Classical non-homologous end-joining pathway utilizes nascent RNA for error-free double-strand break repair of transcribed genes

Nat Commun. 2016 Oct 5:7:13049. doi: 10.1038/ncomms13049.

Abstract

DNA double-strand breaks (DSBs) leading to loss of nucleotides in the transcribed region can be lethal. Classical non-homologous end-joining (C-NHEJ) is the dominant pathway for DSB repair (DSBR) in adult mammalian cells. Here we report that during such DSBR, mammalian C-NHEJ proteins form a multiprotein complex with RNA polymerase II and preferentially associate with the transcribed genes after DSB induction. Depletion of C-NHEJ factors significantly abrogates DSBR in transcribed but not in non-transcribed genes. We hypothesized that nascent RNA can serve as a template for restoring the missing sequences, thus allowing error-free DSBR. We indeed found pre-mRNA in the C-NHEJ complex. Finally, when a DSB-containing plasmid with several nucleotides deleted within the E. coli lacZ gene was allowed time to repair in lacZ-expressing mammalian cells, a functional lacZ plasmid could be recovered from control but not C-NHEJ factor-depleted cells, providing important mechanistic insights into C-NHEJ-mediated error-free DSBR of the transcribed genome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA Breaks, Double-Stranded*
  • DNA End-Joining Repair*
  • DNA-Binding Proteins / metabolism
  • Escherichia coli / metabolism
  • Gene Expression Regulation, Bacterial
  • HEK293 Cells
  • Humans
  • Lac Operon
  • Plasmids
  • RNA / genetics*
  • RNA Polymerase II / metabolism
  • RNA, Small Interfering / metabolism
  • Reproducibility of Results
  • Ribonuclease H / metabolism
  • Transcription, Genetic

Substances

  • DNA-Binding Proteins
  • RNA, Small Interfering
  • RNA
  • RNA Polymerase II
  • Ribonuclease H