ATR and ATM differently regulate WRN to prevent DSBs at stalled replication forks and promote replication fork recovery.

Accurate response to replication arrest is crucial to preserve genome stability and requires both the ATR and ATM functions. The Werner syndrome protein (WRN) is implicated in the recovery of stalled replication forks, and although an ATR/ATM-dependent phosphorylation of WRN was observed after replication arrest, the function of such modifications ...
during the response to perturbed replication is not yet appreciated. Here, we report that WRN is directly phosphorylated by ATR at multiple C-terminal S/TQ residues. Suppression of ATR-mediated phosphorylation of WRN prevents proper accumulation of WRN in nuclear foci, co-localisation with RPA and causes breakage of stalled forks. On the other hand, inhibition of ATM kinase activity or expression of an ATM-unphosphorylable WRN allele leads to retention of WRN in nuclear foci and impaired recruitment of RAD51 recombinase resulting in reduced viability after fork collapse. Altogether, our findings indicate that ATR and ATM promote recovery from perturbed replication by differently regulating WRN at defined moments of the response to replication fork arrest.
Mesh Terms:
Ataxia Telangiectasia Mutated Proteins, Blotting, Western, Cell Cycle, Cell Cycle Proteins, Cell Nucleus, DNA Breaks, Double-Stranded, DNA Repair, DNA Replication, DNA-Binding Proteins, Exodeoxyribonucleases, Flow Cytometry, Fluorescent Antibody Technique, Humans, Immunoprecipitation, Phosphorylation, Protein Serine-Threonine Kinases, RNA, Messenger, RNA, Small Interfering, Rad51 Recombinase, RecQ Helicases, Reverse Transcriptase Polymerase Chain Reaction, Tumor Suppressor Proteins, Werner Syndrome Helicase
EMBO J
Date: Sep. 15, 2010
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