Ubiquitylation in DNA double-strand break repair

被引:9
|
作者
Tang, Mengfan [1 ]
Li, Siting [1 ]
Chen, Junjie [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Expt Radiat Oncol, Houston, TX 77030 USA
关键词
Double strand break; DNA damage response; ubiquitylation; homologous recombination (HR); non-homologous end joining (NHEJ); DEPENDENT SIGNALING CASCADE; UBIQUITIN E3 LIGASE; HOMOLOGOUS-RECOMBINATION; DAMAGE RESPONSE; END RESECTION; POLY(ADP-RIBOSE) POLYMERASE; HISTONE UBIQUITYLATION; V(D)J RECOMBINATION; CELLULAR-RESPONSE; RAP80; INTERACTS;
D O I
10.1016/j.dnarep.2021.103129
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genome integrity is constantly challenged by various DNA lesions with DNA double-strand breaks (DSBs) as the most cytotoxic lesions. In order to faithfully repair DSBs, DNA damage response (DDR) signaling networks have evolved, which organize many multi-protein complexes to deal with the encountered DNA damage. Spatiotemporal dynamics of these protein complexes at DSBs are mainly modulated by post-translational modifications (PTMs). One of the most well-studied PTMs in DDR is ubiquitylation which can orchestrate cellular responses to DSBs, promote accurate DNA repair, and maintain genome integrity. Here, we summarize the recent advances of ubiquitin-dependent signaling in DDR and discuss how ubiquitylation crosstalks with other PTMs to control fundamental biological processes in DSB repair.
引用
收藏
页数:9
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