Mammalian IAP gene family, primers, probes, and detection methods

BACKGROUND OF THE INVENTION
There are two general ways by which cells die. An easily recognized pathway is necrosis, a process of cell death usually resulting from severe and sudden injury. In necrosis, changes in cellular homeostasis occur with loss of membrane integrity. Dysregulation of osmotic pressure results and, as a consequence, the cells swell and finally rupture. The cellular contents are then spilled into the surrounding tissue space and, usually, an inflammation response ensues. A second form of cell death is apoptosis. This cell "suicide" pathway or programmed cell death often occurs so rapidly that in some biological systems the apoptotic process is difficult to ascertain. Indeed, it has been only in the past few years that the involvement of apoptosis in a wide spectrum of biological processes has become recognized. Apoptosis is a fundamental physiological pathway of cell death, highly conserved throughout evolution, and playing a major role in development, viral pathogenesis, cancer, autoimmune diseases and neurodegenerative disorders.
Inappropriate increases in apoptosis may cause or contribute to a variety of diseases, including AIDS, neurodegenerative diseases (e.g. Alzheimer's Disease, Parkinson's Disease, Amyotrophic Lateral Sclerosis (ALS), retinitis pigmentosa and other diseases of the retina, myelodysplastic syndrome (e.g., aplastic anemia), toxin-induced liver disease (e.g., alcoholism) and ischemic injury (e.g., myocardial infarction, stroke, and reperfusion injury). In addition, disruption of normally occurring apoptosis has been implicated in the development of some cancers (e.g. follicular lymphoma, p53 carcinomas, and hormone dependent tumors), autoimmune disorders (e.g., lupus erythematosis and multiple sclerosis) and viral infections (e.g., herpes virus, poxvirus, and adenovirus infections).
Mature CD4.sup.+ T-lymphocytes in patients with HIV-1 have been observed to respond to stimulation with mitogens or super-antigens by undergoing increased apoptosis. The great majority of these cells are not infected and similar inappropriate antigen-induced apoptosis could be very important in the destruction of this vital part of the immune system early in HIV infection.
Baculoviruses encode inhibitors of apoptosis proteins (IAPs). These proteins inhibit the apoptosis which otherwise occurs when insect cells are infected by the virus. Baculovirus IAP proteins work in a manner which is thought to be independent of other viral proteins. The baculovirus IAP genes include sequences encoding a ring zinc finger-like motif which is presumed to be involved in the direct binding of DNA.
SUMMARY OF THE INVENTION
In general, the invention features substantially pure DNA (for example, genomic DNA, cDNA, or synthetic DNA) encoding a mammalian IAP polypeptide as defined below. In related aspects, the invention also features a vector, a cell (e.g., a mammalian, yeast or bacterial cell), and a transgenic animal or embryo thereof which includes such a substantially pure DNA encoding an IAP polypeptide.
In preferred embodiments, an IAP gene is the xiap (including human xiap and its murine homolog, m-xiap), hiap1 (including human hiap1 and m-hiap1), or the hiap2 gene (including human hiap2 and m-hiap2). In most preferred embodiments the IAP gene is a human IAP gene. In other various preferred embodiments, the cell is a transformed cell. In related aspects, the invention features a transgenic animal containing a transgene which encodes an IAP polypeptide that is expressed in or delivered to tissue normally susceptible to apoptosis.
In yet another aspect, the invention features DNA encoding fragments of IAP polypeptides including the BIR domains and the RZF domains provided herein.
In specific embodiments, the invention features DNA sequences substantially identical to the DNA sequences shown in FIGS. 1-6.
In another aspect, the invention also features RNA which is encoded by the DNA described herein. Preferably, the RNA is mRNA. In another embodiment the RNA is antisense RNA.
In another aspect, the invention features a substantially pure polypeptide having a sequence substantially identical to one of the IAP amino acid sequences shown in FIGS. 1-6.
In a second aspect, the invention features a substantially pure DNA which includes a promoter capable of expressing the IAP gene in a cell susceptible to apoptosis. In preferred embodiments, the IAP gene is xiap (including the human or murine xiap), hiap1 (preferably the human or murine hiap1), or hiap2 (preferably the human or murine hiap2). hiap2 may be the full length gene, as shown in FIG. 3, or the truncated variant having the sequence boxed in FIG. 3 deleted.
In preferred embodiments, the promoter is the promoter native to an IAP gene. Additionally, transcriptional and translational regulatory regions are preferably native to an IAP gene.
In another aspect, the invention provides transgenic cell lines and transgenic animals. The transgenic cells of the invention are preferably cells which are susceptible to apoptosis. In preferred embodiments, the transgenic cell is a fibroblast, neuronal cell, a lymphocyte cell, or an insect cell. Most preferably, the neuron is a motor neuron and the lymphocyte is a CD4.sup.+ T-cell.
In another aspect, the invention features a method of inhibiting apoptosis which involves producing a transgenic cell having a transgene encoding an IAP polypeptide wherein the transgene is integrated into the genome of the cell and is positioned for expression in the cell and wherein the IAP transgene is expressed in the cell at a level sufficient to inhibit apoptosis.
In a related aspect, the invention features a transgenic animal, preferably a mammal, more preferably a rodent, and most preferably a mouse, having either increased copies of IAP genes inserted into the genome or a knockout of an IAP gene in the genome. The transgenic animals may express an increased amount of IAP polypeptide or may express a decreased amount of an IAP polypeptide, respectively. In related embodiments, the invention provides a method of utilizing the IAP nucleic acid to engineer a knockout mutation in an IAP gene and a method of making an animal with increased expression by insertion of IAP gene into the genome.
In another aspect, the invention features a method of detecting an IAP in a cell involving: (a) contacting the IAP gene or a portion thereof greater than 9 nucleic acids, preferably greater than 18 nucleic acids in length with a preparation of genomic DNA from the cell under hybridization conditions providing detection of DNA sequences having about 50% or greater nucleotide sequence identity to the amino acid encoding DNA sequences of hiap1, hiap2, or xiap IAP polypeptides.
In another aspect, the invention features a method of producing an IAP polypeptide which involves: (a) providing a cell transformed with DNA encoding an IAP polypeptide positioned for expression in the cell; (b) culturing the cell under conditions for expressing the DNA; and (c) isolating the IAP polypeptide. In preferred embodiments the IAP polypeptide is expressed by DNA which has a constituative or inducible promotor. In our embodiment, the promotor is a heterologous promotor.
In another aspect, the invention features substantially pure mammalian IAP polypeptide. Preferably, the polypeptide includes a greater than 50 amino acid sequence substantially identical to a greater than 50 amino acid sequence shown in any one of FIGS. 1-4. Most preferably, the polypeptide is the human or murine XIAP, HIAP1, or HIAP2 polypeptide. Fragments including BIR domains and RZF-domains provided herein are also a part of the invention.
In another aspect, the invention features a recombinant mammalian polypeptide capable of modulating apoptosis wherein the polypeptide includes at least a ring zinc finger domain and a BIR domain as defined herein. In preferred embodiments, the invention features a substantially pure polypeptide and an oligonucleotide encoding said polypeptide, the polypeptide including a ring zinc finger (RZF) having the sequence:
Glu Xaa1 Xaa1 Xaa1 Xaa1 Xaa1 Xaa1 Xaa2 Xaa1 Xaa1 Xaa1 Cys Lys Xaa3 Cys Met Xaa1 Xaa1 Xaa1 Xaa1 Xaa1 Xaa3 Xaa1 Phe Xaa1 Pro Cys Gly His Xaa1 Xaa1 Xaa1 Cys Xaa1 Xaa1 Cys Ala Xaa1 Xaa1 Xaa1 Xaa1 Xaa1 Cys Pro Xaa1 Cys, wherein Xaa1 is any amino acid, Xaa2 is Glu or Asp, Xaa3 is Val or Ile (SEQ ID NO:1); and at least one BIR domain having the sequence: Xaa1 Xaa1 Xaa1 Arg Leu Xaa1 Thr Phe Xaa1 Xaa1 Trp Pro Xaa2 Xaa1 Xaa1 Xaa2 Xaa2 Xaa1 Xaa1 Xaa1 Xaa1 Leu Ala Xaa1 Ala Gly Phe Tyr Tyr Xaa1 Gly Xaa1 Xaa1 Asp Xaa1 Val Xaa1 Cys Phe Xaa1 Cys Xaa1 Xaa1 Xaa1 Xaa1 Xaa1 Xaa1 Trp Xaa1 Xaa1 Xaa1 Asp Xaa1 Xaa1 Xaa1 Xaa1 Xaa1 His Xaa1 Xaa1 Xaa1 Xaa1 Pro Xaa1 Cys Xaa1 Phe Val, wherein Xaa1 may be any amino acid and Xaa2 may be any amino acid or may be absent (SEQ ID NO:2).
In various preferred embodiments the protein has at least two or, more preferably at least three BIR domains, the RZF domain has one of the IAP sequences shown in FIG. 6, and the BIR domains are comprised of BIR domains shown in FIG. 5. In other preferred embodiments the BIR domains are at the amino terminal end of the protein relative to the RZF domain, which is at or near the carboxy terminus of the polypeptide.
In another aspect, the invention features an IAP gene isolated according to the method involving: (a) providing a sample of DNA; (b) providing a pair of oligonucleotides having sequence homology to a conserved region of an IAP gene; (c) combining the pair of oligonucleotides with the cell DNA sample under conditions suitable for polymerase chain reaction-mediated DNA amplification; and (d) isolating the amplified IAP gene or fragment thereof.
In preferred embodiments, the amplification is carried out using a reverse-transcription polymerase chain reaction, for example, the RACE method.
In another aspect, the invention features an IAP gene isolated according to the method involving: (a) providing a preparation of DNA; (b) providing a detectably-labelled DNA sequence having homology to a conserved region of an IAP gene; (c) contacting the preparation of DNA with the detectably-labelled DNA sequence under hybridization conditions providing detection of genes having 50% or greater nucleotide sequence identity; and (d) identifying an IAP gene by its association with the detectable label.
In another aspect, the invention features an IAP gene isolated according to the method involving: (a) providing a cell sample; (b) introducing by transformation into the cell sample a candidate IAP gene; (c) expressing the candidate IAP gene within the cell sample; and (d) determining whether the cell sample exhibits an altered apoptotic response, whereby a response identifies an IAP gene.
In another aspect, the invention features a method of identifying an IAP gene in a cell, involving: (a) providing a preparation of cellular DNA (for example, from the human genome or a cDNA library (such as a cDNA library isolated from a cell type which undergoes apoptosis); (b) providing a detectably-labelled DNA sequence (for example, prepared by the methods of the invention) having homology to a conserved region of an IAP gene; (c) contacting the preparation of cellular DNA with the detectably-labelled DNA sequence under hybridization conditions providing detection of genes having 50% nucleotide or greater sequence identity; and (d) identifying an IAP gene by its association with the detectable label.
In another aspect, the invention features a method of isolating an IAP gene from a recombinant library, involving: (a) providing a recombinant library; (b) contacting the library with a detectably-labelled gene fragment produced according to the PCR method of the invention under hybridization conditions providing detection of genes having 50% or greater nucleotide sequence identity; and (c) isolating an IAP gene by its association with the detectable label.
In another aspect, the invention features a method of identifying an IAP gene involving: (a) providing a cell tissue sample; (b) introducing by transformation into the cell sample a candidate IAP gene; (c) expressing the candidate IAP gene within the cell sample; and (d) determining whether the cell sample exhibits inhibition of apoptosis, whereby a change in (i.e. modulation of) apoptosis identifies an IAP gene.
Preferably, the cell sample is a cell type which may be assayed for apoptosis (e.g., lymphocytes, T-cells and B-cells, neuronal cells, baculovirus infected insect cells and fibroblast cells); the candidate IAP gene is obtained from a cDNA expression library; and the apoptosis response is the inhibition of apoptosis.
In another aspect, the invention features a method of inhibiting apoptosis in a mammal wherein the method includes: (a) providing DNA encoding at least one IAP polypeptide to a cell which is susceptible to apoptosis; wherein the DNA is integrated into the genome of the cell and is positioned for expression in the cell; and the IAP gene is under the control of regulatory sequences suitable for controlled expression of the gene(s); wherein the IAP transgene is expressed at a level sufficient to inhibit apoptosis relative to a cell lacking the IAP transgene. It will be appreciated that IAP polypeptides also may be administered directly to inhibit any undesirable apoptosis.
In a related aspect, the invention features a method of inhibiting apoptosis wherein the method involves: (a) producing a cell having integrated in the genome a transgene containing the IAP gene under the control of a promoter providing constitutive expression of the IAP gene.
In yet another related aspect, the invention features a method of inhibiting apoptosis wherein the method involves: (a) producing a cell having integrated in the genome a transgene containing the IAP gene under the control of a promoter providing controllable expression of the IAP gene; and (b) regulating the environment of the cell so that the IAP transgene is controllably expressed in the cell. In preferred embodiments, the IAP gene is expressed using a tissue-specific or cell type-specific promoter, or by a promoter that is activated by the introduction of an external signal or agent, such as a chemical signal or agent. In preferred embodiments the cell is a lymphocyte or B-cell, a neuronal cell, or a fibroblast. In other embodiments the cell is a cell in an HIV infected human, or a mammal with a neurodegenerative disease, ischemia, toxin induced liver disease, or a myelodysplastic syndrome.
In a related aspect, the invention provides a method of inhibiting apoptosis in a mammal by providing an apoptosis-inhibiting amount of IAP polypeptide.
In another aspect, the invention features a purified antibody which binds specifically to an IAP family protein. Such an antibody may be used in any standard immunodetection method for the identification of an IAP polypeptide. Preferably, the antibody binds specifically to xiap, hiap1 or hiap2. In various embodiments the antibody may react with other IAP polypeptides or may be specific for one or a few IAP polypeptides. The antibody may be a monoclonal polyclonal antibody. Preferably, the antibody reacts specifically with only one of the IAP polypeptides, for example, reacts with murine and human xiap, but not with hiap1 or hiap2 from mammalian species.
In another aspect, the invention features a method of identifying a compound which modulates apoptosis. The method includes (a) providing a cell expressing an IAP polypeptide; and (b) contracting the cell with a candidate compound, and monitoring the expression of an IAP gene. An alteration in the level of expression of the IAP gene indicates the presence of a compound which modulates apoptosis. The compound may be an inhibitor or an enhancer of apoptosis. In various preferred embodiments, the cell is a fibroblast, a neuronal cell, a lymphocyte (T-cell or B-cell), or an insect cell; the polypeptide expression being monitored is XIAP, HIAP1, or HIAP2 (e.g., human or murine).
In a related aspect, the invention features methods of detecting compounds which modulate apoptosis using the interaction trap technology and IAP polypeptides or fragments thereof as a component of the bait. In preferred embodiments, the compound being tested as a modulator of apoptosis is also a polypeptide.
In another aspect, the invention features a method for diagnosing a cell proliferation disease, or an increased liklihood of such a disease, using an IAP nucleic acid probe or antibody. Preferably, the disease is a cancer. Most preferably, the disease is selected from the group consisting of promyelocytic leukemia, a Hela-type carcinoma, chronic myelogenous leukemia (preferably using xiap or hiap2 related probes), lymphoblastic leukemia (preferably using a xiap related probe), Burkitt's lymphoma (preferably using an hiap1 related probe), colorectal adenocarcinoma, lung carcinoma, and melanoma (preferably using a xiap probe). Preferably, a diagnosis is indicated by a 2-fold increase in expression or activity, more preferably, at least a 10-fold increase in expression or activity.
By "IAP gene" is meant a gene encoding a polypeptide having at least one BIR domain and a ring zinc finger domain which is capable of modulating (inhibiting or enhancing) apoptosis in a cell or tissue when provided by other intracellular or extracellular delivery methods. In preferred embodiments the IAP gene is a gene having about 50% or greater nucleotide sequence identity to at least one of the IAP amino acid encoding sequences of FIGS. 1-4 or portions thereof. Preferably, the region of sequence over which identity is measured is a region encoding at least one BIR domain and a ring zinc finger domain. Mammalian IAP genes include nucleotide sequences isolated from any mammalian source. Preferably, the mammal is a human.
By an "IAP gene" is also meant any member of the family of apoptosis inhibitory genes characterized by their ability to modulate apoptosis and having at least 20%, preferably 30%, and most preferably 50% amino acid sequence identity to at least one of the conserved regions of one of the IAP members described herein (i.e., either the BIR or ring zinc finger domains from the human or murine xiap, hiap1 and hiap2). Representative members of the IAP gene family include, without limitation, the human and murine xiap, hiap1, and hiap2 genes. By "IAP protein" is meant a polypeptide encoded by an IAP gene.
By "BIR domain" is meant a domain having the amino acid sequence of the consensus sequence: Xaa1 Xaa1 Xaa1 Arg Leu Xaa1 Thr Phe Xaa1 Xaa1 Trp Pro Xaa2 Xaa1 Xaa1 Xaa2 Xaa2 Xaa1 Xaa1 Xaa1 Xaa1 Leu Ala Xaa1 Ala Gly Phe Tyr Tyr Xaa1 Gly Xaa1 Xaa1 Asp Xaa1 Val Xaa1 Cys Phe Xaa1 Cys Xaa1 Xaa1 Xaa1 Xaa1 Xaa1 Xaa1 Trp Xaa1 Xaa1 Xaa1 Asp Xaa1 Xaa1 Xaa1 Xaa1 Xaa1 His Xaa1 Xaa1 Xaa1 Xaa1 Pro Xaa1 Cys Xaa1 Phe Val, wherein Xaa1 is any amino acid and Xaa2 is any amino acid or is absent (SEQ ID NO:2). Preferably, the sequence is substantially identical to one of the BIR domain sequences provided for xiap, hiap1, hiap2 herein.
By "ring zinc finger" or "RZF" is meant a domain having the amino acid sequence of the consensus sequence: Glu Xaa1 Xaa1 Xaa1 Xaa1 Xaa1 Xaa1 Xaa2 Xaa1 Xaa1 Xaa1 Cys Lys Xaa3 Cys Met Xaa1 Xaa1 Xaa1 Xaa1 Xaa1 Xaa3 Xaa1 Phe Xaa1 Pro Cys Gly His Xaa1 Xaa1 Xaa1 Cys Xaa1 Xaa1 Cys Ala Xaa1 Xaa1 Xaa1 Xaa1 Xaa1 Cys Pro Xaa1 Cys, wherein Xaa1 is any amino acid, Xaa2 is Glu or Asp, and Xaa3 is Val or Ile (SEQ ID NO:1). Preferably, the sequence is substantially identical to the RZF domains provided herein for the human or murine xiap, hiap1, or hiap2.
By "modulating apoptosis" or "altering apoptosis" is meant increasing or decreasing the number of cells which undergo apoptosis in a given cell population. Preferably, the cell population is selected from a group including T-cells, neuronal cells, fibroblasts, or any other cell line known to undergo apoptosis in a laboratory setting (e.g., the baculovirus infected insect cells). It will be appreciated that the degree of modulation provided by an IAP or modulating compound in a given assay will vary, but that one skilled in the art can determine the statistically significant change in the level of apoptosis which identifies an IAP or a compound which modulates an IAP.
By "inhibiting apoptosis" is meant any decrease in the number of cells which undergo apoptosis relative to an untreated control. Preferably, the decrease is at least 25%, more preferably the decrease is 50%, and most preferably the decrease is at least one-fold.
By "polypeptide" is meant any chain of amino acids, regardless of length or post-translational modification (e.g., glycosylation or phosphorylation).
By "substantially identical" is meant a polypeptide or nucleic acid exhibiting at least 50%, preferably 85%, more preferably 90%, and most preferably 95% homology to a reference amino acid or nucleic acid sequence. For polypeptides, the length of comparison sequences will generally be at least 16 amino acids, preferably at least 20 amino acids, more preferably at least 25 amino acids, and most preferably 35 amino acids. For nucleic acids, the length of comparison sequences will generally be at least 50 nucleotides, preferably at least 60 nucleotides, more preferably at least 75 nucleotides, and most preferably 110 nucleotides.
Sequence identity is typically measured using sequence analysis software (e.g., Sequence Analysis Software Package of the Genetics Computer Group, University of Wisconsin Biotechnology Center, 1710 University Avenue, Madison, Wis. 53705). Such software matches similar sequences by assigning degrees of homology to various substitutions, deletions, and other modifications. Conservative substitutions typically include substitutions within the following groups: glycine, alanine, valine, isoleucine, leucine; aspartic acid, glutamic acid, asparagine, glutamine; serine, threonine; lysine, arginine; and phenylalanine, tyrosine.
By a "substantially pure polypeptide" is meant an IAP polypeptide which has been separated from components which naturally accompany it. Typically, the polypeptide is substantially pure when it is at least 60%, by weight, free from the proteins and naturally-occurring organic molecules with which it is naturally associated. Preferably, the preparation is at least 75%, more preferably at least 90%, and most preferably at least 99%, by weight, IAP polypeptide. A substantially pure IAP polypeptide may be obtained, for example, by extraction from a natural source (e.g., a fibroblast, neuronal cell, or lymphocyte cell); by expression of a recombinant nucleic acid encoding an IAP polypeptide; or by chemically synthesizing the protein. Purity can be measured by any appropriate method, e.g., those described in column chromatography, polyacrylamide gel electrophoresis, or by HPLC analysis.
A protein is substantially free of naturally associated components when it is separated from those contaminants which accompany it in its natural state. Thus, a protein which is chemically synthesized or produced in a cellular system different from the cell from which it naturally originates will be substantially free from its naturally associated components. Accordingly, substantially pure polypeptides include those derived from eukaryotic organisms but synthesized in E. coli or other prokaryotes.
By "substantially pure DNA" is meant DNA that is free of the genes which, in the naturally-occurring genome of the organism from which the DNA of the invention is derived, flank the gene. The term therefore includes, for example, a recombinant DNA which is incorporated into a vector; into an autonomously replicating plasmid or virus; or into the genomic DNA of a prokaryote or eukaryote; or which exists as a separate molecule (e.g., a cDNA or a genomic or cDNA fragment produced by PCR or restriction endonuclease digestion) independent of other sequences. It also includes a recombinant DNA which is part of a hybrid gene encoding additional polypeptide sequence.
By "transformed cell" is meant a cell into which (or into an ancestor of which) has been introduced, by means of recombinant DNA techniques, a DNA molecule encoding (as used herein) an IAP polypeptide.
By "transgene" is meant any piece of DNA which is inserted by artifice into a cell, and becomes part of the genome of the organism which develops from that cell. Such a transgene may include a gene which is partly or entirely heterologous (i.e., foreign) to the transgenic organism, or may represent a gene homologous to an endogenous gene of the organism.
By "transgenic" is meant any cell which includes a DNA sequence which is inserted by artifice into a cell and becomes part of the genome of the organism which develops from that cell. As used herein, the transgenic organisms are generally transgenic mammalian (e.g., rodents such as rats or mice) and the DNA (transgene) is inserted by artifice into the nuclear genome.
By "transformation" is meant any method for introducing foreign molecules into a cell. Lipofection, calcium phosphate precipitation, retroviral deliver, electroporation and biolistic transformation are just a few of the teachings which may be used. For example, Biolistic transformation is a method for introducing foreign molecules into a cell using velocity driven microprojectiles such as tungsten or gold particles. Such velocity-driven methods originate from pressure bursts which include, but are not limited to, helium-driven, air-driven, and gunpowder-driven techniques. Biolistic transformation may be applied to the transformation or transfection of a wide variety of cell types and intact tissues including, without limitation, intracellular organelles (e.g., and mitochondria and chloroplasts), bacteria, yeast, fungi, algae, animal tissue, and cultured cells.
By "positioned for expression" is meant that the DNA molecule is positioned adjacent to a DNA sequence which directs transcription and translation of the sequence (i.e., facilitates the production of, e.g., an IAP polypeptide, a recombinant protein or a RNA molecule).
By "reporter gene" is meant a gene whose expression may be assayed; such genes include, without limitation, .beta.-glucuronidase (GUS), luciferase, chloramphenicol transacetylase (CAT), and .beta.-galactosidase.
By "promoter" is meant minimal sequence sufficient to direct transcription. Also included in the invention are those promoter elements which are sufficient to render promoter-dependent gene expression controllable for cell-type specific, tissue-specific or inducible by external signals or agents; such elements may be located in the 5' or 3' regions of the native gene.
