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PtdIns 3-Kinase Orchestrates Autophagosome Formation in Yeast

Eukaryotic cells can massively transport their own cytoplasmic contents into a lytic compartment, the vacuole/lysosome, for recycling through a conserved system called autophagy. The key process in autophagy is the sequestration of cytoplasmic contents within a double-membrane structure, the autopha...

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Detalles Bibliográficos
Autores principales: Obara, Keisuke, Ohsumi, Yoshinori
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3067060/
https://www.ncbi.nlm.nih.gov/pubmed/21490802
http://dx.doi.org/10.1155/2011/498768
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author Obara, Keisuke
Ohsumi, Yoshinori
author_facet Obara, Keisuke
Ohsumi, Yoshinori
author_sort Obara, Keisuke
collection PubMed
description Eukaryotic cells can massively transport their own cytoplasmic contents into a lytic compartment, the vacuole/lysosome, for recycling through a conserved system called autophagy. The key process in autophagy is the sequestration of cytoplasmic contents within a double-membrane structure, the autophagosome. Autophagosome formation requires the elaborate cooperation of Atg (autophagy-related) proteins and lipid molecules. Phosphorylation of phosphatidylinositol (PtdIns) by a PtdIns 3-kinase, Vps34, is a key step in coordinating Atg proteins and lipid molecules. Vps34 forms two distinct protein complexes, only one of which is involved in generating autophagic membranes. Upon induction of autophagy, PtdIns(3)P, the enzymatic product of PtdIns 3-kinase, is massively transported into the lumen of the vacuole via autophagy. PtdIns(3)P is enriched on the inner membrane of the autophagosome. PtdIns(3)P recruits the Atg18−Atg2 complex and presumably other Atg proteins to autophagic membranes, thereby coordinating lipid molecules and Atg proteins.
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spelling pubmed-30670602011-04-13 PtdIns 3-Kinase Orchestrates Autophagosome Formation in Yeast Obara, Keisuke Ohsumi, Yoshinori J Lipids Review Article Eukaryotic cells can massively transport their own cytoplasmic contents into a lytic compartment, the vacuole/lysosome, for recycling through a conserved system called autophagy. The key process in autophagy is the sequestration of cytoplasmic contents within a double-membrane structure, the autophagosome. Autophagosome formation requires the elaborate cooperation of Atg (autophagy-related) proteins and lipid molecules. Phosphorylation of phosphatidylinositol (PtdIns) by a PtdIns 3-kinase, Vps34, is a key step in coordinating Atg proteins and lipid molecules. Vps34 forms two distinct protein complexes, only one of which is involved in generating autophagic membranes. Upon induction of autophagy, PtdIns(3)P, the enzymatic product of PtdIns 3-kinase, is massively transported into the lumen of the vacuole via autophagy. PtdIns(3)P is enriched on the inner membrane of the autophagosome. PtdIns(3)P recruits the Atg18−Atg2 complex and presumably other Atg proteins to autophagic membranes, thereby coordinating lipid molecules and Atg proteins. Hindawi Publishing Corporation 2011 2011-01-04 /pmc/articles/PMC3067060/ /pubmed/21490802 http://dx.doi.org/10.1155/2011/498768 Text en Copyright © 2011 K. Obara and Y. Ohsumi. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Obara, Keisuke
Ohsumi, Yoshinori
PtdIns 3-Kinase Orchestrates Autophagosome Formation in Yeast
title PtdIns 3-Kinase Orchestrates Autophagosome Formation in Yeast
title_full PtdIns 3-Kinase Orchestrates Autophagosome Formation in Yeast
title_fullStr PtdIns 3-Kinase Orchestrates Autophagosome Formation in Yeast
title_full_unstemmed PtdIns 3-Kinase Orchestrates Autophagosome Formation in Yeast
title_short PtdIns 3-Kinase Orchestrates Autophagosome Formation in Yeast
title_sort ptdins 3-kinase orchestrates autophagosome formation in yeast
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3067060/
https://www.ncbi.nlm.nih.gov/pubmed/21490802
http://dx.doi.org/10.1155/2011/498768
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