Laminin chains: diagnostic and therapeutic use

BACKGROUND OF THE INVENTION
Laminins are a family of basement membrane proteins which function in cell differentiation, adhesion, and migration, in addition to being true structural components (Tryggvason K, Curr. Opn. Cell Biol., 1993, 5:877-882, this and all following references are hereby incorporated by reference). The laminin molecule is a cross-shaped heterotrimer consisting of one heavy .alpha. chain (.about.400 kd) and two light chains, .beta. and .gamma.(130-200 kd) (nomenclature according to Burgeson et al., Matrix Biol., 1994, 14:209-211). Laminin exists in numerous isoforms that are formed by different combinations of laminin chain varients which currently amount to at least nine.
Kalinin/laminin 5 (most likely also identical to the adhesion molecule nicein) is a recently identified laminin isoform which is a functional adhesion component for epithelial cells (Tryggvason, 1993, supra.; Burgeson et al., 1994, supra.; Rousselle et al., J. Cell Bio., 1991, 114:567-576; Kallunki et al., J. Cell Biol., 1992, 119:679-693; Marinkovich et al., J. Biol. Chem., 1992, 267:17900-17906; Vailly et al., Eur. J. Biochem., 1994, 219:209-218). Kalinin/laminin 5 contains unique laminin varient chains, one of which, the .gamma.2 chain, has recently been cloned and sequenced (Kallunki et al., 1992, supra., previously named B2t). The .gamma.2 chain has a mass of .about.130 kd and is thus smaller than the "classical".about.200 kd .beta.1 and .gamma.1 light chains of laminin. The domain structure of the .gamma.2 chain also differs from that of the .gamma.1 chain in that it lacks the amino-terminal globular domain (domain VI) believed to function in intermolecular cross-linking of laminin molecules to form networks (Yurcheno and O'Rear, in Molecular and Cellular Aspects of Basement Membranes, 1993, (ed. Rohrbach and Timpl, Academic Press, San Diego, pp. 20-47). In addition, domains III, IV, and V (containing EGF-like repeats) in .gamma.2 are shorter than in the .gamma.1 chain (Kallunki et al., 1992, supra.).
By in situ hybridization the .gamma.2 chain was found to be expressed in epithelial cells of many embryonic tissues such as those of skin, lung, and kidney (Kallunki et al., 1992, supra.), and antibodies to kalinin/laminin 5, react with basement membranes of the same tissues (Rousselle et al., 1991, supra.; Verrando et al., Lab. Invest., 1991, 64:85-92).
The different laminin chains have been shown to have quite varying tissue distribution as determined by immunohistological studies, Northern, and in situ hybridization analyses. For example, the A and M chains on the one hand, and the B 1 (.beta.1) and S (.beta.2) chains on the other, have been shown to be mutually exclusive (see for example Vuolteenaho et al., J. Cell Biol., 1994, 124:381-394). In vitro studies have indicated that laminin mediates a variety of biological functions such as stimulation of cell proliferation, cell adhesion, differentiation, and neurite outgrowth. The cellular activities are thought to be mediated by cell membrane receptors, many of which are members of the integrin family (Ruoslahti, E. J. Clin. Invest., 1991, 87:1-5; Mecham, R. P. FASEB J., 1991, 5:2538-2546; Hynes, R. Cell, 1992, 69:11-25).
Recently a new nomenclature for describing laminins has been agreed to as in the following Table 1 (after Burgeson et al., 1994, supra.)
TABLE 1______________________________________laminin chains and genes heterotrimers of lamininNew Previous Gene New Chains Previous______________________________________.alpha.1 A, Ae LAMA1 laminin-1 .alpha.1.beta.1.gamma.1 EHS laminin .alpha.2 M, Am LAMA2 laminin-2 .alpha.2.beta.1.gamma.1 merosin .alpha.3 200 kDa LAMA3 laminin-3 .alpha.1.beta.2.gamma.1 s-laminin .beta.1 B1, B1e LAMB1 laminin-4 .alpha.2.beta.2.gamma.1 s-merosin .beta.2 S, B1s LAMB2 laminin-5 .alpha.3.beta.3.gamma.2 kalinin/nice in .beta.3 140 kDa LAMB3 laminin-6 .alpha.3.beta.1.gamma.1 k-laminin .gamma.1 B2, B2e LAMC1 laminin-7 .alpha.3.beta.2.gamma.1 ks-laminin .gamma.2 B2t LAMC2______________________________________
SUMMARY OF THE INVENTION
The instant invention provides for methods of detecting kalinin/laminin 5 expression in tissue comprising detecting a signal from assayed tissue, such signal resulting from specifically hybridizing tissue with an effective amount of a nucleic acid probe, which probe contains a sense or antisense portion of kalinin/laminin 5 gamma-2 nucleic acid sequence (Kallunki et al., 1992, supra.). In particular, where the nucleic acid probe is DNA, RNA, radiolabelled, enzyme labelled, chemiluminescent labelled, avidin or biotin labelled, derived from human kalinin/laminin 5 gamma-2 nucleic acid sequence, incorporated into an extrachromasomal self-replicating vector, a viral vector, is linear, circularized, or contains modified nucleotides. In the preferred embodiment the probes are linearized specific regions of the .gamma.2 gene.
The instant invention also provides for methods for detecting the presence of invasive cells in tissue comprising detecting a signal from assayed tissue, such signal resulting from contacting tissue with an effective amount of a nucleic acid probe, which probe contains a sense or antisense portion of kalinin/laminin 5 gamma-2 nucleic acid sequence (Kallunki et al., 1992, supra.). In particular, where the nucleic acid probe is DNA, RNA, radiolabelled, enzyme labelled, chemiluminescent labelled, avidin or biotin labelled, derived from human kalinin/laminin 5 gamma-2 nucleic acid sequence, incorporated into an extrachromasomal self-replicating vector, a viral vector, is linear, circularized, or contains modified nucleotides. In the preferred embodiment the probes are linearized specific regions of the .gamma.2 gene. The instant method also provides for the diagnosis of the absence of .gamma.2 chain expression, useful for the monitoring of therapies, and the progress of malignant cell transformation leading to accurate determination of the extent of invasive cell activity.
The instant invention further provides for a method for detecting kalinin/laminin 5 expression in tissue comprising detecting a signal from assayed tissue, such signal resulting from contacting tissue with an effective amount of a labeled probe, which probe contains an antibody immunoreactive with a portion of kalinin/laminin 5 gamma-2 protein.
Further provided is a method for detecting invasive cells in tissue comprising detecting a signal from assayed tissue, such signal resulting from contacting tissue with an effective amount of a labeled probe, which probe contains an antibody immunoreactive with a portion of kalinin/laminin 5 gamma-2 protein. Also provided is a method for detecting kalinin/laminin 5 in tissue comprising detecting a signal from assayed tissue, such signal resulting from contacting tissue with an effective amount of a labeled probe, which probe contains an antibody immunoreactive with a portion of kalinin/laminin 5 gamma-2 protein. Thus the method of the instant invention provides for the absence of such signal as diagnostic for the absence of invasive cells.

BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 shows In situ hybridization of a specimen of colon adenocarcinoma for .gamma.2 chain mRNA using a S-35 labeled anti-sense RNA probe derived from plasmid pbb2r-02. Magnification:1A.times.100; 1B-1D.times.640.
FIG. 2 shows In situ hybridization for .gamma.2 chain mRNA on sections of ductal mammary carcinoma (2A), malignant melanoma (2B), squamous cell carcinoma of the skin (2C-2D), and squamous cell carcinoma of the vulva (2E-2G). Magnification: 2C.times.100, all others.times.640.
FIG. 3 is incisionally wounded mouse skin (72 hours after wounding) showing signal for .gamma.2 chain in keratinocytes at the leading edge of the migrating epithelium (curved arrow). Magnification:.times.640.
FIG. 4 shows the nucleic acid sequence for the .gamma.2 chain cDNA and the derived amino acid sequence. FIG. 4A is the full cDNA for the 5,200 base pair sequence, available from EMB/GenBank/DDBJ under the accession number Z15008. FIG. 4B is the nucleotide and derived amino acid sequence of the alternative 3' end sequence from cDNA clones providing a sequence of 4,316 base pairs, available from EMB/GenBank/DDBJ under the accession number Z15009. (Kallunki et al., 1992, supra.).

DETAILED DESCRIPTION OF THE INVENTION
Epidermolysis bullosa (EB) is a group of mechano-bullous disorders characterized by fragility of the skin and mucous membranes (see Lin & Carter eds., Epidermolysis bullosa, Basic and clinical aspects, 1992, Springer Verlag, N.Y.; Fine et al., J. Am. Acad. Dermatol., 1991, 24:119-135). The junctional forms of EB (JEB) are characterized by tissue separation at the level of the lamina lucida within the dermal-epidermal basement membrane, and no specific mutation had yet to be reported. Recently it has been proposed that the genes for a lamina lucida protein kalinin/nicein/epiligin may be a candidate in some forms of JEB (Verrando et al., 1991, supra.). Several lines of evidence suggest that anchoring filament proteins could be defective in some forms of JEB. First, attenuation or absence of immunoreactivity with anti-kalinin(epiligrin) antibodies has been noted in the skin of patients with the most severe (Herlitz) type of JEB. The immunofluorescence staining patterns may be of prognostic value in classifying JEB, and these immunoreagents have been used for prenatal diagnosis of JEB using fetal skin biopsy specimins. Second, the kalinin/laminin 5 .gamma.2 chain is expressed in epithelial cells of the skin, trachea and kidneys, tissues which are frequently affected by JEB.
Since the majority of cases are of the generalized (Herlitz) phenotype (H-JEB), JEB patients have been classified into Herlitz and non-Herlitz types. Clinical features of H-JEB include mechanical fragility of the skin, with widespread blistering and erosions, rapid deterioration and neonatal death, often from sepsis. Longterm survival is rare.
Efforts to identify the basic defect in JEB began with the observation that a monoclonal antibody that binds to the lamina lucida of the epidermal basement membrane zone of normal skin, fails to react with the lamina lucida of H-JEB skin (Verrando et al., 1991, supra.). The antigen recognized by this antibody was purified from keratinocyte culture medium and termed BM600/nicein. Keratinocytes cultured from the skin of H-JEB patients attach poorly to substrate and fail to accumulate immunologically detectable nicein. Further experiments with antibodies specific for the .alpha.3 chain of nicein, demonstrated that they were capable of inducing the rounding and detachment of adherent keratinocytes without affecting fibroblasts (Rousselle et al., 1991, supra.). Thus the correlation in vivo and in vitro of the dermoepidermal separation with deficient nicein/kalinin/laminin 5 immunoreactivity and the separation induced by anti-nicein antibody have made the genes encoding this protein strong candidates for the site of H-JEB mutations.
The importance of the .gamma.2 chain of nicein/kalinin/laminin 5 in JEB, and epithelial tissues prompted the investigation into the role such adhesion contacts between epithelial cells may play in abberant cells. Of primary interest was the role .gamma.2 chain of nicein/kalinin/laminin 5 abberant expression may play in cancer tissue, and a possible role in cancer dissemination.
It has been recently shown that in colon adenocarcinoma, a significant positive correlation between the degree of tumor budding and the recurrence of tumors following curative surgery exists, and that this fact is likely to reflect a higher invasive potential of budding cancer cells as compared with cancer cells located deeper in the tumor (Hase et al., Dis. Colon Rectum, 1993, 36:627-635). Therefore, as demonstrated in Example 3 below, the instant invention allows for the useful prognostic determination of success of surgery, means for monitoring progression of tumor budding and subsequent prognosis.
The identification of the role of .gamma.2 chain allows for the novel use of kalinin/laminin 5 .gamma.2 chain and its ligand, as diagnostic probes of the tumor cell/basement membrane adhesion interface that is crucial for the invasion of non-malignant tissues, and identifies invasive cells.
Thus the identification of the role of .gamma.2 chain allows for the novel therapeutic intervention of binding of kalinin/laminin 5 to its ligand, and thereby reducing the tumor cell/basement membrane adhesion that is crucial for the invasion of non-malignant tissues, and method for inhibiting the budding of tumor masses, and a means for determining the level of .gamma.2 chain expression as a measure of budding activity of a given tumor.
As demonstrated in Example 3 below, the .gamma.2 chain of kalinin/laminin 5 is preferentially expressed by invasively growing malignant cells in human carcinomas. Furthermore, migrating keratinocytes in wound healing also expressed this gene, pointing to a role of .gamma.2 chain in epithelial cell migration both in malignant and in nonmalignant pathological conditions. The consistent expression of the .gamma.2 chain gene in invading cancer cells reflects a functional importance of this molecule in vivo in establishing contacts between the invading malignant cells and a provisional matrix in the immediate surroundings of the cancer cells. The instant invention provides methods for the identification of, and diagnosis of invasive cells and tissues, and for the monitoring of the progress of therapeutic treatments.
In a preferred embodiment of this aspect of the instant invention the nucleic acid probe comprise a specifically hybridizing fragment of the .gamma.2 chain cDNA nucleic acid sequence. In this embodiment, the nucleic acid sequence comprises all or a specifically hybridizing fragment of an open reading frame of the nucleic acid sequence for the .gamma.2 chain (FIG. 4) encoding the amino acid sequence of the .gamma.2 chain (FIG. 4). It will be understood that the term "specifically hybridizing" when used to describe a fragment of nucleic acid encoding a human laminin .gamma.2 chain gene is intended to mean that, nucleic acid hybridization of such a fragment is stable under high stringency conditions of hybridization and washing as the term "high stringency" would be understood by those having skill in the molecular biological arts.
Further, the instant invention provides for the therapeutic treatment of such invasive tissues by using .gamma.2 chain or biologically active fragments thereof to interfere with the interactions between abberant .gamma.2 chain and surrounding tissues. The instant invention also provides for the intervention of .gamma.2 chain interaction with surrounding tissues by using specific anti-.gamma.2 chain antibodies (monoclonal or polyclonal) to inhibit the .gamma.2 chain biological activity.
The instant disclosure also allows one to ablate the invasive cell phenotypic .gamma.2 chain expression by using genetic manipulation to "knock-out" the functional expression of the .gamma.2 chain gene in cancer cells, or to completely "knock-out" the functional .gamma.2 chain gene in the genome of cancer cells. Such knock-outs can be accomplished by using genetic molecular biological techniques for inserting homologous recombination into genomic DNA, targeted transposon insertion, or random insertion/deletion mutations in the genomic DNA.
The instant disclosure also allows for the therapeutic treatment of invasive cell phenotype by the inhibition of functional .gamma.2 chain expression in targeted cells by using anti-sense technology, such methods for anti-sense production, stabilization, delivery, and therapeutic approaches are reviewed in Uhlmann et al., 1990, Chem. Reviews 90:543-584).
Thus the instant invention provides for a method of detection, diagnosis, prognosis, monitoring, and therapeutic treatment of invasive cell phenotypes.
The examples below are meant by way of illustration, and are not meant to be limiting as to the scope of the instant disclosure.
