DNA repair goes hip-hop: SMARCA and CHD chromatin remodellers join the break dance

Proper signalling and repair of DNA double-strand breaks (DSB) is critical to prevent genome instability and diseases such as cancer. The packaging of DNA into chromatin, however, has evolved as a mere obstacle to these DSB responses. Posttranslational modifications and ATP-dependent chromatin remod...

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Published inPhilosophical transactions of the Royal Society of London. Series B. Biological sciences Vol. 372; no. 1731; p. 20160285
Main Authors Rother, Magdalena B., van Attikum, Haico
Format Journal Article
LanguageEnglish
Published England The Royal Society 05.10.2017
The Royal Society Publishing
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Summary:Proper signalling and repair of DNA double-strand breaks (DSB) is critical to prevent genome instability and diseases such as cancer. The packaging of DNA into chromatin, however, has evolved as a mere obstacle to these DSB responses. Posttranslational modifications and ATP-dependent chromatin remodelling help to overcome this barrier by modulating nucleosome structures and allow signalling and repair machineries access to DSBs in chromatin. Here we recap our current knowledge on how ATP-dependent SMARCA- and CHD-type chromatin remodellers alter chromatin structure during the signalling and repair of DSBs and discuss how their dysfunction impacts genome stability and human disease. This article is part of the themed issue ‘Chromatin modifiers and remodellers in DNA repair and signalling’.
Bibliography:Theme issue ‘Chromatin modifiers and remodellers in DNA repair and signalling’ compiled and edited by Penelope A. Jeggo, Jessica A. Downs and Susan M. Gasser
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One contribution of 14 to a theme issue ‘Chromatin modifiers and remodellers in DNA repair and signalling’.
ISSN:0962-8436
1471-2970
DOI:10.1098/rstb.2016.0285