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不只是焦点:DNA 损伤的染色质反应及其在基因组完整性维持中的作用。

More than just a focus: The chromatin response to DNA damage and its role in genome integrity maintenance.

机构信息

Centre for Genotoxic Stress Research, Institute of Cancer Biology, Danish Cancer Society, Strandboulevarden 49, DK-2100 Copenhagen, Denmark.

出版信息

Nat Cell Biol. 2011 Oct 3;13(10):1161-9. doi: 10.1038/ncb2344.


DOI:10.1038/ncb2344
PMID:21968989
Abstract

Following the discovery in 1998 of γ-H2AX, the first histone modification induced by DNA damage, interest in the changes to chromatin induced by DNA damage has exploded, and a vast amount of information has been generated. However, there has been a discrepancy between our rapidly advancing knowledge of how chromatin responds to DNA damage and the understanding of why cells mobilize large segments of chromatin to protect the genome against destabilizing effects posed by tiny DNA lesions. Recent research has provided insights into these issues and suggests that chromatin responses induced by DNA damage are not simply the accumulation of 'nuclear foci' but are mechanisms required to guard genome integrity.

摘要

自 1998 年发现第一个由 DNA 损伤诱导的组蛋白修饰 γ-H2AX 以来,人们对 DNA 损伤诱导的染色质变化产生了浓厚的兴趣,相关信息量呈爆炸式增长。然而,我们对于染色质如何响应 DNA 损伤的认识的快速发展与理解细胞为什么调动大片段染色质以保护基因组免受微小 DNA 损伤带来的不稳定影响之间存在差异。最近的研究为解决这些问题提供了新的见解,并表明 DNA 损伤诱导的染色质反应不仅仅是“核焦点”的积累,而是保护基因组完整性所需的机制。

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本文引用的文献

[1]
DNA-damage response and repair activities at uncapped telomeres depend on RNF8.

Nat Cell Biol. 2011-8-21

[2]
Wolf-Hirschhorn syndrome candidate 1 is involved in the cellular response to DNA damage.

Proc Natl Acad Sci U S A. 2011-7-25

[3]
Chfr and RNF8 synergistically regulate ATM activation.

Nat Struct Mol Biol. 2011-6-26

[4]
The ubiquitin- and SUMO-dependent signaling response to DNA double-strand breaks.

FEBS Lett. 2011-6-12

[5]
KAP-1 phosphorylation regulates CHD3 nucleosome remodeling during the DNA double-strand break response.

Nat Struct Mol Biol. 2011-6-5

[6]
Genomic instability, defective spermatogenesis, immunodeficiency, and cancer in a mouse model of the RIDDLE syndrome.

PLoS Genet. 2011-4-28

[7]
Regulation of DNA end joining, resection, and immunoglobulin class switch recombination by 53BP1.

Mol Cell. 2011-5-6

[8]
MDC1 directs chromosome-wide silencing of the sex chromosomes in male germ cells.

Genes Dev. 2011-5-1

[9]
MDC1 collaborates with TopBP1 in DNA replication checkpoint control.

J Cell Biol. 2011-4-11

[10]
HP1alpha recruitment to DNA damage by p150CAF-1 promotes homologous recombination repair.

J Cell Biol. 2011-4-4

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