Characterized BRCA1 and BRCA2 proteins and screening and therapeutic methods based on characterized BRCA1 and BRCA2 proteins

UTILITY STATEMENT
Both the BRCA1 and BRCA2 proteins have been identified as inhibitors of the growth of breast and ovarian cancer cells and thus a DNA segment encoding the BRCA1 protein and a DNA segment encoding the BRCA2 protein can be used in a gene therapy methods for the treatment of breast cancer and for the treatment of ovarian cancer.
The discovery and purification of the BRCA1 protein has broad utility. The purified BRCA1 protein can be used in treating breast or ovarian cancer. Moreover, since it has been determined that the BRCA1 protein is secreted, the BRCA1 protein can be also be used to identify the BRCA1 receptor. Once the BRCA1 receptor is identified, BRCA1 protein-mimetic agents which act on the receptor can be identified. Such agents are also useful in the treatment of breast and ovarian cancer.
The BRCA2 protein is also a secreted protein and can be used to identify the BRCA2 receptor. Once the BRCA2 receptor is identified, BRCA2 protein-mimetic agents which act on the receptor can be identified. Such agents are also useful in the treatment of breast and ovarian cancer.
ACTIVITY STATEMENT
The BRCA1 gene product is an inhibitor of the growth and proliferation of human breast and ovarian cancer cells. The BRCA1 gene product is a secreted protein, thus indicating that it acts on a receptor to produce this activity.
The BRCA2 protein is an inhibitor of the growth and proliferation of human breast and ovarian cancer cells. The BRCA2 protein is a secreted protein, thus indicating that it acts on a receptor to produce this activity.
BACKGROUND OF THE INVENTION
The present invention relates generally to purified and isolated proteins and DNA molecules; to methods of screening for receptors; and to methods of treatment of ovarian and breast cancer, and more particularly to a purified and isolated BRCA1 protein cleavage products; and to gene therapy methods using the BRCA1 gene and the BRCA2 gene in the treatment of breast and ovarian cancer; and to methods for identifying the receptors of the BRCA1 protein and the BRCA2 protein.
The human breast and ovarian cancer susceptibility gene BRCA1 is mutated in the germline and lost in tumor tissue in hereditary breast and ovarian cancer (Hall et al., 1990, Science 250, 1684-1689; Miki et al., 1995 Science 266, 66-71; Smith et al., 1992; Cornelius et al., 1995, The Breast Cancer Linkage Consortium. Genes Chrom Cancer 13: 203-210).
Despite much excitement with the discovery of BRCA1, mutations were only found in the germline which accounts for only a small minority of breast cancers (Futreal et al., 1994, Science 266, 120-121). In addition, BRCA1 was found to be expressed at the same levels in normal individuals and sporadic breast cancers (Miki et al., 1994, Science 266, 66-71). Thus, the initial excitement over BRCA1 was followed by great disappointment.
The BRCA2 breast and ovarian cancer susceptibility gene has also recently been identified. (Wooster, R., et al., Nature 379: 789-792, 1995).
To date all tumor suppressors discovered encode proteins which are not secreted. Steeg, (review article), 1996, Nature Genetics 12:223. To treat the cancer associated with these tumor suppressors requires expressing the normal protein in the affected cell. Thus, these cancers have not been treatable with extracellular administration of the normal protein encoded by the tumor suppressor gene. For this reason, gene therapy has been proposed as the most likely means to supply a normal functional tumor suppressor protein.
This invention significantly modifies the state of the BRCA art by providing that the BRCAs are secreted and thus are amenable to direct therapy or prevention by contacting the BRCA receptor on the cell surface. In addition, the invention provides that BRCA1 is indeed underexpressed in sporadic breast cancer and thus sporadic breast cancer is amendable to therapy and prevention by correcting the BRCA deficiency. Other embodiments are also provided.
SUMMARY OF THE INVENTION
An aspect of this invention concerns a purified and isolated BRCA1 cleavage protein; and biologically functional and structural equivalents thereof.
Another aspect of this invention is that the BRCA1 protein is a secreted tumor suppressor/growth inhibitor protein that exhibits tissue-specific tumor suppression/growth inhibition activity.
Important aspects of the present invention concern isolated DNA segments and recombinant vectors encoding the BRCA1 and the BRCA2 proteins, and the creation and use of recombinant host cells through the application of DNA technology, which express the BRCA1 and BRCA2 proteins.
The present invention concerns DNA segments, isolatable from human breast and ovarian tissue, which are free from genomic DNA and which are capable of conferring tumor suppressor/growth inhibitor activity in a recombinant host cell when incorporated into the recombinant host cell. As used herein, the term "breast or ovarian tissue" refers to normal and cancerous ovarian breast tissues, as exemplified, but not limited to, by HMEC or MCF-7 cell lines. DNA segments capable of conferring tumor suppressor activity may encode complete BRCA1 and BRCA2 proteins, cleavage products and biologically actively functional domains thereof.
As used herein, the term "DNA segment" refers to a DNA molecule which has been isolated free of total genomic DNA of a particular species. Furthermore, a DNA segment encoding a BRCA1 protein or encoding a BRCA2 protein refers to a DNA segment which contains BRCA1 coding sequences or contains BRCA2 coding sequences, yet is isolated away from, or purified free from, total genomic DNA of Homo sapiens. Included within the term "DNA segment", are DNA segments and smaller fragments of such segments, and also recombinant vectors, including, for example, plasmids, cosmids, phage, viruses, and the like.
Similarly, a DNA segment comprising an isolated or purified BRCA1 gene or BRCA2 gene refers to a DNA segment including BRCA1 coding sequences isolated substantially away from other naturally occurring genes or protein encoding sequences or including BRCA2 coding sequences isolated substantially away from other naturally occurring genes or protein encoding sequences. In this respect, the term "gene" is used for simplicity to refer to a functional protein, polypeptide or peptide encoding unit. As will be understood by those in the art, this functional term includes both genomic sequences and cDNA sequences. "Isolated substantially away from other coding sequences" means that the gene of interest, in this case, the BRCA1 gene or the BRCA2 gene, forms the significant part of the coding region of the DNA segment, and that the DNA segment does not contain large portions of naturally-occurring coding DNA, such as large chromosomal fragments or other functional genes or cDNA coding regions. Of course, this refers to the DNA segment as originally isolated, and does not exclude genes or coding regions later added to the segment by the hand of man.
In particular embodiments, the invention concerns isolated DNA segments and recombinant vectors incorporating DNA sequences which encode a BRCA1 protein that includes within its amino acid sequence the amino acid sequence of SEQ ID NO:2. In other particular embodiments, the invention concerns isolated DNA segments and recombinant vectors incorporating DNA sequences which encode a protein that includes within its amino acid sequence the amino acid sequence of the BRCA1 protein corresponding to human breast or ovarian tissue.
In particular embodiments, the invention concerns isolated DNA segments and recombinant vectors incorporating DNA sequences which encode a BRCA2 protein that includes within its amino acid sequence the amino acid sequence of SEQ ID NO:4. In other particular embodiments, the invention concerns isolated DNA segments and recombinant vectors incorporating DNA sequences which encode a protein that includes within its amino acid sequence the amino acid sequence of the BRCA2 protein corresponding to human breast or ovarian tissue.
It will also be understood that this invention is not limited to the particular nucleic acid and amino acid sequences of SEQ ID NOS: 1, 2, 3 and 4. Recombinant vectors and isolated DNA segments may therefore variously include the BRCA1 and BRCA2 encoding regions themselves, coding regions bearing selected alterations or modifications in the basic coding region, or they may encode larger polypeptides which nevertheless include BRCA1 or BRCA2 encoding regions or may encode biologically functional equivalent proteins or peptides which have variant amino acid sequences.
In certain embodiments, the invention concerns isolated DNA segments and recombinant vectors which encode a protein or peptide that includes within its amino acid sequence an amino acid sequence essentially as set forth in SEQ ID NO:2 or SEQ ID NO:4, and methods of treating breast or ovarian cancer using these DNA segments. Naturally, where the DNA segment or vector encodes a full length BRCA1 or BRCA2 protein, or is intended for use in expressing the BRCA1 or BRCA2 protein, the most preferred sequences are those which are essentially as set forth in SEQ ID NO:1 and SEQ ID NO:3 and which encode a protein that exhibits tumor suppressor activity in human breast and ovarian cancer cells, as may be determined by the breast and ovarian cancer cell growth inhibition experiments, as disclosed herein.
The term "a sequence essentially as set forth in SEQ ID NO:2" means that the sequence substantially corresponds to a portion of SEQ ID NO:2 and has relatively few amino acids which are not identical to, or a biologically functional equivalent of, the amino acids of SEQ ID NO:2. The term "biologically functional equivalent" is well understood in the art and is further defined in detail herein. Accordingly, sequences which have between about 70% and about 80%; or more preferably, between about 81% and about 90%; or even more preferably, between about 91% and about 99%; of amino acids which are identical or functionally equivalent to the amino acids of SEQ ID NO:2 will be sequences which are "essentially as set forth in SEQ ID NO:2". The term "a sequence essentially as set forth in SEQ ID NO:4" has a similar meaning.
In particular embodiments, the invention concerns gene therapy methods that use isolated DNA segments and recombinant vectors incorporating DNA sequences which encode a protein that includes within its amino acid sequence an amino acid sequence in accordance with SEQ ID NO:2 or in accordance with SEQ ID NO:4, SEQ ID NO:2 and SEQ ID NO:4 derived from breast or ovarian tissue from Homo sapiens. In other particular embodiments, the invention concerns isolated DNA sequences and recombinant DNA vectors incorporating DNA sequences which encode a protein that includes within its amino acid sequence the amino acid sequence of the BRCA1 protein from human breast or ovarian tissue, or which encode a protein that includes within its amino acid sequence the amino acid sequence of the BRCA2 protein from human breast or ovarian tissue.
In certain other embodiments, the invention concerns isolated DNA segments and recombinant vectors that include within their sequence a nucleic acid sequence essentially as set forth in SEQ ID NO:1, or a nucleic acid sequence essentially as set forth in SEQ ID NO:3, and methods of treating breast or ovarian cancer using these sequences. The term "essentially as set forth in SEQ ID NO:1" is used in the same sense as described above and means that the nucleic acid sequence substantially corresponds to a portion of SEQ ID NO:1, respectively, and has relatively few codons which are not identical, or functionally equivalent, to the codons of SEQ ID NO:1, respectively. Again, DNA segments which encode proteins exhibiting tumor suppression activity of the BRCA1 and BRCA2 proteins will be most preferred. The term "functionally equivalent codon" is used herein to refer to codons that encode the same amino acid, such as the six codons for arginine or serine, and also refers to codons that encode biologically equivalent amino acids (see FIG. 2). The term "essentially as set forth in SEQ ID NO:3" has a similar meaning.
The nucleic acid segments of the present invention, regardless of the length of the coding sequence itself, may be combined with other DNA sequences, such as promoters, polyadenylation signals, additional restriction enzyme sites, multiple cloning sites, other coding segments, and the like, such that their overall length may vary considerably. It is therefore contemplated that a nucleic acid fragment of almost any length may be employed, with the total length preferably being limited by the ease of preparation and use in the intended recombinant DNA protocol. For example, nucleic acid fragments may be prepared which include a short stretch complementary to SEQ ID NO:1 or SEQ ID NO:3, such as about 10 nucleotides, and which are up to 10,000 or 5,000 base pairs in length, with segments of 3,000 being preferred in certain cases. DNA segments with total lengths of about 1,000, 500, 200, 100 and about 50 base pairs in length are also contemplated to be useful.
The DNA segments of the present invention encompass biologically functional equivalent BRCA1 and BRCA2 proteins and peptides. Such sequences may rise as a consequence of codon redundancy and functional equivalency which are known to occur naturally within nucleic acid sequences and the proteins thus encoded. Alternatively, functionally equivalent proteins or peptides may be created via the application of recombinant DNA technology, in which changes in the protein structure may be engineered, based on considerations of the properties of the amino acids being exchanged. Changes designed by man may be introduced through the application of site-directed mutagenesis techniques, e.g., to introduce improvements to the antigenicity of the protein or to test BRCA1 and BRCA2 mutants in order to examine tumor suppression activity at the molecular level.
If desired, one may also prepare fusion proteins and peptides, e.g., where the BRCA1 or BRCA2 coding regions are aligned within the same expression unit with other proteins or peptides having desired functions, such as for purification or immunodetection purposes (e.g., proteins which may be purified by affinity chromatography and enzyme label coding regions, respectively).
Recombinant vectors form important further aspects of the present invention. Particularly useful vectors are contemplated to be those vectors in which the coding portion of the DNA segment is positioned under the control of a promoter. The promoter may be in the form of the promoter which is naturally associated with the BRCA1 or BRCA2 gene(s), e.g., in breast or ovarian cancer cells, as may be obtained by isolating the 5' non-coding sequences located upstream of the coding segment or exon, for example, using recombinant cloning and/or PCR technology, in connection with the compositions disclosed herein.
In other embodiments, it is contemplated that certain advantages will be gained by positioning the coding DNA segment under the control of a recombinant, or heterologous, promoter. As used herein, a recombinant or heterologous promoter is intended to refer to a promoter that is not normally associated with a BRCA1 or BRCA2 gene in its natural environment. Such promoters may include promoters isolated from bacterial, viral, eukaryotic, or mammalian cells. Naturally, it will be important to employ a promoter that effectively directs the expression of the DNA segment in the cell type chosen for expression. The use of promoter and cell type combinations for protein expression is generally known to those of skill in the art of molecular biology, for example, see Sambrook et al., 1989, Molecular Cloning Laboratory Manual, 2d Edition. The promoters employed may be constitutive, or inducible, and can be used under the appropriate conditions to direct high level expression of the introduced DNA segment, such as is advantageous in the large-scale production of recombinant proteins or peptides. Appropriate promoter systems contemplated for use in high-level expression include, but are not limited to, a breast selective MMTV promoter and the LXSN promoter, which are more fully described below.
As mentioned above, in connection with expression embodiments to prepare recombinant BRCA1 and BRCA2 proteins and peptides, it is contemplated that longer DNA segments will most often be used, with DNA segments encoding the entire BRCA1 or BRCA2 protein, functional domains or cleavage products thereof, being most preferred. However, it will be appreciated that the use of shorter DNA segments to direct the expression of BRCA1 and BRCA2 peptides or epitopic core regions, such as may be used to generate anti-BRCA1 or anti-BRCA2 antibodies, also falls within the scope of the invention.
DNA segments which encode peptide antigens from about 15 to about 50 amino acids in length, or more preferably, from about 15 to about 30 amino acids in length are contemplated to be particularly useful. DNA segments encoding peptides will generally have a minimum coding length in the order of about 45 to about 150, or to about 90 nucleotides. DNA segments encoding full length proteins may have a minimum coding length on the order of about 5,600 nucleotides for a protein in accordance with SEQ ID NO:2 or a minimum coding length on the order of about 10,300 nucleotides for a protein in accordance with SEQ ID NO:4.
Naturally, the present invention also encompasses DNA segments which are complementary, or essentially complementary, to the sequence set forth in SEQ ID NO:1 or the sequence set forth in SEQ ID NO:4. Nucleic acid sequences which are "complementary" are those which are capable of base-pairing according to the standard Watson-Crick complementarity rules. As used herein, the term "complementary sequences" means nucleic acid sequences which are substantially complementary, as may be assessed by the same nucleotide comparison set forth above, or as defined as being capable of base pairing to codons that encode the same amino acid, such as the six codons for arginine or serine, and also refers to codons that encode biologically equivalent amino acids (See FIG. 2).
It will also be understood that amino acid and nucleic acid sequences may include additional residues, such as additional N- or C-terminal amino acids or 5' or 3' sequences, and yet still be essentially as set forth in one of the sequences disclosed herein, so long as the sequence meets the criteria set forth above, including the maintenance of biological protein activity where protein expression is concerned. The addition of terminal sequences particularly applies to nucleic acid sequences which may, for example, include various non-coding sequences flanking either of the 5' or 3' portions of the coding region or may include various internal sequences, i.e., introns, which are known to occur within genes.
Excepting intronic or flanking regions, and allowing for the degeneracy of the genetic code, sequences which have between about 20% and about 50%; or more preferably, between about 50% and about 70%; or even more preferably, between about 70% and about 99%; of nucleotides which are identical to the nucleotides of SEQ ID NO:1 or to the nucleotides of SEQ ID NO:3, will be sequences which are "essentially as set forth in SEQ ID NO:1" and will be sequences which are "essentially as set forth in SEQ ID NO:3". Sequences which are essentially the same as those set forth in SEQ ID NO:1 or as those set forth in SEQ ID NO:3 may also be functionally defined as sequences which are capable of hybridizing to a nucleic acid segment containing the complement of SEQ ID NO:1 or to a nucleic acid segment containing the complement of SEQ ID NO:3 under relatively stringent conditions. Suitable relatively stringent hybridization conditions will be well known to those of skill in the art (Sambrook et al, 1989, Molecular Cloning Laboratory Manual, 2d Edition).
______________________________________List of Abbreviations______________________________________MCF-7 An immortalized cell line derived from a metastasis of human breast cancerHMEC A primary (non-immortalized) cell line derived from breast epithelial cells obtained during reduction mammoplastyMDA-MB-468 An immortalized cell line derived from a metastasis of human breast cancerSf9 Insect cells widely used in the art with baculovirus vectorscDNA Complementary DNA obtained from an RNA templateDNA Deoxyribonucleic AcidRT-PCR Reverse Transcriptase-Polymerase Chain Reaction______________________________________

BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 lists the C-terminal and N-terminal amino acid sequences [SEQ ID NOs:5, 6, 7] used as antigens to generate antibodies for the purified and isolated BRCA1 protein described herein.
FIG. 2 is a table of the genetic code.
FIG. 3 is a diagram showing structural features of the human BRCA1 protein [SEQ ID NO:2] covering 1864 amino acids.
FIG. 4 is a diagram showing sequence alignment of the granin region of selected granin family members compared with BRCA1.
FIG. 5 is a diagram showing sequence alignment of the granin region of selected granin family members compared with BRCA1 and BRCA2.
FIG. 6 is Table I, which shows inherited BRCA1 mutations and type of cancer.
FIG. 7 is Table II, which shows effect of BRCA1 Expression Vectors on growth.
FIG. 8 is Table III, which shows inhibition of tumorigenesis by BRCA1.
FIGS. 9A-9D show the sequence of the BRCA1 gene [SEQ ID NO:1].
FIGS. 10A-10F show the sequence of the BRCA2 gene [SEQ ID NO:3].
FIGS. 11A-11C show the sequence of the BRCA2 protein [SEQ ID NO:4].
FIG. 12 is an immunoblot analysis of spleen and HMEC cell whole cell lysates probed with preimmune, immune, and immune plus peptide for C-19 antisera and C-20 affinity purified antibody and antibody plus peptide.
FIG. 13 is an immunoprecipitation/immunoblot analysis of MDA-MB-468 cell lysates with C-19 antisera.
FIG. 14 is a C-20 immunoblot analysis of recombinant Baculovirus produced BRCA1 (marked by arrow) compared with uninfected Sf9 cells (Control).
FIG. 15 is a V8 Protease Map of Native and Recombinant BRCA1.
FIG. 16 is a Pulse-Chase Analysis of MDA-MB-468 Cells.
FIG. 17 is an immunoblot analysis of nuclear, cytoplasmic and membrane fractions of HMEC cells paired with corresponding whole cell lysate and probed for BRCA1 (C-19), c-myc, and PDGFR beta.
FIG. 18 is an immunoblot analysis of nuclear, cytoplasmic and membrane fractions of HMEC cells paired with corresponding whole cell lysate and probed with D-20 N-terminal antibody plus and minus peptide.
FIG. 19 is an immunoblot analysis of nuclear, cytoplasmic and membrane fractions of MDA-MB-468 cells paired with corresponding whole cell lysate probed with C-20 antibody.
FIG. 20 depicts assay of MDA-MB-468 cell fractions produced by sucrose gradient for synaptophysin and BRCA1 immunoreactivity.
FIG. 21 depicts estrogen regulation of BRCA1 protein.
FIG. 22 depicts N-Linked glycosylation of BRCA1 protein.
FIG. 23 depicts heat solubility of BRCA1 protein.
FIG. 24 is a Western blot of HMEC cell lysates: control; stimulated with 10 mM forskolin 0.5 hours post stimulation; and 48 hours post stimulation and also includes radioimmunoprecipitation of BRCA1 From conditioned media (lane 4).

DESCRIPTION OF THE PREFERRED EMBODIMENT
For the purposes of the subsequent description, the following definitions will be used:
Nucleic acid sequences which are "complementary" are those which are capable of base-pairing according to the standard Watson-Crick complementarity rules. That is, that the larger purines will always base pair with the smaller pyrimidines to form only combinations of Guanine paired with Cytosine (G:C) and Adenine paired with either Thymine (A:T) in the case of DNA or Adenine paired with Uracil (A:U) in the case of RNA.
"Hybridization techniques" refer to molecular biological techniques which involve the binding or hybridization of a probe to complementary sequences in a polynucleotide. Included among these techniques are northern blot analysis, southern blot analysis, nuclease protection assay, etc.
"Hybridization" and "binding" in the context of probes and denatured DNA are used interchangeably. Probes which are hybridized or bound to denatured DNA are aggregated to complementary sequences in the polynucleotide. Whether or not a particular probe remains aggregated with the polynucleotide depends on the degree of complementarity, the length of the probe, and the stringency of the binding conditions. The higher the stringency, the higher must be the degree of complementarity and/or the longer the probe.
"Probe" refers to an oligonucleotide or short fragment of DNA designed to be sufficiently complementary to a sequence in a denatured nucleic acid to be probed and to be bound under selected stringency conditions.
"Label" refers to a modification to the probe nucleic acid that enables the experimenter to identify the labeled nucleic acid in the presence of unlabeled nucleic acid. Most commonly, this is the replacement of one or more atoms with radioactive isotopes. However, other labels include covalently attached chromophores, fluorescent moieties, enzymes, antigens, groups with specific reactivity, chemiluminescent moieties, and electrochemically detectable moieties, etc.
"Tissuemizer" describes a tissue homogenization probe.
"PCR technique" describes a method of gene amplification which involves sequenced-based hybridization of primers to specific genes within a DNA sample (or library) and subsequent amplification involving multiple rounds of annealing, elongation and denaturation using a heat-stable DNA polymerase.
"RT-PCR" is an abbreviation for reverse transcriptase-polymerase chain reaction. Subjecting mRNA to the reverse transcriptase enzyme results in the production of cDNA which is complementary to the base sequences of the mRNA. Large amounts of selected cDNA can then be produced by means of the polymerase chain reaction which relies on the action of heat-stable DNA polymerase produced by Thermus aquaticus for its amplification action.
"Nuclease protection assay" refers to a method of RNA quantitation which employs strand specific nucleases to identify specific RNAs by detection of duplexes.
"In situ hybridization of RNA" refers to the use of labeled DNA probes employed in conjunction with histological sections on which RNA is present and with which the labeled probe can hybridize allowing an investigator to visualize the location of the specific RNA within the cell.
"Cloning" describes separation and isolation of single genes.
"Sequencing" describes the determination of the specific order of nucleic acids in a gene or polynucleotide.
The term "BRCA1 targeted growth inhibitor agent", as used herein and in the claims, is defined as the BRCA1 protein characterized herein, whether isolated and purified directly from a natural source such as mammalian ovarian or breast cells, or produced using recombinant methods; the targeted growth inhibitor having the biological activity of tumor suppression and/or growth inhibition activity in mammalian breast or ovarian cancer cells and which binds the BRCA1 receptor; and the term "BRCA1 targeted growth inhibitor agent" also including biologically functional equivalents of the BRCA1 protein characterized herein, the term biologically functional equivalent defined herein to include, among others, proteins and protein fragments in which biologically functionally equivalent amino acids have been inserted and peptidomimetics.
The term "BRCA2 targeted growth inhibitor agent" is used herein as "BRCA1 targeted growth inhibitor agent" above but applies to BRCA2.
The term "homology" describes a mathematically based comparison of sequence similarities which is used to identify genes or proteins with similar functions or motifs.
The term "cleavage product" is defined as a polypeptide fragment produced from the targeted growth inhibitor described above by natural proteolytic processes. Preferably such a cleavage product will have biological activity including, but not limited to, tumor suppression and/or growth inhibition activity in mammalian breast or ovarian cancer cells. This term also includes such polypeptide fragments when produced via recombinant techniques and also includes biological functional equivalents of such fragments, the term biologically functional equivalent defined herein to include, among others, proteins in which biologically functionally equivalent amino acids have been inserted and peptidomimetics.
The term "granin box domain" is defined as the consensus granin box domain of amino acids set forth in FIGS. 3 and 5.
The term "recombinant host cell" is defined as a single cell or multiple cells within a cell line which are capable of undergoing genetic manipulation through well-known and art recognized techniques of transformation, transfection, transduction and the like. Examples of contemplated recombinant host cells include, but are not limited to, cell lines derived from normal or cancerous mammalian breast or ovarian tissue, other eukaryotic cells, and microorganisms. Specific examples of recombinant host cells described herein include Sf9 cells and HMEC cells.
The phrase "substantially identical to the carboxyl terminus of an amino acid sequence as essentially set forth in SEQ ID NO:2" is defined as an amino acid sequence including amino acids identical to the C-terminal amino acids in the amino acid sequence set forth in SEQ ID NO:2, or biologically functional equivalents of these amino acids. Preferred examples of the amino acid sequences are set forth in FIG. 1.
EXAMPLE 1
BRCA1 Encodes a 190 kDa Protein Expressed in Breast Epithelial Cells
As an initial step in the biochemical characterization of the BRCA1 gene product, antibodies were developed and the expression, localization, and function of BRCA1 protein were studied. These studies demonstrate that BRCA1 is a secreted, selectively growth inhibitory and represents a new member of the granin gene family.
To enable BRCA1 protein expression studies a polyclonal rabbit antisera was raised against a peptide from the C-terminal portion of the predicted BRCA1 protein [SEQ ID NO:2]. This peptide corresponded to the last 19 C-terminal amino acids (C-19) [SEQ ID NO:5], which is listed in FIG. 1. The results produced by this antibody, which are more fully described below, were confirmed with antibodies against peptides from the last 20 C-terminal amino acids (C-20) [SEQ ID NO:6] and from the first 20 N-terminal amino acids (D-20) [SEQ ID NO:7] of the predicted BRCA1 protein [SEQ ID NO:2]. These antibodies were purchased from Santa Cruz Biotechnology, Santa Cruz, Calif., and the peptide sequences are also are listed in FIG. 1. A search of the SWISS PROT protein sequence database for the N-terminal and C-terminal 20 amino acid peptides at the 60% homology level revealed no entries other than BRCA1. Initially these antisera were screened using Western blot analysis of whole cell lysates from normal human mammary epithelial cells (HMEC-Clonetics, (Stampfer et al., 1980, Growth of Normal Human Mammary Cells in Culture. 16, 415-425)) and normal human spleen. Spleen was chosen as a negative control because Northern analysis demonstrated no expression of BRCA1 in spleen (Miki et al., 1994, Science 266, 66-71). The results of the experiments with the C-terminal antibodies were obtained with an immunoblot analysis of spleen and HMEC cell whole cell lysates probed with preimmune, immune, and immune plus peptide for C-19 antisera and C-20 affinity purified antibody and antibody plus peptide (FIG. 12). An immunoreactive band that is blocked by the addition of corresponding peptide is present at 190 kDa in the HMEC cells for both the C-19 and C-20 anti-peptide antisera. Note that the C-19 blot has been probed with immune ser um diluted 1:200 and that the C-20 blot has been probed with affinity purified antibody. No specific immunoreactivity is detected in the C-19 preimmune sera, and as expected no specific bands are detected in the spleen whole cell lysate by either C-19 or C-20. Several non-specific bands are present in the immune sera that do not block with the addition of peptide, but affinity purified C-20 antibody exhibits minimal non-specific cross reactivity. A minor band at approximately 70 kDa is identified, but appears to block with peptide indicating that this band represents a processed C-terminal fragment of the 190 kDa band. Similar studies were performed on antisera from three separate rabbits, raised against the C-terminal 19 peptide, and in each case, essentially similar results were seen, with some variation in the non-specific bands among individual rabbits, but all three react with a band at approximately 190 kDa that is not present in preimmune serum and is blocked with peptide.
