcgatc tcagtttcaa atttcaacat ttgcccacat 2640tttgttacca ttctaagttt gcttttgttt caccaacatc attgcgacct gaaagaagtt 2700gtaataaatg ttcctctatt aactcttaag acttcacatt ctatactttg ttcattacca 2760ggttaaaaaa aaaaaaaaaa aaaaaaaaaa aaa 2793 10 670 DNA Helianthus annuus 10acgagcagcc atgaagcaaa atgcatcagt gacattgttg gtacaatttc ttctaggctt 60tcttcactaa atacaaacga taataaagac ctcatcggaa tagagacccg cttacaagat 120cttatatcaa agttggaaat cgagtcaggt ggtgtgcgca tggttggaat atggggagtt 180gggggtggtg gtaagactac tctcgcatct gctgcctata tggaaatttc tcacctattc 240gaaggttgtt gtcttcttga aaatattcgt gaggaatcaa gcaaacaggg tttgaaaaag 300ttgcaagaaa attttctctc acttgttttg aaaaccgatg tgaaggtagg gaatgagata 360ataggaagga gcatgataaa aagtaggcta tctcacaaaa ggtttttagt tgttctcgat 420gatgttgata attttgagca acttgaggcg ttggcgggat cccacgattg gtttggtgag 480gggagccgga taataattac gactagagat gtgcatttgc tatccagcag ggcgcaaacg 540atttatgaag tgaatttgtt atcacaagat gaagcaatca agctcttaaa aagatatgca 600tatcataaag ataaacctgt tgaagagtat gagatgcttg cagaagaggt agtttcttat 660gctggtgggc 670 11 1200 DNA Helianthus annuus 11atg cag aaa tct ctc acc gat ttg aag gtc act gcc ttc ttc aaa ata 48tcc gtg agg gag tca aac aag cat ggt ttg gaa aag cta caa gaa aaa 96ttt ctc tca ctc att ttg aaa gca gat gtg aag gta ggg aat gag ata 144gaa gga aga agc att ata gaa aga agg tta cgt aat aaa agc gta tta 192gtt gtt ctt gac gat gtt gat gac cat aag caa cta gag gct cta gcc 240gga tca cat gct tgg ttt ggt aag ggg agc agg ata ata att acg acg 288agg gat gag cat ttg cta acc cgc cat gca gac atg ata tat gaa gtg 336agt ttg tta tca cat gac gag gct atg gag ctc ttc aac aaa cat gca 384tat cgg aaa gat aaa cct ata gaa gat tac gag atg ctt tca aac gat 432gta gtt tct tat gct agt ggg ctc cca tta gca ctt gaa att cta ggt 480tct ttt cta tat gac aaa aac aag gat gag tgg aag agt gca ttg gca 528agt taa aat gca tcc caa atg tta aag tca ccg aaa gac tca aaa taa 576gtt atg atg gac ttg aac ccg acc atc aaa aaa ata ttc tta gat att 624gct tgt ttt tgg agg aga caa cac atg gat gag gca atg atg gtg ctt 672gat gct tgt aat tta cac cct tgt ata ggg gtg aag gtg ttg att caa 720aaa tct ctc ata aaa gtt tca gat gat gta ttt ggt gat aaa ata gtt 768gat atg cat gac ttg gtg gaa gaa atg gct cac tac att gtt aga ggg 816gca cac cct aat cat cct gaa aag cat agt aga att tgg aag gag gag 864gat ata gca tac ctc tgt gat atg ggg gca gat gca gtg cca atg gaa 912act gaa gta gaa gct ttg tgt tct tat gat gtt ccg gat cta tct gat 960gtg gtt gca aac atg aag aaa ctt cgg tgg att cgt ttt gat cag tat 1008cag aca tct tca ttc cca tca aat ttt cag cca aca gag ctt tgt tgt 1056cta gag ttg cat aag agc caa caa aaa gaa ctg tgg cat ggg tat aag 1104ctt cta cca aat ttg aaa att ctt gat ctt agg aga tca tca aaa cta 1152atc acg aca cca aaa ttt tga tgg cct tcc atg tct gaa aag att gat 1200 12 3456 DNA Helianthus annuus CDS (15)...(1442) misc_feature (1)...(3456) n = A,T,C or G 12ggcacgagtg aaca atg gct gtt gga ctt atg gag act ctg aaa gaa gct 50 Met Ala Val Gly Leu Met Glu Thr Leu Lys Glu Ala 1 5 10ata acc gcc tac acc gga ctc tct ccc act act ttc ttc act gtt ctc 98Ile Thr Ala Tyr Thr Gly Leu Ser Pro Thr Thr Phe Phe Thr Val Leu 15 20 25gcc gcc ggt gtc acc gtc tac tac atc gtt tcc gtt ctg ttc atg aga 146Ala Ala Gly Val Thr Val Tyr Tyr Ile Val Ser Val Leu Phe Met Arg 30 35 40ggc tcc tcc gat cac cat caa caa cac agc caa atg tct tcc gaa gaa 194Gly Ser Ser Asp His His Gln Gln His Ser Gln Met Ser Ser Glu Glu 45 50 55 60gac aga tca gcg gca tct tct tcg tcc gct tct cac tca att tct gcc 242Asp Arg Ser Ala Ala Ser Ser Ser Ser Ala Ser His Ser Ile Ser Ala 65 70 75tct act tct caa tca tgg aat cat gat gta ttt ctg agc ttt cgg gga 290Ser Thr Ser Gln Ser Trp Asn His Asp Val Phe Leu Ser Phe Arg Gly 80 85 90gaa gac acc cgt aat agc ttt gtg gat cat ctc tat gcg gct ctt gca 338Glu Asp Thr Arg Asn Ser Phe Val Asp His Leu Tyr Ala Ala Leu Ala 95 100 105caa caa gga atc cag gcg tac aag gat gac gaa aca ctt cct cgg ggt 386Gln Gln Gly Ile Gln Ala Tyr Lys Asp Asp Glu Thr Leu Pro Arg Gly 110 115 120gag cga atc ggt cca gcc ctc ttg aaa gct atc caa gaa tca