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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...

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Autores principales: Jose, Mini, Tollis, Sylvain, Nair, Deepak, Mitteau, Romain, Velours, Christophe, Massoni-Laporte, Aurelie, Royou, Anne, Sibarita, Jean-Baptiste, McCusker, Derek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2015
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.
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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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