A number of normal tissues and breast cancer cell lines were surveyed for the immunoreactive 190 kDa protein and the majority exhibited a decreased relative expression of BRCA1 in comparison to HMEC cells. The cell line MDA-MB-468 exhibited a very high level of BRCA1 expression, but the majority of other cells tested showed very low to absent (MCF-7, MB-157, MB-361) levels of expression. To analyze the ability of the antisera to immunoprecipitate the 190 kDa protein, radiolabelled whole cell lysates from MDA-MB-468 cells were immunoprecipitated with C-20 antisera (FIG. 13). The 190 kDa and 70 kDa species in the HMEC lane are blocked with the addition of peptide, but a number of non-specific bands including a 220 kDa species (Chen, et al, 1995, Science 270:789-791) are not blocked. Immunoprecipitation of MDA-MB-468 cells demonstrates a 190 kDa protein that is not present in the peptide addition control. In addition, the 70 kDa species is immunoprecipitated with antibody and blocked by the addition of peptide. It is noted that several other bands are identified that are not blocked with peptide, in particular at 205 and 220 kDa. This indicates that despite the 207 kDa size predicted from the BRCA1 coding sequence, the 205 kDa and 220 kDa bands do not represent BRCA1. These results are consistent with the 185 kDa estrogen-regulated protein reported by Gudas (Gudas, et al. 1995, Cancer Res., 55:4561-4565) but differ from the 220 kDa ubiquitous protein reported by Chen, particularly because the 220 kDa protein does not block with peptide.
While these results strongly suggested that the antisera was specific for a 190 kDa protein present in breast epithelial cells, further experiments were performed to demonstrate that this protein corresponded to BRCA1. A concern was that the full length coding sequence for BRCA1 predicts a protein of 207 kDa molecular weight and the protein that the antisera recognized was definitely less than 200 kDa, and approximately 190 kDa.
Therefore to confirm that the antisera recognized BRCA1 a full length BRCA1 cDNA was constructed and cloned into the baculovirus transfer vector pAcSG2 (PharMingen). This plasmid was subsequently utilized to produce recombinant BRCA1 baculovirus by co-transfection and homologous recombination. The antisera was then tested for its ability to recognize baculovirus expressed recombinant BRCA1. The results of these experiments were that the antibodies recognize a 180 kDa band in the BRCA1 recombinant virus infected cell lysates that is not present in the no infection control (FIG. 14). The recognition of this band is blocked by the addition of peptide and it is not present in the preimmune serum blot. To verify that the native 190 kDa protein and the recombinant 180 kDa protein were in fact the same protein, peptide mapping of the 190 kDa band from MDA-MB-468 cells and the 180 kDa protein from BRCA1 recombinant S89 cell lysates was performed as described in the methods. The digests were loaded onto a 4-20% gradient SDS-PAGE gel and immunoblotted with C-20 (FIG. 16). In FIG. 15, Lanes 1 through 3 and 4 through 6 represent increasing concentrations of V8 protease. The arrows at right indicate four identical sized molecular weight bands in lanes 3 and 6 that document that recombinant BRCA1 and the 190 kD band from MDA-MB-468 cells are identical proteins. This data confirmed that the antibodies are specific for BRCA1 protein. The difference in molecular weight between the recombinant and native protein is likely to be due to differences in glycosylation. These experiments demonstrate that the immunoreactive band completely blocks with peptide and is not present in control wild type virus infected lysates.
To characterize the 70 kDa species a pulse-chase experiment was performed that demonstrates that this band is a proteolytic fragment derived from the 190 kDa form. MDA-MB-468 cells were starved in cysteine and methionine deficient media and then pulsed with 35S labelled cysteine and methionine containing media with 3% dialyzed fetal bovine serum for three hours. The cells were then chased in L-15 media with 10% fetal bovine serum for increasing periods of time and harvested in lysis buffer. The lysates were immunoprecipitated, electrophoresed and the dried gel was autoradiographed (FIG. 16). In this experiment, it was shown that BRCA1 is initially synthesized as a 185 kDa form that is subsequently processed to a 190 kDa species. This represents glycosylation of the newly synthesized protein. Initially, no 70 kDa form is present, but co-incident with the appearance of the fully glycosylated form, the 70 kDa form appears. Subsequently, as the 190 kDa signal decreases with time post-labelling, the 70 kDa band increases in intensity. These findings indicate that the 70 kDa band is a proteolytic fragment, or cleavage product, of the 190 kDa protein. Other cleavage products were also isolated, including a 110 kDa species and a 130 kDa species.
Having demonstrated that the antibodies recognize BRCA1 protein, immunohistochemical analysis on formalin fixed, paraffin-embedded normal breast tissue were performed to analyze the distribution of BRCA1 within the breast. The results demonstrated that luminal epithelial cells (Page and Anderson, 1987, Nature Genetics 2, 128-131) within breast acini and ducts stain positively but myoepithelial cells and supporting stromal cells did not stain. No staining was observed when either primary antibody was deleted or peptide was added to the incubation. Staining was present diffusely throughout the cytoplasm and was not localized to the nucleus.
In summary, then, a 190 kDa protein was demonstrated to be the BRCA1 gene product by a number of independent criteria: 1) three different antibodies directed against two different regions of the predicted gene product react specifically in western blots and are blocked by appropriate peptides; 2) The C-20 antibody specifically immunoprecipitates the protein; 3) The C-20 antibody specifically recognizes the recombinant protein expressed in baculovirus; 4) Peptide mapping experiments definitely demonstrate that the 190 kDa protein recognized in MDA-MB-468 cells and the recombinant virus infected Sf9 cells are the same. Immunohistochemical studies indicate that BRCA1 protein is present in the luminal epithelial cells which are presumed be the cells of origin for the vast majority of hereditary and sporadic breast cancers.
EXAMPLE 2
BRCA1 is Predominately Localized in the Membrane Fraction of Breast Epithelial Cells
Due to the immunohistochemical studies, a series of experiments to determine more precisely the localization of BRCA1 within the cell was initiated. The first such experiment was a cell fractionation experiment designed to segregate nuclear, cytoplasmic, and membrane compartments of HMEC cells. As shown in FIG. 17, the cell fractionation analysis included immunoblot analysis of nuclear, cytoplasmic and membrane fractions of HMEC cells paired with corresponding whole cell lysate and probed for BRCA1 (C-19 antibody), c-myc, and PDGFR beta; and identical fractions as above probed with D-20 N-terminal antibody plus and minus peptide (FIG. 18). The cell fractionation analysis also included immunoblot analysis of nuclear, cytoplasmic and membrane fractions of MDA-MB-468 cells paired with corresponding whole cell lysate probed with C-20 antibody (FIG. 19). The results of this cell fractionation experiment clearly demonstrate that the 190 kDa species of BRCA1 is present and greatly enriched for in the membrane fraction of HMEC cells. Essentially no 190 kDa BRCA1 could be detected in either the nuclear or cytoplasmic fractions, although the 70 kDa protein is present in the nuclear fraction. As a control for the fractionation procedure parallel blots were probed with antisera for c-myc and platelet-derived growth factor receptor beta (PDGFR). These blots demonstrated that the nuclear fraction is greatly enriched for the 67 and 64 kDa c-myc proteins (Alexandrova et al., 1995, Mol. Cell. Biol. 15:5188-5195) and the cytosolic and membrane fractions show PDGFR as expected. These results were confirmed with the antibody to the N-terminal portion of BRCA1 (D-20). This antibody detects the 190 kDa form of BRCA1 and an additional 165 kDa species in HMEC cells. Both of these bands are blocked with the addition of peptide and are present in the membrane fraction exclusively. Note that this antibody does not detect the 70 kDa species identified in the C-terminal peptide blots.
To investigate the possibility that subcellular localization of BRCA1 might be altered in malignant breast cells, fractionation studies on MDA-MB-468 cells that express high levels of BRCA1 protein were performed (FIG. 19). These studies demonstrated that in parallel with findings in HMEC cells the 190 kDa form of BRCA1 is also greatly enriched in the membrane fraction of MDA-MB-468 cells. In contrast to HMEC cells however, there appears to be a small amount of the 190 kDa species in the nuclear fraction of MDA-MB-468 cells. It is also noted that in contrast to HMEC cells, the 70 kDa species is present exclusively in the cytosolic fraction of MDA-MB-468 cells.
To further investigate the precise subcellular localization of BRCA1 confocal microscopy utilizing the affinity purified C-20 antisera was employed. These experiments indicated that the C-20 antibody exhibits diffuse granular staining that is predominately localized in the cytoplasm of HMEC cells. The nucleus and Golgi compartment were localized in these experiments, and this provided the capability to identify co-localization of BRCA1 in both the nucleus and Golgi complex. Simultaneous triple staining for the nucleus, Golgi complex and BRCA1 again demonstrated a predominant granular cytoplasmic distribution for BRCA1, with co-localization in both the nucleus and Golgi complex. These findings are in agreement with the cell fractionation studies of HMEC cells, despite the inability of those studies to detect the 190 kDa BRCA1 form in the nucleus, because the 70 kDa form was present in the nuclear fraction and would be expected to be detected by C-terminal antibody.
In summary, then, the above studies demonstrate that the majority of BRCA1 protein is non-nuclear and membrane-associated. Cell fractionation studies show the 190 kDa BRCA1 protein resides primarily in the membrane-associated fraction, but the p70 protein is localized in the nucleus of normal breast cells and the cytoplasm of MB-486 breast cancer cells. The distinct membrane-associated and nuclear localization patterns result from the unprocessed and the 70 kDa processed form, respectively. There is definite co-localization with the 190 kDa BRCA1 protein and the Golgi marker supporting the trafficking of BRCA1 through the Golgi prior to its packaging into secretory granules.
EXAMPLE 3
BRCA1 is a Member of the Granin Family of Secretory Proteins and Localizes to Secretory Vesicles
Having identified BRCA1 as being present in the membrane fraction of breast epithelial cells and having a large granular cytoplasmic pattern of staining, a homology search of BRCA1 was performed, focusing on motifs that might explain the apparent membrane localization of BRCA1. A search on the SWISS PROT database of the MacDNAsis PRO v3.0 software package was performed and several features of biologic and functional importance were identified, as shown in FIG. 3. In FIG. 3, (-) and (+) mark location of charged residues and glyc shows potential N-linked glycosylation sites. RING finger and granin (amino acids 1214-1223) consensus are shown by open and closed boxes. Predicted protease cleavage sites for renin, kallikrein, thrombin, and trypsin are shown as thin lines. Regions deleted in the internal deletion mutants are shown as shaded boxes below (343-1081 and 515-1092).
The SWISS PROT search revealed that BRCA1 has homology to the granin consensus site as shown in FIG. 4. In FIG. 4, consensus sequence is shown in bold at the bottom. Sequences are human unless otherwise stated. The granin motif spans amino acids 1214-1223 of BRCA1. Note that human BRCA1 completely satisfies the ten amino acid granin consensus and exhibits the other structural features of the family. The probability that BRCA1 would exhibit a perfect granin consensus by chance alone is 0.0018 (or one in 555). The rationale for this calculation is given at the bottom of FIG. 4.
To investigate the hypothesis that BRCA1 behaves biochemically as a granin, the following series of experiments were executed. To document the presence of BRCA1 in secretory vesicles, cell organelles from MDA-MB-468 cells were fractionated by sucrose gradient centrifugation and the fractions were assayed for synaptophysin (a highly specific marker for secretory vesicles) and BRCA1 immunoreactivity. As seen in FIG. 20, coordinate expression of BRCA1 and synaptophysin was noted, which indicates the co-localization of these proteins in secretory vesicles. These results document the co-localization of synaptophysin and BRCA1 in fractions expected to contain secretory vesicles.
Since granins have been shown to be regulated by estrogens (Fischer-Colbrie et al., 1991, J. Neuroendoctinol. 121, 125-130) HMEC cells were stimulated with estrogen and tamoxifen and increased expression of BRCA1 was demonstrated, as reported previously by others (Gudas, et al. 1995, Cancer Res., 55:4561-4565; Marquis et al. ,1995, Nature Genetics 11, 17-26; Lane et al., 1995, Genes & Development 9, 2712-2722). The dose response was consistent with estrogen regulation of BRCA1 expression. As presented in FIG. 21, cell lysates from HMEC cells treated for 24 hours with tamoxifen (TAM), indicated concentrations of estrogen (E2), or ethanol control (ETOH). Note E2 dosage effect.
HMEC cell membrane fractions were then treated with sequential deglycosylation enzymes (NANase II>O-Glycosidase DS>PNGase F to remove a2-3 and a2-6 N-acetylneuraminic acid, serine/threonine glycosylation (FIG. 22). N-linked glycosylation). A shift of protein following PNGase F treatment was noted, confirming N-linked glycosylation. Thus, BRCA1 exhibits N-linked glycosylation as predicted from the sequence analysis and shows little Ser/Thr glycosylation.
In addition, a heat stable fraction was prepared from recombinant baculovirus BRCA1 in a modification of the procedure of Thompson et al., (1992b), Mol. Brain Res. 12, 195-202, where cell pellets of infected Sf9 cells were sonicated, centrifuged, boiled for five minutes, and then centrifuged again. This heat soluble fraction was then analyzed by immunoblotting.
BRCA1 remained soluble after boiling, which is characteristic of granins. As seen in FIG. 23, the immunoblots included cell lysates from uninfected Sf9 cells, wild-type infected cells (control), BRCA1 infected cells, HMEC cells, and heat soluble fraction of Baculovirus produced recombinant BRCA1. Recombinant BRCA1 remains soluble after boiling.
Additionally, HMEC cells were treated with 10 mM forskolin and a marked decrease in BRCA1 levels in whole cell lysates after 0.5 hours of treatment and a return to normal levels 48 hours later was observed. This data is consistent with forskolin stimulated release of secretory granules and subsequent replenishment. As seen in FIG. 24, the Western blot of HMEC cell lysates included: control, stimulated with 10 mM forskolin 0.5 hours post stimulation and 48 hours post stimulation. The Western blot also included a lane marked Media, which showed the results of radioimmunoprecipitation of 24 hour conditioned media from 35S-labelled MDA-MB-468 cells. These results indicate the presence of BRCA1 protein at 190 kDa. Media was supplemented with aprotinin, PMSF, leupeptin, and pepstatin.
To confirm that BRCA1 is in fact secreted MDA-MB-468 cells were metabolically labelled and the 190 k-Da band was immunoprecipitated from a 24 hour collection of labelled conditioned media. Finally, immunogold electron microscopy was performed with C-20 antibody on MDA-MB-468 cells and it was demonstrated that BRCA1 immunoreactivity localizes to secretory vesicles. These secretory vesicles were primarily located in the apical cytoplasm and were often found at the tips of microvilli extending into the extracellular space. A vesicle actively undergoing secretion was identified. These findings confirm that BRCA1 is a member of the granin family of secretory proteins.
In summary, then, BRCA1 has a granin box which shows 100% homology to the consensus (Huttner et al., 1991, Trends Biochem. Sci. 16, 27-30) and has the expected number of acidic residues and predicted isoelectric point of granin family members. Additional evidence that BRCA1 is a granin includes 1) Presence in secretory vesicle fractions; 2) Induction by estradiol; 3) Glycosylation which occurs on secretory proteins as they are transported through the rough endoplasmic reticulum (Kornfeld & Kornfeld, 1985, Annu. Rev. Biochem. 54, 631-664); 4) Solubility of boiled protein, a biochemical feature of the granin family; 5) Release of BRCA1 protein by forskolin induction of regulated secretion; and 6) localization in secretory vesicles by immunogold electron microscopy.
As more fully described below, internal deletions which eliminate key structural elements and glycosylation sites destroy growth inhibition and tumor suppression, thus indicating that BRCA1 tumor suppression and growth inhibition are mediated through its granin-like properties.
EXAMPLE 4
Normal BRCA1 inhibits growth of breast and ovarian cancer cells
Experiments to determine whether BRCA1 could function as a growth inhibitor or tumor suppressor were performed. Analysis of BRCA1 protein levels in human breast cancer cell lines indicated that MCF-7 cells had little or no BRCA1 protein. Analysis of MCF-7 cells for allelic loss at markers in the BRCA1 region indicates loss of at least 2 Mb including the BRCA1 region on one chromosome 17q21, and that the coding sequence of the retained BRCA1 allele was normal. Sal I linkered BRCA1 cDNA was cloned into the unique Xho I site of the retroviral vector LXSN for transfection studies. To rule out trivial effects on localization or stability, two in-frame internal deletion mutants were constructed which eliminated much of the region of BRCA1 containing acidic residues and putative glycosylation sites (D343-1081 and D515-1092), but preserved the granin homology region. Two termination codon mutants were constructed which resulted in predicted proteins containing 1835 and 340 amino acids.
Table I shows that transfection of the LXSN vector or the internal deletion mutants resulted in similar numbers of G418-resistant stable clones in a number of human cell lines.
Transfection of LXSN-BRCA1 into MCF-7 cells or Caov-4 ovarian cancer cells resulted in fewer clones which could not be expanded beyond 30 cells per clone. Some of these clones can be expanded in an enriched growth media containing GMSA, 10% fetal calf serum and 5 ng/ml EGF. This growth inhibitory effect of BRCA1 was confined to these cell types since fibroblast, lung cancer cells, and colon cancer cells were not growth inhibited by LXSN-BRCA1. The 340-amino acid truncated protein did not inhibit growth of any cell line. However, the 1835 amino acid protein significantly inhibited growth of ovarian cancer cells but not breast cancer cells. This indicates that distinct mechanisms mediate growth inhibition of ovarian cancer cells and breast cancer cells and that this difference depends on the length of the truncated protein.
EXAMPLE 5
Ovarian cancer susceptibility is differentially associated with protein truncations 5' of the granin region
To determine whether the differential effects of short versus long truncated proteins on Caov-4 ovarian cancer cells were paralleled in human patients, the relative frequency of ovarian versus breast cancer among 166 patients in a series inheriting BRCA1 mutations was calculated (Table II). Mutations inherited by 19 patients were nonsense alterations leading to transcript instability and no mutant protein. Mutations inherited by 13 patients were missense alterations in the RING finger leading to complete but aberrant protein. All other mutations were protein-truncating mutations at sites throughout the gene. The difference in ovarian and breast cancer distribution between the two groups was statistically significant: ovarian cancer formed a significantly lower proportion (2%) of the cancers in patients with mutant proteins that would include the granin motif compared to the proportion (25%) of cancers in patients with more severely truncated proteins (X2=11.12, P<0.001). This result is consistent with the observation that the site of BRCA1 mutation is associated with relative susceptibility to ovarian versus breast cancer (Gayther et al., 1995, Nature Genet 11: 428-433). The analysis of Gayther et al., indicated that the correlation between genotype and phenotype was better described by a "change point" in the BRCA1 sequence than by a linear trend in locale of mutation. The granin consensus motif at codons 1214-1223 is well within the confidence limit for the estimated location (codons 1235-1243) of the optimal change point in that analysis.
EXAMPLE 6
BRCA1 Inhibits Breast but not Colon Tumorigenesis
BRCA1 gene transfer into MCF-7 cells inhibits tumorigenesis employing retroviral gene transfer. Supernatants containing 5.times.10.sup.7 vector particles from LXSN and LXSN-BRCA1 PA317 producer clones were used to transduce 5.times.10.sup.7 MCF-7 cells or OK3 colon cancer cells in culture which were subsequently injected into the flanks of six nude mice for each vector. The cells were not treated with G418 before injection because prior G418 treatment inhibits tumorigenesis in this model, but southern blots have demonstrated that 70-80% of MCF-7 cells are transduced by this protocol. Four weeks after injection there were MCF-7 tumors in 5/6 LXSN control mice but no tumors in LXSN-BRCA1 mice. Retroviral transduction by BRCA1 had no effect on colon tumor formation (Table III, FIG. 8). Tumors ultimately developed in all of the control mice and 4/6 LXSN-BRCA1 mice but the tumors in LXSN-BRCA1 mice were significantly smaller (XSN: 569 grams+60; LXSN-BRCA1: 60 grams+24) as illustrated in Table III, FIG. 8. Molecular analysis of tumor RNAs showed that the vector neo gene was present and expressed in all MCF tumors and that BRCA1 was detectable only in the four LXSN-BRCA1 transduced tumors. Because the ex vivo transduction strategy could inhibit tumor establishment but not necessarily inhibit growth of already established tumors, whether in vivo injection of LXSN-BRCA1 into established MCF-7 intraperitoneal tumors could inhibit the growth rate and improve survival was tested. This experimental approach results in retroviral vector integration into 20-40% of tumor cells. The results showed that while all five of the mice given the mutant BRCA1 retrovirus died in less than two weeks, the five mice injected with LXSN-BRCA1 survived from 15-41 days because the injection decreased the size and sequelae of the intraperitoneal tumors (Table III, FIG. 8).
The above studies were confirmed with stable transfectants expressing BRCA1. Using an enriched growth media MCF-7 transfectants containing the transferred BRCA1 gene were obtained. Although these clones grow at 1/3 the rate of mutant BRCA1 transfected clones in vitro, whether they would form tumors in nude mice was determined. Three distinct clones transfected with D343-1081 and four distinct clones transfected with BRCA1 (five mice per clone) were injected with the MCF-7 transfectants. The results show that 0/20 mice injected with BRCA1 transfectants developed tumors while 13/15 mice injected with mutant BRCA1 transfectants developed tumors, providing confirmation that BRCA1 inhibits tumorigenesis in nude mice (Table III). RT-PCR analysis demonstrated that the transfectants expressed the expected transfected BRCA1 or mutant BRCA1 mRNA.
Lactation is the most important secretory process in the breast and is defining for mammals. Indeed, the human breast is unique in that it does not fully differentiate until the first pregnancy and active lactation is followed by involution (Battersby et al., 1994, Histopathology 15:415-433). Thus during each lactation, cell numbers must be increased with the end of proliferation coinciding with the gain of secretory function. Following cessation of lactation the cell numbers must decrease to allow breast involution. Pairing secretion feedback with cell proliferation and growth inhibition mechanisms is reasonable and to be expected in this setting.
The identification of BRCA1 as a member of the granin family of secreted proteins indicates that it functions as a novel type of tumor suppressor gene.
Analysis of BRCA1 mutations shows that near full-length proteins do not protect against breast cancer, but far less often lead to ovarian cancer (Table II). Analysis of transfection experiments shows that near full-length BRCA1 proteins do not inhibit growth of breast cancer cells but do inhibit growth of ovarian cancer cells. This indicates that the mechanism of tumor suppression by BRCA1 differs for breast versus ovarian cancer.
Pregnancy and lactation are important protective factors for breast cancer. Although the epidemiologic basis of this is well-demonstrated, molecular correlates are lacking. The demonstration that BRCA1 mRNA is induced during mouse pregnancies and this work showing a secretory function for BRCA1 link a tumor suppressor gene with a epidemiologically-defined tumor suppression activity, early pregnancy.
EXAMPLE 7
Method of Screening for BRCA1 or BRCA2 Receptor
That BRCA1 is secreted has important implications for lactation and growth regulation of normal and malignant breast cells. The secreted BRCA1 protein acts on a cell surface receptor. The interaction between the BRCA1 protein and the receptor produces the beneficial effects, i.e. tumor suppression, in the target breast or ovarian tissue. Methods for isolating the BRCA1 receptor follow. The BRCA2 receptor can be similarly isolated.
Baculovirus BRCA1 can be purified from the insect cells with the C20 antibody and then labelled with radioactive iodine by standard methods. Cys61Gly and termination codon mutant BRCA1 proteins are prepared and labelled as a control. The labelled BRCA1 can then be used to perform binding studies to identify cells with BRCA1 receptors using Scatchard analysis; and to perform cross-linking studies which demonstrate the BRCA1 receptor(s) on polyacrylamide gels. These initial characterization methods are used to identify cells with high and low numbers of BRCA1 receptor(s) for purification and isolation studies. Once a cell line with high levels of BRCA1 receptor has been identified, then the protein is purified by the following approaches:
Approach A: Biochemical purification
The cell line which expresses high levels of BRCA1 receptor is lysed and the protein from cell lysates or membrane preparations is purified by gel filtration followed by purification of the receptor with a column containing the BRCA1 ligand bound to a solid phase such as sepharose. The purified receptor protein can then be microsequenced and the gene cloned using degenerate oligonucleotides derived from the protein sequence.
Approach B:
Ligand is radiolabeled with 125I and then used to screen cell lines or tissues for specific binding by Scatchard analysis. Once such binding is identified, a cDNA library is constructed from that tissue or cell line and transfected into a cell line that does not exhibit specific binding. These transfected cells are then screened for newly acquired specific binding which indicates they have been transfected with a construct containing the gene for the BRCA1 receptor. Plasmid DNA from positive clones is then isolated and sequenced for identification. This single construct is then transfected back into the null cells to verify that binding of ligand is mediated by the transfected gene. (Kluzen et al, Proc Natl Acad Sci USA 89:4618-4622 (1992).
Alternatively, chimeric BRCA1 and immunoglobulin Fc molecules can be constructed. (LaRochelle et al, J Cell Biol 129:357-366 (1995)). These chimeric molecules are then be used to screen for binding to BRCA1 receptor on whole cells via flow cytometry. Alternatively, due to the presence of the immunoglobulin component of the molecule, cell lysates are screened by immunoblotting or by immunoprecipitation of metabolically labelled cells. This technique can identify BRCA1 binding proteins by a variety of different methods. Peptide digests of the identified proteins are then generated so that the peptides can be sequenced and the whole molecule cloned by a degenerative oligonucleotide approach.
EXAMPLE 8
Screen for BRCA1 Protein Mimetic Agents
Classical methods for identifying compounds which activate receptors are greatly facilitated by the prior identification of the receptor. However, knowledge of ligand structure domains and deletion and minimization methods allow the identification of active ligand mimetic drugs without first finding the receptor. As more fully described above, certain regions of the BRCA1 gene have been deleted to show which regions are essential for growth inhibitory activity. These studies can be continued in a systematic manner, revealing the regions of the molecule needed for its key activities. Upon identification of a small protein that can produce growth inhibition, systematic structural and functional analysis of the minimal protein can be performed as per the methods described in Li, et al., Science 270: 1657, 1995. Drugs can then be screened for and/or synthesized which mimic the peptide structure and consequently produce the desired effect.
Thus, provided also is a method of screening a compound for tumor suppressor activity comprising contacting the compounds with the BRCA1 or BRCA2 receptor, a compound which binds the receptor indicating a compound having potential tumor suppressor activity. Binding can be detected by well-known methods in the art, including, among others, radioimmunoassays and fluorescence assays.
EXAMPLE 9
Therapy method for ovarian cancer using the BRCA1 Gene.
Viral vectors containing a DNA sequence that codes for a protein having an amino acid sequence as essentially set forth in SEQ ID NO:2 can be constructed using techniques that are well known in the art. This sequence includes the BRCA1 protein. Viral vectors containing a DNA sequence essentially as set forth in SEQ ID NO:1 (the BRCA1 gene) can be also constructed using techniques that are well known in the art. Retroviral vectors such as the LXSN vector described above, adenoviral vectors, or adeno-associated viral vectors are all useful methods for delivering genes into ovarian cancer cells. The viral vector is constructed by cloning the DNA sequence essentially as set forth in SEQ ID:1 into a retroviral vector such as an ovarian selective vector. Most preferably, the full-length (coding region) cDNA for BRCA1 is cloned into the retroviral vector. The retroviral vector would then be transfected into virus producing cells in the following manner: Viruses are prepared by transfecting PA317 cells with retroviral vector DNAs which are purified as described in Wong et al., 1988, Proceeding of the UCLA Symposia on Biology of Leukemias and Lymphomas., Golde D. (ed.), Alan R. Liss, Inc. 61:553-566. Following transfection, the PA317 cells are split and then treated with G418 until individual clones can be identified and expanded. Each clone is then screened for its titer by analyzing its ability to transfer G418 resistance (since the retroviral vector contains a Neomycin resistance gene). The clones which have the highest titer are then frozen in numerous aliquots and tested for sterility, presence of replication-competent retrovirus, and presence of mycoplasma. Methods generally employed for construction and production of retroviral vectors have been described above and in Miller, et al., 1990, Methods in Enzym. 217:581-599.
