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Exploratory polarization facilitates mating partner selection in Saccharomyces cerevisiae
Yeast decode pheromone gradients to locate mating partners, providing a model for chemotropism. How yeast polarize toward a single partner in crowded environments is unclear. Initially, cells often polarize in unproductive directions, but then they relocate the polarity site until two partners’ pola...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8101489/ https://www.ncbi.nlm.nih.gov/pubmed/33689470 http://dx.doi.org/10.1091/mbc.E21-02-0068 |
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author | Clark-Cotton, Manuella R. Henderson, Nicholas T. Pablo, Michael Ghose, Debraj Elston, Timothy C. Lew, Daniel J. |
author_facet | Clark-Cotton, Manuella R. Henderson, Nicholas T. Pablo, Michael Ghose, Debraj Elston, Timothy C. Lew, Daniel J. |
author_sort | Clark-Cotton, Manuella R. |
collection | PubMed |
description | Yeast decode pheromone gradients to locate mating partners, providing a model for chemotropism. How yeast polarize toward a single partner in crowded environments is unclear. Initially, cells often polarize in unproductive directions, but then they relocate the polarity site until two partners’ polarity sites align, whereupon the cells “commit” to each other by stabilizing polarity to promote fusion. Here we address the role of the early mobile polarity sites. We found that commitment by either partner failed if just one partner was defective in generating, orienting, or stabilizing its mobile polarity sites. Mobile polarity sites were enriched for pheromone receptors and G proteins, and we suggest that such sites engage in an exploratory search of the local pheromone landscape, stabilizing only when they detect elevated pheromone levels. Mobile polarity sites were also enriched for pheromone secretion factors, and simulations suggest that only focal secretion at polarity sites would produce high pheromone concentrations at the partner’s polarity site, triggering commitment. |
format | Online Article Text |
id | pubmed-8101489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-81014892021-07-16 Exploratory polarization facilitates mating partner selection in Saccharomyces cerevisiae Clark-Cotton, Manuella R. Henderson, Nicholas T. Pablo, Michael Ghose, Debraj Elston, Timothy C. Lew, Daniel J. Mol Biol Cell Articles Yeast decode pheromone gradients to locate mating partners, providing a model for chemotropism. How yeast polarize toward a single partner in crowded environments is unclear. Initially, cells often polarize in unproductive directions, but then they relocate the polarity site until two partners’ polarity sites align, whereupon the cells “commit” to each other by stabilizing polarity to promote fusion. Here we address the role of the early mobile polarity sites. We found that commitment by either partner failed if just one partner was defective in generating, orienting, or stabilizing its mobile polarity sites. Mobile polarity sites were enriched for pheromone receptors and G proteins, and we suggest that such sites engage in an exploratory search of the local pheromone landscape, stabilizing only when they detect elevated pheromone levels. Mobile polarity sites were also enriched for pheromone secretion factors, and simulations suggest that only focal secretion at polarity sites would produce high pheromone concentrations at the partner’s polarity site, triggering commitment. The American Society for Cell Biology 2021-05-01 /pmc/articles/PMC8101489/ /pubmed/33689470 http://dx.doi.org/10.1091/mbc.E21-02-0068 Text en © 2021 Clark-Cotton et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/3.0/This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License. |
spellingShingle | Articles Clark-Cotton, Manuella R. Henderson, Nicholas T. Pablo, Michael Ghose, Debraj Elston, Timothy C. Lew, Daniel J. Exploratory polarization facilitates mating partner selection in Saccharomyces cerevisiae |
title | Exploratory polarization facilitates mating partner selection in Saccharomyces cerevisiae |
title_full | Exploratory polarization facilitates mating partner selection in Saccharomyces cerevisiae |
title_fullStr | Exploratory polarization facilitates mating partner selection in Saccharomyces cerevisiae |
title_full_unstemmed | Exploratory polarization facilitates mating partner selection in Saccharomyces cerevisiae |
title_short | Exploratory polarization facilitates mating partner selection in Saccharomyces cerevisiae |
title_sort | exploratory polarization facilitates mating partner selection in saccharomyces cerevisiae |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8101489/ https://www.ncbi.nlm.nih.gov/pubmed/33689470 http://dx.doi.org/10.1091/mbc.E21-02-0068 |
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