cgc atc 434Glu Arg Ile Gly Pro Ala Leu Leu Lys Ala Ile Gln Glu Ser Arg Ile125 130 135 140gcc gtt gtt gtg ttc tct caa aac tat gcg gat tca tct tgg tgc ttg 482Ala Val Val Val Phe Ser Gln Asn Tyr Ala Asp Ser Ser Trp Cys Leu 145 150 155gac gag ctt gca cat att atg gag tgc atg gac acg aga ggg cag atc 530Asp Glu Leu Ala His Ile Met Glu Cys Met Asp Thr Arg Gly Gln Ile 160 165 170gtg att ccc ata ttt tat ttt gta gat cca tcg gat gtt aga aaa caa 578Val Ile Pro Ile Phe Tyr Phe Val Asp Pro Ser Asp Val Arg Lys Gln 175 180 185aag ggg aaa tat gga aaa gca ttt aga aaa cgt aag agg gaa aat agg 626Lys Gly Lys Tyr Gly Lys Ala Phe Arg Lys Arg Lys Arg Glu Asn Arg 190 195 200caa aaa gtt gaa tca tgg aga aaa gct ctg gaa aag gct ggc aat ctt 674Gln Lys Val Glu Ser Trp Arg Lys Ala Leu Glu Lys Ala Gly Asn Leu205 210 215 220tct gga tgg gtc atc aat gaa aac agt cac gaa gca aaa tgc atc aaa 722Ser Gly Trp Val Ile Asn Glu Asn Ser His Glu Ala Lys Cys Ile Lys 225 230 235gaa att gtt gct aca att tct agt agg ctg cct aca cta agt aca aac 770Glu Ile Val Ala Thr Ile Ser Ser Arg Leu Pro Thr Leu Ser Thr Asn 240 245 250gtc aat aaa gac ctc att gga ata gag aca cgc tta caa gat ctg aaa 818Val Asn Lys Asp Leu Ile Gly Ile Glu Thr Arg Leu Gln Asp Leu Lys 255 260 265tca aag ttg aaa atg gag tca ggt gat gta cgc att att gga ata tgg 866Ser Lys Leu Lys Met Glu Ser Gly Asp Val Arg Ile Ile Gly Ile Trp 270 275 280gga gtt ggg ggt ggt ggt aag act act ctc gca tct gct gct tat gcg 914Gly Val Gly Gly Gly Gly Lys Thr Thr Leu Ala Ser Ala Ala Tyr Ala285 290 295 300gaa atc tct cgc cga ttt gaa gct cac tgc ctt ctt caa aat atc cgt 962Glu Ile Ser Arg Arg Phe Glu Ala His Cys Leu Leu Gln Asn Ile Arg 305 310 315gag gag tca aac aag cat ggt ttg gaa aaa cta caa gaa aaa att ctc 1010Glu Glu Ser Asn Lys His Gly Leu Glu Lys Leu Gln Glu Lys Ile Leu 320 325 330tca ctt gtt ttg aaa aca aaa gat gtt gtg gta ggg agt gag ata gaa 1058Ser Leu Val Leu Lys Thr Lys Asp Val Val Val Gly Ser Glu Ile Glu 335 340 345gga aga agc atg ata gaa aga agg tta cgt aat aaa agc gta tta gtt 1106Gly Arg Ser Met Ile Glu Arg Arg Leu Arg Asn Lys Ser Val Leu Val 350 355 360gtt ctt gac gat gtt gat gac ctc aag caa cta gag gct cta gcc gga 1154Val Leu Asp Asp Val Asp Asp Leu Lys Gln Leu Glu Ala Leu Ala Gly365 370 375 380tca cat gct tgg ttt ggt aag ggg agc agg ata ata att acg acg agg 1202Ser His Ala Trp Phe Gly Lys Gly Ser Arg Ile Ile Ile Thr Thr Arg 385 390 395gat gag cat ttg cta acc cgc cat gca gac atg ata tat gaa gtg agt 1250Asp Glu His Leu Leu Thr Arg His Ala Asp Met Ile Tyr Glu Val Ser 400 405 410ttg tta tca cat gac gag gct atg gag ctc ttc aac aaa cat gca tat 1298Leu Leu Ser His Asp Glu Ala Met Glu Leu Phe Asn Lys His Ala Tyr 415 420 425cgg aaa gat aaa cct ata gaa gat tac gag atg ctt tca aac gat gta 1346Arg Lys Asp Lys Pro Ile Glu Asp Tyr Glu Met Leu Ser Asn Asp Val 430 435 440gtt tct tat gct agt ggg ctc cca tta gca ctt gaa att cta ggt tct 1394Val Ser Tyr Ala Ser Gly Leu Pro Leu Ala Leu Glu Ile Leu Gly Ser445 450 455 460ttt cta tat gac aaa aac aag gat gag tgg aag agt gca ttg gca agt 1442Phe Leu Tyr Asp Lys Asn Lys Asp Glu Trp Lys Ser Ala Leu Ala Ser 465 470 475taaaatgcat cccaaatgtt aaagtcaccg aaagactcaa aataagttat gatggacttg 1502aacccaacat caaaaaatat cctaaataat gctgtttgga ggaacacaca tggatgaggc 1562atgatgggct tgagctggaa ttacaccctg gtaaggggaa gggttttcaa accccaaaat 1622gttatagggt taaaggtgtt ggaacaaaaa tccctcataa aagtttcaaa aaaaggaaga 1682tttgagatgc atgacttgat agaagaaatg gcccactaca ttgttagagg ggaacaccct 1742aataatcctg aaaagcatag caggatttgg aatagggaag atttggaaga gctttgtgct 1802atgggagcag ctgcaccctc aatggaaaat gaagtattag ctaatttgcc aatgtatata 1862attagccatc caggtctact acttgatgtt gttccaaaca tgaagaacct tcgatggata 1922atgttgattg gtcatgggga tccgtcatct tcattcccat caaattttca gccaacaaag 1982cttcgttgtc tctaatcacg acaccaaatt ttgatgccct tccatgtctt gaaagattga 2042ttttaagaga ttgtaagagt ttagaagaga ttcatccatc aattggacat cacaaaaggc 2102ttgtttacgt gagtgtgagc tactgttcaa gccttaaaag ctttccaccc atcatacaga 2162tgcaaatgtt gaagactctt attctctctt attgctatca acttcaacag