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A quantitative imaging-based screen reveals the exocyst as a network hub connecting endocytosis and exocytosis
The coupling of endocytosis and exocytosis underlies fundamental biological processes ranging from fertilization to neuronal activity and cellular polarity. However, the mechanisms governing the spatial organization of endocytosis and exocytosis require clarification. Using a quantitative imaging-ba...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4571305/ https://www.ncbi.nlm.nih.gov/pubmed/25947137 http://dx.doi.org/10.1091/mbc.E14-11-1527 |
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author | Jose, Mini Tollis, Sylvain Nair, Deepak Mitteau, Romain Velours, Christophe Massoni-Laporte, Aurelie Royou, Anne Sibarita, Jean-Baptiste McCusker, Derek |
author_facet | Jose, Mini Tollis, Sylvain Nair, Deepak Mitteau, Romain Velours, Christophe Massoni-Laporte, Aurelie Royou, Anne Sibarita, Jean-Baptiste McCusker, Derek |
author_sort | Jose, Mini |
collection | PubMed |
description | The coupling of endocytosis and exocytosis underlies fundamental biological processes ranging from fertilization to neuronal activity and cellular polarity. However, the mechanisms governing the spatial organization of endocytosis and exocytosis require clarification. Using a quantitative imaging-based screen in budding yeast, we identified 89 mutants displaying defects in the localization of either one or both pathways. High-resolution single-vesicle tracking revealed that the endocytic and exocytic mutants she4∆ and bud6∆ alter post-Golgi vesicle dynamics in opposite ways. The endocytic and exocytic pathways display strong interdependence during polarity establishment while being more independent during polarity maintenance. Systems analysis identified the exocyst complex as a key network hub, rich in genetic interactions with endocytic and exocytic components. Exocyst mutants displayed altered endocytic and post-Golgi vesicle dynamics and interspersed endocytic and exocytic domains compared with control cells. These data are consistent with an important role for the exocyst in coordinating endocytosis and exocytosis. |
format | Online Article Text |
id | pubmed-4571305 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-45713052015-09-29 A quantitative imaging-based screen reveals the exocyst as a network hub connecting endocytosis and exocytosis Jose, Mini Tollis, Sylvain Nair, Deepak Mitteau, Romain Velours, Christophe Massoni-Laporte, Aurelie Royou, Anne Sibarita, Jean-Baptiste McCusker, Derek Mol Biol Cell Articles The coupling of endocytosis and exocytosis underlies fundamental biological processes ranging from fertilization to neuronal activity and cellular polarity. However, the mechanisms governing the spatial organization of endocytosis and exocytosis require clarification. Using a quantitative imaging-based screen in budding yeast, we identified 89 mutants displaying defects in the localization of either one or both pathways. High-resolution single-vesicle tracking revealed that the endocytic and exocytic mutants she4∆ and bud6∆ alter post-Golgi vesicle dynamics in opposite ways. The endocytic and exocytic pathways display strong interdependence during polarity establishment while being more independent during polarity maintenance. Systems analysis identified the exocyst complex as a key network hub, rich in genetic interactions with endocytic and exocytic components. Exocyst mutants displayed altered endocytic and post-Golgi vesicle dynamics and interspersed endocytic and exocytic domains compared with control cells. These data are consistent with an important role for the exocyst in coordinating endocytosis and exocytosis. The American Society for Cell Biology 2015-07-01 /pmc/articles/PMC4571305/ /pubmed/25947137 http://dx.doi.org/10.1091/mbc.E14-11-1527 Text en © 2015 Jose et al. 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 (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. |
spellingShingle | Articles Jose, Mini Tollis, Sylvain Nair, Deepak Mitteau, Romain Velours, Christophe Massoni-Laporte, Aurelie Royou, Anne Sibarita, Jean-Baptiste McCusker, Derek A quantitative imaging-based screen reveals the exocyst as a network hub connecting endocytosis and exocytosis |
title | A quantitative imaging-based screen reveals the exocyst as a network hub connecting endocytosis and exocytosis |
title_full | A quantitative imaging-based screen reveals the exocyst as a network hub connecting endocytosis and exocytosis |
title_fullStr | A quantitative imaging-based screen reveals the exocyst as a network hub connecting endocytosis and exocytosis |
title_full_unstemmed | A quantitative imaging-based screen reveals the exocyst as a network hub connecting endocytosis and exocytosis |
title_short | A quantitative imaging-based screen reveals the exocyst as a network hub connecting endocytosis and exocytosis |
title_sort | quantitative imaging-based screen reveals the exocyst as a network hub connecting endocytosis and exocytosis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4571305/ https://www.ncbi.nlm.nih.gov/pubmed/25947137 http://dx.doi.org/10.1091/mbc.E14-11-1527 |
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