By "operably linked" is meant that a gene and a regulatory sequence(s) are connected in such a way as to permit gene expression when the appropriate molecules (e.g., transcriptional activator proteins) are bound to the regulatory sequence(s).
By "conserved region" is meant any stretch of six or more contiguous amino acids exhibiting at least 30%, preferably 50%, and most preferably 70% amino acid sequence identity between two or more of the IAP family members, (e.g., between human HIAP1, HIAP2, and XIAP). Examples of preferred conserved regions are shown (as boxed or designated sequences) in FIGS. 5-7 and Tables 1 and 2, and include, without limitation, BIR domains and ring zinc finger domains.
By "detectably-labelled" is meant any means for marking and identifying the presence of a molecule, e.g., an oligonucleotide probe or primer, a gene or fragment thereof, or a cDNA molecule. Methods for detectably-labelling a molecule are well known in the art and include, without limitation, radioactive labelling (e.g., with an isotope such as .sup.32 P or .sup.35 S) and nonradioactive labelling (e.g., chemiluminescent labelling, e.g., fluorescein labelling).
By "purified antibody" is meant antibody which is at least 60%, by weight, free from proteins and naturally-occurring organic molecules with which it is naturally associated. Preferably, the preparation is at least 75%, more preferably 90%, and most preferably at least 99%, by weight, antibody, e.g., an IAP specific antibody. A purified antibody may be obtained, for example, by affinity chromatography using recombinantly-produced protein or conserved motif peptides and standard techniques.
By "specifically binds" is meant an antibody which recognizes and binds a protein but which does not substantially recognize and bind other molecules in a sample, e.g., a biological sample, which naturally includes protein.
Other features and advantages of the invention will be apparent from the following description of the preferred embodiments thereof, and from the claims.
DETAILED DESCRIPTION
The drawings will first be described.

DRAWINGS
FIG. 1 is the human xiap cDNA sequence and the XIAP polypeptide sequence (SEQ ID NOS:3, 4).
FIG. 2 is the human hiap1 cDNA sequence and the HIAP1 polypeptide sequence (SEQ ID NOS:5, 6).
FIG. 3 is the human hiap2 cDNA sequence and the HIAP2 polypeptide sequence (SEQ ID NOS:7, 8). The sequence absent in the hiap2-G variant is boxed.
FIG. 4 is the murine xiap cDNA sequence and encoded murine XIAP polypeptide sequence (SEQ ID NOS:9, 10).
FIG. 5 is the murine hiap1 cDNA sequence and the encoded murine HIAP1 polypeptide sequence (SEQ ID NOS:39, 40).
FIG. 6 is the murine hiap2 cDNA sequence and the encoded murine HIAP2 polypeptide SEQ ID NOS:41, 42).
FIG. 7 shows the alignment of the BIR domains of IAP proteins (SEQ ID NOS: 11 and 14-31).
FIG. 8 is the alignment of human IAP polypeptides with diap, cp-iap, and the consensus sequence (SEQ ID NOS:4, 6, 8, 10, 12, and 13).
FIG. 9 shows the alignment of the Ring Zinc Finger domains of IAP proteins (SEQ ID NOS: 32-38).
FIGS. 10A-C are a series of Northern blots showing human hiap1 and hiap2 mRNA expression in human tissues.
FIGS. 11A-C are a series of Northern blots showing human hiap2 mRNA expression in human tissues.
FIGS. 12A-C are a series of Northern blots showing human xiap mRNA expression in human tissues.
FIGS. 13A and 13B are agarose gels showing apoptic DNA ladders and RT PCR products using hiap1 and hiap2 specific probes in HIV infected T cells.
FIGS. 14A-14D are graphs showing apoptosis suppression by XIAP, HIAP1, HIAP2, bcl-2m, smn and 6-myc.

I. IAP POLYPEPTIDES AND GENES ENCODING IAP POLYPEPTIDES
We have discovered a new class of mammalian proteins which modulate apoptosis (IAPs) and the genes which encode these proteins. The IAP proteins are characterized by the presence of a ring zinc finger (RZF) domain (FIG. 9) and at least one BIR domain as defined by the boxed consensus sequences in FIGS. 7 and 8 and by the sequence domains provided in Tables 1 and 2. As examples of the IAP proteins we provide the cDNA sequences and amino acid sequences for these new human and murine apoptosis inhibitors, HIAP1, HIAP2, and XIAP. Additional members of the mammalian IAP family (including homologs from other species and mutant sequences) may be isolated using standard cloning techniques and the conserved amino acid sequences, primers and probes provided herein and known in the art.
This application is related to U.S. Ser. No. 08/511,485, filed Aug. 4, 1995, U.S. Pat. No. 5,919,912. U.S. Ser. No. 08/511,485 is hereby incorporated by reference.
TABLE 1______________________________________NUCLEOTIDE POSITION OF CONSERVED DOMAINS* Ring Zinc BIR-1 BIR-2 BIR-3 Finger______________________________________h-xiap 109-312 520-723 826-1023 1348-1485 m-xiap 202-405 613-816 916-1113 1438-1575 h-hiap1 273-476 693-893 951-1154 1824-1961 m-hiap1 251-453 670-870 928-1131 1795-1932 h-hiap2 373-576 787-987 1042-1245 1915-2052 m-hiap2 215-418 608-808 863-1066 1763-1876______________________________________ *Positions indicate correspond to those shown in FIGS. 1-4.
TABLE 2______________________________________AMINO ACID POSITION OF CONSERVED DOMAINS* Ring Zinc BIR-1 BIR-2 BIR-3 Finger______________________________________h-Xiap 26-93 163-230 265-330 439-484 m-Xiap 26-93 163-230 264-329 438-483 h-Hiap1 29-96 169-235 255-322 546-591 m-Hiap1 29-96 169-235 255-322 544-589 h-Hiap2 46-113 184-250 269-336 560-605 m-Hiap2 25-92 156-222 241-308 541-578______________________________________ *Positions indicate correspond to those shown in FIGS. 1-4.
Recognition of this mammalian IAP family has provided emergent patterns of protein structure. Recognition of these patterns has also allowed us assign the function of a modulator of apoptosis to a drosophila gene product of previously unknown function (Genbank Accession Number M96581). The amino acid sequence of this protein, termed diap, is shown in FIG. 8 for comparison.
The IAP proteins may be used to inhibit the apoptosis which occurs as part of disease or disorder processes. For example, IAP polypeptides or nucleic acid encoding IAP polypeptides may be administered for the treatment of or prevention of apoptosis which occurs as a part of AIDS, neurodegenerative diseases, ischemic injury, toxin-induced liver disease and myelodysplastic syndromes. Nucleic acid encoding the IAP polypeptide may also be provided to inhibit apoptosis.
II. Cloning of IAP Genes
A. XIAP
Our search for human genes potentially involved in apoptosis has resulted in the identification of an x-linked sequence tag site (STS) in the GenBank which demonstrated strong homology with the conserved RZF domain of CpIAP and OpIAP, the two baculovirus genes known to inhibit apoptosis (Clem et al., Mol. Cell Biol., 14:5212-5222, (1994); and Birnbaum et al, J. Virol. 68:2521-8, (1994)). Screening a human fetal brain ZapII cDNA library (Stratagene, La Jolla, Calif.) with this STS resulted in the identification and cloning of xiap (for X-linked Inhibitor of apoptosis protein gene). The human gene has a 1.7 kb coding sequence that includes three BIR (baculovirus inhibitor of apoptosis repeat (Crook et al., J. Virol. 67:2168-74, (1993), Clem et al., Science 254:1388-90, (1991); and Birnbaum et al., J. Virol., 68:2521-8, (1994)) domains and a zinc finger. Northern analysis with xiap reveals a greater than 7 kb message expressed in different tissues particularly liver and kidney (FIG. 12). The large size of the transcript reflects large 5' and 3' untranslated regions.
B. HUMAN HIAP1 and HIAP2
The hiap1 and hiap2 genes were cloned by screening a human liver library (Stratagene) with a probe including the whole xiap coding region at low stringency (40.degree. C. wash, 2.times.ssc, 10% SDS) (FIGS. 2 and 3). hiap1 and hiap2 were also independently detected using a probe derived from a expressed sequence tag (EST) (GenBank Accession No. T96284) which includes a portion of a BIR domain. This EST was originally isolated by the PCR amplification of a cDNA library using the EST-specific primers. The derived probe was then used to screen the human liver cDNA library for full length hiap coding sequences. We have subsequently detected a third DNA which includes the hiap2 sequence which appears to lack one exon, presumably due to alternative mRNA splicing (see boxed region in FIG. 3). FIGS. 8 and 9 show hiap1 and hiap2 expression in human tissues as assayed by Northern Analysis.
C. M-XIAP
Screening of a mouse embryo .lambda.gt11 cDNA library (Clonetech, Palo Alto, Calif.) and a mouse FIX II genomic library with a xiap cDNA clones probe has resulted in the identification of 14 positive cDNA and two hybridizing genomic clones. A cDNA contig spanning 8.0 kb was constructed using 12 overlapping mouse clones. DNA sequencing revealed a coding sequence of about 1.7 kb. The mouse gene called m-xiap (for mouse x-linked inhibitor of apoptosis protein gene) shows striking amino acid homology with xiap at and around the initiation methionine, the stop codon, the three BIR domains and the zinc finger domain. As with the human gene, the mouse homologue contains large 5' and 3' UTRs predicted to result in a transcript as large as 7-8 kb.
Sequencing and restriction mapping of m-xiap can be used to further delineate the structure and genomic organization of m-xiap. Southern blot analysis and inverse PCR technique (Groden et al., Cell 66:589-600 (1991) can be employed to map exons and sequence exon-intron boundaries.
Antisera can be raised against a m-xiap fusion protein expressed in Escherichia coli using a bacterial expression system. The resulting antisera can be used along with Northern blot analysis to analyze the spatial and temporal expression of m-xiap in the mouse.
D. M-HIAP1 and M-HIAP2
The murine homologs to hiap1 and hiap2 were cloned and sequenced in the same general manner as m-xiap using the human hiap1 and hiap2 sequences as probes. Cloning of m-hiap1 and m-hiap2 provide further demonstrations of the case with which homologs from different species may be detected and obtained using the techniques provided herein and those generally known to one skilled in the art of molecular biology.
III. Cloning of Additional IAP Genes
Low stringency Southern blot hybridization of human genomic DNA using probes specific for xiap, hiap1 and hiap2 show bands which correspond to the other known human IAP sequences. In addition, these probes detect sequences which do not correspond to known IAP sequences. This result indicates that additional IAP sequences may be readily identified using low stringency hybridization. Examples of murine and human xiap, hiap1, and hiap2 specific primers which may be used to clone additional genes by RT PCR are shown in Table 5. Standard techniques including PCR and hybridization may be used to clone homologs and additional genes.
IV. Characterization of IAP Apoptosis Modulating Activity
The apoptosis inhibiting capability of IAPs can be defined in an in vitro system know to detect alterations in apoptosis. Mammalian expression constructs carrying IAPs and their truncated forms can be introduced into various cell lines such as CHO, HIH 3T3, HL60, Rat-1, or Jurkart cells, for example. In addition, SF21 insect cells may be used in which case the IAP gene is preferentially expressed using an insect heat shock promotor. Apoptosis will then be induced in transfected cells and controls employing standard methodologies (e.g. serum withdrawal and staurosporine). A survival index (ratio of surviving transfected cells to surviving control cells) will indicate the strength of each IAP construct in inhibiting apoptosis. These experiments can confirm the presence of apoptosis inhibiting or enhancing activity and, can help to determine the minimal functional region of an IAP. These methods may also be used in combination with compounds to identify compounds which modulate apoptosis via their effect on IAP expression.
FIGS. 14A-14D show specific examples of apoptosis suppression assays. FIG. 14A shows CHO survival following serum withdrawal. CHO cells were transfected via Lipofectace with 2 .mu.g of each of the following recombinant plasmids; pCDNA3-6myc-hiap-1, pCDNA3-6myc-hiap-2, pCDNA3-6myc-xiap, pCDNA3-6myc, pCDNA3-HA-smn, and pCDNA3-bcl-2. Oligonucleotide primers were synthesized to allow PCR amplification and cloning of the xiap, hiap-1 and hiap-2. Oligonucleotide primers were synthesized to allow PCR amplification and cloning of the xiap, hiap-1, and hiap-2 ORFs in pCDNA3 (Invitrogen). Each construct was modified to incorporate a synthetic myc tag encoding six repeats of the peptide sequence MEQKLISEEDL (SEQ ID NO:43) allowing detection of myc-IAP fusion proteins via monoclonal anti-myc antiserum (Egan, et al., Nature 363:45-51, 1993). Triplicate samples of cell lines in 24 well dishes were washed 5 times with serum free media and maintained in serum free conditions during the course of the experiment. Trypan blue exclusion counting of viable cells utilizing a hemocytometer was performed on samples at time zero, 24 hrs., 48 hrs., and 72 hrs., post serum withdrawal. Survival was calculated as a percentage of initial numbers. Numbers represent the average of three separate experiments performed in triplicate, +/- average deviation. FIG. 14B shows survival of CHO transfected cell lines following exposure to menadione. Cell lines were plated in 24 well dishes, allowed to grow overnight, then exposed for 1.5 hrs. to [20 mM] menadione (Sigma). Triplicate samples were harvested at the time of exposure and at 24 hrs. post exposure and assessed by trypan blue exclusion for survival. Data represents the average of three independent experiments, +/- average deviation. FIG. 14C shows survival of Rat-1 cells following staurosporine exposure. Rat-1 cells were transfected with the plasmids listed in a), with selection in [800 mg/ml] G418 media for two weeks. Cell lines were assessed for resistance to [1 .mu.M]staurosporine induced apoptosis for 5 hrs. Viable cell counts were obtained 24 hrs. post exposure via trypan blue exclusion counting of samples prepared in triplicate. Numbers represent the average of two independent experiments, +/- average deviation. FIG. 14D shows Rat-1 cell lines were tested for resistance to [10 mM] menadione for 1.5 hrs., then counted at 18 hrs. post exposure. Numbers represent the average of three experiments performed in triplicate, +/- average deviation.
Specific examples of apoptosis assays are also provided in the following references:
Lymphocyte: C. J. Li et al., "Induction of apoptosis in uninfected lymphocytes by HIV-1 Tat protein", Science, 268:429-431 (1995); D. Gibellini et al., "Tat-expressing Jurkat cells show an increased resistance to different apoptotic stimuli, including acute human immunodeficiency virus-type 1 (HIV-1) infection", Br. J. Haematol. 89:24-33, (1995); S. J. Martin et al., "HIV-1 infection of human CD4+ T cells in vitro. Differential induction of apoptosis in these cells." J. Immunol. 152:330-42, (1994); C. Terai et al., "Apoptosis as a mechanism of cell death in cultured T lymphoblasts acutely infected with HIV-1", J. Clin Invest., 87:1710-5, (1991); J. Dhein et al., "Autocrine T-cell suicide mediated by APO-1/(Fas/CD95)", Nature 373:438-441, (1995); P. D. Katsikis et al., "Fas antigen stimulation induces marked apoptosis of T lymphocytes in human immunodeficiency virus-infected individuals", J. Exp. Med. 1815:2029-2036, (1995); Michael O. Westendorp et al., Sensitization of T cells to CD95-mediated apoptosis by HIV-1 Tat and gp120", Nature, 375:497, (1995); DeRossi et al., Virology 198:234-44, (1994).
Fibroblasts: H. Vossbeck et al., "Direct transforming activity of TGF-beta on rat fibroblasts", Int. J. Cancer, 61:92-97, (1995); S. Goruppi et al., "Dissection of c-myc domains involved in S phase induction of NIH3T3 fibroblasts", Oncogene, 9:1537-44, (1994); A. Fernandez et al., "Differential sensitivity of normal and Ha-ras-transformed C3H mouse embryo fibroblasts to tumor necrosis factor: induction of bcl-2, c-myc, and manganese superoxide dismutase in resistant cells", Oncogene, 9:2009-17, (1994); E. A. Harrington et al., "c-Myc-induced apoptosis in fibroblasts in inhibited by specific cytokines", EMBO J., 13:3286-3295, (1994); N. Itoh et al., "A novel protein domain required for apoptosis. Mutational analysis of human Fas antigen", J. Biol. Chem., 268:10932-7, (1993).
Neuronal Cells: G. Melino et al., "Tissue transglutaminase and apoptosis: sense and antisense transfection studies with human neuroblastoma cells", Mol. Cell. Biol., 14:6584-6596, (1994); D. M. Rosenbaum et al., "Evidence for hypoxia-induced, programmed cell death of cultured neurons", Ann. Neurol., 36:864-870, (1994); N. Sato et al., "Neuronal differentiation of PC12 cells as a result of prevention of cell death by bcl-2", J. Neurobiol. 25:1227-1234, (1994); G. Ferrari et al., "N-acetylcysteine (D- and L-stereoisomers) prevents apoptotic death of neuronal cells", J. Neurosci., 1516:2857-2866, (1995); A. K. Talley et al., "Tumor necrosis factor alpha-induced apoptosis in human neuronal cells: protection by the antioxidant N-acetylcysteine and the genes bcl-2 and crmA", Mol. Cell Biol., 1585:2359-2366, (1995); A. K. Talley et al., "Tumor Necrosis Factor Alpha-Induced Apoptosis in Human Neuronal Cells: Protection by the Antioxidant N-Acetylcysteine and the Genes bcl-2 and crmA", Mol. and Cell. Biol., 15:2359-2366, (1995); G. Walkinshaw et al., "Induction of apoptosis in catecholaminergic PC12 cells by L-DOPA. Implications for the treatment of Parkinson's disease.", J. Clin. Invest. 95:2458-2464, (1995).
Insect Cells: R. J. Clem et al., "Prevention of apoptosis by a baculovirus gene during infection of insect cells", Science, 254:1388-90, (1991); N. E. Crook et al., "An apoptosis-inhibiting baculovirus gene with a zinc finger-like motif", J. Virol., 67:2168-74, (1993); S. Rabizadeh et al., "Expression of the baculovirus p35 gene inhibits mammalian neural cell death", J. Neurochem., 61:2318-21, (1993); M. J. Birnbaum et al., "An apoptosis-inhibiting gene from a nuclear polyhidrosis virus encoding a polypeptide with Cys/His sequence motifs", J. Virol. 68:2521-8, (1994); R. J. Clem et al., "Control of programmed cell death by the baculovirus genes p35 and iap", Mol. Cell. Biol., 14:5212-5222, (1994).
V. Construction of a Transgenic Animal
Characterization of IAPs can provide information that allows for the development of an IAP knockout animal model, preferably mammal, most preferably a mouse, by homologous recombination. Similarily, an IAP overproducing animal may be produced by means of DNA sequence integration into the genome.
A replacement type targeting vector to create a knockout can be constructed using an isogenic genomic clone from a mouse strain, e.g. 129/Sv (Strategene LaJolla, Calif.). The targeting vector will be introduced into a J1 line of embryonic stem (ES) cells by electroporation to generate ES cell lines that carry a profoundly truncated form of an IAP. To generate chimeric founder mice, the targeted cell lines will be injected into a mouse blastula stage embryo. Heterozygote offspring will be interbred to homozygosity. Knockout mice may be constructed as a means of screening in vivo for therapeutic compounds which modulate apoptosis.
Animals having enhanced IAP expression may also be constructed using standard transgenic technologies.
VI. IAP Protein Expression
IAP genes may be expressed in both prokaryotic and eukaryotic cell types. For those IAP's which increase apoptosis it may be desirable to express the protein under control of an inducible promotor for the purposes of protein production.
In general, IAP proteins according to the invention may be produced by transformation of a suitable host cell with all or part of a IAP-encoding cDNA fragment (e.g., the cDNA described above) in a suitable expression vehicle.
Those skilled in the field of molecular biology will understand that any of a wide variety of expression systems may be used to provide the recombinant protein. The precise host cell used is not critical to the invention. The IAP protein may be produced in a prokaryotic host (e.g., E. coli) or in a eukaryotic host (e.g., Saccharomyces cerevisiae, insect cells, e.g., Sf21 cells, or mammalian cells, e.g., COS 1, NIH 3T3, or HeLa cells). Such cells are available from a wide range of sources (e.g., the American Type Culture Collection, Rockland, Md.; also, see, e.g., Ausubel et al., Current Protocols in Molecular Biology, John Wiley & Sons, New York, 1994). The method of transformation or transfection and the choice of expression vehicle will depend on the host system selected. Transformation and transfection methods are described, e.g., in Ausubel et al., (supra); expression vehicles may be chosen from those provided, e.g., in Cloning Vectors: A Laboratory Manual (P. H. Pouwels et al., 1985, Supp. 1987).
One preferred expression system is the baculovirus system (using, for example, the vector pBacPAK9) available from Clontech (Palo Alto, Calif.). If desired, this system may be used in conjunction with other protein expression techniques, for example, the myc tag approach described by Evan et al. (Mol. Cell Biol. 5:3610-3616, 1985).
Alternatively, a IAP protein is produced by a stably-transfected mammalian cell line. A number of vectors suitable for stable transfection of mammalian cells are available to the public, e.g., see Pouwels et al. (supra); methods for constructing such cell lines are also publicly available, e.g., in Ausubel et al. (supra). In one example, cDNA encoding the IAP protein is cloned into an expression vector which includes the dihydrofolate reductase (DHFR) gene. Integration of the plasmid and, therefore, the IAP protein-encoding gene into the host cell chromosome is selected for by inclusion of 0.01-300 .mu.M methotrexate in the cell culture medium (as described in Ausubel et al., supra). This dominant selection can be accomplished in most cell types. Recombinant protein expression can be increased by DHFR-mediated amplification of the transfected gene. Methods for selecting cell lines bearing gene amplifications are described in Ausubel et al. (supra); such methods generally involve extended culture in medium containing gradually increasing levels of methotrexate. DHFR-containing expression vectors commonly used for this purpose include pCVSEII-DHFR and pAdD26SV(A) (described in Ausubel et al., supra). Any of the host cells described above or, preferably, a DHFR-deficient CHO cell line (e.g., CHO DHFR.sup.- cells, ATCC Accession No. CRL 9096) are among the host cells preferred for DHFR selection of a stably-transfected cell line or DHFR-mediated gene amplification.
Once the recombinant IAP protein is expressed, it is isolated, e.g., using affinity chromatography. In one example, an anti-IAP protein antibody (e.g., produced as described herein) may be attached to a column and used to isolate the IAP protein. Lysis and fractionation of IAP protein-harboring cells prior to affinity chromatography may be performed by standard methods (see, e.g., Ausubel et al., supra).
Once isolated, the recombinant protein can, if desired, be further purified, e.g., by high performance liquid chromatography (see, e.g., Fisher, Laboratory Techniques In Biochemistry And Molecular Biology, eds., Work and Burdon, Elsevier, 1980).
Polypeptides of the invention, particularly short IAP protein fragments, can also be produced by chemical synthesis (e.g., by the methods described in Solid Phase Peptide Synthesis, 2nd ed., 1984 The Pierce Chemical Co., Rockford, Ill.).
These general techniques of polypeptide expression and purification can also be used to produce and isolate useful IAP fragments or analogs (described herein).
VI. Anti-IAP Antibodies
To generate IAP-specific antibodies, a IAP coding sequence (i.e., amino acids 180-276) can be expressed as a C-terminal fusion with glutathione S-transferase (GST) (Smith et al., Gene 67:31-40, 1988). The fusion protein can be purified on glutathione-Sepharose beads, eluted with glutathione cleaved with thrombin (at the engineered cleavage site), and purified to the degree necessary for immunization of rabbits. Primary immunizations can be carried out with Freund's complete adjuvant and subsequent immunizations with Freund's incomplete adjuvant. Antibody titres are monitored by Western blot and immunoprecipitation analyses using the thrombin-cleaved IAP protein fragment of the GST-IAP fusion protein. Immune sera are affinity purified using CNBr-Sepharose-coupled IAP protein. Antiserum specificity is determined using a panel of unrelated GST proteins (including GSTp53, Rb, HPV-16 E6, and E6-AP) and GST-trypsin (which was generated by PCR using known sequences).
As an alternate or adjunct immunogen to GST fusion proteins, peptides corresponding to relatively unique hydrophilic regions of IAP may be generated and coupled to keyhole limpet hemocyanin (KLH) through an introduced C-terminal lysine. Antiserum to each of these peptides is similarly affinity purified on peptides conjugated to BSA, and specificity tested in ELISA and Western blots using peptide conjugates, and by Western blot and immunoprecipitation using IAP expressed as a GST fusion protein.