tttccggata 2222tccagtcgaa caagagtcta ccaaatttga aaattcttaa tcttgaacaa tgtggaaacc 2282taatcacgac accagatttt gaaggccttc catgtcttga aagattgatt ttatcacatt 2342gtatgagttt agaagagatt catccatcaa ttggatatca caaaaggctt gttttcgtga 2402acctgaactg gtgtagagca cttaaaaggt ttccacccat catacagatg gaaaaattgg 2462agactcttat tctctcttat tgcgagcaac tacaacagtt tccggatatc cagtcgaaca 2522tggatagctt ggtaaccctt gatttgagtg atactggtat agaaataatc ctaccgtcag 2582ctggacgact cccaggtctc aagtatctca atctgtcata ctgcataaac cttgtagaat 2642tgccagacct cccatcaagc atagctattc tcagagcaga tggttgtgac tcacttgaaa 2702ttgtaagaga tttatcagac tataaatggt tgtggaaagt ctctctttgg aggagagcga 2762ataagagggt actactttct atgcttgagg aaaatgcagt taaagaagat cgctttatga 2822gtgtcttact tcccgcgcct gaaccatcaa gcatttatac caaacttgtc acattgcaac 2882ttccacacaa ctggtacagt gactttagtg gatttttatt atcattacgt gctcctgatt 2942cccaatccga tacgtatcgc atagttatta agcaggagat gtccacggat caccctgaag 3002agttcagtga aaattggaaa aattttgacc atgaaagggt gggttatgta ccctttaatt 3062tattgaggca catcccatgg ttcaatccta catacactaa aagtatttca tttaagatgg 3122gtgatgcttg tcttaatgta gaacttgttc gtaggaaaag taaaataggt gatttaaacg 3182aacacctaat cgattactta gagtgttggg atgaagaata tgaagataaa aagacatttg 3242agatcacaaa tgatgcaacg tcttctgaaa ttcagatttt atggagacat cggtagtcga 3302tctcagtttc aaatttcaac atttgcccac attttgttac cattttaagt ttgtttttac 3362ttctccaaca tcattgcaac ctaaaagaag ttgtaataat ttttcctcta ttatctctta 3422agacntcaca ttcaaaaaaa aaaaaaaaaa aaaa 3456 13 476 PRT Helianthus annuus 13Met Ala Val Gly Leu Met Glu Thr Leu Lys Glu Ala Ile Thr Ala Tyr 1 5 10 15Thr Gly Leu Ser Pro Thr Thr Phe Phe Thr Val Leu Ala Ala Gly Val 20 25 30Thr Val Tyr Tyr Ile Val Ser Val Leu Phe Met Arg Gly Ser Ser Asp 35 40 45His His Gln Gln His Ser Gln Met Ser Ser Glu Glu Asp Arg Ser Ala 50 55 60Ala Ser Ser Ser Ser Ala Ser His Ser Ile Ser Ala Ser Thr Ser Gln65 70 75 80Ser Trp Asn His Asp Val Phe Leu Ser Phe Arg Gly Glu Asp Thr Arg 85 90 95Asn Ser Phe Val Asp His Leu Tyr Ala Ala Leu Ala Gln Gln Gly Ile 100 105 110Gln Ala Tyr Lys Asp Asp Glu Thr Leu Pro Arg Gly Glu Arg Ile Gly 115 120 125Pro Ala Leu Leu Lys Ala Ile Gln Glu Ser Arg Ile Ala Val Val Val 130 135 140Phe Ser Gln Asn Tyr Ala Asp Ser Ser Trp Cys Leu Asp Glu Leu Ala145 150 155 160His Ile Met Glu Cys Met Asp Thr Arg Gly Gln Ile Val Ile Pro Ile 165 170 175Phe Tyr Phe Val Asp Pro Ser Asp Val Arg Lys Gln Lys Gly Lys Tyr 180 185 190Gly Lys Ala Phe Arg Lys Arg Lys Arg Glu Asn Arg Gln Lys Val Glu 195 200 205Ser Trp Arg Lys Ala Leu Glu Lys Ala Gly Asn Leu Ser Gly Trp Val 210 215 220Ile Asn Glu Asn Ser His Glu Ala Lys Cys Ile Lys Glu Ile Val Ala225 230 235 240Thr Ile Ser Ser Arg Leu Pro Thr Leu Ser Thr Asn Val Asn Lys Asp 245 250 255Leu Ile Gly Ile Glu Thr Arg Leu Gln Asp Leu Lys Ser Lys Leu Lys 260 265 270Met Glu Ser Gly Asp Val Arg Ile Ile Gly Ile Trp Gly Val Gly Gly 275 280 285Gly Gly Lys Thr Thr Leu Ala Ser Ala Ala Tyr Ala Glu Ile Ser Arg 290 295 300Arg Phe Glu Ala His Cys Leu Leu Gln Asn Ile Arg Glu Glu Ser Asn305 310 315 320Lys His Gly Leu Glu Lys Leu Gln Glu Lys Ile Leu Ser Leu Val Leu 325 330 335Lys Thr Lys Asp Val Val Val Gly Ser Glu Ile Glu Gly Arg Ser Met 340 345 350Ile Glu Arg Arg Leu Arg Asn Lys Ser Val Leu Val Val Leu Asp Asp 355 360 365Val Asp Asp Leu Lys Gln Leu Glu Ala Leu Ala Gly Ser His Ala Trp 370 375 380Phe Gly Lys Gly Ser Arg Ile Ile Ile Thr Thr Arg Asp Glu His Leu385 390 395 400Leu Thr Arg His Ala Asp Met Ile Tyr Glu Val Ser Leu Leu Ser His 405 410 415Asp Glu Ala Met Glu Leu Phe Asn Lys His Ala Tyr Arg Lys Asp Lys 420 425 430Pro Ile Glu Asp Tyr Glu Met Leu Ser Asn Asp Val Val Ser Tyr Ala 435 440 445Ser Gly Leu Pro Leu Ala Leu Glu Ile Leu Gly Ser Phe Leu Tyr Asp 450 455 460Lys Asn Lys Asp Glu Trp Lys Ser Ala Leu Ala Ser465 470 475 14 1360 DNA Helianthus annuus 14ggcacgagtg aacaatggct gttggactta tggagactct gaaagaagct ataaccgcct 60acaccggact ctctcccact actttcttca ctgttctcgc cgccggtgtc accgtctact 120acatcgtttc cgttctgttc atgagaggct cctccgatca ccatcaacaa cacagccaaa 180tgtcttccga agaagacaga tcagcggcat