Protein tyrosine kinase A6

Abstract

A novel protein tyrosine kinase (A6) exhibiting no significant similarity to any known kinase. This protein in widely expressed throughout the body and is present in a variety of vertebrates. The cDNA was expressed in bacteria as a fusion protein which was both autophosphorylated and exhibited kinase activity toward exogenous substrates. Potential uses of this invention include immunodiagnostics and antiproliferative therapeutics.

Description

FIELD OF THE INVENTION

This invention relates to protein tyrosine kinases. More specifically, it relates to the cloning of a human gene encoding a novel protein tyrosine kinase unrelated to any previously identified protein kinase.

BACKGROUND OF THE INVENTION

Protein phosphorylation has been implicated in a number of important physiologic events ranging from normal cell growth and differentiation to malignant transformation. Phosphorylation is mediated by a superfamily of enzymes known as protein kinases. In eukaryotic cells, these enzymes phosphorylate hydroxyl groups of serine (ser), threonine (thr) and tyrosine (tyr) residues by transferring the .lambda. phosphate from ATP using a magnesium or manganese ion cofactor. Tyrosine kinases, unlike ser/thr kinases, prefer manganese ion over magnesium ion. Although the vast majority of kinases are specific to either tyr or ser/thr, several recently-described kinases can phosphorylate all three residues (Ben-David et al., (1991) EMBO J., 10: 317-325; Howell et al., (1991) Mol. Cell. Biol., 11: 568-572). These proteins are called "dual specificity protein kinases" (Lindberg et al., (1992) Trends Biochem. Sci., 17: 114-119).

Tyrosine phosphorylation is an early signal transduction event which occurs after the binding of growth factors, hormones or cytokines to cell surface receptors and is a mechanism by which a number of oncogene products exert their proliferation-inducing effects (Aaronson, (1991) Science, 254: 1146-1153; Hanks et al., (1988) Science, 241: 42-52; Hunter and Cooper, (1985) Annu. Rev. Biochem., 54: 897-930). Oncogenes are mutated forms of normal genes (proto-oncogenes) which have been picked up by retroviruses. Most proto-oncogenes encode proteins mediating events by which growth factors stimulate normal cell division (Cantley et al., (1991) Cell, 64: 281-302). For example, the v-src and v-abl genes encode transforming tyrosine kinases from Rous sarcoma virus and Abelson murine leukemia virus, respectively, which are oncogenic counterparts of the corresponding normal cellular genes. These kinases may be classified as either receptor (v-erb B, v-neu) or nonreceptor (v-src, v-abl) tyrosine kinases.

Changes in tyrosine phosphorylation are believed to be responsible for initiating reaction cascades leading to the covalent modification of proteins. In some instances, these other proteins are kinases. Many of these proteins, including p34.sup.cdc2, and the platelet derived growth factor receptor, are either protein kinases or are regulated by their phosphorylation state. Since several protein kinases, including p34.sup.cac2, regulate entry and progression through the cell cycle, they thus represent important control points in cell growth.

To elucidate the mechanisms involved in the control of cell proliferation, additional novel kinases have been identified by either low stringency hybridization and polymerase chain reaction using primers corresponding to conserved kinase regions (Kraus and Aaronson, (1991) Methods Enzymol., 200: 546-556; Wilks, (1991) Methods Enzymol., 200: 543-546) or by expression cloning (Lindberg et al., (1988) Oncogene, 3: 629-633). Enzymatically active tyrosine kinases undergo autophosphorylation on their own tyrosine residues, allowing their detection by antibodies against phosphotyrosine (pTyr). Since bacteria lack protein tyrosine kinases (PTKs), antibodies to pTyr have been particularly useful in the identification and characterization of several novel kinases isolated from bacterial expression systems (Kornbluth et al., (1988) Mol. Cell Biol., 8: 5541-5544; Letwin et al., (1988) Oncogene, 3: 621-627). Most recently, two novel protein kinases called TIK and TTK have been described (Icely et al., (1991) J. Biol. Chem., 266: 16073-16077; Mills et al., (1992) J. Biol. Chem., 267: 16000-16006). TIK is a ser/thr kinase containing consensus ser/thr kinase catalytic residues while TTK is predominantly a ser/thr kinase with a low level of tyrosine phosphorylation activity and is associated with cell proliferation.

BRIEF DESCRIPTION OF THE FIGURE

FIG. 1 shows the sequence alignment of amino acids 85-114 of the A6 sequence shown in SEQ. ID NO: 2 with homologous regions in cofilin, (SEQ. ID NO: 5) actophorin (SEQ. ID NO: 6) and actin depolymerizing factor (ADF). (SEQ ID NO: 7) Conserved amino acids are boxed.

SUMMARY OF THE INVENTION

One embodiment of the present invention is an isolated polynucleotide encoding the human A6 protein tyrosine kinase. Preferably, this polynucleotide has the sequence corresponding to the coding region of SEQ ID NO: 1. In another aspect of this preferred embodiment, there is provided an isolated nucleotide sequence having homology to at least 18 contiguous nucleotides of this polynucleotide. Another aspect of the invention provides non-human species variations of the isolated tyrosine kinase.

According to another embodiment of the invention, there is provided a recombinant construct comprising the coding region of SEQ ID NO: 1 operably linked to a heterologous promoter in an expression vector. Advantageously, this recombinant construct is expressed in cells. Preferably, these cells are prokaryotic; most preferably, they are E. coli Y1089 cells. According to another aspect of this preferred embodiment, the expression vector is .lambda.pCEVlacz which contains the .beta.-galactosidase promoter and gene sequence. Preferably, the sequence corresponding to SEQ ID NO: 1 is adjacent to the .beta.-galactosidase gene, and upon expression the protein encoded by SEQ ID NO: 1 and .beta.-galactosidase form a fusion protein.

In accordance with another aspect of the invention, there is provided a completely new human protein tyrosine kinase having a molecular weight of about 40,000 daltons, designated A6, in isolated form. Preferably, this kinase has the amino acid sequence corresponding to SEQ ID NO: 2. In another aspect of this preferred embodiment, there are provided non-human species variations of the A6 kinase.

Still another embodiment of the present invention is isolated antibodies against the A6 protein tyrosine kinase. Preferably, these isolated antibodies are monoclonal; most preferably, they are either BF2 or DA6. According to another aspect of this preferred embodiment, the antibodies are polyclonal.