Alternatively, monoclonal antibodies may be prepared using the IAP proteins described above and standard hybridoma technology (see, e.g., Kohler et al., Nature 256:495, 1975; Kohler et al., Eur. J. Immunol. 6:511, 1976; Kohler et al., Eur. J. Immunol. 6:292, 1976; Hammerling et al., In Monoclonal Antibodies and T Cell Hybridomas, Elsevier, N.Y., 1981; Ausubel et al., supra). Once produced, monoclonal antibodies are also tested for specific IAP recognition by Western blot or immunoprecipitation analysis (by the methods described in Ausubel et al., supra). Antibodies which specifically recognize IAP are considered to be useful in the invention; such antibodies may be used, e.g., in an immunoassay to monitor the level of IAP produced by a mammal (for example, to determine the amount or subcellular location of IAP).
Preferably, antibodies of the invention are produced using fragments of the IAP protein which lie outside highly conserved regions and appear likely to be antigenic, by criteria such as those provided by the Peptidestructure program of the Genetics Computer Group Sequence Analysis Package (Program Manual for the GCG Package, Version 7, 1991) using the algorithm of Jameson and Wolf (CABIOS 4:181 1988)). Specifically these regions, which are found between BIR1 and BIR2 of all the IAP proteins, are in hiap1 from amino acid 99 to 170, hiap2 from amino acid 123 to 184, xiap from 116 to 133 and m-xiap from 116 to 133. In one specific example, such fragments are generated by standard techniques of PCR and cloned into the pGEX expression vector (Ausubel et al., supra). Fusion proteins are expressed in E. coli and purified using a glutathione agarose affinity matrix as described in Ausubel et al. (supra). To attempt to minimize the potential problems of low affinity or specificity of antisera, two or three such fusions are generated for each protein, and each fusion is injected into at least two rabbits. Antisera are raised by injections in a series, preferably including at least three booster injections.
VII. Identification of Molecules that Modulate IAP Protein Expression
Isolation of the IAP cDNAs also facilitates the identification of molecules which increase or decrease IAP expression. According to one approach, candidate molecules are added at varying concentrations to the culture medium of cells expressing IAP mRNA. IAP expression is then measured, for example, by standard Northern blot analysis (Ausubel et al., supra) using a IAP cDNA (or cDNA fragment) as a hybridization probe (see also Table 5). The level of IAP expression in the presence of the candidate molecule is compared to the level measured for the same cells in the same culture medium but in the absence of the candidate molecule.
If desired, the effect of candidate modulators on expression may, in the alternative, be measured at the level of IAP protein production using the same general approach and standard immunological detection techniques, such as Western blotting or immunoprecipitation with a IAP-specific antibody (for example, the IAP antibody described herein).
Candidate modulators may be purified (or substantially purified) molecules or may be one component of a mixture of compounds (e.g., an extract or supernatant obtained from cells; Ausubel et al., supra). In a mixed compound assay, IAP expression is tested against progressively smaller subsets of the candidate compound pool (e.g., produced by standard purification techniques, e.g., HPLC or FPLC) until a single compound or minimal compound mixture is demonstrated to modulate IAP expression.
Alternatively, or in addition, candidate compounds may be screened for those which modulate IAP apoptosis inhibiting activity. In this approach, the degree of apoptosis in the presence of a candidate compound is compared to the degree of apoptosis in its absence, under equivalent conditions. Again, such a screen may begin with a pool of candidate compounds, from which one or more useful modulator compounds are isolated in a step-wise fashion. Apoptosis activity may be measured by any standard assay, for example, those described herein.
Another method for detecting compounds which modulate IAP polypeptide activity is to screen for compounds which physically interact with a given IAP polypeptide. Such compounds may be detected using adaptations of the interaction trap expression systems known in the art. Such systems detect protein interactions using a transcriptional activation assay and are generally described in Gyuris et al., Cell 75:791-803 (1993), and Field and Song, Nature 340:245-246, (1989), and are commercially available from Clonetech (Palo Alto, Calif.). In addition, PCT Publication WO 95/28497 (hereby incorporated by reference) describe a method for detecting proteins involved in apoptosis by virtue of their interaction with Bcl-2 using such an interaction trap assay. A similar method may be exploited to identify proteins and other compounds which interact with the IAP polypeptides.
Candidate IAP modulators include peptide as well as non-peptide molecules (e.g., peptide or non-peptide molecules found, e.g., in a cell extract, mammalian serum, or growth medium on which mammalian cells have been cultured).
A molecule which promotes an increase in IAP expression or IAP activity is considered particularly useful in the invention; such a molecule may be used, for example, as a therapeutic to increase cellular levels of IAP and thereby exploit the effect of IAP polypeptides for the inhibition of apoptosis.
A molecule which decreases IAP activity (e.g., by decreasing gene expression or polypeptide activity) may be useful for decreasing cell proliferation. Such uses include treatment of neoplasms (see Table 3, below) or other cell proliferative diseases.
Modulators found to be effective at the level of IAP expression or activity may be confirmed as useful in animal models and, if successful, may be used as anti-cancer therapeutics for either the inhibition or the enhancement of apoptosis, as appropriate.
IX. IAP Therapy
Because expression levels of IAP genes correlates with the levels of apoptosis, the IAP gene also finds use in anti-apoptosis gene therapy. In particular, to sustain neuronal cells, lymphocytes (T-cells and B-cells), or cells exposed to ischemic injury, a functional IAP gene may be introduced into cells at the sites predicted to undergo undesirable apoptosis.
Retroviral vectors, adenoviral vectors, adeno-associated viral vectors, or other viral vectors with the appropriate tropism for cells likely to be involved in apoptosis (for example, epithelial cells) may be used as a gene transfer delivery system for a therapeutic IAP gene construct. Numerous vectors useful for this purpose are generally known (Miller, Human Gene Therapy 15-14, 1990; Friedman, Science 244:1275-1281, 1989; Eglitis and Anderson, BioTechniques 6:608-614, 1988; Tolstoshev and Anderson, Current Opinion in Biotechnology 1:55-61, 1990; Sharp, The Lancet 337:1277-1278, 1991; Cornetta et al., Nucleic Acid Research and Molecular Biology 36:311-322, 1987; Anderson, Science 226:401-409, 1984; Moen, Blood Cells 17:407-416, 1991; and Miller and Rosman, Biotechniques 7:980-990, 1989; Le Gal La Salle et al., Science 259:988-990, 1993; and Johnson, Chest 107:77S-83S, 1995). Retroviral vectors are particularly well developed and have been used in clinical settings (Rosenberg et al., N. Engl. J. Med. 323:370, 1990; Anderson et al., U.S. Pat. No. 5,399,346).
Non-viral approaches may also be employed for the introduction of therapeutic DNA into cells otherwise predicted to undergo apoptosis. For example, IAP may be introduced into a neuronal cell or a T-cell by the techniques of lipofection (Felgner et al., Proc. Natl. Acad. Sci. USA 84:7413, 1987; Ono et al., Neuroscience Lett 117:259, 1990; Brigham et al., Am. J. Med. Sci. 298:278, 1989; Staubinger and Papahadjopoulos, Meth. Enz. 101:512, 1983); asialorosonucoid-polylysine conjugation (Wu and Wu, J. Biol. Chem. 263:14621, 1988; Wu et al., J. Biol. Chem. 264:16985, 1989); or, less preferably, microinjection under surgical conditions (Wolff et al., Science 247:1465, 1990).
For any of the above approaches, the therapeutic IAP DNA construct is preferably applied to the site of the predicted apoptosis event (for example, by injection), but may also be applied to tissue in the vicinity of the predicted apoptosis event or even to a blood vessel supplying the cells predicted to undergo apoptosis.
In the gene therapy constructs, IAP cDNA expression is directed from any suitable promoter (e.g., the human cytomegalovirus, simian virus 40, or metallothionein promoters), and its production is regulated by any desired mammalian regulatory element. For example, if desired, enhancers known to direct preferential gene expression in neural cells or T-cells may be used to direct IAP expression. Such enhancers include, without limitation, those enhancers which are characterized as tissue or cell specific in their expression.
Alternatively, if a IAP genomic clone is utilized as a therapeutic construct (for example, following its isolation by hybridization with the IAP cDNA described above), IAP expression is regulated by its cognate regulatory sequences or, if desired, by regulatory sequences derived from a heterologous source, e.g., any of the promoters or regulatory elements described above.
Less preferably, IAP gene therapy is accomplished by direct administration of the IAP mRNA to a cell predicted to undergo apoptosis. This mRNA may be produced and isolated by any standard technique, but is most readily produced by in vitro transcription using a IAP cDNA under the control of a high efficiency promoter (e.g., the T7 promoter). Administration of IAP mRNA to malignant cells is carried out by any of the methods for direct nucleic acid administration described above.
Ideally, the production of IAP protein by any gene therapy approach described above results in a cellular level of IAP that is at least equivalent to the normal, cellular level of IAP in an unaffected individual. Treatment by any IAP-mediated gene therapy approach may be combined with more traditional therapies.
Another therapeutic approach included within the invention involves direct administration of recombinant IAP protein, either to the site of a predicted apoptosis event (for example, by injection) or systemically by any conventional recombinant protein administration technique. The actual dosage of IAP depends on a number of factors, including the size and health of the individual patient, but, generally, between 0.1 mg and 100 mg inclusive are administered per day to an adult in any pharmaceutically-acceptable formulation.
X. Administration of IAP Polypeptides, IAP Genes, or Modulators of IAP Synthesis or Function
A IAP protein, gene, or modulator may be administered with a pharmaceutically-acceptable diluent, carrier, or excipient, in unit dosage form. Conventional pharmaceutical practice may be employed to provide suitable formulations or compositions to administer IAP to patients suffering from or presymptomatic for a IAP-associated carcinoma. Any appropriate route of administration may be employed, for example, parenteral, intravenous, subcutaneous, intramuscular, intracranial, intraorbital, ophthalmic, intraventricular, intracapsular, intraspinal, intracisternal, intraperitoneal, intranasal, aerosol, or oral administration. Therapeutic formulations may be in the form of liquid solutions or suspensions; for oral administration, formulations may be in the form of tablets or capsules; and for intranasal formulations, in the form of powders, nasal drops, or aerosols.
Methods well known in the art for making formulations are found in, for example, "Remington's Pharmaceutical Sciences." Formulations for parenteral administration may, for example, contain excipients, sterile water, or saline, polyalkylene glycols such as polyethylene glycol, oils of vegetable origin, or hydrogenated napthalenes. Biocompatible, biodegradable lactide polymer, lactide/glycolide copolymer, or polyoxyethylene-polyoxypropylene copolymers may be used to control the release of the compounds. Other potentially useful parenteral delivery systems for IAP modulatory compounds include ethylene-vinyl acetate copolymer particles, osmotic pumps, implantable infusion systems, and liposomes. Formulations for inhalation may contain excipients, for example, lactose, or may be aqueous solutions containing, for example, polyoxyethylene-9-lauryl ether, glycocholate and deoxycholate, or may be oily solutions for administration in the form of nasal drops, or as a gel.
If desired, treatment with a IAP protein, gene, or modulatory compound may be combined with more traditional therapies for the disease such as surgery, radiation, or chemotherapy for cancers; surgery, steroid therapy, and chemotherapy for autoimmune diseases; antiviral therapies for AIDS; and for example, TPA for ischemic injury.
XI. Detection of a Condition Involving Altered Apoptosis
IAP polypeptides and nucleic acid sequences find diagnostic use in the detection or monitoring of conditions involving aberrant levels of apoptosis. For example, decrease expression of IAP may be correlated with enhanced apoptosis in humans (see XII, below). Accordingly, a decrease or increase in the level of IAP production may provide an indication of a deleterious condition. Levels of IAP expression may be assayed by any standard technique. For example, its expression in a biological sample (e.g., a biopsy) may be monitored by standard Northern blot analysis or may be aided by PCR (see, e.g., Ausubel et al., supra; PCR Technology: Principles and Applications for DNA Amplification, ed., H. A. Ehrlich, Stockton Press, N.Y.; and Yap and McGee, Nucl. Acids. Res. 19:4294, 1991).
Alternatively, a patient sample may be analyzed for one or more mutations in the IAP sequences using a mismatch detection approach. Generally, these techniques involve PCR amplification of nucleic acid from the patient sample, followed by identification of the mutation (i.e., mismatch) by either altered hybridization, aberrant electrophoretic gel migration, binding or cleavage mediated by mismatch binding proteins, or direct nucleic acid sequencing. Any of these techniques may be used to facilitate mutant IAP detection, and each is well known in the art; examples of particular techniques are described, without limitation, in Orita et al., Proc. Natl. Acad. Sci. USA 86:2766-2770, (1989); and Sheffield et al., Proc. Natl. Acad. Sci. USA 86:232-236, (1989).
In yet another approach, immunoassays are used to detect or monitor IAP protein in a biological sample. IAP-specific polyclonal or monoclonal antibodies (produced as described above) may be used in any standard immunoassay format (e.g., ELISA, Western blot, or RIA assay) to measure IAP polypeptide levels; again comparison is to wild-type IAP levels, and a decrease in IAP production is indicative of a condition involving increased apoptosis. Examples of immunoassays are described, e.g., in Ausubel et al., supra. Immunohistochemical techniques may also be utilized for IAP detection. For example, a tissue sample may be obtained from a patient, and a section stained for the presence of IAP using an anti-IAP antibody and any standard detection system (e.g., one which includes a secondary antibody conjugated to horseradish peroxidase). General guidance regarding such techniques can be found in, e.g., Bancroft and Stevens (Theory and Practice of Histological Techniques, Churchill Livingstone, 1982) and Ausubel et al. (supra).
In one preferred example, a combined diagnostic method may be employed that begins with an evaluation of IAP protein production (for example, by immunological techniques or the protein truncation test (Hogerrorst, F. B. L., et al., Nature Genetics 10:208-212 (1995) and also includes a nucleic acid-based detection technique designed to identify more subtle IAP mutations (for example, point mutations). As described above, a number of mismatch detection assays are available to those skilled in the art, and any preferred technique may be used (see above). By this approach, mutations in IAP may be detected that either result in loss of IAP expression or loss of IAP biological activity. In a variation of this combined diagnostic method, IAP biological activity is measured as protease activity using any appropriate protease assay system (for example, those described above).
Mismatch detection assays also provide the opportunity to diagnose a IAP-mediated predisposition to diseases of apoptosis. For example, a patient heterozygous for an IAP mutation may show no clinical symptoms and yet possess a higher than normal probability of developing one or more types of neurodegenerative, myelodysplastic or ischemic diseases. Given this diagnosis, a patient may take precautions to minimize their exposure to adverse environmental factors (for example, UV exposure or chemical mutagens) and to carefully monitor their medical condition (for example, through frequent physical examinations). This type of IAP diagnostic approach may also be used to detect IAP mutations in prenatal screens.
The IAP diagnostic assays described above may be carried out using any biological sample (for example, any biopsy sample or bodily fluid or tissue) in which IAP is normally expressed (for example, the inhibition of apoptosis). Identification of a mutant IAP gene may also be assayed using these sources for test samples. Alternatively, a IAP mutation, particularly as part of a diagnosis for predisposition to IAP-associated degenerative disease, may be tested using a DNA sample from any cell, for example, by mismatch detection techniques; preferably, the DNA sample is subjected to PCR amplification prior to analysis.
To demonstrate the utility of IAP gene sequences as diagnostics and prognostics for cancer we probed the Clonetech (La Jolla) Human Cancer Cell Line Multiple Tissue Northern Blot (#7757-1). As Table 3 shows, all cancer lines tested showed increased IAP expression relative to samples from non-cancerous control cell lines. xiap expression was particularly high in HeLa (S-3), chronic myelogenous leukemia (K-562), colorectal adenocarcinoma (SW-480) and melanoma (G-361) lines. hiap1 expression was extremely high in Burkitt's lymphoma and was also elevated in colorectal adenocarcinoma. hiap2 expression was particularly high in chronic myelogenous leukemia (K-562) and colorectal adenocarcinoma (SW-480).
In addition, we note that we have mapped hiap1 and hiap2 to human chromosome 11g23. This is a known hotspot for cancer causing mutations.
TABLE 3______________________________________Northern Blot IAP RNA levels in Cancer Cells* xiap hiap1 hiap2______________________________________Promylocytic Leukemia HL-60 + + + Hela S-3 + + + Chronic Myclogenous Leukemia +++ + +++ K-562 Lymphoblastic Leukemia MDLT- +++ + + 4 Burkitt's Lymphoma Raji + +(.times.10) + Colorectal Adenocarcinoma +++ +++ +++ SW-480 Lung Carcinoma A-549 + + + Melanoma G-361 +++ + +______________________________________ *Levels are indicated by a (+) and are the approximate increase in RNA levels relative to Northern blots of RNA from noncancerous control cell lines. A single plus indicates an estimated increase of at least 1fold
XII. Treatment of HIV Infected Individuals
We have found that hiap1 and hiap 2 expression is decreased significantly in HIV infected human cells. This decrease precedes apoptosis. The result indicates that administration of HIAP1, HIAP2, genes encoding these proteins, or compounds which upregulate these genes can be used to prevent T-cell attrition in HIV infected patients. The following assay may also be used to screen for compounds which alter hiap1 and hiap2 expression and which also prevent apoptosis.
The experiments were preformed as follows: Cultured mature lymphocyte CD-4.sup.+ T-cell lines (H9 labelled "a"; CEM/CM-3 labelled "b"; 6T-CEM labelled "c"; and Jurkat labelled "d" in FIGS. 13A and 13B) were examined for apoptosis (FIG. 13A) and hiap gene expression (FIG. 13B). Control conditions are labelled as lane 1 in FIG. 13A and FIG. 13B. Lane 2 shows the result 24 hours after PHA/PMH (phytohemagglutinin, phorbol ester) mitogen stimulation. Lane 3 shows the result 24 hours after HIV strain III.sub.B infection. The "M" refers to standard DNA markers, the 123 bp ladder (Gibco-BRL) in FIG. 13B, and lambda HindIII ladder (Gibco-BRL) in FIG. A.
In FIG. 13A is a picture of ethidium bromide stained gel showing the presence of DNA ladders (as assayed by the test of Prigent et al., J. of Immun. Methods, 160:139-140, (1993), indicative of apoptosis. The sensitivity and degree of apoptosis of the four T-cell lines varies following mitogen stimulation and HIV infection.
For the experiment examining hiap gene expression, total RNA was prepared from the cultured cells and subject to a reverse transcriptase reaction using oligo-dT priming. The RT cDNA products were PCR amplified using specific primers (as shown in Table 5) for the detection of hiap2a, hiap2b and hiap 1. PCR conditions were routine (94.degree. C. melting for 1 minute, 55.degree. C. annealing for 2 minutes and 72.degree. C. extension for 1.5 minutes for 35 cycles) using a Perkin-Elmer 480 thermocycler. The FIG. 13B shows a picture of the RT-PCR products run on a 1% agarose gel stained with ethidium bromide. Absence of hiap2 transcripts is noted in all four cell lines 24 hours after HIV infection. In three of four cell lines (all except H9), the hiap1 gene is also dramatically down-regulated after HIV infection. PHA/PMA mitogen stimulation also appears to decrease hiap gene expression, particularly for hiap2 and to a lesser extent, for hiap1.
The data from these experiments is summarized in the accompanying Table 5. The .beta.-action gene expression was consistent in all cell lines tested, indicating that a flow in the RT-PCR assay does not account for the decreases in hiap gene expression.
TABLE 4______________________________________Oligonucleotide primers for the specific RT-PCR amplification of unique IAP genes. Forward Primer Reverse Primer Size of IAP Gene (nucleotide position*) (nucleotide position*) Product (bp)______________________________________h-xiap p2415 (876-896) p2449 (1291-1311) 435 m-xiap p2566 (458-478) p2490 (994-1013) 555 h-hiap1 p2465 (827-847) p2464 (1008-1038) 211 m-hiap1 p2687 (747-767) p2684 (1177-1197) 450 hiap2 p2595 (1562-1585) p2578 (2339-2363) .sup. 801.sup.a .sup. 618.sup.b m-hiap2 p2693 (1751-1772) p2734 (2078-2100) 349______________________________________ *Nucleotide position as determined from FIGS. 1-4 for each IAP gene .sup.a PCR product size of hiap2a .sup.b PCR product size of hiap2b
TABLE 5______________________________________Apoptosis and hiap gene expression in cultured T-cells following mitogen stimulation or HIV infection. Cell Line Condition Apoptosis hiap1 hiap2______________________________________H9 not stimulated - + +/- PHA/PMA stimulated +++ + +/- HIV infected ++ + - CEM/CM-3 not stimulated - + +/- PHA/PMA stimulated +/- + - HIV infected +/- - - 6T-CEM not stimulated - + + PHA/PMA stimulated +/- - - HIV infected + - - Jurkat not stimulated - + ++ PHA/PMA stimulated + + + HIV infected +/- - -______________________________________
XIII. Preventive Anti-apoptotic Therapy
In a patient diagnosed to be heterozygous for an IAP mutation or to be susceptible to IAP mutations (even if those mutations do not yet result in alteration or loss of IAP biological activity), or a patent diagnosed as HIV positive, any of the above therapies may be administered before the occurrence of the disease phenotype. For example, the therapies may be provided to a patient who is HIV positive but does not yet show a diminished T-cell count or other signs of full-blown AIDS. In particular, compounds shown to increase IAP expression or IAP biological activity may be administered by any standard dosage and route of administration (see above). Alternatively, gene therapy using an IAP expression construct may be undertaken to reverse or prevent the cell defect prior to the development of the degenerative disease.
The methods of the instant invention may be used to reduce or diagnose the disorders described herein in any mammal, for example, humans, domestic pets, or livestock. Where a non-human mammal is treated or diagnosed, the IAP polypeptide, nucleic acid, or antibody employed is preferably specific for that species.
OTHER EMBODIMENTS
In other embodiments, the invention includes any protein which is substantially identical to a mammalian IAP polypeptides (FIGS. 1-6; SEQ ID NO:1-42); such homologs include other substantially pure naturally-occurring mammalian IAP proteins as well as allelic variants; natural mutants; induced mutants; DNA sequences which encode proteins and also hybridize to the IAP DNA sequences of FIGS. 1-6 (SEQ ID NOS:1-42) under high stringency conditions or, less preferably, under low stringency conditions (e.g., washing at 2.times. SSC at 40.degree. C. with a probe length of at least 40 nucleotides); and proteins specifically bound by antisera directed to a IAP polypeptide. The term also includes chimeric polypeptides that include a IAP portion.
The invention further includes analogs of any naturally-occurring IAP polypeptide. Analogs can differ from the naturally-occurring IAP protein by amino acid sequence differences, by post-translational modifications, or by both. Analogs of the invention will generally exhibit at least 85%, more preferably 90%, and most preferably 95% or even 99% identity with all or part of a naturally-occurring IAP amino acid sequence. The length of sequence comparison is at least 15 amino acid residues, preferably at least 25 amino acid residues, and more preferably more than 35 amino acid residues. Modifications include in vivo and in vitro chemical derivatization of polypeptides, e.g., acetylation, carboxylation, phosphorylation, or glycosylation; such modifications may occur during polypeptide synthesis or processing or following treatment with isolated modifying enzymes. Analogs can also differ from the naturally-occurring IAP polypeptide by alterations in primary sequence. These include genetic variants, both natural and induced (for example, resulting from random mutagenesis by irradiation or exposure to ethanemethylsulfate or by site-specific mutagenesis as described in Sambrook, Fritsch and Maniatis, Molecular Cloning: A Laboratory Manual (2d ed.), CSH Press, 1989, or Ausubel et al., supra). Also included are cyclized peptides, molecules, and analogs which contain residues other than L-amino acids, e.g., D-amino acids or non-naturally occurring or synthetic amino acids, e.g., .beta. or .gamma. amino acids.
In addition to full-length polypeptides, the invention also includes IAP polypeptide fragments. As used herein, the term "fragment," means at least 20 contiguous amino acids, preferably at least 30 contiguous amino acids, more preferably at least 50 contiguous amino acids, and most preferably at least 60 to 80 or more contiguous amino acids. Fragments of IAP polypeptides can be generated by methods known to those skilled in the art or may result from normal protein processing (e.g., removal of amino acids from the nascent polypeptide that are not required for biological activity or removal of amino acids by alternative mRNA splicing or alternative protein processing events).