EXAMPLE 1
Mutation in the .gamma.2 Chain Gene LAMC2 is Critical in Some Cases of JEB
A unique scanning strategy using RT-PCR amplification of LAMC2 sequences was devised to detect truncated forms of .gamma.2 chain gene transcripts (Pulkkinen et al., Nature Genetics, 1994, 6:293-298). The 3.6 kilobase coding sequence of the LAMC2 mRNA, was reverse transcribed and amplified with eight pairs of primers, producing overlapping PCR amplimers designated A-H. The PCR products were then examined by agarose gel electrophoresis, followed by MDE heteroduplex analysis. If bands with altered mobility were detected, the PCR products were sequenced, and compared with normal sequences from unaffected family members or unrelated individuals. Intron/exon borders were identified by PCR analysis of genomic DNA, deduced by comparison with cDNA sequences.
A Point Mutation Produces Exon Skipping
When a panel of five unrelated JEB patients were analysed, the primers used to amplify segment C (nt 1046-1537) produced markedly shortened band of 273 base pairs, as compared with the normal 491 base pairs. No evidence of the normal sized band was noted, suggesting that the patient was homozygous for this allele. Direct sequencing revealed that the shortened product resulted from the deletion of 219 base pairs corresponding to nucleotides 1184-1402 in the cDNA, thus exon 9 was deleted. The remaining nucleotide sequences within this and other PCR products did not reveal any additional mutations upon MDE analysis.
Subsequent examination of the genomic DNA revealed that the sequences for exons 8, 9 and 10 were present, however a homozygous G for A substitution at the 3' acceptor splice site at the junction of intron 8 and exon 9, abolished the obligatory splice site sequence (AG).
Examination of another patient revealed that PCR product F (nt 2248-2777) corresponding to domains I and II of the .gamma.2 chain, was a band with altered mobility. Sequencing the abnormal product revealed a 20 bp deletion, followed by a single base pair (G) insertion in the coding region corresponding to exon 16. This mutation causes a frameshift which results in a premature stop codon 51 base pairs downstream from the deletion-insertion, predicting a truncated kalinin/laminin 5 .gamma.2 chain terminating at residue 830.
RT-PCR and MDE Analyses
RNA isolated from fibroblast cell cultures of JEB patients was used as template for RT-PCR of the LAMC2 mRNA. (Epidermal keratinocytes can also be used). cDNA was prepared from 50 .mu.g of total RNA in a volume of 100 .mu.L according to manufacturer's recommendations (BRL), and oligonucleotide primers were synthesized on the basis of the cDNA sequence (FIG. 4; Kallunki et al., 1992, supra.), to generate .about.500 base pair products, which spanned the entire coding region.
For PCR amplification, 1 .mu.L of cDNA was used as template and amplification conditions were 94 C. for 5 min followed by 95 C. for 45 sec, 60 C. for 45 sec and 72 C. for 45 sec for 35 cycles in an OmniGene thermal cycler (Marsh Scientific). Amplification was performed in a total volume of 25 .mu.L containing 1.5 mM MgCl.sub.2, and 2 U Taq polymerase (Boehringer Mannheim). Aliquots of 5 .mu.L were analysed on 2% agarose gels and MDE heteroduplex analysis was performed according to the manufacturer's recommendation (AT Biochemicals). Heteroduplexes were visualized by staining with ethidium bromide. If a band of altered mobility was detected in heteroduplex analysis, the PCR product was subcloned into the TA vector (Invitrogen), and sequenced by standard techniques.
DNA isolated either from fibroblast cultures or from specimens obtained from buccal smears, was used as template for amplification of genomic sequences. For amplification of introns 8 and 16,.about.500 ng of genomic DNA was used as template and the following oligomer primers were utilized.
______________________________________ 5' GGCTCACCAAGACTTACACA 3'; - 5' GAATCACTGAGCAGCTGAAC 3'; - 5' CAGTACCAGAACCGAGTTCG 3'; - 5' CTGGTTACCAGGCTTGAGAG 3'; - 5' TTACTGCGGAATCTCACAGC 3'; - 5' TACACTGTTCAACCCAGGGT 3'; - 5' AAACAAGCCCTCTCACTGGT 3'; - 5' GCGGAGACTGTGCTGATAAG 3'; - 5' CATACCTCTCTACATGGCAT 3'; - 5' AGTCTCGCTGAATCTCTCTT 3'; - 5' TTACAACTAGCATGGTGCCC 3'.______________________________________
Amplification conditions were 94 C. for 7 min followed by 95 C. for 1.5 min, 56 C. (intron 8) or 58 C. (intron 16) for 1 min and 72 C. for 1.5 min for 35 cycles in an OmniGene thermal cycler (Marsh Scientific). Amplification was performed in a total volume of 25 .mu.L containing 1.5 mM MgCl.sub.2, and 2 U Taq polymerase (Boehringer Mannheim). The PCR products were subcloned and sequenced as above.
Verification of Mutations
The putative mutations detected in the PCR products were verified at the genomic level in both cases. For this purpose, a search for a potential change in restriction endonuclease sites as a result of the mutation was performed.
Amplification conditions were 94 C. for 7 min followed by 94 C. for 1 min, 58 C. for 45 sec and 72 C. for 45 sec for 35 cycles in an OmniGene thermal cycler (Marsh Scientific). PCR products were analysed on 2.5% agarose gels.
The methods described allow for the screening of patients for mutations in the .gamma.2 chain which will correlate with JEB. As demonstrated, the results have identified a homozygous point mutation resulting in exon skipping, and a heterozygous deletion-insertion mutation. This demonstrating the effective screening for, and identification of, .gamma.2 chain mutations which correlate with JEB. The methods are thus useful for diagnosis, prenatal screening, early screening and detection, as well as detailed examination of JEB. Further, the results show that the functional role of .gamma.2 chain expression in epithelial cells is important in determining proper intercellular connectivity, relating to the integrity of tissues and cell interactions.
EXAMPLE 2
Mutation in the .gamma.2 Chain Gene LAMC2 is Critical in H-JEB
The correlation both in vivo and in vitro of the dermo-epidermal separation in H-JEB, with deficient immunoreactivity of anti-nicein/kalinin/laminin 5 antibodies, and the separation induced by anti-nicein/kalinin/laminin 5 antibodies have made the genes encoding this protein strong candidates for the site of H-JEB mutations. In this example, it is demonstrated that the molecular defect which causes H-JEB is linked to the gene encoding nicein/kalinin/laminin 5 .gamma.2 chain. In particular, the occurrence of a homozygous premature termination codon mutation is the specific cause in an examined case of H-JEB (Aberdam et al., Nature Genetics, 1994, 6:299-304).
Expression of mRNA encoding the three nicein subunits by northern analysis of RNA isolated from primary keratinocyte culture of a H-JEB patient was determined as the initial screen. Hybridization with probes for the .alpha.3 and .alpha.3 subunits was normal, but no hybridization with a cDNA encoding the .gamma.2 subunit was detected. Examination of the genomic DNA for gross abnormalities, such as large deletions, insertions or rearrangements, in LAMC2 (the .gamma.2 subunit gene) by Southern blot analysis turned up no abnormalities when the genomic DNA was digested with BamHI, BglI, HindIII, PstI or PvuII and probed with full length LAMC2 cDNA.
Possible mutations in the .gamma.2 subunit were sought by using cDNA reverse transcribed from total RNA purified from cultured keratinocytes of the H-JEB patient, and subjected to PCR amplification. The size of the amplified products was checked by electrophoresis on 2% agarose gels and compared with that obtained from healthy controls.
No major differences were detected in the agarose gels, and the PCR products were examined by heteroduplex analysis (MDE). Heteroduplex analysis of the most 5' PCR product (nt 35-726) revealed the presence of a homoduplex in the proband (patient) and the controls. However, when the amplified PCR products from the patient and control were mixed together, an additional band with altered mobility, representing heteroduplexes, was detected, suggesting a homozygous mutation in the patient's LAMC2 cDNA (FIG. 5a). This amplified fragment corresponded to domain V of the .gamma.2 protein (Vailly et al., Eur. J. Biochem., 1994, 219:209-218). Sequencing detected a C to T transition at position +283, leading to a nonsense mutation in which a termination codon TGA replaces an arginine (CGA), perhaps arising as a result of the hypermutability of 5-methyl-cytosine to thymine at CpG nucleotides. This mutation, R95X, leads to truncation of the .gamma.2 subunit polypeptide at amino acid 95 and loss of a TaqI restriction site (TCGA). Digestion of cDNA with TaqI confirmed the presence of a homozygous mutation in the DNA of the H-JEB patient. No other mutations were detected.
To confirm the cosegregation of the mutation with the loss of the TaqI restriction site, eight genotyped individuals of the family of the patient were screened. In each case, a 120 base pair fragment was amplified by PCR using genomic DNA templates and primers flanking the restriction site. Upon digestion of the wild type amplification product, two clevage fragments of 80 and 40 base pairs are generated. Consistent with the presence of a heterozygous mutation in carriers of this genotype, DNA fragments of 120, 80 and 40 base pairs, indicative of a wild type genotype, were found in the paternal grandmother and two other relatives.
Cell Culture
Epidermis was separated from dermis by dispase treatment at 37 C. Keratinocytes were dissociated in 0.25% trypsin at 37 C. and plated onto a feeder layer of irradiated mouse 3T3 cells (ICN) (Rheinwald & Green, Cell, 175, 6:331-334). Keratinocytes were grown in a 1:1 mixture of DMEM and Ham's F12 (BRL) containing 10% Fetal Calf Serum (FCS), 1 mM sodium pyruvate, 2 mM L-glutamine, 10 .mu.g/mL of penicillin and strptomycin, 10 ng/mL transferrin, 180 .mu.M adenine and 20 pM T3 (Simon & Green, Cell, 1985, 40:677-683). H-JEB keratinocytes were expanded after gentle dissociation in 0.05% trypsin, 0.02% EDTA.
Northern Blot Analysis
Total RNA was prepared from H-JEB and normal cultured keratinocytes according to standard methods (Chomzynski & Sacchi, Anal. Biochem., 1987, 162:156-159). RNA was electrophoresed in 1.2% denaturing agarose gels containing 1.2 M formaldehyde and transferred onto Hybond N membrane (Amersham). Membranes were hybridized at high stringency with P-32 labeled cDNA probes corresponding to the different chains of nicein, and then exposed on Hyperfilm MP (Amersham) with intensifying screens. Radiolabeled cDNA probes NA1 (Baudoin et al., J. Invest. Dermatol., 1994, in press), KAL-5.5C (Gerecke et al., Eur. J. Biochem., 1994, in press), and PCR 1.3 (Vailly et al., 1994, supra.), were used to detect the mRNAs for nicein chains .alpha.3, .beta.3 and .gamma.2, respectively.
RT-PCR and Heteroduplex Analysis (MDE)
50 .mu.g of total RNA isolated from cultured keratinocytes from JEB patient, and unrelated healthy controls were reverse transcribed in a volume of 100 .mu.L as recommended by the manufacturer (BRL). 1 .mu.L of the reaction product was used to amplify overlapping regions of the cDNA that spanned the open reading frame. Primer pair used to identify the mutation R95X: (L) 5'-GAGCGCAGAGTGAGAACCAC-3', (R) 5'-ACTGTATTCTGCAGAGCTGC-3'. PCR cycling conditions were: 94 C., 5 min, followed by 94 C., 45 sec; 60 C., 45 sec; 72 C., 45 sec; for 35 cycles, and extension at 72 C. for 5 min. 5 .mu.L aliquots were run in 2% agarose gels. Heteroduplex analysis was performed as recommended by the manufacturer (MDE, AT Biochemicals). Heteroduplexes were visualized under UV light in the presence of ethidium bromide and photographed. Amplified cDNA fragments with altered mobility were subcloned into the TA vector according to the manufacturer's recommendations (Invitrogen). Sequence analysis were then performed using standard techniques.
Verification of the Mutation
PCR reactions on genomic DNA (50 .mu.g) were carried out using the upstream primer 5'-TTCCTTCCCCTACCTTGTG-3' and the downstream primer 5'-TGTGGAAGCCTGGCAGACAT-3', which are located in the intron 2 and exon 3 of LAMC2 respectively. PCR conditions were: 95 C., 5 min, followed by 94 C., 45 sec; 56 C., 45 sec; 72 C., 45 sec; for 35 cycles, and extension at 72 C. for 5 min. PCR products were used for restriction analysis. 20 .mu.L of PCR product obtained from genomic DNA was digested with TaqI for 2 hours (Boehringer Mannheim). Clevage products were electrophoresed (2.4% agarose) stained and visualized under UV light.
Thus the methods allow for the screening of patients for mutations in the .gamma.2 chain which correlate with H-JEB. As demonstrated, the results have identified a nonsense mutation resulting in a truncated .gamma.2 chain, leading to severe H-JEB. This was further confirmed by specific amplification and restriction enzyme analysis of both the patient and relatives. Thus demonstrating the effective screening for, and identification of, .gamma.2 chain mutations which correlate with H-JEB. The methods are thus useful for diagnosis, prenatal screening, early screening and detection, as well as detailed examination of H-JEB. Furthermore, the results demonstrate the significance of the .gamma.2 chain in forming proper cellular contacts.
EXAMPLE 3
.gamma.2 Chain as Diagnostic for Invasive Tissues
In this example, in situ hybridization is used to demonstrate the expression of the kalinin/laminin 5 .gamma.2 chain in a variety of human cancer tissues and in skin wound healing in mice (Pyke et al., Amer. J. Pathol., October 1994, 145(4): 1-10 in press).
Thirty-six routinely processed, formalin-fixed and paraffin wax-embedded specimens from cancer surgery performed from 1991 to 1993 were drawn from pathology department files at Herlev Hospital (Copenhagen, Denmark). The specimens were evaluated according to standard criteria and included 16 cases of moderately or well-differentiated colon adenocarcinomas, 7 cases of ductal mammary carcinomas, 4 squamous cell carcinomas (2 skin, 1 cervix, 1 vulva), 3 malignant melanomas, and 6 sarcomas (3 leiomyosarcomas, 2 malignant fibrous histiocytomas, 1 neurofibrosarcoma).
All samples were selected upon histological examination of a hematoxylin and eosin-stained section to ensure that they showed a well preserved morphology throughout and contained representative areas of both cancerous tissue and surrounding apparently normal, unaffected tissue. The broad zone separating these two tissue compartments is referred to as the invasive front in the following. No estimation of the effect of variations in fixation conditions was attempted, but in a previous study of plasminogen activating system components using specimens of colon adenocarcinomas collected using the same procedures, very little variation in relative mRNA levels was found (Pyke, C. PhD. Thesis, 1993, University of Copenhagen, Denmark). In addition, tissue from incisionally wounded mouse skin prepared as described by Romer et al. (J. Invest. Dermatol., 1994, 102:519-522), was fixed and paraffin-embedded the same way as the human cancer specimens.
For preparation of total RNA from six samples of colon adenocarcinomas, tissues were snap-frozen in liquid nitrogen immediately following resection and RNA was prepared as described by Lund et al., (Biochem. J., 1994, in press).
Probes
Fragments of the cDNA for the .gamma.2 chain of human kalinin/laminin 5 was inserted into RNA transcription vectors by restriction enzyme cutting of clone L15 covering base pairs 2995 to 3840 (FIG. 4; Kallunki et al., 1992, supra.). In brief, plasmids phb2t-01 and phb2t-02 were prepared by insertion of the complete L15 .gamma.2 chain cDNA in sense and anti-sense orientation into the polylinker of plasmid vectors SP64 and SP65 (both Promega, Madison, Wis.), respectively. In addition, two non-overlapping fragments of clone L15 were bluntend cloned into the EcoRV-site of pKS(Bluescript)II(+) (Stratagene, La Jolla, Calif.) transcription vector and the resulting plasmids were verified by dideoxy sequencing according to Sanger et al (PNAS(USA), 1977, 74:5463-5471). Plasmid phb2t-03 cover bases 3003-3239 and phb2t-05 cover bases 3239 to 3839, numbers referring to cDNA sequence Z15008 in the EMBL/GenBank/DDBJ database as reported by Kallunki et al., (1992, supra.; FIG. 4).
