DNA Double Strand Break Repair and Its Control by Nucleosome Remodeling

被引:23
|
作者
Karl, Leonhard Andreas [1 ]
Peritore, Martina [1 ]
Galanti, Lorenzo [1 ]
Pfander, Boris [1 ]
机构
[1] Max Planck Inst Biochem, Res Grp DNA Replicat & Genome Integr, Martinsried, Germany
关键词
nucleosome remodeling; double strand break; DNA repair; DNA end resection; cell cycle; genome stability; DEPENDENT CHROMATIN REMODELERS; HISTONE H2A PHOSPHORYLATION; PROTEIN; 4; CHD4; END-RESECTION; HOMOLOGOUS RECOMBINATION; PROMOTES RESECTION; STRUCTURAL BASIS; CHECKPOINT ACTIVATION; DAMAGED CHROMATIN; NUCLEASE COMPLEX;
D O I
10.3389/fgene.2021.821543
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
DNA double strand breaks (DSBs) are repaired in eukaryotes by one of several cellular mechanisms. The decision-making process controlling DSB repair takes place at the step of DNA end resection, the nucleolytic processing of DNA ends, which generates single-stranded DNA overhangs. Dependent on the length of the overhang, a corresponding DSB repair mechanism is engaged. Interestingly, nucleosomes-the fundamental unit of chromatin-influence the activity of resection nucleases and nucleosome remodelers have emerged as key regulators of DSB repair. Nucleosome remodelers share a common enzymatic mechanism, but for global genome organization specific remodelers have been shown to exert distinct activities. Specifically, different remodelers have been found to slide and evict, position or edit nucleosomes. It is an open question whether the same remodelers exert the same function also in the context of DSBs. Here, we will review recent advances in our understanding of nucleosome remodelers at DSBs: to what extent nucleosome sliding, eviction, positioning and editing can be observed at DSBs and how these activities affect the DSB repair decision.
引用
收藏
页数:15
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