Esteban, V.Blanco, M.Cueille, N.Simanis, V.Moreno, S.Bueno, A.2008-10-212008-10-212008-10-21200410.1242/jcs.01107https://infoscience.epfl.ch/handle/20.500.14299/30372The Schizosaccaromyces pombe protein Flp1p belongs to a conserved family of serine-threonine-phosphatases. The founding member of this family, Saccharomyces cerevisiae Cdc14p, is required for inactivation of mitotic CDKs and reversal of CDK mediated phosphorylation at the end of mitosis, thereby bringing about the M-G1 transition. Initial studies of Flp1p suggest that it may play a different role to Cdc14p. Here we show that Flp1p is required for rapid degradation of the mitotic inducer Cdc25p at the end of mitosis, and that Cdc25p is a substrate of Flp1p in vitro. Down-regulation of Cdc25p activity by Flp1p may ensure a prompt inactivation of mitotic CDK complexes to trigger cell division. Our results suggest a regulatory mechanism, and a universal role, for Cdc14p like proteins in coordination of cytokinesis with other cell cycle events.*Cell CycleCell Cycle Proteins/*genetics/metabolismCytokinesisDown-RegulationGene Expression RegulationEnzymologicGene Expression RegulationFungalGenesFungalGlutathione Transferase/metabolismMitosisMutationPhosphoprotein Phosphatases/genetics/*metabolismProtein Tyrosine PhosphatasesRecombinant Proteins/metabolismSchizosaccharomyces/cytology/*enzymology/metabolismSchizosaccharomyces pombe Proteins/genetics/*metabolismSubstrate Specificitycdc25 Phosphatases/genetics/*metabolismtext::journal::journal article::research article