Similarly, cDNA fragments of other human laminin chains were prepared in RNA transcription vectors, yielding the following plasmid constructs (numbers in brackets refer to base pair numbers in the EMBL/GenBank/DDBJ sequence database by the listed accession numbers); chain .alpha.1: plasmid phae-01 (3244-3584 (accession No. X58531, Nissinen et al., Biochem. J., 1991, 276:369-379) in pKS(Bluescript)II(+)); chain .beta.1: plasmid phb1e-01 (3460-4366 (accession No. J02778, Pikkarainen et al., J. Biol. Chem., 1987, 262:10454-10462) in pKS(Bluescript)II(+)); chain .gamma.1: plasmids A1PSP64 and A1PSP65 (919-1535 (accession No. M55210, Pikkarainen et al., J. Biol. Chem., 1988, 263:6751-6758) in SP64 and SP65 respectively (sense and anti-sense orientation)).
All plasmids were linearized for transcription using restriction endonucleases and 5 .mu.g of the linearized plasmids was extracted with phenol and with chloroform/isoamyl alcohol (25:1), precipitated with ethanol, and redissolved in water. Each transcription reaction contained 1 .mu.g linearized DNA template, and transcriptions were performed essentially as recommended by the manufacturer of the polymerases. The RNA was hydrolyzed in 0.1 mol/L sodium carbonate buffer, pH 10.2, containing 10 mmol/L dithiothreitol (DTT) to an average size of 100 bases. RNA probes transcribed from opposite strands of the same plasmid template, yielding sense and anti-sense transcripts, were adjusted to 1.times.10.sup.6 cpm/.mu.L and stored at -20 C. until used. Probes were applied to tissue sections.
In situ Hybridization
In situ Hybridization was performed as described by Pyke et al., (Am. J. Pathol., 1991, 38:1059-1067) with S.sup.35 labeled RNA probes prepared as described above. In brief, paraffin sections were cut, placed on gelatinized slides, heated to 60 C. for 30 minutes, deparaffinized in xylene, and rehydrated through graded alcohols to PBS (0.01 mol/L sodium phosphate buffer, pH 7.4, containing 0.14 mol/L NaCl). The slides were then washed twice in PBS, incubated with 5 .mu.g/mL proteinase K in 50 mmol/L Tris/HCl, pH 8.0, with 5 mmol/L EDTA for 7.5 minutes, washed in PBS (2 minutes), dehydrated in graded ethanols, and air-dried before the RNA probe (.about.80 pg/.mu.L) was applied. The hybridization solution consisted of deionized formamide (50%), dextran sulfate (10%), tRNA (1 .mu.g/.mu.L), Ficoll 400 (0.02% (w/v)), polyvinylpyrrolidone (0.02% (w/v)), BSA fraction V (0.02% (w/v)), 10 mmol/L DTT, 0.3 M NaCl, 0.5 mmol/L EDTA, 10 mmol/L Tris-HCl, and 10 mmol/L NaPO.sub.4 (pH 6.8). Sections were covered by alcohol-washed, autoclaved coverslips and hybridized at 47 C. overnight (16 to 18 hours) in a chamber humidified with 10 ml of a mixture similar to the hybridization solution, except for the omission of probe, dextran sulfate, DTT, and tRNA (washing mixture). After hybridization, slides were washed in washing mixture for 2.times.1 hour at 50 C., followed by 0.5 mol/L NaCl, 1 mmol/L EDTA, 10 mmol/L Tris-HCl (pH 7.2) (NTE) with 10 mmol/L DTT at 37 C. for 15 minutes. After treatment with RNAse A (20 .mu.g/mL) in NTE at 37 C. for 30 minutes, the sections were washed in NTE at 37 C. (2.times.30 minutes), and in 2 L of 15 mmol/L sodium chloride, 1.5 mmol/L sodium citrate, pH 7.0, with 1 mmol/L DTT for 30 minutes at room temperature with stirring. Sections were then dehydrated and air-dried. Finally, autoradiographic emulsion was applied according to the manufacturer's recommendations, and sections were stored in black airtight boxes at 4 C. until they were developed after 1 to 2 weeks of exposure.
Results: Laminin .alpha.1, .beta.1, .gamma.1, and .gamma.2 chains
All rounds of in situr hybridization include both sense and anti-sense RNA probes for each of the genes studied. As negative controls, sense RNA probes are applied to adjacent sections and these probes consistently are negative. As a positive control of the .gamma.2 chain hybridizations, two anti-sense probes derived from non-overlapping .gamma.2 chain cDNA clones are used on a number of sections. To summarizes the .gamma.2 chain expression found; all carcinomas were positive except for one case of mammary duct carcinoma, and all three cases of leiomyosarcomas, both cases of malignant fibrous histiocytoma, and the only case of neurofibrosarcoma. The positive controls always give similar staining on adjacent sections (see FIG. 2, E and G). Fifteen of the malignant cases and all mouse tissue blocks were hybridized on two or more separate occasions giving the same hybridization pattern. All cell types other than those described below were negative in all cases.
Colon Adenocarcinoma
Sixteen specimens of colon adenocarcinoma were investigated by in situ hybridization for expression of the .gamma.2 chain (FIG. 1). In all of these cases, mRNA for .gamma.2 chain was present exclusively in cancer cells and in most of the cases, staining was confined to a distinct subpopulation of cancer cells at the invasive front (FIG. 1, A-D). A characteristic feature of .gamma.2 chain containing cancer cells at the invasive front was that they appeared to represent cells in the process of branching or dissociating from larger well differentiated epithelial glands, a phenomenon referred to in the literature as tumor budding or tumor-cell dissociation.
In normal-looking colon mucosa distal from the invasive carcinoma, moderate signals for .gamma.2 chain mRNA were observed in two specimens in the epithelial cells of a few mucosal glands that showed clear morphological signs of glandular disintegration and phagocytic cell infiltration. Apart from this, a weak signal was seen in luminal epithelial cells in normal looking colon mucosa in most specimens.
Weak signals for laminin chains .alpha.1, .beta.1, and .gamma.1 mRNAs were detected in cancerous areas of the 6 colon cancers studied for the expression of these genes. The expression of each of the three genes showed a similar distribution. Expression in stromal cells with a fibroblast-like morphology as well as in endothelial cells of smaller vessels was consistently found. In marked contrast to the .gamma.2 chain expression in the same samples, expression of .alpha.1, .beta.1, or .gamma.1 was never found in cancer cells and no correlation between expression of .alpha.1, .beta.1, and .gamma.1 chains with sites of invasion was found. Adjacent normal-looking parts of the samples were negative or only weakly positive for these laminin chains.
FIG. 1 shows In situ hybridization of a specimen of colon adenocarcinoma for .gamma.2 chain mRNA using a S-35 labeled anti-sense RNA probe derived from plasmid pbb2r-02. FIG. 1A is a cluster of heavily labeled cancer cells at the invasive front (open arrow) in close proximity to a well-differentiated glandular structure (straight arrow). FIG. 1B shows a high-magnification view of the area at the open arrow in 1A. Note that the isolated cancer cells show prominent labeling, whereas many coherent cancer cells of an adjacent glandular structure are negative (straight arrow). FIG. 1C shows the same pattern at an invasive focus in another part of the same specimen. FIG. 1D shows strong .gamma.2 chain expression in cancer cells engaged in a bifurcation process (curved arrows). The malignant glandular epithelium from which the .gamma.2 chain-positive cancer cells are branching is negative (straight arrow). Magnification: 1A.times.100: 1B-1D.times.640.
Ductal Mammary Carcinomas
Six of the seven cases showed a prominent signal for .gamma.2 chain in a small subpopulation of cells intimately associated with invasively growing malignant glandular structures. The most prominent signal was seen in cells located at the border between malignant and surrounding stromal tissue in glandular structures that exhibited clear histological signs of active invasion (FIG. 2A). On careful examination it was concluded that the majority of the positive cells were cancer cells but it was not possible to determine if the cells of myoepithelial origin were also positive in some cases. One case was totally negative. Normal-appearing glandular tissue was negative in all cases.
Weak signals for laminin chains .alpha.1, .beta.1, and .gamma.1 mRNAs were detected in fibroblast-like stromal cells throughout cancerous areas in one of the cases.
Malignant Melanoma
In all three cases strong hybridization of .gamma.2 chain was found in a population of cancer cells in the radial growth phase (FIG. 2B). Laminin chains .alpha.1, .beta.1, and .gamma.1 were weakly expressed in the endothelium of small vessels and in fibroblast-like stromal cells throughout the affected areas in the two cases studied for these components. In addition, a weak signal for these chains was seen in sebaceous glands of adjacent normal skin.
Squamous Cell Carcinomas
In all four squamous cell carcinomas investigated, the same pattern of .gamma.2 chain expression was found as in other carcinomas. The signals were found only in cancer cells, and only in areas with signs of ongoing invasion (FIG. 2, C-G).
The four cases were also studied for mRNA of .alpha.1, .beta.1, and .gamma.1 chains. In the two skin cancers, it was found that a very weak signal occurred in malignant cells, and that the weak signal was in all cancer cells and of an equal intensity. This is in clear contrast to the pattern of expression of the .gamma.2 chain. As seen in melanomas, epithelial cells of sebaceous glands present in adjacent unaffected skin were weakly positive for these laminin chains. In the other two cases (cervix and vulva) weak expression of .alpha.1, .beta.1, and .gamma.1 chains were seen only in endothelial and fibroblast-like stromal cells throughout the cancerous areas (FIG. 2F).
FIG. 2 shows In situ hybridization for .gamma.2 chain mRNA on sections of ductal mammary carcinoma (2A), malignant melanoma (2B), squamous cell carcinoma of the skin (2C-2D), and squamous cell carcinoma of the vulva (2E-2G). In 2A, cancer shows prominent signal for .gamma.2 chain mRNA in cells bordering the zone between malignant glandular tissue and surrounding mesenchyme (curved arrows). Cancer cells located more centrally in individual malignant glandular structures are negative for .gamma.2 chain mRNA (straight arrows). Note the wedge shaped form of the invading glandular tissue. (All images marked X' are darkfield images of the respective sections). FIG. 2B shows .gamma.2 chain mRNA signal in a subpopulation of cancer cells of radially growing malignant epithelium (curved arrows). Adjacent malignant epithelium showing a different growth pattern is devoid signal (straight arrow). FIG. 2C shows .gamma.2 chain mRNA containing cancer cells at the invasive front (curved arrow). Note lack of signal in non-invasive areas of the tumor and in adjacent unaffected areas (straight arrow). FIG. 2D is a higher magnification of area of curved arrow of 2C. highlighting the prominent signal in invading cells (curved arrow). Adjacent cancer cells with tumor islets are negative (straight arrow). FIG. 2E shows a strong signal for .gamma.2 chain mRNA is seen in invading cancer cells, using an anti-sense RNA probe derived from plasmid pb2t-03 (curved arrow). A postcapillary venule is negative (straight arrow). FIG. 2F is a near adjacent section hybridized for laminin .gamma.1 chain. Note that the endothelial cells of the venule show signal (straight arrow) whereas the malignant epithelium is negative (curved arrow). FIG. 2G is another near-adjacent section which was hybridized for .gamma.2 chain expression using an anti-sense RNA probe derived from a cDNA plasmid non-overlapping with that used for preparing the probe in 2E (phb2t-05). Note that the hybridization patter is similar to that seen in 2E, with strong signal in invading cancer cells (curved arrow) and absence of signal in a vessel (straight arrow). Magnification: 2C.times.100, all others.times.640.
Sarcomas
All six sarcomas tested in the study were totally negative for .gamma.2 chain mRNA. The expression of other laminin chains was not done.
Mouse Wounded Skin
To compare the gene expression of .gamma.2 chain in cancer tissue with a nonmalignant condition known to contain actively migrating epithelial cells showing a transient invasive phenotype, we hybridized sections of incisionally wounded mouse skin with .gamma.2 chain sense and anti-sense RNA probes. Weak .gamma.2 chain expression was observed in the keratinocytes at the edge of 12-hour old wounds, and at later time points (1-5 days), strong signals for .gamma.2 chain mRNA was seen exclusively in the basal keratinocytes of the epidermal tongue moving under the wound clot (FIG. 3). In adjacent normal-looking skin, keratinocytes were negative for .gamma.2 chain mRNA.
FIG. 3 is incisionally wounded mouse skin (72 hours after wounding) showing signal for .gamma.2 chain in keratinocytes at the leading edge of the migrating epithelium (curved arrow). Whereas buccal keratinocytes located more distant to the site of injury show little or no signal (straight arrow). Note that the signal for .gamma.2 chain stops at the tip of invading keratinocytes (open arrow). A' is a dark field image of 2A. Magnification:.times.640.
RNAse Protection Assay
Plasmid phbt-03 was linearized with EcoRI and a radiolabeled RNA-anti-sense probe was prepared by transcription using P-32 UTP and T3 polymerase (Pyke et al., FEBS Letters, 1993, 326:69-75). RNAse protection assay, using 40 .mu.g ethanol-precipitated and DNAse I-treated total RNA from six samples of colon adenocarcinomas was performed as described in Pyke et al., (1993, supra.). Protected mRNA regions were analyzed on a denaturing polyacrylamide gel and autoradiography.
The RNAse protection assay carried out on total RNA from the six samples confirmed the presence of genuine .gamma.2 chain mRNA in all samples.
These results clearly demonstrate the important correlation of .gamma.2 chain expression and invasive cell phenotype in vivo, as detected in vitro. Thus the instant methods present a novel and important method for the specific identification of invasive cell phenotypes in biopsied tissues. The knowledge of any information diagnostic for the presence or absence of invasive cells is useful for the monitoring and prognosis of continuing anti-carcinoma therapies. Further the identification of the expression or non-expression of the .gamma.2 chain provides important information as to the phenotypic nature of the tissue expanded. Thus the instant example demonstrates the use of probes of .gamma.2 chain for detection of the presence, or absence, of invasive cells.
Those skilled in the art will know, or be able to ascertain, using no more than routine experimentation, many equivalents to the specific embodiments of the invention described herein. These and all other equivalents are intended to be encompassed by the following claims.
