Gurdon Institute and Department of Biochemistry, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK.
Science. 2010 Sep 10;329(5997):1348-53. doi: 10.1126/science.1192049.
SIRT6 belongs to the sirtuin family of protein lysine deacetylases, which regulate aging and genome stability. We found that human SIRT6 has a role in promoting DNA end resection, a crucial step in DNA double-strand break (DSB) repair by homologous recombination. SIRT6 depletion impaired the accumulation of replication protein A and single-stranded DNA at DNA damage sites, reduced rates of homologous recombination, and sensitized cells to DSB-inducing agents. We identified the DSB resection protein CtIP [C-terminal binding protein (CtBP) interacting protein] as a SIRT6 interaction partner and showed that SIRT6-dependent CtIP deacetylation promotes resection. A nonacetylatable CtIP mutant alleviated the effect of SIRT6 depletion on resection, thus identifying CtIP as a key substrate by which SIRT6 facilitates DSB processing and homologous recombination. These findings further clarify how SIRT6 promotes genome stability.
SIRT6 属于蛋白赖氨酸去乙酰化酶的 sirtuin 家族,该家族可调节衰老和基因组稳定性。我们发现人类 SIRT6 可促进 DNA 末端切除,这是同源重组修复 DNA 双链断裂(DSB)的关键步骤。SIRT6 缺失会削弱复制蛋白 A 和单链 DNA 在 DNA 损伤部位的积累,降低同源重组的速度,并使细胞对 DSB 诱导剂敏感。我们鉴定出 DSB 切除蛋白 CtIP(C 端结合蛋白(CtBP)相互作用蛋白)为 SIRT6 的相互作用伙伴,并表明 SIRT6 依赖性 CtIP 去乙酰化可促进切除。非乙酰化的 CtIP 突变体减轻了 SIRT6 缺失对切除的影响,从而鉴定出 CtIP 是 SIRT6 促进 DSB 加工和同源重组的关键底物。这些发现进一步阐明了 SIRT6 如何促进基因组稳定性。