Scientific Article
previous document  unige:43636  next document
add to browser collection

Histone acetylation by Trrap-Tip60 modulates loading of repair proteins and repair of DNA double-strand breaks

Loizou, Joanna I
Yang, Yun-Gui
Cuenin, Cyrille
Li, Hai
Wang, Zhao-Qi
Herceg, Zdenko
Published in Nature cell biology. 2006, vol. 8, no. 1, p. 91-9
Abstract DNA is packaged into chromatin, a highly compacted DNA-protein complex; therefore, all cellular processes that use the DNA as a template, including DNA repair, require a high degree of coordination between the DNA-repair machinery and chromatin modification/remodelling, which regulates the accessibility of DNA in chromatin. Recent studies have implicated histone acetyltransferase (HAT) complexes and chromatin acetylation in DNA repair; however, the precise underlying mechanism remains poorly understood. Here, we show that the HAT cofactor Trrap and Tip60 HAT bind to the chromatin surrounding sites of DNA double-strand breaks (DSBs) in vivo. Trrap depletion impairs both DNA-damage-induced histone H4 hyperacetylation and accumulation of repair molecules at sites of DSBs, resulting in defective homologous recombination (HR) repair, albeit with the presence of a functional ATM-dependent DNA-damage signalling cascade. Importantly, the impaired loading of repair proteins and the defect in DNA repair in Trrap-deficient cells can be counteracted by chromatin relaxation, indicating that the DNA-repair defect that was observed in the absence of Trrap is due to impeded chromatin accessibility at sites of DNA breaks. Thus, these data reveal that cells may use the same basic mechanism involving HAT complexes to regulate distinct cellular processes, such as transcription and DNA repair.
Keywords AcetylationAdaptor Proteins, Signal TransducingAnimalsCells, CulturedChromatin/metabolismChromatin Assembly and DisassemblyDNA DamageDNA Repair/drug effectsDeoxyribonucleases, Type II Site-Specific/genetics/metabolismElectroporationHeLa CellsHistone Acetyltransferases/metabolismHistones/metabolismHumansMaleMiceMice, TransgenicNuclear Proteins/genetics/metabolismRNA, Small InterferingRecombination, GeneticReverse Transcriptase Polymerase Chain ReactionSaccharomyces cerevisiae ProteinsTransfection
PMID: 16341205
Full text
Article (Published version) (1.1 MB) - document accessible for UNIGE members only Limited access to UNIGE
(ISO format)
MURR, Rabih et al. Histone acetylation by Trrap-Tip60 modulates loading of repair proteins and repair of DNA double-strand breaks. In: Nature cell biology, 2006, vol. 8, n° 1, p. 91-9. doi: 10.1038/ncb1343

455 hits

0 download


Deposited on : 2014-12-17

Export document
Format :
Citation style :