Unraveling the mechanism of BRCA2 in homologous recombination

被引:165
作者
Holloman, William K. [1 ]
机构
[1] Weill Cornell Med Coll, Weill Cornell Canc Ctr, Dept Microbiol & Immunol, New York, NY USA
基金
美国国家卫生研究院;
关键词
CANCER SUSCEPTIBILITY GENE; STRAND-BREAK REPAIR; RAD51 FILAMENT FORMATION; D-LOOP FORMATION; DNA-REPAIR; USTILAGO-MAYDIS; RADIATION HYPERSENSITIVITY; IONIZING-RADIATION; VERTEBRATE CELLS; BRH2; PROTEIN;
D O I
10.1038/nsmb.2096
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
BRCA2 is the product of a breast cancer susceptibility gene in humans and the founding member of an emerging family of proteins present throughout the eukaryotic domain that serve in homologous recombination. The function of BRCA2 in recombination is to control RAD51, a protein that catalyzes homologous pairing and DNA strand exchange. By physically interacting with both RAD51 and single-stranded DNA, BRCA2 mediates delivery of RAD51 preferentially to sites of single-stranded DNA (ssDNA) exposed as a result of DNA damage or replication problems. Through its action, BRCA2 helps restore and maintain integrity of the genome. This review highlights recent studies on BRCA2 and its orthologs that have begun to illuminate the molecular mechanisms by which these proteins control homologous recombination.
引用
收藏
页码:748 / 754
页数:7
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