Functional Analysis of Breast Cancer Susceptibility Gene BRCA2

Abstract

Two monoclonal antibodies against different regions of BRCA2 (mAb B 1 and mAb B3) were characterized. Both of them specifically recognized wild type BRCA2, and mAb B 1 can also specifically recognize C-terminal truncated BRCA2 protein in Capan-1 cell. I detected the interaction between BRCA2 and 3 Rad51-related proteins which are involved in DNA repair and demonstrated that BRCA2 coexists in biochemical complex with hsDMC1, a human meiosis- specific RecA homologue, but not with XRCC2, Rad51D or the replication Protein (RPA). The specific interaction of BRCA2 and hsDMCl suggests that BRCA2 may be involved in DNA recombination and repair both in germ and somatic cells. I have involved in a new BRCA2 associated protein, BRAF35, and demonstrated that: 1) it is a nuclear protein. 2) it interacts specifically with BRCA2 in mammalian cells. Turns of the functional relationship between BRCA2 and BRAF35 is under investigation.

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Document Details

Document Type
Technical Report
Publication Date
Aug 01, 1999
Accession Number
ADA386437

Entities

People

  • Stuart Aaronson
  • Yingcai Wang

Organizations

  • Icahn School of Medicine at Mount Sinai

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • Biomedical Research
  • Breast Cancer
  • Carrier Proteins
  • Cell Line
  • Cells
  • Functional Analysis
  • Genetic Code
  • Genetic Structures
  • Laboratory Animals
  • Materials
  • Molecules
  • Neoplasms
  • New York
  • Proteins
  • Recombinant Dna
  • Terminals
  • Tissue Extracts

Fields of Study

  • Biology

Readers

  • Immunology
  • Molecular Genetics
  • Molecular and genetic basis of cancer.

Technology Areas

  • Biotechnology
  • Biotechnology - Cancer Biotech