Chromatin dynamics in DNA double-strand break repair

Biochim Biophys Acta. 2012 Jul;1819(7):811-9. doi: 10.1016/j.bbagrm.2012.01.002. Epub 2012 Jan 17.

Abstract

DNA double-strand breaks (DSBs) occur in the context of a highly organized chromatin environment and are, thus, a significant threat to the epigenomic integrity of eukaryotic cells. Changes in break-proximal chromatin structure are thought to be a prerequisite for efficient DNA repair and may help protect the structural integrity of the nucleus. Unlike most bona fide DNA repair factors, chromatin influences the repair process at several levels: the existing chromatin context at the site of damage directly affects the access and kinetics of the repair machinery; DSB induced chromatin modifications influence the choice of repair factors, thereby modulating repair outcome; lastly, DNA damage can have a significant impact on chromatin beyond the site of damage. We will discuss recent findings that highlight both the complexity and importance of dynamic and tightly orchestrated chromatin reorganization to ensure efficient DSB repair and nuclear integrity. This article is part of a Special Issue entitled: Chromatin in time and space.

Publication types

  • Research Support, N.I.H., Intramural
  • Review

MeSH terms

  • Animals
  • Cell Nucleus / metabolism
  • Cellular Senescence
  • Chromatin Assembly and Disassembly*
  • DNA Breaks, Double-Stranded*
  • DNA Repair*
  • DNA Replication
  • Heterochromatin / genetics
  • Heterochromatin / metabolism
  • Histones / metabolism
  • Humans
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Intracellular Signaling Peptides and Proteins / physiology
  • Nucleosomes / genetics
  • Nucleosomes / metabolism
  • Protein Processing, Post-Translational
  • Tumor Suppressor p53-Binding Protein 1

Substances

  • Heterochromatin
  • Histones
  • Intracellular Signaling Peptides and Proteins
  • Nucleosomes
  • TP53BP1 protein, human
  • Tumor Suppressor p53-Binding Protein 1