染色质
生物
组蛋白
DNA损伤
染色质重塑
细胞生物学
DNA
抄写(语言学)
DNA修复
组蛋白修饰酶
分子生物学
遗传学
语言学
哲学
作者
Christoffel Dinant,Giannis Ampatziadis-Michailidis,Hannes Lans,Maria Tresini,Anna Lagarou,M. Grosbart,Arjan F. Theil,Wiggert A. van Cappellen,Hiroshi Kimurâ,Jiří Bártek,Maria Fousteri,Adriaan B. Houtsmuller,Wim Vermeulen,Jurgen A. Marteijn
出处
期刊:Molecular Cell
[Elsevier]
日期:2013-08-01
卷期号:51 (4): 469-479
被引量:134
标识
DOI:10.1016/j.molcel.2013.08.007
摘要
Chromatin remodeling is tightly linked to all DNA-transacting activities. To study chromatin remodeling during DNA repair, we established quantitative fluorescence imaging methods to measure the exchange of histones in chromatin in living cells. We show that particularly H2A and H2B are evicted and replaced at an accelerated pace at sites of UV-induced DNA damage. This accelerated exchange of H2A/H2B is facilitated by SPT16, one of the two subunits of the histone chaperone FACT (facilitates chromatin transcription) but largely independent of its partner SSRP1. Interestingly, SPT16 is targeted to sites of UV light-induced DNA damage-arrested transcription and is required for efficient restart of RNA synthesis upon damage removal. Together, our data uncover an important role for chromatin dynamics at the crossroads of transcription and the UV-induced DNA damage response.
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