A genome-wide screening uncovers the role of CCAR2 as an antagonist of DNA end resection

Nat Commun. 2016 Aug 9:7:12364. doi: 10.1038/ncomms12364.

Abstract

There are two major and alternative pathways to repair DNA double-strand breaks: non-homologous end-joining and homologous recombination. Here we identify and characterize novel factors involved in choosing between these pathways; in this study we took advantage of the SeeSaw Reporter, in which the repair of double-strand breaks by homology-independent or -dependent mechanisms is distinguished by the accumulation of green or red fluorescence, respectively. Using a genome-wide human esiRNA (endoribonuclease-prepared siRNA) library, we isolate genes that control the recombination/end-joining ratio. Here we report that two distinct sets of genes are involved in the control of the balance between NHEJ and HR: those that are required to facilitate recombination and those that favour NHEJ. This last category includes CCAR2/DBC1, which we show inhibits recombination by limiting the initiation and the extent of DNA end resection, thereby acting as an antagonist of CtIP.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism*
  • Carrier Proteins / metabolism
  • Cell Line, Tumor
  • Chromatin / metabolism
  • DNA Damage
  • DNA End-Joining Repair*
  • Endodeoxyribonucleases
  • Gene Regulatory Networks
  • Genome, Human*
  • Humans
  • Models, Biological
  • Nuclear Proteins / metabolism
  • Protein Binding
  • Recombinational DNA Repair

Substances

  • Adaptor Proteins, Signal Transducing
  • CCAR2 protein, human
  • Carrier Proteins
  • Chromatin
  • Nuclear Proteins
  • Endodeoxyribonucleases
  • RBBP8 protein, human