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Convergence of secretory, endosomal, and autophagic routes in trans-Golgi–associated lysosomes
At the trans-Golgi, complex traffic connections exist to the endolysosomal system additional to the main Golgi-to–plasma membrane secretory route. Here, we investigated three hits in a Drosophila screen displaying secretory cargo accumulation in autophagic vesicles: ESCRT-III component Vps20, SNARE-...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9577102/ https://www.ncbi.nlm.nih.gov/pubmed/36239631 http://dx.doi.org/10.1083/jcb.202203045 |
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author | Zhou, Lingjian Xue, Xutong Yang, Ke Feng, Zhi Liu, Min Pastor-Pareja, José C. |
author_facet | Zhou, Lingjian Xue, Xutong Yang, Ke Feng, Zhi Liu, Min Pastor-Pareja, José C. |
author_sort | Zhou, Lingjian |
collection | PubMed |
description | At the trans-Golgi, complex traffic connections exist to the endolysosomal system additional to the main Golgi-to–plasma membrane secretory route. Here, we investigated three hits in a Drosophila screen displaying secretory cargo accumulation in autophagic vesicles: ESCRT-III component Vps20, SNARE-binding Rop, and lysosomal pump subunit VhaPPA1-1. We found that Vps20, Rop, and lysosomal markers localize near the trans-Golgi. Furthermore, we document that the vicinity of the trans-Golgi is the main cellular location for lysosomes and that early, late, and recycling endosomes associate as well with a trans-Golgi–associated degradative compartment where basal microautophagy of secretory cargo and other materials occurs. Disruption of this compartment causes cargo accumulation in our hits, including Munc18 homolog Rop, required with Syx1 and Syx4 for Rab11-mediated endosomal recycling. Finally, besides basal microautophagy, we show that the trans-Golgi–associated degradative compartment contributes to the growth of autophagic vesicles in developmental and starvation-induced macroautophagy. Our results argue that the fly trans-Golgi is the gravitational center of the whole endomembrane system. |
format | Online Article Text |
id | pubmed-9577102 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-95771022023-04-14 Convergence of secretory, endosomal, and autophagic routes in trans-Golgi–associated lysosomes Zhou, Lingjian Xue, Xutong Yang, Ke Feng, Zhi Liu, Min Pastor-Pareja, José C. J Cell Biol Article At the trans-Golgi, complex traffic connections exist to the endolysosomal system additional to the main Golgi-to–plasma membrane secretory route. Here, we investigated three hits in a Drosophila screen displaying secretory cargo accumulation in autophagic vesicles: ESCRT-III component Vps20, SNARE-binding Rop, and lysosomal pump subunit VhaPPA1-1. We found that Vps20, Rop, and lysosomal markers localize near the trans-Golgi. Furthermore, we document that the vicinity of the trans-Golgi is the main cellular location for lysosomes and that early, late, and recycling endosomes associate as well with a trans-Golgi–associated degradative compartment where basal microautophagy of secretory cargo and other materials occurs. Disruption of this compartment causes cargo accumulation in our hits, including Munc18 homolog Rop, required with Syx1 and Syx4 for Rab11-mediated endosomal recycling. Finally, besides basal microautophagy, we show that the trans-Golgi–associated degradative compartment contributes to the growth of autophagic vesicles in developmental and starvation-induced macroautophagy. Our results argue that the fly trans-Golgi is the gravitational center of the whole endomembrane system. Rockefeller University Press 2022-10-14 /pmc/articles/PMC9577102/ /pubmed/36239631 http://dx.doi.org/10.1083/jcb.202203045 Text en © 2022 Zhou et al. https://creativecommons.org/licenses/by-nc-sa/4.0/http://www.rupress.org/terms/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 | Article Zhou, Lingjian Xue, Xutong Yang, Ke Feng, Zhi Liu, Min Pastor-Pareja, José C. Convergence of secretory, endosomal, and autophagic routes in trans-Golgi–associated lysosomes |
title | Convergence of secretory, endosomal, and autophagic routes in trans-Golgi–associated lysosomes |
title_full | Convergence of secretory, endosomal, and autophagic routes in trans-Golgi–associated lysosomes |
title_fullStr | Convergence of secretory, endosomal, and autophagic routes in trans-Golgi–associated lysosomes |
title_full_unstemmed | Convergence of secretory, endosomal, and autophagic routes in trans-Golgi–associated lysosomes |
title_short | Convergence of secretory, endosomal, and autophagic routes in trans-Golgi–associated lysosomes |
title_sort | convergence of secretory, endosomal, and autophagic routes in trans-golgi–associated lysosomes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9577102/ https://www.ncbi.nlm.nih.gov/pubmed/36239631 http://dx.doi.org/10.1083/jcb.202203045 |
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