Salicylic acid induced map kinase and its use for enhanced disease resistance in plants

Abstract

A salicylic acid-induced protein (SIP) kinase is disclosed. The kinase has a molecular weight of about 48 kDa and is activated in response to salicylic acid, H.sub.2 O.sub.2 and infection with tobacco mosaic virus. The activation and enzymatic properties of the purified protein have been characterized. The partial amino acid sequence and complete nucleotide sequence of a cDNA encoding the SIP kinase demonstrate that it is a unique member of the mitogen-activated protein (MAP) kinase family. The novel SIP kinase may play a critical role in signal transduction for activation of plant defenses against microbial pathogens.

Description

FIELD OF THE INVENTION

This invention relates to the fields of molecular biology and genetic transformation in higher plants. More specifically, the invention relates to novel genes and their encoded proteins that participate in the enhanced disease resistance pathway in multicellular plants.

BACKGROUND OF THE INVENTION

Several publications are referenced in this application in parentheses in order to more fully describe the state of the art to which this invention pertains. Full citations for these references are found at the end of the specification. The disclosure of each of these publications is incorporated by reference herein.

Activation of tobacco defense responses by tobacco mosaic virus (TMV) infection includes both local resistance, manifested as necrotic lesion formation resulting from host cell death at the site of infection (hypersensitive response, HR), and systemic resistance induced in the surrounding and distal uninfected parts of the plant (systemic acquired resistance, SAR) (Ryals et al., 1994; Dempsey and Klessig, 1995). Numerous studies have demonstrated that salicylic acid (SA) is an endogenous signal for the activation of several plant defense responses including synthesis of pathogenesis-related (PR) proteins (Ryals et al., 1994, Dempsey and Klessig, 1995). However, the components which transduce the signal between SA and PR genes remain to be elucidated.

Protein kinases and phosphatases play pivotal roles in regulating and coordinating many signal transduction pathways in living organisms, including but not limited to, cell division, cell differentiation, and responses to environmental stimuli (Hunter, 1995). In plants, protein phosphorylation has been implicated in responses to many signals, such as light, hormones, pathogen attack, temperature stress, and nutrient starvation (Stone and Walker, 1995). Several genes which encode putative protein kinases, including CTR1 (Kieber et al., 1993), ETR1 (Chang et al., 1993) and Pto (Martin et al., 1993) appear to participate in the transmission of signals generated by extracellular stimuli. The CTR1 and ETR1 protein kinases of Arabidopsis thaliana play a role in the ethylene signaling pathway. CTR1 is homologous to the mammalian Raf protein kinase which participates in the mitogen-activated protein (MAP) kinase cascade (Kieber et al., 1993). The Pto protein kinase from tomato, as well as its downstream kinase Pti1 which is phosphorylated by Pto, participate in conferring resistance to the pathogenic bacterium Pseudomonas syringae (Martin et al., 1993; Zhou et al., 1995).

The MAP kinase cascade is a major signaling system by which cells transduce extracellular stimuli into intracellular responses (Herskowitz 1995; Seger and Krebs, 1995; Votjek and Cooper, 1995; Kyriakis and Avruch, 1996). Extracellular signal-regulated protein kinases (ERKs) 1 and 2 were the first of the MAP kinase family to be cloned; they are activated by diverse extracellular stimuli. Other related mammalian MAP kinases include Jun N-terminal kinase/stress-activated protein kinases (JNK/SAPK) and p38 kinases (Seger and Krebs, 1995). MAP kinases are activated by phosphorylation on both threonine (T) and tyrosine (Y) residues within a TXY phosphorylation motif, where X can be Glu (E), Pro (P), or Gly (G). Three subfamilies of MAP kinases have been defined based on their phosphorylation motifs TEY, TPY, and TGY, which correspond to ERK1/2, JNK/SAPK, and p38 subfamilies, respectively (Kyriakis and Avruch, 1996).

The MAP kinase family is present in a diverse array of organisms including mammals, Xenopus, Drosophila, yeast, Dictyostelium, and plants. An increasing body of evidence suggests that MAP kinases play important roles in plants (Nishihama, et al., 1995). Seven MAP kinases have been identified in Arabidopsis. AtMPK1 and AtMPK2 are thought to be involved in cell proliferation (Mizoguchi, et al., 1993; Mizoguchi, et al., 1994), while AtMPK3 appears to play a role in responding to touch, cold and salinity stress (Mizoguchi et al., 1996). Several kinases upstream of the MAP kinase in the cascade have also been identified including cATMEKK1 from Arabidopsis and NPK1 from tobacco (Nishihama, et al., 1995; Mizoguchi, et al., 1996).

Several kinase activities, believed to be MAP kinases based on the fact that they preferentially phosphorylate myelin basic protein (MBP) and are themselves phosphorylated on tyrosine residues, have been shown to be activated by stress or phytohormones. These include the cutting (wounding)-induced p46 kinase (Usami et al., 1995; Seo et al., 1995), the fungal elicitor-induced p47 kinase from tobacco (Suzuki et al., 1995), and the abscisic acid-induced kinase from barley (Knetsch et al., 1996).

Protein phosphorylation/dephosphorylation events have been correlated with the activation of defense responses in a number of plants (Dietrich et al., 1990; Felix et al., 1991; Viard et al., 1994; Conrath et al., 1997). More recently, it has been shown that the activation of the potato PR-10a gene requires the phosphorylation of the nuclear factor PBF-1 (Despros et al., 1994). In addition, protein kinase inhibitors were able to block both the fungal elicitor-induced oxidative burst and the H.sub.2 O.sub.2 -mediated activation of defense genes in soybean suspension cells (Levine et al., 1994). Kinase(s) and/or phosphatase(s) also appear to regulate the activation of defense responses in tobacco, since lesion formation after TMV infection was inhibited by the phosphatase inhibitor okadaic acid (Dunigan et al., 1995). Okadaic acid also blocked the SA-mediated induction of PR-1 gene expression (Conrath et al., 1997). The kinase(s) and/or phosphatase(s) involved in these processes, however, remain to be identified.

It has been shown that the MAP kinases associated with several different signaling pathways are activated by H.sub.2 O.sub.2 or other oxidative stresses in mammalian systems. These include JNK, ERK2, and the big mitogen-activated protein kinase 1 (BMK1; Abe et al., 1996; Lo et al., 1996; Guyton et al., 1996; Sundaresan et al., 1995). Thus, H.sub.2 O.sub.2 appears to regulate a wide variety of different processes. In neutrophils, reactive oxygen species produced by the NADPH oxidase induce tyrosine phosphorylation, in addition to their role in bacterial killing (Fialko et al., 1994; Brumell et al., 1996). The prominent 42-44 kDa tyrosine-phosphorylated polypeptide induced by H.sub.2 O.sub.2 was later shown to be MAP kinase that is phosphorylated on both tyrosine and threonine by a redox-sensitive MAP kinase kinase (MEK; Fialkow et al., 1994). In plants, H.sub.2 O.sub.2 has been implicated in both the action of SA (Chen et al., 1993) and the induction of defense responses after pathogen invasion, exposure to ozone or UV light (Medhy, 1994; Levine et al., 1994; Kangasjarvi et al., 1994; Green and Fluhr, 1995).

SUMMARY OF THE INVENTION

A new member of the mitogen-activated protein (MAP) kinase family of enzymes has been discovered in accordance with the present invention. Referred to herein as salicylic acid-induced protein (SIP) kinase, the enzyme is structurally distinct from other MAP kinases. Another unique feature of SIP kinase is that it is activated by microbial pathogens, as well as by secondary plant defense signaling molecules, as described in greater detail below.

According to one aspect of the invention, an isolated MAP kinase protein of the invention is provided, which is activated by an agent that induces a disease defense response in plants. The protein comprises certain structural features such as (1) kinase subdomains I through XI of serine/threonine kinases, the (2) an N-terminal amino acid sequence which is residues 1-24 of Sequence I.D. No. 2 herein; and (3) sequence I.D. No. 12 within serine/threonine kinase subdomain VIII. In a preferred embodiment, the protein possesses an amino acid sequence greater than 93% homologous to Sequence I.D. No. 2, and most preferably possesses Sequence I.D. No. 2.

For purposes of this invention, a "disease defense response" means an change in metabolism, biosynthetic activity or gene expression that enhances the plant's ability to suppress the replication and spread of a microbial pathogen (i.e., to resist the microbial pathogen). Plants exhibit disease defense responses by way of several signal transduction pathways, as described in greater detail herein. Some of these pathways are at least partially dependent on salicylic acid as a secondary defense signaling molecule.

In another aspect of the invention, an isolated MAP kinase protein is provided which is activated by an agent that induces a disease defense response in plants by way of a signal transduction pathway that is at least partially dependent on salicylic acid as the secondary signaling defense molecule. Preferably, the protein is produced by a method comprising (1) exposing plant cells to an amount of salicylic acid effective to activate the protein to exhibit its kinase activity, (2) identifying the protein exhibiting the kinase activity, and (3) isolating the protein from the plant cells.

According to another aspect of the invention, an isolated protein having Sequence I.D. No. 2 is provided.

According to another aspect of the invention, there is provided a polypeptide produced by expression of an isolated nucleic acid sequence selected from: (a) Sequence I.D. No. 1; (b) an allelic variant of Sequence I.D. No. 1; (c) a natural mutant of Sequence I.D. No. 1; (d) a sequence hybridizing with part or all of a sequence complementary to Sequence I.D. No. 1 and encoding a polypeptide substantially the same as part or all of a polypeptide encoded by sequence I.D. No. 1; and (e) a sequence encoding part or all of a polypeptide having amino acid sequence I.D. No. 2.

According to another aspect of the invention, antibodies are provided that are immunologically specific for part or all of the proteins of the invention.

In yet another aspect of the present invention, an isolated nucleic acid molecule is provided, which includes an open reading frame encoding a MAP kinase protein that comprises kinase subdomains I through XI of serine/threonine kinases, the protein having an N-terminal amino acid sequence which is residues 1-24 of Sequence I.D. No. 2 herein and further comprising sequence I.D. No. 12 within serine/threonine kinase subdomain VIII, the protein also being activated by an agent that induces a disease defense response in plants. The nucleic acid molecule may be genomic DNA, cDNA or RNA. The open reading frame preferably encodes a protein having greater than 93% sequence homology with sequence I.D. No. 2.

According to yet another aspect of the invention, an isolated nucleic acid molecule is provided, which has a sequence selected from: (a) Sequence I.D. No. 1; (b) an allelic variant of Sequence I.D. No. 1; (c) a natural mutant of Sequence I.D. No. 1; (d) a sequence hybridizing with part or all of a sequence complementary to Sequence I.D. No. 1 and encoding a polypeptide substantially the same as part or all of a polypeptide encoded by sequence I.D. No. 1; and (e) a sequence encoding part or all of a polypeptide having amino acid sequence I.D. No. 2.

Also provided in accordance with the invention are oligonucleotides that specifically hybridize with the nucleic acid sequences set forth above, and recombinant DNA molecules comprising the nucleic acid molecules set forth above, operably linked to a vector.

According to yet another aspect of the invention, plant cells transformed with the aforementioned recombinant DNA molecules are provided. Transgenic plants comprising those recombinant DNA molecules are also provided.

The new MAP kinase described in greater detail below may play a key role in signal transduction for activation of plant defenses against microbial pathogens. Accordingly, the novel nucleic acid molecules, proteins, antibodies, plant cells and plants of the invention offer a significant advance in the field of plant molecular biology, as it pertains to enhancing the plant disease resistance response.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1A-1E are a series of autoradiographs and two graphs illustrating the phosphorylation events catalyzed by the SA-induced protein (SIP) kinase of the present invention. The results presented indicate that salicylic acid activates a 48 kDa kinase which preferentially uses myelin basic protein (MBP) as a substrate. Tobacco suspension culture cells were treated by addition of either 250 .mu.M of SA (FIG. 1A) or an equal volume of water (FIG. 1B) as a negative control. Aliquots of each culture were taken at the indicated times, and kinase activity in total cell extracts was tested with an in-gel kinase activity assay using MBP as a substrate. In FIG. 1C, the same extracts from SA- or water-treated cells were tested using casein as a substrate. Only the results from SA-treated cells are shown. The position of the p48 SIP kinase is indicated by an asterisk (*). Molecular mass markers at left are given in kDa. In FIG. 1D, the p48 SIP kinase activities (.circle-solid., SA-treated; .largecircle., water-treated) were quantitated using a phosphoimager and the relative activities were plotted against time. Kinase activities were normalized to the level present at the zero time point, which was assigned a value of 1. In FIG. 1E, the dose response of p48 SIP kinase activation in tobacco suspension cells was plotted. Cells were treated with different concentrations of SA. Aliquots of culture were taken at 0 (before treatment) and 5 min, and p48 SIP kinase activities were assayed using myelin basic protein (MBP) as a substrate. Data presented are fold of induction relative to the basal kinase activity at time zero. Data presented in all panels described above are from one of at least three independent experiments with similar results.

FIG. 2 is an autoradiograph illustrating that only biologically active analogues of SA activate the p48 SIP kinase. Cells were treated with 250 .mu.M of SA or its analogues, 4-chloroSA (4-CSA), 5-CSA, 3-hydroxybenzoic acid (3-HBA), and 4-HBA for 5 minutes. Total cell extracts were prepared, and kinase activities were assayed using MBP as a substrate. The asterisk (*) indicates the position of the p48 SIP kinase. Molecular mass markers at left are given in kDa.

FIG. 3 is an autoradiograph illustrating that hydrogen peroxide treatment activates several kinases, including the p48 SIP kinase. Cells were treated with different concentrations of H.sub.2 O.sub.2 for varying lengths of time as indicated. Total cell extracts were prepared and kinase activities were assayed using MBP as a substrate. The asterisk (*) indicates the position of the p48 SIP kinase. Molecular mass markers at left are given in kilodaltons. With a long exposure of the autoradiogram, two weakly induced kinase activity bands were also detected at 200 kDa and 75 kDa.

FIGS. 4A and 4B are a pair of autoradiographs showing that activation of the p48 SIP kinase by SA or H.sub.2 O.sub.2 is associated with phosphorylation of tyrosine residues in the kinase. In FIG. 4A, extracts prepared from cells treated with 250 .mu.M SA or 2 mM H.sub.2 O.sub.2 for 10 minutes or 30 minutes were separated on a 10% SDS-PAGE gel. Proteins were then transferred to nitrocellulose membranes and phosphotyrosine-containing proteins were detected by immunoblot analysis using the phosphotyrosine-specific monoclonal antibody 4G10. The band corresponding to the p48 SIP kinase is marked with an asterisk (*) while bands corresponding to other proteins of 58 kDa, 52 kDa, and 40 kDa are marked with a dot (.cndot.). In FIG. 4B, phosphorylation of tyrosine residues of the p48 SIP kinase was confirmed and the specificity of the phosphotyrosine monoclonal antibody 4G10 was tested by immunoprecipitation coupled with the in-gel kinase activity assay. Phosphotyrosine-containing proteins in total cell extracts were immunoprecipitated with 4G10 in the absence of competitor (lanes 1 to 6) or in the presence of 1 mM of either phosphoserine (P-Ser, lanes 7 and 10), phosphothreonine (P-Thr, lanes 8 and 11), or phosphotyrosine (P-Tyr, lanes 9 and 12). Kinase activities in the complexes were determined using the in-gel kinase assay. When the 4G10 antibody was omitted from the precipitation reaction, no kinase activity was precipitated from the protein extracts. Molecular mass markers at left are given in kDa.

FIGS. 5A-5D are a pair of autoradiographs and a pair of graphs showing the induction of p48 SIP kinase following injection of tobacco leaves with SA and/or water. In FIG. 5A tobacco leaves were injected with either 500 .mu.M SA or water. At the indicated times leaf discs were taken and total protein extracts were prepared. Kinase activities were monitored with MBP as a substrate. FIG. 5B shows the results of a double injection experiment in which tobacco leaves were first injected with water and 4 hours later the same leaves were injected with either SA or water. Leaf discs were taken at the indicated times and kinase activities were assayed. In FIG. 5C, quantitation of the p48 kinase activities shown in FIG. 5A were performed with a phosphoimager (.circle-solid., SA injected; .largecircle., water injected). Kinase activities were normalized to the level detected at zero time, which was assigned a value of 1. In FIG. 5D the 48 kDa kinase activities shown in FIG. 5B were quantitated with a phosphoimager (.circle-solid., second injection was SA; .largecircle., second injection was water). The slightly lower band of kinase activity seen in FIG. 5A and FIG. 5B at about 44 kDa (compare FIG. 6), which is poorly resolved from 48 kDa kinase, was not included in quantitation for FIGS. 5C and 5D. Arrows indicate the time of injection.