cttcttcgtc cgcttctcac tcaatttctg 240cctctacttc tcaatcatgg aatcatgatg tatttctgag ctttcgggga gaagacaccc 300gtaatagctt tgtggatcat ctctatgcgg ctcttgcaca acaaggaatc caggcgtaca 360aggatgacga aacacttcct cggggtgagc gaatcggtcc agccctcttg aaagctatcc 420aagaatcacg catcgccgtt gttgtgttct ctcaaaacta tgcggattca tcttggtgct 480tggacgagct tgcacatatt atggagtgca tggacacgag agggcagatc gtgattccca 540tattttattt tgtagatcca tcggatgtta gaaaacaaaa ggggaaatat ggaaaagcat 600ttagaaaacg taagagggaa aataggcaaa aagttgaatc atggagaaaa gctctggaaa 660aggctggcaa tctttctgga tgggtcatca atgaaaacag tcacgaagca aaatgcatca 720aagaaattgt tgctacaatt tctagtaggc tgcctacact aagtacaaac gtcaataaag 780acctcattgg aatagagaca cgcttacaag atctgaaatc aaagttgaaa atggagtcag 840gtgatgtacg cattattgga atatggggag ttgggggtgg tggtaagact actctcgcat 900ctgctgctta tgcggaaatc tctcgccgat ttgaagctca ctgccttctt caaaatatcc 960gtgaggagtc aaacaagcat ggtttggaaa aactacaaga aaaaattctc tcacttgttt 1020tgaaaacaaa agatgttgtg gtagggagtg agatagaagg aagaagcatg atagaaagaa 1080ggttacgtaa taaaagcgta ttagttgttc ttgacgatgt tgatgacctc aagcaactag 1140aggctctagc cggatcacat gcttggtttg gtaaggggag caggataata attacgacga 1200gggatgagca tttgctaacc cgccatgcag acatgatata tgaagtgagt ttgttatcac 1260atgacgaggc tatggagctc ttcaacaaac atgcatatcg gaaagataaa cctatagaag 1320attacgagat gctttcaaac gatgtagttt cttatgctag 1360 15 20 DNA Artificial Sequence oligonucleotide primer 15ggnggnrtng gnaanacnac 20 16 17 DNA Artificial Sequence misc_feature (1)...(17) n = A,T,C or G 16agngynagng gnagncc 17 17 17 DNA Artificial Sequence misc_feature (1)...(17) n = A,T,C or G 17agngynagng gnaancc 17 18 17 DNA Artificial Sequence misc_feature (1)...(17) n = A,T,C or G 18agngynaang gnagncc 17 19 17 DNA Artificial Sequence misc_feature (1)...(17) n = A,T,C or G 19agngynaang gnaancc 17 20 17 DNA Artificial Sequence misc_feature (1)...(17) n = A,T,C or G 20aangynagng gnagncc 17 21 17 DNA Artificial Sequence misc_feature (1)...(17) n = A,T,C or G 21aangynagng gnaancc 17 22 17 DNA Artificial Sequence misc_feature (1)...(17) n = A,T,C or G 22aangynaang gnagncc 17 23 17 DNA Artificial Sequence misc_feature (1)...(17) n = A,T,C or G 23aangynaang gnaancc 17 24 20 DNA Artificial Sequence misc_feature (1)...(20) n = A,T,C or G 24ggnttyggnr angtntayaa 20 25 20 DNA Artificial Sequence misc_feature (1)...(20) n = A,T,C or G 25ggnttyggnr angtntayag 20 26 17 DNA Artificial Sequence misc_feature (1)...(17) n = A,T,C or G 26trnccnykng cngcncc 17 27 17 DNA Artificial Sequence misc_feature (1)...(17) n = A,T,C or G 27ccraansyrt anacrtc 17 28 22 DNA Artificial Sequence Oligonucleotide primer 28cgatgtgaag gtagggaatg ag 22 29 24 DNA Artificial Sequence Oligonucleotide primer 29gggagtgaga taataggaag gagc 24 30 24 DNA Artificial Sequence Oligonucleotide primer 30ggtagggagt gagatagaag gaag 24 31 23 DNA Artificial Sequence Oligonucleotide primer 31tatgaagtga atttgttatc aca 23 32 23 DNA Artificial Sequence Oligonucleotide primer 32tatgaagtga gtttgttatc aca 23 33 26 DNA Artificial Sequence Oligonucleotide primer 33aagacgactc tcgcatctgc tgccta 26 34 26 DNA Artificial Sequence Oligonucleotide primer 34gaagacgact ctcgcatctg ctgctt 26 35 22 DNA Artificial Sequence Oligonucleotide primer 35gccaccagca taagaaacta cc 22 36 22 DNA Artificial Sequence Oligonucleotide primer 36ggccgtcagc ataagaaact ac 22 37 22 DNA Artificial Sequence Oligonucleotide primer 37ggaggccact agcataagaa ac 22 38 26 DNA Artificial Sequence Oligonucleotide primer 38ggggaggcca ccagcataag aaacta 26 39 26 DNA Artificial Sequence Oligonucleotide primer 39cgaaggggag gccactagca taagaa 26 40 26 DNA Artificial Sequence Oligonucleotide primer 40caattattat ccggctcccc tcacca 26 41 26 DNA Artificial Sequence Oligonucleotide primer 41tcttatatcg tgtctgcatg gcgggt 26 42 26 DNA Artificial Sequence Oligonucleotide primer 42cacttcataa atcgtttgcg ccctgc 26 43 26 DNA Artificial Sequence Oligonucleotide primer 43gcagcggtca gattgtagct gtcaaa 26 44 26 DNA Artificial Sequence Oligonucleotide primer 44gccagccgct atcttcattc ttgtgt 26 45 