Preferable fragments or analogs according to the invention are those which facilitate specific detection of a IAP nucleic acid or amino acid sequence in a sample to be diagnosed. Particularly useful IAP fragments for this purpose include, without limitation, the amino acid fragments shown in Table 2.
All publications and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each independent publication or patent application was specifically and individually indicated to be incorporated by reference.
__________________________________________________________________________# SEQUENCE LISTING - - - - (1) GENERAL INFORMATION: - - (iii) NUMBER OF SEQUENCES: 68 - - - - (2) INFORMATION FOR SEQ ID NO:1: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 46 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (ix) FEATURE: (D) OTHER INFORMATION: - #Xaa at positons 2, 3, 4, 5, 6, 7, - #9, 10, 11, 17, 18, 19, 20, 21, 23, 25, 30 - #,31, 32, 34, 35, - #38, 39, 40, 41, 42, and 45 may be any ami -#no acid. Xaa at - #position 8 is Glu or Asp. Xaa at positions -#14 & 22 is - #Val or Ile. - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:1: - - Glu Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xa - #a Cys Lys Xaa CysMet 1 5 - # 10 - # 15 - - Xaa Xaa Xaa Xaa Xaa Xaa Xaa Phe Xaa Pro Cy - #s Gly His Xaa Xaa Xaa 20 - # 25 - # 30 - - Cys Xaa Xaa Cys Ala Xaa Xaa Xaa Xaa Xaa Cy - #s Pro Xaa Cys 35 - # 40 - # 45 - - - - (2) INFORMATION FOR SEQ ID NO:2: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 68 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (ix) FEATURE: (D) OTHER INFORMATION: - #Xaa at positions 1, 2, 3, 6, 9, - #10, 14, 15, 18, 19, 20, 21, 24, 30, 32, 3 - #3,35, 37, 40, 42, - #43, 44, 45, 46, 47, 49, 50, 51, 53, 54, 5 -#5, 56, 57, 59, - #60, 61, 62, 64 and 66 may be any amino ac -#id. Xaa at - #positions 13, 16 and 17 may be any amino aci -#d or may be - #absent. - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2: - - Xaa Xaa Xaa Arg Leu Xaa Thr Phe Xaa Xaa Tr - #p Pro Xaa Xaa Xaa Xaa 1 5 - # 10 - # 15 - - Xaa Xaa Xaa Xaa Xaa Leu Ala Xaa Ala Gly Ph - #e Tyr Tyr Xaa Gly Xaa 20 - # 25 - # 30 - - Xaa Asp Xaa Val Xaa Cys Phe Xaa Cys Xaa Xa - #a Xaa Xaa Xaa Xaa Trp 35 - # 40 - # 45 - - Xaa Xaa Xaa Asp Xaa Xaa Xaa Xaa Xaa His Xa - #a Xaa Xaa Xaa Pro Xaa 50 - # 55 - # 60 - - Cys Xaa Phe Val 65 - - - - (2) INFORMATION FOR SEQ ID NO:3: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 2540 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: both (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:3: - - GAAAAGGTGG ACAAGTCCTA TTTTCAAGAG AAGATGACTT TTAACAGTTT TG -#AAGGATCT 60 - - AAAACTTGTG TACCTGCAGA CATCAATAAG GAAGAAGAAT TTGTAGAAGA GT -#TTAATAGA 120 - - TTAAAAACTT TTGCTAATTT TCCAAGTGGT AGTCCTGTTT CAGCATCAAC AC -#TGGCACGA 180 - - GCAGGGTTTC TTTATACTGG TGAAGGAGAT ACCGTGCGGT GCTTTAGTTG TC -#ATGCAGCT 240 - - GTAGATAGAT GGCAATATGG AGACTCAGCA GTTGGAAGAC ACAGGAAAGT AT -#CCCCAAAT 300 - - TGCAGATTTA TCAACGGCTT TTATCTTGAA AATAGTGCCA CGCAGTCTAC AA -#ATTCTGGT 360 - - ATCCAGAATG GTCAGTACAA AGTTGAAAAC TATCTGGGAA GCAGAGATCA TT -#TTGCCTTA 420 - - GACAGGCCAT CTGAGACACA TGCAGACTAT CTTTTGAGAA CTGGGCAGGT TG -#TAGATATA 480 - - TCAGACACCA TATACCCGAG GAACCCTGCC ATGTATTGTG AAGAAGCTAG AT -#TAAAGTCC 540 - - TTTCAGAACT GGCCAGACTA TGCTCACCTA ACCCCAAGAG AGTTAGCAAG TG -#CTGGACTC 600 - - TACTACACAG GTATTGGTGA CCAAGTGCAG TGCTTTTGTT GTGGTGGAAA AC -#TGAAAAAT 660 - - TGGGAACCTT GTGATCGTGC CTGGTCAGAA CACAGGCGAC ACTTTCCTAA TT -#GCTTCTTT 720 - - GTTTTGGGCC GGAATCTTAA TATTCGAAGT GAATCTGATG CTGTGAGTTC TG -#ATAGGAAT 780 - - TTCCCAAATT CAACAAATCT TCCAAGAAAT CCATCCATGG CAGATTATGA AG -#CACGGATC 840 - - TTTACTTTTG GGACATGGAT ATACTCAGTT AACAAGGAGC AGCTTGCAAG AG -#CTGGATTT 900 - - TATGCTTTAG GTGAAGGTGA TAAAGTAAAG TGCTTTCACT GTGGAGGAGG GC -#TAACTGAT 960 - - TGGAAGCCCA GTGAAGACCC TTGGGAACAA CATGCTAAAT GGTATCCAGG GT -#GCAAATAT 1020 - - CTGTTAGAAC AGAAGGGACA AGAATATATA AACAATATTC ATTTAACTCA TT -#CACTTGAG 1080 - - GAGTGTCTGG TAAGAACTAC TGAGAAAACA CCATCACTAA CTAGAAGAAT TG -#ATGATACC 1140 - - ATCTTCCAAA ATCCTATGGT ACAAGAAGCT ATACGAATGG GGTTCAGTTT CA -#AGGACATT 1200 - - AAGAAAATAA TGGAGGAAAA AATTCAGATA TCTGGGAGCA ACTATAAATC AC -#TTGAGGTT 1260 - - CTGGTTGCAG ATCTAGTGAA TGCTCAGAAA GACAGTATGC AAGATGAGTC AA -#GTCAGACT 1320 - - TCATTACAGA AAGAGATTAG TACTGAAGAG CAGCTAAGGC GCCTGCAAGA GG -#AGAAGCTT 1380 - - TGCAAAATCT GTATGGATAG AAATATTGCT ATCGTTTTTG TTCCTTGTGG AC -#ATCTAGTC 1440 - - ACTTGTAAAC AATGTGCTGA AGCAGTTGAC AAGTGTCCCA TGTGCTACAC AG -#TCATTACT 1500 - - TTCAAGCAAA AAATTTTTAT GTCTTAATCT AACTCTATAG TAGGCATGTT AT -#GTTGTTCT 1560 - - TATTACCCTG ATTGAATGTG TGATGTGAAC TGACTTTAAG TAATCAGGAT TG -#AATTCCAT 1620 - - TAGCATTTGC TACCAAGTAG GAAAAAAAAT GTACATGGCA GTGTTTTAGT TG -#GCAATATA 1680 - - ATCTTTGAAT TTCTTGATTT TTCAGGGTAT TAGCTGTATT ATCCATTTTT TT -#TACTGTTA 1740 - - TTTAATTGAA ACCATAGACT AAGAATAAGA AGCATCATAC TATAACTGAA CA -#CAATGTGT 1800 - - ATTCATAGTA TACTGATTTA ATTTCTAAGT GTAAGTGAAT TAATCATCTG GA -#TTTTTTAT 1860 - - TCTTTTCAGA TAGGCTTAAC AAATGGAGCT TTCTGTATAT AAATGTGGAG AT -#TAGAGTTA 1920 - - ATCTCCCCAA TCACATAATT TGTTTTGTGT GAAAAAGGAA TAAATTGTTC CA -#TGCTGGTG 1980 - - GAAAGATAGA GATTGTTTTT AGAGGTTGGT TGTTGTGTTT TAGGATTCTG TC -#CATTTTCT 2040 - - TGTAAAGGGA TAAACACGGA CGTGTGCGAA ATATGTTTGT AAAGTGATTT GC -#CATTGTTG 2100 - - AAAGCGTATT TAATGATAGA ATACTATCGA GCCAACATGT ACTGACATGG AA -#AGATGTCA 2160 - - GAGATATGTT AAGTGTAAAA TGCAAGTGGC GGGACACTAT GTATAGTCTG AG -#CCAGATCA 2220 - - AAGTATGTAT GTTGTTAATA TGCATAGAAC GAGAGATTTG GAAAGATATA CA -#CCAAACTG 2280 - - TTAAATGTGG TTTCTCTTCG GGGAGGGGGG GATTGGGGGA GGGGCCCCAG AG -#GGGTTTTA 2340 - - GAGGGGCCTT TTCACTTTCG ACTTTTTTCA TTTTGTTCTG TTCGGATTTT TT -#ATAAGTAT 2400 - - GTAGACCCCG AAGGGTTTTA TGGGAACTAA CATCAGTAAC CTAACCCCCG TG -#ACTATCCT 2460 - - GTGCTCTTCC TAGGGAGCTG TGTTGTTTCC CACCCACCAC CCTTCCCTCT GA -#ACAAATGC 2520 - - CTGAGTGCTG GGGCACTTTN - # - # 254 - #0 - - - - (2) INFORMATION FOR SEQ ID NO:4: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 497 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:4: - - Met Thr Phe Asn Ser Phe Glu Gly Ser Lys Th - #r Cys Val Pro Ala Asp 1 5 - # 10 - # 15 - - Ile Asn Lys Glu Glu Glu Phe Val Glu Glu Ph - #e Asn Arg Leu Lys Thr 20 - # 25 - # 30 - - Phe Ala Asn Phe Pro Ser Gly Ser Pro Val Se - #r Ala Ser Thr Leu Ala 35 - # 40 - # 45 - - Arg Ala Gly Phe Leu Tyr Thr Gly Glu Gly As - #p Thr Val Arg Cys Phe 50 - # 55 - # 60 - - Ser Cys His Ala Ala Val Asp Arg Trp Gln Ty - #r Gly Asp Ser Ala Val 65 - #70 - #75 - #80 - - Gly Arg His Arg Lys Val Ser Pro Asn Cys Ar - #g Phe Ile Asn Gly Phe 85 - # 90 - # 95 - - Tyr Leu Glu Asn Ser Ala Thr Gln Ser Thr As - #n Ser Gly Ile Gln Asn 100 - # 105 - # 110 - - Gly Gln Tyr Lys Val Glu Asn Tyr Leu Gly Se - #r Arg Asp His Phe Ala 115 - # 120 - # 125 - - Leu Asp Arg Pro Ser Glu Thr His Ala Asp Ty - #r Leu Leu Arg Thr Gly 130 - # 135 - # 140 - - Gln Val Val Asp Ile Ser Asp Thr Ile Tyr Pr - #o Arg Asn Pro Ala Met 145 1 - #50 1 - #55 1 -#60 - - Tyr Cys Glu Glu Ala Arg Leu Lys Ser Phe Gl - #n Asn Trp Pro AspTyr 165 - # 170 - # 175 - - Ala His Leu Thr Pro Arg Glu Leu Ala Ser Al - #a Gly Leu Tyr Tyr Thr 180 - # 185 - # 190 - - Gly Ile Gly Asp Gln Val Gln Cys Phe Cys Cy - #s Gly Gly Lys Leu Lys 195 - # 200 - # 205 - - Asn Trp Glu Pro Cys Asp Arg Ala Trp Ser Gl - #u His Arg Arg His Phe 210 - # 215 - # 220 - - Pro Asn Cys Phe Phe Val Leu Gly Arg Asn Le - #u Asn Ile Arg Ser Glu 225 2 - #30 2 - #35 2 -#40 - - Ser Asp Ala Val Ser Ser Asp Arg Asn Phe Pr - #o Asn Ser Thr AsnLeu 245 - # 250 - # 255 - - Pro Arg Asn Pro Ser Met Ala Asp Tyr Glu Al - #a Arg Ile Phe Thr Phe 260 - # 265 - # 270 - - Gly Thr Trp Ile Tyr Ser Val Asn Lys Glu Gl - #n Leu Ala Arg Ala Gly 275 - # 280 - # 285 - - Phe Tyr Ala Leu Gly Glu Gly Asp Lys Val Ly - #s Cys Phe His Cys Gly 290 - # 295 - # 300 - - Gly Gly Leu Thr Asp Trp Lys Pro Ser Glu As - #p Pro Trp Glu Gln His 305 3 - #10 3 - #15 3 -#20 - - Ala Lys Trp Tyr Pro Gly Cys Lys Tyr Leu Le - #u Glu Gln Lys GlyGln 325 - # 330 - # 335 - - Glu Tyr Ile Asn Asn Ile His Leu Thr His Se - #r Leu Glu Glu Cys Leu 340 - # 345 - # 350 - - Val Arg Thr Thr Glu Lys Thr Pro Ser Leu Th - #r Arg Arg Ile Asp Asp 355 - # 360 - # 365 - - Thr Ile Phe Gln Asn Pro Met Val Gln Glu Al - #a Ile Arg Met Gly Phe 370 - # 375 - # 380 - - Ser Phe Lys Asp Ile Lys Lys Ile Met Glu Gl - #u Lys Ile Gln Ile Ser 385 3 - #90 3 - #95 4 -#00 - - Gly Ser Asn Tyr Lys Ser Leu Glu Val Leu Va - #l Ala Asp Leu ValAsn 405 - # 410 - # 415 - - Ala Gln Lys Asp Ser Met Gln Asp Glu Ser Se - #r Gln Thr Ser Leu Gln 420 - # 425 - # 430 - - Lys Glu Ile Ser Thr Glu Glu Gln Leu Arg Ar - #g Leu Gln Glu Glu Lys 435 - # 440 - # 445 - - Leu Cys Lys Ile Cys Met Asp Arg Asn Ile Al - #a Ile Val Phe Val Pro 450 - # 455 - # 460 - - Cys Gly His Leu Val Thr Cys Lys Gln Cys Al - #a Glu Ala Val Asp Lys 465 4 - #70 4 - #75 4 -#80 - - Cys Pro Met Cys Tyr Thr Val Ile Thr Phe Ly - #s Gln Lys Ile PheMet 485 - # 490 - # 495 - - Ser - - - - (2) INFORMATION FOR SEQ ID NO:5: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 2676 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: both (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:5: - - TCCTTGAGAT GTATCAGTAT AGGATTTAGG ATCTCCATGT TGGAACTCTA AA -#TGCATAGA 60 - - AATGGAAATA ATGGAAATTT TTCATTTTGG CTTTTCAGCC TAGTATTAAA AC -#TGATAAAA 120 - - GCAAAGCCAT GCACAAAACT ACCTCCCTAG AGAAAGGCTA GTCCCTTTTC TT -#CCCCATTC 180 - - ATTTCATTAT GAACATAGTA GAAAACAGCA TATTCTTATC AAATTTGATG AA -#AAGCGCCA 240 - - ACACGTTTGA ACTGAAATAC GACTTGTCAT GTGAACTGTA CCGAATGTCT AC -#GTATTCCA 300 - - CTTTTCCTGC TGGGGTTCCT GTCTCAGAAA GGAGTCTTGC TCGTGCTGGT TT -#CTATTACA 360 - - CTGGTGTGAA TGACAAGGTC AAATGCTTCT GTTGTGGCCT GATGCTGGAT AA -#CTGGAAAA 420 - - GAGGAGACAG TCCTACTGAA AAGCATAAAA AGTTGTATCC TAGCTGCAGA TT -#CGTTCAGA 480 - - GTCTAAATTC CGTTAACAAC TTGGAAGCTA CCTCTCAGCC TACTTTTCCT TC -#TTCAGTAA 540 - - CACATTCCAC ACACTCATTA CTTCCGGGTA CAGAAAACAG TGGATATTTC CG -#TGGCTCTT 600 - - ATTCAAACTC TCCATCAAAT CCTGTAAACT CCAGAGCAAA TCAAGAATTT TC -#TGCCTTGA 660 - - TGAGAAGTTC CTACCCCTGT CCAATGAATA ACGAAAATGC CAGATTACTT AC -#TTTTCAGA 720 - - CATGGCCATT GACTTTTCTG TCGCCAACAG ATCTGGCACG AGCAGGCTTT TA -#CTACATAG 780 - - GACCTGGAGA CAGAGTGGCT TGCTTTGCCT GTGGTGGAAA ATTGAGCAAT TG -#GGAACCGA 840 - - AGGATAATGC TATGTCAGAA CACCTGAGAC ATTTTCCCAA ATGCCCATTT AT -#AGAAAATC 900 - - AGCTTCAAGA CACTTCAAGA TACACAGTTT CTAATCTGAG CATGCAGACA CA -#TGCAGCCC 960 - - GCTTTAAAAC ATTCTTTAAC TGGCCCTCTA GTGTTCTAGT TAATCCTGAG CA -#GCTTGCAA 1020 - - GTGCGGGTTT TTATTATGTG GGTAACAGTG ATGATGTCAA ATGCTTTTGC TG -#TGATGGTG 1080 - - GACTCAGGTG TTGGGAATCT GGAGATGATC CATGGGTTCA ACATGCCAAG TG -#GTTTCCAA 1140 - - GGTGTGAGTA CTTGATAAGA ATTAAAGGAC AGGAGTTCAT CCGTCAAGTT CA -#AGCCAGTT 1200 - - ACCCTCATCT ACTTGAACAG CTGCTATCCA CATCAGACAG CCCAGGAGAT GA -#AAATGCAG 1260 - - AGTCATCAAT TATCCATTTG GAACCTGGAG AAGACCATTC AGAAGATGCA AT -#CATGATGA 1320 - - ATACTCCTGT GATTAATGCT GCCGTGGAAA TGGGCTTTAG TAGAAGCCTG GT -#AAAACAGA 1380 - - CAGTTCAGAG AAAAATCCTA GCAACTGGAG AGAATTATAG ACTAGTCAAT GA -#TCTTGTGT 1440 - - TAGACTTACT CAATGCAGAA GATGAAATAA GGGAAGAGGA GAGAGAAAGA GC -#AACTGAGG 1500 - - AAAAAGAATC AAATGATTTA TTATTAATCC GGAAGAATAG AATGGCACTT TT -#TCAACATT 1560 - - TGACTTGTGT AATTCCAATC CTGGATAGTC TACTAACTGC CGGAATTATT AA -#TGAACAAG 1620 - - AACATGATGT TATTAAACAG AAGACACAGA CGTCTTTACA AGCAAGAGAA CT -#GATTGATA 1680 - - CGATTTTAGT AAAAGGAAAT ATTGCAGCCA CTGTATTCAG AAACTCTCTG CA -#AGAAGCTG 1740 - - AAGCTGTGTT ATATGAGCAT TTATTTGTGC AACAGGACAT AAAATATATT CC -#CACAGAAG 1800 - - ATGTTTCAGA TCTACCAGTG GAAGAACAAT TGCGGAGACT ACCAGAAGAA AG -#AACATGTA 1860 - - AAGTGTGTAT GGACAAAGAA GTGTCCATAG TGTTTATTCC TTGTGGTCAT CT -#AGTAGTAT 1920 - - GCAAAGATTG TGCTCCTTCT TTAAGAAAGT GTCCTATTTG TAGGAGTACA AT -#CAAGGGTA 1980 - - CAGTTCGTAC ATTTCTTTCA TGAAGAAGAA CCAAAACATC GTCTAAACTT TA -#GAATTAAT 2040 - - TTATTAAATG TATTATAACT TTAACTTTTA TCCTAATTTG GTTTCCTTAA AA -#TTTTTATT 2100 - - TATTTACAAC TCAAAAAACA TTGTTTTGTG TAACATATTT ATATATGTAT CT -#AAACCATA 2160 - - TGAACATATA TTTTTTAGAA ACTAAGAGAA TGATAGGCTT TTGTTCTTAT GA -#ACGAAAAA 2220 - - GAGGTAGCAC TACAAACACA ATATTCAATC CAAATTTCAG CATTATTGAA AT -#TGTAAGTG 2280 - - AAGTAAAACT TAAGATATTT GAGTTAACCT TTAAGAATTT TAAATATTTT GG -#CATTGTAC 2340 - - TAATACCGGG AACATGAAGC CAGGTGTGGT GGTATGTACC TGTAGTCCCA GG -#CTGAGGCA 2400 - - AGAGAATTAC TTGAGCCCAG GAGTTTGAAT CCATCCTGGG CAGCATACTG AG -#ACCCTGCC 2460 - - TTTAAAAACN AACAGNACCA AANCCAAACA CCAGGGACAC ATTTCTCTGT CT -#TTTTTGAT 2520 - - CAGTGTCCTA TACATCGAAG GTGTGCATAT ATGTTGAATC ACATTTTAGG GA -#CATGGTGT 2580 - - TTTTATAAAG AATTCTGTGA GNAAAAATTT AATAAAGCAA CCAAATTACT CT -#TAAAAAAA 2640 - - AAAAAAAAAA AAAAAACTCG AGGGGCCCGT ACCAAT - #- # 2676 - - - - (2) INFORMATION FOR SEQ ID NO:6: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 604 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:6: - - Met Asn Ile Val Glu Asn Ser Ile Phe Leu Se - #r Asn Leu Met LysSer 1 5 - # 10 - # 15 - - Ala Asn Thr Phe Glu Leu Lys Tyr Asp Leu Se - #r Cys Glu Leu Tyr Arg 20 - # 25 - # 30 - - Met Ser Thr Tyr Ser Thr Phe Pro Ala Gly Va - #l Pro Val Ser Glu Arg 35 - # 40 - # 45 - - Ser Leu Ala Arg Ala Gly Phe Tyr Tyr Thr Gl - #y Val Asn Asp Lys Val 50 - # 55 - # 60 - - Lys Cys Phe Cys Cys Gly Leu Met Leu Asp As - #n Trp Lys Arg Gly Asp 65 - #70 - #75 - #80 - - Ser Pro Thr Glu Lys His Lys Lys Leu Tyr Pr - #o Ser Cys Arg Phe Val 85 - # 90 - # 95 - - Gln Ser Leu Asn Ser Val Asn Asn Leu Glu Al - #a Thr Ser Gln Pro Thr 100 - # 105 - # 110 - - Phe Pro Ser Ser Val Thr His Ser Thr His Se - #r Leu Leu Pro Gly Thr 115 - # 120 - # 125 - - Glu Asn Ser Gly Tyr Phe Arg Gly Ser Tyr Se - #r Asn Ser Pro Ser Asn 130 - # 135 - # 140 - - Pro Val Asn Ser Arg Ala Asn Gln Glu Phe Se - #r Ala Leu Met Arg Ser 145 1 - #50 1 - #55 1 -#60 - - Ser Tyr Pro Cys Pro Met Asn Asn Glu Asn Al - #a Arg Leu Leu ThrPhe 165 - # 170 - # 175 - - Gln Thr Trp Pro Leu Thr Phe Leu Ser Pro Th - #r Asp Leu Ala Arg Ala 180 - # 185 - # 190 - - Gly Phe Tyr Tyr Ile Gly Pro Gly Asp Arg Va - #l Ala Cys Phe Ala Cys 195 - # 200 - # 205 - - Gly Gly Lys Leu Ser Asn Trp Glu Pro Lys As - #p Asn Ala Met Ser Glu 210 - # 215 - # 220 - - His Leu Arg His Phe Pro Lys Cys Pro Phe Il - #e Glu Asn Gln Leu Gln 225 2 - #30 2 - #35 2 -#40 - - Asp Thr Ser Arg Tyr Thr Val Ser Asn Leu Se - #r Met Gln Thr HisAla 245 - # 250 - # 255 - - Ala Arg Phe Lys Thr Phe Phe Asn Trp Pro Se - #r Ser Val Leu Val Asn 260 - # 265 - # 270 - - Pro Glu Gln Leu Ala Ser Ala Gly Phe Tyr Ty - #r Val Gly Asn Ser Asp 275 - # 280 - # 285 - - Asp Val Lys Cys Phe Cys Cys Asp Gly Gly Le - #u Arg Cys Trp Glu Ser 290 - # 295 - # 300 - - Gly Asp Asp Pro Trp Val Gln His Ala Lys Tr - #p Phe Pro Arg Cys Glu 305 3 - #10 3 - #15 3 -#20 - - Tyr Leu Ile Arg Ile Lys Gly Gln Glu Phe Il - #e Arg Gln Val GlnAla 325 - # 330 - # 335 - - Ser Tyr Pro His Leu Leu Glu Gln Leu Leu Se - #r Thr Ser Asp Ser Pro 340 - # 345 - # 350 - - Gly Asp Glu Asn Ala Glu Ser Ser Ile Ile Hi - #s Leu Glu Pro Gly Glu 355 - # 360 - # 365 - - Asp His Ser Glu Asp Ala Ile Met Met Asn Th - #r Pro Val Ile Asn Ala 370 - # 375 - # 380 - - Ala Val Glu Met Gly Phe Ser Arg Ser Leu Va - #l Lys Gln Thr Val Gln 385 3 - #90 3 - #95 4 -#00 - - Arg Lys Ile Leu Ala Thr Gly Glu Asn Tyr Ar - #g Leu Val Asn AspLeu 405 - # 410 - # 415 - - Val Leu Asp Leu Leu Asn Ala Glu Asp Glu Il - #e Arg