__________________________________________________________________________# SEQUENCE LISTING - - - - (1) GENERAL INFORMATION: - - (iii) NUMBER OF SEQUENCES: 19 - - - - (2) INFORMATION FOR SEQ ID NO:1: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 20 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: other nucleic acid (A) DESCRIPTION: /desc - #= "oligomer primers" - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:1: - - GGCTCACCAA GACTTACACA - # - # - # 20 - - - - (2) INFORMATION FOR SEQ ID NO:2: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 20 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: other nucleic acid (A) DESCRIPTION: /desc - #= "OLIGOMER PRIMER" - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2: - - GAATCACTGA GCAGCTGAAC - # - # - # 20 - - - - (2) INFORMATION FOR SEQ ID NO:3: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 20 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: other nucleic acid (A) DESCRIPTION: /desc - #= "OLIGOMER PRIMER" - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:3: - - CAGTACCAGA ACCGAGTTCG - # - # - # 20 - - - - (2) INFORMATION FOR SEQ ID NO:4: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 20 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: other nucleic acid (A) DESCRIPTION: /desc - #= "OLIGOMER PRIMER" - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:4: - - CTGGTTACCA GGCTTGAGAG - # - # - # 20 - - - - (2) INFORMATION FOR SEQ ID NO:5: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 20 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: other nucleic acid (A) DESCRIPTION: /desc - #= "OLIGOMER PRIMER" - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:5: - - TTACTGCGGA ATCTCACAGC - # - # - # 20 - - - - (2) INFORMATION FOR SEQ ID NO:6: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 20 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: other nucleic acid (A) DESCRIPTION: /desc - #= "OLIGOMER PRIMER" - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:6: - - TACACTGTTC AACCCAGGGT - # - # - # 20 - - - - (2) INFORMATION FOR SEQ ID NO:7: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 20 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: other nucleic acid (A) DESCRIPTION: /desc - #= "OLIGOMER PRIMER" - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:7: - - AAACAAGCCC TCTCACTGGT - # - # - # 20 - - - - (2) INFORMATION FOR SEQ ID NO:8: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 20 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: other nucleic acid (A) DESCRIPTION: /desc - #= "OLIGOMER PRIMER" - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:8: - - GCGGAGACTG TGCTGATAAG - # - # - # 20 - - - - (2) INFORMATION FOR SEQ ID NO:9: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 20 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: other nucleic acid (A) DESCRIPTION: /desc - #= "OLIGOMER PRIMER" - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:9: - - CATACCTCTC TACATGGCAT - # - # - # 20 - - - - (2) INFORMATION FOR SEQ ID NO:10: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 20 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: other nucleic acid (A) DESCRIPTION: /desc - #= "OLIGOMER PRIMER" - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:10: - - AGTCTCGCTG AATCTCTCTT - # - # - # 20 - - - - (2) INFORMATION FOR SEQ ID NO:11: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 20 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: other nucleic acid (A) DESCRIPTION: /desc - #= "OLIGOMER PRIMER" - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:11: - - TTACAACTAG CATGGTGCCC - # - # - # 20 - - - - (2) INFORMATION FOR SEQ ID NO:12: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 5200 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide (B) LOCATION: 118..183 - - (ix) FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 118..3699 - - (ix) FEATURE: (A) NAME/KEY: polyA.sub.-- - #site (B) LOCATION: 4433 - - (ix) FEATURE: (A) NAME/KEY: polyA.sub.-- - #site (B) LOCATION: 5195 - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:12: - - GACCACCTGA TCGAAGGAAA AGGAAGGCAC AGCGGAGCGC AGAGTGAGAA CC -#ACCAACCG 60 - - AGGCGCCGGG CAGCGACCCC TGCAGCGGAG ACAGAGACTG AGCGGCCCGG CA - #CCGCC 117 - - ATG CCT GCG CTC TGG CTG GGC TGC TGC CTC TG - #C TTC TCG CTC CTC CTG 165 Met Pro Ala Leu Trp Leu Gly Cys Cys Leu Cy - #s Phe Ser Leu Leu Leu 1 5 - # 10 - # 15 - - CCC GCA GCC CGG GCC ACC TCC AGG AGG GAA GT - #C TGT GAT TGC AAT GGG 213 Pro Ala Ala Arg Ala Thr Ser Arg Arg Glu Va - #l Cys Asp Cys Asn Gly 20 - # 25 - # 30 - - AAG TCC AGG CAG TGT ATC TTT GAT CGG GAA CT - #T CAC AGA CAA ACT GGT 261 Lys Ser Arg Gln Cys Ile Phe Asp Arg Glu Le - #u His Arg Gln Thr Gly 35 - # 40 - # 45 - - AAT GGA TTC CGC TGC CTC AAC TGC AAT GAC AA - #C ACT GAT GGC ATT CAC 309 Asn Gly Phe Arg Cys Leu Asn Cys Asn Asp As - #n Thr Asp Gly Ile His 50 - # 55 - # 60 - - TGC GAG AAG TGC AAG AAT GGC TTT TAC CGG CA - #C AGA GAA AGG GAC CGC 357 Cys Glu Lys Cys Lys Asn Gly Phe Tyr Arg Hi - #s Arg Glu Arg Asp Arg 65 - # 70 - # 75 - # 80 - - TGT TTG CCC TGC AAT TGT AAC TCC AAA GGT TC - #T CTT AGT GCT CGA TGT 405 Cys Leu Pro Cys Asn Cys Asn Ser Lys Gly Se - #r Leu Ser Ala Arg Cys 85 - # 90 - # 95 - - GAC AAC TCT GGA CGG TGC AGC TGT AAA CCA GG - #T GTG ACA GGA GCC AGA 453 Asp Asn Ser Gly Arg Cys Ser Cys Lys Pro Gl - #y Val Thr Gly Ala Arg 100 - # 105 - # 110 - - TGC GAC CGA TGT CTG CCA GGC TTC CAC ATG CT - #C ACG GAT GCG GGG TGC 501 Cys Asp Arg Cys Leu Pro Gly Phe His Met Le - #u Thr Asp Ala Gly Cys 115 - # 120 - # 125 - - ACC CAA GAC CAG AGA CTG CTA GAC TCC AAG TG - #T GAC TGT GAC CCA GCT 549 Thr Gln Asp Gln Arg Leu Leu Asp Ser Lys Cy - #s Asp Cys Asp Pro Ala 130 - # 135 - # 140 - - GGC ATC GCA GGG CCC TGT GAC GCG GGC CGC TG - #T GTC TGC AAG CCA GCT 597 Gly Ile Ala Gly Pro Cys Asp Ala Gly Arg Cy - #s Val Cys Lys Pro Ala 145 1 - #50 1 - #55 1 -#60 - - GTT ACT GGA GAA CGC TGT GAT AGG TGT CGA TC - #A GGT TAC TAT AATCTG 645 Val Thr Gly Glu Arg Cys Asp Arg Cys Arg Se - #r Gly Tyr Tyr Asn Leu 165 - # 170 - # 175 - - GAT GGG GGG AAC CCT GAG GGC TGT ACC CAG TG - #T TTC TGC TAT GGG CAT 693 Asp Gly Gly Asn Pro Glu Gly Cys Thr Gln Cy - #s Phe Cys Tyr Gly His 180 - # 185 - # 190 - - TCA GCC AGC TGC CGC AGC TCT GCA GAA TAC AG - #T GTC CAT AAG ATC ACC 741 Ser Ala Ser Cys Arg Ser Ser Ala Glu Tyr Se - #r Val His Lys Ile Thr 195 - # 200 - # 205 - - TCT ACC TTT CAT CAA GAT GTT GAT GGC TGG AA - #G GCT GTC CAA CGA AAT 789 Ser Thr Phe His Gln Asp Val Asp Gly Trp Ly - #s Ala Val Gln Arg Asn 210 - # 215 - # 220 - - GGG TCT CCT GCA AAG CTC CAA TGG TCA CAG CG - #C CAT CAA GAT GTG TTT 837 Gly Ser Pro Ala Lys Leu Gln Trp Ser Gln Ar - #g His Gln Asp Val Phe 225 2 - #30 2 - #35 2 -#40 - - AGC TCA GCC CAA CGA CTA GAT CCT GTC TAT TT - #T GTG GCT CCT GCCAAA 885 Ser Ser Ala Gln Arg Leu Asp Pro Val Tyr Ph - #e Val Ala Pro Ala Lys 245 - # 250 - # 255 - - TTT CTT GGG AAT CAA CAG GTG AGC TAT GGG CA - #A AGC CTG TCC TTT GAC 933 Phe Leu Gly Asn Gln Gln Val Ser Tyr Gly Gl - #n Ser Leu Ser Phe Asp 260 - # 265 - # 270 - - TAC CGT GTG GAC AGA GGA GGC AGA CAC CCA TC - #T GCC CAT GAT GTG ATC 981 Tyr Arg Val Asp Arg Gly Gly Arg His Pro Se - #r Ala His Asp Val Ile 275 - # 280 - # 285 - - CTG GAA GGT GCT GGT CTA CGG ATC ACA GCT CC - #C TTG ATG CCA CTT GGC 1029 Leu Glu Gly Ala Gly Leu Arg Ile Thr Ala Pr - #o Leu Met Pro Leu Gly 290 - # 295 - # 300 - - AAG ACA CTG CCT TGT GGG CTC ACC AAG ACT TA - #C ACA TTC AGG TTA AAT 1077 Lys Thr Leu Pro Cys Gly Leu Thr Lys Thr Ty - #r Thr Phe Arg Leu Asn 305 3 - #10 3 - #15 3 -#20 - - GAG CAT CCA AGC AAT AAT TGG AGC CCC CAG CT - #G AGT TAC TTT GAGTAT 1125 Glu His Pro Ser Asn Asn Trp Ser Pro Gln Le - #u Ser Tyr Phe Glu Tyr 325 - # 330 - # 335 - - CGA AGG TTA CTG CGG AAT CTC ACA GCC CTC CG - #C ATC CGA GCT ACA TAT 1173 Arg Arg Leu Leu Arg Asn Leu Thr Ala Leu Ar - #g Ile Arg Ala Thr Tyr 340 - # 345 - # 350 - - GGA GAA TAC AGT ACT GGG TAC ATT GAC AAT GT - #G ACC CTG ATT TCA GCC 1221 Gly Glu Tyr Ser Thr Gly Tyr Ile Asp Asn Va - #l Thr Leu Ile Ser Ala 355 - # 360 - # 365 - - CGC CCT GTC TCT GGA GCC CCA GCA CCC TGG GT - #T GAA CAG TGT ATA TGT 1269 Arg Pro Val Ser Gly Ala Pro Ala Pro Trp Va - #l Glu Gln Cys Ile Cys 370 - # 375 - # 380 - - CCT GTT GGG TAC AAG GGG CAA TTC TGC CAG GA - #T TGT GCT TCT GGC TAC 1317 Pro Val Gly Tyr Lys Gly Gln Phe Cys Gln As - #p Cys Ala Ser Gly Tyr 385 3 - #90 3 - #95 4 -#00 - - AAG AGA GAT TCA GCG AGA CTG GGG CCT TTT GG - #C ACC TGT ATT CCTTGT 1365 Lys Arg Asp Ser Ala Arg Leu Gly Pro Phe Gl - #y Thr Cys Ile Pro Cys 405 - # 410 - # 415 - - AAC TGT CAA GGG GGA GGG GCC TGT GAT CCA GA - #C ACA GGA GAT TGT TAT 1413 Asn Cys Gln Gly Gly Gly Ala Cys Asp Pro As - #p Thr Gly Asp Cys Tyr 420 - # 425 - # 430 - - TCA GGG GAT GAG AAT CCT GAC ATT GAG TGT GC - #T GAC TGC CCA ATT GGT 1461 Ser Gly Asp Glu Asn Pro Asp Ile Glu Cys Al - #a Asp Cys Pro Ile Gly 435 - # 440 - # 445 - - TTC TAC AAC GAT CCG CAC GAC CCC CGC AGC TG - #C AAG CCA TGT CCC TGT 1509 Phe Tyr Asn Asp Pro His Asp Pro Arg Ser Cy - #s Lys Pro Cys Pro Cys 450 - # 455 - # 460 - - CAT AAC GGG TTC AGC TGC TCA GTG ATT CCG GA - #G ACG GAG GAG GTG GTG 1557 His Asn Gly Phe Ser Cys Ser Val Ile Pro Gl - #u Thr Glu Glu Val Val 465 4 - #70 4 - #75 4 -#80 - - TGC AAT AAC TGC CCT CCC GGG GTC ACC GGT GC - #C CGC TGT GAG CTCTGT 1605 Cys Asn Asn Cys Pro Pro Gly Val Thr Gly Al - #a Arg Cys Glu Leu Cys 485 - # 490 - # 495 - - GCT GAT GGC TAC TTT GGG GAC CCC TTT GGT GA - #A CAT GGC CCA GTG AGG 1653 Ala Asp Gly Tyr Phe Gly Asp Pro Phe Gly Gl - #u His Gly Pro