Cargando…

ESCRT-III drives the final stages of CUPS maturation for unconventional protein secretion

The unconventional secretory pathway exports proteins that bypass the endoplasmic reticulum. In Saccharomyces cerevisiae, conditions that trigger Acb1 secretion via this pathway generate a Grh1 containing compartment composed of vesicles and tubules surrounded by a cup-shaped membrane and collective...

Descripción completa

Detalles Bibliográficos
Autores principales: Curwin, Amy J, Brouwers, Nathalie, Alonso Y Adell, Manuel, Teis, David, Turacchio, Gabriele, Parashuraman, Seetharaman, Ronchi, Paolo, Malhotra, Vivek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4868542/
https://www.ncbi.nlm.nih.gov/pubmed/27115345
http://dx.doi.org/10.7554/eLife.16299
_version_ 1782432179612024832
author Curwin, Amy J
Brouwers, Nathalie
Alonso Y Adell, Manuel
Teis, David
Turacchio, Gabriele
Parashuraman, Seetharaman
Ronchi, Paolo
Malhotra, Vivek
author_facet Curwin, Amy J
Brouwers, Nathalie
Alonso Y Adell, Manuel
Teis, David
Turacchio, Gabriele
Parashuraman, Seetharaman
Ronchi, Paolo
Malhotra, Vivek
author_sort Curwin, Amy J
collection PubMed
description The unconventional secretory pathway exports proteins that bypass the endoplasmic reticulum. In Saccharomyces cerevisiae, conditions that trigger Acb1 secretion via this pathway generate a Grh1 containing compartment composed of vesicles and tubules surrounded by a cup-shaped membrane and collectively called CUPS. Here we report a quantitative assay for Acb1 secretion that reveals requirements for ESCRT-I, -II, and -III but, surprisingly, without the involvement of the Vps4 AAA-ATPase. The major ESCRT-III subunit Snf7 localizes transiently to CUPS and this was accelerated in vps4Δ cells, correlating with increased Acb1 secretion. Microscopic analysis suggests that, instead of forming intraluminal vesicles with the help of Vps4, ESCRT-III/Snf7 promotes direct engulfment of preexisting Grh1 containing vesicles and tubules into a saccule to generate a mature Acb1 containing compartment. This novel multivesicular / multilamellar compartment, we suggest represents the stable secretory form of CUPS that is competent for the release of Acb1 to cells exterior. DOI: http://dx.doi.org/10.7554/eLife.16299.001
format Online
Article
Text
id pubmed-4868542
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-48685422016-05-18 ESCRT-III drives the final stages of CUPS maturation for unconventional protein secretion Curwin, Amy J Brouwers, Nathalie Alonso Y Adell, Manuel Teis, David Turacchio, Gabriele Parashuraman, Seetharaman Ronchi, Paolo Malhotra, Vivek eLife Cell Biology The unconventional secretory pathway exports proteins that bypass the endoplasmic reticulum. In Saccharomyces cerevisiae, conditions that trigger Acb1 secretion via this pathway generate a Grh1 containing compartment composed of vesicles and tubules surrounded by a cup-shaped membrane and collectively called CUPS. Here we report a quantitative assay for Acb1 secretion that reveals requirements for ESCRT-I, -II, and -III but, surprisingly, without the involvement of the Vps4 AAA-ATPase. The major ESCRT-III subunit Snf7 localizes transiently to CUPS and this was accelerated in vps4Δ cells, correlating with increased Acb1 secretion. Microscopic analysis suggests that, instead of forming intraluminal vesicles with the help of Vps4, ESCRT-III/Snf7 promotes direct engulfment of preexisting Grh1 containing vesicles and tubules into a saccule to generate a mature Acb1 containing compartment. This novel multivesicular / multilamellar compartment, we suggest represents the stable secretory form of CUPS that is competent for the release of Acb1 to cells exterior. DOI: http://dx.doi.org/10.7554/eLife.16299.001 eLife Sciences Publications, Ltd 2016-04-26 /pmc/articles/PMC4868542/ /pubmed/27115345 http://dx.doi.org/10.7554/eLife.16299 Text en © 2016, Curwin et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Curwin, Amy J
Brouwers, Nathalie
Alonso Y Adell, Manuel
Teis, David
Turacchio, Gabriele
Parashuraman, Seetharaman
Ronchi, Paolo
Malhotra, Vivek
ESCRT-III drives the final stages of CUPS maturation for unconventional protein secretion
title ESCRT-III drives the final stages of CUPS maturation for unconventional protein secretion
title_full ESCRT-III drives the final stages of CUPS maturation for unconventional protein secretion
title_fullStr ESCRT-III drives the final stages of CUPS maturation for unconventional protein secretion
title_full_unstemmed ESCRT-III drives the final stages of CUPS maturation for unconventional protein secretion
title_short ESCRT-III drives the final stages of CUPS maturation for unconventional protein secretion
title_sort escrt-iii drives the final stages of cups maturation for unconventional protein secretion
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4868542/
https://www.ncbi.nlm.nih.gov/pubmed/27115345
http://dx.doi.org/10.7554/eLife.16299
work_keys_str_mv AT curwinamyj escrtiiidrivesthefinalstagesofcupsmaturationforunconventionalproteinsecretion
AT brouwersnathalie escrtiiidrivesthefinalstagesofcupsmaturationforunconventionalproteinsecretion
AT alonsoyadellmanuel escrtiiidrivesthefinalstagesofcupsmaturationforunconventionalproteinsecretion
AT teisdavid escrtiiidrivesthefinalstagesofcupsmaturationforunconventionalproteinsecretion
AT turacchiogabriele escrtiiidrivesthefinalstagesofcupsmaturationforunconventionalproteinsecretion
AT parashuramanseetharaman escrtiiidrivesthefinalstagesofcupsmaturationforunconventionalproteinsecretion
AT ronchipaolo escrtiiidrivesthefinalstagesofcupsmaturationforunconventionalproteinsecretion
AT malhotravivek escrtiiidrivesthefinalstagesofcupsmaturationforunconventionalproteinsecretion