The shieldin complex mediates 53BP1-dependent DNA repair

Nature. 2018 Aug;560(7716):117-121. doi: 10.1038/s41586-018-0340-7. Epub 2018 Jul 18.


53BP1 is a chromatin-binding protein that regulates the repair of DNA double-strand breaks by suppressing the nucleolytic resection of DNA termini1,2. This function of 53BP1 requires interactions with PTIP3 and RIF14-9, the latter of which recruits REV7 (also known as MAD2L2) to break sites10,11. How 53BP1-pathway proteins shield DNA ends is currently unknown, but there are two models that provide the best potential explanation of their action. In one model the 53BP1 complex strengthens the nucleosomal barrier to end-resection nucleases12,13, and in the other 53BP1 recruits effector proteins with end-protection activity. Here we identify a 53BP1 effector complex, shieldin, that includes C20orf196 (also known as SHLD1), FAM35A (SHLD2), CTC-534A2.2 (SHLD3) and REV7. Shieldin localizes to double-strand-break sites in a 53BP1- and RIF1-dependent manner, and its SHLD2 subunit binds to single-stranded DNA via OB-fold domains that are analogous to those of RPA1 and POT1. Loss of shieldin impairs non-homologous end-joining, leads to defective immunoglobulin class switching and causes hyper-resection. Mutations in genes that encode shieldin subunits also cause resistance to poly(ADP-ribose) polymerase inhibition in BRCA1-deficient cells and tumours, owing to restoration of homologous recombination. Finally, we show that binding of single-stranded DNA by SHLD2 is critical for shieldin function, consistent with a model in which shieldin protects DNA ends to mediate 53BP1-dependent DNA repair.

Publication types

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

MeSH terms

  • Animals
  • CRISPR-Cas Systems
  • Cell Line
  • DNA Breaks, Double-Stranded
  • DNA Repair*
  • DNA, Single-Stranded / genetics
  • Female
  • Genes, BRCA1
  • Humans
  • Immunoglobulin Class Switching / genetics
  • Mice
  • Models, Biological
  • Multiprotein Complexes / chemistry
  • Multiprotein Complexes / deficiency
  • Multiprotein Complexes / genetics
  • Multiprotein Complexes / metabolism*
  • Poly(ADP-ribose) Polymerase Inhibitors / pharmacology
  • Telomere-Binding Proteins / metabolism
  • Tumor Suppressor Protein p53 / deficiency
  • Tumor Suppressor p53-Binding Protein 1 / metabolism*


  • DNA, Single-Stranded
  • Multiprotein Complexes
  • Poly(ADP-ribose) Polymerase Inhibitors
  • Rif1 protein, human
  • Telomere-Binding Proteins
  • Trp53 protein, mouse
  • Tumor Suppressor Protein p53
  • Tumor Suppressor p53-Binding Protein 1