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Evidence for ESCRT- and clathrin-dependent microautophagy

Microautophagy refers to a mode of autophagy in which the lysosomal or vacuolar membrane invaginates and directly engulfs target components. The molecular machinery of membrane dynamics driving microautophagy is still elusive. Using immunochemical monitoring of yeast vacuolar transmembrane proteins,...

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Detalles Bibliográficos
Autores principales: Oku, Masahide, Maeda, Yuichiro, Kagohashi, Yoko, Kondo, Takeshi, Yamada, Mai, Fujimoto, Toyoshi, Sakai, Yasuyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626533/
https://www.ncbi.nlm.nih.gov/pubmed/28838958
http://dx.doi.org/10.1083/jcb.201611029
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author Oku, Masahide
Maeda, Yuichiro
Kagohashi, Yoko
Kondo, Takeshi
Yamada, Mai
Fujimoto, Toyoshi
Sakai, Yasuyoshi
author_facet Oku, Masahide
Maeda, Yuichiro
Kagohashi, Yoko
Kondo, Takeshi
Yamada, Mai
Fujimoto, Toyoshi
Sakai, Yasuyoshi
author_sort Oku, Masahide
collection PubMed
description Microautophagy refers to a mode of autophagy in which the lysosomal or vacuolar membrane invaginates and directly engulfs target components. The molecular machinery of membrane dynamics driving microautophagy is still elusive. Using immunochemical monitoring of yeast vacuolar transmembrane proteins, Vph1 and Pho8, fused to fluorescent proteins, we obtained evidence showing an induction of microautophagy after a diauxic shift in the yeast Saccharomyces cerevisiae. Components of the endosomal sorting complex required for transport machinery were found to be required for this process, and the gateway protein of the machinery, Vps27, was observed to change its localization onto the vacuolar membrane after a diauxic shift. We revealed the functional importance of Vps27’s interaction with clathrin in this microautophagy that also contributed to uptake of lipid droplets into the vacuole. This study sheds light on the molecular mechanism of microautophagy, which does not require the core Atg proteins.
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spelling pubmed-56265332018-04-02 Evidence for ESCRT- and clathrin-dependent microautophagy Oku, Masahide Maeda, Yuichiro Kagohashi, Yoko Kondo, Takeshi Yamada, Mai Fujimoto, Toyoshi Sakai, Yasuyoshi J Cell Biol Research Articles Microautophagy refers to a mode of autophagy in which the lysosomal or vacuolar membrane invaginates and directly engulfs target components. The molecular machinery of membrane dynamics driving microautophagy is still elusive. Using immunochemical monitoring of yeast vacuolar transmembrane proteins, Vph1 and Pho8, fused to fluorescent proteins, we obtained evidence showing an induction of microautophagy after a diauxic shift in the yeast Saccharomyces cerevisiae. Components of the endosomal sorting complex required for transport machinery were found to be required for this process, and the gateway protein of the machinery, Vps27, was observed to change its localization onto the vacuolar membrane after a diauxic shift. We revealed the functional importance of Vps27’s interaction with clathrin in this microautophagy that also contributed to uptake of lipid droplets into the vacuole. This study sheds light on the molecular mechanism of microautophagy, which does not require the core Atg proteins. The Rockefeller University Press 2017-10-02 /pmc/articles/PMC5626533/ /pubmed/28838958 http://dx.doi.org/10.1083/jcb.201611029 Text en © 2017 Oku et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Oku, Masahide
Maeda, Yuichiro
Kagohashi, Yoko
Kondo, Takeshi
Yamada, Mai
Fujimoto, Toyoshi
Sakai, Yasuyoshi
Evidence for ESCRT- and clathrin-dependent microautophagy
title Evidence for ESCRT- and clathrin-dependent microautophagy
title_full Evidence for ESCRT- and clathrin-dependent microautophagy
title_fullStr Evidence for ESCRT- and clathrin-dependent microautophagy
title_full_unstemmed Evidence for ESCRT- and clathrin-dependent microautophagy
title_short Evidence for ESCRT- and clathrin-dependent microautophagy
title_sort evidence for escrt- and clathrin-dependent microautophagy
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626533/
https://www.ncbi.nlm.nih.gov/pubmed/28838958
http://dx.doi.org/10.1083/jcb.201611029
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