FIGS. 6A-6C depict a pair of autoradiographs, and graph showing that TMV infection of tobacco induces the p48 SIP kinase, along with a p44 kinase. Tobacco leaves were either inoculated with TMV, see FIG. 6A, or mock inoculated, see FIG. 6B. After 48 hours at 32.degree. C. tobacco plants were shifted to 22.degree. C. and leaf discs were collected at the indicated times post shift. Total protein extracts were prepared and kinase activities were assayed with MBP as a substrate. In FIG. 6C, quantitation of p48 SIP kinase activities (.circle-solid., TMV inoculated; .largecircle., mock inoculated) and 44 kDa kinase activities (.tangle-solidup., TMV inoculated; .DELTA., mock inoculated) shown in FIG. 6A and FIG. 6B was performed with a phosphoimager. Kinase activities were normalized to the level of the p48 kinase present at zero time, which was assigned a value of 1. The position of the p48 SIP kinase is denoted with an asterisk (*) while that of the 44 kDa kinase is marked with a dot (.cndot.). Molecular mass markers at left are given in kDa.

FIGS. 7A-7F depict elution profiles of protein concentration (A.sub.280 nm) and kinase activity from each chromatography step in the purification of tobacco SIP kinase, as follows: Q-Sepharose anion exchange column (FIG. 7A); Phenyl-Sepharose HP hydrophobic interaction column (FIG. 7B); MonoQ HR 5/5 anion exchange fast protein liquid chromatography column (FIG. 7C); MBP-Sepharose affinity column (FIG. 7D); Poly-L-lysine-agarose column (FIG. 7E); and Superdex 200 HR 10/30 gel filtration fast protein liquid chromatography column (FIG. 7F). The position of the molecular mass markers in kDa is indicated at the top. Dashed lines indicate the NaCl gradient profiles (as described in Example 2), except in FIG. 7B, where it represents the ethylene glycol gradient. The kinase activity (.circle-solid.) was determined by the in-solution kinase assay, with MBP as substrate.

FIGS. 8A and 8B show an elution profile (FIG. 8A) and kinase activity gel (FIG. 8B) illustrating that the major MBP kinase peak eluted from the Q-Sepharose column corresponds to the p48 SIP kinase. FIG. 8A: after the ultracentrifugation step, protein samples prepared simultaneously from either SA-treated cells (.circle-solid.) or control water-treated cells (.largecircle.) were loaded onto a HiTrapQ column connected to a fast protein liquid chromatography system. The column was then eluted with a NaCl gradient, depicted by the dashed lines. Kinase activity was determined by the in-solution kinase assay, using MBP as substrate. FIG. 8B: selected fractions from the HiTrapQ column chromatography of the protein sample from SA-treated cells were assayed by the in-gel kinase method, with MBP as the substrate. The position of the molecular mass markers in kDa is indicated at left.

FIGS. 9A-9C show analyses of protein composition (FIG. 9A), the size of the purified kinase (FIG. 9B) and phosphotyrosine-containing polypeptides at different purification steps (FIG. 9C). FIG. 9A: for protein composition analysis, an aliquot of protein sample from each step of the purification was separated on a 10% SDS-polyacrylamide gel and stained with Coomassie blue. Lane 1 contains the 10-kDa size marker (Gibco BRL); lane 2, crude extract (20 .mu.g); lane 3, 0 to 30% ammonium sulfate fraction (10 .mu.g); lane 4, supernatant after 130,000 g ultracentrifugation (10 .mu.g); lane 5, pooled fractions from the Q-Sepharose column (5 .mu.g); lane 6, pooled fractions from the phenyl-Sepharose column (5 .mu.g); lane 7, pooled fractions from the MonoQ HR 5/5 column (2.5 .mu.g); lane 8, pooled fractions from the MBP-Sepharose affinity column (1 .mu.g); lane 9, pooled fractions from the poly-L-lysine agarose (1 .mu.g); and lane 10, pooled fractions from the Superdex 200 HR 10/30 column (0.5 .mu.g). The position of molecular mass markers in kDa is indicated at left. FIG. 9B: to determine the size of the purified enzyme, 1 unit was loaded on a 10% SDS-polyacrylamide gel embedded with MBP, and the kinase activity was detected by using an in-gel assay. FIG. 9C: For analysis of phosphotyrosine-containing proteins, samples from each purification step were subjected to SDS-PAGE, blotted, and probed with anti-phosphotyrosine monoclonal antibody 4G10. Lane 1 contains crude extract (5 .mu.g); lane 2, 0 to 30% ammonium sulfate fraction (5 .mu.g); lane 3, supernatant after 130,000 g ultracentrifugation (5 .mu.g); lane 4, pooled fractions from the Q-Sepharose column (5 .mu.g); lane 5, pooled fractions from the phenyl-Sepharose column (1 .mu.g); lane 6, pooled fractions from the MonoQ HR 5/5 column (0.5 .mu.g); lane 7, pooled fractions from the MBP-Sepharose affinity column (5 units, .about.47 ng); lane 8, pooled fractions from the poly-L-lysine agarose (5 units, .about.29 ng); and lane 9, pooled fractions from the Superdex 200 HR 10/30 column (5 units, .about.15 ng).

FIGS. 10A and 10B show a pair of graphs illustrating the effect of pH (FIG. 10A), Mg.sup.2+ and Mn.sup.2+ (FIG. 10B) on p48 SIP kinase activity. Approximately 0.5 unit of partially purified enzyme was used in each test. Buffers used for measuring the effect of pH were 50 mM 2-[N-morpholino]ethanesulfonic acid (Mes, pH 5.0-8.0, .circle-solid.), 50 mM Tris (pH 6.0-9.5, .tangle-solidup.), and 50 mM 3-[cyclohexylamino]-1-propanesulfonic acid (Caps, pH 9.0-12.0, .box-solid.). For testing the effects of Mg.sup.2+ (.circle-solid.), and Mn.sup.2+ (.tangle-solidup.), buffer B from the last purification step was first exchanged to Mg.sup.2+ -free buffer using a desalting column. Mg.sup.2+ was not added in reactions for testing the effect of Mn.sup.2+.

FIG. 11 is a graph depicting the protein substrate preference of the p48 SIP kinase. About 0.5 unit of partially purified enzyme was used in each reaction. The assay conditions were as described below in Example 1, except various concentrations of MBP (.circle-solid.), histone (.tangle-solidup.), and casein (.box-solid.) were used.

FIG. 12 is an autoradiograph identifying the amino acid phosphorylated by the p48 SIP kinase in MBP. Two and one-half units of partially purified p48 SIP kinase were used to phosphorylate MBP under standard conditions. The reaction was stopped by the addition of 1/10 volume of 100% trichloroacetic acid (TCA). After incubation on ice for 30 minutes, the precipitated protein was collected by centrifugation, and washed with 10% TCA and ethanol. The protein was acid hydrolyzed, and the phospho-amino acid was detected as described below in Example 2.

FIG. 13 is a histogram showing inactivation of p48 SIP kinase by phosphatase treatment. Approximately 20 units of the SIP kinase was treated with either the serine/threonine-specific phosphatase PPI (0.1 units) or the tyrosine-specific protein phosphatase YOP (0.5 units) for 10 min (bars 2 to 5) or 30 min (bars 7 to 10) at 30.degree. C. in the presence or absence of a phosphatase inhibitor. Bars 1 and 6 represent the control without phosphatase or phosphatase inhibitor; bars 2 and 7, PPI; bars 3 and 8, PPI plus okadaic acid (1 .mu.M); bars 4 and 9, YOP; bars 5 and 10, YOP plus Na.sub.3 VO.sub.4 (1 mM). Before assaying for SIP kinase activity, the phosphatase inhibitors were added to all of the reactions to the same final concentrations.

FIG. 14 illustrates an alignment of the deduced amino acid sequence of the SIP kinase (SIPK) with other members of the tobacco MAP kinase family, as well as stress-related MAP kinases from other plants. The amino acid sequences of Ntf3, Ntf4, Ntf6 (Wilson et al., 1993, 1995) and WIPK (Seo et al., 1995) from tobacco, MsK7 (Duerr et al., 1993; Jonak et al., 1993) and MMK4 (Jonak et al., 1996) from alfalfa, and AtMPK3 (Mizoguchi et al., 1993) from Arabidopsis were deduced from cDNA sequences. Numbers within parentheses indicate the percentage of identity to the SIP kinase. Dots represent amino acid residues that match the SIP kinase, and dashes indicate gaps introduced to maximize alignment. The conserved TEY phosphorylation motif for MAP kinase in underlined. The unique proline residue in the conserved kinase subdomain VIII of SIP kinase is marked with an asterisk. Roman numerals indicate the 11 major conserved subdomains of serine/threonine protein kinases. The six peptide sequences obtained by miscrosequencing are shown on top of the SIP kinase sequence. The boundary between peptides 5 and 6 is indicated by a vertical line.

DETAILED DESCRIPTION OF THE INVENTION

The present invention is directed to a novel protein kinase isolated from plants which is rapidly and transiently activated by salicylic acid, as well as by hydrogen peroxide or infection with tobacco mosaic virus (TMV). Transgenic plants with altered expression of this kinase are expected to demonstrate enhanced disease resistance to certain pathogens. The novel protein kinase of the present invention is sometimes referred to herein as "SIP kinase" or "p48 SIP kinase" to denote its novel functional features (activatable by agents, such as SA, that induce a resistance response) and approximate molecular weight as isolated from tobacco.

I. Definitions

Various terms relating to the biological molecules of the present invention are used hereinabove and also throughout the specifications and claims. The terms "substantially the same," "percent similarity" and "percent identity" are defined in detail below.

With reference to nucleic acids of the invention, the term "isolated nucleic acid" is sometimes used. This term, when applied to DNA, refers to a DNA molecule that is separated from sequences with which it is immediately contiguous (in the 5' and 3' directions) in the naturally occurring genome of the organism from which it was derived. For example, the "isolated nucleic acid" may comprise a DNA molecule inserted into a vector, such as a plasmid or virus vector, or integrated into the genomic DNA of a procaryote or eucaryote. An "isolated nucleic acid molecule" may also comprise a cDNA molecule.

With respect to RNA molecules of the invention the term "isolated nucleic acid" primarily refers to an RNA molecule encoded by an isolated DNA molecule as defined above. Alternatively, the term may refer to an RNA molecule that has been sufficiently separated from RNA molecules with which it would be associated in its natural state (i.e., in cells or tissues), such that it exists in a "substantially pure" form (the term "substantially pure" is defined below).

With respect to protein, the term "isolated protein" or "isolated and purified protein" is sometimes used herein. This term refers primarily to a protein produced by expression of an isolated nucleic acid molecule of the invention. Alternatively, this term may refer to a protein which has been sufficiently separated from other proteins with which it would naturally be associated, so as to exist in "substantially pure" form.

The term "substantially pure" refers to a preparation comprising at least 50-60% by weight the compound of interest (e.g., nucleic acid, oligonucleotide, protein, etc.). More preferably, the preparation comprises at least 75% by weight, and most preferably 90-99% by weight, the compound of interest. Purity is measured by methods appropriate for the compound of interest (e.g. chromatographic methods, agarose or polyacrylamide gel electrophoresis, HPLC analysis, and the like).

With respect to antibodies of the invention, the term "immunologically specific" refers to antibodies that bind to one or more epitopes of a protein of interest (e.g., SIP kinase), but which do not substantially recognize and bind other molecules in a sample containing a mixed population of antigenic biological molecules.

With respect to oligonucleotides, the term "specifically hybridizing" refers to the association between two single-stranded nucleotide molecules of sufficiently complementary sequence to permit such hybridization under pre-determined conditions generally used in the art (sometimes termed "substantially complementary"). In particular, the term refers to hybridization of an oligonucleotide with a substantially complementary sequence contained within a single-stranded DNA or RNA molecule of the invention, to the substantial exclusion of hybridization of the oligonucleotide with single-stranded nucleic acids of non-complementary sequence.

The term "pathogen-inoculated" refers to the inoculation of a plant with a pathogen.

The term "promoter region" refers to the 5' regulatory regions of a gene. In the present invention, the use of CaMV 35S gene promoters and/or tetracycline repressor/operator gene promoters is contemplated.

The term "selectable" marker gene refers to a gene product that when expressed confers a selectable phenotype such as antibiotic resistance on a transformed cell or plant.

The term "operably linked" means that the regulatory sequences necessary for expression of the coding sequence are placed in the DNA molecule in the appropriate positions relative to the coding sequence so as to effect expression of the coding sequence. This same definition is sometimes applied to the arrangement of transcription units and other transcription control elements (e.g. enhancers) in an expression vector.

The term "DNA construct" refers to genetic sequence used to transform plants and generate progeny transgenic plants. These constructs may be administered to plants in a viral or plasmid vector. Other methods of delivery such as Agrobacterium T-DNA mediated transformation and transformation using the biolistic process are also contemplated to be within the scope of the present invention. The transforming DNA may be prepared according to standard protocols such as those set forth in "Current Protocols in Molecular Biology", eds. Frederick M. Ausubel et al., John Wiley & Sons, 1995.

II. Characterization of SA-Induced MAP Kinase (SIP Kinase)

Numerous studies have demonstrated that SA is an endogenous signal for the activation of several plant defense responses, including the synthesis of PR proteins (Klessig and Malamy, 1994; Ryals et al., 1994, 1996). However, many of the components in the SA signal transduction pathway remain to be elucidated. It has now been discovered in accordance with the present invention that a plant protein kinase of about 48 kDa in molecular weight is rapidly activated by treatment with SA.

The activation of p48 SIP kinase by SA was rapid and transient, with activity returning to basal levels within 45 minutes after stimulation. A second addition of SA at up to 4 hr after the initial treatment did not reactivate the SIP kinase, suggesting that the activation pathway was desensitized. Without the invention being limited by any proposed mechanism, it is possible that a negative regulatory loop is responsible for the transient nature of the activation and the subsequent refractory period. In mammalian systems, inactivation of MAP kinases is performed by a dual specificity protein (MAP kinase phosphatases), which simultaneously dephosphorylate both the threonine and tyrosine residues of MAP kinases with high efficiency (Keyse, 1995; Groom et al., 1996). Transcription of these MAP kinase phosphatases is quickly activated by the MAP kinase signaling pathway (Bokemeyer et al., 1996).

Several kinases were activated in cells exposed to exogenous H.sub.2 O.sub.2. See FIG. 3. In addition, at least four proteins were phosphorylated on tyrosine residues in response to H.sub.2 O.sub.2. See FIG. 4. Using immunoprecipitation coupled with an in-gel kinase assay, it was demonstrated that one of these proteins is the p48 SIP kinase. The sizes of the other H.sub.2 O.sub.2 -activated kinases (58 kDa, 52 kDa and 40 kDa) as shown in FIG. 3, were consistent with those of tyrosine phosphorylated proteins; however in contrast to the SIP kinase, they were not immunoprecipitable with the anti-phosphotyrosine antibody.

The mechanism by which SA activates the p48 SIP kinase has not yet been fully elucidated. However, without being limited by the following hypothesis, it is believed that, since SA can inhibit the two major H.sub.2 O.sub.2 -scavenging enzymes (Chen et al., 1993; Durner and Klessig, 1995) and generate radicals (Durner and Klessig 1996), as well as function as an antioxidant (Halliwell et al., 1995), it may activate the SIP kinase by altering the redox status of the cell.

The p48 SIP kinase can be activated by TMV infection. The TMV-induced elevation in p48 SIP kinase activity correlates with increases in endogenous SA levels. Thus, this p48 SA-inducible kinase is involved in the signaling pathway that regulates the induction of certain defense responses after pathogen attack.

Several lines of evidence indicate that the SIP kinase of the invention is a member of the MAP kinase family: (1) activation of the SIP kinase is associated with phosphorylation of a tyrosine residue(s); (2) the SIP kinase preferentially phosphorylates the myelin basic protein (MBP); (3) the SIP kinase is unable to use GTP as a phosphate donor; (4) the SIP kinase lacks a calcium requirement for activity; and (5) the size of the SIP kinase (about 48 kDa as isolated from tobacco) is within the 38 to 55 kDa size range of known members of the MAP kinase family from many organisms (Seger and Krebs, 1995).

To confirm that the SIP kinase is indeed a novel MAP kinase, the kinase was purified and the amino acid sequence of several tryptic peptides were used to isolate its encoding cDNA. The nucleotide and deduced amino acid sequence of the SIP kinase-encoding cDNA exhibits high homology to other cloned MAP kinases, particularly the tobacco Ntf4 MAP kinase. Furthermore, SIP kinase contains the TEY phosphorylation sequence and conserved kinase catalytic domain associated with serine/threonine kinases. However, SIP kinase possesses a unique amino-terminal sequence, as well as a proline in place of alanine in the conserved kinase subdomain VIII (see FIG. 14). All other MAP kinases cloned from plants, yeast and mammals have an alanine at this position. Thus, SIP kinase clearly is a new member of the MAP kinase family.

