Unknown

Dataset Information

0

Inactivation of Cdh1 by synergistic action of Cdk1 and polo kinase is necessary for proper assembly of the mitotic spindle.


ABSTRACT: Separation of duplicated centrosomes (spindle-pole bodies or SPBs in yeast) is a crucial step in the biogenesis of the mitotic spindle. In vertebrates, centrosome separation requires the BimC family kinesin Eg5 and the activities of Cdk1 and polo kinase; however, the roles of these kinases are not fully understood. In Saccharomyces cerevisiae, SPB separation also requires activated Cdk1 and the plus-end kinesins Cin8 (homologous to vertebrate Eg5) and Kip1. Here we report that polo kinase has a role in the separation of SPBs. We show that adequate accumulation of Cin8 and Kip1 requires inactivation of the anaphase-promoting complex-activator Cdh1 through sequential phosphorylation by Cdk1 and polo kinase. In this process, Cdk1 functions as a priming kinase in that Cdk1-mediated phosphorylation creates a binding site for polo kinase,which further phosphorylates Cdh1. Thus, Cdh1 inactivation through the synergistic action of Cdk1 and polo kinase provides a new model for inactivation of cell-cycle effectors.

SUBMITTER: Crasta K 

PROVIDER: S-EPMC2677644 | biostudies-literature | 2008 Jun

REPOSITORIES: biostudies-literature

altmetric image

Publications

Inactivation of Cdh1 by synergistic action of Cdk1 and polo kinase is necessary for proper assembly of the mitotic spindle.

Crasta Karen K   Lim Hong Hwa HH   Giddings Thomas H TH   Winey Mark M   Surana Uttam U  

Nature cell biology 20080525 6


Separation of duplicated centrosomes (spindle-pole bodies or SPBs in yeast) is a crucial step in the biogenesis of the mitotic spindle. In vertebrates, centrosome separation requires the BimC family kinesin Eg5 and the activities of Cdk1 and polo kinase; however, the roles of these kinases are not fully understood. In Saccharomyces cerevisiae, SPB separation also requires activated Cdk1 and the plus-end kinesins Cin8 (homologous to vertebrate Eg5) and Kip1. Here we report that polo kinase has a  ...[more]

Similar Datasets

| S-EPMC4013160 | biostudies-literature
| S-EPMC10432340 | biostudies-literature
| S-EPMC6726907 | biostudies-literature
| S-SCDT-EMBOR-2018-47495-T | biostudies-other
| S-EPMC6765185 | biostudies-literature
| S-EPMC3969148 | biostudies-literature
| S-EPMC7406356 | biostudies-literature
| S-EPMC1636773 | biostudies-literature
| S-EPMC5549795 | biostudies-literature
| S-EPMC6520610 | biostudies-literature