DETAILED DESCRIPTION OF THE INVENTION

The present invention discloses the prokaryotic expression cloning and in vitro characterization of a novel human protein tyrosine kinase. This protein kinase is highly divergent from previously described members of this important class of regulatory molecules. Nucleotide sequence analysis revealed that the predicted protein lacked consensus amino acid sequences commonly found in protein kinases. This kinase may be important in the regulation of cellular growth control pathways.

The human A6 gene sequence, fragments thereof, vectors containing this sequence or fragments thereof, cells transfected with this sequence or fragments thereof and protein purified from these cells are useful for studying the cellular distribution and expression of the A6 protein kinase. The expressed recombinant A6 protein is useful as a reagent for converting Tyr to pTyr. One of ordinary skill in the art who desires a particular tyrosine-phosphorylated protein can combine the expressed protein or .beta.-galactosidase fusion protein in a reaction container with ATP, magnesium or manganese ion and the protein to be phosphorylated, as shown in Examples 3 and 4. Fragments of the A6 protein kinase gene consisting of at least 18 consecutive nucleotides unique to A6 are useful as polymerase chain reaction (PCR) probes for isolating other members of this new kinase family as well as the corresponding receptor gene from other species (See Example 10). These oligonucleotides are also useful for in situ hybridization and for probing Northern blots of RNA isolated from various tissues by well known methods to determine the A6 protein kinase distribution.

In addition, DNA sequences of 18 nucleotides correspond to six amino acids. Those of ordinary skill in the art will appreciate that a six amino acid peptide, when coupled to an immunogenic carrier protein such as keyhole limpet hemocyanin (KLH) or ovalbumin, can be utilized as an immunogen to raise antibodies against A6 kinase epitopes. Alternatively, the A6 kinase cDNA or fragments thereof can be expressed and the resulting polypeptide recovered and used as an immunogen. Antibodies against the A6 protein will allow immuno-histochemical localization of the protein in cells, tissues and body fluids.

The use of a number of prokaryotic expression vectors in addition to .lambda.pCevlacz is also within the scope of the present invention. Although the A6 kinase was expressed as a lacz fusion protein, the expression of the protein itself by minor technical modifications known to one of ordinary skill in the art, is also envisioned. In addition, the use of eukaryotic expression vectors and transfection of eukaryotic cells is also contemplated. However, eukaryotic cells possess endogenous kinase activity, so mock-transfected cell protein kinase activity must be subtracted from transfected cell protein kinase activity to determine true A6 kinase activity.

One of ordinary skill in the art will appreciate that the A6 gene sequence can be rapidly incorporated into almost any desired vector. In the present invention, the most preferable expression vectors are prokaryotic, although the use of yeast and viral, particularly baculoviral, expression vectors is also within the scope of the present invention, as is the production of the A6 kinase or fragments thereof in these cell types.

Antibodies generated against the A6 protein tyrosine kinase will be useful in the production of diagnostic kits for determining the level of the A6 kinase in both normal and neoplastic tissue to correlate its activity with cell proliferation. Antibodies against A6 will also be useful in cellular localization of the A6 kinase by immunocytochemistry. Further, these antibodies can be used for affinity chromatography to isolate large quantities of the expressed protein.

Inhibitors of the A6 kinase will be useful in controlling A6-mediated cell growth. Any of the known tyrosine kinase inhibitors may exhibit particular specificity toward the A6 kinase as described in Example 9. With the gene sequence determined, mutations can now be introduced in order to study structure-function relationships as they relate to ATP and pTyr binding and to effector system coupling. This information will be useful in the design of inhibitors able to specifically block A6 kinase activity which may inhibit aberrant cellular growth processes including neoplastic growth, atherosclerosis and psoriasis. Identification and characterization of this novel protein kinase will help elucidate the processes controlling both normal and aberrant cell growth.

The recombinantly expressed kinase will also be useful in screening new kinase inhibitors both in vitro and in vivo. The bacterial system is especially well-suited for this purpose since the lack of endogenous protein tyrosine kinases will greatly decrease background binding of the potential inhibitors to endogenous proteins. Any background binding may be attributed to inhibition of endogenous ser/thr kinases, although this background binding is expected to be very low since bacteria contain low levels of these proteins.

To identify novel tyrosine kinases unrelated to previously identified members of the PTK superfamily, a human lung fibroblast cDNA library was screened with a monoclonal antibody to pTyr as described in the following example.

EXAMPLE 1

cDNA library construction and screening

Human lung fibroblast M426 cells were developed in the laboratory of Stuart Aaronson, National Cancer Institute, National Institutes of Health, Bethesda, Md. An expression library was constructed by well known methods using oligo (dT)-primed M426 human lung fibroblast cDNA packaged into the prokaryotic expression vector .lambda.pCEVlacz which contains the .beta.-galactosidase (lacz) promoter and gene sequence (Ishibashi et al., (1992) Proc. Natl. Acad. Sci. U.S.A., 89: 12170-12174). For library screening, the bacterial strain Y1090 was infected with phage (2.times.10.sup.4 per 150 mm plate) and plated on agar plates containing 50 .mu.g/ml ampicillin. The plates were incubated for 4 hours at 37.degree. C., overlayed with nitrocellulose filters pretreated with 10 mM isopropyl-1-thio-.beta.-D-galactopyranoside (IPTG) and incubated for 6 hours at 37.degree. C. Filters were rinsed in TTBS (25 mM Tris-HCl, pH 7.5, 150 mM NaCl, 0.05% Tween-20) and nonspecific binding sites were blocked with 3% nonfat dry milk in TTBS for 1 hour at room temperature. The filters were probed with the mouse monoclonal anti-pTyr antibody 4G10 (Upstate Biotechnology, Inc., Lake Placid, N.Y.) overnight, washed twice with TTBS and positive clones were detected with [.sup.125 I] labeled protein A for 1 hour. Filters were washed four times with TTBS, air-dried and exposed to Kodak XAR film (Eastman Kodak, Rochester, N.Y.) overnight at -70.degree. C. Positive plaques were isolated and subjected to secondary and tertiary screenings, resulting in pure plaques.

The cDNA inserts from plaque-purified clones were sequenced using Sequenase.TM. (United States Biochemical, Cleveland, Ohio). The majority of the positive clones were identified as the tyrosine kinases src or fyn based on the molecular weights of the deduced encoded proteins. However, one clone, designated A6, contained a 3 kilobase insert designated as SEQ ID NO: 1 whose deduced amino acid sequence exhibited little or no sequence similarity to any known protein.

