Requirement of the Prolyl Isomerase Pin1 for the Replication Checkpoint

Author:

Winkler Katharine E.1,Swenson Katherine I.1,Kornbluth Sally1,Means Anthony R.1

Affiliation:

1. Department of Pharmacology and Cancer Biology, Duke University Medical Center, Box 3813, Durham, NC 27710, USA.

Abstract

The peptidyl-prolyl isomerase Pin1 has been implicated in regulating cell cycle progression. Pin1 was found to be required for the DNA replication checkpoint in Xenopus laevis . Egg extracts depleted of Pin1 inappropriately transited from the G 2 to the M phase of the cell cycle in the presence of the DNA replication inhibitor aphidicolin. This defect in replication checkpoint function was reversed after the addition of recombinant wild-type Pin1, but not an isomerase-inactive mutant, to the depleted extract. Premature mitotic entry in the absence of Pin1 was accompanied by hyperphosphorylation of Cdc25, activation of Cdc2/cyclin B, and generation of epitopes recognized by the mitotic phosphoprotein antibody, MPM-2. Therefore, Pin1 appears to be required for the checkpoint delaying the onset of mitosis in response to incomplete replication.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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