Once high titer viral vector producing clones have been identified, then patients with ovarian cancer can be treated by the following protocol: Viral vector expressing BRCA1 is infused into either solid tumors or infused into malignant effusions as a means for altering the growth of the tumor (since it is shown above that the BRCA1 protein decreases the growth rate of ovarian cancer cells). Because viral vectors can efficiently transduce a high percentage of cancer cells, the tumors will be growth inhibited.
EXAMPLE 10
The protein encoded by the BRCA2 breast and ovarian cancer susceptibility gene is a granin and a secreted tumor suppressor.
The protein encoded by the BRCA2 breast and ovarian cancer susceptibility gene (Wooster, R., et al., Nature 379: 789-792, 1995) includes a domain similar to the granin consensus at the C-terminus of the protein. As seen in FIG. 5, the sequence at amino acids 3334-3344 of Genbank locus HUS43746 matches six of the seven constrained sites of the granin consensus. BRCA2 and murine BRCA1 differ from the consensus at the same site. The granin motif in BRCA2 lies at the extreme C-terminal end of the protein, a locale characteristic of a known granin. This indicates that the protein encoded by the BRCA2 gene is also a secreted growth inhibitor. Use of both the BRCA1 and BRCA2 genes offer the opportunity for a unified approach to the treatment of inherited and sporadic breast cancer. Accordingly, the examples set forth above depicting the treatment of ovarian cancer, are equally applicable to the BRCA2 gene and the BRCA2 protein.
The identification of BRCA1 and BRCA2 as granins indicated that there is a granin superfamily of which consists of the subfamilies of chromogranins (chromogranins A, B and C); secretogranins (secretogranins III-V) and the BROCAgranins (BRCA1, BRCA2 and other tumor suppressor genes). This classification of granins into these subclasses is based on greater similarities within the subfamilies than with the superfamily as a whole. For example, the chromogranins share an additional region of homology besides the granin consensus and exhibit similar expression patterns; the secretogranins show less homology to the granin consensus than either chromogranins or BROCAgranins; the BROCAgranins BRCA1 and BRCA2 are cancer susceptibility genes, contain additional regions of homology, and are significantly larger (two-twenty times larger) than other granins described to date.
Thus, the invention provides in Example 3 and in this example a granin box consensus sequence shown in FIG. 5. Thus, provided is a family of proteins which share the consensus sequence that are tumor suppressor genes. BRCA1 and BRCA2 are members of this family. Other members may be identified and purified as tumor suppressor genes by genetic methods, by DNA-based searches for granin homology; or by cloning and characterization of granins in ovarian or breast cancer cells by biochemical methods. Such biochemical methods include the isolation and purification of proteins from secretory vesicles or Golgi by physical isolation methods, followed by development of antibodies to determine which proteins, followed by cloning of genes for secreted proteins after protein sequencing and cloning with degenerate oligonucleotide primers. A example of this method is described in Colomer et al., 1996, J. Biological Chemistry 271:48-55. Thus, other BROCA granins are contemplated to be within the scope of this invention.
EXAMPLE 11
Gene Therapy method using the BRCA2 Gene
Viral vectors containing a DNA sequence that codes for a protein having an amino acid sequence as essentially set forth in SEQ ID NO:4 can be constructed using techniques that are well known in the art, and as are more fully described above. This sequence includes the BRCA2 protein. Viral vectors containing a DNA sequence essentially as set forth in SEQ ID NO:3 (the BRCA2 gene) can be also constructed using techniques that are well known in the art. Retroviral vectors, adenoviral vectors, or adeno-associated viral vectors are all useful methods for delivering genes into breast cancer cells. An excellent candidate for use in breast cancer gene therapy is a Moloney-based retroviral vector with a breast selective MMTV promoter (Wong et al., 1988, Proceeding of the UCLA Symposia on Biology of Leukemias and Lymphomas., Golde D. (ed.), Alan R. Liss, Inc. 61:553-566). The viral vector is constructed by cloning the DNA sequence essentially as set forth in SEQ ID NO:3 into a retroviral vector such as a breast selective vector. Most preferably, the full-length (coding region) cDNA for BRCA2 is cloned into the retroviral vector. The retroviral vector is then transfected into virus producing cells in the following manner: Viruses are prepared by transfecting PA317 cells with retroviral vector DNAs which are purified as described in Wong et al. Following transfection, the PA317 cells are split and then treated with G418 until individual clones can be identified and expanded. Each clone is then screened for its titer by analyzing its ability to transfer G418 resistance (since the retroviral vector contains a Neomycin resistance gene). The clones which have the highest titer are then frozen in numerous aliquots and tested for sterility, presence of replication-competent retrovirus, and presence of mycoplasm. The methods generally employed for construction and production of retroviral vectors have been described above and in Miller, et al., 1990, Methods in Enzym. 217:581-599.
Once high titer viral vector producing clones have been identified, then patients with breast cancer can be treated by the following protocol: Viral vector expressing BRCA2 protein is infused into either solid tumors or infused into malignant effusions as a means for altering the growth of the tumor. Because viral vectors can efficiently transduce a high percentage of cancer cells, the tumors will be growth inhibited.
EXAMPLE 12
Gene Transfer Using Liposomes
An alternative method of gene therapy using the BRCA1 and BRCA2 gene includes the use of liposome to deliver the DNA into the cells. By this method, the above described LXSN-BRCA1 plasmid would be incubated with a liposome preparation such as cationic liposomes and then the DNA liposome mix is added to cells or injected into an animal or patient. Generally, the liposome transfection method is of a lower efficiency than viral gene transfer methods. This method is useful because the BRCA1 and BRCA2 proteins are secreted proteins. Thus, if only a few percent of cells take up the DNA-liposome combination, it is likely that enough BRCA1 or BRCA2 protein will be produced and secreted from these cells to growth inhibit other cells. Liposomal transfection of nucleic acids into host cells is described in U.S. Pat. Nos. 5,279,833 and 5,286,634, the contents of each of which are herein incorporated by reference.
EXAMPLE 13
Anti-Sense Inhibition of the Production of BRCA1 Protein
The antisense inhibition of BRCA1 is described as follows. Antisense methods were used to demonstrate that BRCA1 expression inhibits cell growth. Unmodified 18 base deoxyribonucleotide complementary to the BRCA1 translation initiation site were synthesized and added to cultures of primary mammary epithelial cells (Stampfer et al. 1980, In Vitro 16: 415-425 (1980)) or MCF-7 breast cancer cells (Soule and McGrath, 1980, Cancer Letters 10, 177-189 (1980)).
The morphologic appearance of the cell lines was not noticeably changed by addition of antisense oligonucleotide, but the proliferative rate was faster. Incubation of cells with 40 uM anti-BRCA1 oligonucleotide produced accelerated growth of both normal and malignant mammary cells, but did not affect the growth of human retinal pigmented epithelial cells. An intermediate dose of anti-BRCA1 oligonucleotide produced a less pronounced but significant 310 increase in cell growth rate. This was not a toxic effect of the oligonucleotide since a control "sense" oligomer with the same GC content did not increase the proliferation rate, and because an addition of a 10 fold excess of sense oligomer to the anti-BRCA1 oligomer reversed the growth activation.
Thus, antisense inhibition of BRCA1 accelerates the growth of breast cancer cells. Because chemotherapy is most effective in cancer cells which are rapidly dividing, it is possible then to treat breast or ovarian cancer by accelerating growth of cancer cells by antisense inhibition of BRCA1 protein expression and by treating with chemotherapeutic drugs using standard chemotherapy protocols.
EXAMPLE 14
Biological Functional Equivalent Proteins and Peptides
Modification and changes may be made in the structure of the BRCA1 protein and the BRCA2 protein, or in cleavage products of these proteins, and still obtain a molecule having like or otherwise desirable characteristics. For example, certain amino acids may be substituted for other amino acids in a protein structure without appreciable loss of interactive binding capacity with structures such as, for example, antigen-binding regions of antibodies or binding sites on substrate molecules or receptors, specifically the BRCA1 or BRCA2 receptor. Since it is the interactive capacity and nature of a protein that defines that protein's biological functional activity, certain amino acid sequence substitutions can be made in a protein sequence (or, of course, its underlying DNA coding sequence) and nevertheless obtain a protein with like (agonistic) properties. Equally, the same considerations may be employed to create a protein or polypeptide with counterveiling (e.g., antagonistic) properties. It is thus contemplated by the inventors that various changes may be made in the sequence of the BRCA1 and BRCA2 proteins or peptides (or underlying DNA) without appreciable loss of their biological utility or activity.
Two designations for amino acids are used interchangeably throughout this application, as is common practice in the art. Alanine=Ala (A); Arginine=Arg (R); Aspartate=Asp (D); Asparagine=Asn (N); Cysteine=Cys (C); Glutamate=Glu (E); Glutamine=Gln (Q); Glycine=Gly (G); Histidine=His (H); Isoleucine=Ile (1); Leucine=Leu (L); Lysine=Lys (K); Methionine=Met (M); Phenylalanine=Phe (F): Proline=Pro (P); Serine=Ser (S); Threonine=Thr (T); Tryptophan=Trp (W); Tyrosine=Tyr (Y); Valine=Val (V).
It is also well understood by the skilled artisan that, inherent in the definition of a biologically functional equivalent protein or peptide, is the concept that there is a limit to the number of changes that may be made within a defined portion of the molecule and still result in a molecule with an acceptable level of equivalent biological activity. Biologically functional equivalent peptides are thus defined herein as those peptides in which certain, not most or all, of the amino acids may be substituted. Of course, a plurality of distinct proteins/peptides with different substitutions may easily be made and used in accordance with this invention.
It is also well understood that where certain residues are shown to be particularly important to the biological or structural properties of a protein or peptide, e.g., residues in active sites, such residues may not generally be exchanged. This is the case in the present invention where an exchange in the granin box domain may alter the fact that the BRCA1 and BRCA2 proteins are secreted.
Amino acid substitutions are generally based on the relative similarity of the amino acid side-chain substituents, for example, their hydrophobicity, hydrophilicity, charge, size, and the like. An analysis of the size, shape and type of the amino acid side-chain substituents reveals that arginine, lysine, and histidine are all positively charged residues; that alanine, glycine and serine are all a similar size; and that phenylalanine, tryptophan and tyrosine all have a generally similar shape. Therefore, based upon these considerations, arginine, lysine and histidine; alanine, glycine and serine; and phenylalanine, tryptophan and tyrosine; are defined herein as biologically functional equivalents.
In making such changes, the hydropathic index of amino acids may be considered. Each amino acid has been assigned a hydropathic index on the basis of their hydrophobicity and charge characteristics, these are: isoleucine (+4.5); valine (+4.2); leucine (+3.8); phenylalanine (+2.8); cysteine/cystine (+2.5); methionine (+1.9); alanine (+1.8); glycine (-0.4); threonine (-0.7); serine (-0.8); tryptophan (-0.9); tyrosine (-1.3); proline (-1.6); histidine (-3.2); glutamate (-3.5); glutamine (-3.5); aspartate (-3.5); asparagine (-3.5); lysine (-3.9); and arginine (-4.5).
The importance of the hydropathic amino acid index in conferring interactive biological function on a protein is generally understood in the art (Kyte & Doolittle, 1982, incorporated herein by reference). It is known that certain amino acids may be substituted for another amino acids having a similar hydropathic index or score and still retain a similar biological activity. In making changes based upon the hydropathic index, the substitution of amino acids whose hydropathic indices are within .+-.1 are particularly preferred, and those within .+-.2 is preferred, those which are within .+-.0.5 are even more particularly preferred.
It is also understood in the art that the substitution of like amino acids can be made effectively on the basis of hydrophilicity, particularly where the biological functional equivalent protein or peptide thereby created is intended for use in immunological embodiments. U.S. Pat. No. 4,554,101, incorporated herein by reference, states that the greatest local average hydrophilicity of a protein, as governed by the hydrophilicity of its adjacent amino acids, correlates with its immunogenicity and antigenicity, i.e. with a biological property of the protein. It is understood that an amino acid can be substituted for another having a similar hydrophilicity value and still obtain a biologically equivalent, and in particular, an immunologically equivalent protein.
As detailed in U.S. Pat. No. 4,554,101, the following hydrophilicity values have been assigned to amino acid residues: arginine (+3.0); lysine (+3.0); aspartate (+3.0.+-.1); glutamate (+3.0.+-.1); serine (+0.3); asparagine (+0.2); glutamine (+0.2); glycine (0); threonine (-0.4); proline (-0.5+1); alanine (-0.5); histidine (-0.5); cysteine (-1.0); methionine (-1.3); valine (-1.5); leucine (-1.8); isoleucine (-1.8); tyrosine (-2.3); phenylalanine (-2.5); tryptophan (-3.4).
In making changes based upon similar hydrophilicity values, the substitution of amino acids hose hydrophilicity values are within .+-.2 is preferred, those which are within .+-.1 are particularly preferred, and those within .+-.0.5 are even more particularly preferred.
As outlined above, amino acid substitutions are generally therefore based on the relative similarity of the amino acid side-chain substituents, for example, their hydrophobicity, hydrophilicity, charge, size, and the like. Exemplary substitutions which take various of the foregoing characteristics into consideration are well known to those of skill in the art and include: arginine and lysine; glutamate and aspartate; serine and threonine; glutamine and asparagine; and valine, leucine and isoleucine.
While discussion has focused on functionally equivalent polypeptides arising from amino acid changes, it will be appreciated that these changes may be effected by alteration of the encoding DNA; taking into consideration also that the genetic code is degenerate and that two or more codons may code for the same amino acid.
Kyte & Doolittle, J. Mol. Biol., 157:105-132, 1982; Hopp, U.S. Pat. No. 4,554,101.
In addition to the peptidyl compounds described herein, the inventors also contemplate that other sterically similar compounds may be formulated to mimic the key portions of the peptide structure. Such compounds, which may be termed peptidomimetics, may be used in the same manner as the peptides of the invention and hence are also functional equivalents. The generation of a structural functional equivalent may be achieved by the techniques of modelling and chemical design known to those of skill in the art. It will be understood that all such sterically similar constructs fall within the scope of the present invention.
U.S. Pat. No. 4,554,101 (Hopp, incorporated herein by reference) teaches the identification and preparation of epitopes from primary amino acid sequences on the basis of hydrophilicity. Through identify epitopes from within an amino acid sequence such as the BRCA1 and BRCA2 sequences disclosed herein (SEQ ID NOs:2, 4). These regions are also referred to as "epitopic core regions".
Numerous scientific publications have been devoted to the prediction of secondary structure, and to the identification of epitopes, from analyses of amino acid sequences (Chou & Fasman, 1974a,b; 1978a,b 1979). Any of these may be used, if desired, to supplement the teachings of Hopp in U.S. Pat. No. 4,554,101. Moreover, computer programs are currently available to assist with predicting antigenic portions and epitopic core regions of proteins. Examples include those programs based upon the Jameson-Wolf analysis (Jameson & Wolf, 1998; Wolf et al., 1988), the program PepPlot.RTM. (Brutlag et al., 1990; Weinberger et al., 1985), and other new programs for protein tertiary structure prediction (Fetrow & Bryant, 1993).
EXAMPLE 15
Treatment of Breast or Ovarian Cancer using Purified BRCA1 or BRCA2 Protein
Alternatively, breast or ovarian cancer be treated by the administration of a therapeutically effective amount of the BRCA1 or BRCA2 protein via an efficient method, such as injection into a tumor. A therapeutically effective amount can be determined by one having ordinary skill in the art using well-known protocols.
It is important to note that breast and ovarian cancer cells have surface receptors which must be contacted by the BRCA1 or BRCA2. Thus, the BRCA1 or BRCA2 protein, an active fragment, or a small molecule mimetic binds directly to a receptor on the surface of the breast or ovarian cancer cells.
EXAMPLE 16
Method of Treating Breast or Ovarian Cancer Comprising Introducing the BRCA1 Receptor Gene and the BRCA1 protein into a Breast or Ovarian Cancer Cell
The loss of the BRCA1 receptor in breast and ovarian cancer cells will lead to the proliferation and tumorigenesis in these cells. Thus, breast and ovarian cancer can be treated by introducing the BRCA1 receptor gene into breast or ovarian cancer cells using the gene therapy methods described above. This step will be followed by the administration of a therapeutically effective amount of the BRCA1 protein so that the BRCA1 protein contacts a receptor on a surface of the breast or ovarian cells. A therapeutically effective amount can be determined by one having ordinary skill in the art using well-known protocols.
EXAMPLE 17
Method of Preventing Breast or Ovarian Cancer using BRCA1 or BRCA2 Protein
It is a well-established epidemiologic fact that parity and particularly early parity has a protective effect in regards to both breast and ovarian cancer risk. Because of various changes in the structure of society it is now quite common for women to delay childbirth and lose this natural protective effect. Since it is known that BRCA1 is induced in pregnancy and lactation, and it is demonstrated herein that BRCA1 is a secreted growth inhibitor that is specific for breast and ovarian cancer, the protective effect of pregnancy and lactation is due to BRCA1 expression. BRCA1 mediation of this effect for both breast and ovarian cancer presents a variety of strategies that are useful in decreasing breast and ovarian cancer risk, particularly in women that did not have a baby in their first twenty years and thus, were at a higher risk to develop breast or ovarian cancer. Thus, one can use a BRCA to prevent the first occurrence or a recurrence of breast and ovarian cancer. Examples of such strategies are presented below. While examples are provided, such strategies should not be limited to the examples.
BRCA1 protein might be used a chemopreventive agent by introducing BRCA1 directly into the peritoneal cavity of women as the whole protein, as a functional fragment, or as a functional cleavage product. In addition, compounds that induce expression of BRCA1 or activate its receptor, e.g. a small molecule mimetic, could also be introduced. Since BRCA1 is a secreted protein, the introduced BRCA1 will decrease ovarian cancer risk in the same manner that BRCA1 does normally when its expression is induced by pregnancy. The protective effect is also expected where BRCA1 expression is mediated by gene therapy method by either directly or indirectly inducing expression of BRCA1.
A similar rationale can be applied to breast cancer prevention. In this case, the whole BRCA1 protein; a functional fragment or a functional cleavage product thereof; or a pharmacological mimic can be used. In addition, compounds that induce expression of BRCA1 or activate its receptor, e.g. a small molecule mimetic, could also be used. Gene therapy approaches for increasing the expression of BRCA1 in breast directly or indirectly could also be used. Systemic agents that induce expression of BRCA1, or that mimic function and can replace BRCA1, such a peptidomimetic agent, could also be used. The delivery of such agents could take place by directly instilling the agent within the breast by introducing via the nipple. Finally, an implantable time release capsule can be used in a prevention strategy, either by placing such a capsule in the peritoneum for ovarian cancer, by implant such a capsule into the breast for breast cancer.
Since the BRCA2 protein includes a granin sequences and is also a secreted tumor suppressor protein, similar prevention strategies can be applied using the BRCA2 gene and protein.
Experimental Procedures for Examples 1-6
Tissues and Cell Culture
Cryopreserved primary cell lines (Passage 7) of normal human mammary epithelial (HMEC) cells, were obtained from Clonetics, Inc. The cryovial of HMEC was thawed and subcultured according to the instructions provided, which are a slight modification of published procedures (Stampfer et al, 1980, Growth of Normal Human Mammary Cells in Culture. 16, 415-425). Breast cancer cell lines were obtained from American Type Culture Collection (ATCC), Rockville, Md. Sf9 cells were obtained from ATCC.
Antibodies
C-terminal 19 peptide fragment was conjugated to keyhole limpet hemacyanin and injected into New Zealand white rabbits along with Freund's adjuvant according to standard protocols. C-20 and D-20 were provided by Santa Cruz Biotechnology. c-myc and PDGFR antibodies were provided by Steve Hann and William LaRochelle, respectively.
Cell Extracts, Immunoblotting, Immunoprecipitation, Northern blotting Cell lysates, immunoblotting, and immunoprecipitation assays were performed according to previously published methods (Jensen et al, 1992, Biochem. 31: 10887-10892). RNA was isolated by published methods (Jensen et al, 1994, Proc Natl Acad Sci USA 91, 9257-9261) and probed with the T7 labelled EcoRI-Kpn I fragment from exon 11.
Cell Fractionation Studies
Cell fractionations were performed according the method of Fazioli, et al (1993, Mol. Cell. Bio. 13, 5814-5828). Briefly, cells in T175 flasks were washed twice with cold PBS/0.5 mM sodium vanadate, followed by a single washing in cold isotonic fractionation buffer (FB). Then, cold FB+protease inhibitors (PI) are added to the plates. The plates are incubated for 10 min, scraped, and homogenized with a Dounce tissue homogenizer. The nuclei were gently pelleted (375 g) at 4.degree. C. and the supernatant (cytosolic and plasma membrane fraction) was saved. After washing the nuclear pellet with four aliquots of cold FB+PI+0.1% NP40 followed by centrifugation at 4.degree. C., the nuclei were resuspended in cold FB and 2.times. lysis buffer+PI. The cytosolic and plasma membrane fraction was then ultracentrifuged (35,000 g) for 30 min at 4.degree. C. and the supernatant was saved as the cytosolic fraction. The pellet (plasma membrane fraction) was resuspended in FB+PI and solubilized in 2.times. lysis buffer with PI. Following this, the nuclear and plasma membrane fractions are sonicated on ice for 10 seconds three times. They were then spun at 10,000 g at 4.degree. C., and the supernatant was collected and saved as the soluble nuclear and plasma membrane fractions, respectively.
Confocal Imaging Studies
HMEC cells were plated into 35 mm culture dishes with glass bottom cover slips (Mat-Tek) and allowed to grow to 70% confluency. The cells were then rinsed, fixed in 4.0% paraformaldehyde in phosphate buffered saline at 4.degree. C. (PBS, 0.01 M phosphate salts, and 0.15 M NaCl, pH 7.6) for ten minutes, and washed and permeabilized in PBS with 0.2% Triton X-100 for two minutes. Cells were blocked with 5% normal donkey serum in PBS. Primary antibodies were diluted in PBS containing 3.0% bovine serum albumin (BSA) and 0.1% Triton X-100 and consisted of rabbit anti-BRCA-1 (vendor) diluted 1:200 and a mouse monoclonal to a Golgi complex antigen (Biogenex; clone 371-4) diluted 1:10. No antibody and antibody to BRCA-1 pre-adsorbed with the peptide antigen were used as negative controls. Secondary antibodies were from Jackson Immunoresearch and consisted of extensively adsorbed, multiple-labeling grade donkey anti-rabbit-specific IgG conjugated to CY3 (diluted 1:1000) and donkey anti-mouse-specific IgG conjugated to either CY5 (diluted 1:500) or FITC (diluted 1:250). Nuclei were counterstained with YO-PRO1 (Molecular Probes, Inc.) diluted 1:500 for 20 minutes following immunostaining. Double-immunolabeling studies were carried out with all the necessary controls for staining specificity as outlined previously (Jetton et al., 1994, J. Biol. Chem. 269, 3641-3654). Following immunostaining, sections were mounted in Aqua-Polymount (Polysciences) and imaged using a Zeiss LSM 410 confocal microscope using the 488/647 and 543 nm lines of an Ar--Kr and He--Ne laser, respectively. Images were optimized using Adobe Photoshop 3.0 then transferred as TIFF files to a Silicon Graphics Indigo where figures were assembled using SGI Showcase and printed using a Tektronix Phaser IISDX color printer.
Glycosylation Analysis
Glycosylation analysis was performed on aliquots of HMEC membrane fractions with the Enzymatic Deglycosylation Kit from Glyko, Inc. according to the manufacturer's recommended protocol, and the samples were immunoblotted and probed with C-20 antibody.
Isolation of Secretory Vesicles
Secretory vesicles were isolated as described (Tooze and Huttner, 1990, Cell 60, 837-847) with minor modifications. All steps were performed at 4.degree. C. MDA-MB-468 cells were washed with cold PBS containing protease inhibitors. After centrifugation at 700.times. g for 5 min, the pellet was resuspended in homogenization buffer (0.25 M sucrose, 1 mM EDTA, 1 mM Mg acetate, 10 mM HEPES-KOH, pH 7.2) with protease inhibitors and centrifuged at 1700.times. g for 5 min. The pellet was resuspended in 5 times the cell volume of homogenization buffer with protease inhibitors. Cells were passed through a 22 gauge needle 10 times and homogenized with 50 strokes of a Pyrex homogenizer. Unbroken cells and nuclei were pelleted at 1000.times. g for 10 min. One ml of the postnuclear supernatant was loaded onto a 0.3 M-1.2 M sucrose gradient (made in 10 mM HEPES-KOH, pH 7.2) with protease inhibitors and centrifuged at 25,000 rpm in a Beckman SW41 rotor for 15 min. One ml fractions were collected from the bottom and fractions 9-12 were pooled and loaded onto a 0.5 M-2 M sucrose gradient. The gradient was centrifuged at 25,000 rpm in a Beckman SW41 rotor for 16 hours and fractions collected from the bottom. Fractions 4-12 were analyzed by Western blot analysis.
Expression of Recombinant Clones in the Baculovirus Expression System
A full length BRCA1 cDNA containing consensus translation initiation and stop sites was cloned into the baculovirus transfer vector pAcSG2 as a Sal I fragment. Recombinant baculovirus were produced by cotransfecting Sf9 cells with Baculogold (PharMingen) virus DNA and the recombinant vector DNA. The resulting culture supernatants were harvested after four days, screened for homologous recombination by limiting dilution (Jensen et al., 1992, Biochem. 31: 10887-10892), and confirmed by dot-blot hybridization using the 32P-labeled, BRCA1 cDNA probe. Recombinant protein was expressed by infecting with high titer virus at multiplicities of infection of 10:1 or greater.
Peptide Mapping
Whole cell lysates from MDA-MB-468 cells and BRCA1 recombinant virus infected Sf9 cells were electrophoresed and the 190 kDa MDA-MB-468 band and 180 kDa BRCA1 recombinant protein were identified by removing one lane for immunoblotting with C-20 antibody. The bands of interest were then cut out of the gel, eluted on Microcon spin columns (Amicon), and digested with increasing amounts of V8 protease. The digests were re-electrophoresed on 4-20% gradient gels and immunoblotted with C-20.
Immunogold electron microscopy
MDA-MB-468 cells were trypsinized, washed in PBS, and fixed in 4.0% paraformaldehyde+0.1% glutaraldehyde/PBS (pH 7.4) for 10 minutes on ice. The cell pellet was washed in PBS, dehydrated in a graded series of alcohols, and embedded in LR White resin (medium grade; Polysciences, Inc.). Thin sections were mounted on nickel grids and blocked in PBS+1.0% bovine serum albumin (BSA) for two hours at room temperature. The grids were then incubated overnight in 1.0% BSA supplemented with 0.05% Tween with or without the C-20 antibody at a final dilution of 1:200. The grids were then washed in PBS/0.05% Tween and incubated in a 1:100 dilution of a goat anti-rabbit-gold conjugate (15 nm size; Electron Microscopy Sciences) for one hour at room temperature. The grids were washed as above, rinsed in distilled water and lightly counterstained with saturated aqueous uranyl acetate and lead citrate, and imaged with a Hitachi H-800 transmission electron microscope.
Gene Transfer Methods and Nude Mice Studies
MCF-7 cells were transfected by calcium phosphate coprecipitation for cell growth studies, but were transduced with retroviral stocks from PA317 producer clones for the nude mice studies as described in the results. Cultured MCF-7 cells were transduced in vitro and then injected subcutaneously into the left flank of 4 week old female nu/nu mice containing slow-release estrogen pellets (Soule et al., 1980, Cancer Letters 10, 177-189). Tumor size was determined weekly and animals were autopsied at 8 weeks after injection for determination of tumor weight and RT-PCR analysis for gene expression (Thompson et al., 1995, Nature Genetics 9, 444-450). For evaluation of effects of BRCA1 and mutant retroviral vectors on established tumors, 10.sup.7 MCF-7 cells were injected intraperitoneally and the animals were injected intraperitoneally with high titer retroviral vector stock (10.sup.7 virions) once palpable tumors were identified.