Nucleotide and predicted amino acid sequence of A6

The open reading frame (ORF) of SEQ ID NO: 1 encoding the A6 kinase consisted of 1050 base pairs starting with an initiating methionine codon at position 61 and ending with a TAA termination codon at nucleotide 1110. The open reading frame was flanked by 5' and 3' untranslated regions consisting of 60 and 1890 nucleotides, respectively, with a putative polyadenylation signal (AATAAA) at position 2953. Translation of the ORF resulted in a 350 amino acid protein with a calculated molecular weight of 40,285 daltons.

To search for clones containing additional 5' untranslated sequence, the 3 kilobase A6 fragment was used to screen the M426 cDNA library. Analysis of nine additional clones indicated the absence of any additional 5' untranslated sequence.

Computer analysis of the deduced A6 protein sequence

Computer analysis using the Prosite program (Bairoch, (1992) Nucleic Acids Res., 20:2013-2018) revealed that the predicted A6 amino acid sequence lacked an amino terminal secretory signal sequence and a membrane spanning domain. A consensus N-myristoylation site (GEDRKHPFYW-XX-STAGCNP) (SEQ. ID. NO. 8) was found at gly6. N-myristoylation is a post-translational modification of a number of oncogenic tyrosine kinases which allows anchoring to the cell membrane via the myristate lipid moiety. Several potential protein kinase C phosphorylation sites (S/T-X-R/K) were found at thru.sub.107, thru.sub.124, ser.sub.233, ser.sub.265 and ser.sub.274. Two consensus tyrosine kinase phosphorylation sites were found at tyr.sub.236 and tyr.sub.249. The A6 protein was analyzed for similarity to existing sequences using the National Center for Biotechnology Information (NCBI) BLAST network service (Altschul et al., (1990) J. Mol. Biol., 215: 403-410). Searches of NCBI databases (SWISS-PROT 25.0, PIR 36.0 and GenPept-GenBank 76.0) as well as the Protein Kinase Catalytic Domain Data Base (Hanks and Quinn, (1991) Methods Enzymol., 200: 38-62) indicated that A6 showed no significant similarity to any known protein.

The protein kinase family, which includes more than 100 members of eukaryotic origin, all have a discrete catalytic domain that can be divided into twelve different subdomains (Hanks and Quinn, supra.). The conserved features within these subdomains help to define a consensus sequence for protein kinases. The A6 sequence did not exhibit any of the sequence motifs commonly conserved among protein kinases as judged by using the pattern and matching programs of the University of Wisconsin Genetics Computer Group's Motifs, ProfileScan and Profile Gap computer programs (Carrera et al., (1993) Proc. Natl. Acad. Sci. U.S.A., 90: 442-446).

Although proteins exhibiting kinase activity but having little or no similarity to the catalytic domains of protein kinases have been described, computer analysis of the deduced A6 sequence failed to reveal significant similarity with the following "atypical" kinases: BCR (Maru and Witte, (1991) Cell, 67: 459-468), the hepatitis B virus transactivator protein HBx (Wu et al., (1990) Cell, 63: 687-695) and aceK, an isocitrate dehydrogenase kinase/phosphatase specific for ser/thr residues from E. coli (Klumpp et al., (1988) J. Bacteriol., 170: 2763-2769). For further comparison, pairwise alignments between the A6 sequence, representatives of the major protein kinase subfamilies, and the "atypical" kinases BCR and HBx, were generated using the FASTA program (Pearson and Lipman, (1988) Proc. Natl. Acad. Sci. U.S.A., 85: 2444-2448). The RDF2 program was used to judge the statistical significance of the alignments (Pearson and Lipman, supra). Alignment scores generated by the FASTA program are shown in Table 1; scores of 80 and higher reflect significant similarity. Although no significant similarities were observed between the "atypical" kinases and any other protein kinase, relationships between various subfamilies were readily observed. The A6 sequence contained a potential catalytic subdomain I/II motif (Hanks et al., (1988) Science, 241: 42-48) with residues 113-123 representing the glycine-rich region characteristic of a nucleotide binding domain followed by a downstream lysine (lys.sub.135) which is a critical residue for proper phosphotransferase activity (Ben-David et al., (1991) EMBO J., 10: 379 317-325). However, similarity to other subdomains was not observed. Thus, the A6 gene encodes a unique "atypical" kinase.

To determine whether a kinase activity was associated with the protein encoded by the A6 gene, the protein was expressed in bacteria and the recombinant protein analyzed as described below.

TABLE 1__________________________________________________________________________Comparison of the predicted A6 amino acid sequenceto those of the catalytic domains of representative protein kinasesAtypical Dual-Specificity TyrosineA6 BCR HBX CLK DPYK1 MCK1 MIK1 MKK1A C-SRC MET PDGFR-.alpha.__________________________________________________________________________A6 1730BCR 49 1233HBx 39 30 833CLK 29 32 34 1736DPYK1 27 23 31 109 1439MCK1 33 44 37 176 85 1621MIK1 28 27 32 101 113 164 1376MKK1A 30 54 31 109 107 195 207 1147C-SRC 34 28 27 98 200 140 138 171 1330MET 29 33 34 47 113 111 138 171 447 1376PDGFR-.alpha. 41 32 36 82 160 167 97 137 395 414 1809C-MOS 55 32 37 77 119 146 118 146 171 183 155PKC-.gamma. 44 35 30 107 105 191 179 205 222 177 152RKS1-C 69 29 33 132 130 195 36 183 153 126 152__________________________________________________________________________ The A6 sequence was compared to known protein kinases using the FASTA program. The values represent the optimized alignment scores and values o 80 or higher indicate significant similarity. Designations for representative protein kinase catalytic domain sequences were taken from the protein kinase data base of Hanks and Quinn (8) except for BCR (21) and HBx (27).

