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Phosphorylation state defines discrete roles for monopolin in chromosome attachment and spindle elongation.


ABSTRACT: It is unknown how oscillations in Cdk1 activity drive the dramatic changes in chromosome and spindle dynamics that occur at the metaphase/anaphase transition.We show that the Schizosaccharomyces pombe monopolin complex has distinct functions in metaphase and anaphase that are determined by the phosphorylation state of its Mde4 subunit. When Cdk1 activity is high in metaphase, Mde4 is hyperphosphorylated on Cdk1 phosphorylation sites and localizes to kinetochores. A nonphosphorylatable mutant of Mde4 does not localize to kinetochores, appears prematurely on the metaphase spindle, and interferes with spindle dynamics and chromosome segregation, illustrating the importance of Cdk1 phosphorylation in regulating metaphase monopolin activity. When Cdk1 activity drops in anaphase, dephosphorylation of Mde4 triggers monopolin localization to the mitotic spindle, where it promotes spindle elongation and integrity, coupling the late mitotic loss of Cdk1 activity to anaphase spindle dynamics.Together, these findings illustrate how the sequential phosphorylation and dephosphorylation of monopolin helps ensure the orderly execution of discrete steps in mitosis.

SUBMITTER: Choi SH 

PROVIDER: S-EPMC2726783 | biostudies-literature | 2009 Jun

REPOSITORIES: biostudies-literature

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Phosphorylation state defines discrete roles for monopolin in chromosome attachment and spindle elongation.

Choi Sung Hugh SH   Péli-Gulli Marie-Pierre MP   Mcleod Iain I   Sarkeshik Ali A   Yates John R JR   Simanis Viesturs V   McCollum Dannel D  

Current biology : CB 20090611 12


<h4>Background</h4>It is unknown how oscillations in Cdk1 activity drive the dramatic changes in chromosome and spindle dynamics that occur at the metaphase/anaphase transition.<h4>Results</h4>We show that the Schizosaccharomyces pombe monopolin complex has distinct functions in metaphase and anaphase that are determined by the phosphorylation state of its Mde4 subunit. When Cdk1 activity is high in metaphase, Mde4 is hyperphosphorylated on Cdk1 phosphorylation sites and localizes to kinetochore  ...[more]

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