A tobacco clone that encodes an exemplary SIP kinase of the invention is described in detail herein. The nucleotide sequence of a cDNA encoding tobacco SIP kinase is set forth below as Sequence I.D. No. 1. It is believed that Sequence I.D. No. 1 constitutes a full-length SIP kinase-encoding clone as it contains a suitable methionine for initiation of translation. Furthermore, expression of this cDNA in E. coli results in production of a protein that phosphorylates MBP (note MAP kinases have low basal phosphorylation activity in the absence of their activation by the MAP kinase kinases).

The tobacco SIP kinase cDNA shown below is approximately 1.54 kb in length.

Sequence I.D. No. 1 (5' .fwdarw. 3'): - CACAATTCCA CATATTCATT GACATACTAC GGCCCTTCTT - CCCTAATTTT AAGACAAAGG AAAAAAAGTA ATTATTGATT - CTTCTAGGAT TTACAATTTT TGTTGACGAA TTTTCCAAAA - AAAAAAATAT GGATGGTTCT GGTCAGCAGA CGGACACGAT - GATGTCTGAT GCGGGGGCGG AGCAGCCACC TACGGCGCCG - CAGCCGGTGG CCGGTATGGA TAATATTCCG GCGACGTTGA - GCCACGGTGG CAGGTTCATT CAATACAATA TATTTGGTAA - TATATTTGAA GTTACTGCTA AATATAAGCC TCCTATTTTG - CCTATTGGTA AAGGTGCTTA CGGCATCGTT TGTTCTGCTT - TGAACTCGGA GACAATTGAG AACGTAGCGA TAAAGAAAAT - CGCAAATGCT TTTGATAACA AGATTGATGC CAAGAGGACT - TTGAGAGAGA TCAAGCTTCT TCGGCATATG GATCATGAAA - ACATTGTTGC GATCAGAGAT ATAATTCCAC CACCACAGAG - AGAGGCCTTT AATGATGTTT ATATTGCGTA TGAGCTTATG - GATACTGATC TCCATCAAAT TATTCGCTCT AATCAGGGTT - TATCTGAGGA GCACTGTCAG TATTTCTTGT ATCAGATCCT - CCGAGGGTTG AAATACATAC ATTCTGCGAA TGTTCTGCAC - AGGGACTTGA AGCCTAGCAA TCTCCTGTTG AATGCCAACT - GTGATTTAAA GATATGTGAT TTTGGGCTAG CTCGTGTCAC - TTCTGAAACT GACTTTATGA CGGAATATGT TGTGACAAGA - TGGTATCGTC CACCTGAGCT GTTGTTAAAT TCGTCTGACT - ATACTGCAGC AATTGACGTA TGGTCAGTGG GTTGCATTTT - CATGGAATTG ATGGACAGGA AACCCCTATT TCCTGGTAGA - GATCACGTAC ACCAGCTGCG TCTTATTATG GAGTTGATTG - GTACTCCTTC AGAGGCTGAA ATGGAGTTTT TAAATGAGAA - TGCAAAACGA TACATCCGCC AACTTCCTCT TTACCGTCGA - CAATCATTCA CTGAAAAGTT TCCACATGTA CACCCAACTG - CAATTGATCT TGTCGAGAAA ATGCTGACAT TTGATCCTAG - AAGGAGAATA ACAGTTGAAG GTGCACTTGC ACATCCTTAC - CTGAACTCGC TCCACGATAT TAGTGACGAG CCCATTTGCA - TGACTCCCTT TAGCTTCGAC TTTGAACAGC ATGcCCTTAC - GGAGGAACAG ATGAAGGAGC TGATTTACAG GGAGTCGCTT - GCATTTAATC CTGAATACCA GCATATGTGA ATAATTGCTG - GTAAGATTGT TGTCAGTTTG ATCTCCAACT GACAATTTGT - CCCTCCATGT ATATATGTGT GCACTTCGTC CGAAACACGG - ATGGCTTTCT TATGCAAACA CTTAGTTATG AAGCTGATTT - GTGTAAAGAA TTGTTTGATG TATCTGATGA GGTGGATCGC - TTGTATTGGT TCTGTTTTAA TTTACTGAAG TCATAGTGGA - CGAAAAAAAA AAAAAAAAAA AAAA

The amino acid sequence deduced from Sequence I.D. No. 1 is set forth herein as Sequence I.D. No. 2. Sequence I.D. No. 2 is shown in FIG. 14 aligned with amino acid sequences of other cloned MAP kinases. The corresponding Sequence I.D. Numbers are as follows: SIPK is Sequence I.D. No. 2 (as mentioned); Ntf4 is Sequence I.D. No. 3, Msk7 is Sequence I.D. No. 4; WIPK is Sequence I.D. No. 5, MMK4 is Sequence I.D. No. 6; AtMPK3 is Sequence I.D. No. 7; Ntf6 is Sequence I.D. No. 8; and Ntf3 is Sequence I.D. No. 9. FIG. 14 also shows the peptide fragments of purified tobacco SIP kinase obtained by tryptic digestion, as described in Example 2. The Sequence I.D. Numbers of these fragments are as follows: Peptide 1 is Sequence I.D. No. 10; Peptide 2 is Sequence I.D. No. 11, Peptide 3 is Sequence I.D. No. 12, Peptide 4 is sequence I.D. No. 13, Peptide 5 & 6 together are Sequence I.D. No. 14.

Although the tobacco SIP kinase is described and exemplified herein, this invention is intended to encompass nucleic acid sequences and proteins from other species that are sufficiently similar to be used interchangeably with tobacco SIP kinase-encoding nucleic acids and proteins for the purposes described below. Because of the high degree of conservation of genes encoding specific MAP kinases, it will be appreciated by those skilled in the art that SIP kinase-encoding nucleic acids from diverse species, and particularly higher plant species, should possess a sufficient degree of homology with tobacco SIP kinase so as to be interchangeably useful in various applications. The present invention, therefore, is drawn to SIP kinase-encoding nucleic acids and encoded proteins from any species in which they are found, preferably to SIP kinases of plant origin, and most preferably to SIP kinases of higher plant origin. Accordingly, when the terms "SIP kinase" and "p48 SIP kinase" are used herein, they are intended to encompass all SIP kinases falling within the confines of homology set forth below, of which tobacco SIP kinase is an exemplary member.

MAP kinases are activated post-translationally by phosphorylation. The SIP kinase of the invention is also unique in the manner by which it is activated (MAP kinases are activated post-translationally by phosphorylation, but the agents that trigger that activation differ among various MAP kinases). The tobacco SIP kinase exemplified herein is activated by SA, H.sub.2 O.sub.2, and TMV infection, all of which share a common feature of being agents that induce a disease defense response in plants (defined above in the Summary of the Invention). Accordingly, in the same manner that structural homologs of tobacco SIP kinase are considered to be within the scope of this invention, functional homologs, as pertains to activation of the kinase, are also considered to be within the scope of this invention. Such "activation" homologs include SIP kinases that are activated by a variety of agents known to induce a disease defense response in plants, preferably via the salicylic acid signal transduction pathway. Examples of plant disease defense responses include, but are not limited to, production of low molecular weight compounds with antimicrobial activity (referred to as phytoalexins) and induction of expression of defense (or defense-related) genes, whose products include, for example, peroxidases, cell wall proteins, proteinase inhibitors, hydrolytic enzymes, pathogenesis-related (PR) proteins and phytoalexin biosynthetic enzymes, such as phenylalanine ammonia lyase and chalcone synthase (Dempsey and Klessig, 1995). Such defense responses appear to be induced in plants by several signal transduction pathways involving secondary defense signaling molecules produced in plants (see below). Certain of these defense response pathways are SA dependent, while others are partially SA dependent and still others are SA independent. For this reason, the SIP kinases of the present invention preferably are activated by agents which induce a disease defense response via the SA signal transduction pathway in plants.

Agents that induce disease defense responses in plants include, but are not limited to: (1) microbial pathogens, such as fungi, bacteria and viruses; (2) microbial components and other defense response elicitors, such as proteins and protein fragments, small peptides, .beta.-glucans, elicitins and harpins (see Benhamou, 1996), cryptogein (see Ricci et al., 1989) and oligosaccharides (see John et al., 1997); and (3) secondary defense signaling molecules produced by the plant, such as SA, H.sub.2 O.sub.2, ethylene and jasmonates (see Yang et al., 1997).

Allelic variants and natural mutants of Sequence I.D. No. 1 are likely to exist within the plant genome and within the genomes of other species. Because such variants are expected to possess certain differences in nucleotide and amino acid sequence, this invention provides an isolated SIP kinase-encoding nucleic acid molecule having at least about 75% (and preferably over 80%) sequence homology in the coding region with the nucleotide sequence set forth as Sequence I.D. No. 1 (and, most preferably, specifically comprising the coding region of sequence I.D. No. 1). This invention also provides an isolated SIP kinase having at least about 93% (preferably 95% or greater) sequence homology with the amino acid sequence of Sequence I.D. No. 2. Because of the natural sequence variation likely to exist among SIP kinases and nucleic acids encoding them, one skilled in the art would expect to find up to about 25-30% nucleotide sequence variation, while still maintaining the unique properties of the SIP kinase of the present invention. Such an expectation is due in part to the degeneracy of the genetic code, as well as to the known evolutionary success of conservative amino acid sequence variations, which do not appreciably alter the nature of the protein. Accordingly, such variants are considered substantially the same as one another and are included within the scope of the present invention.

For purposes of this invention, the term "substantially the same" refers to nucleic acid or amino acid sequences having sequence variation that do not materially affect the nature of the protein (i.e. its activation by pathogens or other agents, such as SA, that induce plant defense responses, such as PR gene expression, its structure and/or biological activity). With particular reference to nucleic acid sequences, the term "substantially the same" is intended to refer to the coding region and to conserved sequences governing expression, and refers primarily to degenerate codons encoding the same amino acid, or alternate codons encoding conservative substitute amino acids in the encoded polypeptide. With reference to amino acid sequences, the term "substantially the same" refers generally to conservative substitutions and/or variations in regions of the polypeptide not involved in determination of structure, function or activation by disease resistance-inducing pathogens or agents (e.g., SA). The terms "percent identity" and "percent similarity" are also used herein in comparisons among amino acid sequences. These terms are intended to be defined as they are in the UWGCG sequence analysis program (Devereaux et al., Nucl. Acids Res. 12: 387-397, 1984), available from the University of Wisconsin.

The following description sets forth the general procedures involved in practicing the present invention. To the extent that specific materials are mentioned, it is merely for purposes of illustration and is not intended to limit the invention. Unless otherwise specified, general cloning procedures, such as those set forth in Sambrook et al., Molecular Cloning, Cold Spring Harbor Laboratory (1989) (hereinafter "Sambrook et al.") are used.

III. Preparation of SIP Kinase-Encoding Nucleic Acid Molecules, SIP Kinase Protein and Antibodies Against SIP Kinase

A. Nucleic Acid Molecules

Nucleic acid molecules encoding the SIP kinase of the invention may be prepared by two general methods: (1) They may be synthesized from appropriate nucleotide triphosphates, or (2) they may be isolated from biological sources. Both methods utilize protocols well known in the art.

The availability of nucleotide sequence information, such as the full length cDNA having Sequence I.D. No. 1, enables preparation of an isolated nucleic acid molecule of the invention by oligonucleotide synthesis. Synthetic oligonucleotides may be prepared by the phosphoramadite method employed in the Applied Biosystems 38A DNA Synthesizer or similar devices. The resultant construct may be purified according to methods known in the art, such as high performance liquid chromatography (HPLC). Long, double-stranded polynucleotides, such as a DNA molecule of the present invention, must be synthesized in stages, due to the size limitations inherent in current oligonucleotide synthetic methods. Thus, for example, a 1.54 kb double-stranded molecule may be synthesized as several smaller segments of appropriate complementarity. Complementary segments thus produced may be annealed such that each segment possesses appropriate cohesive termini for attachment of an adjacent segment. Adjacent segments may be ligated by annealing cohesive termini in the presence of DNA ligase to construct an entire 1.54 kb double-stranded molecule. A synthetic DNA molecule so constructed may then be cloned and amplified in an appropriate vector.

Nucleic acid sequences encoding SIP kinase may be isolated from appropriate biological sources using methods known in the art. In a preferred embodiment, a cDNA clone is isolated from a tobacco cDNA library. In an alternative embodiment, genomic clones encoding SIP kinase may be isolated. Alternatively, cDNA or genomic clones encoding SIP kinase from other species, preferably higher plant species, may be obtained.

In accordance with the present invention, nucleic acids having the appropriate level sequence homology with the coding region of Sequence I.D. No. 1 may be identified by using hybridization and washing conditions of appropriate stringency. For example, hybridizations may be performed, according to the method of Sambrook et al., using a hybridization solution comprising: 5.times. SSC, 5.times. Denhardt's reagent, 1.0% SDS, 100 .mu.g/ml denatured, fragmented salmon sperm DNA, 0.05% sodium pyrophosphate and up to 50% formamide. Hybridization is carried out at 37-42.degree. C. for at least six hours. Following hybridization, filters are washed as follows: (1) 5 minutes at room temperature in 2.times. SSC and 1% SDS; (2) 15 minutes at room temperature in 2.times. SSC and 0.1% SDS; (3) 30 minutes-1 hour at 37.degree. C. in 1.times. SSC and 1% SDS; (4) 2 hours at 42-65.degree. in 1.times. SSC and 1% SDS, changing the solution every 30 minutes. Alternatively, the hybridization procedure described in Example 2 may be used.

Nucleic acids of the present invention may be maintained as DNA in any convenient cloning vector. In a preferred embodiment, clones are maintained in plasmid cloning/expression vector, such as pGEM-T (Promega Biotech, Madison, Wis.) or pBluescript (Stratagene, La Jolla, Calif.), either of which is propagated in a suitable E. coli host cell.

SIP kinase-encoding nucleic acid molecules of the invention include cDNA, genomic DNA, RNA, and fragments thereof which may be single- or double-stranded. Thus, this invention provides oligonucleotides (sense or antisense strands of DNA or RNA) having sequences capable of hybridizing with at least one sequence of a nucleic acid molecule of the present invention, such as selected segments of the cDNA having Sequence I.D. No. 1. Such oligonucleotides are useful as probes for detecting SIP kinase genes or mRNA in test samples of plant tissue or other biological sources, e.g. by PCR amplification, or for the positive or negative regulation of expression of SIP kinase genes at or before translation of the mRNA into proteins.

B. Proteins

A SIP kinase protein of the present invention may be prepared in a variety of ways, according to known methods. The protein may be purified from appropriate sources, e.g., cultured plant cells or tissues as described in detail in Examples 1 and 2. Those Examples describe the isolation of SIP kinase from cultured tobacco cell suspensions, followed by its purification to apparent homogeneity by ammonium sulfate fractionation, ultracentrifugation and six column chromatography steps.

Alternatively, the availability of nucleic acids molecules encoding SIP kinase enables production of the protein using in vitro expression methods known in the art. For example, a cDNA or gene may be cloned into an appropriate in vitro transcription vector, such a pSP64 or pSP65 for in vitro transcription, followed by cell-free translation in a suitable cell-free translation system, such as wheat germ or rabbit reticulocytes. In vitro transcription and translation systems are commercially available, e.g., from Promega Biotech, Madison, Wis. or BRL, Rockville, Md.

According to a preferred embodiment, larger quantities of SIP kinase may be produced by expression in a suitable procaryotic or eucaryotic system. For example, part or all of a DNA molecule, such as the cDNA having Sequence I.D. No. 1, may be inserted into a plasmid vector adapted for expression in a bacterial cell (such as E. coli) or a yeast cell (such as Saccharomyces cerevisiae), or into a baculovirus vector for expression in an insect cell. Such vectors comprise the regulatory elements necessary for expression of the DNA in the host cell, positioned in such a manner as to permit expression of the DNA in the host cell. Such regulatory elements required for expression include promoter sequences, transcription initiation sequences and, optionally, enhancer sequences.

The SIP kinase produced by gene expression in a recombinant procaryotic or eucyarotic system may be purified according to methods known in the art. In a preferred embodiment, a commercially available expression/secretion system can be used, whereby the recombinant protein is expressed and thereafter secreted from the host cell, to be easily purified from the surrounding medium. If expression/secretion vectors are not used, an alternative approach involves purifying the recombinant protein by affinity separation, such as by immunological interaction with antibodies that bind specifically to the recombinant protein. Such methods are commonly used by skilled practitioners.

The SIP kinase of the invention, prepared by the aforementioned methods, may be analyzed according to standard procedures. Methods for analyzing the physical characteristics and biological activity of SIP kinase are set forth in Examples 1 and 2.

The present invention also provides antibodies capable of immunospecifically binding to proteins of the invention. Polyclonal or monoclonal antibodies directed toward SIP kinase may be prepared according to standard methods. Monoclonal antibodies may be prepared according to general methods of Kohler and Milstein, following standard protocols.