EXAMPLE 2

Bacterial expression of .beta.-gal-A6 fusion protein

The E. coli strain Y1089 was grown to log phase (OD.sub.600 =0.4) in NZY media and infected with the .lambda.pCEVlacz vector from Example 1 containing the A6 gene at a multiplicity of infection of 10:1 (phage:cells). Cells were grown in the presence of 100 .mu.M IPTG for 2 hours at 37.degree. C. to induce expression of the .beta.-galactosidase-A6 fusion protein. For analysis of bacterial lysates, 1 ml aliquots of lysed cells were centrifuged to pellet the membranes and cell debris and resuspended in 100 .mu.l 2.times.SDS sample buffer (0.125 M Tris-HCl, pH 6.8, 4% SDS, 20% glycerol, 0.1M dithiothreitol, 0.2% bromphenol blue). Samples (20-40 .mu.l each) were analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). For immunoprecipitations, cells were resuspended in Nonidet.TM. P-40 (NP-40) lysis buffer (50 mM Tris-HCl, pH 8.0, 150 mM NaCl, 1 mM EDTA, 1% NP-40, 100 mM phenylmethylsulfonylfluoride (PMSF), 10 .mu.g/ml pepstatin) and lysed by sonication. Lysates were clarified by centrifugation at 14,000.times.g for 10 minutes.

SDS-PAGE analysis of bacterial cell lysates infected with .lambda.pCEVlacz-A6 revealed the presence of a 150 kDa protein induced by IPTG. Since the .lambda.pCEVlacz expression vector alone encoded only the 110 kDa .beta.-gal fusion protein, the deduced molecular weight of the A6 expression product itself was approximately 40 kDa, in good agreement with the calculated molecular weight based on the deduced amino acid sequence (Example 1). To confirm that the 150 kDa protein was a .beta.-gal fusion product, bacterial lysates were analyzed by immunoblotting using either a mouse monoclonal anti-.beta.-galactosidase antibody (Promega, Madison, Wis.) or anti-pTyr. Bands were visualized using [.sup.125 I] protein A. The .lambda.pCEVlacz-A6 fusion product was detected as a predominant immunoreactive species of approximately 150 kDa, consistent with the size of the IPTG inducible protein.

EXAMPLE 3

Determination of .beta.-gal-A6 fusion protein kinase activity

To characterize the protein kinase activity of the .beta.-gal-A6 fusion protein, lysates from bacteria expressing .beta.-gal-A6 or .beta.-gal alone were analyzed by immunoblotting with anti-pTyr. A predominant 150 kDa species was detected in .beta.-gal-A6 lysates, consistent with the signal of the .beta.-gal-A6 fusion protein mentioned in Example 2. A number of additional anti-pTyr reactive proteins were also detected in the .beta.-gal-A6 lysates. Although lower molecular weight species may represent degradation products of the fusion protein, immunoreactive proteins greater than 150 kDa were also observed. This indicated that the fusion protein phosphorylated endogenous bacterial proteins. Immunoreactivity of anti-pTyr with the fusion product, as well as with the other proteins, was completely inhibited by pretreatment of cell lysates with alkaline phosphatase which removes phosphate groups, or by preincubation of the antipTyr with the competitive inhibitor phosphotyrosine (1 mM), but not with 1 mM phosphoserine or phosphothreonine. These results strongly suggested that .beta.-gal-A6 was tyrosine phosphorylated in bacteria.

To establish that the A6 protein was a tyrosine kinase, lysates of bacterial cells expressing .beta.-gal-A6 or .beta.-gal alone were immunoprecipitated with anti-.beta.-gal and the immune complexes analyzed by an in vitro kinase assay as described in the following example.

EXAMPLE 4

In vitro kinase assay of .beta.-gal-A6 immunoprecipitates

Cleared lysates were immunoprecipitated with either anti-.beta.-gal or anti-pTyr and washed twice with 1 ml NP-40 lysis buffer and twice with 1 ml kinase reaction buffer (50 mM HEPES, pH 7.4, 1% NP-40). Immunoprecipitates were resuspended in kinase reaction buffer containing 10 mM MnCl.sub.2 followed by addition of 20 .mu.Ci [.gamma.-.sup.32 P] ATP for 20 minutes at room temperature. Myelin basic protein (MBP) and poly(glu-tyr, 4:1) (Sigma, St. Louis, Mo.) were included as exogenous protein kinase substrates where indicated. Reactions were terminated by the addition of 2.times.SDS sample buffer and .sup.32 P labeled proteins were resolved by SDS-PAGE. In some cases proteins were transferred to Immobilon-P membranes (Millipore, Beverly, Mass.). Protein bands were visualized by autoradiography.

SDS-PAGE analysis of immunoprecipitates from .beta.-gal-A6 lysates revealed a .sup.32 P-labeled 150 kDa protein, consistent with the predicted molecular weight of the .beta.-gal fusion protein. In contrast, no .sup.32 P-labeled proteins were detected in immunoprecipitates from lysates expressing .beta.-gal alone. These results indicated an in vitro kinase activity associated with the A6 protein. The ability of the .beta.-gal-A6 fusion protein to phosphorylate MBP and poly (glu-tyr), known in vitro substrates of a variety of tyrosine kinases, was also examined. The .beta.-gal-A6 fusion protein was able to phosphorylate both substrates.

To identify the residues phosphorylated in the A6 protein itself and in the exogenous substrates, phosphoamino acid analysis was performed as described below.

EXAMPLE 5

Phosphoamino acid analysis

Phosphoamino acid analysis was performed as previously described (Haring et al., (1984) Biochemistry, 23: 3298-3306). Briefly, bands of interest were hydrolyzed from Immobilon-P membranes by incubation with 6M HCl for 2 hours at 110.degree. C. Sample volumes were adjusted to 1 ml with water and the HCl was removed under vacuum. Hydrolysates were washed with water, centrifuged under vacuum, resuspended in a mixture of pSer, pThr, and pTyr (1 mg/ml each), and analyzed by thin layer electrophoresis. Two dimensional analysis was performed at pH 1.9 for 60 min at 1 kV (first dimension) and at pH 3.5 for 50 min at 1 kV (second dimension). One dimensional analysis was performed at pH 3.5 for 60 min. Phosphoamino acid standards were visualized by staining with ninhydrin.

The results indicated that the A6 kinase was phosphorylated on both tyrosine and serine residues. However, the exogenous kinase substrates MBP and poly (glu-tyr) were phosphorylated exclusively on tyrosine.

To examine the distribution of A6 gene expression, we performed Northern blot analysis on RNA isolated from a variety of human tissue, as described in the following example.

