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Cell
Article
License: Elsevier Non-Commercial
Data sources: UnpayWall
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Cell
Article . 2007
License: Elsevier Non-Commercial
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Cell
Article . 2007 . Peer-reviewed
License: Elsevier Non-Commercial
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Cell
Article . 2008
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RNF8 Ubiquitylates Histones at DNA Double-Strand Breaks and Promotes Assembly of Repair Proteins

Authors: Mailand, Niels; Bekker-Jensen, Simon; Faustrup, Helene; Melander, Fredrik; Bartek, Jiri; Lukas, Claudia; Lukas, Jiri;

RNF8 Ubiquitylates Histones at DNA Double-Strand Breaks and Promotes Assembly of Repair Proteins

Abstract

Accumulation of repair proteins on damaged chromosomes is required to restore genomic integrity. However, the mechanisms of protein retention at the most destructive chromosomal lesions, the DNA double-strand breaks (DSBs), are poorly understood. We show that RNF8, a RING-finger ubiquitin ligase, rapidly assembles at DSBs via interaction of its FHA domain with the phosphorylated adaptor protein MDC1. This is accompanied by an increase in DSB-associated ubiquitylations and followed by accumulation of 53BP1 and BRCA1 repair proteins. Knockdown of RNF8 or disruption of its FHA or RING domains impaired DSB-associated ubiquitylation and inhibited retention of 53BP1 and BRCA1 at the DSB sites. In addition, we show that RNF8 can ubiquitylate histone H2A and H2AX, and that its depletion sensitizes cells to ionizing radiation. These data suggest that MDC1-mediated and RNF8-executed histone ubiquitylation protects genome integrity by licensing the DSB-flanking chromatin to concentrate repair factors near the DNA lesions.

Related Organizations
Keywords

PROTEINS, Cell Survival, Cell Cycle Proteins, Models, Biological, Histones, Tumor Cells, Cultured, Humans, DNA Breaks, Double-Stranded, Phosphorylation, Adaptor Proteins, Signal Transducing, Binding Sites, Biochemistry, Genetics and Molecular Biology(all), BRCA1 Protein, Intracellular Signaling Peptides and Proteins, Nuclear Proteins, DNA, Chromatin, Protein Structure, Tertiary, DNA-Binding Proteins, DNA Repair Enzymes, SIGNALING, Trans-Activators, Tumor Suppressor p53-Binding Protein 1, Protein Binding

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
1K
Top 0.1%
Top 1%
Top 0.1%
hybrid