Val Arg 500 - # 505 - # 510 - - CCT TGT CAG CCC TGT CAA TGC AAC AGC AAT GT - #G GAC CCC AGT GCC TCT 1701 Pro Cys Gln Pro Cys Gln Cys Asn Ser Asn Va - #l Asp Pro Ser Ala Ser 515 - # 520 - # 525 - - GGG AAT TGT GAC CGG CTG ACA GGC AGG TGT TT - #G AAG TGT ATC CAC AAC 1749 Gly Asn Cys Asp Arg Leu Thr Gly Arg Cys Le - #u Lys Cys Ile His Asn 530 - # 535 - # 540 - - ACA GCC GGC ATC TAC TGC GAC CAG TGC AAA GC - #A GGC TAC TTC GGG GAC 1797 Thr Ala Gly Ile Tyr Cys Asp Gln Cys Lys Al - #a Gly Tyr Phe Gly Asp 545 5 - #50 5 - #55 5 -#60 - - CCA TTG GCT CCC AAC CCA GCA GAC AAG TGT CG - #A GCT TGC AAC TGTAAC 1845 Pro Leu Ala Pro Asn Pro Ala Asp Lys Cys Ar - #g Ala Cys Asn Cys Asn 565 - # 570 - # 575 - - CCC ATG GGC TCA GAG CCT GTA GGA TGT CGA AG - #T GAT GGC ACC TGT GTT 1893 Pro Met Gly Ser Glu Pro Val Gly Cys Arg Se - #r Asp Gly Thr Cys Val 580 - # 585 - # 590 - - TGC AAG CCA GGA TTT GGT GGC CCC AAC TGT GA - #G CAT GGA GCA TTC AGC 1941 Cys Lys Pro Gly Phe Gly Gly Pro Asn Cys Gl - #u His Gly Ala Phe Ser 595 - # 600 - # 605 - - TGT CCA GCT TGC TAT AAT CAA GTG AAG ATT CA - #G ATG GAT CAG TTT ATG 1989 Cys Pro Ala Cys Tyr Asn Gln Val Lys Ile Gl - #n Met Asp Gln Phe Met 610 - # 615 - # 620 - - CAG CAG CTT CAG AGA ATG GAG GCC CTG ATT TC - #A AAG GCT CAG GGT GGT 2037 Gln Gln Leu Gln Arg Met Glu Ala Leu Ile Se - #r Lys Ala Gln Gly Gly 625 6 - #30 6 - #35 6 -#40 - - GAT GGA GTA GTA CCT GAT ACA GAG CTG GAA GG - #C AGG ATG CAG CAGGCT 2085 Asp Gly Val Val Pro Asp Thr Glu Leu Glu Gl - #y Arg Met Gln Gln Ala 645 - # 650 - # 655 - - GAG CAG GCC CTT CAG GAC ATT CTG AGA GAT GC - #C CAG ATT TCA GAA GGT 2133 Glu Gln Ala Leu Gln Asp Ile Leu Arg Asp Al - #a Gln Ile Ser Glu Gly 660 - # 665 - # 670 - - GCT AGC AGA TCC CTT GGT CTC CAG TTG GCC AA - #G GTG AGG AGC CAA GAG 2181 Ala Ser Arg Ser Leu Gly Leu Gln Leu Ala Ly - #s Val Arg Ser Gln Glu 675 - # 680 - # 685 - - AAC AGC TAC CAG AGC CGC CTG GAT GAC CTC AA - #G ATG ACT GTG GAA AGA 2229 Asn Ser Tyr Gln Ser Arg Leu Asp Asp Leu Ly - #s Met Thr Val Glu Arg 690 - # 695 - # 700 - - GTT CGG GCT CTG GGA AGT CAG TAC CAG AAC CG - #A GTT CGG GAT ACT CAC 2277 Val Arg Ala Leu Gly Ser Gln Tyr Gln Asn Ar - #g Val Arg Asp Thr His 705 7 - #10 7 - #15 7 -#20 - - AGG CTC ATC ACT CAG ATG CAG CTG AGC CTG GC - #A GAA AGT GAA GCTTCC 2325 Arg Leu Ile Thr Gln Met Gln Leu Ser Leu Al - #a Glu Ser Glu Ala Ser 725 - # 730 - # 735 - - TTG GGA AAC ACT AAC ATT CCT GCC TCA GAC CA - #C TAC GTG GGG CCA AAT 2373 Leu Gly Asn Thr Asn Ile Pro Ala Ser Asp Hi - #s Tyr Val Gly Pro Asn 740 - # 745 - # 750 - - GGC TTT AAA AGT CTG GCT CAG GAG GCC ACA AG - #A TTA GCA GAA AGC CAC 2421 Gly Phe Lys Ser Leu Ala Gln Glu Ala Thr Ar - #g Leu Ala Glu Ser His 755 - # 760 - # 765 - - GTT GAG TCA GCC AGT AAC ATG GAG CAA CTG AC - #A AGG GAA ACT GAG GAC 2469 Val Glu Ser Ala Ser Asn Met Glu Gln Leu Th - #r Arg Glu Thr Glu Asp 770 - # 775 - # 780 - - TAT TCC AAA CAA GCC CTC TCA CTG GTG CGC AA - #G GCC CTG CAT GAA GGA 2517 Tyr Ser Lys Gln Ala Leu Ser Leu Val Arg Ly - #s Ala Leu His Glu Gly 785 7 - #90 7 - #95 8 -#00 - - GTC GGA AGC GGA AGC GGT AGC CCG GAC GGT GC - #T GTG GTG CAA GGGCTT 2565 Val Gly Ser Gly Ser Gly Ser Pro Asp Gly Al - #a Val Val Gln Gly Leu 805 - # 810 - # 815 - - GTG GAA AAA TTG GAG AAA ACC AAG TCC CTG GC - #C CAG CAG TTG ACA AGG 2613 Val Glu Lys Leu Glu Lys Thr Lys Ser Leu Al - #a Gln Gln Leu Thr Arg 820 - # 825 - # 830 - - GAG GCC ACT CAA GCG GAA ATT GAA GCA GAT AG - #G TCT TAT CAG CAC AGT 2661 Glu Ala Thr Gln Ala Glu Ile Glu Ala Asp Ar - #g Ser Tyr Gln His Ser 835 - # 840 - # 845 - - CTC CGC CTC CTG GAT TCA GTG TCT CCG CTT CA - #G GGA GTC AGT GAT CAG 2709 Leu Arg Leu Leu Asp Ser Val Ser Pro Leu Gl - #n Gly Val Ser Asp Gln 850 - # 855 - # 860 - - TCC TTT CAG GTG GAA GAA GCA AAG AGG ATC AA - #A CAA AAA GCG GAT TCA 2757 Ser Phe Gln Val Glu Glu Ala Lys Arg Ile Ly - #s Gln Lys Ala Asp Ser 865 8 - #70 8 - #75 8 -#80 - - CTC TCA AGC CTG GTA ACC AGG CAT ATG GAT GA - #G TTC AAG CGT ACACAA 2805 Leu Ser Ser Leu Val Thr Arg His Met Asp Gl - #u Phe Lys Arg Thr Gln 885 - # 890 - # 895 - - AAG AAT CTG GGA AAC TGG AAA GAA GAA GCA CA - #G CAG CTC TTA CAG AAT 2853 Lys Asn Leu Gly Asn Trp Lys Glu Glu Ala Gl - #n Gln Leu Leu Gln Asn 900 - # 905 - # 910 - - GGA AAA AGT GGG AGA GAG AAA TCA GAT CAG CT - #G CTT TCC CGT GCC AAT 2901 Gly Lys Ser Gly Arg Glu Lys Ser Asp Gln Le - #u Leu Ser Arg Ala Asn 915 - # 920 - # 925 - - CTT GCT AAA AGC AGA GCA CAA GAA GCA CTG AG - #T ATG GGC AAT GCC ACT 2949 Leu Ala Lys Ser Arg Ala Gln Glu Ala Leu Se - #r Met Gly Asn Ala Thr 930 - # 935 - # 940 - - TTT TAT GAA GTT GAG AGC ATC CTT AAA AAC CT - #C AGA GAG TTT GAC CTG 2997 Phe Tyr Glu Val Glu Ser Ile Leu Lys Asn Le - #u Arg Glu Phe Asp Leu 945 9 - #50 9 - #55 9 -#60 - - CAG GTG GAC AAC AGA AAA GCA GAA GCT GAA GA - #A GCC ATG AAG AGACTC 3045 Gln Val Asp Asn Arg Lys Ala Glu Ala Glu Gl - #u Ala Met Lys Arg Leu 965 - # 970 - # 975 - - TCC TAC ATC AGC CAG AAG GTT TCA GAT GCC AG - #T GAC AAG ACC CAG CAA 3093 Ser Tyr Ile Ser Gln Lys Val Ser Asp Ala Se - #r Asp Lys Thr Gln Gln 980 - # 985 - # 990 - - GCA GAA AGA GCC CTG GGG AGC GCT GCT GCT GA - #T GCA CAG AGG GCA AAG 3141 Ala Glu Arg Ala Leu Gly Ser Ala Ala Ala As - #p Ala Gln Arg Ala Lys 995 - # 1000 - # 1005 - - AAT GGG GCC GGG GAG GCC CTG GAA ATC TCC AG - #T GAG ATT GAA CAG GAG 3189 Asn Gly Ala Gly Glu Ala Leu Glu Ile Ser Se - #r Glu Ile Glu Gln Glu 1010 - # 1015 - # 1020 - - ATT GGG AGT CTG AAC TTG GAA GCC AAT GTG AC - #A GCA GAT GGA GCC TTG 3237 Ile Gly Ser Leu Asn Leu Glu Ala Asn Val Th - #r Ala Asp Gly Ala Leu 1025 1030 - # 1035 - # 1040 - - GCC ATG GAA AAG GGA CTG GCC TCT CTG AAG AG - #T GAG ATG AGG GAA GTG 3285 Ala Met Glu Lys Gly Leu Ala Ser Leu Lys Se - #r Glu Met Arg Glu Val 1045 - # 1050 - # 1055 - - GAA GGA GAG CTG GAA AGG AAG GAG CTG GAG TT - #T GAC ACG AAT ATG GAT 3333 Glu Gly Glu Leu Glu Arg Lys Glu Leu Glu Ph - #e Asp Thr Asn Met Asp 1060 - # 1065 - # 1070 - - GCA GTA CAG ATG GTG ATT ACA GAA GCC CAG AA - #G GTT GAT ACC AGA GCC 3381 Ala Val Gln Met Val Ile Thr Glu Ala Gln Ly - #s Val Asp Thr Arg Ala 1075 - # 1080 - # 1085 - - AAG AAC GCT GGG GTT ACA ATC CAA GAC ACA CT - #C AAC ACA TTA GAC GGC 3429 Lys Asn Ala Gly Val Thr Ile Gln Asp Thr Le - #u Asn Thr Leu Asp Gly 1090 - # 1095 - # 1100 - - CTC CTG CAT CTG ATG GAC CAG CCT CTC AGT GT - #A GAT GAA GAG GGG CTG 3477 Leu Leu His Leu Met Asp Gln Pro Leu Ser Va - #l Asp Glu Glu Gly Leu 1105 1110 - # 1115 - # 1120 - - GTC TTA CTG GAG CAG AAG CTT TCC CGA GCC AA - #G ACC CAG ATC AAC AGC 3525 Val Leu Leu Glu Gln Lys Leu Ser Arg Ala Ly - #s Thr Gln Ile Asn Ser 1125 - # 1130 - # 1135 - - CAA CTG CGG CCC ATG ATG TCA GAG CTG GAA GA - #G AGG GCA CGT CAG CAG 3573 Gln Leu Arg Pro Met Met Ser Glu Leu Glu Gl - #u Arg Ala Arg Gln Gln 1140 - # 1145 - # 1150 - - AGG GGC CAC CTC CAT TTG CTG GAG ACA AGC AT - #A GAT GGG ATT CTG GCT 3621 Arg Gly His Leu His Leu Leu Glu Thr Ser Il - #e Asp Gly Ile Leu Ala 1155 - # 1160 - # 1165 - - GAT GTG AAG AAC TTG GAG AAC ATT AGG GAC AA - #C CTG CCC CCA GGC TGC 3669 Asp Val Lys Asn Leu Glu Asn Ile Arg Asp As - #n Leu Pro Pro Gly Cys 1170 - # 1175 - # 1180 - - TAC AAT ACC CAG GCT CTT GAG CAA CAG TGA AG - #CTGCCATA AATATTTCTC 3719 Tyr Asn Thr Gln Ala Leu Glu Gln Gln * 1185 1190 - - AACTGAGGTT CTTGGGATAC AGATCTCAGG GCTCGGGAGC CATGTCATGT GA -#GTGGGTGG 3779 - - GATGGGGACA TTTGAACATG TTTAATGGGT ATGCTCAGGT CAACTGACCT GA -#CCCCATTC 3839 - - CTGATCCCAT GGCCAGGTGG TTGTCTTATT GCACCATACT CCTTGCTTCC TG -#ATGCTGGG 3899 - - CATGAGGCAG ATAGGCACTG GTGTGAGAAT GATCAAGGAT CTGGACCCCA AA -#GATAGACT 3959 - - GGATGGAAAG ACAAACTGCA CAGGCAGATG TTTGCCTCAT AATAGTCGTA AG -#TGGAGTCC 4019 - - TGGAATTTGG ACAAGTGCTG TTGGGATATA GTCAACTTAT TCTTTGAGTA AT -#GTGACTAA 4079 - - AGGAAAAAAC TTTGACTTTG CCCAGGCATG AAATTCTTCC TAATGTCAGA AC -#AGAGTGCA 4139 - - ACCCAGTCAC ACTGTGGCCA GTAAAATACT ATTGCCTCAT ATTGTCCTCT GC -#AAGCTTCT 4199 - - TGCTGATCAG AGTTCCTCCT ACTTACAACC CAGGGTGTGA ACATGTTCTC CA -#TTTTCAAG 4259 - - CTGGAAGAAG TGAGCAGTGT TGGAGTGAGG ACCTGTAAGG CAGGCCCATT CA -#GAGCTATG 4319 - - GTGCTTGCTG GTGCCTGCCA CCTTCAAGTT CTGGACCTGG GCATGACATC CT -#TTCTTTTA 4379 - - ATGATGCCAT GGCAACTTAG AGATTGCATT TTTATTAAAG CATTTCCTAC CA -#GCAAAGCA 4439 - - AATGTTGGGA AAGTATTTAC TTTTTCGGTT TCAAAGTGAT AGAAAAGTGT GG -#CTTGGGCA 4499 - - TTGAAAGAGG TAAAATTCTC TAGATTTATT AGTCCTAATT CAATCCTACT TT -#TCGAACAC 4559 - - CAAAAATGAT GCGCATCAAT GTATTTTATC TTATTTTCTC AATCTCCTCT CT -#CTTTCCTC 4619 - - CACCCATAAT AAGAGAATGT TCCTACTCAC ACTTCAGCTG GGTCACATCC AT -#CCCTCCAT 4679 - - TCATCCTTCC ATCCATCTTT CCATCCATTA CCTCCATCCA TCCTTCCAAC AT -#ATATTTAT 4739 - - TGAGTACCTA CTGTGTGCCA GGGGCTGGTG GGACAGTGGT GACATAGTCT CT -#GCCCTCAT 4799 - - AGAGTTGATT GTCTAGTGAG GAAGACAAGC ATTTTTAAAA AATAAATTTA AA -#CTTACAAA 4859 - - CTTTGTTTGT CACAAGTGGT GTTTATTGCA ATAACCGCTT GGTTTGCAAC CT -#CTTTGCTC 4919 - - AACAGAACAT ATGTTGCAAG ACCCTCCCAT GGGCACTGAG TTTGGCAAGG AT -#GACAGAGC 4979 - - TCTGGGTTGT GCACATTTCT TTGCATTCCA GCGTCACTCT GTGCCTTCTA CA -#ACTGATTG 5039 - - CAACAGACTG TTGAGTTATG ATAACACCAG TGGGAATTGC TGGAGGAACC AG -#AGGCACTT 5099 - - CCACCTTGGC TGGGAAGACT ATGGTGCTGC CTTGCTTCTG TATTTCCTTG GA -#TTTTCCTG 5159 - - AAAGTGTTTT TAAATAAAGA ACAATTGTTA GATGCCAAAA A - # - # 5200 - - - - (2) INFORMATION FOR SEQ ID NO:13: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 1193 am - #ino acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:13: - - Met Pro Ala Leu Trp Leu Gly Cys Cys Leu Cy - #s Phe Ser Leu Leu Leu 1 5 - # 10 - # 15 - - Pro Ala Ala Arg Ala Thr Ser Arg Arg Glu Va - #l Cys Asp Cys Asn Gly 20 - # 25 - # 30 - - Lys Ser Arg Gln Cys Ile Phe Asp Arg Glu Le - #u His