Protein phosphatase 2A (PP2A) promotes anaphase entry after DNA replication stress in budding yeast.

DNA replication stress activates the S-phase checkpoint that arrests the cell cycle, but it is poorly understood how cells recover from this arrest. Cyclin-dependent kinase (CDK) and protein phosphatase 2A (PP2A) are key cell cycle regulators, and Cdc55 is a regulatory subunit of PP2A in budding yeast. We found that ...
yeast cells lacking functional PP2ACdc55 showed slow growth in the presence of hydroxyurea (HU), a DNA synthesis inhibitor, without obvious viability loss. Moreover, PP2A mutants exhibited delayed anaphase entry and sustained levels of anaphase inhibitor Pds1 after HU treatment. A DNA damage checkpoint Chk1 phosphorylates and stabilizes Pds1. We show that chk1? and mutation of the Chk1 phosphorylation sites in Pds1 largely restored efficient anaphase entry in PP2A mutants after HU treatment. In addition, deletion of SWE1, which encodes the inhibitory kinase for CDK or mutation of the Swe1 phosphorylation site in CDK (cdc28F19), also suppressed the anaphase entry delay in PP2A mutants after HU treatment. Our genetic data suggest that Swe1/CDK acts upstream of Pds1. Surprisingly, cdc55? showed significant suppression to the viability loss of S-phase checkpoint mutants during DNA synthesis block. Together, our results uncover a PP2A-Swe1-CDK-Chk1-Pds1 axis that promotes recovery from DNA replication stress.
Mesh Terms:
Anaphase, CDC2 Protein Kinase, Cell Cycle Proteins, Checkpoint Kinase 1, DNA Replication, Green Fluorescent Proteins, Hydroxyurea, Microorganisms, Genetically-Modified, Mutation, Phosphorylation, Protein Phosphatase 2, Protein-Tyrosine Kinases, S Phase, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins, Securin
Mol Biol Cell
Date: Dec. 01, 2020
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