The chromatin remodeler p400 ATPase facilitates Rad51-mediated repair of DNA double-strand breaks

Céline Courilleau, Catherine Chailleux, Alain Jauneau, Fanny Grimal, Sébastien Briois, Elisa Boutet-Robinet, François Boudsocq, Didier Trouche, Yvan Canitrot

Research output: Contribution to journalArticlepeer-review

Abstract

DNA damage signaling and repair take place in a chromatin context. Consequently, chromatin-modifying enzymes, including adenosine triphosphate-dependent chromatin remodeling enzymes, play an important role in the management of DNA double-strand breaks (DSBs). Here, we show that the p400 ATPase is required for DNA repair by homologous recombination (HR). Indeed, although p400 is not required for DNA damage signaling, DNA DSB repair is defective in the absence of p400. We demonstrate that p400 is important for HR-dependent processes, such as recruitment of Rad51 to DSB (a key component of HR), homology-directed repair, and survival after DNA damage. Strikingly, p400 and Rad51 are present in the same complex and both favor chromatin remodeling around DSBs. Altogether, our data provide a direct molecular link between Rad51 and a chromatin remodeling enzyme involved in chromatin decompaction around DNA DSBs.
Original languageEnglish
Pages (from-to)1067-81
Number of pages15
JournalJournal of Cell Biology
Volume199
Issue number7
DOIs
Publication statusPublished - 24 Dec 2012

Keywords

  • Cell Cycle
  • Cell Line
  • Chromatin Assembly and Disassembly
  • DNA Breaks, Double-Stranded
  • DNA Helicases
  • DNA-Binding Proteins
  • Gene Knockdown Techniques
  • Histones
  • Humans
  • Phosphorylation
  • Protein Binding
  • Protein Processing, Post-Translational
  • Protein Transport
  • RNA Interference
  • Rad51 Recombinase
  • Recombinational DNA Repair
  • Replication Protein A
  • Signal Transduction

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