| Literature DB >> 28591578 |
Lilia Gheghiani1, Damarys Loew2, Bérangère Lombard2, Jörg Mansfeld3, Olivier Gavet4.
Abstract
Commitment to mitosis must be tightly coordinated with DNA replication to preserve genome integrity. While we have previously established that the timely activation of CyclinB1-Cdk1 in late G2 triggers mitotic entry, the upstream regulatory mechanisms remain unclear. Here, we report that Polo-like kinase 1 (Plk1) is required for entry into mitosis during an unperturbed cell cycle and is rapidly activated shortly before CyclinB1-Cdk1. We determine that Plk1 associates with the Cdc25C1 phosphatase and induces its phosphorylation before mitotic entry. Plk1-dependent Cdc25C1 phosphosites are sufficient to promote mitotic entry, even when Plk1 activity is inhibited. Furthermore, we find that activation of Plk1 during G2 relies on CyclinA2-Cdk activity levels. Our findings thus elucidate a critical role for Plk1 in CyclinB1-Cdk1 activation and mitotic entry and outline how CyclinA2-Cdk, an S-promoting factor, poises cells for commitment to mitosis.Entities:
Keywords: Cdc25C; CyclinA2; FRET biosensor; G2 phase; Plk1; mitosis
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Year: 2017 PMID: 28591578 DOI: 10.1016/j.celrep.2017.05.031
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423