Coordinated nuclease activities counteract Ku at single-ended DNA double-strand breaks View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2016-09-19

AUTHORS

Pauline Chanut, Sébastien Britton, Julia Coates, Stephen P. Jackson, Patrick Calsou

ABSTRACT

Repair of single-ended DNA double-strand breaks (seDSBs) by homologous recombination (HR) requires the generation of a 3' single-strand DNA overhang by exonuclease activities in a process called DNA resection. However, it is anticipated that the highly abundant DNA end-binding protein Ku sequesters seDSBs and shields them from exonuclease activities. Despite pioneering works in yeast, it is unclear how mammalian cells counteract Ku at seDSBs to allow HR to proceed. Here we show that in human cells, ATM-dependent phosphorylation of CtIP and the epistatic and coordinated actions of MRE11 and CtIP nuclease activities are required to limit the stable loading of Ku on seDSBs. We also provide evidence for a hitherto unsuspected additional mechanism that contributes to prevent Ku accumulation at seDSBs, acting downstream of MRE11 endonuclease activity and in parallel with MRE11 exonuclease activity. Finally, we show that Ku persistence at seDSBs compromises Rad51 focus assembly but not DNA resection. More... »

PAGES

12889

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/ncomms12889

DOI

http://dx.doi.org/10.1038/ncomms12889

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1022699472

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/27641979


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