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Yeast Cdc42 functions at a late step in exocytosis, specifically during polarized growth of the emerging bud
The Rho family GTPase Cdc42 is a key regulator of cell polarity and cytoskeletal organization in eukaryotic cells. In yeast, the role of Cdc42 in polarization of cell growth includes polarization of the actin cytoskeleton, which delivers secretory vesicles to growth sites at the plasma membrane. We...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2001
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2198861/ https://www.ncbi.nlm.nih.gov/pubmed/11706050 http://dx.doi.org/10.1083/jcb.200106065 |
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author | Adamo, Joan E. Moskow, John J. Gladfelter, Amy S. Viterbo, Domenic Lew, Daniel J. Brennwald, Patrick J. |
author_facet | Adamo, Joan E. Moskow, John J. Gladfelter, Amy S. Viterbo, Domenic Lew, Daniel J. Brennwald, Patrick J. |
author_sort | Adamo, Joan E. |
collection | PubMed |
description | The Rho family GTPase Cdc42 is a key regulator of cell polarity and cytoskeletal organization in eukaryotic cells. In yeast, the role of Cdc42 in polarization of cell growth includes polarization of the actin cytoskeleton, which delivers secretory vesicles to growth sites at the plasma membrane. We now describe a novel temperature-sensitive mutant, cdc42-6, that reveals a role for Cdc42 in docking and fusion of secretory vesicles that is independent of its role in actin polarization. cdc42-6 mutants can polarize actin and deliver secretory vesicles to the bud, but fail to fuse those vesicles with the plasma membrane. This defect is manifested only during the early stages of bud formation when growth is most highly polarized, and appears to reflect a requirement for Cdc42 to maintain maximally active exocytic machinery at sites of high vesicle throughput. Extensive genetic interactions between cdc42-6 and mutations in exocytic components support this hypothesis, and indicate a functional overlap with Rho3, which also regulates both actin organization and exocytosis. Localization data suggest that the defect in cdc42-6 cells is not at the level of the localization of the exocytic apparatus. Rather, we suggest that Cdc42 acts as an allosteric regulator of the vesicle docking and fusion apparatus to provide maximal function at sites of polarized growth. |
format | Text |
id | pubmed-2198861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2001 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21988612008-05-01 Yeast Cdc42 functions at a late step in exocytosis, specifically during polarized growth of the emerging bud Adamo, Joan E. Moskow, John J. Gladfelter, Amy S. Viterbo, Domenic Lew, Daniel J. Brennwald, Patrick J. J Cell Biol Article The Rho family GTPase Cdc42 is a key regulator of cell polarity and cytoskeletal organization in eukaryotic cells. In yeast, the role of Cdc42 in polarization of cell growth includes polarization of the actin cytoskeleton, which delivers secretory vesicles to growth sites at the plasma membrane. We now describe a novel temperature-sensitive mutant, cdc42-6, that reveals a role for Cdc42 in docking and fusion of secretory vesicles that is independent of its role in actin polarization. cdc42-6 mutants can polarize actin and deliver secretory vesicles to the bud, but fail to fuse those vesicles with the plasma membrane. This defect is manifested only during the early stages of bud formation when growth is most highly polarized, and appears to reflect a requirement for Cdc42 to maintain maximally active exocytic machinery at sites of high vesicle throughput. Extensive genetic interactions between cdc42-6 and mutations in exocytic components support this hypothesis, and indicate a functional overlap with Rho3, which also regulates both actin organization and exocytosis. Localization data suggest that the defect in cdc42-6 cells is not at the level of the localization of the exocytic apparatus. Rather, we suggest that Cdc42 acts as an allosteric regulator of the vesicle docking and fusion apparatus to provide maximal function at sites of polarized growth. The Rockefeller University Press 2001-11-12 /pmc/articles/PMC2198861/ /pubmed/11706050 http://dx.doi.org/10.1083/jcb.200106065 Text en Copyright © 2001, The Rockefeller University Press 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 | Article Adamo, Joan E. Moskow, John J. Gladfelter, Amy S. Viterbo, Domenic Lew, Daniel J. Brennwald, Patrick J. Yeast Cdc42 functions at a late step in exocytosis, specifically during polarized growth of the emerging bud |
title | Yeast Cdc42 functions at a late step in exocytosis, specifically during polarized growth of the emerging bud |
title_full | Yeast Cdc42 functions at a late step in exocytosis, specifically during polarized growth of the emerging bud |
title_fullStr | Yeast Cdc42 functions at a late step in exocytosis, specifically during polarized growth of the emerging bud |
title_full_unstemmed | Yeast Cdc42 functions at a late step in exocytosis, specifically during polarized growth of the emerging bud |
title_short | Yeast Cdc42 functions at a late step in exocytosis, specifically during polarized growth of the emerging bud |
title_sort | yeast cdc42 functions at a late step in exocytosis, specifically during polarized growth of the emerging bud |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2198861/ https://www.ncbi.nlm.nih.gov/pubmed/11706050 http://dx.doi.org/10.1083/jcb.200106065 |
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