4.7 Article

On the assembly of the mitotic spindle, bistability and hysteresis

Journal

CELLULAR AND MOLECULAR LIFE SCIENCES
Volume 80, Issue 4, Pages -

Publisher

SPRINGER BASEL AG
DOI: 10.1007/s00018-023-04727-6

Keywords

Spindle assembly; i-Cdk1; Checkpoint; Genome stability; Chromosome segregation; Cell cycle progression

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During cell division, the activation of the cyclin B-cdk1 (Cdk1) complex plays a crucial role in transitioning from interphase to mitosis. Positive Cdk1 activation loops and inhibition of Cdk1 counteracting phosphatases ensure the irreversible establishment of mitosis. Mitosis is a bistable state that shows hysteresis, enabling cells to tolerate moderate drops in Cdk1 activity without exiting mitosis. Recent evidence suggests that stable mitosis and hysteresis are also necessary for the assembly of the mitotic spindle, contributing to the forward progression of mitosis.
During cell division, the transition from interphase to mitosis is dictated by activation of the cyclin B-cdk1 (Cdk1) complex, master mitotic kinase. During interphase, Cdk1 accumulates in an inactive state (pre-Cdk1). When Cdk1 overcomes a certain threshold of activity upon initial activation of pre-Cdk1, then the stockpiled pre-Cdk1 is rapidly converted into overshooting active Cdk1, and mitosis is established irreversibly in a switch-like fashion. This is granted by positive Cdk1 activation loops and the concomitant inactivation of Cdk1 counteracting phosphatases, empowering Cdk1 activity and favoring the Cdk1-dependent phosphorylations that are required to establish mitosis. These circuitries prevent backtracking and ensure unidirectionality so that interphase and mitosis are considered bistable states. Mitosis also shows hysteresis, meaning that the levels of Cdk1 activity needed to establish mitosis are higher than those required to maintain it; therefore, once in mitosis cells can tolerate moderate drops in Cdk1 activity without exiting mitosis. Whether these features have other functional implications in addition to the general action of preventing backtracking is unknown. Here, we contextualize these concepts in the view of recent evidence indicating that loss of activity of small and compartmentalized amounts of Cdk1 within mitosis is necessary to assemble the mitotic spindle, the structure required to segregate replicated chromosomes. We further propose that, in addition to prevent backtracking, the stability and hysteresis properties of mitosis are also essential to move forward in mitosis by allowing cells to bear small, localized, drops in Cdk1 activity that are necessary to build the mitotic spindle.

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