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Plant AtEH/Pan1 proteins drive autophagosome formation at ER-PM contact sites with actin and endocytic machinery

The Arabidopsis EH proteins (AtEH1/Pan1 and AtEH2/Pan1) are components of the endocytic TPLATE complex (TPC) which is essential for endocytosis. Both proteins are homologues of the yeast ARP2/3 complex activator, Pan1p. Here, we show that these proteins are also involved in actin cytoskeleton regula...

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Autores principales: Wang, Pengwei, Pleskot, Roman, Zang, Jingze, Winkler, Joanna, Wang, Jie, Yperman, Klaas, Zhang, Tong, Wang, Kun, Gong, Jinli, Guan, Yajie, Richardson, Christine, Duckney, Patrick, Vandorpe, Michael, Mylle, Evelien, Fiserova, Jindriska, Van Damme, Daniel, Hussey, Patrick J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6853982/
https://www.ncbi.nlm.nih.gov/pubmed/31723129
http://dx.doi.org/10.1038/s41467-019-12782-6
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author Wang, Pengwei
Pleskot, Roman
Zang, Jingze
Winkler, Joanna
Wang, Jie
Yperman, Klaas
Zhang, Tong
Wang, Kun
Gong, Jinli
Guan, Yajie
Richardson, Christine
Duckney, Patrick
Vandorpe, Michael
Mylle, Evelien
Fiserova, Jindriska
Van Damme, Daniel
Hussey, Patrick J.
author_facet Wang, Pengwei
Pleskot, Roman
Zang, Jingze
Winkler, Joanna
Wang, Jie
Yperman, Klaas
Zhang, Tong
Wang, Kun
Gong, Jinli
Guan, Yajie
Richardson, Christine
Duckney, Patrick
Vandorpe, Michael
Mylle, Evelien
Fiserova, Jindriska
Van Damme, Daniel
Hussey, Patrick J.
author_sort Wang, Pengwei
collection PubMed
description The Arabidopsis EH proteins (AtEH1/Pan1 and AtEH2/Pan1) are components of the endocytic TPLATE complex (TPC) which is essential for endocytosis. Both proteins are homologues of the yeast ARP2/3 complex activator, Pan1p. Here, we show that these proteins are also involved in actin cytoskeleton regulated autophagy. Both AtEH/Pan1 proteins localise to the plasma membrane and autophagosomes. Upon induction of autophagy, AtEH/Pan1 proteins recruit TPC and AP-2 subunits, clathrin, actin and ARP2/3 proteins to autophagosomes. Increased expression of AtEH/Pan1 proteins boosts autophagosome formation, suggesting independent and redundant pathways for actin-mediated autophagy in plants. Moreover, AtEHs/Pan1-regulated autophagosomes associate with ER-PM contact sites (EPCS) where AtEH1/Pan1 interacts with VAP27-1. Knock-down expression of either AtEH1/Pan1 or VAP27-1 makes plants more susceptible to nutrient depleted conditions, indicating that the autophagy pathway is perturbed. In conclusion, we identify the existence of an autophagy-dependent pathway in plants to degrade endocytic components, starting at the EPCS through the interaction among AtEH/Pan1, actin cytoskeleton and the EPCS resident protein VAP27-1.
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spelling pubmed-68539822019-11-18 Plant AtEH/Pan1 proteins drive autophagosome formation at ER-PM contact sites with actin and endocytic machinery Wang, Pengwei Pleskot, Roman Zang, Jingze Winkler, Joanna Wang, Jie Yperman, Klaas Zhang, Tong Wang, Kun Gong, Jinli Guan, Yajie Richardson, Christine Duckney, Patrick Vandorpe, Michael Mylle, Evelien Fiserova, Jindriska Van Damme, Daniel Hussey, Patrick J. Nat Commun Article The Arabidopsis EH proteins (AtEH1/Pan1 and AtEH2/Pan1) are components of the endocytic TPLATE complex (TPC) which is essential for endocytosis. Both proteins are homologues of the yeast ARP2/3 complex activator, Pan1p. Here, we show that these proteins are also involved in actin cytoskeleton regulated autophagy. Both AtEH/Pan1 proteins localise to the plasma membrane and autophagosomes. Upon induction of autophagy, AtEH/Pan1 proteins recruit TPC and AP-2 subunits, clathrin, actin and ARP2/3 proteins to autophagosomes. Increased expression of AtEH/Pan1 proteins boosts autophagosome formation, suggesting independent and redundant pathways for actin-mediated autophagy in plants. Moreover, AtEHs/Pan1-regulated autophagosomes associate with ER-PM contact sites (EPCS) where AtEH1/Pan1 interacts with VAP27-1. Knock-down expression of either AtEH1/Pan1 or VAP27-1 makes plants more susceptible to nutrient depleted conditions, indicating that the autophagy pathway is perturbed. In conclusion, we identify the existence of an autophagy-dependent pathway in plants to degrade endocytic components, starting at the EPCS through the interaction among AtEH/Pan1, actin cytoskeleton and the EPCS resident protein VAP27-1. Nature Publishing Group UK 2019-11-13 /pmc/articles/PMC6853982/ /pubmed/31723129 http://dx.doi.org/10.1038/s41467-019-12782-6 Text en © Crown 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wang, Pengwei
Pleskot, Roman
Zang, Jingze
Winkler, Joanna
Wang, Jie
Yperman, Klaas
Zhang, Tong
Wang, Kun
Gong, Jinli
Guan, Yajie
Richardson, Christine
Duckney, Patrick
Vandorpe, Michael
Mylle, Evelien
Fiserova, Jindriska
Van Damme, Daniel
Hussey, Patrick J.
Plant AtEH/Pan1 proteins drive autophagosome formation at ER-PM contact sites with actin and endocytic machinery
title Plant AtEH/Pan1 proteins drive autophagosome formation at ER-PM contact sites with actin and endocytic machinery
title_full Plant AtEH/Pan1 proteins drive autophagosome formation at ER-PM contact sites with actin and endocytic machinery
title_fullStr Plant AtEH/Pan1 proteins drive autophagosome formation at ER-PM contact sites with actin and endocytic machinery
title_full_unstemmed Plant AtEH/Pan1 proteins drive autophagosome formation at ER-PM contact sites with actin and endocytic machinery
title_short Plant AtEH/Pan1 proteins drive autophagosome formation at ER-PM contact sites with actin and endocytic machinery
title_sort plant ateh/pan1 proteins drive autophagosome formation at er-pm contact sites with actin and endocytic machinery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6853982/
https://www.ncbi.nlm.nih.gov/pubmed/31723129
http://dx.doi.org/10.1038/s41467-019-12782-6
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