Dynamics of DNA damage response proteins at DNA breaks: a focus on protein modifications

被引:860
作者
Polo, Sophie E. [1 ]
Jackson, Stephen P. [1 ]
机构
[1] Univ Cambridge, Dept Biochem, Gurdon Inst, Cambridge CB2 1QN, England
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
checkpoint; DNA breaks; DNA damage foci; post-translational modifications; repair; DOUBLE-STRAND BREAKS; CHROMATIN-REMODELING COMPLEXES; KINASE CATALYTIC SUBUNIT; HOMOLOGOUS RECOMBINATION REPAIR; HISTONE H2AX PHOSPHORYLATION; MAINTAINS GENOMIC STABILITY; FANCONI-ANEMIA PATHWAY; END-JOINING REPAIR; CROSS-LINK REPAIR; CELL-CYCLE;
D O I
10.1101/gad.2021311
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Genome integrity is constantly monitored by sophisticated cellular networks, collectively termed the DNA damage response (DDR). A common feature of DDR proteins is their mobilization in response to genotoxic stress. Here, we outline how the development of various complementary methodologies has provided valuable insights into the spatiotemporal dynamics of DDR protein assembly/disassembly at sites of DNA strand breaks in eukaryotic cells. Considerable advances have also been made in understanding the underlying molecular mechanisms for these events, with post-translational modifications of DDR factors being shown to play prominent roles in controlling the formation of foci in response to DNA-damaging agents. We review these regulatory mechanisms and discuss their biological significance to the DDR.
引用
收藏
页码:409 / 433
页数:25
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