About: RNF8 Ubiquitylates Histones at DNA Double-Strand Breaks and Promotes Assembly of Repair Proteins     Goto   Sponge   NotDistinct   Permalink

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  • 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 DSBassociated 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
  • 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 DSBassociated 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 (en)
Title
  • RNF8 Ubiquitylates Histones at DNA Double-Strand Breaks and Promotes Assembly of Repair Proteins
  • RNF8 Ubiquitylates Histones at DNA Double-Strand Breaks and Promotes Assembly of Repair Proteins (en)
skos:prefLabel
  • RNF8 Ubiquitylates Histones at DNA Double-Strand Breaks and Promotes Assembly of Repair Proteins
  • RNF8 Ubiquitylates Histones at DNA Double-Strand Breaks and Promotes Assembly of Repair Proteins (en)
skos:notation
  • RIV/61989592:15110/07:00009720!RIV10-MSM-15110___
http://linked.open...avai/riv/aktivita
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  • Z(MSM6198959216)
http://linked.open...iv/cisloPeriodika
  • 5
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http://linked.open...aciTvurceVysledku
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  • 448052
http://linked.open...ai/riv/idVysledku
  • RIV/61989592:15110/07:00009720
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • Genomic integrity; DNA damage; DNA repair; homologous recombination; DNA double-strand breaks; histone ubiquitylation (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • US - Spojené státy americké
http://linked.open...ontrolniKodProRIV
  • [79D1D0A25B7F]
http://linked.open...i/riv/nazevZdroje
  • Cell
http://linked.open...in/vavai/riv/obor
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http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 131
http://linked.open...iv/tvurceVysledku
  • Bártek, Jiří
  • Bekker-Jensen, Simon
  • Lukas, Claudia
  • Faustrup, Helene
  • Lukas, Jiří
  • Mailand, Niels
  • Melander, Fredrik
http://linked.open...n/vavai/riv/zamer
issn
  • 0092-8674
number of pages
http://localhost/t...ganizacniJednotka
  • 15110
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