__________________________________________________________________________# SEQUENCE LISTING- (1) GENERAL INFORMATION:- (iii) NUMBER OF SEQUENCES: 29- (2) INFORMATION FOR SEQ ID NO:1:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 5712 (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: cDNA to mRNA- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Homo sapi - #ens (C) INDIVIDUAL ISOLATE:#adult (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: female - # breast#carcinoma in situ, invasivetal breast ca - #ncer and normal breast tissue (H) CELL LINE: not d - #erived from a cell line (I) ORGANELLE: no- (vii) IMMEDIATE SOURCE: (A) LIBRARY: cDNA libra - #ry derived from human (B) CLONE: obtained usi - #ng published sequence- (viii) POSITION IN GENOME: (A) CHROMOSOME/SEGMENT: un - #known (B) MAP POSITION: unkno - #wn (C) UNITS: unknown- (ix) FEATURE: (A) NAME/KEY: BRCA1 (B) LOCATION: GenBank a - #ccession no. U14680 (C) IDENTIFICATION METHOD: - # microscopicallydirected#and nuclease protection assay#gene encoding BRCA1 proteinION:- (x) PUBLICATION INFORMATION:#Y., et. al.) AUTHORS: Miki,#candidate gene for the breast and ovarian c - #ancer susceptibility gene BRCA1. (C) JOURNAL: Science (D) VOLUME: 266 (E) PAGES: 66-71 (F) DATE: 1994 (K) RELEVANT RESIDUES I - #N SEQ ID NO:1:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #1:- agctcgctga gacttcctgg accccgcacc aggctgtggg gtttctcaga ta - #actgggcc 60- cctgcgctca ggaggccttc accctctgct ctgggtaaag ttcattggaa ca - #gaaagaa 119- atg gat tta tct gct ctt cgc gtt gaa gaa gt - #a caa aat gtc att aat 167Met Asp Leu Ser Ala Leu Arg Val Glu Glu Va - #l Gln Asn Val Ile Asn# 15- gct atg cag aaa atc tta gag tgt ccc atc tg - #t ctg gag ttg atc aag 215Ala Met Gln Lys Ile Leu Glu Cys Pro Ile Cy - #s Leu Glu Leu Ile Lys# 30- gaa cct gtc tcc aca aag tgt gac cac ata tt - #t tgc aaa ttt tgc atg 263Glu Pro Val Ser Thr Lys Cys Asp His Ile Ph - #e Cys Lys Phe Cys Met# 45- ctg aaa ctt ctc aac cag aag aaa ggg cct tc - #a cag tgt cct tta tgt 311Leu Lys Leu Leu Asn Gln Lys Lys Gly Pro Se - #r Gln Cys Pro Leu Cys# 60- aag aat gat ata acc aaa agg agc cta caa ga - #a agt acg aga ttt agt 359Lys Asn Asp Ile Thr Lys Arg Ser Leu Gln Gl - #u Ser Thr Arg Phe Ser#80- caa ctt gtt gaa gag cta ttg aaa atc att tg - #t gct ttt cag ctt gac 407Gln Leu Val Glu Glu Leu Leu Lys Ile Ile Cy - #s Ala Phe Gln Leu Asp# 95- aca ggt ttg gag tat gca aac agc tat aat tt - #t gca aaa aag gaa aat 455Thr Gly Leu Glu Tyr Ala Asn Ser Tyr Asn Ph - #e Ala Lys Lys Glu Asn# 110- aac tct cct gaa cat cta aaa gat gaa gtt tc - #t atc atc caa agt atg 503Asn Ser Pro Glu His Leu Lys Asp Glu Val Se - #r Ile Ile Gln Ser Met# 125- ggc tac aga aac cgt gcc aaa aga ctt cta ca - #g agt gaa ccc gaa aat 551Gly Tyr Arg Asn Arg Ala Lys Arg Leu Leu Gl - #n Ser Glu Pro Glu Asn# 140- cct tcc ttg cag gaa acc agt ctc agt gtc ca - #a ctc tct aac ctt gga 599Pro Ser Leu Gln Glu Thr Ser Leu Ser Val Gl - #n Leu Ser Asn Leu Gly145 1 - #50 1 - #55 1 -#60- act gtg aga act ctg agg aca aag cag cgg at - #a caa cct caa aag acg 647Thr Val Arg Thr Leu Arg Thr Lys Gln Arg Il - #e Gln Pro Gln Lys Thr# 175- tct gtc tac att gaa ttg gga tct gat tct tc - #t gaa gat acc gtt aat 695Ser Val Tyr Ile Glu Leu Gly Ser Asp Ser Se - #r Glu Asp Thr Val Asn# 190- aag gca act tat tgc agt gtg gga gat caa ga - #a ttg tta caa atc acc 743Lys Ala Thr Tyr Cys Ser Val Gly Asp Gln Gl - #u Leu Leu Gln Ile Thr# 205- cct caa gga acc agg gat gaa atc agt ttg ga - #t tct gca aaa aag gct 791Pro Gln Gly Thr Arg Asp Glu Ile Ser Leu As - #p Ser Ala Lys Lys Ala# 220- gct tgt gaa ttt tct gag acg gat gta aca aa - #t act gaa cat cat caa 839Ala Cys Glu Phe Ser Glu Thr Asp Val Thr As - #n Thr Glu His His Gln225 2 - #30 2 - #35 2 -#40- ccc agt aat aat gat ttg aac acc act gag aa - #g cgt gca gct gag agg 887Pro Ser Asn Asn Asp Leu Asn Thr Thr Glu Ly - #s Arg Ala Ala Glu Arg# 255- cat cca gaa aag tat cag ggt agt tct gtt tc - #a aac ttg cat gtg gag 935His Pro Glu Lys Tyr Gln Gly Ser Ser Val Se - #r Asn Leu His Val Glu# 270- cca tgt ggc aca aat act cat gcc agc tca tt - #a cag cat gag aac agc 983Pro Cys Gly Thr Asn Thr His Ala Ser Ser Le - #u Gln His Glu Asn Ser# 285- agt tta tta ctc act aaa gac aga atg aat gt - #a gaa aag gct gaa ttc1031Ser Leu Leu Leu Thr Lys Asp Arg Met Asn Va - #l Glu Lys Ala Glu Phe# 300- tgt aat aaa agc aaa cag cct ggc tta gca ag - #g agc caa cat aac aga1079Cys Asn Lys Ser Lys Gln Pro Gly Leu Ala Ar - #g Ser Gln His Asn Arg305 3 - #10 3 - #15 3 -#20- tgg gct gga agt aag gaa aca tgt aat gat ag - #g cgg act ccc agc aca1127Trp Ala Gly Ser Lys Glu Thr Cys Asn Asp Ar - #g Arg Thr Pro Ser Thr# 335- gaa aaa aag gta gat ctg aat gct gat ccc ct - #g tgt gag aga aaa gaa1175Glu Lys Lys Val Asp Leu Asn Ala Asp Pro Le - #u Cys Glu Arg Lys Glu# 350- tgg aat aag cag aaa ctg cca tgc tca gag aa - #t cct aga gat act gaa1223Trp Asn Lys Gln Lys Leu Pro Cys Ser Glu As - #n Pro Arg Asp Thr Glu# 365- gat gtt cct tgg ata aca cta aat agc agc at - #t cag aaa gtt aat gag1271Asp Val Pro Trp Ile Thr Leu Asn Ser Ser Il - #e Gln Lys Val Asn Glu# 380- tgg ttt tcc aga agt gat gaa ctg tta ggt tc - #t gat gac tca cat gat1319Trp Phe Ser Arg Ser Asp Glu Leu Leu Gly Se - #r Asp Asp Ser His Asp385 3 - #90 3 - #95 4 -#00- ggg gag tct gaa tca aat gcc aaa gta gct ga - #t gta ttg gac gtt cta1367Gly Glu Ser Glu Ser Asn Ala Lys Val Ala As - #p Val Leu Asp Val Leu# 415- aat gag gta gat gaa tat tct ggt tct tca ga - #g aaa ata gac tta ctg1415Asn Glu Val Asp Glu Tyr Ser Gly Ser Ser Gl - #u Lys Ile Asp Leu Leu# 430- gcc agt gat cct cat gag gct tta ata tgt aa - #a agt gaa aga gtt cac1463Ala Ser Asp Pro His Glu Ala Leu Ile Cys Ly - #s Ser Asp Arg Val His# 445- tcc aaa tca gta gag agt aat att gaa gac aa - #a ata ttt ggg aaa acc1511Ser Lys Ser Val Glu Ser Asp Ile Glu Asp Ly - #s Ile Phe Gly Lys Thr# 460- tat cgg aag aag gca agc ctc ccc aac tta ag - #c cat gta act gaa aat1559Tyr Arg Lys Lys Ala Ser Leu Pro Asn Leu Se - #r His Val Thr Glu Asn465 4 - #70 4 - #75 4 -#80- cta att ata gga gca ttt gtt act gag cca ca - #g ata ata caa gag cgt1607Leu Ile Ile Gly Ala Phe Val Ser Glu Pro Gl - #n Ile Ile Gln Glu Arg# 495- ccc ctc aca aat aaa tta aag cgt aaa agg ag - #a cct aca tca ggc ctt1655Pro Leu Thr Asn Lys Leu Lys Arg Lys Arg Ar - #g Pro Thr Ser Gly Leu# 510- cat cct gag gat ttt atc aag aaa gca gat tt - #g gca gtt caa aag act1703His Pro Glu Asp Phe Ile Lys Lys Ala Asp Le - #u Ala Val Gln Lys Thr# 525- cct gaa atg ata aat cag gga act aac caa ac - #g gag cag aat ggt caa1751Pro Glu Met Ile Asn Gln Gly Thr Asn Gln Th - #r Glu Gln Asn Gly Gln# 540- gtg atg aat att act aat agt ggt cat gag aa - #t aaa aca aaa ggt gat1799Val Met Asn Ile Thr Asn Ser Gly His Glu As - #n Lys Thr Lys Gly Asp545 5 - #50 5 - #55 5 -#60- tct att cag aat gag aaa aat cct aac cca at - #a gaa tca ctc gaa aaa1847Ser Ile Gln Asn Glu Lys Asn Pro Asn Pro Il - #e Glu Ser Leu Glu Lys# 575- gaa tct gct ttc aaa acg aaa gct gaa cct at - #a agc agc agt ata agc1895Glu Ser Ala Phe Lys Thr Lys Ala Glu Pro Il - #e Ser Ser Ser Ile Ser# 590- aat atg gaa ctc gaa tta aat atc cac aat tc - #a aaa gca cct aaa aag1943Asn Glu Leu Glu Leu Asn Ile Met His Asn Se - #r Lys Ala Pro Lys Lys# 605- aat agg ctg agg agg aag tct tct acc agg ca - #t att cat gcg ctt gaa1991Asn Arg Leu Arg Arg Lys Ser Ser Thr Arg Hi - #s Ile His Ala Leu Glu# 620- cta gta gtc agt aga aat cta agc cca cct aa - #t tgt act gaa ttg caa2039Leu Val Val Ser Arg Asn Leu Ser Pro Pro As - #n Cys Thr Glu Leu Gln625 6 - #30 6 - #35 6 -#40- att gat agt tgt tct agc agt gaa gag ata aa - #g aaa aaa aag tac aac2087Ile Asp Ser Cys Ser Ser Ser Glu Glu Ile Ly - #s Lys Lys Lys Tyr Asn# 655- caa atg cca gtc agg cac agc aga aac cta ca - #a ctc atg gaa ggt aaa2135Gln Met Pro Val Arg His Ser Arg Asn Leu Gl - #n Leu Met Glu Gly Lys# 670- gaa cct gca act gga gcc aag aag agt aac aa - #g cca aat gaa cag aca2183Glu Pro Ala Thr Gly Ala Lys Lys Ser Asn Ly - #s Pro Asn Glu Gln Thr# 685- agt aaa aga cat gac agc gat act ttc cca ga - #g ctg aag tta aca aat2231Ser Lys Arg His Asp Ser Asp Thr Phe Pro Gl - #u Leu Lys Leu Thr Asn# 700- gca cct ggt tct ttt act aag tgt tca aat ac - #c agt gaa ctt aaa gaa2279Ala Pro Gly Ser Phe Thr Lys Cys Ser Asn Th - #r Ser Glu Leu Lys Glu705 7 - #10 7 - #15 7 -#20- ttt gtc aat cct agc ctt cca aga gaa gaa aa - #a gaa gag aaa cta gaa2327Phe Val Asn Pro Ser Leu Pro Arg Glu Glu Ly - #s Glu Glu Lys Leu Glu# 735- aca gtt aaa gtg tct aat aat gct gaa gac cc - #c aaa gat ctc atg tta2375Thr Val Lys Val Ser Asn Asn Ala Glu Asp Pr - #o Lys Asp Leu Met Leu# 750- agt gga gaa agg gtt ttg caa act gaa aga tc - #t gta gag agt agc agt2423Ser Gly Glu Arg Val Leu Gln Thr Glu Arg Se - #r Val Glu Ser Ser Ser# 765- att tca ttg gta cct ggt act gat tat ggc ac - #t cag gaa agt atc tcg2471Ile Ser Leu Val Pro Gly Thr Asp Tyr Gly Th - #r Gln Glu Ser Ile Ser# 780- tta ctg gaa gtt agc act cta ggg aag gca aa - #a aca gaa cca aat aaa2519Leu Leu Glu Val Ser Thr Leu Gly Lys Ala Ly - #s Thr Glu Pro Asn Lys785 7 - #90 7 - #95 8 -#00- tgt gtg agt cag tgt gca gca ttt gaa aac cc - #c aag gga cta att cat2567Cys Val Ser Gln Cys Ala Ala Phe Glu Asn Pr - #o Lys Gly Leu Ile His# 815- ggt tgt tcc aaa gat aat aga aat gac aca ga - #a ggc ttt aag tat cca2615Gly Cys Ser Lys Asp Asn Arg Asn Asp Thr Gl - #u Gly Phe Lys Tyr Pro# 830- ttg gga cat gaa gtt aac cac agt cgg gaa ac - #a agc ata gaa atg gaa2663Leu Gly His Glu Val Asn His Ser Arg Glu Th - #r Ser Ile Glu Met Glu# 845- gaa agt gaa ctt gat gct cag tat ttg cag aa - #t aca ttc aag gtt tca2711Glu Ser Glu Leu Asp Ala Gln Tyr Leu Gln As - #n Thr Phe Lys Val Ser# 860- aag cgc cag tca ttt gct ccg ttt tca aat cc - #a gga aat gca gaa gag2759Lys Arg Gln Ser Phe Ala Pro Phe Ser Asn Pr - #o Gly Asn Ala Glu Glu865 8 - #70 8 - #75 8 -#80- gaa tgt gca aca ttc tct gcc cac tct ggg tc - #c tta aag aaa caa agt2807Glu Cys Ala Thr Phe Ser Ala His Ser Gly Se - #r Leu Lys Lys Gln Ser# 895- cca aaa gtc act ttt gaa tgt gaa caa aag ga - #a gaa aat caa gga aag2855Pro Lys Val Thr Phe Glu Cys Glu Gln Lys Gl - #u Glu Asn Gln Gly Lys# 910- aat gag tct aat atc aag cct gta cag aca gt - #t aat atc act gca ggc2903Asn Glu Ser Asn Ile Lys Pro Val Gln Thr Va - #l Asn Ile Thr Ala Gly# 925- ttt cct gtg gtt ggt cag aaa gat aag cca gt - #t gat aat gcc aaa tgt2951Phe Pro Val Val Gly Gln Lys Asp Lys Pro Va - #l Asp Asn Ala Lys Cys# 940- agt atc aaa gga ggc tct agg ttt tgt cta tc - #a tct cag ttc aga ggc2999Ser Ile Lys Gly Gly Ser Arg Phe Cys Leu Se - #r Ser Gln Phe Arg Gly945 9 - #50 9 - #55 9 -#60- aac gaa act gga ctc att act cca aat aaa ca - #t gga ctt tta caa aac3047Asn Glu Thr Gly Leu Ile Thr Pro Asn Lys Hi - #s Gly Leu Leu Gln Asn# 975- cca tat cgt ata cca cca ctt ttt ccc atc aa - #g tca ttt gtt aaa act3095Pro Tyr Arg Ile Pro Pro Leu Phe Pro Ile Ly - #s Ser Phe Val Lys Thr# 990- aaa tgt aag aaa aat ctg cta gag gaa aac tt - #t gag gaa cat tca atg3143Lys Cys Lys Lys Asn Leu Leu Glu Glu Asn Ph - #e Glu Glu His Ser Met# 10050- tca cct gaa aga gaa atg gga aat gag aac at - #t cca agt aca gtg agc3191Ser Pro Glu Arg Glu Met Gly Asn Glu Asn Il - #e Pro Ser Thr Val Ser# 10205- aca att agc cgt aat aac att aga gaa aat gt - #t ttt aaa gaa gcc agc3239Thr Ile Ser Arg Asn Asn Ile Arg Glu Asn Va - #l Phe Lys Glu Ala Ser# 10401030 - # 1035- tca agc aat att aat gaa gta ggt tcc agt ac - #t aat gaa gtg ggc tcc3287Ser Ser Asn Ile Asn Glu Val Gly Ser Ser Th - #r Asn Glu Val Gly Ser# 10550- agt att aat gaa ata ggt tcc agt gat gaa aa - #c att caa gca gaa cta3335Ser Ile Asn Glu Ile Gly Ser Ser Asp Glu As - #n Ile Gln Ala Glu Leu# 10705- ggt aga aac aga ggg cca aaa ttg aat gct at - #g ctt aga tta ggg gtt3383Gly Arg Asn Arg Gly Pro Lys Leu Asn Ala Me - #t Leu Arg Leu Gly Val# 10850- ttg caa cct gag gtc tat aaa caa agt ctt cc - #t gga agt aat tgt aag3431Leu Gln Pro Glu Val Tyr Lys Gln Ser Leu Pr - #o Gly Ser Asn Cys Lys# 11005- cat cct gaa ata aaa aag caa gaa tat gaa ga - #a gta gtt cag act gtt3479His Pro Glu Ile Lys Lys Gln Glu Tyr Glu Gl - #u Val Val Gln Thr Val# 11201110 - # 1115- aat aca gat ttc tct cca tat ctg att tca ga - #t aac tta gaa cag cct3527Asn Thr Asp Phe Ser Pro Tyr Leu Ile Ser As - #p Asn Leu Glu Gln Pro# 11350- atg gga agt agt cat gca tct cag gtt tgt tc - #t gag aca cct gat gac3575Met Gly Ser Ser His Ala Ser Gln Val Cys Se - #r Glu Thr Pro Asp Asp# 11505- ctg tta gat gat ggt gaa ata aag gaa gat ac - #t agt ttt gct gaa aat3623Leu Leu Asp Asp Gly Glu Ile Lys Glu Asp Th - #r Ser Phe Ala Glu Asn# 11650- gac att aag gaa agt tct gct gtt ttt agc aa - #a agc gtc cag aaa gga3671Asp Ile Lys Glu Ser Ser Ala Val Phe Ser Ly - #s Ser Val Gln Lys Gly# 11805- gag ctt agc agg agt cct agc cct ttc acc ca - #t aca cat ttg gct cag3719Glu Leu Ser Arg Ser Pro Ser Pro Phe Thr Hi - #s Thr His Leu Ala Gln# 12001190 - # 1195- ggt tac cga aga ggg gcc aag aaa tta gag tc - #c tca gaa gag aac tta3767Gly Tyr Arg Arg Gly Ala Lys Lys Leu Glu Se - #r Ser Glu Glu Asn Leu# 12150- tct agt gag gat gaa gag ctt ccc tgc ttc ca - #a cac ttg tta ttt ggt3815Ser Ser Glu Asp Glu Glu Leu Pro Cys Phe Gl - #n His Leu Leu Phe Gly# 12305- aaa gta aac aat ata cct tct cag tct act ag - #g cat agc acc gtt gct3863Lys Val Asn Asn Ile Pro Ser Gln Ser Thr Ar - #g His Ser Thr Val Ala# 12450- acc gag tgt ctg tct aag aac aca gag gag aa - #t tta tta tca ttg aag3911Thr Glu Cys Leu Ser Lys Asn Thr Glu Glu As - #n Leu Leu Ser Leu Lys# 12605- aat agc tta aat gac tgc agt aac cag gta at - #a ttg gca aag gca tct3959Asn Ser Leu Asn Asp Cys Ser Asn Gln Val Il - #e Leu Ala Lys Ala Ser# 12801270 - # 1275- cag gaa cat cac ctt agt gag gaa aca aaa tg - #t tct gct agc ttg ttt4007Gln Glu His His Leu Ser Glu Glu Thr Lys Cy - #s Ser Ala Ser Leu Phe# 12950- tct tca cag tgc agt gaa ttg gaa gac ttg ac - #t gca aat aca aac acc4055Ser Ser Gln Cys Ser Glu Leu Glu Asp Leu Th - #r Ala Asn Thr Asn Thr# 13105- cag gat cct ttc ttg att ggt tct tcc aaa ca - #a atg agg cat cag tct4103Gln Asp Pro Phe Leu Ile Gly Ser Ser Lys Gl - #n Met Arg His Gln Ser# 13250- gaa agc cag gga gtt ggt ctg agt gac aag ga - #a ttg gtt tca gat gat4151Glu Ser Gln Gly Val Gly Leu Ser Asp Lys Gl - #u Leu Val Ser Asp Asp# 13405- gaa gaa aga gga acg ggc ttg gaa gaa aat aa - #t caa gaa gag caa agc4199Glu Glu Arg Gly Thr Gly Leu Glu Glu Asn As - #n Gln Glu Glu Gln Ser# 13601350 - # 1355- atg gat tca aac tta ggt gaa gca gca tct gg - #g tgt gag agt gaa aca4247Met Asp Ser Asn Leu Gly Glu Ala Ala Ser Gl - #y Cys Glu Ser Glu Thr# 13750- agc gtc tct gaa gac tgc tca ggg cta tcc tc - #t cag agt gac att tta4295Ser Val Ser Glu Asp Cys Ser Gly Leu Ser Se - #r Gln Ser Asp Ile Leu# 13905- acc act cag cag agg gat acc atg caa cat aa - #c ctg ata aag ctc cag4343Thr Thr Gln Gln Arg Asp Thr Met Gln His As - #n Leu Ile Lys Leu Gln# 14050- cag gaa atg gct gaa cta gaa gct gtg tta ga - #a cag cat ggg agc cag4391Gln Glu Met Ala Glu Leu Glu Ala Val Leu Gl - #u Gln His Gly Ser Gln# 14205- cct tct aac agc tac cct tcc atc ata agt ga - #c tct tct gcc ctt gag4439Pro Ser Asn Ser Tyr Pro Ser Ile Ile Ser As - #p Ser Ser Ala Leu Glu# 14401430 - # 1435- gac ctg cga aat cca gaa caa agc aca tca ga - #a aaa gca gta tta act4487Asp Leu Arg Asn Pro Glu Gln Ser Thr Ser Gl - #u Lys Val Leu Gln Thr# 14550- tca cag aaa agt agt gaa tac cct ata agc ca - #g aat cca gaa ggc ctt4535Ser Gln Lys Ser Ser Glu Tyr Pro Ile Ser Gl - #n Asn Pro Glu Gly Xaa# 14705- tct gct gac aag ttt gag gtg tct gca gat ag - #t tct acc agt aaa aat4583Ser Ala Asp Lys Phe Glu Val Ser Ala Asp Se - #r Ser Thr Ser Lys Asn# 14850- aaa gaa cca gga gtg gaa agg tca tcc cct tc - #t aaa tgc cca tca tta4631Lys Glu Pro Gly Val Glu Arg Ser Ser Pro Se - #r Lys Cys Pro Ser Leu# 15005- gat gat agg tgg tac atg cac agt tgc tct gg - #g agt ctt cag aat aga4679Asp Asp Arg Trp Tyr Met His Ser Cys Ser Gl - #y Ser Leu Gln Asn Arg# 15201510 - # 1515- aac tac cca tct caa gag gag ctc att aag gt - #t gtt gat gtg gag gag4727Asn Tyr Pro Pro Gln Glu Glu Leu Ile Lys Va - #l Val Asp Val Glu Glu# 15350- caa cag ctg gaa gag tct ggg cca cac gat tt - #g acg gaa aca tct tac4775Gln Gln Leu Glu Glu Ser Gly Pro His Asp Le - #u Thr Glu Thr Ser Tyr# 15505- ttg cca agg caa gat cta gag gga acc cct ta - #c ctg gaa tct gga atc4823Leu Pro Arg Gln Asp Leu Glu Gly Thr Pro Ty - #r Leu Glu Ser Gly Ile# 15650- agc ctc ttc tct gat gac cct gaa tct gat cc - #t tct gaa gac aga gcc4871Ser Leu Phe Ser Asp Asp Pro Glu Ser Asp Pr - #o Ser Glu Asp Arg Ala# 15805- cca gag tca gct cgt gtt ggc aac ata cca tc - #t tca acc tct gca ttg4919Pro Glu Ser Ala Arg Val Gly Asn Ile Pro Se - #r Ser Thr Ser Ala Leu# 16001590 - # 1595- aaa gtt ccc caa ttg aaa gtt gca gaa tct gc - #c cag agt cca gct gct4967Lys Val Pro Gln Leu Lys Val Ala Glu Ser Al - #a Gln Ser Pro Ala Ala# 16150- gct cat act act gat act gct ggg tat aat gc - #a atg gaa gaa agt gtg5015Ala His Thr Thr Asp Thr Ala Gly Tyr Asn Al - #a Met Glu Glu Ser Val# 16305- agc agg gag aag cca gaa ttg aca gct tca ac - #a gaa agg gtc aac aaa5063Ser Arg Glu Lys Pro Glu Leu Thr Ala Ser Th - #r Glu Arg Val Asn Lys# 16450- aga atg tcc atg gtg gtg tct ggc ctg acc cc - #a gaa gaa ttt atg ctc5111Arg Met Ser Met Val Val Ser Gly Leu Thr Pr - #o Glu Glu Phe Met Leu# 16605- gtg tac aag ttt gcc aga aaa cac cac atc ac - #t tta act aat cta att5159Val Tyr Lys Phe Ala Arg Lys His His Ile Th - #r Leu Thr Asn Leu Ile# 16801670 - # 1675- act gaa gag act act cat gtt gtt atg aaa ac - #a gat gct gag ttt gtg5207Thr Glu Glu Thr Thr His Val Val Met Lys Th - #r Asp Ala Glu Phe Val# 16950- tgt gaa cgg aca ctg aaa tat ttt cta gga at - #t gcg gga gga aaa tgg5255Cys Glu Arg Thr Leu Lys Tyr Phe Leu Gly Il - #e Ala Gly Gly Lys Trp# 17105- gta gtt agc tat ttc tgg gtg acc cag tct at - #t aaa gaa aga aaa atg5303Val Val Ser Tyr Phe Trp Val Thr Gln Ser Il - #e Lys Glu Arg Lys Met# 17250- ctg aat gag cat gat ttt gaa gtc aga gga ga - #t gtg gtc aat gga aga5351Leu Asn Glu His Asp Phe Glu Val Arg Gly As - #p Val Val Asn Gly Arg# 17405- aac cac caa ggt cca aag cga gca aga gaa tc - #c cag gac aga aag atc5399Asn His Gln Gly Pro Lys Arg Ala Arg Glu Se - #r Gln Asp Arg Lys Ile# 17601750 - # 1755- ttc agg ggg cta gaa atc tgt tgc tat ggg cc - #c ttc acc aac atg ccc5447Phe Arg Gly Leu Glu Ile Cys Cys Tyr Gly Pr - #o Phe Thr Asn Met Pro# 17750- aca gat caa ctg gaa tgg atg gta cag ctg tg - #t ggt gct tct gtg gtg5495Thr Asp Gln Leu Glu Trp Met Val Gln Leu Cy - #s Gly Ala Ser Val Val# 1790- aag gag ctt tca tca ttc acc ctt ggc aca gg - #t gtc cac cca att gtg5543Lys Glu Leu Ser Ser Phe Thr Leu Gly Thr Gl - #y Val His Pro Ile Val# 18050- gtt gtg cag cca gat gcc tgg aca gag gac aa - #t ggc ttc cat gca att5591Val Val Gln Pro Asp Ala Trp Thr Glu Asp As - #n Gly Phe His Ala Ile# 18205- ggg cag atg tgt gag gca cct gtg gtg acc cg - #a gag tgg gtg ttg gac5639Gly Gln Met Cys Glu Ala Pro Val Val Thr Ar - #g Glu Trp Val Leu Asp# 18401830 - # 1835- agt gta gca ctc tac cag tgc cag gag ctg ga - #c acc tac ctg ata ccc5687Ser Val Ala Leu Tyr Gln Cys Gln Glu Leu As - #p Thr Tyr Leu Ile Pro# 18550# 5712 gc cac tac tgatGln Ile Pro His Ser His Tyr 1860- (2) INFORMATION FOR SEQ ID NO:2:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 1863 (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: protein- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Homo sapi - #ens (C) INDIVIDUAL ISOLATE:#adult (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: female - # breast#carcinoma in situ, invasivetal breast ca - #ncer and normal breast tissue (H) CELL LINE: not d - #erived from a cell line (I) ORGANELLE: no- (vii) IMMEDIATE SOURCE: (A) LIBRARY: cDNA libra - #ry derived from human (B) CLONE: obtained usi - #ng published sequence- (viii) POSITION IN GENOME: (A) CHROMOSOME/SEGMENT: un - #known (B) MAP POSITION: unkno - #wn (C) UNITS: unknown- (ix) FEATURE: (A) NAME/KEY: BRCA1 pro - #tein (B) LOCATION: 1 to 1 - #863 (C) IDENTIFICATION METHOD: - # observation of mRNA and#inhibition of BRCA1 gene#BRCA1 protein has a negativeON:#effect on growth of human mammary cells.