In a preferred embodiment, antibodies are prepared, which react immunospecifically with various epitopes of SIP kinase. In a particularly preferred embodiment, polyclonal antibodies have been generated against each of two synthetic peptide corresponding to (1) the tobacco SIP kinase N-terminal sequence (residues 1-24 of Sequence I.D. No. 2; FIG. 14) or (2) the tobacco SIP kinase C-terminal sequence (residues 376-393 of Sequence I.D. No. 2; FIG. 14). The anti-N-terminus antibody was found to be immunologically specific for SIP kinase (it did not recognize Ntf4 or WIPK). The anti C-terminus antibody is immunologically specific for SIP kinase and for Ntf4, but does not recognize WIPK.

Polyclonal or monoclonal antibodies that immunospecifically interact with SIP kinase can be utilized for identifying and purifying such proteins. For example, antibodies may be utilized for affinity separation of proteins with which they immunospecifically interact. Antibodies may also be used to immunoprecipitate proteins from a sample containing a mixture of proteins and other biological molecules. Other uses of anti-SIP kinase antibodies are described below.

IV. Uses of SIP Kinase-Encoding Nucleic Acids, SIP Kinase Protein and Antibodies

The potential of recombinant genetic engineering methods to enhance disease resistance in agronomically important plants has received considerable attention in recent years. Protocols are currently available for the stable introduction of genes into plants, as well as for augmentation of gene expression. The present invention provides nucleic acid molecules which, upon stable introduction into a recipient plant, enhance the plant's ability to resist pathogen attack. SIP kinase proteins of the invention may also be used as a research tool to identify other proteins involved in the hypersensitive response and/or systemic acquired resistance response in plants.

A. SIP Kinase-Encoding Nucleic Acids

SIP kinase-encoding nucleic acids may be used for a variety of purposes in accordance with the present invention. SIP kinase-encoding DNA, RNA, or fragments thereof may be used as probes to detect the presence of and/or expression of genes encoding SIP kinase. Methods in which SIP kinase-encoding nucleic acids may be utilized as probes for such assays include, but are not limited to: (1) in situ hybridization; (2) Southern hybridization (3) northern hybridization; and (4) assorted amplification reactions such as polymerase chain reactions (PCR).

The SIP kinase-encoding nucleic acids of the invention may also be utilized as probes to identify related genes either from plants or from other species. As is well known in the art, hybridization stringencies may be adjusted to allow hybridization of nucleic acid probes with complementary sequences of varying degrees of homology. Thus, SIP kinase-encoding nucleic acids may be used to advantage to identify and characterize other genes of varying degrees of relation to SIP kinase, thereby enabling further characterization the signalling cascade involved in the disease resistance response in plants. Additionally, they may be used to identify genes encoding proteins that interact with SIP kinase (e.g., by the "interaction trap" technique), which should further accelerate elucidation of these cellular signalling mechanisms.

Nucleic acid molecules, or fragments thereof, encoding SIP kinase may also be utilized to control the production of SIP kinase, thereby regulating the amount of protein available to participate in disease resistance signalling pathways. Alterations in the physiological amount of SIP kinase may act synergistically with other agents used to protect plants during pathogen attack. In one embodiment, the nucleic acid molecules of the invention may be used to decrease expression of SIP kinase in plant cells. In this embodiment, full-length antisense molecules are employed which are targeted to SIP kinase, or antisense oligonucleotides, targeted to specific regions of SIP kinase-encoding genes that are critical for gene expression, are used. The use of antisense molecules to decrease expression levels of a pre-determined gene is known in the art. In a preferred embodiment, antisense oligonucleotides are modified in various ways to increase their stability and membrane permeability, so as to maximize their effective delivery to target cells in vitro and in vivo. Such modifications include the preparation of phosphorothioate or methylphosphonate derivatives, among many others, according to procedures known in the art.

In another embodiment, overexpression of SIP kinase is induced to generate a co-suppression effect. This excess expression serves to promote down-regulation of both endogenous and exogenous SIP kinase-encoding genes. Under other circumstances, overexpression can lead to overproduction of SIP kinase. Overproduction of SIP kinase in transgenic plants may be assessed by immunofluorescence or other standard techniques known in the art. Alternatively, overproduction of SIP kinase in transgenic plants or plant cells may facilitate the isolation and characterization of other components involved in protein-protein complex formation occurring during the disease resistance response in plants.

As described above, SIP kinase-encoding nucleic acids are also used to advantage to produce large quantities of substantially pure SIP kinase protein, or selected portions thereof.

B. SIP Kinase Protein and Antibodies

Purified SIP kinase, or fragments thereof, may be used to produce polyclonal or monoclonal antibodies which also may serve as sensitive detection reagents for the presence and accumulation of SIP kinase (or complexes containing SIP kinase) in cultured plant cells or tissues and in intact plants. Recombinant techniques enable expression of fusion proteins containing part or all of the SIP kinase protein. The full length protein or fragments of the protein may be used to advantage to generate an array of monoclonal or polyclonal antibodies specific for various epitopes of the protein, thereby providing even greater sensitivity for detection of the protein in cells or tissue.

Polyclonal or monoclonal antibodies immunologically specific for SIP kinase may be used in a variety of assays designed to detect and quantitate the protein. Such assays include, but are not limited to: (1) flow cytometric analysis; (2) immunochemical localization of SIP kinase in cultured cells or tissues; and (3) immunoblot analysis (e.g., dot blot, Western blot) of extracts from various cells and tissues. Additionally, as described above, anti-SIP kinase can be used for purification of SIP kinase (e.g., affinity column purification, immunoprecipitation).

C. Transgenic Plants

Transgenic plants constitutively expressing SIP kinase gene would be generated using standard transformation methods known to those skilled in the art. Presumably, these plants would have altered resistance to pathogens as the SIP kinase has been shown to be activated during a resistance response to TMV infection. The SIP kinase gene would be placed under a powerful constitutive promoter like the Cauliflower Mosaic Virus (CaMV) 35S promoter and introduced into plants using procedures such as Agrobacterium-mediated transformation. Expression of the kinase would be modified by ectopic, overexpression of the gene under control of the CaMV 35S promoter.

Alternatively SIP kinase expression would also be disrupted by the expression of the gene in an antisense orientation under the CaMV 35S promoter.

Transgenic plants expressing the SIP kinase gene under an inducible promoter are also contemplated to be within the scope of the present invention. Inducible plant promoters include the tetracycline repressor/operator controlled promoter.

Optionally, transgenic plants would be created containing mutations in the region encoding the active site of SIP kinase. This embodiment is preferred over the use of anti-sense constructs due to the very high homology between MAP kinases. For example, a mutated p48 SIP kinase with a Lys to Arg change in the kinase subdomain II has been made, and could be introduced into wild tobacco plants. This mutation would block the phosphate transfer from ATP to the protein substrate, thereby rendering the kinase permanently inactive (the Lys to Arg mutant SIP kinase produced in E. coli has lost the basal phosphorylation activity found with its wildtype counterpart recombinant protein). Since the mutant p48 kinase would still serve as the substrate for upstream MAP kinase kinase and physically compete with the wild-type p48 SIP kinase, but would not transduce signal to downstream components, it may be possible to specifically block the pathway without affecting other MAP kinase cascades.

From the foregoing discussion, it can be seen that SIP kinase-encoding nucleic acids and SIP kinase proteins and antibodies of the invention can be used to detect SIP kinase gene expression and protein accumulation for purposes of assessing the genetic and protein interactions involved in the plant disease resistance response. It is also anticipated that SIP kinase-encoding nucleic acid molecules and transgenic plants containing them will be useful for the regulation of the disease resistance pathway in plants and for enhancing resistance to plant pathogens.

The following examples are intended to illustrate embodiments of the invention. They are not intended to limit the scope of the invention in any way.

EXAMPLE I

IDENTIFICATION AND CHARACTERIZATION OF SIP KINASE FROM TOBACCO

This example describes the identification of SIP kinase protein from tobacco suspension cultures, and characterization of its activity.

MATERIALS AND METHODS

A. Treatment of Tobacco Cell Suspension Culture

The cell suspension culture was derived from callus tissue originated from leaves of Nicotiana tabacum cv Xanthi nc and grown in MS medium supplemented with 1 mg/L .alpha.-naphthaleneacetic acid, 0.1 mg/L 2,4-dichlorophenoxyacetic acid, 0.1 mg/L benzyladenine, and 3% sucrose. Log phase cells were used three days after a 1:10 dilution. Treatment with H.sub.2 O.sub.2, SA and its analogues was performed in the original flasks in the dark to avoid any stresses associated with transfer. At various times, 10 mL cells (approximately 0.2 to 0.3 g fresh weight of cells) were harvested by filtration. The cells were quickly frozen in liquid nitrogen and stored at -80.degree. C. until analysis.

B. Infection and Treatment of Tobacco Leaves

Tobacco plants (N. tabacum cv Xanthi nc) were grown at 22.degree. C. in a growth room programmed for a 14-hr light cycle. Plants approximately 7-8 weeks old were used for experiments. For temperature-shift experiments, plants were transferred to a 32.degree. C. chamber one day before inoculation. TMV strain U1 was used at a concentration of 1 .mu.g/mL in 50 mM phosphate buffer, pH 7.0; mock inoculation was done with buffer only. After 48 hours infected plants were shifted back to 22.degree. C. and leaf discs (1 cm in diameter) were taken at the indicated times. For water or SA treatment, one leaf from each plant was injected with solution using a syringe until the entire leaf was infiltrated. At various times, leaf discs were taken, quickly frozen in liquid nitrogen, and stored at -80.degree. C. until analysis.

C. Preparation of Protein Extracts

Leaf discs were first ground to a fine powder in 1.5 ml microcentrifuge tubes using small plastic pestles. After adding 0.25 mL extraction buffer (100 mM Hepes, pH 7.5, 5 mM EDTA, 5 mM EGTA, 10 mM DTT, 10 mM Na.sub.3 VO.sub.4, 10 mM NaF, 50 mM .beta.-glycerolphosphate, 1 mM phenylmethylsulfonyl fluoride, 5 .mu.g/mL antipain, 5 .mu.g/mL aprotinin, 5 .mu.g/mL leupeptin, 10% glycerol, 7.5% polyvinylpolypyrrolidone), the mixture was sonicated for 15 seconds with a W-375 Sonicator (Heat System-Ultrasonics, Inc., N.Y.) fitted with a microprobe at setting 4 and 80% duty cycle. To prepare extracts from treated cells, cells were mixed with two volumes (w/v) of extraction buffer and were then sonicated twice for 15 seconds each in 1.5 mL microcentrifuge tube. After centrifugation at 13,000 rpm for 20 minutes, supernatants were transferred into clean tubes, quickly frozen in liquid nitrogen and stored at -80.degree. C.

D. Protein Concentration Assay

The concentration of protein extracts was determined using the Bio-Rad protein assay kit (Bio-Rad, CA) according to manufacturer's instructions with BSA as standard.

E. In-gel Kinase Activity Assay

The in-gel kinase assay was performed as described previously (Zhang et al., 1993). Extracts containing 10 .mu.g protein were electrophoresed on 10% SDS-polyacrylamide gels imbedded with either 1 mg/mL of casein, 1 mg/mL histone (Type III-SS, Sigma, MO), 1 mg/mL BSA, or 0.25 mg/mL of MBP in the separating gel as substrate for the kinase. After electrophoresis, SDS was removed by washing the gel with washing buffer (25 mM Tris, pH 7.5, 0.5 mM DTT, 0.1 mM Na.sub.3 VO.sub.4, 5 mM NaF, 0.5 mg/mL BSA, 0.1% Triton X-100 [v/v]). The buffer was changed three times, each for 30 minutes at room temperature. The kinases were allowed to renature in 25 mM Tris, pH 7.5, 1 mM DTT, 0.1 mM Na.sub.3 VO.sub.4, 5 mM NaF at 4.degree. C. overnight with three changes of buffer. The gel was then incubated at room temperature in 30 mL reaction buffer (25 mM Tris, pH 7.5, 2 mM EGTA, 12 mM MgCl.sub.2, 1 mM DTT, 0.1 mM Na.sub.3 VO.sub.4) with 200 nM ATP plus 50 .mu.Ci .gamma.-.sup.32 P-ATP (3000 Ci/mmole) for 60 minutes. The reaction was stopped by transferring the gel into 5% TCA (w/v)/1% NaPPi (w/v). The unincorporated .gamma.-.sup.32 P-ATP was removed by washing in the same solution for at least 6 hours with 5 changes of buffer. The gel was dried onto 3 MM paper and exposed to Kodak XAR-5 film. Prestained size markers (Bio-Rad, CA) were used to calculate the size of the kinases. Quantitation of the relative kinase activities were done using a phosphoimager (Molecular Dynamics Inc., CA).

F. Immunoblot Analysis With Anti-phosphotyrosine Antibody

Protein extracts were separated by SDS-PAGE on 10% acrylamide gels, and the proteins were transferred to nitrocellulose membrane by semidry electroblotting. The membrane was blocked for 2 hours in TBS buffer (20 mM Tris, pH 7.5, 150 mM NaCl, 0.1% Tween 20, 0.1 mM Na.sub.3 VO.sub.4) with 10% BSA at room temperature, and then incubated with the phosphotyrosine-specific monoclonal antibody 4G10 (Upstate Biotechnology Incorporated, NY) in TBS buffer with BSA for 1 hr. After the blot was incubated with horseradish peroxidase-conjugated secondary antibody, the complexes were visualized using an enhanced chemiluminescence kit (DuPont, MA) following the manufacture's instructions.

G. Immunoprecipitation-kinase Activity Assay

Protein extract (50 .mu.g) with or without phospho-amino acid (1 mM final concentration) competitor was incubated with the 4G10 antibody in immunoprecipitation buffer (20 mM Tris, pH 7.5, 150 mM NaCl, 1 mM EDTA, 1 mM EGTA, 1 mM Na.sub.3 VO.sub.4, 1 mM NaF, 10 mM .beta.-glycerophosphate, 2 .mu.g/mL antipain, 2 .mu.g/mL aprotinin, 2 .mu.g/mL leupeptin, 0.5% Triton X-100, 0.5% Nonidet P-40) at 4.degree. C. for 4 hours on a rocker. About 25 .mu.L packed volume of protein A-agarose was added, and the incubation was continued for another 2 hours. Agarose bead-protein complexes were pelleted by brief centrifugation. After washing with immunoprecipitation buffer three times, 1.times. SDS sample buffer was added and the sample boiled for 3 minutes. After centrifugation, the supernatant fraction was electrophoresed on 10% SDS-PAGE gel, and the in-gel kinase assay was performed.

RESULTS

A. SA and its Biologically Active Analogues Induce a 48 kDa Protein Kinase.

Previous studies have demonstrated that in tobacco, both protein phosphorylation and dephosphorylation are required for the activation of the HR and PR gene expression in response to TMV infection or SA treatment (Conrath et al., 1997; Dunigan and Madlener, 1995). To search for the kinase(s) involved in the pathway, an in-gel kinase activity assay was utilized. Various kinase substrates, including casein, MBP, histone and BSA, were imbedded in the separating gel and kinase activities were tested under different reaction conditions. Treatment of tobacco suspension cells with 250 .mu.M SA activated a 48 kDa kinase that efficiently used MBP as an artificial substrate, as shown in FIG. 1A, while the same kinase was not activated by addition of water, as shown in FIG. 1B. This kinase is called the p48 SIP kinase for SA-induced protein kinase. Activation of the p48 SIP kinase was very rapid and transient, peaking within 5 minutes and returning to basal level in about 45 minutes, then decreasing further thereafter. See FIGS. 1A and 1D. The p48 SIP kinase activity in SA-treated cells increased from 15 to 25 fold in different experiments. The minimum concentration of SA required to activate this p48 kinase was 100 .mu.M under our experimental conditions, with maximum activity obtained at 500 .mu.M (FIG. 1E). When casein, histone, or BSA were used as the substrate, no increases in kinase activities were detected in extracts from SA-treated cells (only casein as substrate is shown in FIG. 1C).

To assess the biological relevance of SA induction of the p48 SIP kinase, analogues of SA were tested. Biologically active analogues of SA, such as 4-chloroSA (4-CSA) and 5-CSA (Conrath et al., 1995) which induce PR gene expression and enhanced disease resistance in tobacco, activated the SIP kinase to similar extents as SA at 250 .mu.M. See FIG. 2. However, both analogues induced a more sustained activation of the SIP kinase than SA (data not shown). This sustained activation may arise due to the inability of these cells to metabolize these compounds efficiently. In contrast, the biologically inactive analogues, 3-hydroxybenzoic acid (3-HBA) and 4-HBA, were poor activators of this kinase as shown in FIG. 2.