Arg Gln Thr Gly 35 - # 40 - # 45 - - Asn Gly Phe Arg Cys Leu Asn Cys Asn Asp As - #n Thr Asp Gly Ile His 50 - # 55 - # 60 - - Cys Glu Lys Cys Lys Asn Gly Phe Tyr Arg Hi - #s Arg Glu Arg Asp Arg 65 - # 70 - # 75 - # 80 - - Cys Leu Pro Cys Asn Cys Asn Ser Lys Gly Se - #r Leu Ser Ala Arg Cys 85 - # 90 - # 95 - - Asp Asn Ser Gly Arg Cys Ser Cys Lys Pro Gl - #y Val Thr Gly Ala Arg 100 - # 105 - # 110 - - Cys Asp Arg Cys Leu Pro Gly Phe His Met Le - #u Thr Asp Ala Gly Cys 115 - # 120 - # 125 - - Thr Gln Asp Gln Arg Leu Leu Asp Ser Lys Cy - #s Asp Cys Asp Pro Ala 130 - # 135 - # 140 - - Gly Ile Ala Gly Pro Cys Asp Ala Gly Arg Cy - #s Val Cys Lys Pro Ala 145 1 - #50 1 - #55 1 -#60 - - Val Thr Gly Glu Arg Cys Asp Arg Cys Arg Se - #r Gly Tyr Tyr AsnLeu 165 - # 170 - # 175 - - Asp Gly Gly Asn Pro Glu Gly Cys Thr Gln Cy - #s Phe Cys Tyr Gly His 180 - # 185 - # 190 - - Ser Ala Ser Cys Arg Ser Ser Ala Glu Tyr Se - #r Val His Lys Ile Thr 195 - # 200 - # 205 - - Ser Thr Phe His Gln Asp Val Asp Gly Trp Ly - #s Ala Val Gln Arg Asn 210 - # 215 - # 220 - - Gly Ser Pro Ala Lys Leu Gln Trp Ser Gln Ar - #g His Gln Asp Val Phe 225 2 - #30 2 - #35 2 -#40 - - Ser Ser Ala Gln Arg Leu Asp Pro Val Tyr Ph - #e Val Ala Pro AlaLys 245 - # 250 - # 255 - - Phe Leu Gly Asn Gln Gln Val Ser Tyr Gly Gl - #n Ser Leu Ser Phe Asp 260 - # 265 - # 270 - - Tyr Arg Val Asp Arg Gly Gly Arg His Pro Se - #r Ala His Asp Val Ile 275 - # 280 - # 285 - - Leu Glu Gly Ala Gly Leu Arg Ile Thr Ala Pr - #o Leu Met Pro Leu Gly 290 - # 295 - # 300 - - Lys Thr Leu Pro Cys Gly Leu Thr Lys Thr Ty - #r Thr Phe Arg Leu Asn 305 3 - #10 3 - #15 3 -#20 - - Glu His Pro Ser Asn Asn Trp Ser Pro Gln Le - #u Ser Tyr Phe GluTyr 325 - # 330 - # 335 - - Arg Arg Leu Leu Arg Asn Leu Thr Ala Leu Ar - #g Ile Arg Ala Thr Tyr 340 - # 345 - # 350 - - Gly Glu Tyr Ser Thr Gly Tyr Ile Asp Asn Va - #l Thr Leu Ile Ser Ala 355 - # 360 - # 365 - - Arg Pro Val Ser Gly Ala Pro Ala Pro Trp Va - #l Glu Gln Cys Ile Cys 370 - # 375 - # 380 - - Pro Val Gly Tyr Lys Gly Gln Phe Cys Gln As - #p Cys Ala Ser Gly Tyr 385 3 - #90 3 - #95 4 -#00 - - Lys Arg Asp Ser Ala Arg Leu Gly Pro Phe Gl - #y Thr Cys Ile ProCys 405 - # 410 - # 415 - - Asn Cys Gln Gly Gly Gly Ala Cys Asp Pro As - #p Thr Gly Asp Cys Tyr 420 - # 425 - # 430 - - Ser Gly Asp Glu Asn Pro Asp Ile Glu Cys Al - #a Asp Cys Pro Ile Gly 435 - # 440 - # 445 - - Phe Tyr Asn Asp Pro His Asp Pro Arg Ser Cy - #s Lys Pro Cys Pro Cys 450 - # 455 - # 460 - - His Asn Gly Phe Ser Cys Ser Val Ile Pro Gl - #u Thr Glu Glu Val Val 465 4 - #70 4 - #75 4 -#80 - - Cys Asn Asn Cys Pro Pro Gly Val Thr Gly Al - #a Arg Cys Glu LeuCys 485 - # 490 - # 495 - - Ala Asp Gly Tyr Phe Gly Asp Pro Phe Gly Gl - #u His Gly Pro Val Arg 500 - # 505 - # 510 - - Pro Cys Gln Pro Cys Gln Cys Asn Ser Asn Va - #l Asp Pro Ser Ala Ser 515 - # 520 - # 525 - - Gly Asn Cys Asp Arg Leu Thr Gly Arg Cys Le - #u Lys Cys Ile His Asn 530 - # 535 - # 540 - - Thr Ala Gly Ile Tyr Cys Asp Gln Cys Lys Al - #a Gly Tyr Phe Gly Asp 545 5 - #50 5 - #55 5 -#60 - - Pro Leu Ala Pro Asn Pro Ala Asp Lys Cys Ar - #g Ala Cys Asn CysAsn 565 - # 570 - # 575 - - Pro Met Gly Ser Glu Pro Val Gly Cys Arg Se - #r Asp Gly Thr Cys Val 580 - # 585 - # 590 - - Cys Lys Pro Gly Phe Gly Gly Pro Asn Cys Gl - #u His Gly Ala Phe Ser 595 - # 600 - # 605 - - Cys Pro Ala Cys Tyr Asn Gln Val Lys Ile Gl - #n Met Asp Gln Phe Met 610 - # 615 - # 620 - - Gln Gln Leu Gln Arg Met Glu Ala Leu Ile Se - #r Lys Ala Gln Gly Gly 625 6 - #30 6 - #35 6 -#40 - - Asp Gly Val Val Pro Asp Thr Glu Leu Glu Gl - #y Arg Met Gln GlnAla 645 - # 650 - # 655 - - Glu Gln Ala Leu Gln Asp Ile Leu Arg Asp Al - #a Gln Ile Ser Glu Gly 660 - # 665 - # 670 - - Ala Ser Arg Ser Leu Gly Leu Gln Leu Ala Ly - #s Val Arg Ser Gln Glu 675 - # 680 - # 685 - - Asn Ser Tyr Gln Ser Arg Leu Asp Asp Leu Ly - #s Met Thr Val Glu Arg 690 - # 695 - # 700 - - Val Arg Ala Leu Gly Ser Gln Tyr Gln Asn Ar - #g Val Arg Asp Thr His 705 7 - #10 7 - #15 7 -#20 - - Arg Leu Ile Thr Gln Met Gln Leu Ser Leu Al - #a Glu Ser Glu AlaSer 725 - # 730 - # 735 - - Leu Gly Asn Thr Asn Ile Pro Ala Ser Asp Hi - #s Tyr Val Gly Pro Asn 740 - # 745 - # 750 - - Gly Phe Lys Ser Leu Ala Gln Glu Ala Thr Ar - #g Leu Ala Glu Ser His 755 - # 760 - # 765 - - Val Glu Ser Ala Ser Asn Met Glu Gln Leu Th - #r Arg Glu Thr Glu Asp 770 - # 775 - # 780 - - Tyr Ser Lys Gln Ala Leu Ser Leu Val Arg Ly - #s Ala Leu His Glu Gly 785 7 - #90 7 - #95 8 -#00 - - Val Gly Ser Gly Ser Gly Ser Pro Asp Gly Al - #a Val Val Gln GlyLeu 805 - # 810 - # 815 - - Val Glu Lys Leu Glu Lys Thr Lys Ser Leu Al - #a Gln Gln Leu Thr Arg 820 - # 825 - # 830 - - Glu Ala Thr Gln Ala Glu Ile Glu Ala Asp Ar - #g Ser Tyr Gln His Ser 835 - # 840 - # 845 - - Leu Arg Leu Leu Asp Ser Val Ser Pro Leu Gl - #n Gly Val Ser Asp Gln 850 - # 855 - # 860 - - Ser Phe Gln Val Glu Glu Ala Lys Arg Ile Ly - #s Gln Lys Ala Asp Ser 865 8 - #70 8 - #75 8 -#80 - - Leu Ser Ser Leu Val Thr Arg His Met Asp Gl - #u Phe Lys Arg ThrGln 885 - # 890 - # 895 - - Lys Asn Leu Gly Asn Trp Lys Glu Glu Ala Gl - #n Gln Leu Leu Gln Asn 900 - # 905 - # 910 - - Gly Lys Ser Gly Arg Glu Lys Ser Asp Gln Le - #u Leu Ser Arg Ala Asn 915 - # 920 - # 925 - - Leu Ala Lys Ser Arg Ala Gln Glu Ala Leu Se - #r Met Gly Asn Ala Thr 930 - # 935 - # 940 - - Phe Tyr Glu Val Glu Ser Ile Leu Lys Asn Le - #u Arg Glu Phe Asp Leu 945 9 - #50 9 - #55 9 -#60 - - Gln Val Asp Asn Arg Lys Ala Glu Ala Glu Gl - #u Ala Met Lys ArgLeu 965 - # 970 - # 975 - - Ser Tyr Ile Ser Gln Lys Val Ser Asp Ala Se - #r Asp Lys Thr Gln Gln 980 - # 985 - # 990 - - Ala Glu Arg Ala Leu Gly Ser Ala Ala Ala As - #p Ala Gln Arg Ala Lys 995 - # 1000 - # 1005 - - Asn Gly Ala Gly Glu Ala Leu Glu Ile Ser Se - #r Glu Ile Glu Gln Glu 1010 - # 1015 - # 1020 - - Ile Gly Ser Leu Asn Leu Glu Ala Asn Val Th - #r Ala Asp Gly Ala Leu 1025 1030 - # 1035 - # 1040 - - Ala Met Glu Lys Gly Leu Ala Ser Leu Lys Se - #r Glu Met Arg Glu Val 1045 - # 1050 - # 1055 - - Glu Gly Glu Leu Glu Arg Lys Glu Leu Glu Ph - #e Asp Thr Asn Met Asp 1060 - # 1065 - # 1070 - - Ala Val Gln Met Val Ile Thr Glu Ala Gln Ly - #s Val Asp Thr Arg Ala 1075 - # 1080 - # 1085 - - Lys Asn Ala Gly Val Thr Ile Gln Asp Thr Le - #u Asn Thr Leu Asp Gly 1090 - # 1095 - # 1100 - - Leu Leu His Leu Met Asp Gln Pro Leu Ser Va - #l Asp Glu Glu Gly Leu 1105 1110 - # 1115 - # 1120 - - Val Leu Leu Glu Gln Lys Leu Ser Arg Ala Ly - #s Thr Gln Ile Asn Ser 1125 - # 1130 - # 1135 - - Gln Leu Arg Pro Met Met Ser Glu Leu Glu Gl - #u Arg Ala Arg Gln Gln 1140 - # 1145 - # 1150 - - Arg Gly His Leu His Leu Leu Glu Thr Ser Il - #e Asp Gly Ile Leu Ala 1155 - # 1160 - # 1165 - - Asp Val Lys Asn Leu Glu Asn Ile Arg Asp As - #n Leu Pro Pro Gly Cys 1170 - # 1175 - # 1180 - - Tyr Asn Thr Gln Ala Leu Glu Gln Gln 1185 1190 - - - - (2) INFORMATION FOR SEQ ID NO:14: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 4316 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (ix) FEATURE: (A) NAME/KEY: sig.sub.-- - #peptide (B) LOCATION: 118..183 - - (ix) FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 118..3453 - - (ix) FEATURE: (A) NAME/KEY: repeat.sub.-- - #unit (B) LOCATION: 4021..4316 (D) OTHER INFORMATION: - #/rpt.sub.-- type= "other" /rpt.sub.-- - #family= "HUMAN ALU" - - (ix) FEATURE: (A) NAME/KEY: polyA.sub.-- - #site (B) LOCATION: 4296 - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:14: - - GACCACCTGA TCGAAGGAAA AGGAAGGCAC AGCGGAGCGC AGAGTGAGAA CC -#ACCAACCG 60 - - AGGCGCCGGG CAGCGACCCC TGCAGCGGAG ACAGAGACTG AGCGGCCCGG CA - #CCGCC 117 - - ATG CCT GCG CTC TGG CTG GGC TGC TGC CTC TG - #C TTC TCG CTC CTC CTG 165 Met Pro Ala Leu Trp Leu Gly Cys Cys Leu Cy - #s Phe Ser Leu Leu Leu 1195 1200 - # 1205 - # 1210 - - CCC GCA GCC CGG GCC ACC TCC AGG AGG GAA GT - #C TGT GAT TGC AAT GGG 213 Pro Ala Ala Arg Ala Thr Ser Arg Arg Glu Va - #l Cys Asp Cys Asn Gly 1215 - # 1220 - # 1225 - - AAG TCC AGG CAG TGT ATC TTT GAT CGG GAA CT - #T CAC AGA CAA ACT GGT 261 Lys Ser Arg Gln Cys Ile Phe Asp Arg Glu Le - #u His Arg Gln Thr Gly 1230 - # 1235 - # 1240 - - AAT GGA TTC CGC TGC CTC AAC TGC AAT GAC AA - #C ACT GAT GGC ATT CAC 309 Asn Gly Phe Arg Cys Leu Asn Cys Asn Asp As - #n Thr Asp Gly Ile His 1245 - # 1250 - # 1255 - - TGC GAG AAG TGC AAG AAT GGC TTT TAC CGG CA - #C AGA GAA AGG GAC CGC 357 Cys Glu Lys Cys Lys Asn Gly Phe Tyr Arg Hi - #s Arg Glu Arg Asp Arg 1260 - # 1265 - # 1270 - - TGT TTG CCC TGC AAT TGT AAC TCC AAA GGT TC - #T CTT AGT GCT CGA TGT 405 Cys Leu Pro Cys Asn Cys Asn Ser Lys Gly Se - #r Leu Ser Ala Arg Cys 1275 1280 - # 1285 - # 1290 - - GAC AAC TCT GGA CGG TGC AGC TGT AAA CCA GG - #T GTG ACA GGA GCC AGA 453 Asp Asn Ser Gly Arg Cys Ser Cys Lys Pro Gl - #y Val Thr Gly Ala Arg 1295 - # 1300 - # 1305 - - TGC GAC CGA TGT CTG CCA GGC TTC CAC ATG CT - #C ACG GAT GCG GGG TGC 501 Cys Asp Arg Cys Leu Pro Gly Phe His Met Le - #u Thr Asp Ala Gly Cys 1310 - # 1315 - # 1320 - - ACC CAA GAC CAG AGA CTG CTA GAC TCC AAG TG - #T GAC TGT GAC CCA GCT 549 Thr Gln Asp Gln Arg Leu Leu Asp Ser Lys Cy - #s Asp Cys Asp Pro Ala 1325 - # 1330 - # 1335 - - GGC ATC GCA GGG CCC TGT GAC GCG GGC CGC TG - #T GTC TGC AAG CCA GCT 597 Gly Ile Ala Gly Pro Cys Asp Ala Gly Arg Cy - #s Val Cys Lys Pro Ala 1340 - # 1345 - # 1350 - - GTT ACT GGA GAA CGC TGT GAT AGG TGT CGA TC - #A GGT TAC TAT AAT CTG 645 Val Thr Gly Glu Arg Cys Asp Arg Cys Arg Se - #r Gly Tyr Tyr Asn Leu 1355 1360 - # 1365 - # 1370 - - GAT GGG GGG AAC CCT GAG GGC TGT ACC CAG TG - #T TTC TGC TAT GGG CAT 693 Asp Gly Gly Asn Pro Glu Gly Cys Thr Gln Cy - #s Phe Cys Tyr Gly His 1375 - # 1380 - # 1385 - - TCA