RNF8 transduces the DNA-damage signal via histone ubiquitylation and checkpoint protein assembly

Cell. 2007 Nov 30;131(5):901-14. doi: 10.1016/j.cell.2007.09.041. Epub 2007 Nov 20.

Abstract

DNA-damage signaling utilizes a multitude of posttranslational modifiers as molecular switches to regulate cell-cycle checkpoints, DNA repair, cellular senescence, and apoptosis. Here we show that RNF8, a FHA/RING domain-containing protein, plays a critical role in the early DNA-damage response. We have solved the X-ray crystal structure of the FHA domain structure at 1.35 A. We have shown that RNF8 facilitates the accumulation of checkpoint mediator proteins BRCA1 and 53BP1 to the damaged chromatin, on one hand through the phospho-dependent FHA domain-mediated binding of RNF8 to MDC1, on the other hand via its role in ubiquitylating H2AX and possibly other substrates at damage sites. Moreover, RNF8-depleted cells displayed a defective G2/M checkpoint and increased IR sensitivity. Together, our study implicates RNF8 as a novel DNA-damage-responsive protein that integrates protein phosphorylation and ubiquitylation signaling and plays a critical role in the cellular response to genotoxic stress.

Publication types

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

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Amino Acid Motifs
  • BRCA1 Protein / metabolism
  • Binding Sites
  • Cell Cycle / radiation effects
  • Cell Cycle Proteins / metabolism*
  • Cells, Cultured
  • DNA Damage / physiology*
  • DNA-Binding Proteins / chemistry
  • DNA-Binding Proteins / metabolism
  • DNA-Binding Proteins / physiology*
  • Histones / metabolism*
  • Histones / physiology
  • Humans
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Models, Biological
  • Models, Molecular
  • Nuclear Proteins / physiology
  • Phosphorylation
  • Protein Binding
  • Protein Structure, Tertiary
  • Signal Transduction
  • Trans-Activators / physiology
  • Tumor Suppressor p53-Binding Protein 1
  • Ubiquitin-Protein Ligases
  • Ubiquitination* / physiology

Substances

  • Adaptor Proteins, Signal Transducing
  • BRCA1 Protein
  • BRCA1 protein, human
  • Cell Cycle Proteins
  • DNA-Binding Proteins
  • H2AX protein, human
  • Histones
  • Intracellular Signaling Peptides and Proteins
  • MDC1 protein, human
  • Nuclear Proteins
  • RNF8 protein, human
  • TP53BP1 protein, human
  • Trans-Activators
  • Tumor Suppressor p53-Binding Protein 1
  • Ubiquitin-Protein Ligases