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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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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 |
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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 |
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