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Inhibition of Cdc42 during mitotic exit is required for cytokinesis

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TLDR
A decrease in Cdc42 activation during mitotic exit is necessary to allow localization of key cytokinesis regulators and proper septum formation.
Abstract
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.

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Journal ArticleDOI

Cell Polarity in Yeast.

TL;DR: Findings from budding and fission yeasts that reveal both a conserved core polarity circuit and several adaptations that each organism exploits to fulfill the needs of its lifestyle are reviewed.
Journal ArticleDOI

Distinct roles of Rho1, Cdc42, and Cyk3 in septum formation and abscission during yeast cytokinesis

TL;DR: Rho1 inactivation by Cyk3 promotes primary septum formation and cleavage-furrow ingression, whereas Rho1 activation or Cdc42 inactivation promotes secondary septal formation and abscission.
Journal ArticleDOI

Cell cycle entry triggers a switch between two modes of Cdc42 activation during yeast polarization

TL;DR: Using optogenetics, yeast polarization is probed and it is found that local recruitment of Cdc24 or Bem1 is sufficient to induce polarization by triggering self-sustaining Cdc42 activity, however, the response to these perturbations depends on the recruited molecule, the cell cycle stage, and existing polarization sites.
Journal ArticleDOI

Cell-cycle control of cell polarity in yeast.

TL;DR: It is reported that yeast daughter cells can polarize Cdc42 before CDK activation at start, and it is shown that G1 cyclin‐dependent kinase activity enables localization of a subset of CDC42 effectors to sites enriched for C dc42.
Journal ArticleDOI

The final cut: cell polarity meets cytokinesis at the bud neck in S. cerevisiae

TL;DR: This review recapitulates how budding yeast cells undergo polarized processes at the bud neck for cell division, and divides asymmetrically, producing two cells with distinct sizes and fates.
References
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Book ChapterDOI

Getting started with yeast.

TL;DR: The yeast Saccharomyces cerevisiae is now recognized as a model system representing a simple eukaryote whose genome can be easily manipulated and made particularly accessible to gene cloning and genetic engineering techniques.
Journal ArticleDOI

Genetic Control of the Cell Division Cycle in Yeast

TL;DR: Two features which distinguish the cell cycle of Saccharomyces cerevisiae from most other eukaryotes are particularly useful for an analysis of the gene functions that control the cell division cycle.
Journal ArticleDOI

A chemical switch for inhibitor-sensitive alleles of any protein kinase

TL;DR: A chemical genetic strategy for sensitizing protein kinases to cell-permeable molecules that do not inhibit wild-type kinases is described, allowing for rapid functional characterization of members of this important gene family.
Journal ArticleDOI

Targets of the cyclin-dependent kinase Cdk1

TL;DR: The identities of these substrates reveal that Cdk1 employs a global regulatory strategy involving phosphorylation of other regulatory molecules as well as phosphorylated of the molecular machines that drive cell-cycle events.
Journal ArticleDOI

Overview of manual and automated DNA sequencing by the dideoxy chain termination method

TL;DR: A brief evaluation of commercial efforts to automate DNA sample preparation, separation, and data acquisition is presented, including instruments currently available as well as new concepts potentially amenable to automation.
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