B. Hydrogen Peroxide Activates the p48 SIP Kinase, as Well as Several Other Kinases

Since H.sub.2 O.sub.2 is implicated in both the action of SA (Chen et al., 1993) and several defense responses of plants against pathogens (Mehdy, 1994; Levine et al., 1994), the effect of H.sub.2 O.sub.2 on SIP kinase activity was also examined. As shown in FIG. 3, H.sub.2 O.sub.2 at 1 mM and 2 mM induced several kinase activities including the p48 SIP kinase. The sizes of the other activated kinases were 58 kDa, 52 kDa, and 40 kDa. Activation of the SIP kinase by H.sub.2 O.sub.2 was more sustained compared to that induced by SA; even at 60 minutes after addition of H.sub.2 O.sub.2, kinase activities remained at peak levels.

C. Activation of the p48 SIP Kinase by SA and H.sub.2 O.sub.2 is Associated with Phosphorylation of Tyrosine Residue on the Kinase

The use of MBP as a preferred substrate suggested that the p48 SIP kinase might be a MAP kinase. Another characteristic of MAP kinases is their activation via simultaneous phosphorylation of tyrosine and threonine residues by MAP kinase kinases (Seger and Krebs, 1995). To determine if the SIP kinase was similarly activated, extracts from SA- or H.sub.2 O.sub.2 -treated cells were subjected to immunoblot analysis using the phosphotyrosine-specific monoclonal antibody 4G10. See FIG. 4A. Increases in the amount of a phosphotyrosine-containing 48 kDa polypeptide were associated with both the SA- and H.sub.2 O.sub.2 -induced activation of the p48 SIP kinase. SA induced a transient activation of the p48 kinase, which correlates with the transient increase in the level of a phosphotyrosine-containing 48 kDa protein. Compare FIG. 1A with FIG. 4A. Hydrogen peroxide induced both sustained activation of the p48 kinase, as shown in FIG. 3, and prolonged phosphorylation of tyrosine residue(s) on a 48 kDa protein, as shown in FIG. 4A. These results suggest that the p48 SIP kinase is a MAP kinase.

To confirm these results, as well as demonstrate the specificity of the 4G10 monoclonal antibody for phosphotyrosine, immunoprecipitation of phosphotyrosine-containing proteins was coupled with the in-gel kinase activity assay. Phosphotyrosine-containing polypeptides were first immunoprecipitated from extracts of SA- or H.sub.2 O.sub.2 -treated cells and then subjected to the in-gel kinase activity assay. See FIG. 4B. Again, the immunoprecipitated 48 kDa kinase activity, as can be seen in FIG. 4B, lanes 1 to 6, correlates with the p48 SIP kinase activity in the cell extracts (FIGS. 1A and 3), as well as with the amount of a phosphotyrosine-containing 48 kDa protein detected by immunoblot analysis (FIG. 4A). To confirm that the antibody specifically recognized a phosphorylated tyrosine residue in the SIP kinase, phosphoserine, phosphothreonine and phosphotyrosine were used as competitors in the immunoprecipitation experiments described above. See FIG. 4B, lanes 7-12. Only phosphotyrosine inhibited precipitation of the p48 SIP kinase, confirming the specificity of the antibody.

D. Tobacco Leaves Injected with SA have Elevated p48 Kinase Activity

Activation of the p48 SIP kinase was next monitored in tobacco plants after injection of SA into their leaves. See FIG. 5A and 5C. Injection of 500 .mu.M SA resulted in the rapid activation of a kinase whose activity decreased to basal level in about 30 minutes. This was followed by a second, more prolonged activation of a kinase of the same size which peaked at approximately 3 hours. Using the in-gel kinase assay with crude protein extracts, both activities were observed as a 46 kDa polypeptide, which is the same size as the cutting-induced MAP kinase (termed PMSAP kinase) reported by Usami et al., 1995. However, after immunoprecipitation with the anti-phosphotyrosine monoclonal antibody, both activities migrated as a 48 kDa protein, identical in size to that present in extracts from tobacco suspension cells (data not shown). Coomassie staining of the gel revealed that there was a very abundant protein of about 48 kDa present in leaf but not suspension cell extracts which likely was responsible for the aberrant migration of the p48 kinase activities.

The very rapidly and transiently induced kinase activity was also present in leaves injected with water, suggesting that only the second peak of activity was SA related. See FIG. 5A and 5C. This is consistent with the induction of the first (rapid, transient) peak of activity by biologically inactive as well as active analogues of SA. In contrast, the second peak was induced only by active analogues (data not shown). Thus, the first peak of activity is probably brought about by mechanical and/or osmotic stress.

To separate the two kinase activation responses elicited by injection of SA, double-injection experiments were performed. Leaves were first injected with water, and 1, 2 or 4 hours later injected a second time with water or SA. The first injection of water desensitized the mechanical and/or osmotic stress response since a second injection of water failed to activate the 48 kDa kinase again (only the second injection of water at 4 hours is shown in FIG. 5B). In contrast, a second injection of SA led to a dramatic activation of the p48 SIP kinase. This activation occurred more rapidly, was stronger, and less prolonged than the second peak of kinase activity elicited by a single SA injection. Compare FIGS. 5B and 5D with 5A and 5C. It is unclear whether the wounding and/or osmotic stress-induced activity and SA-induced activity were due to the same kinase. The activation of the p48 SIP kinase activity by a second injection of SA, but not of water, in the double-injection experiment suggests that either SIP kinase is distinct from the p48 wounding and/or osmotic stress-induced kinase, or they are the same kinase with different upstream signaling components.

E. TMV Infection Activates the p48 SIP Kinase

As TMV infection of resistant tobacco plants leads to elevated levels of endogenous SA (Malamy et al., 1992), p48 SIP kinase activity was monitored after TMV infection. To more readily follow changes in kinase activity, advantage was taken of the reversible, high temperature inhibition of defense responses to TMV in resistant tobacco. At 32.degree. C. TMV-infected tobacco fails to (i) produce elevated levels of SA, (ii) synthesize PR proteins, (iii) restrict virus multiplication and spread, and (iv) develop necrotic lesions. Upon shifting these plants to lower temperatures (22.degree. C.) all of the above defense responses are rapidly and strongly induced (Malamy et al., 1992). In the experiments shown here, plants were infected with TMV and then maintained at 32.degree. C. for 48 hours before shifting to 22.degree. C. Under these conditions, SA levels rise several fold between 0 and 4 hours and then 10-50 fold more by 6 hours after the shift (Malamy et al., 1992; Guo and Klessig, unpublished). The increase in p48 SIP kinase activity paralleled the rise in SA. See FIG. 6. Activity of this kinase began to increase at about 3.5 hours, peaked approximately 10 fold above basal level at 4.5 hours, and then declined.

The activity of a second, slightly smaller kinase (approximately 44 kDa) was also induced by TMV infection. See FIG. 6. Its activation was delayed until 4.5 hours and then rose dramatically from an undetectable basal level. Activation of this p44 kinase was also evident after SA treatment of tobacco plants (FIGS. 5A and 5B) but not suspension cells (FIG. 1A). The identity of this kinase is unknown, but based on its substrate preference, it may be another MAP kinase.

EXAMPLE 2

PURIFICATION AND CLONING OF TOBACCO SIP KINASE

In this Example, the purification of the p48 SIP kinase from tobacco is described. The cloning and characterization of a cDNA encoding the tobacco SIP kinase is also described.

MATERIALS AND METHODS

A. Purification of p48 SIP Kinase

All purification procedures were carried out in a cold room or in a 4.degree. C. chamber. Protein extract from about 200 grams of SA-treated cells was first fractionated by (NH.sub.4).sub.2 SO.sub.4 precipitation. Saturated ammonium sulfate solution was slowly added to total protein extract to 30% of final concentration. After slowly stirring for 30 minutes, the precipitate was collected by centrifugation at 23,000.times.g for 10 minutes. The pellets were then dissolved in a total of 30 mL of buffer A (25 mM Tris, pH 7.5, 1 mM EGTA, 10 mM .beta.-glycerolphosphate, 0.1 mM Na.sub.3 VO.sub.4, 1 mM DTT, 5% glycerol) plus 1 mM phenylmethylsulfonyl fluoride, 5 .mu.g/mL each of antipain, aprotinin, and leupeptin. After centrifugation at 130,000.times.g for 1 hour, the S130 supernatant was dialyzed against 1000 mL of buffer A for 4 hours in the cold room and loaded onto a 10 mL Q-Sepharose column (two tandemly connected 5 mL HiTrapQ columns) equilibrated with buffer A plus 50 mM NaCl. After washing with 30 mL of buffer A, with 50 mM NaCl, the column was eluted with a 150 mL linear gradient of 50 to 400 mM NaCl in buffer A. The p48 SIP kinase activity eluted at about 250 mM. The pooled fractions were adjusted to 300 mM final concentration of NaCl, and loaded onto a 15 mL phenyl-Sepharose/High Performance column (1.6 cm.times.7.5 cm) equilibrated with buffer A plus 300 mM NaCl. The column was washed with 50 mL buffer A plus 300 mM NaCl and eluted with 100 mL linear gradient of 0-60% ethylene glycol and 300-0 mM NaCl in buffer A. The active fractions (eluting around 40% ethylene glycol) were pooled and diluted with equal volume of buffer A, and then loaded to a MonoQ HR 5/5 FPLC column equilibrated with buffer A plus 100 mM NaCl. After washing with 5 mL buffer A plus 100 mM NaCl, the column was eluted with 30 mL gradient of 100-400 mM NaCl in buffer A. The pooled fractions containing the p48 SIP kinase (about 3 mL) were adjusted to 10 mM MgCl.sub.2 final concentration and diluted with equal volume of buffer B (25 mM Tris, pH 7.5, 10 mM MgCl.sub.2, 1 mM EGTA, 1 mM DTT, 10 mM .beta.-glycerolphosphate, 0.1 mM Na.sub.3 VO.sub.4, and 0.02% Triton X-100). The sample was then loaded onto a MBP-Sepharose affinity column (1 mL) and equilibrated with buffer B plus 50 mM NaCl. The column was step-eluted with 5 mL each of buffer B plus 100 mM NaCl, 500 mM NaCl, and 1000 mM NaCl. The pooled fractions containing the p48 SIP kinase (about 2.5 mL) were diluted with 3 volumes of buffer B and loaded to a 3.5 mL poly-L-lysine-agarose column (0.9 cm.times.5.5 cm). After washing with buffer B plus 50 mM NaCl, the column was eluted with 50 mL gradient of 50-800 mM NaCl in buffer B. The active fractions were pooled and concentrated with a Centricon concentrator (10,000 molecular weight cut-off, Amicon, Mass.). To determine the native molecular weight or to further purify the p48 SIP kinase, the concentrated sample was loaded onto a Superdex 200 HR 10/30 FPLC column equilibrated with buffer B plus 250 mM NaCl, and the column was eluted with the same buffer at 0.5 mL/min.

B. Assay of Kinase Activity

Unless specifically indicated, assays were performed at room temperature for 20 minutes in a final volume of 15 .mu.l containing 0.5 mg/mL of MBP, 50 .mu.M of .gamma.-.sup.32 P-ATP (about 3000-6000 cpm/pmole), 25 mM Tris pH 7.5, 5 mM MgCl.sub.2, 1 mM EGTA, 1 mM DTT, and enzyme. The reaction was terminated by the addition of equal volume of 150 mM H.sub.3 PO.sub.4. Twenty .mu.L of the mixture was spotted onto an 8-well phosphocellulose filter strip (Pierce, Ill.). After washing with 150 mM H.sub.3 PO.sub.4 extensively, the phospho-protein was eluted with 0.4 mL of 1 N NaOH, and the radioactivity was determined by liquid scintillation counting. Total cpm in the reaction mixture was also determined in order to calculate the specific activity of the enzyme preparation. One unit of p48 SIP kinase was defined as the amount of enzyme that will catalyze the transfer of 1 pmole of phosphate from ATP to MBP in 1 minute.

C. Identification of Phosphorylated Amino Acids in the Substrates

The procedure followed was identical to that described earlier (Zhang et al., 1993), except that two-dimensional thin-layer electrophoresis was used. Phosphorylated substrates were precipitated using 10% (w/v) TCA. After washing with 10% (w/v) TCA and ethanol, the pellets were hydrolyzed in 6 N HCl for 2 hours at 110.degree. C., dried in a Speed-Vac evaporator, and then dissolved in 10 .mu.L phospho-amino acids standard (1 mg/mL each of L-phosphoserine, L-phosphothreonine and L-phosphotyrosine). The phospho-amino acids were separated by two-dimensional high voltage thin-layer electrophoresis as previously described (Sefton, 1996). The position of the standards was visualized by ninhydrin (0.2% (w/v) in acetone), and the labeled amino acids were detected by autoradiography.

D. Treatment of the p48 SIP Kinase with Phosphatases

The phosphatase inhibitors present in the purified p48 SIP kinase preparation were first removed by dialysis against buffer B lacking .beta.-glycerophosphate and Na.sub.3 VO.sub.4 in a 0.5-mL 10 K dialysis cassette (Slide-A-Lyzer; Pierce). For treatment with serine/threonine protein phosphatase PP1 (Calbiochem, San Diego, Calif.), MnCl.sub.2, DTT, and BSA were added to aliquots of the SIP kinase preparation to final concentrations of 200 .mu.m, 5 mM and 100 .mu.g/mL respectively. Then 0.1 unit of PP1 was added, and the reaction mixture was incubated at 30.degree. C. in the presence or absence of 1 .mu.M of the phosphatase inhibitor okadaic acid (Calbiochem). For treatment with the tyrosine-specific protein phosphatase YOP (Calbiochem), NaCl, DTT, and BSA were added to purified SIP kinase to final concentrations of 150 mM, 5 mM and 100 .mu.g/mL, respectively. Then 0.5 unit of YOP was added, and the reaction was incubated at 30.degree. C. in the presence or absence of 1 mM of the tyrosine phosphatase inhibitor Na.sub.3 VO.sub.4. Before assaying for the SIP kinase activity, the phosphatase inhibitors were brought to the same final concentration.B.

E. Microsequencing of Internal Tryptic Peptides

The protein in the active fractions eluted from the poly-L-lysine column was concentrated and precipitated with acetone. The pellets were then dissolved in SDS-Laemmli sample buffer and separated on a 10% SDS-polyacrylamide gel. After Coomassie Brilliant Blue R 250 staining, the 48-kDa band was excised and sent to the W.M. Keck Foundation Biotechnology Resource Laboratory (Yale University, New Haven, Conn.) for amino acid composition and sequence analysis. Briefly, for sequence analysis, the p48 SIP kinase was subjected to in-gel digestion with trypsin, and the resultant peptides were separated by reverse-phase HPLC. After determination of molecular mass and purity using matrix-assisted laser desorption ionization (MALDI) mass spectrometry, selected peptides were sequenced using standard methods.

F. Cloning of Tobacco SIP Kinase cDNA

Two primers, 5'-AAYATHTTYGARGTNACNGC-3' and 5'-CKNCCNGGRAANARNGGYTT-3' (where H is A,T and C; K is T and G; N is A, T, C and G; R is A and G; and Y is T and C), which correspond to peptide 1 and peptide 4 (FIG. 14), respectively, were used to amplify by polymerase chain reaction (PCR) the cDNA that was reverse transcribed from poly(A) RNA prepared from tobacco cell suspension culture. A reverse transcription/PCR product of .about.600 bp was cloned into pGEM-T vector (Promega) and sequenced. A clone whose deduced amino acid sequence matched the internal peptide 2 and peptide 3 (FIG. 14) was labeled with .alpha.-.sup.32 P-dCTP and used to screen a tobacco cDNA library under high stringency. Briefly, nylon membranes (Duralon-UV; Stratagene, La Jolla, Calif.), each with 5.times.10.sup.4 plaque-forming units, were hybridized at 42.degree. C. for 20 hr in solution containing 20 mM Pipes, pH 6.5, 0.8 M NaCl, 50% formamide, 1% (w/v) SDS, 100 .mu.g/mL denatured salmon sperm DNA, plus 10.sup.6 cpm/mL of probe. After hybridization, the filters were washed once with 1.times. SSC (0.15 M NaCl, 0.015 M sodium citrate), 0.1% (w/v) SDS at room temperature, and three times, each for 15 min, with 0.1.times. SSC, 0.1% (w/v) SDS at 55.degree. C. More than 10 positive clones were obtained by screening .about.10.sup.6 plaque-forming units. Both strands of the clone containing the longest insert were sequenced using the Sequenase 2.0 kit (Amersham).

RESULTS

A. Purification of SIP Kinase

Purification of p48 SIP kinase from SA-treated tobacco suspension cells is summarized in Table I, with typical elution profiles from the column chromatography steps shown in FIG. 7 (FIGS. 7A-7F). The 0 to 30% (NH.sub.4).sub.2 SO.sub.4 fraction contained almost all of the p48 SIP kinase activity. Several kinases with similar molecular weight but much lower activity, as determined by the in-gel kinase activity assay, were present in 30% to 75% fractions from both SA-treated and control water-treated cell extracts (data not shown). The 0 to 30% (NH.sub.4).sub.2 SO.sub.4 fraction was initially fractionated on a Q-Sepharose anion exchange column (FIG. 7A). The major peak of kinase activity that eluted from this column corresponded to the p48 SIP kinase, based on its absence in the protein preparation obtained from control tobacco cells treated with water (FIG. 8A). Its identity was confirmed by the in-gel kinase activity assay which revealed a major kinase of 48 kDa in the Q-Sepharose fractions with high kinase activity (FIG. 8B). In all of the subsequent chromatographic steps, only a single major kinase activity peak was detected by the in-solution assay using MBP as the substrate (FIG. 7).

