Cargando…

High-resolution secretory timeline from vesicle formation at the Golgi to fusion at the plasma membrane in S. cerevisiae

Most of the components in the yeast secretory pathway have been studied, yet a high-resolution temporal timeline of their participation is lacking. Here, we define the order of acquisition, lifetime, and release of critical components involved in late secretion from the Golgi to the plasma membrane....

Descripción completa

Detalles Bibliográficos
Autores principales: Gingras, Robert M, Sulpizio, Abigail M, Park, Joelle, Bretscher, Anthony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671497/
https://www.ncbi.nlm.nih.gov/pubmed/36331188
http://dx.doi.org/10.7554/eLife.78750
_version_ 1784832565383790592
author Gingras, Robert M
Sulpizio, Abigail M
Park, Joelle
Bretscher, Anthony
author_facet Gingras, Robert M
Sulpizio, Abigail M
Park, Joelle
Bretscher, Anthony
author_sort Gingras, Robert M
collection PubMed
description Most of the components in the yeast secretory pathway have been studied, yet a high-resolution temporal timeline of their participation is lacking. Here, we define the order of acquisition, lifetime, and release of critical components involved in late secretion from the Golgi to the plasma membrane. Of particular interest is the timing of the many reported effectors of the secretory vesicle Rab protein Sec4, including the myosin-V Myo2, the exocyst complex, the lgl homolog Sro7, and the small yeast-specific protein Mso1. At the trans-Golgi network (TGN) Sec4’s GEF, Sec2, is recruited to Ypt31-positive compartments, quickly followed by Sec4 and Myo2 and vesicle formation. While transported to the bud tip, the entire exocyst complex, including Sec3, is assembled on to the vesicle. Before fusion, vesicles tether for 5 s, during which the vesicle retains the exocyst complex and stimulates lateral recruitment of Rho3 on the plasma membrane. Sec2 and Myo2 are rapidly lost, followed by recruitment of cytosolic Sro7, and finally the SM protein Sec1, which appears for just 2 s prior to fusion. Perturbation experiments reveal an ordered and robust series of events during tethering that provide insights into the function of Sec4 and effector exchange.
format Online
Article
Text
id pubmed-9671497
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-96714972022-11-18 High-resolution secretory timeline from vesicle formation at the Golgi to fusion at the plasma membrane in S. cerevisiae Gingras, Robert M Sulpizio, Abigail M Park, Joelle Bretscher, Anthony eLife Cell Biology Most of the components in the yeast secretory pathway have been studied, yet a high-resolution temporal timeline of their participation is lacking. Here, we define the order of acquisition, lifetime, and release of critical components involved in late secretion from the Golgi to the plasma membrane. Of particular interest is the timing of the many reported effectors of the secretory vesicle Rab protein Sec4, including the myosin-V Myo2, the exocyst complex, the lgl homolog Sro7, and the small yeast-specific protein Mso1. At the trans-Golgi network (TGN) Sec4’s GEF, Sec2, is recruited to Ypt31-positive compartments, quickly followed by Sec4 and Myo2 and vesicle formation. While transported to the bud tip, the entire exocyst complex, including Sec3, is assembled on to the vesicle. Before fusion, vesicles tether for 5 s, during which the vesicle retains the exocyst complex and stimulates lateral recruitment of Rho3 on the plasma membrane. Sec2 and Myo2 are rapidly lost, followed by recruitment of cytosolic Sro7, and finally the SM protein Sec1, which appears for just 2 s prior to fusion. Perturbation experiments reveal an ordered and robust series of events during tethering that provide insights into the function of Sec4 and effector exchange. eLife Sciences Publications, Ltd 2022-11-04 /pmc/articles/PMC9671497/ /pubmed/36331188 http://dx.doi.org/10.7554/eLife.78750 Text en © 2022, Gingras et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Gingras, Robert M
Sulpizio, Abigail M
Park, Joelle
Bretscher, Anthony
High-resolution secretory timeline from vesicle formation at the Golgi to fusion at the plasma membrane in S. cerevisiae
title High-resolution secretory timeline from vesicle formation at the Golgi to fusion at the plasma membrane in S. cerevisiae
title_full High-resolution secretory timeline from vesicle formation at the Golgi to fusion at the plasma membrane in S. cerevisiae
title_fullStr High-resolution secretory timeline from vesicle formation at the Golgi to fusion at the plasma membrane in S. cerevisiae
title_full_unstemmed High-resolution secretory timeline from vesicle formation at the Golgi to fusion at the plasma membrane in S. cerevisiae
title_short High-resolution secretory timeline from vesicle formation at the Golgi to fusion at the plasma membrane in S. cerevisiae
title_sort high-resolution secretory timeline from vesicle formation at the golgi to fusion at the plasma membrane in s. cerevisiae
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671497/
https://www.ncbi.nlm.nih.gov/pubmed/36331188
http://dx.doi.org/10.7554/eLife.78750
work_keys_str_mv AT gingrasrobertm highresolutionsecretorytimelinefromvesicleformationatthegolgitofusionattheplasmamembraneinscerevisiae
AT sulpizioabigailm highresolutionsecretorytimelinefromvesicleformationatthegolgitofusionattheplasmamembraneinscerevisiae
AT parkjoelle highresolutionsecretorytimelinefromvesicleformationatthegolgitofusionattheplasmamembraneinscerevisiae
AT bretscheranthony highresolutionsecretorytimelinefromvesicleformationatthegolgitofusionattheplasmamembraneinscerevisiae