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Electrochemical Regulation of Budding Yeast Polarity

Cells are naturally surrounded by organized electrical signals in the form of local ion fluxes, membrane potential, and electric fields (EFs) at their surface. Although the contribution of electrochemical elements to cell polarity and migration is beginning to be appreciated, underlying mechanisms a...

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Autores principales: Haupt, Armin, Campetelli, Alexis, Bonazzi, Daria, Piel, Matthieu, Chang, Fred, Minc, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4280105/
https://www.ncbi.nlm.nih.gov/pubmed/25548923
http://dx.doi.org/10.1371/journal.pbio.1002029
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author Haupt, Armin
Campetelli, Alexis
Bonazzi, Daria
Piel, Matthieu
Chang, Fred
Minc, Nicolas
author_facet Haupt, Armin
Campetelli, Alexis
Bonazzi, Daria
Piel, Matthieu
Chang, Fred
Minc, Nicolas
author_sort Haupt, Armin
collection PubMed
description Cells are naturally surrounded by organized electrical signals in the form of local ion fluxes, membrane potential, and electric fields (EFs) at their surface. Although the contribution of electrochemical elements to cell polarity and migration is beginning to be appreciated, underlying mechanisms are not known. Here we show that an exogenous EF can orient cell polarization in budding yeast (Saccharomyces cerevisiae) cells, directing the growth of mating projections towards sites of hyperpolarized membrane potential, while directing bud emergence in the opposite direction, towards sites of depolarized potential. Using an optogenetic approach, we demonstrate that a local change in membrane potential triggered by light is sufficient to direct cell polarization. Screens for mutants with altered EF responses identify genes involved in transducing electrochemical signals to the polarity machinery. Membrane potential, which is regulated by the potassium transporter Trk1p, is required for polarity orientation during mating and EF response. Membrane potential may regulate membrane charges through negatively charged phosphatidylserines (PSs), which act to position the Cdc42p-based polarity machinery. These studies thus define an electrochemical pathway that directs the orientation of cell polarization.
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spelling pubmed-42801052015-01-07 Electrochemical Regulation of Budding Yeast Polarity Haupt, Armin Campetelli, Alexis Bonazzi, Daria Piel, Matthieu Chang, Fred Minc, Nicolas PLoS Biol Research Article Cells are naturally surrounded by organized electrical signals in the form of local ion fluxes, membrane potential, and electric fields (EFs) at their surface. Although the contribution of electrochemical elements to cell polarity and migration is beginning to be appreciated, underlying mechanisms are not known. Here we show that an exogenous EF can orient cell polarization in budding yeast (Saccharomyces cerevisiae) cells, directing the growth of mating projections towards sites of hyperpolarized membrane potential, while directing bud emergence in the opposite direction, towards sites of depolarized potential. Using an optogenetic approach, we demonstrate that a local change in membrane potential triggered by light is sufficient to direct cell polarization. Screens for mutants with altered EF responses identify genes involved in transducing electrochemical signals to the polarity machinery. Membrane potential, which is regulated by the potassium transporter Trk1p, is required for polarity orientation during mating and EF response. Membrane potential may regulate membrane charges through negatively charged phosphatidylserines (PSs), which act to position the Cdc42p-based polarity machinery. These studies thus define an electrochemical pathway that directs the orientation of cell polarization. Public Library of Science 2014-12-30 /pmc/articles/PMC4280105/ /pubmed/25548923 http://dx.doi.org/10.1371/journal.pbio.1002029 Text en © 2014 Haupt et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Haupt, Armin
Campetelli, Alexis
Bonazzi, Daria
Piel, Matthieu
Chang, Fred
Minc, Nicolas
Electrochemical Regulation of Budding Yeast Polarity
title Electrochemical Regulation of Budding Yeast Polarity
title_full Electrochemical Regulation of Budding Yeast Polarity
title_fullStr Electrochemical Regulation of Budding Yeast Polarity
title_full_unstemmed Electrochemical Regulation of Budding Yeast Polarity
title_short Electrochemical Regulation of Budding Yeast Polarity
title_sort electrochemical regulation of budding yeast polarity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4280105/
https://www.ncbi.nlm.nih.gov/pubmed/25548923
http://dx.doi.org/10.1371/journal.pbio.1002029
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