- (x) PUBLICATION INFORMATION:#Y., et. al.) AUTHORS: Miki,#candidate gene for the breast and ovarian c - #ancer susceptibility gene BRCA1. (C) JOURNAL: Science (D) VOLUME: 266 (E) PAGES: 66-71 (F) DATE: 1994 (K) RELEVANT RESIDUES I - #N SEQ ID NO:2: granin box domain at - # amino acids 1214-1223- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2:- Met Asp Leu Ser Ala Leu Arg Val Glu Glu Va - #l Gln Asn Val Ile Asn# 15- Ala Met Gln Lys Ile Leu Glu Cys Pro Ile Cy - #s Leu Glu Leu Ile Lys# 30- Glu Pro Val Ser Thr Lys Cys Asp His Ile Ph - #e Cys Lys Phe Cys Met# 45- Leu Lys Leu Leu Asn Gln Lys Lys Gly Pro Se - #r Gln Cys Pro Leu Cys# 60- Lys Asn Asp Ile Thr Lys Arg Ser Leu Gln Gl - #u Ser Thr Arg Phe Ser#80- Gln Leu Val Glu Glu Leu Leu Lys Ile Ile Cy - #s Ala Phe Gln Leu Asp# 95- Thr Gly Leu Glu Tyr Ala Asn Ser Tyr Asn Ph - #e Ala Lys Lys Glu Asn# 110- Asn Ser Pro Glu His Leu Lys Asp Glu Val Se - #r Ile Ile Gln Ser Met# 125- Gly Tyr Arg Asn Arg Ala Lys Arg Leu Leu Gl - #n Ser Glu Pro Glu Asn# 140- Pro Ser Leu Gln Glu Thr Ser Leu Ser Val Gl - #n Leu Ser Asn Leu Gly145 1 - #50 1 - #55 1 -#60- Thr Val Arg Thr Leu Arg Thr Lys Gln Arg Il - #e Gln Pro Gln Lys Thr# 175- Ser Val Tyr Ile Glu Leu Gly Ser Asp Ser Se - #r Glu Asp Thr Val Asn# 190- Lys Ala Thr Tyr Cys Ser Val Gly Asp Gln Gl - #u Leu Leu Gln Ile Thr# 205- Pro Gln Gly Thr Arg Asp Glu Ile Ser Leu As - #p Ser Ala Lys Lys Ala# 220- Ala Cys Glu Phe Ser Glu Thr Asp Val Thr As - #n Thr Glu His His Gln225 2 - #30 2 - #35 2 -#40- Pro Ser Asn Asn Asp Leu Asn Thr Thr Glu Ly - #s Arg Ala Ala Glu Arg# 255- His Pro Glu Lys Tyr Gln Gly Ser Ser Val Se - #r Asn Leu His Val Glu# 270- Pro Cys Gly Thr Asn Thr His Ala Ser Ser Le - #u Gln His Glu Asn Ser# 285- Ser Leu Leu Leu Thr Lys Asp Arg Met Asn Va - #l Glu Lys Ala Glu Phe# 300- Cys Asn Lys Ser Lys Gln Pro Gly Leu Ala Ar - #g Ser Gln His Asn Arg305 3 - #10 3 - #15 3 -#20- Trp Ala Gly Ser Lys Glu Thr Cys Asn Asp Ar - #g Arg Thr Pro Ser Thr# 335- Glu Lys Lys Val Asp Leu Asn Ala Asp Pro Le - #u Cys Glu Arg Lys Glu# 350- Trp Asn Lys Gln Lys Leu Pro Cys Ser Glu As - #n Pro Arg Asp Thr Glu# 365- Asp Val Pro Trp Ile Thr Leu Asn Ser Ser Il - #e Gln Lys Val Asn Glu# 380- Trp Phe Ser Arg Ser Asp Glu Leu Leu Gly Se - #r Asp Asp Ser His Asp385 3 - #90 3 - #95 4 -#00- Gly Glu Ser Glu Ser Asn Ala Lys Val Ala As - #p Val Leu Asp Val Leu# 415- Asn Glu Val Asp Glu Tyr Ser Gly Ser Ser Gl - #u Lys Ile Asp Leu Leu# 430- Ala Ser Asp Pro His Glu Ala Leu Ile Cys Ly - #s Ser Asp Arg Val His# 445- Ser Lys Ser Val Glu Ser Asp Ile Glu Asp Ly - #s Ile Phe Gly Lys Thr# 460- Tyr Arg Lys Lys Ala Ser Leu Pro Asn Leu Se - #r His Val Thr Glu Asn465 4 - #70 4 - #75 4 -#80- Leu Ile Ile Gly Ala Phe Val Ser Glu Pro Gl - #n Ile Ile Gln Glu Arg# 495- Pro Leu Thr Asn Lys Leu Lys Arg Lys Arg Ar - #g Pro Thr Ser Gly Leu# 510- His Pro Glu Asp Phe Ile Lys Lys Ala Asp Le - #u Ala Val Gln Lys Thr# 525- Pro Glu Met Ile Asn Gln Gly Thr Asn Gln Th - #r Glu Gln Asn Gly Gln# 540- Val Met Asn Ile Thr Asn Ser Gly His Glu As - #n Lys Thr Lys Gly Asp545 5 - #50 5 - #55 5 -#60- Ser Ile Gln Asn Glu Lys Asn Pro Asn Pro Il - #e Glu Ser Leu Glu Lys# 575- Glu Ser Ala Phe Lys Thr Lys Ala Glu Pro Il - #e Ser Ser Ser Ile Ser# 590- Asn Glu Leu Glu Leu Asn Ile Met His Asn Se - #r Lys Ala Pro Lys Lys# 605- Asn Arg Leu Arg Arg Lys Ser Ser Thr Arg Hi - #s Ile His Ala Leu Glu# 620- Leu Val Val Ser Arg Asn Leu Ser Pro Pro As - #n Cys Thr Glu Leu Gln625 6 - #30 6 - #35 6 -#40- Ile Asp Ser Cys Ser Ser Ser Glu Glu Ile Ly - #s Lys Lys Lys Tyr Asn# 655- Gln Met Pro Val Arg His Ser Arg Asn Leu Gl - #n Leu Met Glu Gly Lys# 670- Glu Pro Ala Thr Gly Ala Lys Lys Ser Asn Ly - #s Pro Asn Glu Gln Thr# 685- Ser Lys Arg His Asp Ser Asp Thr Phe Pro Gl - #u Leu Lys Leu Thr Asn# 700- Ala Pro Gly Ser Phe Thr Lys Cys Ser Asn Th - #r Ser Glu Leu Lys Glu705 7 - #10 7 - #15 7 -#20- Phe Val Asn Pro Ser Leu Pro Arg Glu Glu Ly - #s Glu Glu Lys Leu Glu# 735- Thr Val Lys Val Ser Asn Asn Ala Glu Asp Pr - #o Lys Asp Leu Met Leu# 750- Ser Gly Glu Arg Val Leu Gln Thr Glu Arg Se - #r Val Glu Ser Ser Ser# 765- Ile Ser Leu Val Pro Gly Thr Asp Tyr Gly Th - #r Gln Glu Ser Ile Ser# 780- Leu Leu Glu Val Ser Thr Leu Gly Lys Ala Ly - #s Thr Glu Pro Asn Lys785 7 - #90 7 - #95 8 -#00- Cys Val Ser Gln Cys Ala Ala Phe Glu Asn Pr - #o Lys Gly Leu Ile His# 815- Gly Cys Ser Lys Asp Asn Arg Asn Asp Thr Gl - #u Gly Phe Lys Tyr Pro# 830- Leu Gly His Glu Val Asn His Ser Arg Glu Th - #r Ser Ile Glu Met Glu# 845- Glu Ser Glu Leu Asp Ala Gln Tyr Leu Gln As - #n Thr Phe Lys Val Ser# 860- Lys Arg Gln Ser Phe Ala Pro Phe Ser Asn Pr - #o Gly Asn Ala Glu Glu865 8 - #70 8 - #75 8 -#80- Glu Cys Ala Thr Phe Ser Ala His Ser Gly Se - #r Leu Lys Lys Gln Ser# 895- Pro Lys Val Thr Phe Glu Cys Glu Gln Lys Gl - #u Glu Asn Gln Gly Lys# 9105- Asn Glu Ser Asn Ile Lys Pro Val Gln Thr Va - #l Asn Ile Thr Ala Gly# 925- Phe Pro Val Val Gly Gln Lys Asp Lys Pro Va - #l Asp Asn Ala Lys Cys# 940- Ser Ile Lys Gly Gly Ser Arg Phe Cys Leu Se - #r Ser Gln Phe Arg Gly945 9 - #50 9 - #55 9 -#60- Asn Glu Thr Gly Leu Ile Thr Pro Asn Lys Hi - #s Gly Leu Leu Gln Asn# 975- Pro Tyr Arg Ile Pro Pro Leu Phe Pro Ile Ly - #s Ser Phe Val Lys Thr# 990- Lys Cys Lys Lys Asn Leu Leu Glu Glu Asn Ph - #e Glu Glu His Ser Met# 10050- Ser Pro Glu Arg Glu Met Gly Asn Glu Asn Il - #e Pro Ser Thr Val Ser# 10205- Thr Ile Ser Arg Asn Asn Ile Arg Glu Asn Va - #l Phe Lys Glu Ala Ser# 10401030 - # 1035- Ser Ser Asn Ile Asn Glu Val Gly Ser Ser Th - #r Asn Glu Val Gly Ser# 10550- Ser Ile Asn Glu Ile Gly Ser Ser Asp Glu As - #n Ile Gln Ala Glu Leu# 10705- Gly Arg Asn Arg Gly Pro Lys Leu Asn Ala Me - #t Leu Arg Leu Gly Val# 10850- Leu Gln Pro Glu Val Tyr Lys Gln Ser Leu Pr - #o Gly Ser Asn Cys Lys# 11005- His Pro Glu Ile Lys Lys Gln Glu Tyr Glu Gl - #u Val Val Gln Thr Val# 11201110 - # 1115- Asn Thr Asp Phe Ser Pro Tyr Leu Ile Ser As - #p Asn Leu Glu Gln Pro# 11350- Met Gly Ser Ser His Ala Ser Gln Val Cys Se - #r Glu Thr Pro Asp Asp# 11505- Leu Leu Asp Asp Gly Glu Ile Lys Glu Asp Th - #r Ser Phe Ala Glu Asn# 11650- Asp Ile Lys Glu Ser Ser Ala Val Phe Ser Ly - #s Ser Val Gln Lys Gly# 11805- Glu Leu Ser Arg Ser Pro Ser Pro Phe Thr Hi - #s Thr His Leu Ala Gln# 12001190 - # 1195- Gly Tyr Arg Arg Gly Ala Lys Lys Leu Glu Se - #r Ser Glu Glu Asn Leu# 12150- Ser Ser Glu Asp Glu Glu Leu Pro Cys Phe Gl - #n His Leu Leu Phe Gly# 12305- Lys Val Asn Asn Ile Pro Ser Gln Ser Thr Ar - #g His Ser Thr Val Ala# 12450- Thr Glu Cys Leu Ser Lys Asn Thr Glu Glu As - #n Leu Leu Ser Leu Lys# 12605- Asn Ser Leu Asn Asp Cys Ser Asn Gln Val Il - #e Leu Ala Lys Ala Ser# 12801270 - # 1275- Gln Glu His His Leu Ser Glu Glu Thr Lys Cy - #s Ser Ala Ser Leu Phe# 12950- Ser Ser Gln Cys Ser Glu Leu Glu Asp Leu Th - #r Ala Asn Thr Asn Thr# 13105- Gln Asp Pro Phe Leu Ile Gly Ser Ser Lys Gl - #n Met Arg His Gln Ser# 13250- Glu Ser Gln Gly Val Gly Leu Ser Asp Lys Gl - #u Leu Val Ser Asp Asp# 13405- Glu Glu Arg Gly Thr Gly Leu Glu Glu Asn As - #n Gln Glu Glu Gln Ser# 13601350 - # 1355- Met Asp Ser Asn Leu Gly Glu Ala Ala Ser Gl - #y Cys Glu Ser Glu Thr# 13750- Ser Val Ser Glu Asp Cys Ser Gly Leu Ser Se - #r Gln Ser Asp Ile Leu# 13905- Thr Thr Gln Gln Arg Asp Thr Met Gln His As - #n Leu Ile Lys Leu Gln# 14050- Gln Glu Met Ala Glu Leu Glu Ala Val Leu Gl - #u Gln His Gly Ser Gln# 14205- Pro Ser Asn Ser Tyr Pro Ser Ile Ile Ser As - #p Ser Ser Ala Leu Glu# 14401430 - # 1435- Asp Leu Arg Asn Pro Glu Gln Ser Thr Ser Gl - #u Lys Val Leu Gln Thr# 14550- Ser Gln Lys Ser Ser Glu Tyr Pro Ile Ser Gl - #n Asn Pro Glu Gly Xaa# 14705- Ser Ala Asp Lys Phe Glu Val Ser Ala Asp Se - #r Ser Thr Ser Lys Asn# 14850- Lys Glu Pro Gly Val Glu Arg Ser Ser Pro Se - #r Lys Cys Pro Ser Leu# 15005- Asp Asp Arg Trp Tyr Met His Ser Cys Ser Gl - #y Ser Leu Gln Asn Arg# 15201510 - # 1515- Asn Tyr Pro Pro Gln Glu Glu Leu Ile Lys Va - #l Val Asp Val Glu Glu# 15350- Gln Gln Leu Glu Glu Ser Gly Pro His Asp Le - #u Thr Glu Thr Ser Tyr# 15505- Leu Pro Arg Gln Asp Leu Glu Gly Thr Pro Ty - #r Leu Glu Ser Gly Ile# 15650- Ser Leu Phe Ser Asp Asp Pro Glu Ser Asp Pr - #o Ser Glu Asp Arg Ala# 15805- Pro Glu Ser Ala Arg Val Gly Asn Ile Pro Se - #r Ser Thr Ser Ala Leu# 16001590 - # 1595- Lys Val Pro Gln Leu Lys Val Ala Glu Ser Al - #a Gln Ser Pro Ala Ala# 16150- Ala His Thr Thr Asp Thr Ala Gly Tyr Asn Al - #a Met Glu Glu Ser Val# 16305- Ser Arg Glu Lys Pro Glu Leu Thr Ala Ser Th - #r Glu Arg Val Asn Lys# 16450- Arg Met Ser Met Val Val Ser Gly Leu Thr Pr - #o Glu Glu Phe Met Leu# 16605- Val Tyr Lys Phe Ala Arg Lys His His Ile Th - #r Leu Thr Asn Leu Ile# 16801670 - # 1675- Thr Glu Glu Thr Thr His Val Val Met Lys Th - #r Asp Ala Glu Phe Val# 16950- Cys Glu Arg Thr Leu Lys Tyr Phe Leu Gly Il - #e Ala Gly Gly Lys Trp# 17105- Val Val Ser Tyr Phe Trp Val Thr Gln Ser Il - #e Lys Glu Arg Lys Met# 17250- Leu Asn Glu His Asp Phe Glu Val Arg Gly As - #p Val Val Asn Gly Arg# 17405- Asn His Gln Gly Pro Lys Arg Ala Arg Glu Se - #r Gln Asp Arg Lys Ile# 17601750 - # 1755- Phe Arg Gly Leu Glu Ile Cys Cys Tyr Gly Pr - #o Phe Thr Asn Met Pro# 17750- Thr Asp Gln Leu Glu Trp Met Val Gln Leu Cy - #s Gly Ala Ser Val Val# 1790- Lys Glu Leu Ser Ser Phe Thr Leu Gly Thr Gl - #y Val His Pro Ile Val# 18050- Val Val Gln Pro Asp Ala Trp Thr Glu Asp As - #n Gly Phe His Ala Ile# 18205- Gly Gln Met Cys Glu Ala Pro Val Val Thr Ar - #g Glu Trp Val Leu Asp# 18401830 - # 1835- Ser Val Ala Leu Tyr Gln Cys Gln Glu Leu As - #p Thr Tyr Leu Ile Pro# 18550- Gln Ile Pro His Ser His Tyr 1860- (2) INFORMATION FOR SEQ ID NO:3:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 11283 (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: cDNA to mRNA- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Homo sapi - #ens sapiens (C) INDIVIDUAL ISOLATE:#adult (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: female - # breast#and cancerous breast cellsrmal (H) CELL LINE: MCF-7 (I) ORGANELLE: no- (vii) IMMEDIATE SOURCE: (A) LIBRARY: cDNA libra - #ry derived from human (B) CLONE: obtained usi - #ng published sequence- (viii) POSITION IN GENOME: (A) CHROMOSOME/SEGMENT: un - #known (B) MAP POSITION: unkno - #wn (C) UNITS: unknown- (ix) FEATURE: (A) NAME/KEY: BRCA2 (B) LOCATION: (C) IDENTIFICATION METHOD:#gene encoding BRCA2 proteinION:- (x) PUBLICATION INFORMATION:#Wooster, R. et al.RS: (B) TITLE: Identificat - #ion of the breast cancer susceptabili - #ty gene BRCA2#Nature (C) JOURNAL:# 379 (D) VOLUME:# 789-792(E) PAGES:# 1995 (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:3- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #3:- ggcggagccg ctgtggcact gctgcgcctc tgctgcgcct cgggtgtctt tt - #gcggcggt 60- gggtcgccgc cgggagaagc gtgaggggac agatttgtga ccggcgcggt tt - #ttgtcagc 120- ttactccggc caaaaaagaa ctgcacctct ggagcggact tatttaccaa gc - #attggagg 180# 196- atg cct att gga tcc aaa gag agg cca aca tt - #t ttt gaa att ttt aag 244Met Pro Ile Gly Ser Lys Glu Arg Pro Thr Ph - #e Phe Glu Ile Phe Lys# 15- aca cgc tgc aac aaa gca gat tta gga cca at - #a agt ctt aat tgg ttt 292Thr Arg Cys Asn Lys Ala Asp Leu Gly Pro Il - #e Ser Leu Asn Trp Phe#30- gaa gaa ctt tct tca gaa gct cca ccc tat aa - #t tct gaa cct gca gaa 340Glu Glu Leu Ser Ser Glu Ala Pro Pro Tyr As - #n Ser Glu Pro Ala Glu#45- gaa tct gaa cat aaa aac aac aat tac gaa cc - #a aac cta ttt aaa act 388Glu Ser Glu His Lys Asn Asn Asn Tyr Glu Pr - #o Asn Leu Phe Lys Thr#60- cca caa agg aaa cca tct tat aat cag ctg gc - #t tca act cca ata ata 436Pro Gln Arg Lys Pro Ser Tyr Asn Gln Leu Al - #a Ser Thr Pro Ile Ile#80- ttc aaa gag caa ggg ctg act ctg ccg ctg ta - #c caa tct cct gta aaa 484Phe Lys Glu Gln Gly Leu Thr Leu Pro Leu Ty - #r Gln Ser Pro Val Lys#95- gaa tta gat aaa ttc aaa tta gac tta gga ag - #g aat gtt ccc aat agt 532Glu Leu Asp Lys Phe Lys Leu Asp Leu Gly Ar - #g Asn Val Pro Asn Ser100 1 - #05 1 - #10- aga cat aaa agt ctt cgc aca gtg aaa act aa - #a atg gat caa gca gat 580Arg His Lys Ser Leu Arg Thr Val Lys Tyr Ly - #s Met Asp Gln Ala Asp115 1 - #20 1 - #25- gat gtt tcc tgt cca ctt cta aat tct tgt ct - #t agt gaa agt cct gtt 628Asp Val Ser Cys Pro Leu Leu Asn Ser Cys Le - #u Ser Glu Ser Pro Val130 1 - #35 1 - #40- gtt cta caa tgt aca cat gta aca cca caa ag - #a gat aag tca gtg gta 676Val Leu Gln Cys Thr His Val Thr Pro Gln Ar - #g Asp Lys Ser Val Val145 1 - #50 1 - #55 1 -#60- tgt ggg agt ttg ttt cat aca cca aag ttt gt - #g aag ggt cgt cag aca 724Cys Gly Ser Leu Phe His Thr Pro Lys Phe Va - #l Lys Gly Arg Gln Thr165 1 - #70 1 - #75- cca aaa cat att tct gaa agt cta gga gct ga - #g gtg gat cct gat atg 772Pro Lys His Ile Ser Glu Ser Leu Gly Ala Gl - #u Val Asp Pro Asp Met180 1 - #85 1 - #90- tct tgg tca agt tct tta gct aca cca ccc ac - #c ctt agt tct act gtg 820Ser Trp Ser Ser Ser Leu Ala Thr Pro Pro Th - #r Leu Ser Ser Thr Val195 2 - #00 2 - #05- ctc ata gtc aga aat gaa gaa gca tct gaa ac - #t gta ttt cct cat gat 868Leu Ile Val Arg Asn Glu Glu Ala Ser Glu Th - #r Val Phe Pro His Asp210 2 - #15 2 - #20- act act gct aat gtg aaa agc tat ttt tcc aa - #t cat gat gaa agt ctg 916Thr Thr Ala Asn Val Lys Ser Tyr Phe Ser As - #n His Asp Glu Ser Leu225 2 - #30 2 - #35 2 -#40- aag aaa aat gat aga ttt atc gct tct gtg ac - #a gac agt gaa aac aca 964Lys Lys Asn Asp Arg Phe Ile Ala Ser Val Th - #r Asp Ser Glu Asn Thr245 2 - #50 2 - #55- aat caa aga gaa gct gca agt cat gga ttt gg - #a aaa aca tca ggg aat1012Asn Gln Arg Glu Ala Ala Ser His Gly Phe Gl - #y Lys Thr Ser Gly Asn260 2 - #65 2 - #70- tca ttt aaa gta aat agc tgc aaa gac cac at - #t gga aag tca atg cca1060Ser Phe Lys Val Asn Ser Cys Lys Asp His Il - #e Gly Lys Ser Met Pro275 2 - #80 2 - #85- aat gtc cta gaa gat gaa gta tat gaa aca gt - #t gta gat acc tct gaa1108Asn Val Leu Glu Asp Glu Val Tyr Glu Thr Va - #l Val Asp Thr Ser Glu290 2 - #95 3 - #00- gaa gat agt ttt tca tta tgt ttt tct aaa tg - #t aga aca aaa aat cta1156Glu Asp Ser Phe Ser Leu Cys Phe Ser Lys Cy - #s Arg Thr Lys Asn Leu305 3 - #10 3 - #15 3 -#20- caa aaa gta aga act agc aag act agg aaa aa - #a att ttc cat gaa gca1204Gln Lys Val Arg Thr Ser Lys Thr Arg Lys Ly - #s Ile Phe His Glu Ala325 3 - #30 3 - #35- aac gct gat gaa tgt gaa aaa tct aaa aac ca - #a gtg aaa gaa aaa tac1252Asn Ala Asp Glu Cys Glu Lys Ser Lys Asn Gl - #n Val Lys Glu Lys Tyr340 3 - #45 3 - #50- tca ttt gta tct gaa gtg gaa cca aat gat ac - #t gat cca tta gat tca1300Ser Phe Val Ser Glu Val Glu Pro Asn Asp Th - #r Asp Pro Leu Asp Ser355 3 - #60 3 - #65- aat gta gca cat cag aag ccc ttt gag agt gg - #a agt gac aaa atc tcc1348Asn Val Ala His Gln Lys Pro Phe Glu Ser Gl - #y Ser Asp Lys Ile Ser370 3 - #75 3 - #80- aag gaa gtt gta ccg tct ttg gcc tgt gaa tg - #g tct caa cta acc ctt1396Lys Glu Val Val Pro Ser Leu Ala Cys Glu Tr - #p Ser Gln Leu Thr Leu385 3 - #90 3 - #95 4 -#00- tca ggt cta aat gga gcc cag atg gag aaa at - #a ccc cta ttg cat att1444Ser Gly Leu Asn Gly Ala Gln Met Glu Lys Il - #e Pro Leu Leu His Ile405 4 - #10 4 - #15- tct tca tgt gac caa aat att tca gaa aaa ga - #c cta tta gac aca gag1492Ser Ser Cys Asp Gln Asn Ile Ser Glu Lys As - #p Leu Leu Asp Thr Glu420 4 - #25 4 - #30- aac aaa aga aag aaa gat ttt ctt act tca ga - #g aat tct ttg cca cgt1540Asn Lys Arg Lys Lys Asp Phe Leu Thr Ser Gl - #u Asn Ser Leu Pro Arg435 4 - #40 4 - #45- att tct agc cta cca aaa tca gag aag cca tt - #a aat gag gaa aca gtg1588Ile Ser Ser Leu Pro Lys Ser Glu Lys Pro Le - #u Asn Glu Glu Thr Val450 4 - #55 4 - #60- gta aat aag aga gat gaa gag cag cat ctt ga - #a tct cat aca gac tgc1636Val Asn Lys Arg Asp Glu Glu Gln His Leu Gl - #u Ser His Thr Asp Cys465 4 - #70 4 - #75 4 -#80- att ctt gca gta aag cag gca ata tct gga ac - #t tct cca gtg gct tct1684Ile Leu Ala Val Lys Gln Ala Ile Ser Gly Th - #r Ser Pro Val Ala Ser485 4 - #90 4 - #95- tca ttt cag ggt atc aaa aag tct ata ttc ag - #a ata aga gaa tca cct1732Ser Phe Gln Gly Ile Lys Lys Ser Ile Phe Ar - #g Ile Arg Glu Ser Pro500 5 - #05 5 - #10- aaa gag act ttc aat gca agt ttt tca ggt ca - #t atg act gat cca aac1780Lys Glu Thr Phe Asn Ala Ser Phe Ser Gly Hi - #s Met Thr Asp Pro Asn515 5 - #20 5 - #25- ttt aaa aaa gaa act gaa gcc tct gaa agt gg - #a ctg gaa ata cat act1828Phe Lys Lys Glu Thr Glu Ala Ser Glu Ser Gl - #y Leu Glu Ile His Thr530 5 - #35 5 - #40- gtt tgc tca cag aag gag gac tcc tta tgt cc - #a aat tta att gat aat1876Val Cys Ser Gln Lys Glu Asp Ser Leu Cys Pr - #o Asn Leu Ile Asp Asn545 5 - #50 5 - #55 5 -#60- gga agc tgg cca gcc acc acc aca cag aat tc - #t gta gct ttg aag aat1924Gly Ser Trp Pro Ala Thr Thr Thr Gln Asn Se - #r Val Ala Leu Lys Asn565 5 - #70 5 - #75- gca ggt tta ata tcc act ttg aaa aag aaa ac - #a aat aag ttt att tat1972Ala Gly Leu Ile Ser Thr Leu Lys Lys Lys Th - #r Asn Lys Phe Ile Tyr580 5 - #85 5 - #90- gct ata cat gat gaa aca ttt tat aaa gga aa - #a aaa ata ccg aaa gac2020Ala Ile His Asp Glu Thr Phe Tyr Lys Gly Ly - #s Lys Ile Pro Lys Asp595 6 - #00 6 - #05- caa aaa tca gaa cta att aac tgt tca gcc ca - #g ttt gaa gca aat gct2068Gln Lys Ser Glu Leu Ile Asn Cys Ser Ala Gl - #n Phe Glu Ala Asn Ala610 6 - #15 6 - #20- ttt gaa gca cca ctt aca ttt gca aat gct ga - #t tca ggt tta ttg cat2116Phe Glu Ala Pro Leu Thr Phe Ala Asn Ala As - #p Ser Gly Leu Leu His625 6 - #30 6 - #35 6 -#40- tct tct gtg aaa aga agc tgt tca cag aat ga - #t tct gaa gaa cca act2164Ser Ser Val Lys Arg Ser Cys Ser Gln Asn As - #p Ser Glu Glu Pro Thr645 6 - #50 6 - #55- ttg tcc tta act agc tct ttt ggg aca att ct - #g agg aaa tgt tct aga2212Leu Ser Leu Thr Ser Ser Phe Gly Thr Ile Le - #u Arg Lys Cys Ser Arg660 6 - #65 6 - #70- aat gaa aca tgt tct aat aat aca gta atc tc - #t cag gat ctt gat tat2260Asn Glu Thr Cys Ser Asn Asn Thr Val Ile Se - #r Gln Asp Leu Asp Tyr675 6 - #80 6 - #85- aaa gaa gca aaa tgt aat aag gaa aaa cta ca - #g tta ttt att acc cca2308Lys Glu Ala Lys Cys Asn Lys Glu Lys Leu Gl - #n Leu Phe Ile Thr Pro# 700- gaa gct gat tct ctg tca tgc ctg cag gaa gg - #a cag tgt gaa aat gat2356Glu Ala Asp Ser Leu Ser Cys Leu Gln Glu Gl - #y Gln Cys Glu Asn Asp705 7 - #10 7 - #15 7 -#20- cca aaa agc aaa aaa gtt tca gat ata aaa ga - #a gag gtc ttg gct gca2404Pro Lys Ser Lys Lys Val Ser Asp Ile Lys Gl - #u Glu Val Leu Ala Ala725 7 - #30 7 - #35- gca tgt cac cca gta caa cat tca aaa gtg ga - #a tac agt gat act gac2452Ala Cys His Pro Val Gln His Ser Lys Val Gl - #u Tyr Ser Asp Thr Asp740 7 - #45 7 - #50- ttt caa tcc cag aaa agt ctt tta tat gat ca - #t gaa aat gcc agc act2500Phe Gln Ser Gln Lys Ser Leu Leu Tyr Asp Hi - #s Glu Asn Ala Ser Thr755 7 - #60 7 - #65- ctt att tta act cct act