DNA Damage Response

  1. Wim Vermeulen1
  1. 1Department of Genetics, Erasmus University Medical Center, Dr Molewaterplein 50, 3015 GE Rotterdam, The Netherlands
  2. 2Department of Cancer Biology, Institute of Pharmacology and Structural Biology, CNRS, 205 route de Narbonne, 31077 Toulouse, France
  3. 3Université de Toulouse Paul Sabatier, 31000, Toulouse, France
  4. 4Core Research Laboratory, Istituto Toscano Tumori, Villa delle Rose, Via Cosimo il Vecchio 2, 50139 Firenze, Italy
  1. Correspondence: w.vermeulen{at}erasmusmc.nl

Abstract

Structural changes to DNA severely affect its functions, such as replication and transcription, and play a major role in age-related diseases and cancer. A complicated and entangled network of DNA damage response (DDR) mechanisms, including multiple DNA repair pathways, damage tolerance processes, and cell-cycle checkpoints safeguard genomic integrity. Like transcription and replication, DDR is a chromatin-associated process that is generally tightly controlled in time and space. As DNA damage can occur at any time on any genomic location, a specialized spatio-temporal orchestration of this defense apparatus is required.

Footnotes

  • Editors: Tom Misteli and David L. Spector

  • Additional Perspectives on The Nucleus available at www.cshperspectives.org



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      1. Cold Spring Harb. Perspect. Biol. 3: a000745 Copyright © 2011 Cold Spring Harbor Laboratory Press; all rights reserved

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