GCC AGC TGC CGC AGC TCT GCA GAA TAC AG - #T GTC CAT AAG ATC ACC 741 Ser Ala Ser Cys Arg Ser Ser Ala Glu Tyr Se - #r Val His Lys Ile Thr 1390 - # 1395 - # 1400 - - TCT ACC TTT CAT CAA GAT GTT GAT GGC TGG AA - #G GCT GTC CAA CGA AAT 789 Ser Thr Phe His Gln Asp Val Asp Gly Trp Ly - #s Ala Val Gln Arg Asn 1405 - # 1410 - # 1415 - - GGG TCT CCT GCA AAG CTC CAA TGG TCA CAG CG - #C CAT CAA GAT GTG TTT 837 Gly Ser Pro Ala Lys Leu Gln Trp Ser Gln Ar - #g His Gln Asp Val Phe 1420 - # 1425 - # 1430 - - AGC TCA GCC CAA CGA CTA GAT CCT GTC TAT TT - #T GTG GCT CCT GCC AAA 885 Ser Ser Ala Gln Arg Leu Asp Pro Val Tyr Ph - #e Val Ala Pro Ala Lys 1435 1440 - # 1445 - # 1450 - - TTT CTT GGG AAT CAA CAG GTG AGC TAT GGG CA - #A AGC CTG TCC TTT GAC 933 Phe Leu Gly Asn Gln Gln Val Ser Tyr Gly Gl - #n Ser Leu Ser Phe Asp 1455 - # 1460 - # 1465 - - TAC CGT GTG GAC AGA GGA GGC AGA CAC CCA TC - #T GCC CAT GAT GTG ATC 981 Tyr Arg Val Asp Arg Gly Gly Arg His Pro Se - #r Ala His Asp Val Ile 1470 - # 1475 - # 1480 - - CTG GAA GGT GCT GGT CTA CGG ATC ACA GCT CC - #C TTG ATG CCA CTT GGC 1029 Leu Glu Gly Ala Gly Leu Arg Ile Thr Ala Pr - #o Leu Met Pro Leu Gly 1485 - # 1490 - # 1495 - - AAG ACA CTG CCT TGT GGG CTC ACC AAG ACT TA - #C ACA TTC AGG TTA AAT 1077 Lys Thr Leu Pro Cys Gly Leu Thr Lys Thr Ty - #r Thr Phe Arg Leu Asn 1500 - # 1505 - # 1510 - - GAG CAT CCA AGC AAT AAT TGG AGC CCC CAG CT - #G AGT TAC TTT GAG TAT 1125 Glu His Pro Ser Asn Asn Trp Ser Pro Gln Le - #u Ser Tyr Phe Glu Tyr 1515 1520 - # 1525 - # 1530 - - CGA AGG TTA CTG CGG AAT CTC ACA GCC CTC CG - #C ATC CGA GCT ACA TAT 1173 Arg Arg Leu Leu Arg Asn Leu Thr Ala Leu Ar - #g Ile Arg Ala Thr Tyr 1535 - # 1540 - # 1545 - - GGA GAA TAC AGT ACT GGG TAC ATT GAC AAT GT - #G ACC CTG ATT TCA GCC 1221 Gly Glu Tyr Ser Thr Gly Tyr Ile Asp Asn Va - #l Thr Leu Ile Ser Ala 1550 - # 1555 - # 1560 - - CGC CCT GTC TCT GGA GCC CCA GCA CCC TGG GT - #T GAA CAG TGT ATA TGT 1269 Arg Pro Val Ser Gly Ala Pro Ala Pro Trp Va - #l Glu Gln Cys Ile Cys 1565 - # 1570 - # 1575 - - CCT GTT GGG TAC AAG GGG CAA TTC TGC CAG GA - #T TGT GCT TCT GGC TAC 1317 Pro Val Gly Tyr Lys Gly Gln Phe Cys Gln As - #p Cys Ala Ser Gly Tyr 1580 - # 1585 - # 1590 - - AAG AGA GAT TCA GCG AGA CTG GGG CCT TTT GG - #C ACC TGT ATT CCT TGT 1365 Lys Arg Asp Ser Ala Arg Leu Gly Pro Phe Gl - #y Thr Cys Ile Pro Cys 1595 1600 - # 1605 - # 1610 - - AAC TGT CAA GGG GGA GGG GCC TGT GAT CCA GA - #C ACA GGA GAT TGT TAT 1413 Asn Cys Gln Gly Gly Gly Ala Cys Asp Pro As - #p Thr Gly Asp Cys Tyr 1615 - # 1620 - # 1625 - - TCA GGG GAT GAG AAT CCT GAC ATT GAG TGT GC - #T GAC TGC CCA ATT GGT 1461 Ser Gly Asp Glu Asn Pro Asp Ile Glu Cys Al - #a Asp Cys Pro Ile Gly 1630 - # 1635 - # 1640 - - TTC TAC AAC GAT CCG CAC GAC CCC CGC AGC TG - #C AAG CCA TGT CCC TGT 1509 Phe Tyr Asn Asp Pro His Asp Pro Arg Ser Cy - #s Lys Pro Cys Pro Cys 1645 - # 1650 - # 1655 - - CAT AAC GGG TTC AGC TGC TCA GTG ATT CCG GA - #G ACG GAG GAG GTG GTG 1557 His Asn Gly Phe Ser Cys Ser Val Ile Pro Gl - #u Thr Glu Glu Val Val 1660 - # 1665 - # 1670 - - TGC AAT AAC TGC CCT CCC GGG GTC ACC GGT GC - #C CGC TGT GAG CTC TGT 1605 Cys Asn Asn Cys Pro Pro Gly Val Thr Gly Al - #a Arg Cys Glu Leu Cys 1675 1680 - # 1685 - # 1690 - - GCT GAT GGC TAC TTT GGG GAC CCC TTT GGT GA - #A CAT GGC CCA GTG AGG 1653 Ala Asp Gly Tyr Phe Gly Asp Pro Phe Gly Gl - #u His Gly Pro Val Arg 1695 - # 1700 - # 1705 - - CCT TGT CAG CCC TGT CAA TGC AAC AGC AAT GT - #G GAC CCC AGT GCC TCT 1701 Pro Cys Gln Pro Cys Gln Cys Asn Ser Asn Va - #l Asp Pro Ser Ala Ser 1710 - # 1715 - # 1720 - - GGG AAT TGT GAC CGG CTG ACA GGC AGG TGT TT - #G AAG TGT ATC CAC AAC 1749 Gly Asn Cys Asp Arg Leu Thr Gly Arg Cys Le - #u Lys Cys Ile His Asn 1725 - # 1730 - # 1735 - - ACA GCC GGC ATC TAC TGC GAC CAG TGC AAA GC - #A GGC TAC TTC GGG GAC 1797 Thr Ala Gly Ile Tyr Cys Asp Gln Cys Lys Al - #a Gly Tyr Phe Gly Asp 1740 - # 1745 - # 1750 - - CCA TTG GCT CCC AAC CCA GCA GAC AAG TGT CG - #A GCT TGC AAC TGT AAC 1845 Pro Leu Ala Pro Asn Pro Ala Asp Lys Cys Ar - #g Ala Cys Asn Cys Asn 1755 1760 - # 1765 - # 1770 - - CCC ATG GGC TCA GAG CCT GTA GGA TGT CGA AG - #T GAT GGC ACC TGT GTT 1893 Pro Met Gly Ser Glu Pro Val Gly Cys Arg Se - #r Asp Gly Thr Cys Val 1775 - # 1780 - # 1785 - - TGC AAG CCA GGA TTT GGT GGC CCC AAC TGT GA - #G CAT GGA GCA TTC AGC 1941 Cys Lys Pro Gly Phe Gly Gly Pro Asn Cys Gl - #u His Gly Ala Phe Ser 1790 - # 1795 - # 1800 - - TGT CCA GCT TGC TAT AAT CAA GTG AAG ATT CA - #G ATG GAT CAG TTT ATG 1989 Cys Pro Ala Cys Tyr Asn Gln Val Lys Ile Gl - #n Met Asp Gln Phe Met 1805 - # 1810 - # 1815 - - CAG CAG CTT CAG AGA ATG GAG GCC CTG ATT TC - #A AAG GCT CAG GGT GGT 2037 Gln Gln Leu Gln Arg Met Glu Ala Leu Ile Se - #r Lys Ala Gln Gly Gly 1820 - # 1825 - # 1830 - - GAT GGA GTA GTA CCT GAT ACA GAG CTG GAA GG - #C AGG ATG CAG CAG GCT 2085 Asp Gly Val Val Pro Asp Thr Glu Leu Glu Gl - #y Arg Met Gln Gln Ala 1835 1840 - # 1845 - # 1850 - - GAG CAG GCC CTT CAG GAC ATT CTG AGA GAT GC - #C CAG ATT TCA GAA GGT 2133 Glu Gln Ala Leu Gln Asp Ile Leu Arg Asp Al - #a Gln Ile Ser Glu Gly 1855 - # 1860 - # 1865 - - GCT AGC AGA TCC CTT GGT CTC CAG TTG GCC AA - #G GTG AGG AGC CAA GAG 2181 Ala Ser Arg Ser Leu Gly Leu Gln Leu Ala Ly - #s Val Arg Ser Gln Glu 1870 - # 1875 - # 1880 - - AAC AGC TAC CAG AGC CGC CTG GAT GAC CTC AA - #G ATG ACT GTG GAA AGA 2229 Asn Ser Tyr Gln Ser Arg Leu Asp Asp Leu Ly - #s Met Thr Val Glu Arg 1885 - # 1890 - # 1895 - - GTT CGG GCT CTG GGA AGT CAG TAC CAG AAC CG - #A GTT CGG GAT ACT CAC 2277 Val Arg Ala Leu Gly Ser Gln Tyr Gln Asn Ar - #g Val Arg Asp Thr His 1900 - # 1905 - # 1910 - - AGG CTC ATC ACT CAG ATG CAG CTG AGC CTG GC - #A GAA AGT GAA GCT TCC 2325 Arg Leu Ile Thr Gln Met Gln Leu Ser Leu Al - #a Glu Ser Glu Ala Ser 1915 1920 - # 1925 - # 1930 - - TTG GGA AAC ACT AAC ATT CCT GCC TCA GAC CA - #C TAC GTG GGG CCA AAT 2373 Leu Gly Asn Thr Asn Ile Pro Ala Ser Asp Hi - #s Tyr Val Gly Pro Asn 1935 - # 1940 - # 1945 - - GGC TTT AAA AGT CTG GCT CAG GAG GCC ACA AG - #A TTA GCA GAA AGC CAC 2421 Gly Phe Lys Ser Leu Ala Gln Glu Ala Thr Ar - #g Leu Ala Glu Ser His 1950 - # 1955 - # 1960 - - GTT GAG TCA GCC AGT AAC ATG GAG CAA CTG AC - #A AGG GAA ACT GAG GAC 2469 Val Glu Ser Ala Ser Asn Met Glu Gln Leu Th - #r Arg Glu Thr Glu Asp 1965 - # 1970 - # 1975 - - TAT TCC AAA CAA GCC CTC TCA CTG GTG CGC AA - #G GCC CTG CAT GAA GGA 2517 Tyr Ser Lys Gln Ala Leu Ser Leu Val Arg Ly - #s Ala Leu His Glu Gly 1980 - # 1985 - # 1990 - - GTC GGA AGC GGA AGC GGT AGC CCG GAC GGT GC - #T GTG GTG CAA GGG CTT 2565 Val Gly Ser Gly Ser Gly Ser Pro Asp Gly Al - #a Val Val Gln Gly Leu 1995 2000 - # 2005 - # 2010 - - GTG GAA AAA TTG GAG AAA ACC AAG TCC CTG GC - #C CAG CAG TTG ACA AGG 2613 Val Glu Lys Leu Glu Lys Thr Lys Ser Leu Al - #a Gln Gln Leu Thr Arg 2015 - # 2020 - # 2025 - - GAG GCC ACT CAA GCG GAA ATT GAA GCA GAT AG - #G TCT TAT CAG CAC AGT 2661 Glu Ala Thr Gln Ala Glu Ile Glu Ala Asp Ar - #g Ser Tyr Gln His Ser 2030 - # 2035 - # 2040 - - CTC CGC CTC CTG GAT TCA GTG TCT CCG CTT CA - #G GGA GTC AGT GAT CAG 2709 Leu Arg Leu Leu Asp Ser Val Ser Pro Leu Gl - #n Gly Val Ser Asp Gln 2045 - # 2050 - # 2055 - - TCC TTT CAG GTG GAA GAA GCA AAG AGG ATC AA - #A CAA AAA GCG GAT TCA 2757 Ser Phe Gln Val Glu Glu Ala Lys Arg Ile Ly - #s Gln Lys Ala Asp Ser 2060 - # 2065 - # 2070 - - CTC TCA AGC CTG GTA ACC AGG CAT ATG GAT GA - #G TTC AAG CGT ACA CAA 2805 Leu Ser Ser Leu Val Thr Arg His Met Asp Gl - #u Phe Lys Arg Thr Gln 2075 2080 - # 2085 - # 2090 - - AAG AAT CTG GGA AAC TGG AAA GAA GAA GCA CA - #G CAG CTC TTA CAG AAT 2853 Lys Asn Leu Gly Asn Trp Lys Glu Glu Ala Gl - #n Gln Leu Leu Gln Asn 2095 - # 2100 - # 2105 - - GGA AAA AGT GGG AGA GAG AAA TCA GAT CAG CT - #G CTT TCC CGT GCC AAT 2901 Gly Lys Ser Gly Arg Glu Lys Ser Asp Gln Le - #u Leu Ser Arg Ala Asn 2110 - # 2115 - # 2120 - - CTT GCT AAA AGC AGA GCA CAA GAA GCA CTG AG - #T ATG GGC AAT GCC ACT 2949 Leu Ala Lys Ser Arg Ala Gln Glu Ala Leu Se - #r Met Gly Asn Ala Thr 2125 - # 2130 - # 2135 - - TTT TAT GAA GTT GAG AGC ATC CTT AAA AAC CT - #C AGA GAG TTT GAC CTG 2997 Phe Tyr Glu Val Glu Ser Ile Leu Lys Asn Le - #u Arg Glu Phe Asp Leu 2140 - # 2145 - # 2150 - - CAG GTG GAC AAC AGA AAA GCA GAA GCT GAA GA - #A GCC ATG AAG AGA CTC 3045 Gln Val Asp Asn Arg Lys Ala Glu Ala Glu Gl - #u Ala Met Lys Arg Leu 2155 2160 - # 2165 - # 2170 - - TCC TAC ATC AGC CAG AAG GTT TCA GAT GCC AG - #T GAC AAG ACC CAG CAA 3093 Ser Tyr Ile Ser Gln Lys Val Ser Asp Ala Se - #r Asp Lys Thr Gln Gln 2175 - # 2180 - # 2185 - - GCA GAA AGA GCC CTG GGG AGC GCT GCT GCT GA - #T GCA CAG AGG GCA AAG 3141 Ala Glu Arg Ala Leu Gly Ser Ala Ala Ala As - #p Ala Gln Arg Ala Lys 2190 - # 2195 - # 2200 - - AAT GGG GCC GGG GAG GCC CTG GAA ATC TCC AG - #T GAG ATT GAA CAG GAG 3189 Asn Gly Ala Gly Glu Ala Leu Glu Ile Ser Se - #r Glu Ile Glu Gln Glu 2205 - # 2210 - # 2215 - - ATT GGG AGT CTG AAC TTG GAA GCC AAT GTG AC - #A GCA GAT GGA GCC TTG 3237 Ile Gly Ser Leu Asn Leu Glu Ala Asn Val Th - #r Ala Asp Gly Ala Leu 2220 - # 2225 - # 2230 - - GCC ATG GAA AAG GGA CTG GCC TCT CTG AAG AG - #T GAG ATG AGG GAA GTG 3285 Ala Met Glu Lys Gly Leu Ala Ser Leu Lys Se - #r Glu Met Arg Glu Val 2235 2240 - # 2245 - # 2250 - - GAA GGA GAG CTG GAA AGG AAG GAG CTG GAG TT - #T GAC ACG AAT ATG GAT 3333 Glu Gly Glu Leu Glu Arg Lys Glu Leu Glu Ph - #e Asp Thr Asn Met Asp 2255 - # 2260 - # 2265 - - GCA GTA CAG ATG GTG ATT ACA GAA GCC CAG AA - #G GTT GAT ACC AGA GCC 3381 Ala Val Gln Met Val Ile Thr Glu Ala Gln Ly - #s Val Asp Thr Arg Ala 2270 - # 2275 - # 2280 - - AAG AAC GCT GGG GTT ACA ATC CAA GAC ACA CT - #C