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Global Proximity Interactome of the Human Macroautophagy Pathway
Macroautophagy is a highly conserved eukaryotic cellular pathway involving the engulfment of macromolecules, organelles, and invading microbes by a double-membrane compartment and subsequent lysosomal degradation. The mechanisms that regulate macroautophagy, and the interaction of its components wit...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9196747/ https://www.ncbi.nlm.nih.gov/pubmed/34524948 http://dx.doi.org/10.1080/15548627.2021.1965711 |
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author | Tu, Yi Xin (Iris) Sydor, Andrew M. Coyaud, Etienne Laurent, Estelle M. N. Dyer, Diana Mellouk, Nora St-Germain, Jonathan Vernon, Robert M. Forman-Kay, Julie D. Li, Taoyingnan Hua, Rong Zhao, Kexin Ridgway, Neale D. Kim, Peter K. Raught, Brian Brumell, John H. |
author_facet | Tu, Yi Xin (Iris) Sydor, Andrew M. Coyaud, Etienne Laurent, Estelle M. N. Dyer, Diana Mellouk, Nora St-Germain, Jonathan Vernon, Robert M. Forman-Kay, Julie D. Li, Taoyingnan Hua, Rong Zhao, Kexin Ridgway, Neale D. Kim, Peter K. Raught, Brian Brumell, John H. |
author_sort | Tu, Yi Xin (Iris) |
collection | PubMed |
description | Macroautophagy is a highly conserved eukaryotic cellular pathway involving the engulfment of macromolecules, organelles, and invading microbes by a double-membrane compartment and subsequent lysosomal degradation. The mechanisms that regulate macroautophagy, and the interaction of its components with other cellular pathways, have remained unclear. Here, we performed proximity-dependent biotin identification (BioID) on 39 core human macroautophagy proteins, identifying over 700 unique high confidence proximity interactors with new putative connections between macroautophagic and essential cellular processes. Of note, we identify members of the OSBPL (oxysterol binding protein like) family as Atg8-family protein interactors. We subsequently conducted comprehensive screens of the OSBPL family for LC3B-binding and roles in xenophagy and aggrephagy. OSBPL7 and OSBPL11 emerged as novel lipid transfer proteins required for macroautophagy of selective cargo. Altogether, our proximity interaction map provides a valuable resource for the study of autophagy and highlights the critical role of membrane contact site proteins in the pathway. ABBREVIATIONS: BioID: proximity-dependent biotin identification; GO: gene ontology; OSBPL: oxysterol binding protein like; VAPA: VAMP associated protein A; VAPB: VAMP associated protein B and C |
format | Online Article Text |
id | pubmed-9196747 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-91967472022-06-15 Global Proximity Interactome of the Human Macroautophagy Pathway Tu, Yi Xin (Iris) Sydor, Andrew M. Coyaud, Etienne Laurent, Estelle M. N. Dyer, Diana Mellouk, Nora St-Germain, Jonathan Vernon, Robert M. Forman-Kay, Julie D. Li, Taoyingnan Hua, Rong Zhao, Kexin Ridgway, Neale D. Kim, Peter K. Raught, Brian Brumell, John H. Autophagy Resource Macroautophagy is a highly conserved eukaryotic cellular pathway involving the engulfment of macromolecules, organelles, and invading microbes by a double-membrane compartment and subsequent lysosomal degradation. The mechanisms that regulate macroautophagy, and the interaction of its components with other cellular pathways, have remained unclear. Here, we performed proximity-dependent biotin identification (BioID) on 39 core human macroautophagy proteins, identifying over 700 unique high confidence proximity interactors with new putative connections between macroautophagic and essential cellular processes. Of note, we identify members of the OSBPL (oxysterol binding protein like) family as Atg8-family protein interactors. We subsequently conducted comprehensive screens of the OSBPL family for LC3B-binding and roles in xenophagy and aggrephagy. OSBPL7 and OSBPL11 emerged as novel lipid transfer proteins required for macroautophagy of selective cargo. Altogether, our proximity interaction map provides a valuable resource for the study of autophagy and highlights the critical role of membrane contact site proteins in the pathway. ABBREVIATIONS: BioID: proximity-dependent biotin identification; GO: gene ontology; OSBPL: oxysterol binding protein like; VAPA: VAMP associated protein A; VAPB: VAMP associated protein B and C Taylor & Francis 2021-09-15 /pmc/articles/PMC9196747/ /pubmed/34524948 http://dx.doi.org/10.1080/15548627.2021.1965711 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
spellingShingle | Resource Tu, Yi Xin (Iris) Sydor, Andrew M. Coyaud, Etienne Laurent, Estelle M. N. Dyer, Diana Mellouk, Nora St-Germain, Jonathan Vernon, Robert M. Forman-Kay, Julie D. Li, Taoyingnan Hua, Rong Zhao, Kexin Ridgway, Neale D. Kim, Peter K. Raught, Brian Brumell, John H. Global Proximity Interactome of the Human Macroautophagy Pathway |
title | Global Proximity Interactome of the Human Macroautophagy Pathway |
title_full | Global Proximity Interactome of the Human Macroautophagy Pathway |
title_fullStr | Global Proximity Interactome of the Human Macroautophagy Pathway |
title_full_unstemmed | Global Proximity Interactome of the Human Macroautophagy Pathway |
title_short | Global Proximity Interactome of the Human Macroautophagy Pathway |
title_sort | global proximity interactome of the human macroautophagy pathway |
topic | Resource |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9196747/ https://www.ncbi.nlm.nih.gov/pubmed/34524948 http://dx.doi.org/10.1080/15548627.2021.1965711 |
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