ATR kinase activation in G1 phase facilitates the repair of ionizing radiation-induced DNA damage.

ABSTRACT: The kinase ATR is activated by RPA-coated single-stranded DNA generated at aberrant replicative structures and resected double strand breaks. While many hundred candidate ATR substrates have been identified, the essential role of ATR in the replicative stress response has impeded the study of ATR kinase-dependent signalling. Using recently developed selective drugs, we show that ATR inhibition has a significantly more potent effect than ATM inhibition on ionizing radiation (IR)-mediated cell killing. Transient ATR inhibition for a short interval after IR has long-term consequences that include an accumulation of RPA foci and a total abrogation of Chk1 S345 phosphorylation. We show that ATR kinase activity in G1 phase cells is important for survival after IR and that ATR colocalizes with RP

SUBMITTER: Gamper AM 

PROVIDER: S-EPMC3905881 | biostudies-literature | 2013 Dec

REPOSITORIES: biostudies-literature