Analysis of the pooled fractions from each purification step by SDS-PAGE revealed that the p48 SIP kinase was purified to apparent homogeneity after the final gel filtration step (FIG. 9A, lane 10). More than 25,000-fold purification was required to obtain enzyme of this purity (Table 1). This result indicated that the p48 SIP kinase was approximately 0.004% of the total soluble protein. The final purified enzyme had a molecular weight of 48 kDa (FIGS. 6A and 6B) and a specific activity of 340 nmol min.sup.-1 mg.sup.-1, which is higher than purified MAP kinases obtained from most other sources (Childs and Mak, 1993a and b). To ensure that the 48-kDa band detected on the Coomassie blue-stained SDS-PAGE gels corresponded to the p48 SIP kinase, several precautions were taken. In addition to demonstrating that the p48 SIP kinase activity is present only in protein preparations from SA-treated tobacco cells, we followed the purification of both the 48-kDa band (detected by Coomassie blue-staining of SDS-PAGE gels) and the p48 SIP kinase (monitored by the in-gel activity assay) through the last three steps of purification (data not shown). Their co-purification strongly argues that they are the same protein. Moreover, since the activation of MAP kinases requires phosphorylation of a tyrosine residue in the TXY motif between subdomains VII and VIII of the kinase catalytic domain, the presence of a phosphorylated tyrosine residue in the 48-kDa protein would provide further evidence that it is a MAP kinase. Immunoblot analysis of pooled fractions from each purification step using an anti-phosphotyrosine monoclonal antibody indicated that the 48-kDa polypeptide was heavily phosphorylated on tyrosine residue(s) (FIG. 9C). Furthermore, the enrichment of tyrosine-phosphorylated 48-kDa protein correlated with the purification of p48 SIP kinase activity. Thus, we conclude that the purified 48-kDa protein is the p48 SIP kinase described above.

TABLE I______________________________________Purification of the p48 SIP kinase from tobacco suspension culture cells Total Specific Activity Activity Purifi- Protein (pmol (pmol min .sup.-1 Recovery cation Fraction (mg) min.sup.-1) mg.sup.-1) (%) (fold)______________________________________Total extract.sup.a 1600 20943 13.1 100 1 30% (NH.sub.4).sub.2 SO.sub.4 149 17082 114.6 81.6 9 130,000 .times. g 116 16582 142.9 79.2 11 Q-Sepharose 12 13950 1162.5 66.6 89 Phenyl- 1.482 8072 5446.7 38.5 416 Sepharose/HP MonoQ 0.572 7231 12641.6 34.5 965 MBP-Sepharose 0.065.sup.b 6870 105692.3 32.8 8068 Poly-L-lysine- 0.030.sup.b 5094 169800.0 24.3 12962 agarose Superdex 200 0.005.sup.b 1698 339600.0 8.0 25924 HR 10/30______________________________________ .sup.a The starting total extract was prepared from 200 g of cells. .sup.b Protein amount estimated by comparing to known standards on Commassie bluestained SDSPAGE gel. B. Characterization of Purified Tobacco p48 SIP Kinase

Purification of the p48 SIP kinase by the protocol outlined in Table 1 through the poly-L-lysine agarose chromatography step removed all other contaminant kinases and therefore allowed the characterization of the p48 SIP kinase by in-solution kinase assay. All further characterization described in FIGS. 10-13, and Table III and IV utilized this partially purified enzyme. The native molecular mass as calculated from size-exclusive FPLC chromatography was 50 kDa (FIG. 7F), which is close to the 48 kDa estimated by SDS-PAGE gel. This result indicates that the p48 SIP kinase is a monomeric enzyme, as are all other MAP kinases. Purified p48 SIP kinase had a very broad optimum pH. See FIG. 10A. Even at pH of 5.5 or 10, it retained more than 50% activity. The enzyme exhibited an absolute requirement for Mg.sup.2+ ; Mn.sup.2+ could not substitute for Mg.sup.2+. See FIG. 10B. Kinase activity was strongly stimulated by MgCl.sub.2 up to a total concentration of 2 mM, and then decrease slightly as the concentration of MgCl.sub.2 increase. Stimulation by Mg.sup.2+ in excess of the amount necessary for the formation of a stable Mg.sup.2+ -ATP complex suggests an additional function for this metal ion. The purified p48 SIP kinase could not use Mg.sup.2+ -GTP as a phospho-donor (data not shown). The absolute Km and Vmax of the enzyme for Mg.sup.2+ -ATP was estimated to be of 24 .mu.M and 0.39 .mu.mole min.sup.-1 mg.sup.-1, respectively. See Table II. Of the proteins tested for their ability to serve as in vitro substrates, only MBP proved to be good phosphate acceptor. See FIG. 11. The absolute Km for MBP was 0.19 mg mL.sup.-1. See Table II. Phospho-amino acid analysis by two-dimensional thin-layer electrophoresis demonstrated that only threonine was phosphorylated on MBP. See FIG. 12.

TABLE II______________________________________Structural and kinetic properties of the p48 SIP kinase Parameter Value______________________________________Structural parameters Native molecular weight .sup.a 50,000 Denatured molecular weight.sup.b 48,000 Kinetic parameters Mg.sup.2+ -ATP K.sub.m (.mu.M) 24 V.sub.max (.mu.mole min.sup.-1 mg.sup.-1) 0.39 MBP K.sub.m (mg mL.sup.-1) 0.19 V.sub.max (.mu.mole min.sup.-1 mg.sup.-1) 0.42______________________________________ .sup.a Measured relative to internal standards using a Superdex 200 HR 10/30 FPLC column. .sup.b Measured relative to known standards by SDSPAGE. C. Effectors of p48 SIP Kinase Activity

Under standard assay conditions, none of the compounds tested could significantly stimulate the activity of the partially purified p48 SIP kinase. See Table III. The p48 SIP kinase was very sensitive to the general kinase inhibitor K252a and staurosporine, with I.sub.50 of 12 nM and 60 nM, respectively. In contrast, EGTA, genistein, protein kinase A peptide inhibitor, and protein kinase C peptide inhibitor had no effect on its activity. See Table III. At high concentrations, both Ca.sup.2+ and Zn.sup.2+ inhibited the enzyme. Several poly-ions, including poly-L-Lys, poly-L-Glu, protamine and heparin showed inhibitory effects, while poly-L-Gln and spermidine showed no effect at the concentrations tested. See Table III.

TABLE III______________________________________Effects of various reagents on p48 SIP kinase activity Relative Activity Reagents Concentration % of control.sup.a______________________________________Kinase Inhibitors EGTA 10 mM 100 PKA peptide inhibitor 10 .mu.M 100 PKC peptide inhibitor 10 .mu.M 100 Genistein 20 .mu.M 100 K-252a 12 nM 50 Staurosporine 60 nM 50 Metal ions Na.sup.+ 100 mM 100 Na.sup.+ 750 mM 50 Ca.sup.2+ 0.5 mM 100 Ca.sup.2+ 5.0 mM 50 Zn.sup.2+ 0.10 mM 100 Zn.sup.2+ 0.25 mM 50 Poly-L-lysine 25 .mu.g mL.sup.-1 50 Poly-L-glutamate 500 .mu.g mL.sup.-1 50 Poly-L-glutamine 500 .mu.g mL.sup.-1 100 Protamine 25 .mu.g mL.sup.-1 50 Heparin 50 .mu.g mL.sup.-1 50 Spermidine 1 mM 100 SH-modifying compounds DTT 5 mM 100 Diamide 5 mM 50______________________________________ .sup.a For each reagent, a dose response curve was measured under standar assay conditions. About 0.5 unit of enzyme was used for each reaction. Control was the enzyme activity in the absence of reagent. D. Phosphorylation of Both Tyrosine and Serine/threonine Residues are Required for p48 SIP Kinase Activity

To assess whether phosphorylation is required for p48 SIP kinase activation, the kinase was treated with either the tyrosine-specific protein phosphatase YOP or the serine/threonine-specific protein phosphatase PP1. Both phosphatases inactivated the SIP kinase (FIG. 13). Furthermore, the inactivation of the SIP kinase by PP1 and YOP, respectively, could be prevented by the addition of okadaic acid, a PP1 inhibitor, or Na.sub.3 VO.sub.4, a tyrosine phosphatase inhibitor. These results confirm that the inactivation of the purified SIP kinase was due to the presence of these phosphatases.

E. Characterization of a cDNA Encoding the Tobacco p48 SIP Kinase

The purified p48 SIP kinase shares several characteristics with MAP kinases, including phosphorylation of a tyrosine residue upon activation, preference for MBP as a substrate, a monomeric structure, and a molecular mass within the range of 38 to 55 kDa. To confirm that SIP kinase is a MAP kinase, partial amino acid sequence was obtained by microsequencing of several internal tryptic peptides (FIG. 14). The sequences from two of the peptides were then used to design primers, and a fragment of the SIP kinase gene was cloned by reverse transcription and PCR amplification. A full-length cDNA clone, which contains all of the peptide sequence obtained by microsequencing of the purified protein (FIG. 14), was obtained by screening of a tobacco cDNA library.

The DNA sequence of the tobacco SIP-kinase cDNA is set forth herein as Sequence I.D. No. 1. The deduced amino acid Sequence (Seq. I.D. No. 2) is shown in FIG. 14. Analysis of these sequences shows that it contains all 11 conserved kinase subdomains found in serine/threonine kinases (Hanks and Hunter, 1995) and has the MAP kinase signature phosphorylation motif TXY preceding subdomain VIII (FIG. 14). The SIP kinase shares 93% amino acid sequence identity with Ntf4 (FIG. 14), a tobacco MAP kinase of unknown function previously isolated by PCR-based homology cloning (Wilson et al., 1995). However, the nucleotide sequence identity of these two genes is only 74%. Although the SIP kinase is definitely a MAP kinase, it differs from all other cloned plant MAP kinases at its N terminus. Furthermore, in conserved subdomain VIII of the kinase catalytic domain, the SIP kinase contains a proline in place of alanine, which is conserved in all other MAP kinases cloned in plants as well as in yeast and mammals.

The SIP kinase is also clearly distinct from WIPK, another member of the tobacco MAP kinase family that has been implicated in the wounding response (Seo et al., 1995). They share only 73% amino acid sequence identity and 51% nucleotide sequence identity. These findings suggest that different MAP kinases are responsible for different stress responses in plants.

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While certain of the preferred embodiments of the present invention have been described and specifically exemplified above, it is not intended that the invention be limited to such embodiments. Various modifications may be made thereto without departing from the scope and spirit of the present invention, as set forth in the following claims.

