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Spatial segregation of polarity factors into distinct cortical clusters is required for cell polarity control
Cell polarity is regulated by evolutionarily conserved polarity factors whose precise higher-order organization at the cell cortex is largely unknown. Here we image frontally the cortex of live fission yeast cells using time-lapse and super-resolution microscopy. Interestingly, we find that polarity...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3674234/ https://www.ncbi.nlm.nih.gov/pubmed/23673619 http://dx.doi.org/10.1038/ncomms2813 |
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author | Dodgson, James Chessel, Anatole Yamamoto, Miki Vaggi, Federico Cox, Susan Rosten, Edward Albrecht, David Geymonat, Marco Csikasz-Nagy, Attila Sato, Masamitsu Carazo-Salas, Rafael E. |
author_facet | Dodgson, James Chessel, Anatole Yamamoto, Miki Vaggi, Federico Cox, Susan Rosten, Edward Albrecht, David Geymonat, Marco Csikasz-Nagy, Attila Sato, Masamitsu Carazo-Salas, Rafael E. |
author_sort | Dodgson, James |
collection | PubMed |
description | Cell polarity is regulated by evolutionarily conserved polarity factors whose precise higher-order organization at the cell cortex is largely unknown. Here we image frontally the cortex of live fission yeast cells using time-lapse and super-resolution microscopy. Interestingly, we find that polarity factors are organized in discrete cortical clusters resolvable to ~50–100 nm in size, which can form and become cortically enriched by oligomerization. We show that forced co-localization of the polarity factors Tea1 and Tea3 results in polarity defects, suggesting that the maintenance of both factors in distinct clusters is required for polarity. However, during mitosis, their co-localization increases, and Tea3 helps to retain the cortical localization of the Tea1 growth landmark in preparation for growth reactivation following mitosis. Thus, regulated spatial segregation of polarity factor clusters provides a means to spatio-temporally control cell polarity at the cell cortex. We observe similar clusters in Saccharomyces cerevisiae and Caenorhabditis elegans cells, indicating this could be a universal regulatory feature. |
format | Online Article Text |
id | pubmed-3674234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-36742342013-06-06 Spatial segregation of polarity factors into distinct cortical clusters is required for cell polarity control Dodgson, James Chessel, Anatole Yamamoto, Miki Vaggi, Federico Cox, Susan Rosten, Edward Albrecht, David Geymonat, Marco Csikasz-Nagy, Attila Sato, Masamitsu Carazo-Salas, Rafael E. Nat Commun Article Cell polarity is regulated by evolutionarily conserved polarity factors whose precise higher-order organization at the cell cortex is largely unknown. Here we image frontally the cortex of live fission yeast cells using time-lapse and super-resolution microscopy. Interestingly, we find that polarity factors are organized in discrete cortical clusters resolvable to ~50–100 nm in size, which can form and become cortically enriched by oligomerization. We show that forced co-localization of the polarity factors Tea1 and Tea3 results in polarity defects, suggesting that the maintenance of both factors in distinct clusters is required for polarity. However, during mitosis, their co-localization increases, and Tea3 helps to retain the cortical localization of the Tea1 growth landmark in preparation for growth reactivation following mitosis. Thus, regulated spatial segregation of polarity factor clusters provides a means to spatio-temporally control cell polarity at the cell cortex. We observe similar clusters in Saccharomyces cerevisiae and Caenorhabditis elegans cells, indicating this could be a universal regulatory feature. Nature Pub. Group 2013-05-14 /pmc/articles/PMC3674234/ /pubmed/23673619 http://dx.doi.org/10.1038/ncomms2813 Text en Copyright © 2013, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Article Dodgson, James Chessel, Anatole Yamamoto, Miki Vaggi, Federico Cox, Susan Rosten, Edward Albrecht, David Geymonat, Marco Csikasz-Nagy, Attila Sato, Masamitsu Carazo-Salas, Rafael E. Spatial segregation of polarity factors into distinct cortical clusters is required for cell polarity control |
title | Spatial segregation of polarity factors into distinct cortical clusters is required for cell polarity control |
title_full | Spatial segregation of polarity factors into distinct cortical clusters is required for cell polarity control |
title_fullStr | Spatial segregation of polarity factors into distinct cortical clusters is required for cell polarity control |
title_full_unstemmed | Spatial segregation of polarity factors into distinct cortical clusters is required for cell polarity control |
title_short | Spatial segregation of polarity factors into distinct cortical clusters is required for cell polarity control |
title_sort | spatial segregation of polarity factors into distinct cortical clusters is required for cell polarity control |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3674234/ https://www.ncbi.nlm.nih.gov/pubmed/23673619 http://dx.doi.org/10.1038/ncomms2813 |
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