25 DNA Artificial Sequence Oligonucleotide primer 45ggataggaac gggctgcagg gtaac 25 46 26 DNA Artificial Sequence Oligonucleotide primer 46tttggtcacc atcagcacag tatccg 26 47 26 DNA Artificial Sequence Oligonucleotide primer 47cttgggtttg gggaggtgta cagagg 26 48 26 DNA Artificial Sequence Oligonucleotide primer 48cttggatgct gcaattaagc gactgg 26 49 25 DNA Artificial Sequence Oligonucleotide primer 49ggcggcgcct atgcatattt tgagt 25 50 26 DNA Artificial Sequence Oligonucleotide primer 50cttcaaaacc ggggtctgga gtcgtt 26 51 26 DNA Artificial Sequence Oligonucleotide primer 51cggagactcc atgttagcgg ttgaaa 26 52 29 DNA Artificial Sequence Oligonucleotide primer 52aactatgtct ttccatacca gtcacccgg 29 53 26 DNA Artificial Sequence Oligonucleotide primer 53tcggagactc catgttagcg gttgaa 26 54 26 DNA Artificial Sequence Oligonucleotide primer 54gaccgttcct tcaattaatg ggttgc 26 55 26 DNA Artificial Sequence Oligonucleotide primer 55gcgattaagt tgggtaacgc cagggt 26 56 26 DNA Artificial Sequence Oligonucleotide primer 56tccggctcgt atgttgtgtg gaattg 26 57 389 PRT Arabidopsis thaliana 57Met Gly Gly Cys Phe Ser Asn Arg Ile Lys Thr Asp Ile Ala Ser Ser 1 5 10 15Thr Trp Leu Ser Ser Lys Phe Leu Ser Arg Asp Gly Ser Lys Gly Ser 20 25 30Ser Thr Ala Ser Phe Ser Tyr Met Pro Arg Thr Glu Gly Glu Ile Leu 35 40 45Gln Asn Ala Asn Leu Lys Asn Phe Ser Leu Ser Glu Leu Lys Ser Ala 50 55 60Thr Arg Asn Phe Arg Pro Asp Ser Val Val Gly Glu Gly Gly Phe Gly65 70 75 80Cys Val Phe Lys Gly Trp Ile Asp Glu Ser Ser Leu Ala Pro Ser Lys 85 90 95Pro Gly Thr Gly Ile Val Ile Ala Val Lys Arg Leu Asn Gln Glu Gly 100 105 110Phe Gln Gly His Arg Glu Trp Leu Ala Glu Ile Asn Tyr Leu Gly Gln 115 120 125Leu Asp His Pro Asn Leu Val Lys Leu Ile Gly Tyr Cys Leu Glu Glu 130 135 140Glu His Arg Leu Leu Val Tyr Glu Phe Met Thr Arg Gly Ser Leu Glu145 150 155 160Asn His Leu Phe Arg Arg Gly Thr Phe Tyr Gln Pro Leu Ser Trp Asn 165 170 175Thr Arg Val Arg Met Ala Leu Gly Ala Ala Arg Gly Leu Ala Phe Leu 180 185 190His Asn Ala Gln Pro Gln Val Ile Tyr Arg Asp Phe Lys Ala Ser Asn 195 200 205Ile Leu Leu Asp Ser Asn Tyr Asn Ala Lys Leu Ser Asp Phe Gly Leu 210 215 220Ala Arg Asp Gly Pro Met Gly Asp Asn Ser His Val Ser Thr Arg Val225 230 235 240Met Gly Thr Gln Gly Tyr Ala Ala Pro Glu Tyr Leu Ala Thr Gly His 245 250 255Leu Ser Val Lys Ser Asp Val Tyr Ser Phe Gly Val Val Leu Leu Glu 260 265 270Leu Leu Ser Gly Arg Arg Ala Ile Asp Lys Asn Gln Pro Val Val Glu 275 280 285His Asn Leu Val Asp Trp Ala Arg Pro Tyr Leu Thr Asn Lys Arg Arg 290 295 300Leu Leu Arg Val Met Asp Pro Arg Leu Gln Gly Gln Tyr Ser Leu Thr305 310 315 320Arg Ala Leu Lys Ile Ala Val Leu Ala Leu Asp Cys Ile Ser Ile Asp 325 330 335Ala Lys Ser Arg Pro Thr Met Asn Glu Ile Val Lys Thr Met Glu Glu 340 345 350Leu His Ile Gln Lys Glu Ala Ser Lys Glu Gln Gln Asn Pro Gln Ile 355 360 365Ser Ile Asp Asn Ile Ile Asn Lys Ser Pro Gln Ala Val Asn Tyr Pro 370 375 380Arg Pro Ser Ile Met385 58 410 PRT Arabidopsis thaliana 58Met Gly Ile Cys Leu Ser Ala Gln Val Lys Ala Glu Ser Ser Gly Ala 1 5 10 15Ser Thr Lys Tyr Asp Ala Lys Asp Ile Gly Ser Leu Gly Ser Lys Ala 20 25 30Ser Ser Val Ser Val Arg Pro Ser Pro Arg Thr Glu Gly Glu Ile Leu 35 40 45Gln Ser Pro Asn Leu Lys Ser Phe Ser Phe Ala Glu Leu Lys Ser Ala 50 55 60Thr Arg Asn Phe Arg Pro Asp Ser Val Leu Gly Glu Gly Gly Phe Gly65 70 75 80Cys Val Phe Lys Gly Trp Ile Asp Glu Lys Ser Leu Thr Ala Ser Arg 85 90 95Pro Gly Thr Gly Leu Val Ile Ala Val Lys Lys Leu Asn Gln Asp Gly 100 105 110Trp Gln Gly His Gln Glu Trp Leu Ala Glu Val Asn Tyr Leu Gly Gln 115 120 125Phe Ser His Arg His Leu Val Lys Leu Ile Gly Tyr Cys Leu Glu Asp 130 135 140Glu His Arg Leu Leu Val Tyr Glu Phe Met Pro Arg Gly Ser Leu Glu145 150 155 160Asn His Leu Phe Arg Arg Gly Leu Tyr Phe Gln Pro Leu Ser Trp Lys 165 170 175Leu Arg Leu Lys Val Ala Leu Gly Ala Ala Lys Gly Leu Ala Phe Leu 180 185 190His Ser Ser Glu Thr Arg Val Ile Tyr Arg Asp Phe Lys Thr Ser Asn 195 200 205Ile Leu Leu Asp Ser Glu Tyr Asn Ala Lys Leu Ser Asp Phe Gly Leu 210 215 220Ala Lys Asp Gly Pro Ile