Glu Glu Glu Arg 420 - # 425 - # 430 - - Glu Arg Ala Thr Glu Glu Lys Glu Ser Asn As - #p Leu Leu Leu Ile Arg 435 - # 440 - # 445 - - Lys Asn Arg Met Ala Leu Phe Gln His Leu Th - #r Cys Val Ile Pro Ile 450 - # 455 - # 460 - - Leu Asp Ser Leu Leu Thr Ala Gly Ile Ile As - #n Glu Gln Glu His Asp 465 4 - #70 4 - #75 4 -#80 - - Val Ile Lys Gln Lys Thr Gln Thr Ser Leu Gl - #n Ala Arg Glu LeuIle 485 - # 490 - # 495 - - Asp Thr Ile Leu Val Lys Gly Asn Ile Ala Al - #a Thr Val Phe Arg Asn 500 - # 505 - # 510 - - Ser Leu Gln Glu Ala Glu Ala Val Leu Tyr Gl - #u His Leu Phe Val Gln 515 - # 520 - # 525 - - Gln Asp Ile Lys Tyr Ile Pro Thr Glu Asp Va - #l Ser Asp Leu Pro Val 530 - # 535 - # 540 - - Glu Glu Gln Leu Arg Arg Leu Pro Glu Glu Ar - #g Thr Cys Lys Val Cys 545 5 - #50 5 - #55 5 -#60 - - Met Asp Lys Glu Val Ser Ile Val Phe Ile Pr - #o Cys Gly His LeuVal 565 - # 570 - # 575 - - Val Cys Lys Asp Cys Ala Pro Ser Leu Arg Ly - #s Cys Pro Ile Cys Arg 580 - # 585 - # 590 - - Ser Thr Ile Lys Gly Thr Val Arg Thr Phe Le - #u Ser 595 - # 600 - - - - (2) INFORMATION FOR SEQ ID NO:7: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 2580 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: both (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:7: - - TTAGGTTACC TGAAAGAGTT ACTACAACCC CAAAGAGTTG TGTTCTAAGT AG -#TATCTTGG 60 - - TAATTCAGAG AGATACTCAT CCTACCTGAA TATAAACTGA GATAAATCCA GT -#AAAGAAAG 120 - - TGTAGTAAAT TCTACATAAG AGTCTATCAT TGATTTCTTT TTGTGGTGGA AA -#TCTTAGTT 180 - - CATGTGAAGA AATTTCATGT GAATGTTTTA GCTATCAAAC AGTACTGTCA CC -#TACTCATG 240 - - CACAAAACTG CCTCCCAAAG ACTTTTCCCA GGTCCCTCGT ATCAAAACAT TA -#AGAGTATA 300 - - ATGGAAGATA GCACGATCTT GTCAGATTGG ACAAACAGCA ACAAACAAAA AA -#TGAAGTAT 360 - - GACTTTTCCT GTGAACTCTA CAGAATGTCT ACATATTCAA CTTTCCCCGC CG -#GGGTGCCT 420 - - GTCTCAGAAA GGAGTCTTGC TCGTGCTGGT TTTTATTATA CTGGTGTGAA TG -#ACAAGGTC 480 - - AAATGCTTCT GTTGTGGCCT GATGCTGGAT AACTGGAAAC TAGGAGACAG TC -#CTATTCAA 540 - - AAGCATAAAC AGCTATATCC TAGCTGTAGC TTTATTCAGA ATCTGGTTTC AG -#CTAGTCTG 600 - - GGATCCACCT CTAAGAATAC GTCTCCAATG AGAAACAGTT TTGCACATTC AT -#TATCTCCC 660 - - ACCTTGGAAC ATAGTAGCTT GTTCAGTGGT TCTTACTCCA GCCTTCCTCC AA -#ACCCTCTT 720 - - AATTCTAGAG CAGTTGAAGA CATCTCTTCA TCGAGGACTA ACCCCTACAG TT -#ATGCAATG 780 - - AGTACTGAAG AAGCCAGATT TCTTACCTAC CATATGTGGC CATTAACTTT TT -#TGTCACCA 840 - - TCAGAATTGG CAAGAGCTGG TTTTTATTAT ATAGGACCTG GAGATAGGGT AG -#CCTGCTTT 900 - - GCCTGTGGTG GGAAGCTCAG TAACTGGGAA CCAAAGGATG ATGCTATGTC AG -#AACACCGG 960 - - AGGCATTTTC CCAACTGTCC ATTTTTGGAA AATTCTCTAG AAACTCTGAG GT -#TTAGCATT 1020 - - TCAAATCTGA GCATGCAGAC ACATGCAGCT CGAATGAGAA CATTTATGTA CT -#GGCCATCT 1080 - - AGTGTTCCAG TTCAGCCTGA GCAGCTTGCA AGTGCTGGTT TTTATTATGT GG -#GTCGCAAT 1140 - - GATGATGTCA AATGCTTTGG TTGTGATGGT GGCTTGAGGT GTTGGGAATC TG -#GAGATGAT 1200 - - CCATGGGTAG AACATGCCAA GTGGTTTCCA AGGTGTGAGT TCTTGATACG AA -#TGAAAGGC 1260 - - CAAGAGTTTG TTGATGAGAT TCAAGGTAGA TATCCTCATC TTCTTGAACA GC -#TGTTGTCA 1320 - - ACTTCAGATA CCACTGGAGA AGAAAATGCT GACCCACCAA TTATTCATTT TG -#GACCTGGA 1380 - - GAAAGTTCTT CAGAAGATGC TGTCATGATG AATACACCTG TGGTTAAATC TG -#CCTTGGAA 1440 - - ATGGGCTTTA ATAGAGACCT GGTGAAACAA ACAGTTCTAA GTAAAATCCT GA -#CAACTGGA 1500 - - GAGAACTATA AAACAGTTAA TGATATTGTG TCAGCACTTC TTAATGCTGA AG -#ATGAAAAA 1560 - - AGAGAAGAGG AGAAGGAAAA ACAAGCTGAA GAAATGGCAT CAGATGATTT GT -#CATTAATT 1620 - - CGGAAGAACA GAATGGCTCT CTTTCAACAA TTGACATGTG TGCTTCCTAT CC -#TGGATAAT 1680 - - CTTTTAAAGG CCAATGTAAT TAATAAACAG GAACATGATA TTATTAAACA AA -#AAACACAG 1740 - - ATACCTTTAC AAGCGAGAGA ACTGATTGAT ACCATTTGGG TTAAAGGAAA TG -#CTGCGGCC 1800 - - AACATCTTCA AAAACTGTCT AAAAGAAATT GACTCTACAT TGTATAAGAA CT -#TATTTGTG 1860 - - GATAAGAATA TGAAGTATAT TCCAACAGAA GATGTTTCAG GTCTGTCACT GG -#AAGAACAA 1920 - - TTGAGGAGGT TGCAAGAAGA ACGAACTTGT AAAGTGTGTA TGGACAAAGA AG -#TTTCTGTT 1980 - - GTATTTATTC CTTGTGGTCA TCTGGTAGTA TGCCAGGAAT GTGCCCCTTC TC -#TAAGAAAA 2040 - - TGCCCTATTT GCAGGGGTAT AATCAAGGGT ACTGTTCGTA CATTTCTCTC TT -#AAAGAAAA 2100 - - ATAGTCTATA TTTTAACCTG CATAAAAAGG TCTTTAAAAT ATTGTTGAAC AC -#TTGAAGCC 2160 - - ATCTAAAGTA AAAAGGGAAT TATGAGTTTT TCAATTAGTA ACATTCATGT TC -#TAGTCTGC 2220 - - TTTGGTACTA ATAATCTTGT TTCTGAAAAG ATGGTATCAT ATATTTAATC TT -#AATCTGTT 2280 - - TATTTACAAG GGAAGATTTA TGTTTGGTGA ACTATATTAG TATGTATGTG TA -#CCTAAGGG 2340 - - AGTAGCGTCN CTGCTTGTTA TGCATCATTT CAGGAGTTAC TGGATTTGTT GT -#TCTTTCAG 2400 - - AAAGCTTTGA ANACTAAATT ATAGTGTAGA AAAGAACTGG AAACCAGGAA CT -#CTGGAGTT 2460 - - CATCAGAGTT ATGGTGCCGA ATTGTCTTTG GTGCTTTTCA CTTGTGTTTT AA -#AATAAGGA 2520 - - TTTTTCTCTT ATTTCTCCCC CTAGTTTGTG AGAAACATCT CAATAAAGTG CT -#TTAAAAAG 2580 - - - - (2) INFORMATION FOR SEQ ID NO:8: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 618 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:8: - - Met His Lys Thr Ala Ser Gln Arg Leu Phe Pr - #o Gly Pro Ser TyrGln 1 5 - # 10 - # 15 - - Asn Ile Lys Ser Ile Met Glu Asp Ser Thr Il - #e Leu Ser Asp Trp Thr 20 - # 25 - # 30 - - Asn Ser Asn Lys Gln Lys Met Lys Tyr Asp Ph - #e Ser Cys Glu Leu Tyr 35 - # 40 - # 45 - - Arg Met Ser Thr Tyr Ser Thr Phe Pro Ala Gl - #y Val Pro Val Ser Glu 50 - # 55 - # 60 - - Arg Ser Leu Ala Arg Ala Gly Phe Tyr Tyr Th - #r Gly Val Asn Asp Lys 65 - #70 - #75 - #80 - - Val Lys Cys Phe Cys Cys Gly Leu Met Leu As - #p Asn Trp Lys Leu Gly 85 - # 90 - # 95 - - Asp Ser Pro Ile Gln Lys His Lys Gln Leu Ty - #r Pro Ser Cys Ser Phe 100 - # 105 - # 110 - - Ile Gln Asn Leu Val Ser Ala Ser Leu Gly Se - #r Thr Ser Lys Asn Thr 115 - # 120 - # 125 - - Ser Pro Met Arg Asn Ser Phe Ala His Ser Le - #u Ser Pro Thr Leu Glu 130 - # 135 - # 140 - - His Ser Ser Leu Phe Ser Gly Ser Tyr Ser Se - #r Leu Pro Pro Asn Pro 145 1 - #50 1 - #55 1 -#60 - - Leu Asn Ser Arg Ala Val Glu Asp Ile Ser Se - #r Ser Arg Thr AsnPro 165 - # 170 - # 175 - - Tyr Ser Tyr Ala Met Ser Thr Glu Glu Ala Ar - #g Phe Leu Thr Tyr His 180 - # 185 - # 190 - - Met Trp Pro Leu Thr Phe Leu Ser Pro Ser Gl - #u Leu Ala Arg Ala Gly 195 - # 200 - # 205 - - Phe Tyr Tyr Ile Gly Pro Gly Asp Arg Val Al - #a Cys Phe Ala Cys Gly 210 - # 215 - # 220 - - Gly Lys Leu Ser Asn Trp Glu Pro Lys Asp As - #p Ala Met Ser Glu His 225 2 - #30 2 - #35 2 -#40 - - Arg Arg His Phe Pro Asn Cys Pro Phe Leu Gl - #u Asn Ser Leu GluThr 245 - # 250 - # 255 - - Leu Arg Phe Ser Ile Ser Asn Leu Ser Met Gl - #n Thr His Ala Ala Arg 260 - # 265 - # 270 - - Met Arg Thr Phe Met Tyr Trp Pro Ser Ser Va - #l Pro Val Gln Pro Glu 275 - # 280 - # 285 - - Gln Leu Ala Ser Ala Gly Phe Tyr Tyr Val Gl - #y Arg Asn Asp Asp Val 290 - # 295 - # 300 - - Lys Cys Phe Gly Cys Asp Gly Gly Leu Arg Cy - #s Trp Glu Ser Gly Asp 305 3 - #10 3 - #15 3 -#20 - - Asp Pro Trp Val Glu His Ala Lys Trp Phe Pr - #o Arg Cys Glu PheLeu 325 - # 330 - # 335 - - Ile Arg Met Lys Gly Gln Glu Phe Val Asp Gl - #u Ile Gln Gly Arg Tyr 340 - # 345 - # 350 - - Pro His Leu Leu Glu Gln Leu Leu Ser Thr Se - #r Asp Thr Thr Gly Glu 355 - # 360 - # 365 - - Glu Asn Ala Asp Pro Pro Ile Ile His Phe Gl - #y Pro Gly Glu Ser Ser 370 - # 375 - # 380 - - Ser Glu Asp Ala Val Met Met Asn Thr Pro Va - #l Val Lys Ser Ala Leu 385 3 - #90 3 - #95 4 -#00 - - Glu Met Gly Phe Asn Arg Asp Leu Val Lys Gl - #n Thr Val Leu SerLys 405 - # 410 - # 415 - - Ile Leu Thr Thr Gly Glu Asn Tyr Lys Thr Va - #l Asn Asp Ile Val Ser 420 - # 425 - # 430 - - Ala Leu Leu Asn Ala Glu Asp Glu Lys Arg Gl - #u Glu Glu Lys Glu Lys 435 - # 440 - # 445 - - Gln Ala Glu Glu Met Ala Ser Asp Asp Leu Se - #r Leu Ile Arg Lys Asn 450 - # 455 - # 460 - - Arg Met Ala Leu Phe Gln Gln Leu Thr Cys Va - #l Leu Pro Ile Leu Asp 465 4 - #70 4 - #75 4 -#80 - - Asn Leu Leu Lys Ala Asn Val Ile Asn Lys Gl - #n Glu His Asp IleIle 485 - # 490 - # 495 - - Lys Gln Lys Thr Gln Ile Pro Leu Gln Ala Ar - #g Glu Leu Ile Asp Thr 500 - # 505 - # 510 - - Ile Trp Val Lys Gly Asn Ala Ala Ala Asn Il - #e Phe Lys Asn Cys Leu 515 - # 520 - # 525 - - Lys Glu Ile Asp Ser Thr Leu Tyr Lys Asn Le - #u Phe Val Asp Lys Asn 530 - # 535 - # 540 - - Met Lys Tyr Ile Pro Thr Glu Asp Val Ser Gl - #y Leu Ser Leu Glu Glu 545 5 - #50 5 - #55 5 -#60 - - Gln Leu Arg Arg Leu Gln Glu Glu Arg Thr Cy - #s Lys Val Cys MetAsp 565 - # 570 - # 575 - - Lys Glu Val Ser Val Val Phe Ile Pro Cys Gl - #y His Leu Val Val Cys 580 - # 585 - # 590 - - Gln Glu Cys Ala Pro Ser Leu Arg Lys Cys Pr - #o Ile Cys Arg Gly Ile 595 - # 600 - # 605 - - Ile Lys Gly Thr Val Arg Thr Phe Leu Ser 610 - # 615 - - - - (2) INFORMATION FOR SEQ ID NO:9: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 2100 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: both (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:9: - - GACACTCTGC TGGGCGGCGG GCCGCCCTCC TCCGGGACCT CCCCTCGGGA AC -#CGTCGCCC 60 - - GCGGCGCTTA GTTAGGACTG GAGTGCTTGG CGCGAAAAGG TGGACAAGTC CT -#ATTTTCCA 120 - - GAGAAGATGA CTTTTAACAG TTTTGAAGGA ACTAGAACTT TTGTACTTGC AG -#ACACCAAT 180 - - AAGGATGAAG AATTTGTAGA AGAGTTTAAT AGATTAAAAA CATTTGCTAA CT -#TCCCAAGT 240 - - AGTAGTCCTG TTTCAGCATC AACATTGGCG CGAGCTGGGT TTCTTTATAC CG -#GTGAAGGA 300 - - GACACCGTGC AATGTTTCAG TTGTCATGCG GCAATAGATA GATGGCAGTA TG -#GAGACTCA 360 - - GCTGTTGGAA GACACAGGAG AATATCCCCA AATTGCAGAT TTATCAATGG TT -#TTTATTTT 420 - - GAAAATGGTG CTGCACAGTC TACAAATCCT GGTATCCAAA ATGGCCAGTA CA -#AATCTGAA 480 - - AACTGTGTGG GAAATAGAAA TCCTTTTGCC CCTGACAGGC CACCTGAGAC TC -#ATGCTGAT 540 - - TATCTCTTGA GAACTGGACA GGTTGTAGAT ATTTCAGACA CCATATACCC GA -#GGAACCCT 600 - - GCCATGTGTA GTGAAGAAGC CAGATTGAAG TCATTTCAGA ACTGGCCGGA CT -#ATGCTCAT 660 - - TTAACCCCCA GAGAGTTAGC TAGTGCTGGC CTCTACTACA CAGGGGCTGA TG -#ATCAAGTG 720 - - CAATGCTTTT GTTGTGGGGG AAAACTGAAA AATTGGGAAC CCTGTGATCG TG -#CCTGGTCA 780 - - GAACACAGGA GACACTTTCC CAATTGCTTT TTTGTTTTGG GCCGGAACGT TA -#ATGTTCGA 840 - - AGTGAATCTG GTGTGAGTTC TGATAGGAAT TTCCCAAATT CAACAAACTC TC -#CAAGAAAT 900 - - CCAGCCATGG CAGAATATGA AGCACGGATC GTTACTTTTG GAACATGGAT AT -#ACTCAGTT 960 - - AACAAGGAGC AGCTTGCAAG AGCTGGATTT TATGCTTTAG GTGAAGGCGA TA -#AAGTGAAG 1020 - - TGCTTCCACT GTGGAGGAGG GCTCACGGAT TGGAAGCCAA GTGAAGACCC CT -#GGGACCAG 1080 - - CATGCTAAGT GCTACCCAGG GTGCAAATAC CTATTGGATG AGAAGGGGCA AG -#AATATATA 1140 - - AATAATATTC ATTTAACCCA TCCACTTGAG GAATCTTTGG GAAGAACTGC TG -#AAAAAACA 1200 - - CCACCGCTAA CTAAAAAAAT CGATGATACC ATCTTCCAGA ATCCTATGGT GC -#AAGAAGCT 1260 - - ATACGAATGG GATTTAGCTT CAAGGACCTT AAGAAAACAA TGGAAGAAAA AA -#TCCAAACA 1320 - - TCCGGGAGCA GCTATCTATC ACTTGAGGTC CTGATTGCAG ATCTTGTGAG TG -#CTCAGAAA 1380 - - GATAATACGG AGGATGAGTC AAGTCAAACT TCATTGCAGA AAGACATTAG TA -#CTGAAGAG 1440 - - CAGCTAAGGC GCCTACAAGA GGAGAAGCTT TCCAAAATCT GTATGGATAG AA -#ATATTGCT 1500 - - ATCGTTTTTT TTCCTTGTGG ACATCTGGCC ACTTGTAAAC AGTGTGCAGA AG -#CAGTTGAC 1560 - - AAATGTCCCA TGTGCTACAC CGTCATTACG TTCAACCAAA AAATTTTTAT GT -#CTTAGTGG 1620 - - GGCACCACAT GTTATGTTCT TCTTGCTCTA ATTGAATGTG TAATGGGAGC GA -#ACTTTAAG 1680 - - TAATCCTGCA TTTGCATTCC ATTAGCATCC TGCTGTTTCC AAATGGAGAC CA -#ATGCTAAC 1740 - - AGCACTGTTT CCGTCTAAAC ATTCAATTTC TGGATCTTTC GAGTTATCAG CT -#GTATCATT 1800 - - TAGCCAGTGT TTTACTCGAT TGAAACCTTA GACAGAGAAG CATTTTATAG CT -#TTTCACAT 1860 - - GTATATTGGT AGTACACTGA CTTGATTTCT ATATGTAAGT GAATTCATCA CC -#TGCATGTT 1920 - - TCATGCCTTT TGCATAAGCT TAACAAATGG AGTGTTCTGT ATAAGCATGG AG -#ATGTGATG 1980 - - GAATCTGCCC AATGACTTTA ATTGGCTTAT TGTAAACACG GAAAGAACTG CC -#CCACGCTG 2040 - - CTGGGAGGAT AAAGATTGTT TTAGATGCTC ACTTCTGTGT TTTAGGATTC TG -#CCCATTTA 2100 - - - - (2) INFORMATION FOR SEQ ID NO:10: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 496 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:10: - - Met Thr Phe Asn Ser Phe Glu Gly Thr Arg Th - #r Phe Val Leu AlaAsp 1 5 - # 10 - # 15 - - Thr Asn Lys Asp Glu Glu Phe Val Glu Glu Ph - #e Asn Arg Leu Lys Thr 20 - # 25 - # 30 - - Phe Ala Asn Phe Pro Ser Ser Ser Pro Val Se - #r Ala Ser Thr Leu Ala 35 - # 40 - # 45 - - Arg Ala Gly Phe Leu Tyr Thr Gly Glu Gly As - #p Thr Val Gln Cys Phe 50 - # 55 - # 60 - - Ser Cys His Ala Ala Ile Asp Arg Trp Gln Ty - #r Gly Asp Ser Ala Val 65 - #70 - #75 - #80 - - Gly Arg His Arg Arg Ile Ser Pro Asn Cys Ar - #g Phe Ile Asn Gly Phe 85 - # 90 - # 95 - - Tyr Phe Glu Asn Gly Ala Ala Gln Ser Thr As - #n Pro Gly Ile Gln Asn 100 - # 105 - # 110 - - Gly Gln Tyr Lys Ser Glu Asn Cys Val Gly As - #n Arg Asn Pro Phe Ala 115 - # 120 - # 125 - - Pro Asp Arg Pro Pro Glu Thr His Ala Asp Ty - #r Leu Leu Arg Thr Gly 130 - # 135 - # 140 - - Gln Val Val Asp Ile Ser Asp Thr Ile Tyr Pr - #o Arg Asn Pro Ala Met 145 1 - #50 1 - #55 1 -#60 - - Cys Ser Glu Glu Ala Arg Leu Lys Ser Phe Gl - #n Asn Trp Pro AspTyr 165 - # 170 - # 175 - - Ala His Leu Thr Pro Arg Glu Leu Ala Ser Al - #a Gly Leu Tyr Tyr Thr 180 - # 185 - # 190 - - Gly Ala Asp Asp Gln Val Gln Cys Phe Cys Cy - #s Gly Gly Lys Leu Lys 195 - # 200 - # 205 - - Asn Trp Glu Pro Cys Asp Arg Ala Trp Ser Gl - #u His Arg Arg His Phe 210 - # 215 - # 220 - - Pro Asn Cys Phe Phe Val Leu Gly Arg Asn Va - #l Asn Val Arg Ser Glu 225 2 - #30 2 - #35 2 -#40 - - Ser Gly Val Ser Ser Asp Arg Asn Phe Pro As - #n Ser Thr Asn SerPro 245 - # 250 - # 255 - - Arg Asn Pro Ala Met Ala Glu Tyr Glu Ala Ar - #g Ile Val Thr Phe Gly 260 - # 265 - # 270 - - Thr Trp Ile Tyr Ser Val Asn Lys Glu Gln Le - #u Ala Arg Ala Gly Phe 275 - # 280 - # 285 - - Tyr Ala Leu Gly Glu Gly Asp Lys Val Lys Cy - #s Phe His Cys Gly Gly 290 - # 295 - # 300 - - Gly Leu Thr Asp Trp Lys Pro Ser Glu Asp Pr - #o Trp Asp Gln His Ala 305 3 - #10 3 - #15 3 -#20 - - Lys Cys Tyr Pro Gly Cys Lys Tyr Leu Leu As - #p Glu Lys Gly GlnGlu 325 - # 330 - # 335 - - Tyr Ile Asn Asn Ile His Leu Thr His Pro Le - #u Glu Glu Ser Leu Gly 340 - # 345 - # 350 - - Arg Thr Ala Glu Lys Thr Pro Pro Leu Thr Ly - #s Lys Ile Asp Asp Thr 355 - # 360 - # 365 - - Ile Phe Gln Asn Pro Met Val Gln Glu Ala Il - #e Arg Met Gly Phe Ser 370 - # 375 - # 380 - - Phe Lys Asp Leu Lys Lys Thr Met Glu Glu Ly - #s Ile Gln Thr Ser Gly 385 3 - #90 3 - #95 4 -#00 - - Ser Ser Tyr Leu Ser Leu Glu Val Leu Ile Al - #a Asp Leu Val SerAla 405 - # 410 - # 415 - - Gln Lys Asp Asn Thr Glu Asp Glu Ser Ser Gl - #n Thr Ser Leu Gln Lys 420 - # 425 - # 430 - - Asp Ile Ser Thr Glu Glu Gln Leu Arg Arg Le - #u Gln Glu Glu Lys Leu 435 - # 440 - # 445 - - Ser Lys Ile Cys Met Asp Arg Asn Ile Ala Il - #e Val Phe Phe Pro Cys 450 - # 455 - # 460 - - Gly His Leu Ala Thr Cys Lys Gln Cys Ala Gl - #u Ala Val Asp Lys Cys 465 4 - #70 4 - #75 4 -#80 - - Pro Met Cys Tyr Thr Val Ile Thr Phe Asn Gl - #n Lys Ile Phe MetSer 485 - # 490 - # 495 - - - - (2) INFORMATION FOR SEQ ID NO:11: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 67 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:11: - - Lys Ala Ala Arg Leu Gly Thr Tyr Thr Asn Tr - #p Pro Val Gln Phe Leu 1 5 - # 10 - # 15 - - Glu Pro Ser Arg Met Ala Ala Ser Gly Phe Ty - #r Tyr Leu Gly Arg Gly 20 - # 25 - # 30 - - Asp Glu Val Arg Cys Ala Phe Cys Lys Val Gl - #u Ile Thr Asn Trp Val 35 - # 40 - # 45 - - Arg Gly Asp Asp Pro Glu Thr Asp His Lys Ar - #g Trp Ala Pro Gln Cys 50 - # 55 - # 60 - - Pro Phe Val 65 - - - - (2) INFORMATION FOR SEQ ID NO:12: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 275 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:12: - - Met Ser Asp Leu Arg Leu Glu Glu Val Arg Le - #u Asn Thr Phe Glu Lys 1 5 - # 10 - # 15 - - Trp Pro Val Ser Phe Leu Ser Pro Glu Thr Me - #t Ala Lys Asn Gly Phe 20 - # 25 - # 30 - - Tyr Tyr Leu Gly Arg Ser Asp Glu Val Arg Cy - #s