Ku80型
DNA损伤
细胞生物学
DNA修复
基因组不稳定性
生物
DNA修复蛋白XRCC4
肌动蛋白重塑
DNA
染色质
Ku70型
肌动蛋白细胞骨架
核苷酸切除修复
细胞骨架
遗传学
细胞
DNA结合蛋白
转录因子
基因
作者
Christi Andrin,Darin McDonald,Kathleen M. Attwood,Amélie Rodrigue,Sunita Ghosh,Razmik Mirzayans,Jean‐Yves Masson,Graham Dellaire,Michael J. Hendzel
出处
期刊:Nucleus
[Taylor & Francis]
日期:2012-07-01
卷期号:3 (4): 384-395
被引量:86
摘要
Nuclear actin is involved in several nuclear processes from chromatin remodeling to transcription. Here we examined the requirement for actin polymerization in DNA double-strand break repair. Double-strand breaks are considered the most dangerous type of DNA lesion. Double-strand break repair consists of a complex set of events that are tightly regulated. Failure at any step can have catastrophic consequences such as genomic instability, oncogenesis or cell death. Many proteins involved in this repair process have been identified and their roles characterized. We discovered that some DNA double-strand break repair factors are capable of associating with polymeric actin in vitro and specifically, that purified Ku70/80 interacts with polymerized actin under these conditions. We find that the disruption of polymeric actin inhibits DNA double strand break repair both in vitro and in vivo. Introduction of nuclear targeted mutant actin that cannot polymerize, or the depolymerization of endogenous actin filaments by the addition of cytochalasin D, alters the retention of Ku80 at sites of DNA damage in live cells. Our results suggest that polymeric actin is required for proper DNA double-strand break repair and may function through the stabilization of the Ku heterodimer at the DNA damage site.
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