Cyclin A-cdk1-Dependent Phosphorylation of Bora Is the Triggering Factor Promoting Mitotic Entry

Publication date: 4 June 2018
Source:Developmental Cell, Volume 45, Issue 5
Author(s): Suzanne Vigneron, Lena Sundermann, Jean-Claude Labbé, Lionel Pintard, Ovidiu Radulescu, Anna Castro, Thierry Lorca
Mitosis is induced by the activation of the cyclin B/cdk1 feedback loop that creates a bistable state. The triggering factor promoting active cyclin B/cdk1 switch has been assigned to cyclin B/cdk1 accumulation during G2. However, this complex is rapidly inactivated by Wee1/Myt1-dependent phosphorylation of cdk1 making unlikely a triggering role of this kinase in mitotic commitment. Here we show that cyclin A/cdk1 kinase is the factor triggering mitosis. Cyclin A/cdk1 phosphorylates Bora to promote Aurora A-dependent Plk1 phosphorylation and activation and mitotic entry. We demonstrate that Bora phosphorylation by cyclin A/cdk1 is both necessary and sufficient for mitotic commitment. Finally, we identify a site in Bora whose phosphorylation by cyclin A/cdk1 is required for mitotic entry. We constructed a mathematical model confirming the essential role of this kinase in mitotic commitment. Overall, our results uncover the molecular mechanism by which cyclin A/cdk1 triggers mitotic entry.

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Teaser

Mitotic commitment was thought to depend on the accumulation of cyclin B/cdk1 during G2. Vigneron et al. now revise this view by showing that the key event triggering mitotic entry depends instead on cyclin A/cdk1, which phosphorylates Bora, leading to activation of Plk1 and a cyclin B/cdk positive feedback loop.


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