Gly Asp Lys Ser His Val Ser Thr Arg Val225 230 235 240Met Gly Thr His Gly Tyr Ala Ala Pro Glu Tyr Leu Ala Thr Gly His 245 250 255Leu Thr Thr Lys Ser Asp Val Tyr Ser Phe Gly Val Val Leu Leu Glu 260 265 270Leu Leu Ser Gly Arg Arg Ala Val Asp Lys Asn Arg Pro Ser Gly Glu 275 280 285Arg Asn Leu Val Glu Trp Ala Lys Pro Tyr Leu Val Asn Lys Arg Lys 290 295 300Ile Phe Arg Val Ile Asp Asn Arg Leu Gln Asp Gln Tyr Ser Met Glu305 310 315 320Glu Ala Cys Lys Val Ala Thr Leu Ser Leu Arg Cys Leu Thr Thr Glu 325 330 335Ile Lys Leu Arg Pro Asn Met Ser Glu Val Val Ser His Leu Glu His 340 345 350Ile Gln Ser Leu Asn Ala Ala Ile Gly Gly Asn Met Asp Lys Thr Asp 355 360 365Arg Arg Met Arg Arg Arg Ser Asp Ser Val Val Ser Lys Lys Val Asn 370 375 380Ala Gly Phe Ala Arg Gln Thr Ala Val Gly Ser Thr Val Val Ala Tyr385 390 395 400Pro Arg Pro Ser Ala Ser Pro Leu Tyr Val 405 410 59 426 PRT Arabidopsis thaliana 59Met Gly Asn Cys Leu Asp Ser Ser Ala Lys Val Asp Ser Ser Ser His 1 5 10 15Ser Pro His Ala Asn Ser Ala Ser Leu Ser Ser Arg Val Ser Ser Lys 20 25 30Thr Ser Arg Ser Thr Val Pro Ser Ser Leu Ser Ile Asn Ser Tyr Ser 35 40 45Ser Val Glu Ser Leu Pro Thr Pro Arg Thr Glu Gly Glu Ile Leu Ser 50 55 60Ser Pro Asn Leu Lys Ala Phe Thr Phe Asn Glu Leu Lys Asn Ala Thr65 70 75 80Arg Asn Phe Arg Pro Asp Ser Leu Leu Gly Glu Gly Gly Phe Gly Tyr 85 90 95Val Phe Lys Gly Trp Ile Asp Gly Thr Thr Leu Thr Ala Ser Lys Pro 100 105 110Gly Ser Gly Ile Val Val Ala Val Lys Lys Leu Lys Thr Glu Gly Tyr 115 120 125Gln Gly His Lys Glu Trp Leu Thr Glu Val Asn Tyr Leu Gly Gln Leu 130 135 140Ser His Pro Asn Leu Val Lys Leu Val Gly Tyr Cys Val Glu Gly Glu145 150 155 160Asn Arg Leu Leu Val Tyr Glu Phe Met Pro Lys Gly Ser Leu Glu Asn 165 170 175His Leu Phe Arg Arg Gly Ala Gln Pro Leu Thr Trp Ala Ile Arg Met 180 185 190Lys Val Ala Ile Gly Ala Ala Lys Gly Leu Thr Phe Leu His Asp Ala 195 200 205Lys Ser Gln Val Ile Tyr Arg Asp Phe Lys Ala Ala Asn Ile Leu Leu 210 215 220Asp Ala Glu Phe Asn Ser Lys Leu Ser Asp Phe Gly Leu Ala Lys Ala225 230 235 240Gly Pro Thr Gly Asp Lys Thr His Val Ser Thr Gln Val Met Gly Thr 245 250 255His Gly Tyr Ala Ala Pro Glu Tyr Val Ala Thr Gly Arg Leu Thr Ala 260 265 270Lys Ser Asp Val Tyr Ser Phe Gly Val Val Leu Leu Glu Leu Leu Ser 275 280 285Gly Arg Arg Ala Val Asp Lys Ser Lys Val Gly Met Glu Gln Ser Leu 290 295 300Val Asp Trp Ala Thr Pro Tyr Leu Gly Asp Lys Arg Lys Leu Phe Arg305 310 315 320Ile Met Asp Thr Arg Leu Gly Gly Gln Tyr Pro Gln Lys Gly Ala Tyr 325 330 335Thr Ala Ala Ser Leu Ala Leu Gln Cys Leu Asn Pro Asp Ala Lys Leu 340 345 350Arg Pro Lys Met Ser Glu Val Leu Ala Lys Leu Asp Gln Leu Glu Ser 355 360 365Thr Lys Pro Gly Thr Gly Val Gly Asn Arg Gln Ala Gln Ile Asp Ser 370 375 380Pro Arg Gly Ser Asn Gly Ser Ile Val Gln Lys Ser Pro Arg Arg Tyr385 390 395 400Ser Tyr Asp Arg Pro Leu Leu His Ile Thr Pro Gly Ala Ser Pro Leu 405 410 415Pro Thr His Asn His Ser Pro Arg Val Arg 420 425 60 370 PRT Lycopersicon esculentum 60Met Ser Cys Phe Ser Cys Cys Asp Asp Asp Asp Met His Arg Ala Thr 1 5 10 15Asp Asn Gly Pro Phe Met Ala His Asn Ser Ala Gly Asn Asn Gly Gly 20 25 30Gln Arg Ala Thr Glu Ser Ala Gln Arg Glu Thr Gln Thr Val Asn Ile 35 40 45Gln Pro Ile Ala Val Pro Ser Ile Ala Val Asp Glu Leu Lys Asp Ile 50 55 60Thr Asp Asn Phe Gly Ser Lys Ala Leu Ile Gly Glu Gly Ser Tyr Gly65 70 75 80Arg Val Tyr His Gly Val Leu Lys Ser Gly Arg Ala Ala Ala Ile Lys 85 90 95Lys Leu Asp Ser Ser Lys Gln Pro Asp Arg Glu Phe Leu Ala Gln Val 100 105 110Ser Met Val Ser Arg Leu Lys Asp Glu Asn Val Val Glu Leu Leu Gly 115 120 125Tyr Cys Val Asp Gly Gly Phe Arg Val Leu Ala Tyr Glu Tyr Ala Pro 130 135 140Asn Gly Ser Leu His Asp Ile Leu His Gly Arg Lys Gly Val Lys Gly145 150 155 160Ala Gln Pro Gly Pro Val Leu Ser Trp Ala Gln Arg Val Lys Ile Ala 165 170 175Val Gly Ala Ala Lys Gly Leu Glu Tyr Leu His Glu Lys Ala Gln Pro 180 185 190His Ile Ile His Arg Asp Ile Lys Ser Ser Asn Ile Leu Leu Phe Asp 195 200 205Asp Asp Val Ala Lys Ile Ala Asp Phe Asp Leu Ser Asn Gln Ala Pro 210 215 220Asp Met Ala Ala Arg Leu His