Emerging roles of ATG proteins and membrane lipids in autophagosome formation.

Endoplasmic reticulum Macroautophagy

Journal

Cell discovery
ISSN: 2056-5968
Titre abrégé: Cell Discov
Pays: England
ID NLM: 101661034

Informations de publication

Date de publication:
2020
Historique:
received: 03 12 2019
accepted: 21 03 2020
entrez: 9 6 2020
pubmed: 9 6 2020
medline: 9 6 2020
Statut: epublish

Résumé

Autophagosome biogenesis is a dynamic membrane event, which is executed by the sequential function of autophagy-related (ATG) proteins. Upon autophagy induction, a cup-shaped membrane structure appears in the cytoplasm, then elongates sequestering cytoplasmic materials, and finally forms a closed double membrane autophagosome. However, how this complex vesicle formation event is strictly controlled and achieved is still enigmatic. Recently, there is accumulating evidence showing that some ATG proteins have the ability to directly interact with membranes, transfer lipids between membranes and regulate lipid metabolism. A novel role for various membrane lipids in autophagosome formation is also emerging. Here, we highlight past and recent key findings on the function of ATG proteins related to autophagosome biogenesis and consider how ATG proteins control this dynamic membrane formation event to organize the autophagosome by collaborating with membrane lipids.

Identifiants

pubmed: 32509328
doi: 10.1038/s41421-020-0161-3
pii: 161
pmc: PMC7248066
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

32

Subventions

Organisme : Cancer Research UK
ID : FC001187
Pays : United Kingdom
Organisme : Arthritis Research UK
ID : FC001187
Pays : United Kingdom

Informations de copyright

© The Author(s) 2020.

Déclaration de conflit d'intérêts

Conflict of interestThe authors declare that they have no conflict of interest.

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Auteurs

Taki Nishimura (T)

Molecular Cell Biology of Autophagy, The Francis Crick Institute, London, NW1 1AT UK.

Sharon A Tooze (SA)

Molecular Cell Biology of Autophagy, The Francis Crick Institute, London, NW1 1AT UK.

Classifications MeSH