H4K20me0 marks post-replicative chromatin and recruits the TONSL–MMS22L DNA repair complex

被引:0
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作者
Giulia Saredi
Hongda Huang
Colin M. Hammond
Constance Alabert
Simon Bekker-Jensen
Ignasi Forne
Nazaret Reverón-Gómez
Benjamin M. Foster
Lucie Mlejnkova
Till Bartke
Petr Cejka
Niels Mailand
Axel Imhof
Dinshaw J. Patel
Anja Groth
机构
[1] Biotech Research and Innovation Centre (BRIC) and Centre for Epigenetics,Department of Molecular Biology
[2] Faculty of Health and Medical Sciences,undefined
[3] University of Copenhagen,undefined
[4] Structural Biology Program,undefined
[5] Memorial Sloan-Kettering Cancer Center,undefined
[6] The Novo Nordisk Foundation Center for Protein Research,undefined
[7] University of Copenhagen,undefined
[8] Biomedical Center and Center for Integrated Protein Science Munich,undefined
[9] Ludwig-Maximilians University,undefined
[10] MRC Clinical Sciences Centre (CSC) and Institute of Clinical Sciences (ICS),undefined
[11] Faculty of Medicine,undefined
[12] Imperial College London,undefined
[13] Institute of Molecular Cancer Research,undefined
[14] University of Zurich,undefined
来源
Nature | 2016年 / 534卷
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摘要
We have a limited understanding of how cells mark and identify newly replicated genomic loci that have a sister chromatid; here, unmethylated K20 in the tail of new histone H4 is shown to serve as a signature of post-replicative chromatin, which is specifically recognized by the homologous recombination complex TONSL–MMS22L.
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页码:714 / 718
页数:4
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