EXAMPLE 6

Northern analysis of A6 RNA

M426 cell monolayers in 100 mm culture dishes were washed in PBS, lysed in the presence of the RNase inhibitor RNAzol (TelTest, Inc., Friendswood, Tex.) and extracted with chloroform. Human tissues were pulverized in liquid nitrogen and homogenized in the presence of RNAzol with a polytron. Chloroform (0.2 ml per 2 ml homogenate) was added and the samples were shaken vigorously for 15 seconds and left on ice for 5 minutes. The suspension was centrifuged at 12,000.times.g at 4.degree. C. for 15 minutes. The aqueous phase containing the RNA was transferred to a fresh tube and the RNA was precipitated with an equal volume of isopropanol for 15 min at 4.degree. C. Samples were centrifuged for 15 min at 12,000.times.g at 4.degree. C. The RNA pellet was washed with 75% ethanol, dried briefly under vacuum and dissolved in 10 mM Tris-HCl, pH 7.0, 1 mM EDTA. RNA concentrations were determined by absorbance at 260 nm.

Twenty .mu.g total RNA was analyzed by electrophoresis on 1% agarose gels containing 2.2M formaldehyde and transferred to Nytran (Schleicher and Schuell, Keene, N.H.) nylon membranes. After crosslinking of RNA to the membrane, filters were prehybridized for 2 hours at 42.degree. C. in Hybrisol (50% formamide, 10% dextran sulfate, 1% SDS, 6.times.standard saline citrate (SSC) and blocking agents; Oncor, Gaithersburg, Md.). Filters were then hybridized for 20 hours in the same solution containing the .sup.32 P-labeled 3 kilobase SalI fragment A6 DNA probe. Filters were washed twice for 30 min each at room temperature in 2.times.SSC, 1% SDS, then twice at 50.degree. C. in 0.1.times.SSC, 1% SDS and exposed to Kodak XAR film.

Under stringent hybridization conditions, the A6 cDNA probe revealed a single transcript of approximately 3.4 kilobases in various tissues consistent with its size in M426 cells. The A6 message was expressed at high levels in the colon, testes, uterus, ovary, prostate and lung. Lower levels were found in the brain, bladder and heart with no detectable transcript present in the liver. This distribution indicates the presence of high levels of the A6 kinase in tissues exhibiting a large amount of cell shedding and reproliferation, while lower levels are present in more static tissues. In addition, the A6 cDNA probe detected related genomic DNA fragments in other vertebrates including mice, amphibians and fish. The A6 gene thus appears to be highly conserved in vertebrate evolution.

EXAMPLE 7

Production of polyclonal antibodies against human A6 kinase

Synthetic peptides corresponding to the N- and C-terminal regions of the A6 kinase were synthesized on an Applied Biosystems Model 430A peptide synthesizer. The N-terminal and C-terminal peptides corresponded to amino acids 1-17 and 325-342 of SEQ ID NO: 2, respectively. Peptides were conjugated to the immunogenic carrier protein thyroglobulin as follows: 2 mg peptide was mixed with 24 mg thyroglobulin in 2 ml 0.1M sodium phosphate, pH 7.5 and then incubated with 1 ml 20 mM glutaraldehyde for 30 minutes at room temperature. Thyroglobulin-conjugated peptide (1.5 ml) was removed and mixed with 3.5 ml water, then aliquoted into 10 sterile vials of 0.5 ml each for immunizations. Antigen (100 .mu.g) plus 500 .mu.l phosphate buffered saline (PBS) was emulsified in 500 .mu.l Freund's complete adjuvant. This preparation was used to immunize rabbits at two week intervals. The rabbits were bled at 5 weeks post-injection and the blood was centrifuged to remove blood cells.

Alternatively, a polyclonal antisera designated anti-A6 was developed after immunization of rabbits with the thrombin-cleaved recombinant A6, expressed as a glutathione-S-transferase-A6 fusion protein. The prokaryotic expression vector pGEX-KG containing the glutathione-S-transferase coding region was provided by Dr. Jack Dixon (Guan and Dixon, (1991) Anal. Biochem., 192:262-267). The oligonuclotides used in the polymerase chain reaction were:

5' AATAAGTCGACTCCCACCAGACCGGCATCCAAGCAA 3' (SEQ ID NO: 3) 5' TAATTGTCGACTTAATCAGTAGTAGCTTCAGTTTCC 3' (SEQ ID NO: 4)

The A6 coding sequence was excised from the .beta.-gal-A6 construct and cloned into the prokaryotic expression vector pUC18 by well known methods. The A6 coding region was then amplified by the polymerase chain reaction using oligonucleotides corresponding to SEQ ID NOS: 3 and 4, resulting in the generation of a 1067 base pair fragment encoding amino acids 2-350 of the human A6 protein tyrosine kinase. This fragment was then cloned into XhoI-digested pGEX-KG by well known methods to generate pGEX-A6. Competent E. coli DH5.alpha.F' (Gibco-BRL, Gaithersburg, Md.) were transformed with pGEX-A6. Transformants were grown to an OD.sub.600 =0.8-1.0 and expression of the GST-A6 fusion protein was induced by the addition of 1.0 mM IPTG. After a 3 hour incubation, cells were harvested by centrifugation and resuspended in 10 ml PBST (PBS containing 1% Triton X-100, 2 mM EDTA, 0.1% .beta.-mercaptoethanol (BME) and 1 mM PMSF). Cells were lysed by sonication and clarified be centrifugation. One ml cleared lysate was mixed with 2 ml 50% (v/v) glutathione-agarose beads (Sigma) for 30 min at 4.degree. C. The beads were then washed times with PBST, once with thrombin cleavage buffer (50 mM Tris-HCl, pH 8.0, 150 mM NaCl, 2.5 mM CaCl.sub.2, 0.1% BME) and resuspended in the same buffer. The resuspended beads were mixed with 6 .mu.g thrombin (Sigma) for 20 min at room temperature and centrifuged. The supernatant containing the recombinant A6 protein cleaved from GST was collected and used to immunize rabbits as described above.

The resulting sera were aliquoted and stored at -80.degree. C. The specificity of the antibody was assessed by solid phase ELISA, immunoprecipitation and Western blotting, techniques all well known in the art.

