Requirement of protein phosphatase 5 in DNA-damage-induced ATM activation

Ambereen Ali(Sanford Burnham Prebys Medical Discovery Institute), Ji Zhang(Sanford Burnham Prebys Medical Discovery Institute), Shideng Bao(Sanford Burnham Prebys Medical Discovery Institute), Irene Liu(Sanford Burnham Prebys Medical Discovery Institute), Diane M. Otterness(Sanford Burnham Prebys Medical Discovery Institute), Nicholas M. Dean(Sanford Burnham Prebys Medical Discovery Institute), Robert T. Abraham(Sanford Burnham Prebys Medical Discovery Institute), Xiao-Fan Wang(Sanford Burnham Prebys Medical Discovery Institute)
Genes & Development
February 1, 2004
Cited by 167Open Access
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Abstract

The checkpoint kinase ATM is centrally involved in the cellular response to DNA double-strand breaks. However, the mechanism of ATM activation during genotoxic stress is only partially understood. Here we report a direct regulatory linkage between the protein serine-threonine phosphatase 5 (PP5) and ATM. PP5 interacts with ATM in a DNA-damage-inducible manner. Reduced expression of PP5 attenuated DNA-damage-induced activation of ATM. Expression of a catalytically inactive PP5 mutant inhibited the phosphorylation of ATM substrates and the autophosphorylation of ATM on Ser 1981, and caused an S-phase checkpoint defect in DNA-damaged cells. Together our findings indicate that PP5 plays an essential role in the activation and checkpoint signaling functions of ATM in cells that have suffered DNA double-strand breaks.


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