4.5 Article

Physical interaction between the histone acetyl transferase Tip60 and the DNA double-strand breaks sensor MRN complex

Journal

BIOCHEMICAL JOURNAL
Volume 426, Issue -, Pages 365-371

Publisher

PORTLAND PRESS LTD
DOI: 10.1042/BJ20091329

Keywords

chromatin; DNA repair; histone acetylation; Mre11-Rad50-Nbs1 complex (MRN complex); Tip60

Funding

  1. Association pour la Recherche contra le Cancer (ARC)
  2. Agence Nationale de la Recherche (ANR) [ANR-06-3-13-7148]
  3. Ligue Nationale Contra le Cancer ('equipe labellisee')
  4. Elechicite De France

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Chromatin modifications and chromatin-modifying enzymes are believed to play a major role in the process of DNA repair. The historic acetyl transferase Tip60 is physically recruited to DNA DSBs (double-strand breaks) where it mediates histone acetylation. In the present study, we Show, using a reporter system in mammalian cells, that Tip60 expression is required for homology-driven repair. strongly suggesting that Tip60 participates in DNA DSB repair through homologous recombination. Moreover, Tip60 depletion inhibits the formation of Rad50 loci following ionizing radiation, indicating that Tip60 expression is necessary for the recruitment of the DNA damage sensor MRN (Mre11-Rad50-Nbs1) complex to DNA DSBs. Moreover, we Found that endogenous Tip60 physically Interacts with endogenous MRN proteins in a complex,which is distinct from the classical Tip60 complex. Taken together, our results describe a physical link between a DNA damage sensor and a histone-modifying, enzyme, and provide important new insights into the role and mechanism of action of Tip60 in the process of DNA DSB repair.

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