EXAMPLE 8

Production of monoclonal antibodies against human A6 kinase

For production of monoclonal antibodies, BALB/c mice were injected at two week intervals subcutaneously with 20 .mu.g of recombinant A6 prepared as in Example 7. Three days prior to cell fusion, mice with the highest serum titer against A6 were injected intravenously with 1 .mu.g recombinant A6. On the day of fusion, the mouse was sacrificed and the spleen removed. Fusion of spleen cells and P3-X83 Ag8.653 myeloma cells was performed with polyethylene glycol according to standard techniques (Brown, (1985) Tissue Culture Meth., 9: 137-140) and hybridomas were selected in hypoxanthine-aminopterin-thymidine (HAT) medium. The resulting hybridomas were aliquoted into 96 well tissue culture plates. After approximately 10 to 14 days, the hybridoma supernatants were screened for reactivity with A6 by ELISA. Positive clones were expanded and assayed for reactivity by Western blot analysis. Hybridomas scoring positive were further cloned twice by limiting dilution using 96 well tissue culture plates. Hybridoma supernatants were screened for reactivity with the A6 kinase by ELISA, immunoprecipitation and Western blot analysis. Clones scoring positive were further cloned by limiting dilution. Monoclonal antibodies were isotyped and the ascites purified by protein A-Sepharose chromatography. The resulting antibodies specific for A6 were designated BF2, FG12, GF9, DA6, FH7, EA12, DB7 and BC3. The hybridoma cell lines producing these antibodies are maintained in permanent collection under the same names in the laboratory of Dr. Steven Tronick, National Institutes of Health, National Cancer Institute, Bethesda, Md. Hybridoma cell lines producing the BF2 and DA6 antibodies have been deposited with the American Type Culture Collection (ATCC).

To determine whether any known tyrosine kinase inhibitors could inhibit the A6 kinase, in vitro kinase assays were performed as described in the following example.

EXAMPLE 9

Inhibition of A6 kinase activity

In vitro kinase assays are performed as in Example 4, but in the presence or absence of several known commercially-available (Gibco-BRL, Gaithersburg, Md.; Calbiochem, San Diego, Calif.) tyrosine kinase inhibitors: lavendustin A, genistein, tyrphostin and herbimycin A. Kinase activity in the presence and absence of these inhibitors is compared to determine which is an inhibitor of kinase activity. In addition, the level of inhibition will be compared to that of other known tyrosine kinases to determine whether the A6 inhibition exhibits much greater specificity than that of the other tyrosine kinases. Other tyrosine kinase inhibitors specific to the A6 kinase are also within the scope of the present invention.

Corresponding A6 kinase genes from other species can be readily isolated as described below.

EXAMPLE 10

Isolation of the A6 kinase gene from nonhuman species

Commercially available cDNA libraries from nonhuman species such as mouse (liver, testis, lung) and fish (Stratagene, La Jolla, Calif.) are screened with a labeled human A6 DNA probe derived from restriction digestion of the full length clone described in Example 1 by techniques well known in the art. The clones are plaque-purified and sequenced using, for example, the Sequenase.TM. kit (United States Biochemical). Open reading frames are aligned with the A6 sequence using computer programs such as the NCBI BLAST network service searches of NCBI databases to determine whether the isolated clones encode proteins exhibiting significant homology to the human A6 protein tyrosine kinase.

Several additional features of the A6 protein sequence suggest that this enzyme may be involved in pathways regulating cell proliferation. A short stretch of significant similarity to the actin depolymerizing factors (ADF) and the cofilins, proteins known to bind phosphoinositides, was evident (FIG. 1). Over a 30 amino acid region from phes5 to gly.sub.114, A6 was found to be 77%, 42% and 33% related to the ADF from the plants Lilium longiflorum and Acanthamoeba castellanii and chicken cofilin, respectively. It has been proposed that the corresponding sequence in cofilin (A6 trp.sub.88 to met.sub.99) is responsible for binding to actin and phosphoinositides (Yonezawa et al., (1991) J. Biol. Chem., 266: 17218-17221). Thus, A6 may be linked to the control of cytoskeletal organization mediated by actin polymerization and depolymerization. This organization is important for cell growth and differentiation or phosphoinositide turnover, an important cell signalling pathway occurring in response to a variety of external stimuli. Hormones and growth factor binding to cell surface receptors are examples of some types of external stimuli. In addition, the predicted protein sequence of A6 contains a number of consensus phosphorylation sites for several kinases including protein kinase C, casein kinase and tyrosine kinases. These sequence motifs indicate that A6 activity may be regulated by other kinases known to play a central role in cell signalling pathways. The potential N-myristoylation of the A6 kinase suggests that this protein may have oncogenic capabilities and may exert its effects at the cytoplasmic face of the lipid bilayer. If this is the case, inhibitors of A6 kinase activity can be designed and will have potential antiproliferative effects. Lastly, A6 is a ubiquitous protein expressed in many organs and is highly conserved phylogenetically.

There will be various modifications, improvements and applications of the disclosed invention apparent to those of skill in the art, and the present application is intended to cover such embodiments. It is intended, therefore, that the full scope of these embodiments be measured by the following claims.

