Inhibition of Cdc42 during mitotic exit is required for cytokinesis.

Published

Journal Article

The role of Cdc42 and its regulation during cytokinesis is not well understood. Using biochemical and imaging approaches in budding yeast, we demonstrate that Cdc42 activation peaks during the G1/S transition and during anaphase but drops during mitotic exit and cytokinesis. Cdc5/Polo kinase is an important upstream cell cycle regulator that suppresses Cdc42 activity. Failure to down-regulate Cdc42 during mitotic exit impairs the normal localization of key cytokinesis regulators-Iqg1 and Inn1-at the division site, and results in an abnormal septum. The effects of Cdc42 hyperactivation are largely mediated by the Cdc42 effector p21-activated kinase Ste20. Inhibition of Cdc42 and related Rho guanosine triphosphatases may be a general feature of cytokinesis in eukaryotes.

Full Text

Duke Authors

Cited Authors

  • Atkins, BD; Yoshida, S; Saito, K; Wu, C-F; Lew, DJ; Pellman, D

Published Date

  • July 22, 2013

Published In

Volume / Issue

  • 202 / 2

Start / End Page

  • 231 - 240

PubMed ID

  • 23878274

Pubmed Central ID

  • 23878274

Electronic International Standard Serial Number (EISSN)

  • 1540-8140

Digital Object Identifier (DOI)

  • 10.1083/jcb.201301090

Language

  • eng

Conference Location

  • United States