Cdc42 prevents precocious Rho1 activation during cytokinesis in a Pak1-dependent manner

Author:

Onwubiko Udo N.1,Kalathil Dhanya2,Koory Emma1ORCID,Pokharel Sahara1,Roberts Hayden1,Mitoubsi Ahmad1,Das Maitreyi12ORCID

Affiliation:

1. University of Tennessee 1 Department of Biochemistry & Cellular and Molecular Biology , , Knoxville, TN 37996 , USA

2. Boston College 2 Biology Department , , Chestnut Hill, MA 02467 , USA

Abstract

ABSTRACT During cytokinesis, a series of coordinated events partition a dividing cell. Accurate regulation of cytokinesis is essential for proliferation and genome integrity. In fission yeast, these coordinated events ensure that the actomyosin ring and septum start ingressing only after chromosome segregation. How cytokinetic events are coordinated remains unclear. The GTPase Cdc42 promotes recruitment of certain cell wall-building enzymes whereas the GTPase Rho1 activates these enzymes. We show that Cdc42 prevents early Rho1 activation during fission yeast cytokinesis. Using an active Rho probe, we find that although the Rho1 activators Rgf1 and Rgf3 localize to the division site in early anaphase, Rho1 is not activated until late anaphase, just before the onset of ring constriction. We find that loss of Cdc42 activation enables precocious Rho1 activation in early anaphase. Furthermore, we provide functional and genetic evidence that Cdc42-dependent Rho1 inhibition is mediated by the Cdc42 target Pak1 kinase. Our work proposes a mechanism of Rho1 regulation by active Cdc42 to coordinate timely septum formation and cytokinesis fidelity.

Funder

National Science Foundation

National Institutes of Health

Publisher

The Company of Biologists

Subject

Cell Biology

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