Cargando…

A novel member of the rho family of small GTP-binding proteins is specifically required for cytokinesis

Several members of the rho/rac family of small GTP-binding proteins are known to regulate the distribution of the actin cytoskeleton in various subcellular processes. We describe here a novel rac protein, racE, which is specifically required for cytokinesis, an actomyosin-mediated process. The racE...

Descripción completa

Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2120902/
https://www.ncbi.nlm.nih.gov/pubmed/8682867
_version_ 1782141604179476480
collection PubMed
description Several members of the rho/rac family of small GTP-binding proteins are known to regulate the distribution of the actin cytoskeleton in various subcellular processes. We describe here a novel rac protein, racE, which is specifically required for cytokinesis, an actomyosin-mediated process. The racE gene was isolated in a molecular genetic screen devised to isolate genes required for cytokinesis in Dictyostelium. Phenotypic characterization of racE mutants revealed that racE is not essential for any other cell motility event, including phagocytosis, chemotaxis, capping, or development. Our data provide the first genetic evidence for the essential requirement of a rho-like protein, specifically in cytokinesis, and suggest a role for these proteins in coordinating cytokinesis with the mitotic events of the cell cycle.
format Text
id pubmed-2120902
institution National Center for Biotechnology Information
language English
publishDate 1996
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-21209022008-05-01 A novel member of the rho family of small GTP-binding proteins is specifically required for cytokinesis J Cell Biol Articles Several members of the rho/rac family of small GTP-binding proteins are known to regulate the distribution of the actin cytoskeleton in various subcellular processes. We describe here a novel rac protein, racE, which is specifically required for cytokinesis, an actomyosin-mediated process. The racE gene was isolated in a molecular genetic screen devised to isolate genes required for cytokinesis in Dictyostelium. Phenotypic characterization of racE mutants revealed that racE is not essential for any other cell motility event, including phagocytosis, chemotaxis, capping, or development. Our data provide the first genetic evidence for the essential requirement of a rho-like protein, specifically in cytokinesis, and suggest a role for these proteins in coordinating cytokinesis with the mitotic events of the cell cycle. The Rockefeller University Press 1996-06-02 /pmc/articles/PMC2120902/ /pubmed/8682867 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
A novel member of the rho family of small GTP-binding proteins is specifically required for cytokinesis
title A novel member of the rho family of small GTP-binding proteins is specifically required for cytokinesis
title_full A novel member of the rho family of small GTP-binding proteins is specifically required for cytokinesis
title_fullStr A novel member of the rho family of small GTP-binding proteins is specifically required for cytokinesis
title_full_unstemmed A novel member of the rho family of small GTP-binding proteins is specifically required for cytokinesis
title_short A novel member of the rho family of small GTP-binding proteins is specifically required for cytokinesis
title_sort novel member of the rho family of small gtp-binding proteins is specifically required for cytokinesis
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2120902/
https://www.ncbi.nlm.nih.gov/pubmed/8682867