tcc aag gat gtt ct - #g tca aac cta gtc atg2548Leu Ile Leu Thr Pro Thr Ser Lys Asp Val Le - #u Ser Asn Leu Val Met770 7 - #75 7 - #80- att tct aga ggc aaa gaa tca tac aaa atg tc - #a gac aag ctc aaa ggt2596Ile Ser Arg Gly Lys Glu Ser Tyr Lys Met Se - #r Asp Lys Leu Lys Gly785 7 - #90 7 - #95 8 -#00- aac aat tat gaa tct gat gtt gaa tta acc aa - #a aat att ccc atg gaa2644Asn Asn Tyr Glu Ser Asp Val Glu Leu Thr Ly - #s Asn Ile Pro Met Glu805 8 - #10 8 - #15- aag aat caa gat gta tgt gct tta aat gaa aa - #t tat aaa aac gtt gag2692Lys Asn Gln Asp Val Cys Ala Leu Asn Glu As - #n Tyr Lys Asn Val Glu820 8 - #25 8 - #30- ctg ttg cca cct gaa aaa tac atg aga gta gc - #a tca cct tca aga aag2740Leu Leu Pro Pro Glu Lys Tyr Met Arg Val Al - #a Ser Pro Ser Arg Lys835 8 - #40 8 - #45- gta caa ttc aac caa aac aca aat cta aga gt - #a atc caa aaa aat caa2788Val Gln Phe Asn Gln Asn Thr Asn Leu Arg Va - #l Ile Gln Lys Asn Gln850 8 - #55 8 - #60- gaa gaa act act tca att tca aaa ata act gt - #c aat cca gac tct gaa2836Glu Glu Thr Thr Ser Ile Ser Lys Ile Thr Va - #l Asn Pro Asp Ser Glu865 8 - #70 8 - #75 8 -#80- gaa ctt ttc tca gac aat gag aat aat ttt gt - #c ttc caa gta gct aat2884Glu Leu Phe Ser Asp Asn Glu Asn Asn Phe Va - #l Phe Gln Val Ala Asn885 8 - #90 8 - #95- gaa agg aat aat ctt gct tta gga aat act aa - #g gaa ctt cat gaa aca2932Glu Arg Asn Asn Leu Ala Leu Gly Asn Thr Ly - #s Glu Leu His Glu Thr900 9 - #05 9 - #10- gac ttg act tgt gta aac gaa ccc att ttc aa - #g aac tct acc atg gtt2980Asp Leu Thr Cys Val Asn Glu Pro Ile Phe Ly - #s Asn Ser Thr Met Val915 9 - #20 9 - #25- tta tat gga gac aca ggt gat aaa caa gca ac - #c caa gtg tca att aaa3028Leu Tyr Gly Asp Thr Gly Asp Lys Gln Ala Th - #r Gln Val Ser Ile Lys930 9 - #35 9 - #40- aaa gat ttg gtt tat gtt ctt gca gag gag aa - #c aaa aat agt gta aag3076Lys Asp Leu Val Tyr Val Leu Ala Glu Glu As - #n Lys Asn Ser Val Lys945 9 - #50 9 - #55 9 -#60- cag cat ata aaa atg act cta ggt caa gat tt - #a aaa tcg gac atc tcc3124Gln His Ile Lys Met Thr Leu Gly Gln Asp Le - #u Lys Ser Asp Ile Ser965 9 - #70 9 - #75- ttg aat ata gat aaa ata cca gaa aaa aat aa - #t gat tac atg aac aaa3172Leu Asn Ile Asp Lys Ile Pro Glu Lys Asn As - #n Asp Tyr Met Asn Lys980 9 - #85 9 - #90- tgg gca gga ctc tta ggt cca att tca aat ca - #c agt ttt gga ggt agc3220Trp Ala Gly Leu Leu Gly Pro Ile Ser Asn Hi - #s Ser Phe Gly Gly Ser995 1 - #000 1005- ttc aga aca gct tca aat aag gaa atc aag ct - #c tct gaa cat aac att3268Phe Arg Thr Ala Ser Asn Lys Glu Ile Lys Le - #u Ser Glu His Asn Ile1010 1015 - # 1020- aag aag agc aaa atg ttc ttc aaa gat att ga - #a gaa caa tat cct act3316Lys Lys Ser Lys Met Phe Phe Lys Asp Ile Gl - #u Glu Gln Tyr Pro Thr# 10401030 - # 1035- agt tta gct tgt gtt gaa att gta aat acc tt - #g gca tta gat aat caa3364Ser Leu Ala Cys Val Glu Ile Val Asn Thr Le - #u Ala Leu Asp Asn Gln1045 1050 - # 1055- aag aaa ctg agc aag cct cag tca att aat ac - #t gta tct gca cat tta3412Lys Lys Leu Ser Lys Pro Gln Ser Ile Asn Th - #r Val Ser Ala His Leu1060 1065 - # 1070- cag agt agt gta gtt gtt tct gat tgt aaa aa - #t agt cat ata acc cct3460Gln Ser Ser Val Val Val Ser Asp Cys Lys As - #n Ser His Ile Thr Pro1075 1080 - # 1085- cag atg tta ttt tcc aag cag gat ttt aat tc - #a aac cat aat tta aca3508Gln Met Leu Phe Ser Lys Gln Asp Phe Asn Se - #r Asn His Asn Leu Thr1090 1095 - # 1100- cct agc caa aag gca gaa att aca gaa ctt tc - #t act ata tta gaa gaa3556Pro Ser Gln Lys Ala Glu Ile Thr Glu Leu Se - #r Thr Ile Leu Glu Glu# 11201110 - # 1115- tca gga agt cag ttt gaa ttt act cag ttt ag - #a aaa cca agc tac ata3604Ser Gly Ser Gln Phe Glu Phe Thr Gln Phe Ar - #g Lys Pro Ser Tyr Ile1125 1130 - # 1135- ttg cag aag agt aca ttt gaa gtg cct gaa aa - #c cag atg act atc tta3652Leu Gln Lys Ser Thr Phe Glu Val Pro Glu As - #n Gln Met Thr Ile Leu1140 1145 - # 1150- aag acc act tct gag gaa tgc aga gat gct ga - #t ctt cat gtc ata atg3700Lys Thr Thr Ser Glu Glu Cys Arg Asp Ala As - #p Leu His Val Ile Met1155 1160 - # 1165- aat gcc cca tcg att ggt cag gta gac agc ag - #c aag caa ttt gaa ggt3748Asn Ala Pro Ser Ile Gly Gln Val Asp Ser Se - #r Lys Gln Phe Glu Gly1170 1175 - # 1180- aca gtt gaa att aaa cgg aag ttt gct ggc ct - #g ttg aaa aat gac tgt3796Thr Val Glu Ile Lys Arg Lys Phe Ala Gly Le - #u Leu Lys Asn Asp Cys# 12001190 - # 1195- aac aaa agt gct tct ggt tat tta aca gat ga - #a aat gaa gtg ggg ttt3844Asn Lys Ser Ala Ser Gly Tyr Leu Thr Asp Gl - #u Asn Glu Val Gly Phe1205 1210 - # 1215- agg ggc ttt tat tct gct cat ggc aca aaa ct - #g aat gtt tct act gaa3892Arg Gly Phe Tyr Ser Ala His Gly Thr Lys Le - #u Asn Val Ser Thr Glu1220 1225 - # 1230- gct ctg caa aaa gct gtg aaa ctg ttt agt ga - #t att gag aat att agt3940Ala Leu Gln Lys Ala Val Lys Leu Phe Ser As - #p Ile Glu Asn Ile Ser1235 1240 - # 1245- gag gaa act tct gca gag gta cat cca ata ag - #t tta tct tca agt aaa3988Glu Glu Thr Ser Ala Glu Val His Pro Ile Se - #r Leu Ser Ser Ser Lys1250 1255 - # 1260- tgt cat gat tct gtt gtt tca atg ttt aag at - #a gaa aat cat aat gat4036Cys His Asp Ser Val Val Ser Met Phe Lys Il - #e Glu Asn His Asn Asp# 12801270 - # 1275- aaa act gta agt gaa aaa aat aat aaa tgc ca - #a ctg ata tta caa aat4084Lys Thr Val Ser Glu Lys Asn Asn Lys Cys Gl - #n Leu Ile Leu Gln Asn1285 1290 - # 1295- aat att gaa atg act act ggc act ttt gtt ga - #a gaa att act gaa aat4132Asn Ile Glu Met Thr Thr Gly Thr Phe Val Gl - #u Glu Ile Thr Glu Asn1300 1305 - # 1310- tac aag aga aat act gaa aat gaa gat aac aa - #a tat act gct gcc agt4180Tyr Lys Arg Asn Thr Glu Asn Glu Asp Asn Ly - #s Tyr Thr Ala Ala Ser1315 1320 - # 1325- aga aat tct cat aac tta gaa ttt gat ggc ag - #t gat tca agt aaa aat4228Arg Asn Ser His Asn Leu Glu Phe Asp Gly Se - #r Asp Ser Ser Lys Asn1330 1335 - # 1340- gat act gtt tgt att cat aaa gat gaa acg ga - #c ttg cta ttt act gat4276Asp Thr Val Cys Ile His Lys Asp Glu Thr As - #p Leu Leu Phe Thr Asp# 13601350 - # 1355- cag cac aac ata tgt ctt aaa tta tct ggc ca - #g ttt atg aag gag gga4324Gln His Asn Ile Cys Leu Lys Leu Ser Gly Gl - #n Phe Met Lys Glu Gly1365 1370 - # 1375- aac act cag att aaa gaa gat ttg tca gat tt - #a act ttt ttg gaa gtt4372Asn Thr Gln Ile Lys Glu Asp Leu Ser Asp Le - #u Thr Phe Leu Glu Val1380 1385 - # 1390- gcg aaa gct caa gaa gca tgt cat ggt aat ac - #t tca aat aaa gaa cag4420Ala Lys Ala Gln Glu Ala Cys His Gly Asn Th - #r Ser Asn Lys Glu Gln1395 1400 - # 1405- tta act gct act aaa acg gag caa aat ata aa - #a gat ttt gag act tct4468Leu Thr Ala Thr Lys Thr Glu Gln Asn Ile Ly - #s Asp Phe Glu Thr Ser1410 1415 - # 1420- gat aca ttt ttt cag act gca agt ggg aaa aa - #t att agt gtc gcc aaa4516Asp Thr Phe Phe Gln Thr Ala Ser Gly Lys As - #n Ile Ser Val Ala Lys# 14401430 - # 1435- gag tta ttt aat aaa att gta aat ttc ttt ga - #t cag aaa cca gaa gaa4564Glu Leu Phe Asn Lys Ile Val Asn Phe Phe As - #p Gln Lys Pro Glu Glu1445 1450 - # 1455- ttg cat aac ttt tcc tta aat tct gaa tta ca - #t tct gac ata aga aag4612Leu His Asn Phe Ser Leu Asn Ser Glu Leu Hi - #s Ser Asp Ile Arg Lys1460 1465 - # 1470- aac aaa atg gac att cta agt tat gag gaa ac - #a gac ata gtt aaa cac4660Asn Lys Met Asp Ile Leu Ser Tyr Glu Glu Th - #r Asp Ile Val Lys His1475 1480 - # 1485- aaa ata ctg aaa gaa agt gtc cca gtt ggt ac - #t gga aat caa cta gtg4708Lys Ile Leu Lys Glu Ser Val Pro Val Gly Th - #r Gly Asn Gln Leu Val1490 1495 - # 1500- acc ttc cag gga caa ccc gaa cgt gat gaa aa - #g atc aaa gaa cct act4756Thr Phe Gln Gly Gln Pro Glu Arg Asp Glu Ly - #s Ile Lys Glu Pro Thr# 15201510 - # 1515- ctg ttg ggt ttt cat aca gct agc gga aaa aa - #a gtt aaa att gca aag4804Leu Leu Gly Phe His Thr Ala Ser Gly Lys Ly - #s Val Lys Ile Ala Lys1525 1530 - # 1535- gaa tct ttg gac aaa gtg aaa aac ctt ttt ga - #t gaa aaa gag caa ggt4852Glu Ser Leu Asp Lys Val Lys Asn Leu Phe As - #p Glu Lys Glu Gln Gly1540 1545 - # 1550- act agt gaa atc acc agt ttt agc cat caa tg - #g gca aag acc cta aag4900Thr Ser Glu Ile Thr Ser Phe Ser His Gln Tr - #p Ala Lys Thr Leu Lys1555 1560 - # 1565- tac aga gag gcc tgt aaa gac ctt gaa tta gc - #a tgt gag acc att gag4948Tyr Arg Glu Ala Cys Lys Asp Leu Glu Leu Al - #a Cys Glu Thr Ile Glu1570 1575 - # 1580- atc aca gct gcc cca aag tgt aaa gaa atg ca - #g aat tct ctc aat aat4996Ile Thr Ala Ala Pro Lys Cys Lys Glu Met Gl - #n Asn Ser Leu Asn Asn# 16001590 - # 1595- gat aaa aac ctt gtt tct att gag act gtg gt - #g cca cct aag ctc tta5044Asp Lys Asn Leu Val Ser Ile Glu Thr Val Va - #l Pro Pro Lys Leu Leu1605 1610 - # 1615- agt gat aat tta tgt aga caa act gaa aat ct - #c aaa aca tca aaa agt5092Ser Asp Asn Leu Cys Arg Gln Thr Glu Asn Le - #u Lys Thr Ser Lys Ser1620 1625 - # 1630- atc ttt ttg aaa gtt aaa gta cat gaa aat gt - #a gaa aaa gaa aca gca5140Ile Phe Leu Lys Val Lys Val His Glu Asn Va - #l Glu Lys Glu Thr Ala1635 1640 - # 1645- aaa agt cct gca act tgt tac aca aat cag tc - #c cct tat tca gtc att5188Lys Ser Pro Ala Thr Cys Tyr Thr Asn Gln Se - #r Pro Tyr Ser Val Ile1650 1655 - # 1660- gaa aat tca gcc tta gct ttt tac aca agt tg - #t agt aga aaa act tct5236Glu Asn Ser Ala Leu Ala Phe Tyr Thr Ser Cy - #s Ser Arg Lys Thr Ser# 16801670 - # 1675- gtg agt cag act tca tta ctt gaa gca aaa aa - #a tgg ctt aga gaa gga5284Val Ser Gln Thr Ser Leu Leu Glu Ala Lys Ly - #s Trp Leu Arg Glu Gly1685 1690 - # 1695- ata ttt gat ggt caa cca gaa aga ata aat ac - #t gca gat tat gta gga5332Ile Phe Asp Gly Gln Pro Glu Arg Ile Asn Th - #r Ala Asp Tyr Val Gly1700 1705 - # 1710- aat tat ttg tat gaa aat aat tca aac agt ac - #t ata gct gaa aat gac5380Asn Tyr Leu Tyr Glu Asn Asn Ser Asn Ser Th - #r Ile Ala Glu Asn Asp1715 1720 - # 1725- aaa aat cat ctc tcc gaa aaa caa gat act ta - #t tta agt aac agt agc5428Lys Asn His Leu Ser Glu Lys Gln Asp Thr Ty - #r Leu Ser Asn Ser Ser1730 1735 - # 1740- atg tct aac agc tat tcc tac cat tct gat ga - #g gta tat aat gat tca5476Met Ser Asn Ser Tyr Ser Tyr His Ser Asp Gl - #u Val Tyr Asn Asp Ser# 17601750 - # 1755- gga tat ctc tca aaa aat aaa ctt gat tct gg - #t att gag cca gta ttg5524Gly Tyr Leu Ser Lys Asn Lys Leu Asp Ser Gl - #y Ile Glu Pro Val Leu1765 1770 - # 1775- aag aat gtt gaa gat caa aaa aac act agt tt - #t tcc aaa gta ata tcc5572Lys Asn Val Glu Asp Gln Lys Asn Thr Ser Ph - #e Ser Lys Val Ile Ser1780 1785 - # 1790- aat gta aaa gat gca aat gca tac cca caa ac - #t gta aat gaa gat att5620Asn Val Lys Asp Ala Asn Ala Tyr Pro Gln Th - #r Val Asn Glu Asp Ile1795 1800 - # 1805- tgc gtt gag gaa ctt gtg act agc tct tca cc - #c tgc aaa aat aaa aat5668Cys Val Glu Glu Leu Val Thr Ser Ser Ser Pr - #o Cys Lys Asn Lys Asn1810 1815 - # 1820- gca gcc att aaa ttg tcc ata tct aat agt aa - #t aat ttt gag gta ggg5716Ala Ala Ile Lys Leu Ser Ile Ser Asn Ser As - #n Asn Phe Glu Val Gly# 18401830 - # 1835- cca cct gca ttt agg ata gcc agt ggt aaa at - #c cgt ttg tgt tca cat5764Pro Pro Ala Phe Arg Ile Ala Ser Gly Lys Il - #e Arg Leu Cys Ser His1845 1850 - # 1855- gaa aca att aaa aaa gtg aaa gac ata ttt ac - #a gac agt ttc agc aaa5812Glu Thr Ile Lys Lys Val Lys Asp Ile Phe Th - #r Asp Ser Phe Ser Lys1860 1865 - # 1870- gta att aag gaa aac aac gag aat aaa tca aa - #a att tgc caa acg aaa5860Val Ile Lys Glu Asn Asn Glu Asn Lys Ser Ly - #s Ile Cys Gln Thr Lys1875 1880 - # 1885- att atg gca ggt tgt tac gag gca ttg gat ga - #t tca gag gat att ctt5908Ile Met Ala Gly Cys Tyr Glu Ala Leu Asp As - #p Ser Glu Asp Ile Leu1890 1895 - # 1900- cat aac tct cta gat aat gat gaa tgt agc at - #g cat tca cat aag gtt5956His Asn Ser Leu Asp Asn Asp Glu Cys Ser Me - #t His Ser His Lys Val# 19201910 - # 1915- ttt gct gac att cag agt gaa gaa att tta ca - #a cat aac caa aat atg6004Phe Ala Asp Ile Gln Ser Glu Glu Ile Leu Gl - #n His Asn Gln Asn Met1925 1930 - # 1935- tct gga ttg gag aaa gtt tct aaa ata tca cc - #t tgt gat gtt agt ttg6052Ser Gly Leu Glu Lys Val Ser Lys Ile Ser Pr - #o Cys Asp Val Ser Leu1940 1945 - # 1950- gaa act tca gat ata tgt aaa tgt agt ata gg - #g aag ctt cat aag tca6100Glu Thr Ser Asp Ile Cys Lys Cys Ser Ile Gl - #y Lys Leu His Lys Ser1955 1960 - # 1965- gtc tca tct gca aat act tgt ggg att ttt ag - #c aca gca agt gga aaa6148Val Ser Ser Ala Asn Thr Cys Gly Ile Phe Se - #r Thr Ala Ser Gly Lys1970 1975 - # 1980- tct gtc cag gta tca gat gct tca tta caa aa - #c gca aga caa gtg ttt6196Ser Val Gln Val Ser Asp Ala Ser Leu Gln As - #n Ala Arg Gln Val Phe# 20001990 - # 1995- tct gaa ata gaa gat agt acc aag caa gtc tt - #t tcc aaa gta ttg ttt6244Ser Glu Ile Glu Asp Ser Thr Lys Gln Val Ph - #e Ser Lys Val Leu Phe2005 2010 - # 2015- aaa agt aac gaa cat tca gac cag ctc aca ag - #a gaa gaa aat act gct6292Lys Ser Asn Glu His Ser Asp Gln Leu Thr Ar - #g Glu Glu Asn Thr Ala2020 2025 - # 2030- ata cgt act cca gaa cat tta ata tcc caa aa - #a ggc ttt tca tat aat6340Ile Arg Thr Pro Glu His Leu Ile Ser Gln Ly - #s Gly Phe Ser Tyr Asn2035 2040 - # 2045- gtg gta aat tca tct gct ttc tct gga ttt ag - #t aca gca agt gga aag6388Val Val Asn Ser Ser Ala Phe Ser Gly Phe Se - #r Thr Ala Ser Gly Lys2050 2055 - # 2060- caa gtt tcc att tta gaa agt tcc tta cac aa - #a gtt aag gga gtg tta6436Gln Val Ser Ile Leu Glu Ser Ser Leu His Ly - #s Val Lys Gly Val Leu# 20802070 - # 2075- gag gaa ttt gat tta atc aga act gag cat ag - #t ctt cac tat tca cct6484Glu Glu Phe Asp Leu Ile Arg Thr Glu His Se - #r Leu His Tyr Ser Pro2085 2090 - # 2095- acg tct aga caa aat gta tca aaa ata ctt cc - #t cgt gtt gat aag aga6532Thr Ser Arg Gln Asn Val Ser Lys Ile Leu Pr - #o Arg Val Asp Lys Arg2100 2105 - # 2110- aac cca gag cac tgt gta aac tca gaa atg ga - #a aaa acc tgc agt aaa6580Asn Pro Glu His Cys Val Asn Ser Glu Met Gl - #u Lys Thr Cys Ser Lys2115 2120 - # 2125- gaa ttt aaa tta tca aat aac tta aat gtt ga - #a ggt ggt tct tca gaa6628Glu Phe Lys Leu Ser Asn Asn Leu Asn Val Gl - #u Gly Gly Ser Ser Glu2130 2135 - # 2140- aat aat cac tct att aaa gtt tct cca tat ct - #c tct caa ttt caa caa6676Asn Asn His Ser Ile Lys Val Ser Pro Tyr Le - #u Ser Gln Phe Gln Gln# 21602150 - # 2155- gac aaa caa cag ttg gta tta gga acc aaa gt - #c tca ctt gtt gag aac6724Asp Lys Gln Gln Leu Val Leu Gly Thr Lys Va - #l Ser Leu Val Glu Asn2165 2170 - # 2175- att cat gtt ttg gga aaa gaa cag gct tca cc - #t aaa aac gta aaa atg6772Ile His Val Leu Gly Lys Glu Gln Ala Ser Pr - #o Lys Asn Val Lys Met2180 2185 - # 2190- gaa att ggt aaa act gaa act ttt tct gat gt - #t cct gtg aaa aca aat6820Glu Ile Gly Lys Thr Glu Thr Phe Ser Asp Va - #l Pro Val Lys Thr Asn2195 2200 - # 2205- ata gaa gtt tgt tct act tac tcc aaa gat tc - #a gaa aac tac ttt gaa6868Ile Glu Val Cys Ser Thr Tyr Ser Lys Asp Se - #r Glu Asn Tyr Phe Glu2210 2215 - # 2220- aca gaa gca gta gaa att gct aaa gct ttt at - #g gaa gat gat gaa ctg6916Thr Glu Ala Val Glu Ile Ala Lys Ala Phe Me - #t Glu Asp Asp Glu Leu# 22402230 - # 2235- aca gat tct aaa ctg cca agt cat gcc aca ca - #t tct ctt ttt aca tgt6964Thr Asp Ser Lys Leu Pro Ser His Ala Thr Hi - #s Ser Leu Phe Thr Cys2245 2250 - # 2255- ccc gaa aat gag gaa atg gtt ttg tca aat tc - #a aga att gga aaa aga7012Pro Glu Asn Glu Glu Met Val Leu Ser Asn Se - #r Arg Ile Gly Lys Arg2260 2265 - # 2270- aga gga gag ccc ctt atc tta gtg gga gaa cc - #c tca atc aaa aga aac7060Arg Gly Glu Pro Leu Ile Leu Val Gly Glu Pr - #o Ser Ile Lys Arg Asn2275 2280 - # 2285- tta tta aat gaa ttt gac agg ata ata gaa aa - #t caa gaa aaa tcc tta7108Leu Leu Asn Glu Phe Asp Arg Ile Ile Glu As - #n Gln Glu Lys Ser Leu2290 2295 - # 2300- aag gct tca aaa agc act cca gat ggc aca at - #a aaa gat cga aga ttg7156Lys Ala Ser Lys Ser Thr Pro Asp Gly Thr Il - #e Lys Asp Arg Arg Leu# 23202310 - # 2315- ttt atg cat cat gtt tct tta gag ccg att ac - #c tgt gta ccc ttt cgc7204Phe Met His His Val Ser Leu Glu Pro Ile Th - #r Cys Val Pro Phe Arg2325 2330 - # 2335- aca act aag gaa cgt caa gag ata cag aat cc - #a aat ttt acc gca cct7252Thr Thr Lys Glu Arg Gln Glu Ile Gln Asn Pr - #o Asn Phe Thr Ala Pro2340 2345 - # 2350- ggt caa gaa ttt ctg tct aaa tct cat ttg ta - #t gaa cat ctg act ttg7300Gly Gln Glu Phe Leu Ser Lys Ser His Leu Ty - #r Glu His Leu Thr Leu2355 2360 - # 2365- gaa aaa tct tca agc aat tta gca gtt tca gg - #a cat cca ttt tat caa7348Glu Lys Ser Ser Ser Asn Leu Ala Val Ser Gl - #y His Pro Phe Tyr Gln2370 2375 - # 2380- gtt tct gct aca aga aat gaa aaa atg aga ca - #c ttg att act aca ggc7396Val Ser Ala Thr Arg Asn Glu Lys Met Arg Hi - #s Leu Ile Thr Thr Gly# 24002390 - # 2395- aga cca acc aaa gtc ttt gtt cca cct ttt aa - #a act aaa tca cat ttt7444Arg Pro Thr Lys Val Phe Val Pro Pro Phe Ly - #s Thr Lys Ser His Phe2405 2410 - # 2415- cac aga gtt gaa cag tgt gtt agg aat att aa - #c ttg gag gaa aac aga7492His Arg Val Glu Gln Cys Val Arg Asn Ile As - #n Leu Glu Glu Asn Arg2420 2425 - # 2430- caa aag caa aac att gat gga cat ggc tct ga - #t gat agt aaa aat aag7540Gln Lys Gln Asn Ile Asp Gly His Gly Ser As - #p Asp Ser Lys Asn Lys2435 2440 - # 2445- att aat gac aat gag att cat cag ttt aac aa - #a aac aac tcc aat caa7588Ile Asn Asp Asn Glu Ile His Gln Phe Asn Ly - #s Asn Asn Ser Asn Gln2450 2455 - # 2460- gca gca gct gta act ttc aca aag tgt gaa ga - #a gaa cct tta gat tta7636Ala Ala Ala Val Thr Phe Thr Lys Cys Glu Gl - #u Glu Pro Leu Asp Leu# 24802470 - # 2475- att aca agt ctt cag aat gcc aga gat ata ca - #g gat atg cga att aag7684Ile Thr Ser Leu Gln Asn Ala Arg Asp Ile Gl - #n Asp Met Arg Ile Lys2485 2490 - # 2495- aag aaa caa agg caa cgc gtc ttt cca cag cc - #a ggc agt ctg tat ctt7732Lys Lys Gln Arg Gln Arg Val Phe Pro Gln Pr - #o Gly Ser Leu Tyr Leu2500 2505 - # 2510- gca aaa aca tcc act ctg cct cga atc tct ct - #g aaa gca gca gta gga7780Ala Lys Thr Ser Thr Leu Pro Arg Ile Ser Le - #u Lys Ala Ala Val Gly2515 2520 - # 2525- ggc caa gtt ccc tct gcg tgt tct cat aaa ca - #g ctg tat acg tat ggc7828Gly Gln Val Pro Ser Ala Cys Ser His Lys Gl - #n Leu Tyr Thr Tyr Gly2530 2535 - # 2540- gtt tct aaa cat tgc ata aaa att aac agc aa - #a aat gca gag tct ttt7876Val Ser Lys His Cys Ile Lys Ile Asn Ser Ly - #s Asn Ala Glu Ser Phe# 25602550 - # 2555- cag ttt cac act gaa gat tat ttt ggt aag ga - #a agt tta tgg act gga7924Gln Phe His Thr Glu Asp Tyr Phe Gly Lys Gl - #u Ser Leu Trp Thr Gly2565 2570 - # 2575- aaa gga ata cag ttg gct gat ggt gga tgg ct - #c ata ccc tcc aat gat7972Lys Gly Ile Gln Leu Ala Asp Gly Gly Trp Le - #u Ile Pro Ser Asn Asp2580 2585 - # 2590- gga aag gct gga aaa gaa gaa ttt tat agg gc - #t ctg tgt gac act cca8020Gly Lys Ala Gly Lys Glu Glu Phe Tyr Arg Al - #a Leu Cys Asp Thr Pro2595 2600 - # 2605- ggt gtg gat cca aag ctt att tct aga att tg - #g gtt tat aat cac tat8068Gly Val Asp Pro Lys Leu Ile Ser Arg Ile Tr - #p Val Tyr Asn His Tyr2610 2615 - # 2620- aga tgg atc ata tgg aaa ctg gca gct atg ga - #a tgt gcc ttt cct aag8116Arg Trp Ile Ile Trp Lys Leu Ala Ala Met Gl - #u Cys Ala Phe Pro Lys# 26402630 - # 2635- gaa ttt gct aat aga tgc cta agc cca gaa ag - #g gtg ctt ctt caa cta8164Glu Phe Ala Asn Arg Cys Leu Ser Pro Glu Ar - #g Val Leu Leu Gln Leu2645 2650 - # 2655- aaa tac aga tat gat acg gaa att gat aga ag - #c aga aga tcg gct ata8212Lys Tyr Arg Tyr Asp Thr Glu Ile Asp Arg Se - #r Arg Arg Ser Ala Ile2660 2665 - # 2670- aaa aag ata atg gaa agg gat gac aca gct gc - #a aaa aca ctt gtt ctc8260Lys Lys Ile Met Glu Arg Asp Asp Thr Ala Al - #a Lys Thr Leu Val Leu2675 2680 - # 2685- tgt gtt tct gac ata att tca ttg agc gca aa - #t ata tct gaa act