Yun Maximina H, Hiom Kevin
Division of Protein and Nucleic Acids Chemistry, MRC Laboratory of Molecular Biology, Cambridge, UK.
Biochem Soc Trans. 2009 Jun;37(Pt 3):597-604. doi: 10.1042/BST0370597.
Inheritance of a mutation in BRCA1 (breast cancer 1 early-onset) results in predisposition to early-onset breast and ovarian cancer. Tumours in these individuals arise after somatic mutation or loss of the wild-type allele. Loss of BRCA1 function leads to a profound increase in genomic instability involving the accumulation of mutations, DNA breaks and gross chromosomal rearrangements. Accordingly, BRCA1 has been implicated as an important factor involved in both the repair of DNA lesions and in the regulation of cell-cycle checkpoints in response to DNA damage. However, the molecular mechanism through which BRCA1 functions to preserve genome stability remains unclear. In the present article, we examine the different ways in which BRCA1 might influence the repair of DNA damage and the preservation of genome integrity, taking into account what is currently known about its interactions with other proteins, its biochemical activity and its nuclear localization.
BRCA1(乳腺癌1号,早发型)基因突变的遗传会导致早发型乳腺癌和卵巢癌的易感性。这些个体中的肿瘤是在体细胞突变或野生型等位基因缺失后发生的。BRCA1功能的丧失会导致基因组不稳定性显著增加,包括突变积累、DNA断裂和染色体大片段重排。因此,BRCA1被认为是参与DNA损伤修复和响应DNA损伤时细胞周期检查点调控的重要因素。然而,BRCA1发挥功能以维持基因组稳定性的分子机制仍不清楚。在本文中,我们考虑到目前已知的BRCA1与其他蛋白质的相互作用、其生化活性及其核定位,研究了BRCA1可能影响DNA损伤修复和基因组完整性维持的不同方式。