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Regulation of Cdc42 for polarized growth in budding yeast

The Rho GTPase Cdc42 is a central regulator of cell polarity in diverse cell types. The activity of Cdc42 is dynamically controlled in time and space to enable distinct polarization events, which generally occur along a single axis in response to spatial cues. Our understanding of the mechanisms und...

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Autores principales: Miller, Kristi E., Kang, Pil Jung, Park, Hay-Oak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shared Science Publishers OG 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7328677/
https://www.ncbi.nlm.nih.gov/pubmed/32656257
http://dx.doi.org/10.15698/mic2020.07.722
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author Miller, Kristi E.
Kang, Pil Jung
Park, Hay-Oak
author_facet Miller, Kristi E.
Kang, Pil Jung
Park, Hay-Oak
author_sort Miller, Kristi E.
collection PubMed
description The Rho GTPase Cdc42 is a central regulator of cell polarity in diverse cell types. The activity of Cdc42 is dynamically controlled in time and space to enable distinct polarization events, which generally occur along a single axis in response to spatial cues. Our understanding of the mechanisms underlying Cdc42 polarization has benefited largely from studies of the budding yeast Saccharomyces cerevisiae, a genetically tractable model organism. In budding yeast, Cdc42 activation occurs in two temporal steps in the G1 phase of the cell cycle to establish a proper growth site. Here, we review findings in budding yeast that reveal an intricate crosstalk among polarity proteins for biphasic Cdc42 regulation. The first step of Cdc42 activation may determine the axis of cell polarity, while the second step ensures robust Cdc42 polarization for growth. Biphasic Cdc42 polarization is likely to ensure the proper timing of events including the assembly and recognition of spatial landmarks and stepwise assembly of a new ring of septins, cytoskeletal GTP-binding proteins, at the incipient bud site. Biphasic activation of GTPases has also been observed in mammalian cells, suggesting that biphasic activation could be a general mechanism for signal-responsive cell polarization. Cdc42 activity is necessary for polarity establishment during normal cell division and development, but its activity has also been implicated in the promotion of aging. We also discuss negative polarity signaling and emerging concepts of Cdc42 signaling in cellular aging.
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spelling pubmed-73286772020-07-09 Regulation of Cdc42 for polarized growth in budding yeast Miller, Kristi E. Kang, Pil Jung Park, Hay-Oak Microb Cell Review The Rho GTPase Cdc42 is a central regulator of cell polarity in diverse cell types. The activity of Cdc42 is dynamically controlled in time and space to enable distinct polarization events, which generally occur along a single axis in response to spatial cues. Our understanding of the mechanisms underlying Cdc42 polarization has benefited largely from studies of the budding yeast Saccharomyces cerevisiae, a genetically tractable model organism. In budding yeast, Cdc42 activation occurs in two temporal steps in the G1 phase of the cell cycle to establish a proper growth site. Here, we review findings in budding yeast that reveal an intricate crosstalk among polarity proteins for biphasic Cdc42 regulation. The first step of Cdc42 activation may determine the axis of cell polarity, while the second step ensures robust Cdc42 polarization for growth. Biphasic Cdc42 polarization is likely to ensure the proper timing of events including the assembly and recognition of spatial landmarks and stepwise assembly of a new ring of septins, cytoskeletal GTP-binding proteins, at the incipient bud site. Biphasic activation of GTPases has also been observed in mammalian cells, suggesting that biphasic activation could be a general mechanism for signal-responsive cell polarization. Cdc42 activity is necessary for polarity establishment during normal cell division and development, but its activity has also been implicated in the promotion of aging. We also discuss negative polarity signaling and emerging concepts of Cdc42 signaling in cellular aging. Shared Science Publishers OG 2020-05-19 /pmc/articles/PMC7328677/ /pubmed/32656257 http://dx.doi.org/10.15698/mic2020.07.722 Text en Copyright: © 2020 Miller et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article released under the terms of the Creative Commons Attribution (CC BY) license, which allows the unrestricted use, distribution, and reproduction in any medium, provided the original author and source are acknowledged.
spellingShingle Review
Miller, Kristi E.
Kang, Pil Jung
Park, Hay-Oak
Regulation of Cdc42 for polarized growth in budding yeast
title Regulation of Cdc42 for polarized growth in budding yeast
title_full Regulation of Cdc42 for polarized growth in budding yeast
title_fullStr Regulation of Cdc42 for polarized growth in budding yeast
title_full_unstemmed Regulation of Cdc42 for polarized growth in budding yeast
title_short Regulation of Cdc42 for polarized growth in budding yeast
title_sort regulation of cdc42 for polarized growth in budding yeast
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7328677/
https://www.ncbi.nlm.nih.gov/pubmed/32656257
http://dx.doi.org/10.15698/mic2020.07.722
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