The mechanism of non-homologous end-joining: a synopsis of synapsis

DNA Repair (Amst). 2004 Nov 2;3(11):1425-35. doi: 10.1016/j.dnarep.2004.06.003.

Abstract

Repair of DNA double-strand breaks (DSBs) by non-homologous end-joining (NHEJ) is required for resistance to genotoxic agents, such as ionizing radiation, but also for proper development of the vertebrate immune system. Much progress has been made in identifying the factors that are involved in this repair pathway. We are now entering the phase in which we begin to understand basic concepts of the reaction mechanism and regulation of non-homologous end-joining. This review concentrates on novel insights into damage recognition and subsequent tethering, processing and joining of DNA ends.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • DNA / chemistry
  • DNA / genetics
  • DNA / metabolism
  • DNA Damage
  • DNA Ligase ATP
  • DNA Ligases / metabolism
  • DNA Repair / genetics
  • DNA Repair / immunology
  • DNA Repair / physiology*
  • DNA Repair Enzymes / metabolism
  • DNA-Activated Protein Kinase
  • DNA-Binding Proteins / metabolism
  • Genes, Immunoglobulin
  • Genes, T-Cell Receptor
  • Humans
  • Models, Biological
  • Nuclear Proteins
  • Protein-Serine-Threonine Kinases / metabolism

Substances

  • DNA-Binding Proteins
  • Nuclear Proteins
  • XRCC4 protein, human
  • DNA
  • DNA-Activated Protein Kinase
  • PRKDC protein, human
  • Protein-Serine-Threonine Kinases
  • DNA Ligases
  • DNA Repair Enzymes
  • DNA Ligase ATP