Ala Phe Cys Lys Val 35 - # 40 - # 45 - - Glu Ile Met Arg Trp Lys Glu Gly Glu Asp Pr - #o Ala Ala Asp His Lys 50 - # 55 - # 60 - - Lys Trp Ala Pro Gln Cys Pro Phe Val Lys Gl - #y Ile Asp Val Cys Gly 65 - #70 - #75 - #80 - - Ser Ile Val Thr Thr Asn Asn Ile Gln Asn Th - #r Thr Thr His Asp Thr 85 - # 90 - # 95 - - Ile Ile Gly Pro Ala His Pro Lys Tyr Ala Hi - #s Glu Ala Ala Arg Val 100 - # 105 - # 110 - - Lys Ser Phe His Asn Trp Pro Arg Cys Met Ly - #s Gln Arg Pro Glu Gln 115 - # 120 - # 125 - - Met Ala Asp Ala Gly Phe Phe Tyr Thr Gly Ty - #r Gly Asp Asn Thr Lys 130 - # 135 - # 140 - - Cys Phe Tyr Cys Asp Gly Gly Leu Lys Asp Tr - #p Glu Pro Glu Asp Val 145 1 - #50 1 - #55 1 -#60 - - Pro Trp Glu Gln His Val Arg Trp Phe Asp Ar - #g Cys Ala Tyr ValGln 165 - # 170 - # 175 - - Leu Val Lys Gly Arg Asp Tyr Val Gln Lys Va - #l Ile Thr Glu Ala Cys 180 - # 185 - # 190 - - Val Leu Pro Gly Glu Asn Thr Thr Val Ser Th - #r Ala Ala Pro Val Ser 195 - # 200 - # 205 - - Glu Pro Ile Pro Glu Thr Lys Ile Glu Lys Gl - #u Pro Gln Val Glu Asp 210 - # 215 - # 220 - - Ser Lys Leu Cys Lys Ile Cys Tyr Val Glu Gl - #u Cys Ile Val Cys Phe 225 2 - #30 2 - #35 2 -#40 - - Val Pro Cys Gly His Val Val Ala Cys Ala Ly - #s Cys Ala Leu SerVal 245 - # 250 - # 255 - - Asp Lys Cys Pro Met Cys Arg Lys Ile Val Th - #r Ser Val Leu Lys Val 260 - # 265 - # 270 - - Tyr Phe Ser 275 - - - - (2) INFORMATION FOR SEQ ID NO:13: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 498 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:13: - - Met Thr Glu Leu Gly Met Glu Leu Glu Ser Va - #l Arg Leu Ala Thr Phe 1 5 - # 10 - # 15 - - Gly Glu Trp Pro Leu Asn Ala Pro Val Ser Al - #a Glu Asp Leu Val Ala 20 - # 25 - # 30 - - Asn Gly Phe Phe Ala Thr Gly Lys Trp Leu Gl - #u Ala Glu Cys His Phe 35 - # 40 - # 45 - - Cys His Val Arg Ile Asp Arg Trp Glu Tyr Gl - #y Asp Gln Val Ala Glu 50 - # 55 - # 60 - - Arg His Arg Arg Ser Ser Pro Ile Cys Ser Me - #t Val Leu Ala Pro Asn 65 - #70 - #75 - #80 - - His Cys Gly Asn Val Pro Arg Ser Gln Glu Se - #r Asp Asn Glu Gly Asn 85 - # 90 - # 95 - - Ser Val Val Asp Ser Pro Glu Ser Cys Ser Cy - #s Pro Asp Leu Leu Leu 100 - # 105 - # 110 - - Glu Ala Asn Arg Leu Val Thr Phe Lys Asp Tr - #p Pro Asn Pro Asn Ile 115 - # 120 - # 125 - - Thr Pro Gln Ala Leu Ala Lys Ala Gly Phe Ty - #r Tyr Leu Asn Arg Leu 130 - # 135 - # 140 - - Asp His Val Lys Cys Val Trp Cys Asn Gly Va - #l Ile Ala Lys Trp Glu 145 1 - #50 1 - #55 1 -#60 - - Lys Asn Asp Asn Ala Phe Glu Glu His Lys Ar - #g Phe Phe Pro GlnCys 165 - # 170 - # 175 - - Pro Arg Val Gln Met Gly Pro Leu Ile Glu Ph - #e Ala Thr Gly Lys Asn 180 - # 185 - # 190 - - Leu Asp Glu Leu Gly Ile Gln Pro Thr Thr Le - #u Pro Leu Arg Pro Lys 195 - # 200 - # 205 - - Tyr Ala Cys Val Asp Ala Arg Leu Arg Thr Ph - #e Thr Asp Trp Pro Ile 210 - # 215 - # 220 - - Ser Asn Ile Gln Pro Ala Ser Ala Leu Ala Gl - #n Ala Gly Leu Tyr Tyr 225 2 - #30 2 - #35 2 -#40 - - Gln Lys Ile Gly Asp Gln Val Arg Cys Phe Hi - #s Cys Asn Ile GlyLeu 245 - # 250 - # 255 - - Arg Ser Trp Gln Lys Glu Asp Glu Pro Trp Ph - #e Glu His Ala Lys Trp 260 - # 265 - # 270 - - Ser Pro Lys Cys Gln Phe Val Leu Leu Ala Ly - #s Gly Pro Ala Tyr Val 275 - # 280 - # 285 - - Ser Glu Val Leu Ala Thr Thr Ala Ala Asn Al - #a Ser Ser Gln Pro Ala 290 - # 295 - # 300 - - Thr Ala Pro Ala Pro Thr Leu Gln Ala Asp Va - #l Leu Met Asp Glu Ala 305 3 - #10 3 - #15 3 -#20 - - Pro Ala Lys Glu Ala Leu Thr Leu Gly Ile As - #p Gly Gly Val ValArg 325 - # 330 - # 335 - - Asn Ala Ile Gln Arg Lys Leu Leu Ser Ser Gl - #y Cys Ala Phe Ser Thr 340 - # 345 - # 350 - - Leu Asp Glu Leu Leu His Asp Ile Phe Asp As - #p Ala Gly Ala Gly Ala 355 - # 360 - # 365 - - Ala Leu Glu Val Arg Glu Pro Pro Glu Pro Se - #r Ala Pro Phe Ile Glu 370 - # 375 - # 380 - - Pro Cys Gln Ala Thr Thr Ser Lys Ala Ala Se - #r Val Pro Ile Pro Val 385 3 - #90 3 - #95 4 -#00 - - Ala Asp Ser Ile Pro Ala Lys Pro Gln Ala Al - #a Glu Ala Val SerAsn 405 - # 410 - # 415 - - Ile Ser Lys Ile Thr Asp Glu Ile Gln Lys Me - #t Ser Val Ser Thr Pro 420 - # 425 - # 430 - - Asn Gly Asn Leu Ser Leu Glu Glu Glu Asn Ar - #g Gln Leu Lys Asp Ala 435 - # 440 - # 445 - - Arg Leu Cys Lys Val Cys Leu Asp Glu Glu Va - #l Gly Val Val Phe Leu 450 - # 455 - # 460 - - Pro Cys Gly His Leu Ala Thr Cys Asn Gln Cy - #s Ala Pro Ser Val Ala 465 4 - #70 4 - #75 4 -#80 - - Asn Cys Pro Met Cys Arg Ala Asp Ile Lys Gl - #y Phe Val Arg ThrPhe 485 - # 490 - # 495 - - Leu Ser - - - - (2) INFORMATION FOR SEQ ID NO:14: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 67 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:14: - - Glu Glu Val Arg Leu Asn Thr Phe Glu Lys Tr - #p Pro Val Ser Phe Leu 1 5 - # 10 - # 15 - - Ser Pro Glu Thr Met Ala Lys Asn Gly Phe Ty - #r Tyr Leu Gly Arg Ser 20 - # 25 - # 30 - - Asp Glu Val Arg Cys Ala Phe Cys Lys Val Gl - #u Ile Met Arg Trp Lys 35 - # 40 - # 45 - - Glu Gly Glu Asp Pro Ala Ala Asp His Lys Ly - #s Trp Ala Pro Gln Cys 50 - # 55 - # 60 - - Pro Phe Val 65 - - - - (2) INFORMATION FOR SEQ ID NO:15: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 67 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:15: - - Glu Ala Asn Arg Leu Val Thr Phe Lys Asp Tr - #p Pro Asn Pro Asn Ile 1 5 - # 10 - # 15 - - Thr Pro Gln Ala Leu Ala Lys Ala Gly Phe Ty - #r Tyr Leu Asn Arg Leu 20 - # 25 - # 30 - - Asp His Val Lys Cys Val Trp Cys Asn Gly Va - #l Ile Ala Lys Trp Glu 35 - # 40 - # 45 - - Lys Asn Asp Asn Ala Phe Glu Glu His Lys Ar - #g Phe Phe Pro Gln Cys 50 - # 55 - # 60 - - Pro Arg Val 65 - - - - (2) INFORMATION FOR SEQ ID NO:16: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 68 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:16: - - Glu Phe Asn Arg Leu Lys Thr Phe Ala Asn Ph - #e Pro Ser Ser Ser Pro 1 5 - # 10 - # 15 - - Val Ser Ala Ser Thr Leu Ala Arg Ala Gly Ph - #e Leu Tyr Thr Gly Glu 20 - # 25 - # 30 - - Gly Asp Thr Val Gln Cys Phe Ser Cys His Al - #a Ala Ile Asp Arg Trp 35 - # 40 - # 45 - - Gln Tyr Gly Asp Ser Ala Val Gly Arg His Ar - #g Arg Ile Ser Pro Asn 50 - # 55 - # 60 - - Cys Arg Phe Ile 65 - - - - (2) INFORMATION FOR SEQ ID NO:17: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 68 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:17: - - Glu Phe Asn Arg Leu Lys Thr Phe Ala Asn Ph - #e Pro Ser Gly Ser Pro 1 5 - # 10 - # 15 - - Val Ser Ala Ser Thr Leu Ala Arg Ala Gly Ph - #e Leu Tyr Thr Gly Glu 20 - # 25 - # 30 - - Gly Asp Thr Val Arg Cys Phe Ser Cys His Al - #a Ala Val Asp Arg Trp 35 - # 40 - # 45 - - Gln Tyr Gly Asp Ser Ala Val Gly Arg His Ar - #g Lys Val Ser Pro Asn 50 - # 55 - # 60 - - Cys Arg Phe Ile 65 - - - - (2) INFORMATION FOR SEQ ID NO:18: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 68 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:18: - - Glu Leu Tyr Arg Met Ser Thr Tyr Ser Thr Ph - #e Pro Ala Gly Val Pro 1 5 - # 10 - # 15 - - Val Ser Glu Arg Ser Leu Ala Arg Ala Gly Ph - #e Tyr Tyr Thr Gly Val 20 - # 25 - # 30 - - Asn Asp Lys Val Lys Cys Phe Cys Cys Gly Le - #u Met Leu Asp Asn Trp 35 - # 40 - # 45 - - Lys Arg Gly Asp Ser Pro Thr Glu Lys His Ly - #s Lys Leu Tyr Pro Ser 50 - # 55 - # 60 - - Cys Arg Phe Val 65 - - - - (2) INFORMATION FOR SEQ ID NO:19: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 68 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:19: - - Glu Leu Tyr Arg Met Ser Thr Tyr Ser Thr Ph - #e Pro Ala Gly Val Pro 1 5 - # 10 - # 15 - - Val Ser Glu Arg Ser Leu Ala Arg Ala Gly Ph - #e Tyr Tyr Thr Gly Val 20 - # 25 - # 30 - - Asn Asp Lys Val Lys Cys Phe Cys Cys Gly Le - #u Met Leu Asp Asn Trp 35 - # 40 - # 45 - - Lys Leu Gly Asp Ser Pro Ile Gln Lys His Ly - #s Gln Leu Tyr Pro Ser 50 - # 55 - # 60 - - Cys Ser Phe Ile 65 - - - - (2) INFORMATION FOR SEQ ID NO:20: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 68 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:20: - - Glu Glu Ala Arg Leu Lys Ser Phe Gln Asn Tr - #p Pro Asp Tyr Ala His 1 5 - # 10 - # 15 - - Leu Thr Pro Arg Glu Leu Ala Ser Ala Gly Le - #u Tyr Tyr Thr Gly Ala 20 - # 25 - # 30 - - Asp Asp Gln Val Gln Cys Phe Cys Cys Gly Gl - #y Lys Leu Lys Asn Trp 35 - # 40 - # 45 - - Glu Pro Cys Asp Arg Ala Trp Ser Glu His Ar - #g Arg His Phe Pro Asn 50 - # 55 - # 60 - - Cys Phe Phe Val 65 - - - - (2) INFORMATION FOR SEQ ID NO:21: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 68 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:21: - - Glu Glu Ala Arg Leu Lys Ser Phe Gln Asn Tr - #p Pro Asp Tyr Ala His 1 5 - # 10 - # 15 - - Leu Thr Pro Arg Glu Leu Ala Ser Ala Gly Le - #u Tyr Tyr Thr Gly Ile 20 - # 25 - # 30 - - Gly Asp Gln Val Gln Cys Phe Cys Cys Gly Gl - #y Lys Leu Lys Asn Trp 35 - # 40 - # 45 - - Glu Pro Cys Asp Arg Ala Trp Ser Glu His Ar - #g Arg His Phe Pro Asn 50 - # 55 - # 60 - - Cys Phe Phe Val 65 - - - - (2) INFORMATION FOR SEQ ID NO:22: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 67 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:22: - - Glu Asn Ala Arg Leu Leu Thr Phe Gln Thr Tr - #p Pro Leu Thr Phe Leu 1 5 - # 10 - # 15 - - Ser Pro Thr Asp Leu Ala Arg Ala Gly Phe Ty - #r Tyr Ile Gly Pro Gly 20 - # 25 - # 30 - - Asp Arg Val Ala Cys Phe Ala Cys Gly Gly Ly - #s Leu Ser Asn Trp Glu 35 - # 40 - # 45 - - Pro Lys Asp Asn Ala Met Ser Glu His Leu Ar - #g His Phe Pro Lys Cys 50 - # 55 - # 60 - - Pro Phe Ile 65 - - - - (2) INFORMATION FOR SEQ ID NO:23: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 67 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:23: - - Glu Glu Ala Arg Phe Leu Thr Tyr His Met Tr - #p Pro Leu Thr Phe Leu 1 5 - # 10 - # 15 - - Ser Pro Ser Glu Leu Ala Arg Ala Gly Phe Ty - #r Tyr Ile Gly Pro Gly 20 - # 25 - # 30 - - Asp Arg Val Ala Cys Phe Ala Cys Gly Gly Ly - #s Leu Ser Asn Trp Glu 35 - # 40 - # 45 - - Pro Lys Asp Asp Ala Met Ser Glu His Arg Ar - #g His Phe Pro Asn Cys 50 - # 55 - # 60 - - Pro Phe Leu 65 - - - - (2) INFORMATION FOR SEQ ID NO:24: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 66 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:24: - - Tyr Glu Ala Arg Ile Val Thr Phe Gly Thr Tr - #p Ile Tyr Ser Val Asn 1 5 - # 10 - # 15 - - Lys Glu Gln Leu Ala Arg Ala Gly Phe Tyr Al - #a Leu Gly Glu Gly Asp 20 - # 25 - # 30 - - Lys Val Lys Cys Phe His Cys Gly Gly Gly Le - #u Thr Asp Trp Lys Pro 35 - # 40 - # 45 - - Ser Glu Asp Pro Trp Asp Gln His Ala Lys Cy - #s Tyr Pro Gly Cys Lys 50 - # 55 - # 60 - - Tyr Leu 65 - - - - (2) INFORMATION FOR SEQ ID NO:25: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 66 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:25: - - Tyr Glu Ala Arg Ile Phe Thr Phe Gly Thr Tr - #p Ile Tyr Ser Val Asn 1 5 - # 10 - # 15 - - Lys Glu Gln Leu Ala Arg Ala Gly Phe Tyr Al - #a Leu Gly Glu Gly Asp 20 - # 25 - # 30 - - Lys Val Lys Cys Phe His Cys Gly Gly Gly Le - #u Thr Asp Trp Lys Pro 35 - # 40 - # 45 - - Ser Glu Asp Pro Trp Glu Gln His Ala Lys Tr - #p Tyr Pro Gly Cys Lys 50 - # 55 - # 60 - - Tyr Leu 65 - - - - (2) INFORMATION FOR SEQ ID NO:26: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 68 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:26: - - His Ala Ala Arg Phe Lys Thr Phe Phe Asn Tr - #p Pro Ser Ser Val Leu 1 5 - # 10 - # 15 - - Val Asn Pro Glu Gln Leu Ala Ser Ala Gly Ph - #e Tyr Tyr Val Gly Asn 20 - # 25 - # 30 - - Ser Asp Asp Val Lys Cys Phe Cys Cys Asp Gl - #y Gly Leu Arg Cys Trp 35 - # 40 - # 45 - - Glu Ser Gly Asp Asp Pro Trp Val Gln His Al - #a Lys Trp Phe Pro Arg 50 - # 55 - # 60 - - Cys Glu Tyr Leu 65 - - - - (2) INFORMATION FOR SEQ ID NO:27: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 68 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:27: - - His Ala Ala Arg Met Arg Thr Phe Met Tyr Tr - #p Pro Ser Ser Val Pro 1 5 - # 10 - # 15 - - Val Gln Pro Glu Gln Leu Ala Ser Ala Gly Ph - #e Tyr Tyr Val Gly Arg 20 - # 25 - # 30 - - Asn Asp Asp Val Lys Cys Phe Gly Cys Asp Gl - #y Gly Leu Arg Cys Trp 35 - # 40 - # 45 - - Glu Ser Gly Asp Asp Pro Trp Val Glu His Al - #a Lys Trp Phe Pro Arg 50 - # 55 - # 60 - - Cys Glu Phe Leu 65 - - - - (2) INFORMATION FOR SEQ ID NO:28: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 68 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:28: - - Glu Ala Ala Arg Leu Arg Thr Phe Ala Glu Tr - #p Pro Arg Gly Leu Lys 1 5 - # 10 - # 15 - - Gln Arg Pro Glu Glu Leu Ala Glu Ala Gly Ph - #e Phe Tyr Thr Gly Gln 20 - # 25 - # 30 - - Gly Asp Lys Thr Arg Cys Phe Cys Cys Asp Gl - #y Gly Leu Lys Asp Trp 35 - # 40 - # 45 - - Glu Pro Asp Asp Ala Pro Trp Gln Gln His Al - #a Arg Trp Tyr Asp Arg 50 - # 55 - # 60 - - Cys Glu Tyr Val 65 - - - - (2) INFORMATION FOR SEQ ID NO:29: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 68 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:29: - - Glu Ala Ala Arg Val Lys Ser Phe His Asn Tr - #p Pro Arg Cys Met Lys 1 5 - # 10 - # 15 - - Gln Arg Pro Glu Gln Met Ala Asp Ala Gly Ph - #e Phe Tyr Thr Gly Tyr 20 - # 25 - # 30 - - Gly Asp Asn Thr Lys Cys Phe Tyr Cys Asp Gl - #y Gly Leu Lys Asp Trp 35 - # 40 - # 45 - - Glu Pro Glu Asp Val Pro Trp Glu Gln His Va - #l Arg Trp Phe Asp Arg 50 - # 55 - # 60 - - Cys Ala Tyr Val 65 - - - - (2) INFORMATION FOR SEQ ID NO:30: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 68 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:30: - - Val Asp Ala Arg Leu Arg Thr Phe Thr Asp Tr - #p Pro Ile Ser Asn Ile 1 5 - # 10 - # 15 - - Gln Pro Ala Ser Ala Leu Ala Gln Ala Gly Le - #u Tyr Tyr Gln Lys Ile 20 - # 25 - # 30 - - Gly Asp Gln Val Arg Cys Phe His Cys Asn Il - #e Gly Leu Arg Ser Trp 35 - # 40 - # 45 - - Gln Lys Glu Asp Glu Pro Trp Phe Glu His Al - #a Lys Trp Ser Pro Lys 50 - # 55 - # 60 - - Cys Gln Phe Val 65 - - - - (2) INFORMATION FOR SEQ ID NO:31: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 66 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:31: - - Glu Ser Val Arg Leu Ala Thr Phe Gly Glu Tr - #p Pro Leu Asn Ala Pro 1 5 - # 10 - # 15 - - Val Ser Ala Glu Asp Leu Val Ala Asn Gly Ph - #e Phe Gly Thr Trp Met 20 - # 25 - # 30 - - Glu Ala Glu Cys Asp Phe Cys His Val Arg Il - #e Asp Arg Trp Glu Tyr 35 - # 40 - # 45 - - Gly Asp Leu Val Ala Glu Arg His Arg Arg Se - #r Ser Pro Ile Cys Ser 50 - # 55 - # 60 - - Met Val 65 - - - - (2) INFORMATION FOR SEQ ID NO:32: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 46 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:32: - - Glu Gln Leu Arg Arg Leu Gln Glu Glu Arg Th - #r Cys Lys Val Cys Met 1 5 - # 10 - # 15 - - Asp Lys Glu Val Ser Val Val Phe Ile Pro Cy - #s Gly His Leu Val Val 20 - # 25 - # 30 - - Cys Gln Glu Cys Ala Pro Ser Leu Arg Lys Cy - #s Pro Ile Cys 35 - # 40 - # 45 - - - - (2) INFORMATION FOR SEQ ID NO:33: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 46 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:33: - - Glu Gln Leu Arg Arg Leu Pro Glu Glu Arg Th - #r Cys Lys Val Cys Met 1 5 - # 10 - # 15 - - Asp Lys Glu Val Ser Ile Val Phe Ile Pro Cy - #s Gly His Leu Val Val 20 - # 25 - # 30 - - Cys Lys Asp Cys Ala Pro Ser Leu Arg Lys Cy - #s Pro Ile Cys 35 - # 40 - # 45 - - - - (2) INFORMATION FOR SEQ ID NO:34: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 46 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:34: - - Glu Gln Leu Arg Arg Leu Gln Glu Glu Lys Le - #u Ser Lys Ile Cys Met 1 5 - # 10 - # 15 - - Asp Arg Asn Ile Ala Ile Val Phe Phe Pro Cy - #s Gly His Leu Ala Thr 20 - # 25 - # 30 - - Cys Lys Gln Cys Ala Glu