Protein phosphatase 2A controls the order and dynamics of cell-cycle transitions.. : PP2A Controls Cell-Cycle Transitions

Archive ouverte

Krasinska, Liliana | Rosa Domingo-Sananes, Maria | Kapuy, Orsolya | Parisis, Nikolaos | Harker, Bethany | Moorhead, Gregory | Rossignol, Michel | Novak, Béla | Fisher, Daniel

Edité par CCSD ; Cell Press -

International audience. Bistability of the Cdk1-Wee1-Cdc25 mitotic control network underlies the switch-like transitions between interphase and mitosis. Here, we show by mathematical modeling and experiments in Xenopus egg extracts that protein phosphatase 2A (PP2A), which can dephosphorylate Cdk1 substrates, is essential for this bistability. PP2A inhibition in early interphase abolishes the switch-like response of the system to Cdk1 activity, promoting mitotic onset even with very low levels of Cyclin, Cdk1, and Cdc25, while simultaneously inhibiting DNA replication. Furthermore, even if replication has already initiated, it cannot continue in mitosis. Exclusivity of S and M phases does not depend on bistability only, since partial PP2A inhibition prevents replication without inducing mitotic onset. In these conditions, interphase-level mitotic kinases inhibit Cyclin E-Cdk2 chromatin loading, blocking initiation complex formation. Therefore, by counteracting both Cdk1 activation and activity of mitotic kinases, PP2A ensures robust separation of S phase and mitosis and dynamic transitions between the two states.

Suggestions

Du même auteur

Initiation of DNA replication requires actin dynamics and formin activity

Archive ouverte | Parisis, Nikolaos | CCSD

International audience. Nuclear actin regulates transcriptional programmes in a manner dependent on its levels and polymerisation state. This dynamics is determined by the balance of nucleocytoplasmic shuttling, for...

The cell proliferation antigen Ki-67 organises heterochromatin

Archive ouverte | Sobecki, Michal | CCSD

International audience. Antigen Ki-67 is a nuclear protein expressed in proliferating mammalian cells. It is widely used in cancer histopathology but its functions remain unclear. Here, we show that Ki-67 controls h...

Histone H3 serine-57 is a CHK1 substrate whose phosphorylation affects DNA repair

Archive ouverte | Parisis, Nikolaos | CCSD

International audience. Histone post-translational modifications promote a chromatin environment that controls transcription, DNA replication and repair, but surprisingly few phosphorylations have been documented. W...

Chargement des enrichissements...