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Vac8 spatially confines autophagosome formation at the vacuole in S. cerevisiae
Autophagy is initiated by the formation of a phagophore assembly site (PAS), the precursor of autophagosomes. In mammals, autophagosome formation sites form throughout the cytosol in specialized subdomains of the endoplasmic reticulum (ER). In yeast, the PAS is also generated close to the ER, but al...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899017/ https://www.ncbi.nlm.nih.gov/pubmed/31649143 http://dx.doi.org/10.1242/jcs.235002 |
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author | Hollenstein, David M. Gómez-Sánchez, Rubén Ciftci, Akif Kriegenburg, Franziska Mari, Muriel Torggler, Raffaela Licheva, Mariya Reggiori, Fulvio Kraft, Claudine |
author_facet | Hollenstein, David M. Gómez-Sánchez, Rubén Ciftci, Akif Kriegenburg, Franziska Mari, Muriel Torggler, Raffaela Licheva, Mariya Reggiori, Fulvio Kraft, Claudine |
author_sort | Hollenstein, David M. |
collection | PubMed |
description | Autophagy is initiated by the formation of a phagophore assembly site (PAS), the precursor of autophagosomes. In mammals, autophagosome formation sites form throughout the cytosol in specialized subdomains of the endoplasmic reticulum (ER). In yeast, the PAS is also generated close to the ER, but always in the vicinity of the vacuole. How the PAS is anchored to the vacuole and the functional significance of this localization are unknown. Here, we investigated the role of the PAS–vacuole connection for bulk autophagy in the yeast Saccharomyces cerevisiae. We show that Vac8 constitutes a vacuolar tether that stably anchors the PAS to the vacuole throughout autophagosome biogenesis via the PAS component Atg13. S. cerevisiae lacking Vac8 show inefficient autophagosome–vacuole fusion, and form fewer and smaller autophagosomes that often localize away from the vacuole. Thus, the stable PAS–vacuole connection established by Vac8 creates a confined space for autophagosome biogenesis between the ER and the vacuole, and allows spatial coordination of autophagosome formation and autophagosome–vacuole fusion. These findings reveal that the spatial regulation of autophagosome formation at the vacuole is required for efficient bulk autophagy. |
format | Online Article Text |
id | pubmed-6899017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-68990172019-12-10 Vac8 spatially confines autophagosome formation at the vacuole in S. cerevisiae Hollenstein, David M. Gómez-Sánchez, Rubén Ciftci, Akif Kriegenburg, Franziska Mari, Muriel Torggler, Raffaela Licheva, Mariya Reggiori, Fulvio Kraft, Claudine J Cell Sci Research Article Autophagy is initiated by the formation of a phagophore assembly site (PAS), the precursor of autophagosomes. In mammals, autophagosome formation sites form throughout the cytosol in specialized subdomains of the endoplasmic reticulum (ER). In yeast, the PAS is also generated close to the ER, but always in the vicinity of the vacuole. How the PAS is anchored to the vacuole and the functional significance of this localization are unknown. Here, we investigated the role of the PAS–vacuole connection for bulk autophagy in the yeast Saccharomyces cerevisiae. We show that Vac8 constitutes a vacuolar tether that stably anchors the PAS to the vacuole throughout autophagosome biogenesis via the PAS component Atg13. S. cerevisiae lacking Vac8 show inefficient autophagosome–vacuole fusion, and form fewer and smaller autophagosomes that often localize away from the vacuole. Thus, the stable PAS–vacuole connection established by Vac8 creates a confined space for autophagosome biogenesis between the ER and the vacuole, and allows spatial coordination of autophagosome formation and autophagosome–vacuole fusion. These findings reveal that the spatial regulation of autophagosome formation at the vacuole is required for efficient bulk autophagy. The Company of Biologists Ltd 2019-11-14 /pmc/articles/PMC6899017/ /pubmed/31649143 http://dx.doi.org/10.1242/jcs.235002 Text en © 2019. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Hollenstein, David M. Gómez-Sánchez, Rubén Ciftci, Akif Kriegenburg, Franziska Mari, Muriel Torggler, Raffaela Licheva, Mariya Reggiori, Fulvio Kraft, Claudine Vac8 spatially confines autophagosome formation at the vacuole in S. cerevisiae |
title | Vac8 spatially confines autophagosome formation at the vacuole in S. cerevisiae |
title_full | Vac8 spatially confines autophagosome formation at the vacuole in S. cerevisiae |
title_fullStr | Vac8 spatially confines autophagosome formation at the vacuole in S. cerevisiae |
title_full_unstemmed | Vac8 spatially confines autophagosome formation at the vacuole in S. cerevisiae |
title_short | Vac8 spatially confines autophagosome formation at the vacuole in S. cerevisiae |
title_sort | vac8 spatially confines autophagosome formation at the vacuole in s. cerevisiae |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899017/ https://www.ncbi.nlm.nih.gov/pubmed/31649143 http://dx.doi.org/10.1242/jcs.235002 |
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