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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
来源:
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.
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页数:9
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