__________________________________________________________________________# SEQUENCE LISTING - - - - (1) GENERAL INFORMATION: - - (iii) NUMBER OF SEQUENCES: 14 - - - - (2) INFORMATION FOR SEQ ID NO:1: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 1544 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: both (D) TOPOLOGY: unknown - - (ii) MOLECULE TYPE: cDNA - - (iii) HYPOTHETICAL: NO - - (iv) ANTI-SENSE: NO - - (v) FRAGMENT TYPE: - - (vi) ORIGINAL SOURCE: tobacco - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:1: - - CACAATTCCA CATATTCATT GACATACTAC GGCCCTTCTT CCCTAATTTT AA -#GACAAAGG 60 - - AAAAAAAGTA ATTATTGATT CTTCTAGGAT TTACAATTTT TGTTGACGAA TT -#TTCCAAAA 120 - - AAAAAAATAT GGATGGTTCT GGTCAGCAGA CGGACACGAT GATGTCTGAT GC -#GGGGGCGG 180 - - AGCAGCCACC TACGGCGCCG CAGCCGGTGG CCGGTATGGA TAATATTCCG GC -#GACGTTGA 240 - - GCCACGGTGG CAGGTTCATT CAATACAATA TATTTGGTAA TATATTTGAA GT -#TACTGCTA 300 - - AATATAAGCC TCCTATTTTG CCTATTGGTA AAGGTGCTTA CGGCATCGTT TG -#TTCTGCTT 360 - - TGAACTCGGA GACAATTGAG AACGTAGCGA TAAAGAAAAT CGCAAATGCT TT -#TGATAACA 420 - - AGATTGATGC CAAGAGGACT TTGAGAGAGA TCAAGCTTCT TCGGCATATG GA -#TCATGAAA 480 - - ACATTGTTGC GATCAGAGAT ATAATTCCAC CACCACAGAG AGAGGCCTTT AA -#TGATGTTT 540 - - ATATTGCGTA TGAGCTTATG GATACTGATC TCCATCAAAT TATTCGCTCT AA -#TCAGGGTT 600 - - TATCTGAGGA GCACTGTCAG TATTTCTTGT ATCAGATCCT CCGAGGGTTG AA -#ATACATAC 660 - - ATTCTGCGAA TGTTCTGCAC AGGGACTTGA AGCCTAGCAA TCTCCTGTTG AA -#TGCCAACT 720 - - GTGATTTAAA GATATGTGAT TTTGGGCTAG CTCGTGTCAC TTCTGAAACT GA -#CTTTATGA 780 - - CGGAATATGT TGTGACAAGA TGGTATCGTC CACCTGAGCT GTTGTTAAAT TC -#GTCTGACT 840 - - ATACTGCAGC AATTGACGTA TGGTCAGTGG GTTGCATTTT CATGGAATTG AT -#GGACAGGA 900 - - AACCCCTATT TCCTGGTAGA GATCACGTAC ACCAGCTGCG TCTTATTATG GA -#GTTGATTG 960 - - GTACTCCTTC AGAGGCTGAA ATGGAGTTTT TAAATGAGAA TGCAAAACGA TA -#CATCCGCC 1020 - - AACTTCCTCT TTACCGTCGA CAATCATTCA CTGAAAAGTT TCCACATGTA CA -#CCCAACTG 1080 - - CAATTGATCT TGTCGAGAAA ATGCTGACAT TTGATCCTAG AAGGAGAATA AC -#AGTTGAAG 1140 - - GTGCACTTGC ACATCCTTAC CTGAACTCGC TCCACGATAT TAGTGACGAG CC -#CATTTGCA 1200 - - TGACTCCCTT TAGCTTCGAC TTTGAACAGC ATGCCCTTAC GGAGGAACAG AT -#GAAGGAGC 1260 - - TGATTTACAG GGAGTCGCTT GCATTTAATC CTGAATACCA GCATATGTGA AT -#AATTGCTG 1320 - - GTAAGATTGT TGTCAGTTTG ATCTCCAACT GACAATTTGT CCCTCCATGT AT -#ATATGTGT 1380 - - GCACTTCGTC CGAAACACGG ATGGCTTTCT TATGCAAACA CTTAGTTATG AA -#GCTGATTT 1440 - - GTGTAAAGAA TTGTTTGATG TATCTGATGA GGTGGATCGC TTGTATTGGT TC -#TGTTTTAA 1500 - - TTTACTGAAG TCATAGTGGA CGAAAAAAAA AAAAAAAAAA AAAA - # 154 - #4 - - - - (2) INFORMATION FOR SEQ ID NO:2: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 393 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: protein - - (iii) HYPOTHETICAL: YES - - (iv) ANTI-SENSE: NO - - (v) FRAGMENT TYPE: internal - - (vi) ORIGINAL SOURCE: - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2: - - Met Asp Gly Ser Gly Gln Gln Thr Asp Thr Me - #t Met Ser Asp Ala Gly 1 5 - # 10 - # 15 - - Ala Glu Gln Pro Pro Thr Ala Pro Gln Pro Va - #l Ala Gly Met Asp Asn 20 - # 25 - # 30 - - Ile Pro Ala Thr Leu Ser His Gly Gly Arg Ph - #e Ile Gln Tyr Asn Ile 35 - # 40 - # 45 - - Phe Gly Asn Ile Phe Glu Val Thr Ala Lys Ty - #r Lys Pro Pro Ile Leu 50 - # 55 - # 60 - - Pro Ile Gly Lys Gly Ala Tyr Gly Ile Val Cy - #s Ser Ala Leu Asn Ser 65 - #70 - #75 - #80 - - Glu Thr Ile Glu Asn Val Ala Ile Lys Lys Il - #e Ala Asn Ala Phe Asp 85 - # 90 - # 95 - - Asn Lys Ile Asp Ala Lys Arg Thr Leu Arg Gl - #u Ile Lys Leu Leu Arg 100 - # 105 - # 110 - - His Met Asp His Glu Asn Ile Val Ala Ile Ar - #g Asp Ile Ile Pro Pro 115 - # 120 - # 125 - - Pro Gln Arg Glu Ala Phe Asn Asp Val Tyr Il - #e Ala Tyr Glu Leu Met 130 - # 135 - # 140 - - Asp Thr Asp Leu His Gln Ile Ile Arg Ser As - #n Gln Gly Leu Ser Glu 145 1 - #50 1 - #55 1 -#60 - - Glu His Cys Gln Tyr Phe Leu Tyr Gln Ile Le - #u Arg Gly Leu LysTyr 165 - # 170 - # 175 - - Ile His Ser Ala Asn Val Leu His Arg Asp Le - #u Lys Pro Ser Asn Leu 180 - # 185 - # 190 - - eu Leu Asn Ala Asn Cys Asp Leu Lys Ile Cys - # Asp Phe Gly Leu Ala 195 - # 200 - # 205 - - Arg Val Thr Ser Glu Thr Asp Phe Met Thr Gl - #u Tyr Val Val Thr Arg 210 - # 215 - # 220 - - Trp Tyr Arg Pro Pro Glu Leu Leu Leu Asn Se - #r Ser Asp Tyr Thr Ala 225 2 - #30 2 - #35 2 -#40 - - Ala Ile Asp Val Trp Ser Val Gly Cys Ile Ph - #e Met Glu Leu MetAsp 245 - # 250 - # 255 - - Arg Lys Pro Leu Phe Pro Gly Arg Asp His Va - #l His Gln Leu Arg Leu 260 - # 265 - # 270 - - Ile Met Glu Leu Ile Gly Thr Pro Ser Glu Al - #a Glu Met Glu Phe Leu 275 - # 280 - # 285 - - Asn Glu Asn Ala Lys Arg Tyr Ile Arg Gln Le - #u Pro Leu Tyr Arg Arg 290 - # 295 - # 300 - - Gln Ser Phe Thr Glu Lys Phe Pro His Val Hi - #s Pro Thr Ala Ile Asp 305 3 - #10 3 - #15 3 -#20 - - Leu Val Glu Lys Met Leu Thr Phe Asp Pro Ar - #g Arg Arg Ile ThrVal 325 - # 330 - # 335 - - Glu Gly Ala Leu Ala His Pro Tyr Leu Asn Se - #r Leu His Asp Ile Ser 340 - # 345 - # 350 - - Asp Glu Pro Ile Cys Met Thr Pro Phe Ser Ph - #e Asp Phe Glu Gln His 355 - # 360 - # 365 - - Ala Leu Thr Glu Glu Gln Met Lys Glu Leu Il - #e Tyr Arg Glu Ser Leu 370 - # 375 - # 380 - - Ala Phe Asn Pro Glu Tyr Gln His Met 385 3 - #90 - - - - (2) INFORMATION FOR SEQ ID NO:3: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 393 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: protein - - (iii) HYPOTHETICAL: NO - - (iv) ANTI-SENSE: NO - - (v) FRAGMENT TYPE: internal - - (vi) ORIGINAL SOURCE: - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:3: - - Met Asp Gly Pro Ala His Gln Thr Asp Thr Va - #l Met Ser Asp Ala Ala 1 5 - # 10 - # 15 - - Gly Gln Gln Pro Ala Pro Pro Ser Gln Pro Va - #l Ala Gly Ile Asp Asn 20 - # 25 - # 30 - - Ile Pro Ala Thr Leu Ser His Gly Gly Arg Ph - #e Ile Gln Tyr Asn Ile 35 - # 40 - # 45 - - Phe Gly Asn Ile Phe Glu Val Thr Ala Lys Ty - #r Lys Pro Pro Ile Met 50 - # 55 - # 60 - - Pro Ile Gly Lys Gly Ala Tyr Gly Ile Val Cy - #s Ser Ala Leu Asn Ser 65 - #70 - #75 - #80 - - Glu Thr Asn Glu His Val Ala Ile Lys Lys Il - #e Ala Asn Ala Phe Asp 85 - # 90 - # 95 - - Asn Lys Ile Asp Ala Lys Arg Thr Leu Arg Gl - #u Ile Lys Leu Leu Arg 100 - # 105 - # 110 - - His Met Asp His Glu Asn Ile Val Ala Ile Ar - #g Asp Ile Ile Pro Pro 115 - # 120 - # 125 - - Pro Gln Arg Glu Ala Phe Asn Asp Val Tyr Il - #e Ala Tyr Glu Leu Met 130 - # 135 - # 140 - - Asp Thr Asp Leu His Gln Ile Ile Arg Ser As - #n Gln Gly Leu Ser Glu 145 1 - #50 1 - #55 1 -#60 - - Glu His Cys Gln Tyr Phe Leu Tyr Gln Ile Le - #u Arg Gly Leu LysTyr 165 - # 170 - # 175 - - Ile His Ser Ala Asn Val Leu His Arg Asp Le - #u Lys Pro Ser Asn Leu 180 - # 185 - # 190 - - Leu Leu Asn Ala Asn Cys Asp Leu Lys Ile Cy - #s Asp Phe Gly Leu Ala 195 - # 200 - # 205 - - Arg Val Thr Ser Glu Thr Asp Phe Met Thr Gl - #u Tyr Val Val Thr Arg 210 - # 215 - # 220 - - Trp Tyr Arg Ala Pro Glu Leu Leu Leu Asn Se - #r Ser Asp Tyr Thr Ala 225 2 - #30 2 - #35 2 -#40 - - Ala Ile Asp Val Trp Ser Val Gly Cys Ile Ph - #e Met Glu Leu MetAsp 245 - # 250 - # 255 - - Arg Lys Pro Leu Phe Pro Gly Arg Asp His Va - #l His Gln Leu Arg Leu 260 - # 265 - # 270 - - Leu Met Glu Leu Ile Gly Thr Pro Ser Glu Al - #a Glu Met Glu Phe Leu 275 - # 280 - # 285 - - Asn Glu Asn Ala Lys Arg Tyr Ile Arg Gln Le - #u Pro Leu Tyr Arg Arg 290 - # 295 - # 300 - - Gln Ser Phe Val Glu Lys Phe Pro His Val As - #n Pro Ala Ala Ile Asp 305 3 - #10 3 - #15 3 -#20 - - Leu Val Glu Lys Met Leu Thr Phe Asp Pro Ar - #g Arg Arg Ile ThrVal 325 - # 330 - # 335 - - Glu Asp Ala Leu Ala His Pro Tyr Leu Thr Se - #r Leu His Asp Ile Ser 340 - # 345 - # 350 - - Asp Glu Pro Val Cys Met Thr Pro Phe Asn Ph - #e Asp Phe Glu Gln His 355 - # 360 - # 365 - - Ala Leu Thr Glu Glu Gln Met Lys Glu Leu Il - #e Tyr Arg Glu Gly Leu 370 - # 375 - # 380 - - Ala Phe Asn Pro Glu Tyr Gln His Met 385 3 - #90 - - - - (2) INFORMATION FOR SEQ ID NO:4: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 387 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: protein - - (iii) HYPOTHETICAL: NO - - (iv) ANTI-SENSE: NO - - (v) FRAGMENT TYPE: internal - - (vi) ORIGINAL SOURCE: - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:4: - - Met Glu Gly Gly Gly Ala Pro Pro Ala Asp Th - #r Val Met Ser Asp Ala 1 5 - # 10 - # 15 - - Ala Pro Ala Pro Pro Gln Met Gly Ile Glu As - #n Ile Pro Ala Val Leu 20 - # 25 - # 30 - - Ser His Gly Gly Arg Phe Ile Gln Tyr Asn Il - #e Phe Gly Asn Ile Phe 35 - # 40 - # 45 - - Glu Val Thr Ala Lys Tyr Lys Pro Pro Ile Me - #t Pro Ile Gly Lys Gly 50 - # 55 - # 60 - - Ala Tyr Gly Ile Val Cys Ser Ala His Asn Se - #r Glu Thr Asn Glu His 65 - #70 - #75 - #80 - - Val Ala Val Lys Lys Ile Ala Asn Ala Phe As - #p Asn Lys Ile Asp Ala 85 - # 90 - # 95 - - Lys Arg Thr Leu Arg Glu Ile Lys Leu Leu Ar - #g His Met Asp His Glu 100 - # 105 - # 110 - - Asn Val Val Ala Ile Arg Asp Ile Val Pro Pr - #o Pro Gln Arg Glu Val 115 - # 120 - # 125 - - Phe Asn Asp Val Tyr Ile Ala Tyr Glu Leu Me - #t Asp Thr Asp Leu His 130 - # 135 - # 140 - - Gln Ile Ile Arg Ser Asn Gln Ala Leu Ser Gl - #u Glu His Cys Gln Tyr 145 1 - #50 1 - #55 1 -#60 - - Phe Leu Tyr Gln Ile Leu Arg Gly Leu Lys Ty - #r Ile His Ser AlaAsn 165 - # 170 - # 175 - - Val Leu His Arg Asp Leu Lys Pro Ser Asn Le - #u Leu Leu Asn Ala Asn 180 - # 185 - # 190 - - Cys Asp Leu Lys Ile Cys Asp Phe Gly Leu Al - #a Arg Val Thr Ser Glu 195 - # 200 - # 205 - - Thr Asp Phe Met Thr Glu Tyr Val Val Thr Ar - #g Trp Tyr Arg Ala Pro 210 - # 215 - # 220 - - Glu Leu Leu Leu Asn Ser Ser Asp Tyr Thr Al - #a Ala Ile Asp Val Trp 225 2 - #30 2 - #35 2 -#40 - - Ser Val Gly Cys Ile Phe Met Glu Leu Met As - #p Arg Lys Pro LeuPhe 245 - # 250 - # 255 - - Pro Gly Arg Asp His Val His Gln Leu Arg Le - #u Leu Met Glu Leu Ile 260 - # 265 - # 270 - - Gly Thr Pro Ser Glu Asp Asp Leu Gly Phe Le - #u Asn Glu Asn Ala Lys 275 - # 280 - # 285 - - Arg Tyr Ile Arg Gln Leu Pro Pro Tyr Arg Ar - #g Gln Ser Phe Gln Glu 290 - # 295 - # 300 - - Lys Phe Pro His Val His Pro Glu Ala Ile As - #p Leu Val Glu Lys Met 305 3 - #10 3 - #15 3 -#20 - - Leu Thr Phe Asp Pro Arg Lys Arg Ile Thr Va - #l Glu Asp Ala LeuAla 325 - # 330 - # 335 - - His Pro Tyr Leu Thr Ser Leu His Asp Ile Se - #r Asp Glu Pro Val Cys 340 - # 345 - # 350 - - Met Thr Pro Phe Ser Phe Asp Phe Glu Gln Hi - #s Ala Leu Thr Glu Glu 355 - # 360 - # 365 - - Gln Met Lys Glu Leu Ile Tyr Arg Glu Ala Le - #u Ala Phe Asn Pro Glu 370 - # 375 - # 380 - - Tyr Gln Gln 385 - - - - (2) INFORMATION FOR SEQ ID NO:5: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 375 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: protein - - (iii) HYPOTHETICAL: NO - - (iv) ANTI-SENSE: NO - - (v) FRAGMENT TYPE: internal - - (vi) ORIGINAL SOURCE: - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:5: - - Met Ala Asp Ala Asn Met Gly Ala Gly Gly Gl - #y Gln Phe Pro Asp Phe 1 5 - # 10 - # 15 - - Pro Ser Val Leu Thr His Gly Gly Gln Tyr Va - #l Gln Phe Asp Ile Phe 20 - # 25 - # 30 - - Gly Asn Phe Phe Glu Ile Thr Thr Lys Tyr Ar - #g Pro Pro Ile Met Pro 35 - # 40 - # 45 - - Ile Gly Arg Gly Ala Tyr Gly Ile Val Cys Se - #r Val Leu Asn Thr Glu 50 - # 55 - # 60 - - Leu Asn Glu Met Val Ala Val Lys Lys Ile Al - #a Asn Ala Phe Asp Ile 65 - #70 - #75 - #80 - - Tyr Met Asp Ala Lys Arg Thr Leu Arg Glu Il - #e Lys Leu Leu Arg His 85 - # 90 - # 95 - - Leu Asp His Glu Asn Val Ile Gly Leu Arg As - #p Val Ile Pro Pro Pro 100 - # 105 - # 110 - - Leu Arg Arg Glu Phe Ser Asp Val Tyr Ile Al - #a Thr Glu Leu Met Asp 115 - # 120 - # 125 - - Thr Asp Leu His Gln Ile Ile Arg Ser Asn Gl - #n Gly Leu Ser Glu Asp 130 - # 135 - # 140 - - His Cys Gln Tyr Phe Met Tyr Gln Leu Leu Ar - #g Gly Leu Lys Tyr Ile 145 1 - #50 1 - #55 1 -#60 - - His Ser Ala Asn Val Leu His Arg Asp Leu Ly - #s Pro Ser Asn LeuLeu 165 - # 170 - # 175 - - Val Asn Ala Asn Cys Asp Leu Lys Ile Cys As - #p Phe Gly Leu Ala Arg 180 - # 185 - # 190 - - Pro Asn Ile Glu Asn Glu Asn Met Thr Glu Ty - #r Val Val Thr Arg Trp 195 - # 200 - # 205 - - Tyr Arg Ala Pro Glu Leu Leu Leu Asn Ser Se - #r Asp Tyr Thr Ala Ala 210 - # 215 - # 220 - - Ile Asp Val Trp Ser Val Gly Cys Ile Phe Me - #t Glu Leu Met Asn Arg 225 2 - #30 2 - #35 2 -#40 - - Lys Pro Leu Phe Gly Gly Lys Asp His Val Hi - #s Gln Ile Arg LeuLeu 245 - # 250 - # 255 - - Thr Glu Leu Leu Gly Thr Pro Thr Glu Ala As - #p Leu Gly Phe Leu Gln 260 - # 265 - # 270 - - Asn Glu Asp Ala Lys Arg Tyr Ile Arg Gln Le - #u Pro Gln His Pro Arg 275 - # 280 - # 285 - - Gln Gln Leu Ala Glu Val Phe Pro His Val As - #n Pro Leu Ala Ile Asp 290 - # 295 - # 300 - - Leu Val Asp Lys Met Leu Thr Phe Asp Pro Th - #r Arg Arg Ile Thr Val 305 3 - #10 3 - #15 3 -#20 - - Glu Glu Ala Leu Asp His Pro Tyr Leu Ala Ly - #s Leu His Asp AlaGly 325 - # 330 - # 335 - - Asp Glu Pro Ile Cys Pro Val Pro Phe Ser Ph - #e Asp Phe Glu Gln Gln 340 - # 345 - # 350 - - Gly Ile Gly Glu Glu Gln Ile Lys Asp Met Il - #e Tyr Gln Glu Ala Leu 355 - # 360 - # 365 - - Ser Leu Asn Pro Glu Tyr Ala 370 - # 375 - - - - (2) INFORMATION FOR SEQ ID NO:6: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 371 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: protein - - (iii) HYPOTHETICAL: NO - - (iv) ANTI-SENSE: NO - - (v) FRAGMENT TYPE: internal - - (vi) ORIGINAL SOURCE: - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:6: - - Met Ala Arg Val Asn Gln Asn Gly Val Ala Gl - #u Phe Pro Ala Val Gln 1 5 - # 10 - # 15 - - Thr His Gly Gly Gln Phe Val Gln Tyr Asn Va - #l Phe Gly Asn Leu Phe 20 - # 25 - # 30 - - Glu Val Thr Ala Lys Tyr Arg Pro Pro Ile Me - #t Pro Ile Gly Arg Gly 35 - # 40 - # 45 - - Ala Tyr Gly Ile Val Cys Ser Leu Leu Asn Th - #r Glu Thr Asn Glu Leu 50 - # 55 - # 60 - - Val Ala Val Lys Lys Ile Ala Asn Ala Phe As - #p Asn His Met Asp Ala 65 - #70 - #75 - #80 - - Lys Arg Thr Leu Arg Glu Ile Lys Leu Leu Ar - #g His Leu Asp His Glu 85 - # 90 - # 95 - - Asn Val Ile Gly Leu Arg Asp Val Ile Pro Pr - #o Pro Leu Arg Arg Glu 100 - # 105 - # 110 - - Phe Asn Asp Val Tyr Ile Thr Thr Glu Leu Me - #t Asp Thr Asp Leu His 115 - # 120 - # 125 - - Gln Ile Ile Arg Ser Asn Gln Asn Leu Ser As - #p Glu His Cys Gln Tyr 130 - # 135 - # 140 - - Phe Leu Tyr Gln Ile Leu Arg Gly Leu Arg Ty - #r Ile His Ser Ala Asn 145 1 - #50 1 - #55 1 -#60 - - Ile Ile His Arg Asp Leu Lys Pro Ser Asn Le - #u Leu Leu Asn AlaAsn 165 - # 170 - # 175 - - Cys Asp Leu Lys Ile Ile Asp Phe Gly Leu Al - #a Arg Pro Thr Met Glu 180 - # 185 - # 190 - - Ser Asp Phe Met Thr Glu Tyr Val Val Thr Ar - #g Trp Tyr Arg Ala Pro 195 - # 200 - # 205 - - Glu Leu Leu Leu Asn Ser Ser Asp Tyr Thr Se - #r Ala Ile Asp Val Trp 210 - # 215 - # 220 - - Ser Val Gly Cys Ile Phe Met Glu Leu Met As - #n Lys Lys Pro Leu Phe 225 2 - #30 2 - #35 2 -#40 - - Pro Gly Lys Asp His Val His Gln Met Arg Le - #u Leu Thr Glu LeuLeu 245 - # 250 - # 255 - - Gly Thr Pro Thr Asp Ala Asp Val Gly Leu Va - #l Lys Asn Asp Asp Ala 260 - # 265 - # 270 - - Arg Arg Tyr Ile Arg Gln Leu Pro Gln Tyr Pr - #o Arg Gln Pro Leu Asn 275 - # 280 - # 285 - - Arg Val Phe Pro His Val His Pro Leu Ala Il - #e Asp Leu Val Asp Lys 290 - # 295 - # 300 - - Met Leu Thr Ile Asp Pro Thr Arg Arg Ile Th - #r Val Glu Glu Ala Leu 305 3 - #10 3 - #15 3 -#20 - - Ala His Pro Tyr Leu Glu Lys Leu His Asp Va - #l Ala Asp Glu ProIle 325 - # 330 - # 335 - - Cys Met Glu Pro Phe Ser Phe Glu Phe Glu Gl - #n Gln His Leu Asp Glu 340 - # 345 - # 350 - - Glu Gln Ile Lys Glu Met Ile Tyr Arg Glu Al - #a Leu Ala Leu Asn Pro 355 - # 360 - # 365 - - Glu Tyr Ala 370 - - - - (2) INFORMATION FOR SEQ ID NO:7: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 370 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: protein - - (iii) HYPOTHETICAL: NO - - (iv) ANTI-SENSE: NO - - (v) FRAGMENT TYPE: internal - - (vi) ORIGINAL SOURCE: - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:7: - - Met Asn Thr Gly Gly Gly Gln Tyr Thr Asp Ph - #e Pro Ala Val Asp Thr 1 5 - # 10 - # 15 - - His Gly Gly Gln Phe Ile Ser Tyr Asp Ile Ph - #e Gly Ser Leu Phe Glu 20 - # 25 - # 30 - - Ile Thr Ser Lys Tyr Arg Pro Pro Ile Ile Pr - #o Ile Gly Arg Gly Ala 35 - # 40 - # 45 - - Tyr Gly Ile Val Cys Ser Val Leu Asp Thr Gl - #u Thr Asn Glu Leu Val 50 - # 55 - # 60 - - Ala Met Lys Lys Ile Ala Asn Ala Phe Asp As - #n His Met Asp Ala Lys 65 - #70 - #75 - #80 - - Arg Thr Leu Arg Glu Ile Lys Leu Leu Arg Hi - #s Leu Asp His Glu Asn 85 - # 90 - # 95 - - Ile Ile Ala Ile Arg Asp Val Val Pro Pro Pr - #o Leu Arg Arg Gln Phe 100 - # 105 - # 110 - - Ser Asp Val Tyr Ile Ser Thr Glu Leu Met As - #p Thr Asp Leu His Gln 115 - # 120 - # 125 - - Ile Ile Arg Ser Asn Gln Ser Leu Ser Glu Gl - #u His Cys Gln Tyr Phe 130 - # 135 - # 140 - - Leu Tyr Gln Leu Leu Arg Gly Leu Lys Tyr Il - #e His Ser Ala Asn Ile 145 1 - #50 1 - #55 1 -#60 - - Ile His Arg Asp Leu Lys Pro Ser Asn Leu Le - #u Leu Asn Ala AsnCys 165 - # 170 - # 175 - - Asp Leu Lys Ile Cys Asp Phe Gly Leu Ala Ar - #g Pro Thr Ser Glu Asn 180 - # 185 - # 190 - - Asp Phe Met Thr Glu Tyr Val Val Thr Arg Tr - #p Tyr Arg Ala Pro Glu 195 - # 200 - # 205 - - Leu Leu Leu Asn Ser Ser Asp Tyr Thr Ala Al - #a Ile Asp Val Trp Ser 210 - # 215 - # 220 - - Val Gly Cys Ile Phe Met Glu Leu Met Asn Ar - #g Lys Pro Leu Phe Pro 225 2 - #30 2 - #35 2 -#40 - - Gly Lys Asp His Val His Gln Met Arg Leu Le - #u Thr Glu Leu LeuGly 245 - # 250 - # 255 - - Thr Pro Thr Glu Ser Asp Leu Gly Phe Thr Hi - #s Asn Glu Asp Ala Lys 260 - # 265 - # 270 - - Arg Tyr Ile Arg Gln Leu Pro Asn Phe Pro Ar - #g Gln Pro Leu Ala Lys 275 - # 280 - # 285 - - Leu Phe Ser His Val Asn Pro Met Ala Ile As - #p Leu Val Asp Arg Met 290 - # 295 - # 300 - - Leu Thr Phe Asp Pro Asn Arg Arg Ile Thr Va - #l Glu Gln Ala Leu Asn 305 3 - #10 3 - #15 3 -#20 - - His Gln Tyr Leu Ala Lys Leu His Asp Pro As - #n Asp Glu Pro IleCys 325 - # 330 - # 335 - - Gln Lys Pro Phe Ser Phe Glu Phe Glu Gln Gl - #n Pro Leu Asp Glu Glu 340 - # 345 - # 350 - - Gln Ile Lys Glu Met Ile Tyr Gln Glu Ala Il - #e Ala Leu Asn Pro Thr 355 - # 360 - # 365 - - Tyr Gly 370 - - - - (2) INFORMATION FOR SEQ ID NO:8: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 371 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: protein - - (iii) HYPOTHETICAL: NO - - (iv) ANTI-SENSE: NO - - (v) FRAGMENT TYPE: internal - - (vi) ORIGINAL SOURCE: - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:8: - - Met Glu Asn Glu Thr Asn Glu Lys Leu Glu Il - #e Lys Gly Ile Pro Thr 1 5 - # 10 - # 15 - - His Glu Gly Lys Tyr Val Glu Tyr Asn Val Le - #u Gly Asn Phe Phe Glu 20 - # 25 - # 30 - - Val Thr Ser Lys Tyr Ile Pro Pro Ile Gln Pr - #o Val Gly Arg Gly Ala 35 - # 40 - # 45 - - Tyr Gly Met Val Cys Cys Ala Thr Asn Ser Gl - #u Thr Lys Glu Glu Val 50 - # 55 - # 60 - - Ala Ile Lys Lys Ile Gly Asn Ala Phe Glu As - #n Arg Ile Asp Ala Lys 65 - #70 - #75 - #80 - - Arg Thr Leu Arg Glu Ile Lys Leu Leu Ser Hi - #s Met Asp His Glu Asn 85 - # 90 - # 95 - - Ile Ile Lys Ile Lys Asp Ile Val Arg Pro Pr - #o Asp Arg Glu Glu Phe 100 - # 105 - # 110 - - Asn Asp Val Tyr Ile Val Tyr Glu Leu Met As - #p Thr Asp Leu His Gln 115 - # 120 - # 125 - - Ile Ile Arg Ser Ser Gln Ala Leu Thr Asp As - #p His Cys Gln Tyr Phe 130 - # 135 - # 140 - - Leu Tyr Gln Leu Leu Arg Gly Leu Lys Tyr Va - #l His Ser Ala Asn Val 145 1 - #50 1 - #55 1 -#60 - - Leu His Arg Asp Leu Lys Pro Ser Asn Leu Le - #u Leu Asn Ala AsnCys 165 - # 170 - # 175 - - Asp Leu Lys Ile Cys Asp Phe Gly Leu Ala Ar - #g Thr Thr Ser Glu Ala 180 - # 185 - # 190 - - Asp Phe Met Thr Glu Tyr Val Val Thr Arg Tr - #p Tyr Arg Ala Pro Glu 195 - # 200 - # 205 - - Leu Leu Leu Asn Cys Thr Glu Tyr Thr Ala Al - #a Ile Asp Ile Trp Ser 210 - # 215 - # 220 - - Val Gly Cys Ile Leu Met Glu Leu Ile Lys Ar - #g Glu Pro Leu Phe Pro 225 2 - #30 2 - #35 2 -#40 - - Gly Arg Asp Tyr Ala Gln Gln Leu Gly Leu Il - #e Ile Ala Leu LeuGly 245 - # 250 - # 255 - - Ser Pro Glu Asp Ser Asp Leu Gly Phe Leu Ar - #g Ser Asp Asn Ala Arg 260 - # 265 - # 270 - - Lys Tyr Val Lys His Leu Pro Arg Val Pro Ar - #g His Pro Phe Ser Gln 275 - # 280 - # 285 - - Lys Phe Pro Asp Val Ser Pro Leu Ala Leu As - #p Leu Ala Glu Arg Met 290 - # 295 - # 300 - - Leu Val Phe Asp Pro Ala Lys Arg Ile Thr Va - #l Glu Asp Ala Leu Asn 305 3 - #10 3 - #15 3 -#20 - - His Pro Phe Leu Ile Ser Leu His Glu Ile As - #n Glu Glu Pro ValCys 325 - # 330 - # 335 - - Asp Ser Pro Phe Asn Phe Asp Phe Glu Gln Al - #a Ser Leu Ser Glu Asp 340 - # 345 - # 350 - - Asp Ile Lys Glu Leu Ile Trp Asn Glu Ala Le - #u Lys Phe Asp Pro Asn 355 - # 360 - # 365 - - Thr Met Lys 370 - - - - (2) INFORMATION FOR SEQ ID NO:9: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 372 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: protein - - (iii) HYPOTHETICAL: NO - - (iv) ANTI-SENSE: NO - - (v) FRAGMENT TYPE: internal - - (vi) ORIGINAL SOURCE: - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:9: - - Met Ala Thr Pro Val Glu Pro Pro Asn Gly Il - #e Arg Thr Pro Gly Lys 1 5 - # 10 - # 15 - - His Tyr Tyr Ser Met Trp Gln Ser Leu Phe Gl - #u Ile Asp Thr Lys Tyr 20 - # 25 - # 30 - - Val Pro Ile Lys Pro Ile Gly Arg Gly Ala Ty - #r Gly Ile Val Cys Ser 35 - # 40 - # 45 - - Ser Val Asn Arg Glu Thr Asn Glu Lys Val Al - #a Ile Lys Lys Ile Asn 50 - # 55 - # 60 - - Asn Ala Phe Glu Asn Arg Ile Asp Ala Leu Ar - #g Thr Leu Arg Glu Leu 65 - #70 - #75 - #80 - - Lys Leu Leu Arg His Leu Arg His Glu Asn Va - #l Ile Ala Leu Lys Asp 85 - # 90 - # 95 - - Val Met Met Pro Ile His Arg Arg Ser Phe Ly - #s Asp Val Tyr Leu Val 100 - # 105 - # 110 - - Tyr Glu Leu Met Asp Thr Asp Leu His Gln Il - #e Ile Lys Ser Ser Gln 115 - # 120 - # 125 - - Thr Leu Ser Asn Asp His Cys Gln Tyr Phe Le - #u Phe Gln Leu Leu Arg 130 - # 135 - # 140 - - Gly Leu Lys Tyr Leu His Ser Ala Asn Ile Le - #u His Arg Asp Leu Lys 145 1 - #50 1 - #55 1 -#60 - - Pro Gly Asn Leu Leu Ile Asn Ala Asn Cys As - #p Leu Lys Ile CysAsp 165 - # 170 - # 175 - - Phe Gly Leu Ala Arg Thr Ser Ser Gly Lys As - #p Gln Phe Met Thr Glu 180 - # 185 - # 190 - - Tyr Val Val Thr Arg Trp Tyr Arg Ala Pro Gl - #u Leu Leu Leu Cys Cys 195 - # 200 - # 205 - - Asp Asn Tyr Gly Thr Ser Ile Asp Val Trp Se - #r Val Gly Cys Ile Phe 210 - # 215 - # 220 - - Ala Glu Leu Leu Gly Arg Lys Pro Val Phe Pr - #o Gly Thr Glu Cys Leu 225 2 - #30 2 - #35 2 -#40 - - Asn Gln Leu Lys Leu Ile Ile Asn Ile Leu Gl - #y Ser Gln Arg GluGlu 245 - # 250 - # 255 - - Asp Ile Glu Phe Ile Asp Asn Pro Lys Ala Ar - #g Lys Tyr Ile Lys Ser 260 - # 265 - # 270 - - Leu Pro Tyr Ser Pro Gly Thr Pro Phe Ser Ar - #g Leu Tyr Pro His Ala 275 - # 280 - # 285 - - His Pro Leu Ala Ile Asp Leu Leu Gln Arg Me - #t Leu Val Phe Asp Pro 290 - # 295 - # 300 - - Ser Lys Arg Ile Ser Val Ile Glu Ala Leu Gl - #n His Pro Tyr Met Ser 305 3 - #10 3 - #15 3 -#20 - - Pro Leu Tyr Asp Pro Asn Thr Asp Pro Pro Al - #a Gln Val Pro IleAsn 325 - # 330 - # 335 - - Leu Asp Ile Asp Glu Asp Leu Gly Glu Glu Th - #r Ile Arg Glu Met Met 340 - # 345 - # 350 - - Trp Ser Glu Ile Leu Glu Tyr His Pro Glu Al - #a Ala Thr Ala Ala Met 355 - # 360 - # 365 - - Glu Val Val Leu 370 - - - - (2) INFORMATION FOR SEQ ID NO:10: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 8 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (iii) HYPOTHETICAL: NO - - (iv) ANTI-SENSE: NO - - (v) FRAGMENT TYPE: internal - - (vi) ORIGINAL SOURCE: - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:10: - - Asn Ile Phe Glu Val Thr Ala Lys 1 5 - - - - (2) INFORMATION FOR SEQ ID NO:11: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 12 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (iii) HYPOTHETICAL: NO - - (iv) ANTI-SENSE: NO - - (v) FRAGMENT TYPE: internal - - (vi) ORIGINAL SOURCE: - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:11: - - Asp Leu Lys Pro Ser Asn Leu Leu Leu Asn Al - #a Asn 1 5 - # 10 - - - - (2) INFORMATION FOR SEQ ID NO:12: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (iii) HYPOTHETICAL: NO - - (iv) ANTI-SENSE: NO - - (v) FRAGMENT TYPE: internal - - (vi) ORIGINAL SOURCE: - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:12: - - Trp Tyr Arg Pro Pro Glu Leu Leu Leu Asn 1 5 - # 10 - - - - (2) INFORMATION FOR SEQ ID NO:13: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 7 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (iii) HYPOTHETICAL: NO - - (iv) ANTI-SENSE: NO - - (v) FRAGMENT TYPE: internal - - (vi) ORIGINAL SOURCE: - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:13: - - Lys Pro Leu Phe Pro Gly Arg 1 5 - - - - (2) INFORMATION FOR SEQ ID NO:14: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 14 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (iii) HYPOTHETICAL: NO - - (iv) ANTI-SENSE: NO - - (v) FRAGMENT TYPE: internal - - (vi) ORIGINAL SOURCE: - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:14: - - Ala Ile Asp Leu Val Glu Lys Met Leu Thr Ph - #e Asp Pro Arg 1 5 - # 10__________________________________________________________________________

