The anaphase promoting complex impacts repair choice by protecting ubiquitin signalling at DNA damage sites

Nat Commun. 2017 Jun 12;8:15751. doi: 10.1038/ncomms15751.


Double-strand breaks (DSBs) are repaired through two major pathways, homology-directed recombination (HDR) and non-homologous end joining (NHEJ). While HDR can only occur in S/G2, NHEJ can happen in all cell cycle phases (except mitosis). How then is the repair choice made in S/G2 cells? Here we provide evidence demonstrating that APCCdh1 plays a critical role in choosing the repair pathways in S/G2 cells. Our results suggest that the default for all DSBs is to recruit 53BP1 and RIF1. BRCA1 is blocked from being recruited to broken ends because its recruitment signal, K63-linked poly-ubiquitin chains on histones, is actively destroyed by the deubiquitinating enzyme USP1. We show that the removal of USP1 depends on APCCdh1 and requires Chk1 activation known to be catalysed by ssDNA-RPA-ATR signalling at the ends designated for HDR, linking the status of end processing to RIF1 or BRCA1 recruitment.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anaphase-Promoting Complex-Cyclosome / physiology*
  • Animals
  • Cell Line
  • DNA Breaks, Double-Stranded
  • DNA Damage*
  • DNA Repair / physiology*
  • Genomic Instability
  • HEK293 Cells
  • HeLa Cells
  • Humans
  • Mice
  • Models, Genetic
  • Signal Transduction
  • Ubiquitin / metabolism*


  • Ubiquitin
  • Anaphase-Promoting Complex-Cyclosome