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Review

Phosphatases, DNA Damage Checkpoints and Checkpoint Deactivation

Johanna Heideker, Ewa T. Lis and Floyd E. Romesberg

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Cells have evolved intricate and specialized responses to DNA damage, central to which are the DNA damage checkpoints that arrest cell cycle progression and facilitate the repair process. Activation of these damage checkpoints relies heavily on the activity of Ser/Thr kinases, such as Chk1 and Chk2 (Saccharomyces cerevisiae Rad53), which are themselves activated by phosphorylation. Only more recently have we begun to understand how cells disengage the checkpoints to reenter the cell cycle. Here, we review progress toward understanding the functions of phosphatases in checkpoint deactivation in S. cerevisiae, focusing on the non-redundant roles of the type 2A phosphatase Pph3 and the PP2C phosphatases Ptc2 and Ptc3 in the deactivation of Rad53. We discuss how these phosphatases may specifically recognize different phosphorylated forms of Rad53 and how each may independently regulate different facets of the checkpoint response. In conjunction with the independent dephosphorylation of other checkpoint proteins, such regulation may allow a more tailored response to DNA damage that is coordinated with the repair process, ultimately resulting in the resumption of growth.

Authors

Johanna Heideker

The Scripps Research Institute; La Jolla, CA

Ewa T. Lis

The Scripps Research Institute; La Jolla, CA

Floyd E. Romesberg

The Scripps Research Institute; La Jolla, CA

Purchase article for $19

Subscribe to this journal for $129/year