__________________________________________________________________________SEQUENCE LISTING(1) GENERAL INFORMATION:(iii) NUMBER OF SEQUENCES: 8(2) INFORMATION FOR SEQ ID NO:1:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 3000 base pairs(B) TYPE: nucleic acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: cDNA(iii) HYPOTHETICAL: NO(iv) ANTI-SENSE: NO(ix) FEATURE:(A) NAME/KEY: CDS(B) LOCATION: 61..1113(xi) SEQUENCE DESCRIPTION: SEQ ID NO:1:CCGCCGGCCGGGGCGCCTGGCTGCACTCAGCGCCGGAGCCGGGAGCTAGCGGCCGCCGCC60ATGTCCCACCAGACCGGCATCCAAGCAAGTGAAGATGTTAAAGAGATC108MetSerHisGlnThrGlyIleGlnAlaSerGluAspValLysGluIle151015TTTGCCAGAGCCAGAAATGGAAAGTACAGACTTCTGAAAATATCTATT156PheAlaArgAlaArgAsnGlyLysTyrArgLeuLeuLysIleSerIle202530GAAAATGAGCAACTTGAGATTGGATCATATAGTCAGCCTTCAGATTCC204GluAsnGluGlnLeuGluIleGlySerTyrSerGlnProSerAspSer354045TGGGATAAGGATTATGATTCCTTTGTTTTACCCCTGTTGGAGGACAAA252TrpAspLysAspTyrAspSerPheValLeuProLeuLeuGluAspLys505560CAACCATGCTATATATTATTCAGGTTAGATTCTCAGAATGCCCAGGGA300GlnProCysTyrIleLeuPheArgLeuAspSerGlnAsnAlaGlnGly65707580TATGAATGGATATTCATTGCATGGTCTCCAGATCATTCTCATGTTCGT348TyrGluTrpIlePheIleAlaTrpSerProAspHisSerHisValArg859095CAAAAAATGTTGTATGCAGCAACAAGAGCAACTCTGAAGAAGGAATTT396GlnLysMetLeuTyrAlaAlaThrArgAlaThrLeuLysLysGluPhe100105110GGAGGTGGCCACATTAAAGATGAAGTATTTGGAACAGTAAAGGAAGAT444GlyGlyGlyHisIleLysAspGluValPheGlyThrValLysGluAsp115120125GTATCATTACATGGATATAAAAAATACTTGCTGTCACAATCTTCCCCT492ValSerLeuHisGlyTyrLysLysTyrLeuLeuSerGlnSerSerPro130135140GCCCCACTGACTGCAGCTGAGGAAGAACTACGACAGATTAAAATCAAT540AlaProLeuThrAlaAlaGluGluGluLeuArgGlnIleLysIleAsn145150155160GAGGTACAGACTGACGTGGGTGTGGACACTAAGCATCAAACACTACAA588GluValGlnThrAspValGlyValAspThrLysHisGlnThrLeuGln165170175GGAGTAGCATTTCCCATTTCTCGAGAAGCCTTTCAGGCTTTGGAAAAA636GlyValAlaPheProIleSerArgGluAlaPheGlnAlaLeuGluLys180185190TTGAATAATAGACAGCTCAACTATGTGCAGTTGGAAATAGATATAAAA684LeuAsnAsnArgGlnLeuAsnTyrValGlnLeuGluIleAspIleLys195200205AATGAAATTATAATTTTGGCCAACACAACAAATACAGAACTGAAAGAT732AsnGluIleIleIleLeuAlaAsnThrThrAsnThrGluLeuLysAsp210215220TTGCCAAAGAGGATTCCCAAGGATTCAGCTCGTTACCATTTCTTTCTG780LeuProLysArgIleProLysAspSerAlaArgTyrHisPhePheLeu225230235240TATAAACATTCCCATGAAGGAGACTATTTAGAGTCCATAGTTTTTATT828TyrLysHisSerHisGluGlyAspTyrLeuGluSerIleValPheIle245250255TATTCAATGCCTGGATACACATGCAGTATAAGAGAGCGGATGCTGTAT876TyrSerMetProGlyTyrThrCysSerIleArgGluArgMetLeuTyr260265270TCTAGCTGCAAGAGCCGTCTGCTAGAAATTGTAGAAAGACAACTACAA924SerSerCysLysSerArgLeuLeuGluIleValGluArgGlnLeuGln275280285ATGGATGTAATTAGAAAGATCGAGATAGACAATGGGGATGAGTTGACT972MetAspValIleArgLysIleGluIleAspAsnGlyAspGluLeuThr290295300GCAGACTTCCTTTATGAAGAAGTACATCCCAAGCAGCATGCACACAAG1020AlaAspPheLeuTyrGluGluValHisProLysGlnHisAlaHisLys305310315320CAAAGTTTTGCAAAACCAAAAGGTCCTGCAGGAAAAAGAGGAATTCGA1068GlnSerPheAlaLysProLysGlyProAlaGlyLysArgGlyIleArg325330335AGACTAATTAGGGGCCCAGCGGAAACTGAAGCTACTACTGATTAAAGTCATC1120ArgLeuIleArgGlyProAlaGluThrGluAlaThrThrAsp340345350ACATTAAACATTGTAATACTAGTTTTTTAAAAGTCCAGCTTTTAGTACAGGAGAACTGAA1180ATCATTCCATGTTGATATAAAGTAGGGAAAAAATTTGTACTTTTTGGAAAATAGCACTTT1240TCACTTCTGTGTGTTTTTAAAATTAATGTTATAGAAGACTCATGATTTCTATTTTTGAGT1300TAAAGCTAGAAAAGGGTTCAACATAATGTTTAATTTTGTCACACTGTTTTCATAGCGTTG1360ATTCCACACTTCAAATACTTCTTAAAATTTTATACAGTTGGGCCAGTTCTAGAAAGTCTG1420ATGTCTCAAAGGGTAAACTTACTACTTTCTTGTGGGACAGAAAGACCTTAAAATATTCAT1480ATTACTTAATGAATATGTTAAGGACCAGGCTAGAGTATTTTCTAAGCTGGAAACTTAGTG1540TGCCTTGGAAAAGCCGCAAGTTGCTTACTCCGAGTAGCTGTGCTAGCTCTGTCAGACTGT1600AGGATCATGTCTGCAACTTTTAGAAATAGTGCTTTATATTGCAGCAGTCTTTTATATTTG1660ACTTTTTTTTAATAGCATTAAAATTGCAGATCAGCTCACTCTGAAACTTTAAGGGTACCA1720GATATTTTCTATACTGCAGGATTTCTGATGACATTGAAAGACTTTAAACAGCCTTAGTAA1780ATTATCTTTCTAATGCTCTGTGAGGCCAAACATTTATGTTCAGATTGAAATTTAAATTAA1840TATCATTCAAAAGGAAACAAAAAATGTTGAGTTTTAAAAAATCAGGATTGACTTTTTTCT1900CAAAACCATACATTTATGGGCAAATTGTGTTCTTTATCACTTCCGAGCAAATACTCAGAT1960TTAAAATTACTTTAAAGTCCTGGTACTTAACAGGCTAACGTAGATAAACACCTTAATAAT2020CTCAGTTAATACTGTATTTCAAAACACATTTAACTGTTTTCTAATGCTTTGCATTATCAG2080TTACAACCTAGAGAGATTTTGAGCCTCATATTTCTTTGATACTTGAAATAGAGGGAGCTA2140GAACACTTAATGTTTAATCTGTTAAACCTGCTGCAAGAGCCATAACTTTGAGGCATTTTC2200TAAATGAACTGTGGGGATCCAGGATTTGTAATTTCTTGATCTAAACTTTATGCTGCATAA2260ATCACTTATCGGAAATGCACATTTCATAGTGTGAAGCACTCATTTCTAAACCTTATTATC2320TAAGGTAATATATGCACCTTTCAGAAATTTGTGTTCGAGTAAGTAAAGCATATTAGAATA2380ATTGTGGGTTGACAGATTTTTAAAATAGAATTTAGAGTATTTGGTGTTTTGTTTGTTTAC2440AAATAATCAGACTATAATATTTAAACATGCAAAATAACTGACAATAATGTTGCACTTGTT2500TACTAAAGATATAAGTTGTTCCATGGGTGGACACGTAGACAGACACACATACACCCAAAT2560TATTGCATTAAGAATCCTGGAGCAGACCATAGCTGAAGCTGTTATTTTCAGTCAGGAAGA2620CTACCTGTCATGAAGGTATAAAATAATTTAGAAGTGAATGTTTTTCTGTACCATCTATGT2680GCAATTATACTCTAAATTCCACTACACTACATTAAAGTAAATGGACATTCCAGAATATAG2740ATGTGATTATAGTCTTAAACTAATTATTATTAAACCAATGATTGCTGAAAATCAGTGATG2800CATTTGTTATAGAGTATAACTCATCGTTTACAGTATGTTTTAGTTGGCAGTATCATACCT2860AGATGGTGAATAACATATTCCCAGTAAATTTATATAGCAGGGAAGAATTACATGCCTTCT2920GGTGGACATTTTATAAGTGCATTTTATATCACAATAAAAATTTTTTCTCTTTAAAAAAAA2980AAACAAGAAAAAAAAAAAAA3000(2) INFORMATION