Regulation of DNA Damage Responses by Ubiquitin and SUMO

被引:482
作者
Jackson, Stephen P. [1 ,2 ]
Durocher, Daniel [3 ,4 ]
机构
[1] Univ Cambridge, Gurdon Inst, Cambridge CB2 1QN, England
[2] Univ Cambridge, Dept Biochem, Cambridge CB2 1QN, England
[3] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
[4] Univ Toronto, Dept Med Genet, Toronto, ON M5S 1A8, Canada
基金
欧洲研究理事会; 英国惠康基金;
关键词
RNA-POLYMERASE-II; FANCONI-ANEMIA PATHWAY; DOUBLE-STRAND BREAKS; CROSS-LINK REPAIR; E3; LIGASE; HOMOLOGOUS RECOMBINATION; HISTONE UBIQUITINATION; INDUCED UBIQUITYLATION; SELECTIVE SEGREGASE; 53BP1; RECRUITMENT;
D O I
10.1016/j.molcel.2013.01.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ubiquitylation and sumoylation, the covalent attachment of the polypeptides ubiquitin and SUMO, respectively, to target proteins, are pervasive mechanisms for controlling cellular functions. Here, we summarize the key steps and enzymes involved in ubiquitin and SUMO conjugation and provide an overview of how they are crucial for maintaining genome stability. Specifically, we review research that has revealed how ubiquitylation and sumoylation regulate and coordinate various pathways of DNA damage recognition, signaling, and repair at the biochemical, cellular, and whole-organism levels. In addition to providing key insights into the control and importance of DNA repair and associated processes, such work has established paradigms for regulatory control that are likely to extend to other cellular processes and that may provide opportunities for better understanding and treatment of human disease.
引用
收藏
页码:795 / 807
页数:13
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