Ser Thr Arg Val Leu Gly Thr Phe Gly225 230 235 240Tyr His Ala Pro Glu Tyr Ala Met Thr Gly Gln Leu Ser Ser Lys Ser 245 250 255Asp Val Tyr Ser Phe Gly Val Val Leu Leu Glu Leu Leu Thr Gly Arg 260 265 270Lys Pro Val Asp His Thr Leu Pro Arg Gly Asn Arg Val Cys Tyr Leu 275 280 285Gly Asn Ala Arg Leu Ser Glu Asp Lys Val Lys Gln Cys Val Asp Ala 290 295 300Arg Leu Asn Thr Asp Tyr Pro Pro Lys Ala Ile Ala Lys Met Ala Ala305 310 315 320Val Ala Ala Leu Cys Val Gln Tyr Glu Ala Asp Phe Arg Pro Asn Met 325 330 335Ser Ile Val Val Lys Leu Phe Ser Leu Cys Cys Leu Asp Leu Tyr Gln 340 345 350Val Arg His Gln Ala Cys Glu Phe Ser Pro Tyr Pro Cys Leu Tyr Val 355 360 365Met Lys 370 61 176 PRT Nicotiana tabacum 61Gly Met Gly Gly Val Gly Lys Thr Thr Ile Ala Arg Ala Ile Phe Asp 1 5 10 15Thr Leu Leu Gly Arg Met Asp Ser Ser Tyr Gln Phe Asp Gly Ala Cys 20 25 30Phe Leu Lys Asp Ile Lys Glu Asn Lys Arg Gly Met His Ser Leu Gln 35 40 45Asn Ala Leu Leu Ser Glu Leu Leu Arg Glu Lys Ala Asn Tyr Asn Asn 50 55 60Glu Glu Asp Gly Lys His Gln Met Ala Ser Arg Leu Arg Ser Lys Lys65 70 75 80Val Leu Ile Val Leu Asp Asp Ile Asp Asn Lys Asp His Tyr Leu Glu 85 90 95Tyr Leu Ala Gly Asp Leu Asp Trp Phe Gly Asn Gly Ser Arg Ile Ile 100 105 110Ile Thr Thr Arg Asp Lys His Leu Ile Glu Lys Asn Asp Ile Ile Tyr 115 120 125Glu Val Thr Ala Leu Pro Asp His Glu Ser Ile Gln Leu Phe Lys Gln 130 135 140His Ala Phe Gly Lys Glu Val Pro Asn Glu Asn Phe Glu Lys Leu Ser145 150 155 160Leu Glu Val Val Asn Tyr Ala Lys Gly Leu Pro Leu Ala Leu Lys Val 165 170 175 62 177 PRT Linum usitatissimum 62Gly Met Gly Gly Ile Gly Lys Thr Thr Thr Ala Lys Ala Val Tyr Asn 1 5 10 15Lys Ile Ser Ser His Phe Asp Arg Cys Cys Phe Val Asp Asn Val Arg 20 25 30Ala Met Gln Glu Gln Lys Asp Gly Ile Phe Ile Leu Gln Lys Lys Leu 35 40 45Val Ser Glu Ile Leu Arg Met Asp Ser Val Gly Phe Thr Asn Asp Ser 50 55 60Gly Gly Arg Lys Met Ile Lys Glu Arg Val Ser Lys Ser Lys Ile Leu65 70 75 80Val Val Leu Asp Asp Val Asp Glu Lys Phe Lys Phe Glu Asp Ile Leu 85 90 95Gly Cys Pro Lys Asp Phe Asp Ser Gly Thr Arg Phe Ile Ile Thr Ser 100 105 110Arg Asn Gln Asn Val Leu Ser Arg Leu Asn Glu Asn Gln Cys Lys Leu 115 120 125Tyr Glu Val Gly Ser Met Ser Glu Gln His Ser Leu Glu Leu Phe Ser 130 135 140Lys His Ala Phe Lys Lys Asn Thr Pro Pro Ser Asp Tyr Glu Thr Leu145 150 155 160Ala Asn Asp Ile Val Ser Thr Thr Gly Gly Leu Pro Leu Thr Leu Lys 165 170 175Val 63 165 PRT Arabidopsis thaliana 63Gly Met Ala Gly Ile Gly Lys Thr Thr Leu Ala Arg Ala Ala Tyr Asp 1 5 10 15Gln Leu Ser Arg Asp Phe Glu Ala Ser Cys Phe Ile Glu Asp Phe Asp 20 25 30Arg Glu Phe Gln Glu Lys Gly Phe Phe Gly Leu Leu Glu Lys Gln Leu 35 40 45Gly Val Asn Pro Gln Val Thr Arg Leu Ser Ile Leu Leu Lys Thr Leu 50 55 60Arg Ser Lys Arg Ile Leu Leu Val Leu Asp Asp Val Arg Lys Pro Leu65 70 75 80Gly Ala Thr Ser Phe Leu Cys Glu Phe Asp Trp Leu Gly Pro Gly Ser 85 90 95Leu Ile Ile Val Thr Ser Gln Asp Lys Gln Val Leu Val Gln Cys Gln 100 105 110Val Asn Glu Ile Tyr Lys Val Gln Gly Leu Asn Lys His Glu Ser Leu 115 120 125Gln Leu Phe Ser Arg Cys Ala Phe Gly Lys Asp Val Pro Asp Gln Asn 130 135 140Leu Leu Glu Leu Ser Met Lys Phe Val Asp Tyr Ala Asn Gly Asn Pro145 150 155 160Leu Ala Leu Ser Ile 165 64 173 PRT Arabidopsis thaliana 64Gly Pro Gly Gly Val Gly Lys Thr Thr Leu Met Gln Ser Ile Asn Asn 1 5 10 15Glu Leu Ile Thr Lys Gly His Gln Tyr Asp Val Leu Ile Trp Val Gln 20 25 30Met Ser Arg Glu Phe Gly Glu Cys Thr Ile Gln Gln Ala Val Gly Ala 35 40 45Arg Leu Gly Leu Ser Trp Asp Glu Lys Glu Thr Gly Glu Asn Arg Ala 50 55 60Leu Lys Ile Tyr Arg Ala Leu Arg Gln Lys Arg Phe Leu Leu Leu Leu65 70 75 80Asp Asp Val Trp Glu Glu Ile Asp Leu Glu Lys Thr Gly Val Pro Arg 85 90 95Pro Asp Arg Glu Asn Lys Cys Lys Val Met Phe Thr Thr Arg Ser Ile 100 105 110Ala Leu Cys Asn Asn Met Gly Ala Glu Tyr Lys Leu Arg Val Glu Phe 115 120 125Leu Glu Lys Lys His Ala Trp Glu Leu Phe Cys Ser Lys Val Trp Arg 130 135 140Lys Asp Leu Leu Glu Ser Ser Ser Ile Arg Arg Leu Ala Glu Ile Ile145 150 155 160Val Ser Lys Cys Gly Gly Leu Pro Leu Ala Leu Ile Thr 165 170