Claims

1. An isolated nucleic acid molecule that includes an open reading frame encoding a MAP kinase protein, said protein being activated by an agent that induces a disease defense response in plants, wherein said open reading frame encodes Sequence I.D. No. 2.

2. The nucleic acid molecule of claim 1, which comprises Sequence I.D. No. 1.

3. A recombinant DNA molecule comprising the nucleic acid molecule of claim 1, operably linked to a vector for transforming cells.

4. An isolated single stranded or double stranded nucleic acid molecule having a sequence selected from the group consisting of:

a) Sequence I.D. No. 1;

b) an allelic variant of Sequence I.D. No. 1; and

c) a sequence encoding a polypeptide having amino acid Sequence I.D. No. 2.

5. A recombinant DNA molecule comprising the nucleic acid molecule of claim 4, operably linked to a vector for transforming plant cells.

6. A plant cell transformed with the recombinant DNA molecule of claim 3.

7. A transgenic plant comprising the recombinant DNA molecule of claim 3.

8. A plant cell transformed with the recombinant DNA molecule of claim 5.

9. A transgenic plant comprising the recombinant DNA molecule of claim 5.

10. An isolated nucleic acid molecule that encodes a salicylic acid-activated MAP kinase protein having SEQ ID NO:2, or an allelic variant thereof.