Double strand break repair functions of histone H2AX.

Double strand break repair functions of histone H2AX.
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DOI:
10.1016/j.mrfmmm.2013.07.007
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发表时间:
2013-10
影响因子:
2.3
通讯作者:
Xie, Anyong
Xie, Anyong
中科院分区:
医学4区
文献类型:
--
作者:
Scully, Ralph;Xie, Anyong

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Chromosomal double strand breaks provoke an extensive reaction in neighboring chromatin, characterized by phosphorylation of histone H2AX on serine 139 of its C-terminal tail (to form “γH2AX”). The γH2AX response contributes to the repair of double strand breaks encountered in a variety of different contexts, including those induced by ionizing radiation, physiologically programmed breaks that characterize normal immune cell development and the pathological exposure of DNA ends triggered by telomere dysfunction. γH2AX also participates in the evolutionarily conserved process of sister chromatid recombination, a homologous recombination pathway involved in the suppression of genomic instability during DNA replication and directly implicated in tumor suppression. At a biochemical level, the γH2AX response provides a compelling example of how the “histone code” is adapted to the regulation of double strand break repair. Here, we review progress in research aimed at understanding how γH2AX contributes to double strand break repair in mammalian cells.
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