Claims

1. A method for creating or enhancing disease resistance in a plant, said method comprising:(a) introducing into a plant cell a recombinant expression cassette comprising a sunflower R nucleotide sequence operably linked to a promoter that drives expression in a plant, wherein said R nucleotide sequence is selected from the group consisting of: (i) a nucleotide sequence encoding the amino acid sequence set forth in SEQ ID NO: 2; and (ii) the nucleotide sequence set forth in SEQ ID NO: 1; (b) culturing the plant cell under plant cell growing conditions; and (c) regenerating from the plant cell a whole plant, wherein the plant has enhanced or newly created disease resistance.

2. The method of claim 1, wherein said plant is a monocot.

3. The method of claim 2, wherein said monocot is maize, rice, or wheat.

4. The method of claim 1, wherein said plant is a dicot.

5. The method of claim 4, wherein said dicot is sunflower, soybean, canola or alfalfa.

6. A plant having stably incorporated in its genome a DNA construct, said construct comprising a promoter that drives expression in a plant operably linked to a sunflower R nucleotide sequence, wherein said R nucleotide sequence is selected from the group consisting of:(a) a nucleotide sequence encoding the amino acid sequence set forth in SEQ ID NO: 2; and (b) the nucleotide sequence set forth in SEQ ID NO: 1.

7. The plant of claim 6, wherein said plant is a monocot.

8. The plant of claim 7, wherein said monocot is maize, rice or wheat.

9. The plant of claim 6, wherein said plant is a dicot.

10. The plant of claim 9, wherein said dicot is sunflower, soybean, canola or alfalfa.

11. Transformed seed of the plant of any one of claims 6-10 inclusive, wherein the seed comprise the construct.

12. A plant cell having stably incorporated in its genome a DNA construct, said construct comprising a promoter that drives expression in a plant cell operably linked to a sunflower R nucleotide sequence, wherein said R nucleotide sequence is selected from the group consisting of:(a) a nucleotide sequence encoding the amino acid sequence set forth in SEQ ID NO: 2; and (b) the nucleotide sequence set forth in SEQ ID NO: 1.

13. The plant cell of claim 12, wherein said plant cell is from a monocot.

14. The plant cell of claim 12, wherein said plant cell is from a dicot.

15. An isolated nucleotide sequence said sequence comprising at least one of the nucleotide sequences selected from the group consisting of:(a) a nucleotide sequence encoding the amino acid sequence set forth in SEQ ID NO: 2; and (b) the nucleotide sequence set forth in SEQ ID NO: 1.

16. A chimeric gene comprising a promoter operably linked to the nucleotide sequence of claim 15.

17. A vector comprising the chimeric gene of claim 16.

18. A plant cell transformed with the vector of claim 17.

19. A plant regenerated from the plant cell of claim 18.

20. A method for modulating cellular metabolism in a plant, said method comprising(a) introducing into a plant cell a recombinant expression cassette comprising a promoter that drives expression in a plant cell operably linked to a nucleic acid sequence selected from the group consisting of; (i) a nucleotide sequence encoding the amino acid sequence set forth in SEQ ID NO: 2; and (ii) the nucleotide sequence set forth in SEQ ID NO: 1; (b) culturing the plant cell under plant cell growing conditions; and (c) regenerating from the plant cell a whole plant, wherein the plant has modulated cellular metabolism.

21. A method for creating or enhancing disease resistance in a plant, said method comprising:(a) introducing into a plant cell a recombinant expression cassette comprising a sunflower R nucleotide sequence operably linked to a promoter that drives expression in a plant, wherein said R nucleotide sequence comprises a nucleotide sequence that has at least about 95% sequence identity to the sequence set forth in SEQ ID NO: 1, wherein said nucleotide sequence encodes an R protein; (b) culturing the plant cell under plant cell growing conditions; and (c) regenerating from the plant cell a whole plant, wherein the plant has enhanced or newly created disease resistance.

22. The method of claim 21, wherein said plant is a monocot.

23. The method of claim 22, wherein said monocot is maize, rice, or wheat.

24. The method of claim 21, wherein said plant is a dicot.

25. The method of claim 24, wherein said dicot is sunflower, soybean, canola or alfalfa.

26. A plant having stably incorporated in its genome a DNA construct, said construct comprising a promoter that drives expression in a plant operably linked to a sunflower R nucleotide sequence, wherein said R nucleotide sequence comprises a nucleotide sequence that has at least about 95% sequence identity to the sequence set forth in SEQ ID NO:1, wherein said nucleotide sequence encodes an R protein.

27. The plant of claim 26, wherein said plant is a monocot.

28. The plant of claim 27, wherein said monocot is maize, rice or wheat.

29. The plant of claim 26, wherein said plant is a dicot.

30. The plant of claim 29, wherein said dicot is sunflower, soybean, canola or alfalfa.

31. Transformed seed of the plant of any one of claims 26-30 inclusive, wherein the seed comprise the construct.

32. A plant cell having stably incorporated in its genome a DNA construct, said construct comprising a promoter that drives expression in a plant cell operably linked to a sunflower R nucleotide sequence, wherein said R nucleotide sequence comprises a nucleotide sequence that has at least about 95% sequence identity to the sequence set forth in SEQ ID NO:1, wherein said nucleotide sequence encodes an R protein.

33. The plant cell of claim 32, wherein said plant cell is from a monocot.

34. The plant cell of claim 32, wherein said plant cell is from a dicot.

35. An isolated nucleotide sequence, said sequence comprising a nucleotide sequence that has at least about 95% sequence identity to the sequence set forth in SEQ ID NO:1, wherein said nucleotide sequence encodes an R protein.

36. A chimeric gene comprising a promoter operably linked to the nucleotide sequence of claim 35.

37. A vector comprising the chimeric gene of claim 36.

38. A plant cell transformed with the vector of claim 37.

39. A plant regenerated from the plant cell of claim 38.

40. A method for modulating cellular metabolism in a plant, said method comprising(a) introducing into a plant cell a recombinant expression cassette comprising a promoter that drives expression in a plant cell operably linked to a sunflower R nucleotide sequence, wherein said R nucleotide sequence comprises a nucleotide sequence that has at least about 95% sequence identity to the sequence set forth in SEQ ID NO:1, wherein said nucleotide sequence encodes an R protein; (b) culturing the plant cell under plant cell growing conditions; and (c) regenerating from the plant cell a whole plant, wherein the plant has modulated cellular metabolism.