FOR SEQ ID NO:2:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 350 amino acids(B) TYPE: amino acid(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:2:MetSerHisGlnThrGlyIleGlnAlaSerGluAspValLysGluIle151015PheAlaArgAlaArgAsnGlyLysTyrArgLeuLeuLysIleSerIle202530GluAsnGluGlnLeuGluIleGlySerTyrSerGlnProSerAspSer354045TrpAspLysAspTyrAspSerPheValLeuProLeuLeuGluAspLys505560GlnProCysTyrIleLeuPheArgLeuAspSerGlnAsnAlaGlnGly65707580TyrGluTrpIlePheIleAlaTrpSerProAspHisSerHisValArg859095GlnLysMetLeuTyrAlaAlaThrArgAlaThrLeuLysLysGluPhe100105110GlyGlyGlyHisIleLysAspGluValPheGlyThrValLysGluAsp115120125ValSerLeuHisGlyTyrLysLysTyrLeuLeuSerGlnSerSerPro130135140AlaProLeuThrAlaAlaGluGluGluLeuArgGlnIleLysIleAsn145150155160GluValGlnThrAspValGlyValAspThrLysHisGlnThrLeuGln165170175GlyValAlaPheProIleSerArgGluAlaPheGlnAlaLeuGluLys180185190LeuAsnAsnArgGlnLeuAsnTyrValGlnLeuGluIleAspIleLys195200205AsnGluIleIleIleLeuAlaAsnThrThrAsnThrGluLeuLysAsp210215220LeuProLysArgIleProLysAspSerAlaArgTyrHisPhePheLeu225230235240TyrLysHisSerHisGluGlyAspTyrLeuGluSerIleValPheIle245250255TyrSerMetProGlyTyrThrCysSerIleArgGluArgMetLeuTyr260265270SerSerCysLysSerArgLeuLeuGluIleValGluArgGlnLeuGln275280285MetAspValIleArgLysIleGluIleAspAsnGlyAspGluLeuThr290295300AlaAspPheLeuTyrGluGluValHisProLysGlnHisAlaHisLys305310315320GlnSerPheAlaLysProLysGlyProAlaGlyLysArgGlyIleArg325330335ArgLeuIleArgGlyProAlaGluThrGluAlaThrThrAsp340345350(2) INFORMATION FOR SEQ ID NO:3:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 36 base pairs(B) TYPE: nucleic acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: cDNA(iii) HYPOTHETICAL: NO(iv) ANTI-SENSE: NO(xi) SEQUENCE DESCRIPTION: SEQ ID NO:3:AATAAGTCGACTCCCACCAGACCGGCATCCAAGCAA36(2) INFORMATION FOR SEQ ID NO:4:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 36 base pairs(B) TYPE: nucleic acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: cDNA(iii) HYPOTHETICAL: NO(iv) ANTI-SENSE: NO(xi) SEQUENCE DESCRIPTION: SEQ ID NO:4:TAATTGTCGACTTAATCAGTAGTAGCTTCAGTTTCC36(2) INFORMATION FOR SEQ ID NO:5:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 30 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(xi) SEQUENCE DESCRIPTION: SEQ ID NO:5:PheIlePheTrpAlaProGluSerAlaProLeuLysSerLysMetIle151015TyrAlaSerSerLysAspAlaIleLysLysLysPheThrGly202530(2) INFORMATION FOR SEQ ID NO:6:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 30 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(xi) SEQUENCE DESCRIPTION: SEQ ID NO:6:PheIleLeuTrpAlaProAspSerAlaProIleLysSerLysMetMet151015TyrThrSerThrLysAspSerIleLysLysLysLeuValGly202530(2) INFORMATION FOR SEQ ID NO:7:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 30 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(xi) SEQUENCE DESCRIPTION: SEQ ID NO:7:PheIleSerTrpSerProAspThrSerArgValArgSerLysMetLeu151015TyrAlaSerThrLysAspArgPheLysArgGluLeuAspGly202530(2) INFORMATION FOR SEQ ID NO:8:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 19 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(xi) SEQUENCE DESCRIPTION: SEQ ID NO:8:GlyPheAspArgLysHisProPheTyrTrpXaaXaaSerThrAlaGly151015CysAsnPro__________________________________________________________________________

Claims

1. An isolated polynucleotide encoding the human A6 protein tyrosine kinase.

2. The polynucleotide of claim 1, wherein said polynucleotide has the sequence corresponding to the coding region of SEQ ID NO: 1.

3. A recombinant construct comprising the coding region of SEQ ID NO: 1 operably linked to a heterologous promoter in an expression vector.

4. Isolated cells transfected with the recombinant construct of claim 3.

5. The cells of claim 4 wherein said cells are prokaryotic.

6. The prokaryotic cells of claim 5, wherein said cells are E. coli Y1089 cells.

7. The construct of claim 3, wherein said expression vector is .lambda.pCEVlacz, said vector containing the galactosidase promoter and gene sequence.

8. The construct of claim 7 wherein the sequence corresponding to SEQ ID NO: 1 is adjacent to said .beta.-galactosidase gene, wherein upon expression the protein encoded by said SEQ ID NO: 1 and said .beta.-galactosidase form a fusion protein.

9. Isolated human A6 protein tyrosine kinase having a molecular weight of about 40,000 daltons.

10. The protein kinase of claim 9, wherein said kinase has the sequence corresponding to SEQ ID NO: 2.