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The nucleosome: orchestrating DNA damage signaling and repair within chromatin
被引:24
|作者:
Agarwal, Poonam
[1
]
Miller, Kyle M.
[1
]
机构:
[1] Univ Texas Austin, Inst Cellular & Mol Biol, Dept Mol Biosci, 2506 Speedway Stop A5000, Austin, TX 78712 USA
关键词:
DNA double-strand break repair;
DNA damage response;
nucleosome acidic patch;
chromatin;
histone modifications;
DOUBLE-STRAND BREAKS;
PROMOTES HOMOLOGOUS RECOMBINATION;
HISTONE H2AX;
CRYSTAL-STRUCTURE;
CORE PARTICLE;
GENOMIC INSTABILITY;
H4-K16;
ACETYLATION;
STRUCTURAL BASIS;
REMOVES H2A.Z;
PROTEIN;
D O I:
10.1139/bcb-2016-0017
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:
DNA damage occurs within the chromatin environment, which ultimately participates in regulating DNA damage response (DDR) pathways and repair of the lesion. DNA damage activates a cascade of signaling events that extensively modulates chromatin structure and organization to coordinate DDR factor recruitment to the break and repair, whilst also promoting the maintenance of normal chromatin functions within the damaged region. For example, DDR pathways must avoid conflicts between other DNA-based processes that function within the context of chromatin, including transcription and replication. The molecular mechanisms governing the recognition, target specificity, and recruitment of DDR factors and enzymes to the fundamental repeating unit of chromatin, i.e., the nucleosome, are poorly understood. Here we present our current view of how chromatin recognition by DDR factors is achieved at the level of the nucleosome. Emerging evidence suggests that the nucleosome surface, including the nucleosome acidic patch, promotes the binding and activity of several DNA damage factors on chromatin. Thus, in addition to interactions with damaged DNA and histone modifications, nucleosome recognition by DDR factors plays a key role in orchestrating the requisite chromatin response to maintain both genome and epigenome integrity.
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页码:381 / 395
页数:15
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