AAC ACA TTA GAC GGC 3429 Lys Asn Ala Gly Val Thr Ile Gln Asp Thr Le - #u Asn Thr Leu Asp Gly 2285 - # 2290 - # 2295 - - CTC CTG CAT CTG ATG GGT ATG TGA ACCCACAACC CA - #CAACCTTC CAGCTCCATG 3483 Leu Leu His Leu Met Gly Met * 2300 - # 2305 - - CTCCAGGGCT TTGCTCCAGA ACACTCACTA TACCTAGCCC CAGCAAAGGG GA -#GTCTCAGC 3543 - - TTTCCTTAAG GATATCAGTA AATGTGCTTT GTTTCCAGGC CCAGATAACT TT -#CGGCAGGT 3603 - - TCCCTTACAT TTACTGGACC CTGTTTTACC GTTGCTAAGA TGGGTCACTG AA -#CACCTATT 3663 - - GCACTTGGGG GTAAAGGTCT GTGGGCCAAA GAACAGGTGT ATATAAGCAA CT -#TCACAGAA 3723 - - CACGAGACAG CTTGGGAATC CTGCTAAAGA GTCTGGCCTG GACCCTGAGA AG -#CCAGTGGA 3783 - - CAGTTTTAAG CAGAGGAATA ACATCACCAC TGTATATTTC AGAAAGATCA CT -#AGGGCAGC 3843 - - CGAGTGGAGG AAAGCTTGAA GAGGGGGTTA GAGAGAAGGC AGGTTGAGAC TA -#CTTAAGAT 3903 - - ATTGTTGAAA TAATTGAAGA GAGAAATGAC AGGAGCCTGC TCTAAGGCAG TA -#GAATGGTG 3963 - - GCTGGGAAGA TGTGAAGGAA GATTTTCCCA GTCTGTGAAG TCAAGAATCA CT -#TGCCGGCC 4023 - - GGGTGTGGTG GCTCACGCCT GTAATTCTAG CACTTTGGGA GACTGAAGCG GG -#TGGATCAC 4083 - - CCGAGGTCAG GAGTTGAAGA CCAGCCTGGC CAACATGGTG AAACCCTGTC TC -#TACTAAAA 4143 - - GTACAAAAAT TAGCTGGATG ATGGTGGTGG GCGCCTGTAA TTCCAGCTAC TC -#AGGAGTCT 4203 - - GAGGCAGGAG AATCGCTTGA ACCCAGGAGG CGAGGTTACA GTGAGCCAAG AT -#TGCACCAC 4263 - - TGCTCTTCCA GCCTGGGAAC AGAGAGACTG CCTAAAAAAA AAAAAAAAAA AA - #A 4316 - - - - (2) INFORMATION FOR SEQ ID NO:15: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 1111 am - #ino acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:15: - - Met Pro Ala Leu Trp Leu Gly Cys Cys Leu Cy - #s Phe Ser Leu Leu Leu 1 5 - # 10 - # 15 - - Pro Ala Ala Arg Ala Thr Ser Arg Arg Glu Va - #l Cys Asp Cys Asn Gly 20 - # 25 - # 30 - - Lys Ser Arg Gln Cys Ile Phe Asp Arg Glu Le - #u His Arg Gln Thr Gly 35 - # 40 - # 45 - - Asn Gly Phe Arg Cys Leu Asn Cys Asn Asp As - #n Thr Asp Gly Ile His 50 - # 55 - # 60 - - Cys Glu Lys Cys Lys Asn Gly Phe Tyr Arg Hi - #s Arg Glu Arg Asp Arg 65 - # 70 - # 75 - # 80 - - Cys Leu Pro Cys Asn Cys Asn Ser Lys Gly Se - #r Leu Ser Ala Arg Cys 85 - # 90 - # 95 - - Asp Asn Ser Gly Arg Cys Ser Cys Lys Pro Gl - #y Val Thr Gly Ala Arg 100 - # 105 - # 110 - - Cys Asp Arg Cys Leu Pro Gly Phe His Met Le - #u Thr Asp Ala Gly Cys 115 - # 120 - # 125 - - Thr Gln Asp Gln Arg Leu Leu Asp Ser Lys Cy - #s Asp Cys Asp Pro Ala 130 - # 135 - # 140 - - Gly Ile Ala Gly Pro Cys Asp Ala Gly Arg Cy - #s Val Cys Lys Pro Ala 145 1 - #50 1 - #55 1 -#60 - - Val Thr Gly Glu Arg Cys Asp Arg Cys Arg Se - #r Gly Tyr Tyr AsnLeu 165 - # 170 - # 175 - - Asp Gly Gly Asn Pro Glu Gly Cys Thr Gln Cy - #s Phe Cys Tyr Gly His 180 - # 185 - # 190 - - Ser Ala Ser Cys Arg Ser Ser Ala Glu Tyr Se - #r Val His Lys Ile Thr 195 - # 200 - # 205 - - Ser Thr Phe His Gln Asp Val Asp Gly Trp Ly - #s Ala Val Gln Arg Asn 210 - # 215 - # 220 - - Gly Ser Pro Ala Lys Leu Gln Trp Ser Gln Ar - #g His Gln Asp Val Phe 225 2 - #30 2 - #35 2 -#40 - - Ser Ser Ala Gln Arg Leu Asp Pro Val Tyr Ph - #e Val Ala Pro AlaLys 245 - # 250 - # 255 - - Phe Leu Gly Asn Gln Gln Val Ser Tyr Gly Gl - #n Ser Leu Ser Phe Asp 260 - # 265 - # 270 - - Tyr Arg Val Asp Arg Gly Gly Arg His Pro Se - #r Ala His Asp Val Ile 275 - # 280 - # 285 - - Leu Glu Gly Ala Gly Leu Arg Ile Thr Ala Pr - #o Leu Met Pro Leu Gly 290 - # 295 - # 300 - - Lys Thr Leu Pro Cys Gly Leu Thr Lys Thr Ty - #r Thr Phe Arg Leu Asn 305 3 - #10 3 - #15 3 -#20 - - Glu His Pro Ser Asn Asn Trp Ser Pro Gln Le - #u Ser Tyr Phe GluTyr 325 - # 330 - # 335 - - Arg Arg Leu Leu Arg Asn Leu Thr Ala Leu Ar - #g Ile Arg Ala Thr Tyr 340 - # 345 - # 350 - - Gly Glu Tyr Ser Thr Gly Tyr Ile Asp Asn Va - #l Thr Leu Ile Ser Ala 355 - # 360 - # 365 - - Arg Pro Val Ser Gly Ala Pro Ala Pro Trp Va - #l Glu Gln Cys Ile Cys 370 - # 375 - # 380 - - Pro Val Gly Tyr Lys Gly Gln Phe Cys Gln As - #p Cys Ala Ser Gly Tyr 385 3 - #90 3 - #95 4 -#00 - - Lys Arg Asp Ser Ala Arg Leu Gly Pro Phe Gl - #y Thr Cys Ile ProCys 405 - # 410 - # 415 - - Asn Cys Gln Gly Gly Gly Ala Cys Asp Pro As - #p Thr Gly Asp Cys Tyr 420 - # 425 - # 430 - - Ser Gly Asp Glu Asn Pro Asp Ile Glu Cys Al - #a Asp Cys Pro Ile Gly 435 - # 440 - # 445 - - Phe Tyr Asn Asp Pro His Asp Pro Arg Ser Cy - #s Lys Pro Cys Pro Cys 450 - # 455 - # 460 - - His Asn Gly Phe Ser Cys Ser Val Ile Pro Gl - #u Thr Glu Glu Val Val 465 4 - #70 4 - #75 4 -#80 - - Cys Asn Asn Cys Pro Pro Gly Val Thr Gly Al - #a Arg Cys Glu LeuCys 485 - # 490 - # 495 - - Ala Asp Gly Tyr Phe Gly Asp Pro Phe Gly Gl - #u His Gly Pro Val Arg 500 - # 505 - # 510 - - Pro Cys Gln Pro Cys Gln Cys Asn Ser Asn Va - #l Asp Pro Ser Ala Ser 515 - # 520 - # 525 - - Gly Asn Cys Asp Arg Leu Thr Gly Arg Cys Le - #u Lys Cys Ile His Asn 530 - # 535 - # 540 - - Thr Ala Gly Ile Tyr Cys Asp Gln Cys Lys Al - #a Gly Tyr Phe Gly Asp 545 5 - #50 5 - #55 5 -#60 - - Pro Leu Ala Pro Asn Pro Ala Asp Lys Cys Ar - #g Ala Cys Asn CysAsn 565 - # 570 - # 575 - - Pro Met Gly Ser Glu Pro Val Gly Cys Arg Se - #r Asp Gly Thr Cys Val 580 - # 585 - # 590 - - Cys Lys Pro Gly Phe Gly Gly Pro Asn Cys Gl - #u His Gly Ala Phe Ser 595 - # 600 - # 605 - - Cys Pro Ala Cys Tyr Asn Gln Val Lys Ile Gl - #n Met Asp Gln Phe Met 610 - # 615 - # 620 - - Gln Gln Leu Gln Arg Met Glu Ala Leu Ile Se - #r Lys Ala Gln Gly Gly 625 6 - #30 6 - #35 6 -#40 - - Asp Gly Val Val Pro Asp Thr Glu Leu Glu Gl - #y Arg Met Gln GlnAla 645 - # 650 - # 655 - - Glu Gln Ala Leu Gln Asp Ile Leu Arg Asp Al - #a Gln Ile Ser Glu Gly 660 - # 665 - # 670 - - Ala Ser Arg Ser Leu Gly Leu Gln Leu Ala Ly - #s Val Arg Ser Gln Glu 675 - # 680 - # 685 - - Asn Ser Tyr Gln Ser Arg Leu Asp Asp Leu Ly - #s Met Thr Val Glu Arg 690 - # 695 - # 700 - - Val Arg Ala Leu Gly Ser Gln Tyr Gln Asn Ar - #g Val Arg Asp Thr His 705 7 - #10 7 - #15 7 -#20 - - Arg Leu Ile Thr Gln Met Gln Leu Ser Leu Al - #a Glu Ser Glu AlaSer 725 - # 730 - # 735 - - Leu Gly Asn Thr Asn Ile Pro Ala Ser Asp Hi - #s Tyr Val Gly Pro Asn 740 - # 745 - # 750 - - Gly Phe Lys Ser Leu Ala Gln Glu Ala Thr Ar - #g Leu Ala Glu Ser His 755 - # 760 - # 765 - - Val Glu Ser Ala Ser Asn Met Glu Gln Leu Th - #r Arg Glu Thr Glu Asp 770 - # 775 - # 780 - - Tyr Ser Lys Gln Ala Leu Ser Leu Val Arg Ly - #s Ala Leu His Glu Gly 785 7 - #90 7 - #95 8 -#00 - - Val Gly Ser Gly Ser Gly Ser Pro Asp Gly Al - #a Val Val Gln GlyLeu 805 - # 810 - # 815 - - Val Glu Lys Leu Glu Lys Thr Lys Ser Leu Al - #a Gln Gln Leu Thr Arg 820 - # 825 - # 830 - - Glu Ala Thr Gln Ala Glu Ile Glu Ala Asp Ar - #g Ser Tyr Gln His Ser 835 - # 840 - # 845 - - Leu Arg Leu Leu Asp Ser Val Ser Pro Leu Gl - #n Gly Val Ser Asp Gln 850 - # 855 - # 860 - - Ser Phe Gln Val Glu Glu Ala Lys Arg Ile Ly - #s Gln Lys Ala Asp Ser 865 8 - #70 8 - #75 8 -#80 - - Leu Ser Ser Leu Val Thr Arg His Met Asp Gl - #u Phe Lys Arg ThrGln 885 - # 890 - # 895 - - Lys Asn Leu Gly Asn Trp Lys Glu Glu Ala Gl - #n Gln Leu Leu Gln Asn 900 - # 905 - # 910 - - Gly Lys Ser Gly Arg Glu Lys Ser Asp Gln Le - #u Leu Ser Arg Ala Asn 915 - # 920 - # 925 - - Leu Ala Lys Ser Arg Ala Gln Glu Ala Leu Se - #r Met Gly Asn Ala Thr 930 - # 935 - # 940 - - Phe Tyr Glu Val Glu Ser Ile Leu Lys Asn Le - #u Arg Glu Phe Asp Leu 945 9 - #50 9 - #55 9 -#60 - - Gln Val Asp Asn Arg Lys Ala Glu Ala Glu Gl - #u Ala Met Lys ArgLeu 965 - # 970 - # 975 - - Ser Tyr Ile Ser Gln Lys Val Ser Asp Ala Se - #r Asp Lys Thr Gln Gln 980 - # 985 - # 990 - - Ala Glu Arg Ala Leu Gly Ser Ala Ala Ala As - #p Ala Gln Arg Ala Lys 995 - # 1000 - # 1005 - - Asn Gly Ala Gly Glu Ala Leu Glu Ile Ser Se - #r Glu Ile Glu Gln Glu 1010 - # 1015 - # 1020 - - Ile Gly Ser Leu Asn Leu Glu Ala Asn Val Th - #r Ala Asp Gly Ala Leu 1025 1030 - # 1035 - # 1040 - - Ala Met Glu Lys Gly Leu Ala Ser Leu Lys Se - #r Glu Met Arg Glu Val 1045 - # 1050 - # 1055 - - Glu Gly Glu Leu Glu Arg Lys Glu Leu Glu Ph - #e Asp Thr Asn Met Asp 1060 - # 1065 - # 1070 - - Ala Val Gln Met Val Ile Thr Glu Ala Gln Ly - #s Val Asp Thr Arg Ala 1075 - # 1080 - # 1085 - - Lys Asn Ala Gly Val Thr Ile Gln Asp Thr Le - #u Asn Thr Leu Asp Gly 1090 - # 1095 - # 1100 - - Leu Leu His Leu Met Gly Met 1105 1110 - - - - (2) INFORMATION FOR SEQ ID NO:16: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 20 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: other nucleic acid (A) DESCRIPTION: /desc - #= "oligomer primers" - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:16: - - GAGCGCAGAG TGAGAACCAC - # - # - # 20 - - - - (2) INFORMATION FOR SEQ ID NO:17: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 20 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: other nucleic acid (A) DESCRIPTION: /desc - #= "oligomer primers" - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:17: - - ACTGTATTCT GCAGAGCTGC - # - # - # 20 - - - - (2) INFORMATION FOR SEQ ID NO:18: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 20 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: other nucleic acid (A) DESCRIPTION: /desc - #= "oligomer primers" - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:18: - - TTCCTTTCCCCTACCTTGTG - # - # - # 20 - - - - (2) INFORMATION FOR SEQ ID NO:19: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 20 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: other nucleic acid (A) DESCRIPTION: /desc - #= "OLIGOMER PRIMER" - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:19: - - TGTGGAAGCCTGGCAGACAT - # - # - # 20__________________________________________________________________________

Laminin chains: diagnostic and therapeutic use

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Embase Abstract No: 97163048, 1997.
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