The chromatin-remodeling subunit Baf200 promotes homology-directed DNA repair and regulates distinct chromatin-remodeling complexes

Rodrigo O de Castro, Luciana Previato, Victor Goitea, Anna Felberg, Michel F Guiraldelli, Adrian Filiberti, Roberto J Pezza*

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

Abstract

The efficiency and type of pathway chosen to repair DNA double-strand breaks (DSBs) are critically influenced by the nucleosome packaging and the chromatin architecture surrounding the DSBs. The Swi/Snf (PBAF and BAF) chromatin-remodeling complexes contribute to DNA damage-induced nucleosome remodeling, but the mechanism by which it contributes to this function is poorly understood. Herein, we report how the Baf200 (Arid2) PBAF-defining subunit regulates DSB repair. We used cytological and biochemical approaches to show that Baf200 plays an important function by facilitating homologous recombination-dependent processes, such as recruitment of Rad51 (a key component of homologous recombination) to DSBs, homology-directed repair, and cell survival after DNA damage. Furthermore, we observed that Baf200 and Rad51 are present in the same complex and that this interaction is mediated by C-terminal sequences in both proteins. It has been recognized previously that the interplay between distinct forms of Swi/Snf has profound functional consequences, but we understand little about the composition of complexes formed by PBAF protein subunits. Our biochemical analyses reveal that Baf200 forms at least two distinct complexes. One is a canonical form of PBAF including the Swi/Snf-associated Brg1 catalytic subunit, and the other contains Baf180 but not Brg1. This distinction of PBAF complexes based on their unique composition provides the foundation for future studies on the specific contributions of the PBAF forms to the regulation of DNA repair.

Original languageEnglish
JournalThe Journal of biological chemistry
Volume292
Issue number20
Pages (from-to)8459-8471
ISSN0021-9258
DOIs
Publication statusPublished - May 2017
Externally publishedYes

Keywords

  • Cell Line, Tumor
  • Chromosomal Proteins, Non-Histone/genetics
  • DNA Breaks, Double-Stranded
  • DNA Helicases/genetics
  • Humans
  • Multiprotein Complexes/genetics
  • Nuclear Proteins/genetics
  • Rad51 Recombinase/genetics
  • Recombinational DNA Repair/physiology
  • Transcription Factors/genetics

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