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Chromatin modifications and DNA double-strand breaks: the current state of play
被引:30
作者:
Karagiannis, T. C.
El-Osta, A.
机构:
[1] Alfred Med Res & Educ Precinct, AMREP, Epigenet Human Hlth & Dis Lab, Baker Med Res Inst, Prahran, Vic 3181, Australia
[2] Peter MacCallum Canc Inst, Trescowthick Res Labs, Melbourne, Vic 3000, Australia
[3] Univ Melbourne, Dept Pathol, Parkville, Vic 3052, Australia
来源:
基金:
英国医学研究理事会;
关键词:
double-strand break;
chromatin modification;
histone acetylation;
histone phosphorylation;
histone methylation;
chromatin-remodeling complex;
D O I:
10.1038/sj.leu.2404478
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
The packaging and compaction of DNA into chromatin is important for all DNA-metabolism processes such as transcription, replication and repair. The involvement of chromatin modifications in transcriptional regulation is relatively well characterized, and the distinct patterns of chromatin transitions that guide the process are thought to be the result of a code on the histone proteins ( histone code). In contrast to transcription, the intricate link between chromatin and responses to DNA damage has been given attention only recently. It is now emerging that specific ATP-dependent chromatin remodeling complexes ( including the Ino80, Swi/Snf and RSC remodelers) and certain constitutive ( methylation of lysine 79 of histone H3) and DNA damage-induced covalent histone modifications ( the most well characterized being the rapid phosphorylation of histone H2A) facilitate responses to double-strand breaks. Indeed, evidence is already accumulating for a DNA repair-specific histone code. In this review, the recent advances in our understanding of the relationship between chromatin modifications and double-strand break signaling and repair is discussed.
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页码:195 / 200
页数:6
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