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Transmembrane phospholipid translocation mediated by Atg9 is involved in autophagosome formation

The mechanism of isolation membrane formation in autophagy is receiving intensive study. We recently found that Atg9 translocates phospholipids across liposomal membranes and proposed that this functionality plays an essential role in the expansion of isolation membranes. The distribution of phospha...

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Autores principales: Orii, Minami, Tsuji, Takuma, Ogasawara, Yuta, Fujimoto, Toyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809878/
https://www.ncbi.nlm.nih.gov/pubmed/33439214
http://dx.doi.org/10.1083/jcb.202009194
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author Orii, Minami
Tsuji, Takuma
Ogasawara, Yuta
Fujimoto, Toyoshi
author_facet Orii, Minami
Tsuji, Takuma
Ogasawara, Yuta
Fujimoto, Toyoshi
author_sort Orii, Minami
collection PubMed
description The mechanism of isolation membrane formation in autophagy is receiving intensive study. We recently found that Atg9 translocates phospholipids across liposomal membranes and proposed that this functionality plays an essential role in the expansion of isolation membranes. The distribution of phosphatidylinositol 3-phosphate in both leaflets of yeast autophagosomal membranes supports this proposal, but if Atg9-mediated lipid transport is crucial, symmetrical distribution in autophagosomes should be found broadly for other phospholipids. To test this idea, we analyzed the distributions of phosphatidylcholine, phosphatidylserine, and phosphatidylinositol 4-phosphate by freeze-fracture electron microscopy. We found that all these phospholipids are distributed with comparable densities in the two leaflets of autophagosomes and autophagic bodies. Moreover, de novo–synthesized phosphatidylcholine is incorporated into autophagosomes preferentially and shows symmetrical distribution in autophagosomes within 30 min after synthesis, whereas this symmetrical distribution is compromised in yeast expressing an Atg9 mutant. These results indicate that transbilayer phospholipid movement that is mediated by Atg9 is involved in the biogenesis of autophagosomes.
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spelling pubmed-78098782021-09-01 Transmembrane phospholipid translocation mediated by Atg9 is involved in autophagosome formation Orii, Minami Tsuji, Takuma Ogasawara, Yuta Fujimoto, Toyoshi J Cell Biol Report The mechanism of isolation membrane formation in autophagy is receiving intensive study. We recently found that Atg9 translocates phospholipids across liposomal membranes and proposed that this functionality plays an essential role in the expansion of isolation membranes. The distribution of phosphatidylinositol 3-phosphate in both leaflets of yeast autophagosomal membranes supports this proposal, but if Atg9-mediated lipid transport is crucial, symmetrical distribution in autophagosomes should be found broadly for other phospholipids. To test this idea, we analyzed the distributions of phosphatidylcholine, phosphatidylserine, and phosphatidylinositol 4-phosphate by freeze-fracture electron microscopy. We found that all these phospholipids are distributed with comparable densities in the two leaflets of autophagosomes and autophagic bodies. Moreover, de novo–synthesized phosphatidylcholine is incorporated into autophagosomes preferentially and shows symmetrical distribution in autophagosomes within 30 min after synthesis, whereas this symmetrical distribution is compromised in yeast expressing an Atg9 mutant. These results indicate that transbilayer phospholipid movement that is mediated by Atg9 is involved in the biogenesis of autophagosomes. Rockefeller University Press 2021-01-13 /pmc/articles/PMC7809878/ /pubmed/33439214 http://dx.doi.org/10.1083/jcb.202009194 Text en © 2021 Orii et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/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 Report
Orii, Minami
Tsuji, Takuma
Ogasawara, Yuta
Fujimoto, Toyoshi
Transmembrane phospholipid translocation mediated by Atg9 is involved in autophagosome formation
title Transmembrane phospholipid translocation mediated by Atg9 is involved in autophagosome formation
title_full Transmembrane phospholipid translocation mediated by Atg9 is involved in autophagosome formation
title_fullStr Transmembrane phospholipid translocation mediated by Atg9 is involved in autophagosome formation
title_full_unstemmed Transmembrane phospholipid translocation mediated by Atg9 is involved in autophagosome formation
title_short Transmembrane phospholipid translocation mediated by Atg9 is involved in autophagosome formation
title_sort transmembrane phospholipid translocation mediated by atg9 is involved in autophagosome formation
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809878/
https://www.ncbi.nlm.nih.gov/pubmed/33439214
http://dx.doi.org/10.1083/jcb.202009194
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