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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-...

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Autores principales: Zhou, Lingjian, Xue, Xutong, Yang, Ke, Feng, Zhi, Liu, Min, Pastor-Pareja, José C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2022
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.
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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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