Distinct functions of BRCA1 and BRCA2 in double-strand break repair
被引:81
作者:
Liu, YL
论文数: 0引用数: 0
h-index: 0
机构:
Imperial Canc Res Fund, Clare Hall Labs, Potters Bar EN6 3LD, Herts, EnglandImperial Canc Res Fund, Clare Hall Labs, Potters Bar EN6 3LD, Herts, England
Liu, YL
[1
]
West, SC
论文数: 0引用数: 0
h-index: 0
机构:
Imperial Canc Res Fund, Clare Hall Labs, Potters Bar EN6 3LD, Herts, EnglandImperial Canc Res Fund, Clare Hall Labs, Potters Bar EN6 3LD, Herts, England
West, SC
[1
]
机构:
[1] Imperial Canc Res Fund, Clare Hall Labs, Potters Bar EN6 3LD, Herts, England
BRCA1;
BRCA2;
DNA repair;
homologous recombination;
RAD51;
D O I:
10.1186/bcr417
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Individuals carrying BRCA mutations are predisposed to breast cancer. The BRCA1 and BRCA2 proteins are required for homologous recombination and DNA break repair, leading to the suggestion that they act in concert. However, direct evidence of a stable BRCA1/BRCA2 complex has not been demonstrated. Rather, the two proteins have been found as constituents of discrete, but perhaps nonexclusive complexes that are critical for repair. We discuss the interaction of BRCA1 with the BACH1 and BARD1 proteins, and suggest that the pleiotropic nature of mutations in BRCA1 may be associated with defects in protein-protein interactions In contrast, the role of BRCA2 in DNA repair may be more defined by its direct interaction with the RAD51 recombinase.