tct8308Cys Val Ser Asp Ile Ile Ser Leu Ser Ala As - #n Ile Ser Glu Thr Ser2690 2695 - # 2700- agc aat aaa act agt agt gca gat acc caa aa - #a gtg gcc att att gaa8356Ser Asn Lys Thr Ser Ser Ala Asp Thr Gln Ly - #s Val Ala Ile Ile Glu# 27202710 - # 2715- ctt aca gat ggg tgg tat gct gtt aag gcc ca - #g tta gat cct ccc ctc8404Leu Thr Asp Gly Trp Tyr Ala Val Lys Ala Gl - #n Leu Asp Pro Pro Leu2725 2730 - # 2735- tta gct gtc tta aag aat ggc aga ctg aca gt - #t ggt cag aag att att8452Leu Ala Val Leu Lys Asn Gly Arg Leu Thr Va - #l Gly Gln Lys Ile Ile2740 2745 - # 2750- ctt cat gga gca gaa ctg gtg ggc tct cct ga - #t gcc tgt aca cct ctt8500Leu His Gly Ala Glu Leu Val Gly Ser Pro As - #p Ala Cys Thr Pro Leu2755 2760 - # 2765- gaa gcc cca gaa tct ctt atg tta aag att tc - #t gct aac agt act cgg8548Glu Ala Pro Glu Ser Leu Met Leu Lys Ile Se - #r Ala Asn Ser Thr Arg2770 2775 - # 2780- cct gct cgc tgg tat acc aaa ctt gga ttc tt - #t cct gac cct aga cct8596Pro Ala Arg Trp Tyr Thr Lys Leu Gly Phe Ph - #e Pro Asp Pro Arg Pro# 28002790 - # 2795- ttt cct ctg ccc tta tca tcg ctt ttc agt ga - #t gga gga aat gtt ggt8644Phe Pro Leu Pro Leu Ser Ser Leu Phe Ser As - #p Gly Gly Asn Val Gly2805 2810 - # 2815- tgt gtt gat gta att att caa aga gca tac cc - #t ata cag cgg atg gag8692Cys Val Asp Val Ile Ile Gln Arg Ala Tyr Pr - #o Ile Gln Arg Met Glu2820 2825 - # 2830- aag aca tca tct gga tta tac ata ttt cgc aa - #t gaa aga gag gaa gaa8740Lys Thr Ser Ser Gly Leu Tyr Ile Phe Arg As - #n Glu Arg Glu Glu Glu2835 2840 - # 2845- aag gaa gca gca aaa tat gtg gag gcc caa ca - #a aag aga cta gaa gcc8788Lys Glu Ala Ala Lys Tyr Val Glu Ala Gln Gl - #n Lys Arg Leu Glu Ala2850 2855 - # 2860- tta ttc act aaa att cag gag gaa ttt gaa ga - #a cat gaa gaa aac aca8836Leu Phe Thr Lys Ile Gln Glu Glu Phe Glu Gl - #u His Glu Glu Asn Thr# 28802870 - # 2875- aca aaa cca tat tta cca tca cgt gca cta ac - #a aga cag caa gtt cgt8884Thr Lys Pro Tyr Leu Pro Ser Arg Ala Leu Th - #r Arg Gln Gln Val Arg2885 2890 - # 2895- gct ttg caa gat ggt gca gag ctt tat gaa gc - #a gtg aag aat gca gca8932Ala Leu Gln Asp Gly Ala Glu Leu Tyr Glu Al - #a Val Lys Asn Ala Ala2900 2905 - # 2910- gac cca gct tac ctt gag ggt tat ttc agt ga - #a gag cag tta aga gcc8980Asp Pro Ala Tyr Leu Glu Gly Tyr Phe Ser Gl - #u Glu Gln Leu Arg Ala2915 2920 - # 2925- ttg aat aat cac agg caa atg ttg aat gat aa - #g aaa caa gct cag atc9028Leu Asn Asn His Arg Gln Met Leu Asn Asp Ly - #s Lys Gln Ala Gln Ile2930 2935 - # 2940- cag ttg gaa att agg aag gcc atg gaa tct gc - #t gaa caa aag gaa caa9076Gln Leu Glu Ile Arg Lys Ala Met Glu Ser Al - #a Glu Gln Lys Glu Gln# 29602950 - # 2955- ggt tta tca agg gat gtc aca acc gtg tgg aa - #g ttg cgt att gta agc9124Gly Leu Ser Arg Asp Val Thr Thr Val Trp Ly - #s Leu Arg Ile Val Ser2965 2970 - # 2975- tat tca aaa aaa gaa aaa gat tca gtt ata ct - #g agt att tgg cgt cca9172Tyr Ser Lys Lys Glu Lys Asp Ser Val Ile Le - #u Ser Ile Trp Arg Pro2980 2985 - # 2990- tca tca gat tta tat tct ctg tta aca gaa gg - #a aag aga tac aga att9220Ser Ser Asp Leu Tyr Ser Leu Leu Thr Glu Gl - #y Lys Arg Tyr Arg Ile2995 3000 - # 3005- tat cat ctt gca act tca aaa tct aaa agt aa - #a tct gaa aga gct aac9268Tyr His Leu Ala Thr Ser Lys Ser Lys Ser Ly - #s Ser Glu Arg Ala Asn3010 3015 - # 3020- ata cag tta gca gcg aca aaa aaa act cag ta - #t caa caa cta ccg gtt9316Ile Gln Leu Ala Ala Thr Lys Lys Thr Gln Ty - #r Gln Gln Leu Pro Val# 30403030 - # 3035- tca gat gaa att tta ttt cag att tac cag cc - #a cgg gag ccc ctt cac9364Ser Asp Glu Ile Leu Phe Gln Ile Tyr Gln Pr - #o Arg Glu Pro Leu His3045 3050 - # 3055- ttc agc aaa ttt tta gat cca gac ttt cag cc - #a tct tgt tct gag gtg9412Phe Ser Lys Phe Leu Asp Pro Asp Phe Gln Pr - #o Ser Cys Ser Glu Val3060 3065 - # 3070- gac cta ata gga ttt gtc gtt tct gtt gtg aa - #a aaa aca gga ctt gcc9460Asp Leu Ile Gly Phe Val Val Ser Val Val Ly - #s Lys Thr Gly Leu Ala3075 3080 - # 3085- cct ttc gtc tat ttg tca gac gaa tgt tac aa - #t tta ctg gca ata aag9508Pro Phe Val Tyr Leu Ser Asp Glu Cys Tyr As - #n Leu Leu Ala Ile Lys3090 3095 - # 3100- ttt tgg ata gac ctt aat gag gac att att aa - #g cct cat atg tta att9556Phe Trp Ile Asp Leu Asn Glu Asp Ile Ile Ly - #s Pro His Met Leu Ile# 31203110 - # 3115- gct gca agc aac ctc cag tgg cga cca gaa tc - #c aaa tca ggc ctt ctt9604Ala Ala Ser Asn Leu Gln Trp Arg Pro Glu Se - #r Lys Ser Gly Leu Leu3125 3130 - # 3135- act tta ttt gct gga gat ttt tct gtg ttt tc - #t gct agt cca aaa gag9652Thr Leu Phe Ala Gly Asp Phe Ser Val Phe Se - #r Ala Ser Pro Lys Glu3140 3145 - # 3150- ggc cac ttt caa gag aca ttc aac aaa atg aa - #a aat act gtt gag aat9700Gly His Phe Gln Glu Thr Phe Asn Lys Met Ly - #s Asn Thr Val Glu Asn3155 3160 - # 3165- att gac ata ctt tgc aat gaa gca gaa aac aa - #g ctt atg cat ata ctg9748Ile Asp Ile Leu Cys Asn Glu Ala Glu Asn Ly - #s Leu Met His Ile Leu3170 3175 - # 3180- cat gca aat gat ccc aag tgg tcc acc cca ac - #t aaa gac tgt act tca9796His Ala Asn Asp Pro Lys Trp Ser Thr Pro Th - #r Lys Asp Cys Thr Ser3185 3190 - # 319 - #5 3200- ggg ccg tac act gct caa atc att cct ggt ac - #a gga aac aag ctt ctg9844Gly Pro Tyr Thr Ala Gln Ile Ile Pro Gly Th - #r Gly Asn Lys Leu Leu3205 3210 - # 3215- atg tct tct cct aat tgt gag ata tat tat ca - #a agt cct tta tca ctt9892Met Ser Ser Pro Asn Cys Glu Ile Tyr Tyr Gl - #n Ser Pro Leu Ser Leu3220 3225 - # 3230- tgt atg gcc aaa agg aag tct gtt tcc aca cc - #t gtc tca gcc cag atg9940Cys Met Ala Lys Arg Lys Ser Val Ser Thr Pr - #o Val Ser Ala Gln Met3235 3240 - # 3245- act tca aag tct tgt aaa ggg gag aaa gag at - #t gat gac caa aag aac9988Thr Ser Lys Ser Cys Lys Gly Glu Lys Glu Il - #e Asp Asp Gln Lys Asn3250 3255 - # 3260- tgc aaa aag aga aga gcc ttg gat ttc ttg ag - #t aga ctg cct tta cct10036Cys Lys Lys Arg Arg Ala Leu Asp Phe Leu Se - #r Arg Leu Pro Leu Pro# 32803270 - # 3275- cca cct gtt agt ccc att tgt aca ttt gtt tc - #t ccg gct gca cag aag10084Pro Pro Val Ser Pro Ile Cys Thr Phe Val Se - #r Pro Ala Ala Gln Lys3285 3290 - # 3295- gca ttt cag cca cca agg agt tgt ggc acc aa - #a tac gaa aca ccc ata10132Ala Phe Gln Pro Pro Arg Ser Cys Gly Thr Ly - #s Tyr Glu Thr Pro Ile3300 3305 - # 3310- aag aaa aaa gaa ctg aat tct cct cag atg ac - #t cca ttt aaa aaa ttc10180Lys Lys Lys Glu Leu Asn Ser Pro Gln Met Th - #r Pro Phe Lys Lys Phe3315 3320 - # 3325- aat gaa att tct ctt ttg gaa agt aat tca at - #a gct gac gaa gaa ctt10228Asn Glu Ile Ser Leu Leu Glu Ser Asn Ser Il - #e Ala Asp Glu Glu Leu3330 3335 - # 3340- gca ttg ata aat acc caa gct ctt ttg tct gg - #t tca aca gga gaa aaa10276Ala Leu Ile Asn Thr Gln Ala Leu Leu Ser Gl - #y Ser Thr Gly Glu Lys# 33603350 - # 3355- caa ttt ata tct gtc agt gaa tcc act agg ac - #t gct ccc acc agt tca10324Gln Phe Ile Ser Val Ser Glu Ser Thr Arg Th - #r Ala Pro Thr Ser Ser3365 3370 - # 3375- gaa gat tat ctc aga ctg aaa cga cgt tgt ac - #t aca tct ctg atc aaa10372Glu Asp Tyr Leu Arg Leu Lys Arg Arg Cys Th - #r Thr Ser Leu Ile Lys3380 3385 - # 3390- gaa cag gag agt tcc cag gcc agt acg gaa ga - #a tgt gag aaa aat aag10420Glu Gln Glu Ser Ser Gln Ala Ser Thr Glu Gl - #u Cys Glu Lys Asn Lys3395 3400 - # 3405- cag gac aca att aca act aaa aaa tat atc ta - #agcatttg caaaggcgac10470Gln Asp Thr Ile Thr Thr Lys Lys Tyr Ile3410 3415- aataaattat tgacgcttaa cctttccagt ttataagact ggaatataat tt - #caaaccac10530- acattagtac ttatgttgcm caatgagaaa agaaattagt ttcaaattta cc - #tcagcgtt10590- tgtgtatcgg gcaaaaatcg ttttgcccga ttccgtattg gtatactttt gc - #ctcagttg10650- catatcctaa aactaaatgt aatttattaa ctaatcaaga aaaacatctt tg - #gctgagct10710- cggtggctca tgcctgtaat cccaacactt tgagaagctg aggtgggagg ag - #tgcttgag10770- gccaggagtt caagaccagc ctgggcaaca tagggagacc ccatctttac ga - #agaaaaaa10830- aaaaagggga aaagaaaatc ttttaaatct ttggatttca ctacaagtat ta - #ttttacaa10890- gtgaaataaa cataccattt tcttttagat tgtgtcatta aatggaatga gg - #tctcttag10950- tacagttatt ttgatgcaga taattccttt tagtttagct actattttag gg - #gatttttt11010- ttagaggtaa ctcactatga aatagttccc cttaatgcaa atatgttggt tc - #tgcaatag11070- ttccatcctg ttcaaaartc rggrtgaawa tgaagagtgg tgttyccttt tg - #agcaattc11130- tcatccttaa gtcagcrtga ttataagaaa aatagaaccc ycagtgtaac yc - #taattcct11190- ttttrctatt ccagtgtgat ctctgaaakt aaattacttc mactaaaaat tc - #aaaaactt11250# 11283 awag twgatttatt ttt- (2) INFORMATION FOR SEQ ID NO:4:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 3418 (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: protein- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Homo sapi - #ens sapiens (C) INDIVIDUAL ISOLATE:#adult (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: female - # breast (G) CELL TYPE: norm - #al breast tissue (H) CELL LINE: HMEC (I) ORGANELLE: no- (ix) FEATURE: (A) NAME/KEY: BRCA2 pro - #tein (B) LOCATION: 1 to 3 - #418; Genbank locus HSU43746 (C) IDENTIFICATION METHOD:#BRCA2 protein has a negativeON:#effect on growth of human mammary cells.- (x) PUBLICATION INFORMATION:#R. et al.(A) AUTHORS: Wooster, (B) TITLE: Identificat - #ion of the breast cancer susceptabili - #ty gene BRCA2 (C) JOURNAL: Nature (D) VOLUME: 379 (E) PAGES: 789-792 (F) DATE: 1995 (K) RELEVANT RESIDUES I - #N SEQ ID NO:4: granin box domain at - # amino acids 3334-3344- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #4:- Met Pro Ile Gly Ser Lys Glu Arg Pro Thr Ph - #e Phe Glu Ile Phe Lys# 15- Thr Arg Cys Asn Lys Ala Asp Leu Gly Pro Il - #e Ser Leu Asn Trp Phe# 30- Glu Glu Leu Ser Ser Glu Ala Pro Pro Tyr As - #n Ser Glu Pro Ala Glu# 45- Glu Ser Glu His Lys Asn Asn Asn Tyr Glu Pr - #o Asn Leu Phe Lys Thr# 60- Pro Gln Arg Lys Pro Ser Tyr Asn Gln Leu Al - #a Ser Thr Pro Ile Ile#80- Phe Lys Glu Gln Gly Leu Thr Leu Pro Leu Ty - #r Gln Ser Pro Val Lys# 95- Glu Leu Asp Lys Phe Lys Leu Asp Leu Gly Ar - #g Asn Val Pro Asn Ser# 110- Arg His Lys Ser Leu Arg Thr Val Lys Tyr Ly - #s Met Asp Gln Ala Asp# 125- Asp Val Ser Cys Pro Leu Leu Asn Ser Cys Le - #u Ser Glu Ser Pro Val# 140- Val Leu Gln Cys Thr His Val Thr Pro Gln Ar - #g Asp Lys Ser Val Val145 1 - #50 1 - #55 1 -#60- Cys Gly Ser Leu Phe His Thr Pro Lys Phe Va - #l Lys Gly Arg Gln Thr# 175- Pro Lys His Ile Ser Glu Ser Leu Gly Ala Gl - #u Val Asp Pro Asp Met# 190- Ser Trp Ser Ser Ser Leu Ala Thr Pro Pro Th - #r Leu Ser Ser Thr Val# 205- Leu Ile Val Arg Asn Glu Glu Ala Ser Glu Th - #r Val Phe Pro His Asp# 220- Thr Thr Ala Asn Val Lys Ser Tyr Phe Ser As - #n His Asp Glu Ser Leu225 2 - #30 2 - #35 2 -#40- Lys Lys Asn Asp Arg Phe Ile Ala Ser Val Th - #r Asp Ser Glu Asn Thr# 255- Asn Gln Arg Glu Ala Ala Ser His Gly Phe Gl - #y Lys Thr Ser Gly Asn# 270- Ser Phe Lys Val Asn Ser Cys Lys Asp His Il - #e Gly Lys Ser Met Pro# 285- Asn Val Leu Glu Asp Glu Val Tyr Glu Thr Va - #l Val Asp Thr Ser Glu# 300- Glu Asp Ser Phe Ser Leu Cys Phe Ser Lys Cy - #s Arg Thr Lys Asn Leu305 3 - #10 3 - #15 3 -#20- Gln Lys Val Arg Thr Ser Lys Thr Arg Lys Ly - #s Ile Phe His Glu Ala# 335- Asn Ala Asp Glu Cys Glu Lys Ser Lys Asn Gl - #n Val Lys Glu Lys Tyr# 350- Ser Phe Val Ser Glu Val Glu Pro Asn Asp Th - #r Asp Pro Leu Asp Ser# 365- Asn Val Ala His Gln Lys Pro Phe Glu Ser Gl - #y Ser Asp Lys Ile Ser# 380- Lys Glu Val Val Pro Ser Leu Ala Cys Glu Tr - #p Ser Gln Leu Thr Leu385 3 - #90 3 - #95 4 -#00- Ser Gly Leu Asn Gly Ala Gln Met Glu Lys Il - #e Pro Leu Leu His Ile# 415- Ser Ser Cys Asp Gln Asn Ile Ser Glu Lys As - #p Leu Leu Asp Thr Glu# 430- Asn Lys Arg Lys Lys Asp Phe Leu Thr Ser Gl - #u Asn Ser Leu Pro Arg# 445- Ile Ser Ser Leu Pro Lys Ser Glu Lys Pro Le - #u Asn Glu Glu Thr Val# 460- Val Asn Lys Arg Asp Glu Glu Gln His Leu Gl - #u Ser His Thr Asp Cys465 4 - #70 4 - #75 4 -#80- Ile Leu Ala Val Lys Gln Ala Ile Ser Gly Th - #r Ser Pro Val Ala Ser# 495- Ser Phe Gln Gly Ile Lys Lys Ser Ile Phe Ar - #g Ile Arg Glu Ser Pro# 510- Lys Glu Thr Phe Asn Ala Ser Phe Ser Gly Hi - #s Met Thr Asp Pro Asn# 525- Phe Lys Lys Glu Thr Glu Ala Ser Glu Ser Gl - #y Leu Glu Ile His Thr# 540- Val Cys Ser Gln Lys Glu Asp Ser Leu Cys Pr - #o Asn Leu Ile Asp Asn545 5 - #50 5 - #55 5 -#60- Gly Ser Trp Pro Ala Thr Thr Thr Gln Asn Se - #r Val Ala Leu Lys Asn# 575- Ala Gly Leu Ile Ser Thr Leu Lys Lys Lys Th - #r Asn Lys Phe Ile Tyr# 590- Ala Ile His Asp Glu Thr Phe Tyr Lys Gly Ly - #s Lys Ile Pro Lys Asp# 605- Gln Lys Ser Glu Leu Ile Asn Cys Ser Ala Gl - #n Phe Glu Ala Asn Ala# 620- Phe Glu Ala Pro Leu Thr Phe Ala Asn Ala As - #p Ser Gly Leu Leu His625 6 - #30 6 - #35 6 -#40- Ser Ser Val Lys Arg Ser Cys Ser Gln Asn As - #p Ser Glu Glu Pro Thr# 655- Leu Ser Leu Thr Ser Ser Phe Gly Thr Ile Le - #u Arg Lys Cys Ser Arg# 670- Asn Glu Thr Cys Ser Asn Asn Thr Val Ile Se - #r Gln Asp Leu Asp Tyr# 685- Lys Glu Ala Lys Cys Asn Lys Glu Lys Leu Gl - #n Leu Phe Ile Thr Pro# 700- Glu Ala Asp Ser Leu Ser Cys Leu Gln Glu Gl - #y Gln Cys Glu Asn Asp705 7 - #10 7 - #15 7 -#20- Pro Lys Ser Lys Lys Val Ser Asp Ile Lys Gl - #u Glu Val Leu Ala Ala# 735- Ala Cys His Pro Val Gln His Ser Lys Val Gl - #u Tyr Ser Asp Thr Asp# 750- Phe Gln Ser Gln Lys Ser Leu Leu Tyr Asp Hi - #s Glu Asn Ala Ser Thr# 765- Leu Ile Leu Thr Pro Thr Ser Lys Asp Val Le - #u Ser Asn Leu Val Met# 780- Ile Ser Arg Gly Lys Glu Ser Tyr Lys Met Se - #r Asp Lys Leu Lys Gly785 7 - #90 7 - #95 8 -#00- Asn Asn Tyr Glu Ser Asp Val Glu Leu Thr Ly - #s Asn Ile Pro Met Glu# 815- Lys Asn Gln Asp Val Cys Ala Leu Asn Glu As - #n Tyr Lys Asn Val Glu# 830- Leu Leu Pro Pro Glu Lys Tyr Met Arg Val Al - #a Ser Pro Ser Arg Lys# 845- Val Gln Phe Asn Gln Asn Thr Asn Leu Arg Va - #l Ile Gln Lys Asn Gln# 860- Glu Glu Thr Thr Ser Ile Ser Lys Ile Thr Va - #l Asn Pro Asp Ser Glu865 8 - #70 8 - #75 8 -#80- Glu Leu Phe Ser Asp Asn Glu Asn Asn Phe Va - #l Phe Gln Val Ala Asn# 895- Glu Arg Asn Asn Leu Ala Leu Gly Asn Thr Ly - #s Glu Leu His Glu Thr# 910- Asp Leu Thr Cys Val Asn Glu Pro Ile Phe Ly - #s Asn Ser Thr Met Val# 925- Leu Tyr Gly Asp Thr Gly Asp Lys Gln Ala Th - #r Gln Val Ser Ile Lys# 940- Lys Asp Leu Val Tyr Val Leu Ala Glu Glu As - #n Lys Asn Ser Val Lys945 9 - #50 9 - #55 9 -#60- Gln His Ile Lys Met Thr Leu Gly Gln Asp Le - #u Lys Ser Asp Ile Ser# 975- Leu Asn Ile Asp Lys Ile Pro Glu Lys Asn As - #n Asp Tyr Met Asn Lys# 990- Trp Ala Gly Leu Leu Gly Pro Ile Ser Asn Hi - #s Ser Phe Gly Gly Ser# 10050- Phe Arg Thr Ala Ser Asn Lys Glu Ile Lys Le - #u Ser Glu His Asn Ile# 10205- Lys Lys Ser Lys Met Phe Phe Lys Asp Ile Gl - #u Glu Gln Tyr Pro Thr# 10401030 - # 1035- Ser Leu Ala Cys Val Glu Ile Val Asn Thr Le - #u Ala Leu Asp Asn Gln# 10550- Lys Lys Leu Ser Lys Pro Gln Ser Ile Asn Th - #r Val Ser Ala His Leu# 10705- Gln Ser Ser Val Val Val Ser Asp Cys Lys As - #n Ser His Ile Thr Pro# 10850- Gln Met Leu Phe Ser Lys Gln Asp Phe Asn Se - #r Asn His Asn Leu Thr# 11005- Pro Ser Gln Lys Ala Glu Ile Thr Glu Leu Se - #r Thr Ile Leu Glu Glu# 11201110 - # 1115- Ser Gly Ser Gln Phe Glu Phe Thr Gln Phe Ar - #g Lys Pro Ser Tyr Ile# 11350- Leu Gln Lys Ser Thr Phe Glu Val Pro Glu As - #n Gln Met Thr Ile Leu# 11505- Lys Thr Thr Ser Glu Glu Cys Arg Asp Ala As - #p Leu His Val Ile Met# 11650- Asn Ala Pro Ser Ile Gly Gln Val Asp Ser Se - #r Lys Gln Phe Glu Gly# 11805- Thr Val Glu Ile Lys Arg Lys Phe Ala Gly Le - #u Leu Lys Asn Asp Cys# 12001190 - # 1195- Asn Lys Ser Ala Ser Gly Tyr Leu Thr Asp Gl - #u Asn Glu Val Gly Phe# 12150- Arg Gly Phe Tyr Ser Ala His Gly Thr Lys Le - #u Asn Val Ser Thr Glu# 12305- Ala Leu Gln Lys Ala Val Lys Leu Phe Ser As - #p Ile Glu Asn Ile Ser# 12450- Glu Glu Thr Ser Ala Glu Val His Pro Ile Se - #r Leu Ser Ser Ser Lys# 12605- Cys His Asp Ser Val Val Ser Met Phe Lys Il - #e Glu Asn His Asn Asp# 12801270 - # 1275- Lys Thr Val Ser Glu Lys Asn Asn Lys Cys Gl - #n Leu Ile Leu Gln Asn# 12950- Asn Ile Glu Met Thr Thr Gly Thr Phe Val Gl - #u Glu Ile Thr Glu Asn# 13105- Tyr Lys Arg Asn Thr Glu Asn Glu Asp Asn Ly - #s Tyr Thr Ala Ala Ser# 13250- Arg Asn Ser His Asn Leu Glu Phe Asp Gly Se - #r Asp Ser Ser Lys Asn# 13405- Asp Thr Val Cys Ile His Lys Asp Glu Thr As - #p Leu Leu Phe Thr Asp# 13601350 - # 1355- Gln His Asn Ile Cys Leu Lys Leu Ser Gly Gl - #n Phe Met Lys Glu Gly# 13750- Asn Thr Gln Ile Lys Glu Asp Leu Ser Asp Le - #u Thr Phe Leu Glu Val# 13905- Ala Lys Ala Gln Glu Ala Cys His Gly Asn Th - #r Ser Asn Lys Glu Gln# 14050- Leu Thr Ala Thr Lys Thr Glu Gln Asn Ile Ly - #s Asp Phe Glu Thr Ser# 14205- Asp Thr Phe Phe Gln Thr Ala Ser Gly Lys As - #n Ile Ser Val Ala Lys# 14401430 - # 1435- Glu Leu Phe Asn Lys Ile Val Asn Phe Phe As - #p Gln Lys Pro Glu Glu# 14550- Leu His Asn Phe Ser Leu Asn Ser Glu Leu Hi - #s Ser Asp Ile Arg Lys# 14705- Asn Lys Met Asp Ile Leu Ser Tyr Glu Glu Th - #r Asp Ile Val Lys His# 14850- Lys Ile Leu Lys Glu Ser Val Pro Val Gly Th - #r Gly Asn Gln Leu Val# 15005- Thr Phe Gln Gly Gln Pro Glu Arg Asp Glu Ly - #s Ile Lys Glu Pro Thr# 15201510 - # 1515- Leu Leu Gly Phe His Thr Ala Ser Gly Lys Ly - #s Val Lys Ile Ala Lys# 15350- Glu Ser Leu Asp Lys Val Lys Asn Leu Phe As - #p Glu Lys Glu Gln Gly# 15505- Thr Ser Glu Ile Thr Ser Phe Ser His Gln Tr - #p Ala Lys Thr Leu Lys# 15650- Tyr Arg Glu Ala Cys Lys Asp Leu Glu Leu Al - #a Cys Glu Thr Ile Glu# 15805- Ile Thr Ala Ala Pro Lys Cys Lys Glu Met Gl - #n Asn Ser Leu Asn Asn# 16001590 - # 1595- Asp Lys Asn Leu Val Ser Ile Glu Thr Val Va - #l Pro Pro Lys Leu Leu# 16150- Ser Asp Asn Leu Cys Arg Gln Thr Glu Asn Le - #u Lys Thr Ser Lys Ser# 16305- Ile Phe Leu Lys Val Lys Val His Glu Asn Va - #l Glu Lys Glu Thr Ala# 16450- Lys Ser Pro Ala Thr Cys Tyr Thr Asn Gln Se - #r Pro Tyr Ser Val Ile# 16605- Glu Asn Ser Ala Leu Ala Phe Tyr Thr Ser Cy - #s Ser Arg Lys Thr Ser# 16801670 - # 1675- Val Ser Gln Thr Ser Leu Leu Glu Ala Lys Ly - #s Trp Leu Arg Glu Gly# 16950- Ile Phe Asp Gly Gln Pro Glu Arg Ile Asn Th - #r Ala Asp Tyr Val Gly# 17105- Asn Tyr Leu Tyr Glu Asn Asn Ser Asn Ser Th - #r Ile Ala Glu Asn Asp# 17250- Lys Asn His Leu Ser Glu Lys Gln Asp Thr Ty - #r Leu Ser Asn Ser Ser# 17405- Met Ser Asn Ser Tyr Ser Tyr His Ser Asp Gl - #u Val Tyr Asn Asp Ser# 17601750 - # 1755- Gly Tyr Leu Ser Lys Asn Lys Leu Asp Ser Gl - #y Ile Glu Pro Val Leu# 17750- Lys Asn Val Glu Asp Gln Lys Asn Thr Ser Ph - #e Ser Lys Val Ile Ser# 17905- Asn Val Lys Asp Ala Asn Ala Tyr Pro Gln Th - #r Val Asn Glu Asp Ile# 18050- Cys Val Glu Glu Leu Val Thr Ser Ser Ser Pr - #o Cys Lys Asn Lys Asn# 18205- Ala Ala Ile Lys Leu Ser Ile Ser Asn Ser As - #n Asn Phe Glu Val Gly# 18401830 - # 1835- Pro Pro Ala Phe Arg Ile Ala Ser Gly Lys Il - #e Arg Leu Cys Ser His# 18550- Glu Thr Ile Lys Lys Val Lys Asp Ile Phe Th - #r Asp Ser Phe Ser Lys# 18705- Val Ile Lys Glu Asn Asn Glu Asn Lys Ser Ly - #s Ile Cys Gln Thr Lys# 18850- Ile Met Ala Gly Cys Tyr Glu Ala Leu Asp As - #p Ser Glu Asp Ile Leu# 19005- His Asn Ser Leu Asp Asn Asp Glu Cys Ser Me - #t His Ser His Lys Val# 19201910 - # 1915- Phe Ala Asp Ile Gln Ser Glu Glu Ile Leu Gl - #n His Asn Gln Asn Met# 19350- Ser Gly Leu Glu Lys Val Ser Lys Ile Ser Pr - #o Cys Asp Val Ser Leu# 19505- Glu Thr Ser Asp Ile Cys Lys Cys Ser Ile Gl - #y Lys Leu His Lys Ser# 19650- Val Ser Ser Ala Asn Thr Cys Gly Ile Phe Se - #r Thr Ala Ser Gly Lys# 19805- Ser Val Gln Val Ser Asp Ala Ser Leu Gln As - #n Ala Arg Gln Val Phe# 20001990 - # 1995- Ser Glu Ile Glu Asp Ser Thr Lys Gln Val Ph - #e Ser Lys Val Leu Phe# 20150- Lys Ser Asn Glu His Ser Asp Gln Leu Thr Ar - #g