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Rho Family GTPases in Fission Yeast Cytokinesis

During cytokinesis, actomyosin ring constriction drives furrow formation. In animal cells, Rho GTPases drive this process through the positioning and assembly of the actomyosin ring, and through extracellular matrix remodeling within the furrow. In the fission yeast S. pombe, actomyosin ring constri...

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Detalles Bibliográficos
Autores principales: Hercyk, Brian, Das, Maitreyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6802929/
https://www.ncbi.nlm.nih.gov/pubmed/31666919
http://dx.doi.org/10.1080/19420889.2019.1678453
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author Hercyk, Brian
Das, Maitreyi
author_facet Hercyk, Brian
Das, Maitreyi
author_sort Hercyk, Brian
collection PubMed
description During cytokinesis, actomyosin ring constriction drives furrow formation. In animal cells, Rho GTPases drive this process through the positioning and assembly of the actomyosin ring, and through extracellular matrix remodeling within the furrow. In the fission yeast S. pombe, actomyosin ring constriction and septum formation are concurrent processes. While S. pombe is the primary source from which the mechanics of ring assembly and constriction stem, much less is known about the regulation of Rho GTPases that control these processes. Of the six Rho GTPases encoded in S. pombe, only Rho1, the RhoA homologue, has been shown to be essential for cytokinesis. While Rho3, Rho4, and Cdc42 have defined roles in cytokinesis, Rho2 and Rho5 play minor to no roles in this process. Here we review the roles of the Rho GTPases during cytokinesis, with a focus on their regulation, and discuss whether crosstalk between GTPases, as has been reported in other organisms, exists during cytokinesis in S. pombe.
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spelling pubmed-68029292019-10-30 Rho Family GTPases in Fission Yeast Cytokinesis Hercyk, Brian Das, Maitreyi Commun Integr Biol Mini-Review During cytokinesis, actomyosin ring constriction drives furrow formation. In animal cells, Rho GTPases drive this process through the positioning and assembly of the actomyosin ring, and through extracellular matrix remodeling within the furrow. In the fission yeast S. pombe, actomyosin ring constriction and septum formation are concurrent processes. While S. pombe is the primary source from which the mechanics of ring assembly and constriction stem, much less is known about the regulation of Rho GTPases that control these processes. Of the six Rho GTPases encoded in S. pombe, only Rho1, the RhoA homologue, has been shown to be essential for cytokinesis. While Rho3, Rho4, and Cdc42 have defined roles in cytokinesis, Rho2 and Rho5 play minor to no roles in this process. Here we review the roles of the Rho GTPases during cytokinesis, with a focus on their regulation, and discuss whether crosstalk between GTPases, as has been reported in other organisms, exists during cytokinesis in S. pombe. Taylor & Francis 2019-10-21 /pmc/articles/PMC6802929/ /pubmed/31666919 http://dx.doi.org/10.1080/19420889.2019.1678453 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Mini-Review
Hercyk, Brian
Das, Maitreyi
Rho Family GTPases in Fission Yeast Cytokinesis
title Rho Family GTPases in Fission Yeast Cytokinesis
title_full Rho Family GTPases in Fission Yeast Cytokinesis
title_fullStr Rho Family GTPases in Fission Yeast Cytokinesis
title_full_unstemmed Rho Family GTPases in Fission Yeast Cytokinesis
title_short Rho Family GTPases in Fission Yeast Cytokinesis
title_sort rho family gtpases in fission yeast cytokinesis
topic Mini-Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6802929/
https://www.ncbi.nlm.nih.gov/pubmed/31666919
http://dx.doi.org/10.1080/19420889.2019.1678453
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