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Poly(ADP-ribose) polymerases in double-strand break repair: Focus on PARP1, PARP2 and PARP3

Journal

EXPERIMENTAL CELL RESEARCH
Volume 329, Issue 1, Pages 18-25

Publisher

ELSEVIER INC
DOI: 10.1016/j.yexcr.2014.07.003

Keywords

Homologous recombination; Non homologous end joining; Poly(ADP-ribose) polymerases; DNA repair

Funding

  1. Electricite de France
  2. Ligue Nationale Contre le Cancer (Equipe Labellisee)
  3. Centre National de la Recherche Scientifique
  4. Institut National de la Sante et de la Recherche Medicale
  5. Fondation ARC pour la recherche sur le cancer
  6. Universite de Strasbourg
  7. French government

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Poly(ADP-ribosyl)ation (PARylation) is a post-translational modification of proteins catalysed by Poly(ADP-ribose) polymerases (PARP). A wealth of recent advances in the biochemical and functional characterization of the DNA-dependent PARP family members have highlighted their key contribution in the DNA damage response network, the best characterized being the role of PARP1 and PARP2 in the resolution of single-strand breaks as part of the BER/SSBR process. How PARylation contributes to the repair of double-strand breaks is less well defined but has become recently the subject of significant research in the field. The aim of this review is to provide an overview of the current knowledge concerning the role of the DNA-activated PARP1, PARP2 and PARP3 in cellular response to double-strand breaks (DSB). In addition, we outline the biological significance of these properties in response to programmed DNA lesions formed during physiological processes such as antibody repertoire assembly and diversification. (C) 2014 Elsevier Inc. All rights reserved.

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