Glu Glu Asn Thr Ala# 20305- Ile Arg Thr Pro Glu His Leu Ile Ser Gln Ly - #s Gly Phe Ser Tyr Asn# 20450- Val Val Asn Ser Ser Ala Phe Ser Gly Phe Se - #r Thr Ala Ser Gly Lys# 20605- Gln Val Ser Ile Leu Glu Ser Ser Leu His Ly - #s Val Lys Gly Val Leu# 20802070 - # 2075- Glu Glu Phe Asp Leu Ile Arg Thr Glu His Se - #r Leu His Tyr Ser Pro# 20950- Thr Ser Arg Gln Asn Val Ser Lys Ile Leu Pr - #o Arg Val Asp Lys Arg# 21105- Asn Pro Glu His Cys Val Asn Ser Glu Met Gl - #u Lys Thr Cys Ser Lys# 21250- Glu Phe Lys Leu Ser Asn Asn Leu Asn Val Gl - #u Gly Gly Ser Ser Glu# 21405- Asn Asn His Ser Ile Lys Val Ser Pro Tyr Le - #u Ser Gln Phe Gln Gln# 21602150 - # 2155- Asp Lys Gln Gln Leu Val Leu Gly Thr Lys Va - #l Ser Leu Val Glu Asn# 21750- Ile His Val Leu Gly Lys Glu Gln Ala Ser Pr - #o Lys Asn Val Lys Met# 21905- Glu Ile Gly Lys Thr Glu Thr Phe Ser Asp Va - #l Pro Val Lys Thr Asn# 22050- Ile Glu Val Cys Ser Thr Tyr Ser Lys Asp Se - #r Glu Asn Tyr Phe Glu# 22205- Thr Glu Ala Val Glu Ile Ala Lys Ala Phe Me - #t Glu Asp Asp Glu Leu# 22402230 - # 2235- Thr Asp Ser Lys Leu Pro Ser His Ala Thr Hi - #s Ser Leu Phe Thr Cys# 22550- Pro Glu Asn Glu Glu Met Val Leu Ser Asn Se - #r Arg Ile Gly Lys Arg# 22705- Arg Gly Glu Pro Leu Ile Leu Val Gly Glu Pr - #o Ser Ile Lys Arg Asn# 22850- Leu Leu Asn Glu Phe Asp Arg Ile Ile Glu As - #n Gln Glu Lys Ser Leu# 23005- Lys Ala Ser Lys Ser Thr Pro Asp Gly Thr Il - #e Lys Asp Arg Arg Leu# 23202310 - # 2315- Phe Met His His Val Ser Leu Glu Pro Ile Th - #r Cys Val Pro Phe Arg# 23350- Thr Thr Lys Glu Arg Gln Glu Ile Gln Asn Pr - #o Asn Phe Thr Ala Pro# 23505- Gly Gln Glu Phe Leu Ser Lys Ser His Leu Ty - #r Glu His Leu Thr Leu# 23650- Glu Lys Ser Ser Ser Asn Leu Ala Val Ser Gl - #y His Pro Phe Tyr Gln# 23805- Val Ser Ala Thr Arg Asn Glu Lys Met Arg Hi - #s Leu Ile Thr Thr Gly# 24002390 - # 2395- Arg Pro Thr Lys Val Phe Val Pro Pro Phe Ly - #s Thr Lys Ser His Phe# 24150- His Arg Val Glu Gln Cys Val Arg Asn Ile As - #n Leu Glu Glu Asn Arg# 24305- Gln Lys Gln Asn Ile Asp Gly His Gly Ser As - #p Asp Ser Lys Asn Lys# 24450- Ile Asn Asp Asn Glu Ile His Gln Phe Asn Ly - #s Asn Asn Ser Asn Gln# 24605- Ala Ala Ala Val Thr Phe Thr Lys Cys Glu Gl - #u Glu Pro Leu Asp Leu# 24802470 - # 2475- Ile Thr Ser Leu Gln Asn Ala Arg Asp Ile Gl - #n Asp Met Arg Ile Lys# 24950- Lys Lys Gln Arg Gln Arg Val Phe Pro Gln Pr - #o Gly Ser Leu Tyr Leu# 25105- Ala Lys Thr Ser Thr Leu Pro Arg Ile Ser Le - #u Lys Ala Ala Val Gly# 25250- Gly Gln Val Pro Ser Ala Cys Ser His Lys Gl - #n Leu Tyr Thr Tyr Gly# 25405- Val Ser Lys His Cys Ile Lys Ile Asn Ser Ly - #s Asn Ala Glu Ser Phe# 25602550 - # 2555- Gln Phe His Thr Glu Asp Tyr Phe Gly Lys Gl - #u Ser Leu Trp Thr Gly# 25750- Lys Gly Ile Gln Leu Ala Asp Gly Gly Trp Le - #u Ile Pro Ser Asn Asp# 25905- Gly Lys Ala Gly Lys Glu Glu Phe Tyr Arg Al - #a Leu Cys Asp Thr Pro# 26050- Gly Val Asp Pro Lys Leu Ile Ser Arg Ile Tr - #p Val Tyr Asn His Tyr# 26205- Arg Trp Ile Ile Trp Lys Leu Ala Ala Met Gl - #u Cys Ala Phe Pro Lys# 26402630 - # 2635- Glu Phe Ala Asn Arg Cys Leu Ser Pro Glu Ar - #g Val Leu Leu Gln Leu# 26550- Lys Tyr Arg Tyr Asp Thr Glu Ile Asp Arg Se - #r Arg Arg Ser Ala Ile# 26705- Lys Lys Ile Met Glu Arg Asp Asp Thr Ala Al - #a Lys Thr Leu Val Leu# 26850- Cys Val Ser Asp Ile Ile Ser Leu Ser Ala As - #n Ile Ser Glu Thr Ser# 27005- Ser Asn Lys Thr Ser Ser Ala Asp Thr Gln Ly - #s Val Ala Ile Ile Glu# 27202710 - # 2715- Leu Thr Asp Gly Trp Tyr Ala Val Lys Ala Gl - #n Leu Asp Pro Pro Leu# 27350- Leu Ala Val Leu Lys Asn Gly Arg Leu Thr Va - #l Gly Gln Lys Ile Ile# 27505- Leu His Gly Ala Glu Leu Val Gly Ser Pro As - #p Ala Cys Thr Pro Leu# 27650- Glu Ala Pro Glu Ser Leu Met Leu Lys Ile Se - #r Ala Asn Ser Thr Arg# 27805- Pro Ala Arg Trp Tyr Thr Lys Leu Gly Phe Ph - #e Pro Asp Pro Arg Pro# 28002790 - # 2795- Phe Pro Leu Pro Leu Ser Ser Leu Phe Ser As - #p Gly Gly Asn Val Gly# 28150- Cys Val Asp Val Ile Ile Gln Arg Ala Tyr Pr - #o Ile Gln Arg Met Glu# 28305- Lys Thr Ser Ser Gly Leu Tyr Ile Phe Arg As - #n Glu Arg Glu Glu Glu# 28450- Lys Glu Ala Ala Lys Tyr Val Glu Ala Gln Gl - #n Lys Arg Leu Glu Ala# 28605- Leu Phe Thr Lys Ile Gln Glu Glu Phe Glu Gl - #u His Glu Glu Asn Thr# 28802870 - # 2875- Thr Lys Pro Tyr Leu Pro Ser Arg Ala Leu Th - #r Arg Gln Gln Val Arg# 28950- Ala Leu Gln Asp Gly Ala Glu Leu Tyr Glu Al - #a Val Lys Asn Ala Ala# 29105- Asp Pro Ala Tyr Leu Glu Gly Tyr Phe Ser Gl - #u Glu Gln Leu Arg Ala# 29250- Leu Asn Asn His Arg Gln Met Leu Asn Asp Ly - #s Lys Gln Ala Gln Ile# 29405- Gln Leu Glu Ile Arg Lys Ala Met Glu Ser Al - #a Glu Gln Lys Glu Gln# 29602950 - # 2955- Gly Leu Ser Arg Asp Val Thr Thr Val Trp Ly - #s Leu Arg Ile Val Ser# 29750- Tyr Ser Lys Lys Glu Lys Asp Ser Val Ile Le - #u Ser Ile Trp Arg Pro# 29905- Ser Ser Asp Leu Tyr Ser Leu Leu Thr Glu Gl - #y Lys Arg Tyr Arg Ile# 30050- Tyr His Leu Ala Thr Ser Lys Ser Lys Ser Ly - #s Ser Glu Arg Ala Asn# 30205- Ile Gln Leu Ala Ala Thr Lys Lys Thr Gln Ty - #r Gln Gln Leu Pro Val# 30403030 - # 3035- Ser Asp Glu Ile Leu Phe Gln Ile Tyr Gln Pr - #o Arg Glu Pro Leu His# 30550- Phe Ser Lys Phe Leu Asp Pro Asp Phe Gln Pr - #o Ser Cys Ser Glu Val# 30705- Asp Leu Ile Gly Phe Val Val Ser Val Val Ly - #s Lys Thr Gly Leu Ala# 30850- Pro Phe Val Tyr Leu Ser Asp Glu Cys Tyr As - #n Leu Leu Ala Ile Lys# 31005- Phe Trp Ile Asp Leu Asn Glu Asp Ile Ile Ly - #s Pro His Met Leu Ile# 31203110 - # 3115- Ala Ala Ser Asn Leu Gln Trp Arg Pro Glu Se - #r Lys Ser Gly Leu Leu# 31350- Thr Leu Phe Ala Gly Asp Phe Ser Val Phe Se - #r Ala Ser Pro Lys Glu# 31505- Gly His Phe Gln Glu Thr Phe Asn Lys Met Ly - #s Asn Thr Val Glu Asn# 31650- Ile Asp Ile Leu Cys Asn Glu Ala Glu Asn Ly - #s Leu Met His Ile Leu# 31805- His Ala Asn Asp Pro Lys Trp Ser Thr Pro Th - #r Lys Asp Cys Thr Ser# 32003190 - # 3195- Gly Pro Tyr Thr Ala Gln Ile Ile Pro Gly Th - #r Gly Asn Lys Leu Leu# 32150- Met Ser Ser Pro Asn Cys Glu Ile Tyr Tyr Gl - #n Ser Pro Leu Ser Leu# 32305- Cys Met Ala Lys Arg Lys Ser Val Ser Thr Pr - #o Val Ser Ala Gln Met# 32450- Thr Ser Lys Ser Cys Lys Gly Glu Lys Glu Il - #e Asp Asp Gln Lys Asn# 32605- Cys Lys Lys Arg Arg Ala Leu Asp Phe Leu Se - #r Arg Leu Pro Leu Pro# 32803270 - # 3275- Pro Pro Val Ser Pro Ile Cys Thr Phe Val Se - #r Pro Ala Ala Gln Lys# 32950- Ala Phe Gln Pro Pro Arg Ser Cys Gly Thr Ly - #s Tyr Glu Thr Pro Ile# 33105- Lys Lys Lys Glu Leu Asn Ser Pro Gln Met Th - #r Pro Phe Lys Lys Phe# 33250- Asn Glu Ile Ser Leu Leu Glu Ser Asn Ser Il - #e Ala Asp Glu Glu Leu# 33405- Ala Leu Ile Asn Thr Gln Ala Leu Leu Ser Gl - #y Ser Thr Gly Glu Lys# 33603350 - # 3355- Gln Phe Ile Ser Val Ser Glu Ser Thr Arg Th - #r Ala Pro Thr Ser Ser# 33750- Glu Asp Tyr Leu Arg Leu Lys Arg Arg Cys Th - #r Thr Ser Leu Ile Lys# 33905- Glu Gln Glu Ser Ser Gln Ala Ser Thr Glu Gl - #u Cys Glu Lys Asn Lys# 34050- Gln Asp Thr Ile Thr Thr Lys Lys Tyr Ile# 34150- (2) INFORMATION FOR SEQ ID NO:5:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH:19 (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Homo sapi - #ens sapiens (C) INDIVIDUAL ISOLATE:#adult (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: female - # breast (G) CELL TYPE: norm - #al breast tissue (H) CELL LINE: HMEC (I) ORGANELLE: no- (ix) FEATURE: (A) NAME/KEY: BRCA1 C-1 - #9 antigen#1863 (B) LOCATION: 1845 to (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:5- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #5:- Tyr Gln Cys Gln Glu Leu Asp Thr Tyr Leu Il - #e Pro Gln Ile Pro His# 15- Ser His Tyr- (2) INFORMATION FOR SEQ ID NO:6:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 20 (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Homo sapi - #ens sapiens (C) INDIVIDUAL ISOLATE:#adult (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: female - # breast (G) CELL TYPE: norm - #al breast tissue (H) CELL LINE: HMEC (I) ORGANELLE: no- (ix) FEATURE: (A) NAME/KEY: BRCA1 C-2 - #0 antigen#1863 (B) LOCATION: 1844 to (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:6- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #6:- Leu Tyr Gln Cys Gln Glu Leu Asp Thr Tyr Le - #u Ile Pro Gln Ile Pro# 15- His Ser His Tyr20- (2) INFORMATION FOR SEQ ID NO:7:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 20 (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Homo sapi - #ens sapiens (C) INDIVIDUAL ISOLATE:#adult (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: female - # breast (G) CELL TYPE: norm - #al breast tissue (H) CELL LINE: HMEC (I) ORGANELLE: no- (ix) FEATURE: (A) NAME/KEY: BRCA1 D-2 - #0 antigen (B) LOCATION: 1 to 2 - #0 (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:7- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #7:- Met Asp Leu Ser Ala Leu Arg Val Glu Glu Va - #l Gln Asn Val Ile Asn# 15- Ala Met Gln Lys20- (2) INFORMATION FOR SEQ ID NO:8:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL:- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: Granin Co - #nsensus Sequence (B) LOCATION: (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:8:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #8:- Glu Asn Leu Ser Xaa Xaa Asp Xaa Glu Leu# 10- (2) INFORMATION FOR SEQ ID NO:9:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Human (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: BRCA1 Gra - #nin Sequence (B) LOCATION: amino aci - #ds 1214-1223 of BRCA1 protein (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:9:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #9:- Glu Asn Leu Ser Ser Glu Asp Glu Glu Leu# 10- (2) INFORMATION FOR SEQ ID NO:10:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Rhesus (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: BRCA1 Gra - #nin Sequence (B) LOCATION: (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:10:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #10:- Glu Asn Leu Ser Ser Glu Asp Glu Glu Leu# 10- (2) INFORMATION FOR SEQ ID NO:11:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Mouse (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: BRCA1 Gra - #nin Sequence (B) LOCATION: (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:11:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #11:- Glu Ser Asp Ser Thr Glu Asp Glu Asp Leu# 10- (2) INFORMATION FOR SEQ ID NO:12:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Human (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: BRCA2 Gra - #nin Sequence (B) LOCATION: amino aci - #ds 3334-3344 of BRCA2 protein (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:12:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #12:- Glu Ser Asn Ser Ile Ala Asp Glu Glu Leu# 105- (2) INFORMATION FOR SEQ ID NO:13:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Human (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: Chromogranin - # A Granin Sequence (B) LOCATION: (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:13:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #13:- Glu Ser Leu Ser Ala Ile Glu Ala Glu Leu# 10- (2) INFORMATION FOR SEQ ID NO:14:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Bovine (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: Chromogranin - # A Granin Sequence (B) LOCATION: (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:14:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #14:- Glu Ser Leu Ser Ala Ile Glu Ala Glu Leu# 10- (2) INFORMATION FOR SEQ ID NO:15:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Rat (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: Chromogranin - # A Granin Sequence (B) LOCATION: (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:15:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #15:- Glu Ser Leu Ser Ala Ile Glu Ala Glu Leu# 10- (2) INFORMATION FOR SEQ ID NO:16:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Pig (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: Chromogranin - # A Granin Sequence (B) LOCATION: (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:16:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #16:- Glu Ser Leu Ser Ala Ile Glu Ala Glu Leu# 10- (2) INFORMATION FOR SEQ ID NO:17:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Human (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: Chromogranin - # B Granin Sequence (B) LOCATION: (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:17:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #17:- Glu Asn Leu Ala Ala Met Asp Leu Glu Leu# 10- (2) INFORMATION FOR SEQ ID NO:18:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Bovine (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: Chromogranin - # B Granin Sequence (B) LOCATION: (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:18:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #18:- Glu Asn Leu Ala Ala Met Asp Leu Glu Leu# 10- (2) INFORMATION FOR SEQ ID NO:19:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Mouse (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: Chromogranin - # B Granin Sequence (B) LOCATION: (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:19:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #19:- Glu Asn Leu Ala Ala Met Asp Leu Glu Leu# 10- (2) INFORMATION FOR SEQ ID NO:20:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Human (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: Secretograni - #n II Granin Sequence (B) LOCATION: (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:20:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #20:- Glu Asn Leu Asn Asp Lys Asp Gln Glu Leu# 10- (2) INFORMATION FOR SEQ ID NO:21:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Bovine (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: Secretograni - #n II Granin Sequence (B) LOCATION: (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:21:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #21:- Glu Asn Leu Asn Asp Lys Asp Gln Glu Leu# 10- (2) INFORMATION FOR SEQ ID NO:22:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Rat (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: Secretograni - #n II Granin Sequence (B) LOCATION: (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:22:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #22:- Asp Asn Leu Asn Asp Lys Asp Gln Glu Leu# 10- (2) INFORMATION FOR SEQ ID NO:23:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Mouse (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: Secretograni - #n II Granin Sequence (B) LOCATION: (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:23:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #23:- Glu Asn Leu Asn Xaa Xaa Asp Gln Glu Leu# 10- (2) INFORMATION FOR SEQ ID NO:24:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino aci - #d (C) STRANDEDNESS: sing - #le (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Rat (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: Secretograni - #n III Granin Sequence (B) LOCATION: (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:24:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #24:- Glu Asn Leu Asp Glu Thr Ile Ala Leu Gln# 10- (2) INFORMATION FOR SEQ ID NO:25:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino aci - #d (C) STRANDEDNESS: sing - #le (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Mouse (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: Secretograni - #n III Granin Sequence (B) LOCATION: (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:25:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #25:- Glu Asn Leu Asp Glu Thr Ile Ala Leu Gln# 10- (2) INFORMATION FOR SEQ ID NO:26:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino aci - #d (C) STRANDEDNESS: sing - #le (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Human (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: Secretograni - #n V Granin Sequence (B) LOCATION: (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:26:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #26:- Gly Asn Ile Pro Asn Ile Val Ala Glu Leu# 10- (2) INFORMATION FOR SEQ ID NO:27:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino aci - #d (C) STRANDEDNESS: sing - #le (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Pig (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: Secretograni - #n V Granin Sequence (B) LOCATION: (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:27:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #27:- Gly Asn Ile Pro Asn Ile Val Ala Glu Leu# 10- (2) INFORMATION FOR SEQ ID NO:28:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino aci - #d (C) STRANDEDNESS: sing - #le (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Rat (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: Secretograni - #n V Granin Sequence (B) LOCATION: (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:28:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #28:- Gly Asn Ile Pro Asn Ile Val Ala Glu Leu# 10- (2) INFORMATION FOR SEQ ID NO:29:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 (B) TYPE: amino aci - #d (C) STRANDEDNESS: sing - #le (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (iii) HYPOTHETICAL: no- (iv) ANTI-SENSE: no- (v) ORIGINAL SOURCE: (A) ORGANISM: Xenopus (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (F) TISSUE TYPE: (G) CELL TYPE: (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: Secretograni - #n V Granin Sequence (B) LOCATION: (C) IDENTIFICATION METHOD: (D) OTHER INFORMATION:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) PAGES: (F) DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO:29:- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #29:- Gly Asn Ile Pro Asn Ile Val Ala Glu Leu# 10__________________________________________________________________________
Thus, although there have been described particular embodiments of the present invention of a new and useful Characterized BRCA1 and BRCA2 Proteins and Screening and Therapeutic Methods Based on Characterized BRCA1 and BRCA2 Proteins, it is not intended that such references be construed as limitations upon the scope of this invention except as set forth in the following claims. Further, although there have been described certain examples used in the preferred embodiment, it is not intended that such examples be construed as limitations upon the scope of this invention except as set forth in the following claims.

Number	Name	Date
4675285	Clark et al.	Jun 1987
5399346	Anderson et al.	Mar 1995
5434064	Schlessinger et al.	Jul 1995
5654155	Murphy et al.	Aug 1997
5891857	Holt et al.	Apr 1999

Number	Date	Country
0699754A1	Mar 1996	EPX
0705903A1	Apr 1996	EPX
0705902A1	Apr 1996	EPX
9519369	Jul 1995	WOX
9525813	Sep 1995	WOX
9525429	Sep 1995	WOX
9605307	Feb 1996	WOX
9605308	Feb 1996	WOX
9605306	Feb 1996	WOX
9729213	Aug 1997	WOX
97301308	Aug 1997	WOX

Characterized BRCA1 and BRCA2 proteins and screening and therapeutic methods based on characterized BRCA1 and BRCA2 proteins

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US Referenced Citations (5)

Foreign Referenced Citations (11)

Non-Patent Literature Citations (57)

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Entry
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