Ala Val Asp Lys Cy - #s Pro Met Cys 35 - # 40 - # 45 - - - - (2) INFORMATION FOR SEQ ID NO:35: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 46 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:35: - - Glu Gln Leu Arg Arg Leu Gln Glu Glu Lys Le - #u Cys Lys Ile Cys Met 1 5 - # 10 - # 15 - - Asp Arg Asn Ile Ala Ile Val Phe Val Pro Cy - #s Gly His Leu Val Thr 20 - # 25 - # 30 - - Cys Lys Gln Cys Ala Glu Ala Val Asp Lys Cy - #s Pro Met Cys 35 - # 40 - # 45 - - - - (2) INFORMATION FOR SEQ ID NO:36: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 46 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:36: - - Glu Glu Asn Arg Gln Leu Lys Asp Ala Arg Le - #u Cys Lys Val Cys Leu 1 5 - # 10 - # 15 - - Asp Glu Glu Val Gly Val Val Phe Leu Pro Cy - #s Gly His Leu Ala Thr 20 - # 25 - # 30 - - Cys Asn Gln Cys Ala Pro Ser Val Ala Asn Cy - #s Pro Met Cys 35 - # 40 - # 45 - - - - (2) INFORMATION FOR SEQ ID NO:37: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 46 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:37: - - Glu Lys Glu Pro Gln Val Glu Asp Ser Lys Le - #u Cys Lys Ile Cys Tyr 1 5 - # 10 - # 15 - - Val Glu Glu Cys Ile Val Cys Phe Val Pro Cy - #s Gly His Val Val Ala 20 - # 25 - # 30 - - Cys Ala Lys Cys Ala Leu Ser Val Asp Lys Cy - #s Pro Met Cys 35 - # 40 - # 45 - - - - (2) INFORMATION FOR SEQ ID NO:38: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 46 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: both - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:38: - - Ala Val Glu Ala Glu Val Ala Asp Asp Arg Le - #u Cys Lys Ile Cys Leu 1 5 - # 10 - # 15 - - Gly Ala Glu Lys Thr Val Cys Phe Val Pro Cy - #s Gly His Val Val Ala 20 - # 25 - # 30 - - Cys Gly Lys Cys Ala Ala Gly Val Thr Thr Cy - #s Pro Val Cys 35 - # 40 - # 45 - - - - (2) INFORMATION FOR SEQ ID NO:39: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 2474 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:39: - - GAATTCCGGG AGACCTACAC CCCCGGAGAT CAGAGGTCAT TGCTGGCGTT CA -#GAGCCTAG 60 - - GAAGTGGGCT GCGGTATCAG CCTAGCAGTA AAACCGACCA GAAGCCATGC AC -#AAAACTAC 120 - - ATCCCCAGAG AAAGACTTGT CCCTTCCCCT CCCTGTCATC TCACCATGAA CA -#TGGTTCAA 180 - - GACAGCGCCT TTCTAGCCAA GCTGATGAAG AGTGCTGACA CCTTTGAGTT GA -#AGTATGAC 240 - - TTTTCCTGTG AGCTGTACCG ATTGTCCACG TATTCAGCTT TTCCCAGGGG AG -#TTCCTGTG 300 - - TCAGAAAGGA GTCTGGCTCG TGCTGGCTTT TACTACACTG GTGCCAATGA CA -#AGGTCAAG 360 - - TGCTTCTGCT GTGGCCTGAT GCTAGACAAC TGGAAACAAG GGGACAGTCC CA -#TGGAGAAG 420 - - CACAGAAAGT TGTACCCCAG CTGCAACTTT GTACAGACTT TGAATCCAGC CA -#ACAGTCTG 480 - - GAAGCTAGTC CTCGGCCTTC TCTTCCTTCC ACGGCGATGA GCACCATGCC TT -#TGAGCTTT 540 - - GCAAGTTCTG AGAATACTGG CTATTTCAGT GGCTCTTACT CGAGCTTTCC CT -#CAGACCCT 600 - - GTGAACTTCC GAGCAAATCA AGATTGTCCT GCTTTGAGCA CAAGTCCCTA CC -#ACTTTGCA 660 - - ATGAACACAG AGAAGGCCAG ATTACTCACC TATGAAACAT GGCCATTGTC TT -#TTCTGTCA 720 - - CCAGCAAAGC TGGCCAAAGC AGGCTTCTAC TACATAGGAC CTGGAGATAG AG -#TGGCCTGC 780 - - TTTGCGTGCG ATGGGAAACT GAGCAACTGG GAACGTAAGG ATGATGCTAT GT -#CAGAGCAC 840 - - CAGAGGCATT TCCCCAGCTG TCCGTTCTTA AAAGACTTGG GTCAGTCTGC TT -#CGAGATAC 900 - - ACTGTCTCTA ACCTGAGCAT GCAGACACAC GCAGCCCGTA TTAGAACATT CT -#CTAACTGG 960 - - CCTTCTAGTG CACTAGTTCA TTCCCAGGAA CTTGCAAGTG CGGGCTTTTA TT -#ATACAGGA 1020 - - CACAGTGATG ATGTCAAGTG TTTATGCTGT GATGGTGGGC TGAGGTGCTG GG -#AATCTGGA 1080 - - GATGACCCCT GGGTGGAACA TGCCAAGTGG TTTCCAAGGT GTGAGTACTT GC -#TCAGAATC 1140 - - AAAGGCCAAG AATTTGTCAG CCAAGTTCAA GCTGGCTATC CTCATCTACT TG -#AGCAGCTA 1200 - - TTATCTACGT CAGACTCCCC AGAAGATGAG AATGCAGACG CAGCAATCGT GC -#ATTTTGGC 1260 - - CCTGGAGAAA GTTCGGAAGA TGTCGTCATG ATGAGCACGC CTGTGGTTAA AG -#CAGCCTTG 1320 - - GAAATGGGCT TCAGTAGGAG CCTGGTGAGA CAGACGGTTC AGTGGCAGAT CC -#TGGCCACT 1380 - - GGTGAGAACT ACAGGACCGT CAGTGACCTC GTTATAGGCT TACTCGATGC AG -#AAGACGAG 1440 - - ATGAGAGAGG AGCAGATGGA GCAGGCGGCC GAGGAGGAGG AGTCAGATGA TC -#TAGCACTA 1500 - - ATCCGGAAGA ACAAAATGGT GCTTTTCCAA CATTTGACGT GTGTGACACC AA -#TGCTGTAT 1560 - - TGCCTCCTAA GTGCAAGGGC CATCACTGAA CAGGAGTGCA ATGCTGTGAA AC -#AGAAACCA 1620 - - CACACCTTAC AAGCAAGCAC ACTGATTGAT ACTGTGTTAG CAAAAGGAAA CA -#CTGCAGCA 1680 - - ACCTCATTCA GAAACTCCCT TCGGGAAATT GACCCTGCGT TATACAGAGA TA -#TATTTGTG 1740 - - CAACAGGACA TTAGGAGTCT TCCCACAGAT GACATTGCAG CTCTACCAAT GG -#AAGAACAG 1800 - - TTGCGGCCCC TCCCGGAGGA CAGAATGTGT AAAGTGTGTA TGGACCGAGA GG -#TATCCATC 1860 - - GTGTTCATTC CCTGTGGCCA TCTGGTCGTG TGCAAAGACT GCGCTCCCTC TC -#TGAGGAAG 1920 - - TGTCCCATCT GTAGAGGGAC CATCAAGGGC ACAGTGCGCA CATTTCTCTC CT -#GAACAAGA 1980 - - CTAATGGTCC ATGGCTGCAA CTTCAGCCAG GAGGAAGTTC ACTGTCACTC CC -#AGTTCCAT 2040 - - TCGGAACTTG AGGCCAGCCT GGATAGCACG AGACACCGCC AAACACACAA AT -#ATAAACAT 2100 - - GAAAAACTTT TGTCTGAAGT CAAGAATGAA TGAATTACTT ATATAATAAT TT -#TAATTGGT 2160 - - TTCCTTAAAA GTGCTATTTG TTCCCAACTC AGAAAATTGT TTTCTGTAAA CA -#TATTTACA 2220 - - TACTACCTGC ATCTAAAGTA TTCATATATT CATATATTCA GATGTCATGA GA -#GAGGGTTT 2280 - - TGTTCTTGTT CCTGAAAAGC TGGTTTATCA TCTGATCAGC ATATACTGCG CA -#ACGGGCAG 2340 - - GGCTAGAATC CATGAACCAA GCTGCAAAGA TCTCACGCTA AATAAGGCGG AA -#AGATTTGG 2400 - - AGAAACGAAA GGAAATTCTT TCCTGTCCAA TGTATACTCT TCAGACTAAT GA -#CCTCTTCC 2460 - - TATCAAGCCT TCTA - # - # - # 2474 - - - - (2) INFORMATION FOR SEQ ID NO:40: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 602 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: Not R - #elevant (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:40: - - Met Asn Met Val Gln Asp Ser Ala Phe Leu Al - #a Lys Leu Met Lys Ser 1 5 - # 10 - # 15 - - Ala Asp Thr Phe Glu Leu Lys Tyr Asp Phe Se - #r Cys Glu Leu Tyr Arg 20 - # 25 - # 30 - - Leu Ser Thr Tyr Ser Ala Phe Pro Arg Gly Va - #l Pro Val Ser Glu Arg 35 - # 40 - # 45 - - Ser Leu Ala Arg Ala Gly Phe Tyr Tyr Thr Gl - #y Ala Asn Asp Lys Val 50 - # 55 - # 60 - - Lys Cys Phe Cys Cys Gly Leu Met Leu Asp As - #n Trp Lys Gln Gly Asp 65 - #70 - #75 - #80 - - Ser Pro Met Glu Lys His Arg Lys Leu Tyr Pr - #o Ser Cys Asn Phe Val 85 - # 90 - # 95 - - Gln Thr Leu Asn Pro Ala Asn Ser Leu Glu Al - #a Ser Pro Arg Pro Ser 100 - # 105 - # 110 - - Leu Pro Ser Thr Ala Met Ser Thr Met Pro Le - #u Ser Phe Ala Ser Ser 115 - # 120 - # 125 - - Glu Asn Thr Gly Tyr Phe Ser Gly Ser Tyr Se - #r Ser Phe Pro Ser Asp 130 - # 135 - # 140 - - Pro Val Asn Phe Arg Ala Asn Gln Asp Cys Pr - #o Ala Leu Ser Thr Ser 145 1 - #50 1 - #55 1 -#60 - - Pro Tyr His Phe Ala Met Asn Thr Glu Lys Al - #a Arg Leu Leu ThrTyr 165 - # 170 - # 175 - - Glu Thr Trp Pro Leu Ser Phe Leu Ser Pro Al - #a Lys Leu Ala Lys Ala 180 - # 185 - # 190 - - Gly Phe Tyr Tyr Ile Gly Pro Gly Asp Arg Va - #l Ala Cys Phe Ala Cys 195 - # 200 - # 205 - - Asp Gly Lys Leu Ser Asn Trp Glu Arg Lys As - #p Asp Ala Met Ser Glu 210 - # 215 - # 220 - - His Gln Arg His Phe Pro Ser Cys Pro Phe Le - #u Lys Asp Leu Gly Gln 225 2 - #30 2 - #35 2 -#40 - - Ser Ala Ser Arg Tyr Thr Val Ser Asn Leu Se - #r Met Gln Thr HisAla 245 - # 250 - # 255 - - Ala Arg Ile Arg Thr Phe Ser Asn Trp Pro Se - #r Ser Ala Leu Val His 260 - # 265 - # 270 - - Ser Gln Glu Leu Ala Ser Ala Gly Phe Tyr Ty - #r Thr Gly His Ser Asp 275 - # 280 - # 285 - - Asp Val Lys Cys Leu Cys Cys Asp Gly Gly Le - #u Arg Cys Trp Glu Ser 290 - # 295 - # 300 - - Gly Asp Asp Pro Trp Val Glu His Ala Lys Tr - #p Phe Pro Arg Cys Glu 305 3 - #10 3 - #15 3 -#20 - - Tyr Leu Leu Arg Ile Lys Gly Gln Glu Phe Va - #l Ser Gln Val GlnAla 325 - # 330 - # 335 - - Gly Tyr Pro His Leu Leu Glu Gln Leu Leu Se - #r Thr Ser Asp Ser Pro 340 - # 345 - # 350 - - Glu Asp Glu Asn Ala Asp Ala Ala Ile Val Hi - #s Phe Gly Pro Gly Glu 355 - # 360 - # 365 - - Ser Ser Glu Asp Val Val Met Met Ser Thr Pr - #o Val Val Lys Ala Ala 370 - # 375 - # 380 - - Leu Glu Met Gly Phe Ser Arg Ser Leu Val Ar - #g Gln Thr Val Gln Trp 385 3 - #90 3 - #95 4 -#00 - - Gln Ile Leu Ala Thr Gly Glu Asn Tyr Arg Th - #r Val Ser Asp LeuVal 405 - # 410 - # 415 - - Ile Gly Leu Leu Asp Ala Glu Asp Glu Met Ar - #g Glu Glu Gln Met Glu 420 - # 425 - # 430 - - Gln Ala Ala Glu Glu Glu Glu Ser Asp Asp Le - #u Ala Leu Ile Arg Lys 435 - # 440 - # 445 - - Asn Lys Met Val Leu Phe Gln His Leu Thr Cy - #s Val Thr Pro Met Leu 450 - # 455 - # 460 - - Tyr Cys Leu Leu Ser Ala Arg Ala Ile Thr Gl - #u Gln Glu Cys Asn Ala 465 4 - #70 4 - #75 4 -#80 - - Val Lys Gln Lys Pro His Thr Leu Gln Ala Se - #r Thr Leu Ile AspThr 485 - # 490 - # 495 - - Val Leu Ala Lys Gly Asn Thr Ala Ala Thr Se - #r Phe Arg Asn Ser Leu 500 - # 505 - # 510 - - Arg Glu Ile Asp Pro Ala Leu Tyr Arg Asp Il - #e Phe Val Gln Gln Asp 515 - # 520 - # 525 - - Ile Arg Ser Leu Pro Thr Asp Asp Ile Ala Al - #a Leu Pro Met Glu Glu 530 - # 535 - # 540 - - Gln Leu Arg Pro Leu Pro Glu Asp Arg Met Cy - #s Lys Val Cys Met Asp 545 5 - #50 5 - #55 5 -#60 - - Arg Glu Val Ser Ile Val Phe Ile Pro Cys Gl - #y His Leu Val ValCys 565 - # 570 - # 575 - - Lys Asp Cys Ala Pro Ser Leu Arg Lys Cys Pr - #o Ile Cys Arg Gly Thr 580 - # 585 - # 590 - - Ile Lys Gly Thr Val Arg Thr Phe Leu Ser 595 - # 600 - - - - (2) INFORMATION FOR SEQ ID NO:41: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 2416 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:41: - - CTGTGGTGGA GATCTATTGT CCAAGTGGTG AGAAACTTCA TCTGGAAGTT TA -#AGCGGTCA 60 - - GAAATACTAT TACTACTCAT GGACAAAACT GTCTCCCAGA GACTCGCCCA AG -#GTACCTTA 120 - - CACCCAAAAA CTTAAACGTA TAATGGAGAA GAGCACAATC TTGTCAAATT GG -#ACAAAGGA 180 - - GAGCGAAGAA AAAATGAAGT TTGACTTTTC GTGTGAACTC TACCGAATGT CT -#ACATATTC 240 - - AGCTTTTCCC AGGGGAGTTC CTGTCTCAGA GAGGAGTCTG GCTCGTGCTG GC -#TTTTATTA 300 - - TACAGGTGTG AATGACAAAG TCAAGTGCTT CTGCTGTGGC CTGATGTTGG AT -#AACTGGAA 360 - - ACAAGGGGAC AGTCCTGTTG AAAAGCACAG ACAGTTCTAT CCCAGCTGCA GC -#TTTGTACA 420 - - GACTCTGCTT TCAGCCAGTC TGCAGTCTCC ATCTAAGAAT ATGTCTCCTG TG -#AAAAGTAG 480 - - ATTTGCACAT TCGTCACCTC TGGAACGAGG TGGCATTCAC TCCAACCTGT GC -#TCTAGCCC 540 - - TCTTAATTCT AGAGCAGTGG AAGACTTCTC ATCAAGGATG GATCCCTGCA GC -#TATGCCAT 600 - - GAGTACAGAA GAGGCCAGAT TTCTTACTTA CAGTATGTGG CCTTTAAGTT TT -#CTGTCACC 660 - - AGCAGAGCTG GCCAGAGCTG GCTTCTATTA CATAGGGCCT GGAGACAGGG TG -#GCCTGTTT 720 - - TGCCTGTGGT GGGAAACTGA GCAACTGGGA ACCAAAGGAT TATGCTATGT CA -#GAGCACCG 780 - - CAGACATTTT CCCCACTGTC CATTTCTGGA AAATACTTCA GAAACACAGA GG -#TTTAGTAT 840 - - ATCAAATCTA AGTATGCAGA CACACTCTGC TCGATTGAGG ACATTTCTGT AC -#TGGCCACC 900 - - TAGTGTTCCT GTTCAGCCCG AGCAGCTTGC AAGTGCTGGA TTCTATTACG TG -#GATCGCAA 960 - - TGATGATGTC AAGTGCCTTT GTTGTGATGG TGGCTTGAGA TGTTGGGAAC CT -#GGAGATGA 1020 - - CCCCTGGATA GAACACGCCA AATGGTTTCC AAGGTGTGAG TTCTTGATAC GG -#ATGAAGGG 1080 - - TCAGGAGTTT GTTGATGAGA TTCAAGCTAG ATATCCTCAT CTTCTTGAGC AG -#CTGTTGTC 1140 - - CACTTCAGAC ACCCCAGGAG AAGAAAATGC TGACCCTACA GAGACAGTGG TG -#CATTTTGG 1200 - - CCCTGGAGAA AGTTCGAAAG ATGTCGTCAT GATGAGCACG CCTGTGGTTA AA -#GCAGCCTT 1260 - - GGAAATGGGC TTCAGTAGGA GCCTGGTGAG ACAGACGGTT CAGCGGCAGA TC -#CTGGCCAC 1320 - - TGGTGAGAAC TACAGGACCG TCAATGATAT TGTCTCAGTA CTTTTGAATG CT -#GAAGATGA 1380 - - GAGAAGAGAA GAGGAGAAGG AAAGACAGAC TGAAGAGATG GCATCAGGTG AC -#TTATCACT 1440 - - GATTCGGAAG AATAGAATGG CCCTCTTTCA ACAGTTGACA CATGTCCTTC CT -#ATCCTGGA 1500 - - TAATCTTCTT GAGGCCAGTG TAATTACAAA ACAGGAACAT GATATTATTA GA -#CAGAAAAC 1560 - - ACAGATACCC TTACAAGCAA GAGAGCTTAT TGACACCGTT TTAGTCAAGG GA -#AATGCTGC 1620 - - AGCCAACATC TTCAAAAACT CTCTGAAGGG AATTGACTCC ACGTTATATG AA -#AACTTATT 1680 - - TGTGGAAAAG AATATGAAGT ATATTCCAAC AGAAGACGTT TCAGGCTTGT CA -#TTGGAAGA 1740 - - GCAGTTGCGG AGATTACAAG AAGAACGAAC TTGCAAAGTG TGTATGGACA GA -#GAGGTTTC 1800 - - TATTGTGTTC ATTCCGTGTG GTCATCTAGT AGTCTGCCAG GAATGTGCCC CT -#TCTCTAAG 1860 - - GAAGTGCCCC ATCTGCAGGG GGACAATCAA GGGGACTGTG CGCACATTTC TC -#TCATGAGT 1920 - - GAAGAATGGT CTGAAAGTAT TGTTGGACAT CAGAAGCTGT CAGAACAAAG AA -#TGAACTAC 1980 - - TGATTTCAGC TCTTCAGCAG GACATTCTAC TCTCTTTCAA GATTAGTAAT CT -#TGCTTTAT 2040 - - GAAGGGTAGC ATTGTATATT TAAGCTTAGT CTGTTGCAAG GGAAGGTCTA TG -#CTGTTGAG 2100 - - CTACAGGACT GTGTCTGTTC CAGAGCAGGA GTTGGGATGC TTGCTGTATG TC -#CTTCAGGA 2160 - - CTTCTTGGGA TTTGGGAATT TGGGGAAAGC TTTGGAATCC AGTGATGTGG AG -#CTCAGAAA 2220 - - TCCTGGAACC AGTGACTCTG GTACTCAGTA GATAGGGTAC CCTGTACTTC TT -#GGTGCTTT 2280 - - TCCAGTCTGG GAAATAAGGA GGAATCTGCT GCTGGTAAAA ATTTGCTGGA TG -#TGAGAAAT 2340 - - AGATGAAAGT GTTTCGGGTG GGGGCGTGCA TCAGTGTAGT GTGTGCAGGG AT -#GTATGCAG 2400 - - GCCAAACACT GTGTAG - # - # - # 2416 - - - - (2) INFORMATION FOR SEQ ID NO:42: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 591 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:42: - - Met Glu Lys Ser Thr Ile Leu Ser Asn Trp Th - #r Lys Glu Ser Glu Glu 1 5 - # 10 - # 15 - - Lys Met Lys Phe Asp Phe Ser Cys Glu Leu Ty - #r Arg Met Ser Thr Tyr 20 - # 25 - # 30 - - Ser Ala Phe Pro Arg Gly Val Pro Val Ser Gl - #u Arg Ser Leu Ala Arg 35 - # 40 - # 45 - - Ala Gly Phe Tyr Tyr Thr Gly Val Asn Asp Ly - #s Val Lys Cys Phe Cys 50 - # 55 - # 60 - - Cys Gly Leu Met Leu Asp Asn Trp Lys Gln Gl - #y Asp Ser Pro Val Glu 65 - #70 - #75 - #80 - - Lys His Arg Gln Phe Tyr Pro Ser Cys Ser Ph - #e Val Gln Thr Leu Leu 85 - # 90 - # 95 - - Ser Ala Ser Leu Gln Ser Pro Ser Lys Asn Me - #t Ser Pro Val Lys Ser 100 - # 105 - # 110 - - Arg Phe Ala His Ser Ser Pro Leu Glu Arg Gl - #y Gly Ile His Ser Asn 115 - # 120 - # 125 - - Leu Cys Ser Ser Pro Leu Asn Ser Arg Ala Va - #l Glu Asp Phe Ser Ser 130 - # 135 - # 140 - - Arg Met Asp Pro Cys Ser Tyr Ala Met Ser Th - #r Glu Glu Ala Arg Phe 145 1 - #50 1 - #55 1 -#60 - - Leu Thr Tyr Ser Met Trp Pro Leu Ser Phe Le - #u Ser Pro Ala GluLeu 165 - # 170 - # 175 - - Ala Arg Ala Gly Phe Tyr Tyr Ile Gly Pro Gl - #y Asp Arg Val Ala Cys 180 - # 185 - # 190 - - Phe Ala Cys Gly Gly Lys Leu Ser Asn Trp Gl - #u Pro Lys Asp Tyr Ala 195 - # 200 - # 205 - - Met Ser Glu His Arg Arg His Phe Pro His Cy - #s Pro Phe Leu Glu Asn 210 - # 215 - # 220 - - Thr Ser Glu Thr Gln Arg Phe Ser Ile Ser As - #n Leu Ser Met Gln Thr 225 2 - #30 2 - #35 2 -#40 - - His Ser Ala Arg Leu Arg Thr Phe Leu Tyr Tr - #p Pro Pro Ser ValPro 245 - # 250 - # 255 - - Val Gln Pro Glu Gln Leu Ala Ser Ala Gly Ph - #e Tyr Tyr Val Asp Arg 260 - # 265 - # 270 - - Asn Asp Asp Val Lys Cys Leu Cys Cys Asp Gl - #y Gly Leu Arg Cys Trp 275 - # 280 - # 285 - - Glu Pro Gly Asp Asp Pro Trp Ile Glu His Al - #a Lys Trp Phe Pro Arg 290 - # 295 - # 300 - - Cys Glu Phe Leu Ile Arg Met Lys Gly Gln Gl - #u Phe Val Asp Glu Ile 305 3 - #10 3 - #15 3 -#20 - - Gln Ala Arg Tyr Pro His Leu Leu Glu Gln Le - #u Leu Ser Thr SerAsp 325 - # 330 - # 335 - - Thr Pro Gly Glu Glu Asn Ala Asp Pro Thr Gl - #u Thr Val Val His Phe 340 - # 345 - # 350 - - Gly Pro Gly Glu Ser Ser Lys Asp Val Val Me - #t Met Ser Thr Pro Val 355 - # 360 - # 365 - - Val Lys Ala Ala Leu Glu Met Gly Phe Ser Ar - #g Ser Leu Val Arg Gln 370 - # 375 - # 380 - - Thr Val Gln Arg Gln Ile Leu Ala Thr Gly Gl - #u Asn Tyr Arg Thr Val 385 3 - #90 3 - #95 4 -#00 - - Asn Asp Ile Val Ser Val Leu Leu Asn Ala Gl - #u Asp Glu Arg ArgGlu 405 - # 410 - # 415 - - Glu Glu Lys Glu Arg Gln Thr Glu Glu Met Al - #a Ser Gly Asp Leu Ser 420 - # 425 - # 430 - - Leu Ile Arg Lys Asn Arg Met Ala Leu Phe Gl - #n Gln Leu Thr His Val 435 - # 440 - # 445 - - Leu Pro Ile Leu Asp Asn Leu Leu Glu Ala Se - #r Val Ile Thr Lys Gln 450 - # 455 - # 460 - - Glu His Asp Ile Ile Arg Gln Lys Thr Gln Il - #e Pro Leu Gln Ala Arg 465 4 - #70 4 - #75 4 -#80 - - Glu Leu Ile Asp Thr Val Leu Val Lys Gly As - #n Ala Ala Ala AsnIle 485 - # 490 - # 495 - - Phe Lys Asn Ser Leu Lys Gly Ile Asp Ser Th - #r Leu Tyr Glu Asn Leu 500 - # 505 - # 510 - - Phe Val Glu Lys Asn Met Lys Tyr Ile Pro Th - #r Glu Asp Val Ser Gly 515 - # 520 - # 525 - - Leu Ser Leu Glu Glu Gln Leu Arg Arg Leu Gl - #n Glu Glu Arg Thr Cys 530 - # 535 - # 540 - - Lys Val Cys Met Asp Arg Glu Val Ser Ile Va - #l Phe Ile Pro Cys Gly 545 5 - #50 5 - #55 5 -#60 - - His Leu Val Val Cys Gln Glu Cys Ala Pro Se - #r Leu Arg Lys CysPro 565 - # 570 - # 575 - - Ile Cys Arg Gly Thr Ile Lys Gly Thr Val Ar - #g Thr Phe Leu Ser 580 - # 585 - # 590 - - - - (2) INFORMATION FOR SEQ ID NO:43: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 11 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:43: - - Met Glu Gln Lys Leu Ile Ser Glu Glu Asp Le - #u 1 5 - # 10 - - - - (2) INFORMATION FOR SEQ ID NO:44: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 635 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: protein - - (ix) FEATURE: (A) NAME/KEY: Other (B) LOCATION: 1...1 (D) OTHER INFORMATION: - #Xaa at 1,2,3 and 635 can be anyamino - # acid or - #may be abse - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:44: - - Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xa - #a Xaa Xaa Xaa XaaXaa 1 5 - # 10 - # 15 - - Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Phe Xa - #a Xaa Glu Xaa Xaa Arg 20 - # 25 - # 30 - - Leu Xaa Thr Phe Xaa Xaa Phe Pro Xaa Xaa Xa - #a Pro Val Ser Xaa Xaa 35 - # 40 - # 45 - - Xaa Leu Ala Arg Ala Gly Phe Xaa Tyr Thr Gl - #y Xaa Xaa Asp Xaa Val 50 - # 55 - # 60 - - Xaa Cys Phe Xaa Cys Xaa Xaa Xaa Xaa Asp Xa - #a Trp Xaa Xaa Gly Asp 65 - #70 - #75 - #80 - - Ser Xaa Xaa Xaa Xaa His Xaa Xaa Xaa Xaa Pr - #o Xaa Cys Xaa Phe Ile 85 - # 90 - # 95 - - Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xa - #a Xaa Xaa Xaa Xaa Xaa 100 - # 105 - # 110 - - Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xa - #a Ser Xaa Xaa Xaa Xaa 115 - # 120 - # 125 - - Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Ty - #r Xaa Xaa Xaa Xaa Xaa 130 - # 135 - # 140 - - Xaa Xaa Xaa Xaa Xaa Arg Xaa Xaa Glu Xaa Xa - #a Xaa Xaa Xaa Xaa Xaa 145 1 - #50 1 - #55 1 -#60 - - Xaa Xaa Xaa Xaa Xaa Xaa Asp Xaa Ser Asp Xa - #a Xaa Xaa Xaa XaaXaa 165 - # 170 - # 175 - - Xaa Xaa Xaa Met Xaa Xaa Glu Glu Ala Arg Le - #u Xaa Thr Phe Xaa Xaa 180 - # 185 - # 190 - - Trp Pro Xaa Xaa Xaa Xaa Leu Xaa Pro Xaa Gl - #u Leu Ala Xaa Ala Gly 195 - # 200 - # 205 - - Phe Tyr Tyr Xaa Gly Xaa Xaa Asp Xaa Val Xa - #a Cys Phe Xaa Cys Gly 210 - # 215 - # 220 - - Gly Lys Leu Xaa Asn Trp Glu Pro Xaa Asp Xa - #a Ala Xaa Ser Glu His 225 2 - #30 2 - #35 2 -#40 - - Xaa Arg His Phe Pro Xaa Cys Pro Phe Val Xa - #a Xaa Xaa Xaa XaaXaa 245 - # 250 - # 255 - - Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xa - #a Xaa Xaa Phe Xaa Xaa 260 - # 265 - # 270 - - Ser Xaa Xaa Xaa Pro Xaa Asn Pro Xaa Met Al - #a Xaa Xaa Xaa Ala Arg 275 - # 280 - # 285 - - Xaa Xaa Thr Phe Xaa Xaa Trp Pro Xaa Ser Xa - #a Xaa Val Xaa Xaa Glu 290 - # 295 - # 300 - - Gln Leu Ala Xaa Ala Gly Phe Tyr Tyr Xaa Gl - #y Xaa Gly Asp Xaa Val 305 3 - #10 3 - #15 3 -#20 - - Lys Cys Phe Xaa Cys Xaa Gly Gly Leu Xaa Xa - #a Trp Xaa Xaa XaaAsp 325 - # 330 - # 335 - - Asp Pro Trp Xaa Gln His Ala Lys Trp Phe Pr - #o Xaa Cys Xaa Tyr Leu 340 - # 345 - # 350 - - Xaa Xaa Xaa Lys Gly Gln Glu Tyr Xaa Xaa Xa - #a Xaa Xaa Xaa Xaa Xaa 355 - # 360 - # 365 - - Xaa Xaa Leu Xaa Glu Xaa Leu Xaa Xaa Thr Xa - #a Xaa Xaa Xaa Xaa Xaa 370 - # 375 - # 380 - - Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xa - #a Pro Xaa Xaa Xaa Xaa 385 3 - #90 3 - #95 4 -#00 - - Xaa Xaa Asp Xaa Val Xaa Xaa Xaa Xaa Pro Xa - #a Val Xaa Xaa AlaXaa 405 - # 410 - # 415 - - Xaa Met Gly Phe Xaa Xaa Xaa Xaa Val Lys Xa - #a Xaa Xaa Xaa Xaa Lys 420 - # 425 - # 430 - - Ile Xaa Xaa Xaa Gly Xaa Xaa Tyr Xaa Xaa Xa - #a Xaa Xaa Leu Val Xaa 435 - # 440 - # 445 - - Asp Leu Xaa Xaa Ala Xaa Xaa Xaa Xaa Xaa Xa - #a Xaa Glu Xaa Xaa Xaa 450 - # 455 - # 460 - - Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xa - #a Xaa Xaa Xaa Xaa Xaa 465 4 - #70 4 - #75 4 -#80 - - Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xa - #a Xaa Xaa Xaa XaaXaa 485 - # 490 - # 495 - - Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xa - #a Xaa Xaa Xaa Xaa Xaa 500 - # 505 - # 510 - - Xaa Xaa Xaa Xaa Gln Xaa Xaa Leu Gln Xaa Xa - #a Xaa Xaa Xaa Xaa Xaa 515 - # 520 - # 525 - - Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xa - #a Xaa Xaa Xaa Xaa Xaa 530 - # 535 - # 540 - - Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xa - #a Xaa Xaa Xaa Xaa Xaa 545 5 - #50 5 - #55 5 -#60 - - Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xa - #a Xaa Ser Xaa GluGlu 565 - # 570 - # 575 - - Gln Leu Arg Arg Leu Xaa Glu Glu Xaa Leu Cy - #s Lys Xaa Cys Met Asp 580 - # 585 - # 590 - - Xaa Glu Val Xaa Xaa Val Phe Xaa Pro Cys Gl - #y His Leu Val Xaa Cys 595 - # 600 - # 605 - - Xaa Xaa Cys Ala Xaa Ser Val Xaa Lys Cys Pr - #o Met Cys Arg Xaa Xaa 610 - # 615 - # 620 - - Ile Xaa Xaa Xaa Xaa Xaa Xaa Phe Leu Ser Xa - #a 625 6 - #30 6 - #35 - - - - (2) INFORMATION FOR SEQ ID NO:45: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 204 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (ix) FEATURE: (A) NAME/KEY: Coding Se - #quence (B) LOCATION: 1...0 (D) OTHER INFORMATION: - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:45: - - GAGTTTAATA GATTAAAAAC TTTTGCTAAT TTTCCAAGTG GTAGTCCTGT TT -#CAGCATCA 60 - - ACACTGGCAC GAGCAGGGTT TCTTTATACT GGTGAAGGAG ATACCGTGCG GT -#GCTTTAGT 120 - - TGTCATGCAG CTGTAGATAG ATGGCAATAT GGAGACTCAG CAGTTGGAAG AC -#ACAGGAAA 180 - - GTATCCCCAA ATTGCAGATT TATC - # - # 204 - - - - (2) INFORMATION FOR SEQ ID NO:46: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 204 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:46: - - GAAGAAGCTA GATTAAAGTC CTTTCAGAAC TGGCCAGACT ATGCTCACCT AA -#CCCCAAGA 60 - - GAGTTAGCAA GTGCTGGACT CTACTACACA GGTATTGGTG ACCAAGTGCA GT -#GCTTTTGT 120 - - TGTGGTGGAA AACTGAAAAA TTGGGAACCT TGTGATCGTG CCTGGTCAGA AC -#ACAGGCGA 180 - - CACTTTCCTA ATTGCTTCTT TGTT - # - # 204 - - - - (2) INFORMATION FOR SEQ ID NO:47: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 198 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:47: - - TATGAAGCAC GGATCTTTAC TTTTGGGACA TGGATATACT CAGTTAACAA GG -#AGCAGCTT 60 - - GCAAGAGCTG GATTTTATGC TTTAGGTGAA GGTGATAAAG TAAAGTGCTT TC -#ACTGTGGA 120 - - GGAGGGCTAA CTGATTGGAA GCCCAGTGAA GACCCTTGGG AACAACATGC TA -#AATGGTAT 180 - - CCAGGGTGCA AATATCTG - # - # - # 198 - - - - (2) INFORMATION FOR SEQ ID NO:48: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 138 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:48: - - GAGCAGCTAA GGCGCCTGCA AGAGGAGAAG CTTTGCAAAA TCTGTATGGA TA -#GAAATATT 60 - - GCTATCGTTT TTGTTCCTTG TGGACATCTA GTCACTTGTA AACAATGTGC TG -#AAGCAGTT 120 - - GACAAGTGTC CCATGTGC - # - # - # 138 - - - - (2) INFORMATION FOR SEQ ID NO:49: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 204 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:49: - - GAGTTTAATA GATTAAAAAC ATTTGCTAAC TTCCCAAGTA GTAGTCCTGT TT -#CAGCATCA 60 - - ACATTGGCGC GAGCTGGGTT TCTTTATACC GGTGAAGGAG ACACCGTGCA AT -#GTTTCAGT 120 - - TGTCATGCGG CAATAGATAG ATGGCAGTAT GGAGACTCAG CTGTTGGAAG AC -#ACAGGAGA 180 - - ATATCCCCAA ATTGCAGATT TATC - # - # 204 - - - - (2) INFORMATION FOR SEQ ID NO:50: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 204 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:50: - - GAAGAAGCCA GATTGAAGTC ATTTCAGAAC TGGCCGGACT ATGCTCATTT AA -#CCCCCAGA 60 - - GAGTTAGCTA GTGCTGGCCT CTACTACACA GGGGCTGATG ATCAAGTGCA AT -#GCTTTTGT 120 - - TGTGGGGGAA AACTGAAAAA TTGGGAACCC TGTGATCGTG CCTGGTCAGA AC -#ACAGGAGA 180 - - CACTTTCCCA ATTGCTTTTT TGTT - # - # 204 - - - - (2) INFORMATION FOR SEQ ID NO:51: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 198 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:51: - - TATGAAGCAC GGATCGTTAC TTTTGGAACA TGGATATACT CAGTTAACAA GG -#AGCAGCTT 60 - - GCAAGAGCTG GATTTTATGC TTTAGGTGAA GGCGATAAAG TGAAGTGCTT CC -#ACTGTGGA 120 - - GGAGGGCTCA CGGATTGGAA GCCAAGTGAA GACCCCTGGG ACCAGCATGC TA -#AGTGCTAC 180 - - CCAGGGTGCA AATACCTA - # - # - # 198 - - - - (2) INFORMATION FOR SEQ ID NO:52: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 138 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:52: - - GAGCAGCTAA GGCGCCTACA AGAGGAGAAG CTTTCCAAAA TCTGTATGGA TA -#GAAATATT 60 - - GCTATCGTTT TTTTTCCTTG TGGACATCTG GCCACTTGTA AACAGTGTGC AG -#AAGCAGTT 120 - - GACAAATGTC CCATGTGC - # - # - # 138 - - - - (2) INFORMATION FOR SEQ ID NO:53: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 204 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:53: - - GAACTGTACC GAATGTCTAC GTATTCCACT TTTCCTGCTG GGGTTCCTGT CT -#CAGAAAGG 60 - - AGTCTTGCTC GTGCTGGTTT CTATTACACT GGTGTGAATG ACAAGGTCAA AT -#GCTTCTGT 120 - - TGTGGCCTGA TGCTGGATAA CTGGAAAAGA GGAGACAGTC CTACTGAAAA GC -#ATAAAAAG 180 - - TTGTATCCTA GCTGCAGATT CGTT - # - # 204 - - - - (2) INFORMATION FOR SEQ ID NO:54: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 201 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:54: - - GAAAATGCCA GATTACTTAC TTTTCAGACA TGGCCATTGA CTTTTCTGTC GC -#CAACAGAT 60 - - CTGGCACGAG CAGGCTTTTA CTACATAGGA CCTGGAGACA GAGTGGCTTG CT -#TTGCCTGT 120 - - GGTGGAAAAT TGAGCAATTG GGAACCGAAG GATAATGCTA TGTCAGAACA CC -#TGAGACAT 180 - - TTTCCCAAAT GCCCATTTAT A - # - # 201 - - - - (2) INFORMATION FOR SEQ ID NO:55: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 204 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:55: - - CATGCAGCCC GCTTTAAAAC ATTCTTTAAC TGGCCCTCTA GTGTTCTAGT TA -#ATCCTGAG 60 - - CAGCTTGCAA GTGCGGGTTT TTATTATGTG GGTAACAGTG ATGATGTCAA AT -#GCTTTTGC 120 - - TGTGATGGTG GACTCAGGTG TTGGGAATCT GGAGATGATC CATGGGTTCA AC -#ATGCCAAG 180 - - TGGTTTCCAA GGTGTGAGTA CTTG - # - # 204 - - - - (2) INFORMATION FOR SEQ ID NO:56: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 138 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:56: - - GAACAATTGC GGAGACTACC AGAAGAAAGA ACATGTAAAG TGTGTATGGA CA -#AAGAAGTG 60 - - TCCATAGTGT TTATTCCTTG TGGTCATCTA GTAGTATGCA AAGATTGTGC TC -#CTTCTTTA 120 - - AGAAAGTGTC CTATTTGT - # - # - # 138 - - - - (2) INFORMATION FOR SEQ ID NO:57: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 203 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:57: - - AGCTGTACCG ATTGTCCACG TATTCAGCTT TTCCCAGGGG AGTTCCTGTG TC -#AGAAAGGA 60 - - GTCTGGCTCG TGCTGGCTTT TACTACACTG GTGCCAATGA CAAGGTCAAG TG -#CTTCTGCT 120 - - GTGGCCTGAT GCTAGACAAC TGGAAACAAG GGGACAGTCC CATGGAGAAG CA -#CAGAAAGT 180 - - TGTACCCCAG CTGCAACTTT GTA - # - # 203 - - - - (2) INFORMATION FOR SEQ ID NO:58: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 201 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:58: - - GAGAAGGCCA GATTACTCAC CTATGAAACA TGGCCATTGT CTTTTCTGTC AC -#CAGCAAAG 60 - - CTGGCCAAAG CAGGCTTCTA CTACATAGGA CCTGGAGATA GAGTGGCCTG CT -#TTGCGTGC 120 - - GATGGGAAAC TGAGCAACTG GGAACGTAAG GATGATGCTA TGTCAGAGCA CC -#AGAGGCAT 180 - - TTCCCCAGCT GTCCGTTCTT A - # - # 201 - - - - (2) INFORMATION FOR SEQ ID NO:59: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 204 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:59: - - CACGCAGCCC GTATTAGAAC ATTCTCTAAC TGGCCTTCTA GTGCACTAGT TC -#ATTCCCAG 60 - - GAACTTGCAA GTGCGGGCTT TTATTATACA GGACACAGTG ATGATGTCAA GT -#GTTTATGC 120 - - TGTGATGGTG GGCTGAGGTG CTGGGAATCT GGAGATGACC CCTGGGTGGA AC -#ATGCCAAG 180 - - TGGTTTCCAA GGTGTGAGTA CTTG - # - # 204 - - - - (2) INFORMATION FOR SEQ ID NO:60: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 138 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:60: - - GAACAGTTGC GGCCCCTCCC GGAGGACAGA ATGTGTAAAG TGTGTATGGA CC -#GAGAGGTA 60 - - TCCATCGTGT TCATTCCCTG TGGCCATCTG GTCGTGTGCA AAGACTGCGC TC -#CCTCTCTG 120 - - AGGAAGTGTC CCATCTGT - # - # - # 138 - - - - (2) INFORMATION FOR SEQ ID NO:61: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 204 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:61: - - GAACTCTACA GAATGTCTAC ATATTCAACT TTCCCCGCCG GGGTGCCTGT CT -#CAGAAAGG 60 - - AGTCTTGCTC GTGCTGGTTT TTATTATACT GGTGTGAATG ACAAGGTCAA AT -#GCTTCTGT 120 - - TGTGGCCTGA TGCTGGATAA CTGGAAACTA GGAGACAGTC CTATTCAAAA GC -#ATAAACAG 180 - - CTATATCCTA GCTGTAGCTT TATT - # - # 204 - - - - (2) INFORMATION FOR SEQ ID NO:62: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 201 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:62: - - GAAGAAGCCA GATTTCTTAC CTACCATATG TGGCCATTAA CTTTTTTGTC AC -#CATCAGAA 60 - - TTGGCAAGAG CTGGTTTTTA TTATATAGGA CCTGGAGATA GGGTAGCCTG CT -#TTGCCTGT 120 - - GGTGGGAAGC TCAGTAACTG GGAACCAAAG GATGATGCTA TGTCAGAACA CC -#GGAGGCAT 180 - - TTTCCCAACT GTCCATTTTT G - # - # 201 - - - - (2) INFORMATION FOR SEQ ID NO:63: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 204 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:63: - - CATGCAGCTC GAATGAGAAC ATTTATGTAC TGGCCATCTA GTGTTCCAGT TC -#AGCCTGAG 60 - - CAGCTTGCAA GTGCTGGTTT TTATTATGTG GGTCGCAATG ATGATGTCAA AT -#GCTTTGGT 120 - - TGTGATGGTG GCTTGAGGTG TTGGGAATCT GGAGATGATC CATGGGTAGA AC -#ATGCCAAG 180 - - TGGTTTCCAA GGTGTGAGTT CTTG - # - # 204 - - - - (2) INFORMATION FOR SEQ ID NO:64: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 138 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:64: - - GAACAATTGA GGAGGTTGCA AGAAGAACGA ACTTGTAAAG TGTGTATGGA CA -#AAGAAGTT 60 - - TCTGTTGTAT TTATTCCTTG TGGTCATCTG GTAGTATGCC AGGAATGTGC CC -#CTTCTCTA 120 - - AGAAAATGCC CTATTTGC - # - # - # 138 - - - - (2) INFORMATION FOR SEQ ID NO:65: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 204 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:65: - - GAACTCTACC GAATGTCTAC ATATTCAGCT TTTCCCAGGG GAGTTCCTGT CT -#CAGAGAGG 60 - - AGTCTGGCTC GTGCTGGCTT TTATTATACA GGTGTGAATG ACAAAGTCAA GT -#GCTTCTGC 120 - - TGTGGCCTGA TGTTGGATAA CTGGAAACAA GGGGACAGTC CTGTTGAAAA GC -#ACAGACAG 180 - - TTCTATCCCA GCTGCAGCTT TGTA - # - # 204 - - - - (2) INFORMATION FOR SEQ ID NO:66: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 201 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:66: - - GAAGAGGCCA GATTTCTTAC TTACAGTATG TGGCCTTTAA GTTTTCTGTC AC -#CAGCAGAG 60 - - CTGGCCAGAG CTGGCTTCTA TTACATAGGG CCTGGAGACA GGGTGGCCTG TT -#TTGCCTGT 120 - - GGTGGGAAAC TGAGCAACTG GGAACCAAAG GATTATGCTA TGTCAGAGCA CC -#GCAGACAT 180 - - TTTCCCCACT GTCCATTTCT G - # - # 201 - - - - (2) INFORMATION FOR SEQ ID NO:67: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 204 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:67: - - CACTCTGCTC GATTGAGGAC ATTTCTGTAC TGGCCACCTA GTGTTCCTGT TC -#AGCCCGAG 60 - - CAGCTTGCAA GTGCTGGATT CTATTACGTG GATCGCAATG ATGATGTCAA GT -#GCCTTTGT 120 - - TGTGATGGTG GCTTGAGATG TTGGGAACCT GGAGATGACC CCTGGATAGA AC -#ACGCCAAA 180 - - TGGTTTCCAA GGTGTGAGTT CTTG - # - # 204 - - - - (2) INFORMATION FOR SEQ ID NO:68: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 114 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:68: - - GAACGAACTT GCAAAGTGTG TATGGACAGA GAGGTTTCTA TTGTGTTCAT TC -#CGTGTGGT 60 - - CATCTAGTAG TCTGCCAGGA ATGTGCCCCT TCTCTAAGGA AGTGCCCCAT CT - #GC 114__________________________________________________________________________

Number	Date	Country
WO 9406814	Mar 1994	WOX
WO 9519431	Jul 1995	WOX
WO 9528497	Oct 1995	WOX

Mammalian IAP gene family, primers, probes, and detection methods

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