ISWI chromatin remodeling complexes in the DNA damage response

被引:106
作者
Aydin, Ozge Z. [1 ]
Vermeulen, Wim [1 ]
Lans, Hannes [1 ]
机构
[1] Erasmus MC, Dept Genet, Rotterdam, Netherlands
基金
欧洲研究理事会;
关键词
ATP-dependent chromatin remodeling; ISWI; SMARCA5; SNF2H; WSTF; ACF1; Homologous Recombination; Non-Homologous End-Joining; Nucleotide Excision Repair; DNA damage response; ATP-utilizing Chromatin assembly and remodeling Factor 1; BER; Base Excision Repair; DDR; DNA Damage Response; DSB; Double Strand Break; GG-NER; Global Genome Nucleotide Excision Repair; HR; Imitation SWItch; MRN; MRE11; Rad50; NBS1; NER; NHEJ; Non-Homologous End Joining; PAR; Poly(ADP-Ribose); RNApolII; RNA Polymerase II; RSF1; Remodeling and Spacing Factor 1; SMARCA; SWI-SNF-related Matrix-associated Actin-dependent Regulator of Chromatin A; TC-NER; Transcription-Coupled Nucleotide Excision Repair; Williams Syndrome Transcription Factor; NUCLEOTIDE EXCISION-REPAIR; DOUBLE-STRAND BREAKS; CONCERTED ACTION; HISTONE H2A.X; ATPASE DOMAIN; UV LESIONS; NUCLEOSOME; BASE; PROTEIN; PROMOTES;
D O I
10.4161/15384101.2014.956551
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Regulation of chromatin structure is an essential component of the DNA damage response (DDR), which effectively preserves the integrity of DNA by a network of multiple DNA repair and associated signaling pathways. Within the DDR, chromatin is modified and remodeled to facilitate efficient DNA access, to control the activity of repair proteins and to mediate signaling. The mammalian ISWI family has recently emerged as one of the major ATP-dependent chromatin remodeling complex families that function in the DDR, as it is implicated in at least 3 major DNA repair pathways: homologous recombination, non-homologous end-joining and nucleotide excision repair. In this review, we discuss the various manners through which different ISWI complexes regulate DNA repair and how they are targeted to chromatin containing damaged DNA.
引用
收藏
页码:3016 / 3025
页数:10
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