Atg9 establishes Atg2-dependent contact sites between the endoplasmic reticulum and phagophores

Abstract: The autophagy-related (Atg) proteins play a key role in the formation of autophagosomes, the hallmark of autophagy. The function of the cluster composed by Atg2, Atg18, and transmembrane Atg9 is completely unknown despite their importance in autophagy. In this study, we provide insights into the molecular role of these proteins by identifying and characterizing Atg2 point mutants impaired in Atg9 binding. We show that Atg2 associates to autophagosomal membranes through lipid binding and independently from Atg9. Its interaction with Atg9, however, is key for Atg2 confinement to the growing phagophore extremities and subsequent association of Atg18. Assembly of the Atg9–Atg2–Atg18 complex is important to establish phagophore–endoplasmic reticulum (ER) contact sites. In turn, disruption of the Atg2–Atg9 interaction leads to an aberrant topological distribution of both Atg2 and ER contact sites on forming phagophores, which severely impairs autophagy. Altogether, our data shed light in the interrelationship between Atg9, Atg2, and Atg18 and highlight the possible functional relevance of the phagophore–ER contact sites in phagophore expansion

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch
Anmerkungen
The journal of cell biology. - 217, 8 (2018) , 2743-2763, ISSN: 1540-8140

Ereignis
Veröffentlichung
(wo)
Freiburg
(wer)
Universität
(wann)
2019
Urheber
Gómez-Sánchez, Rubén
Rose, Jaqueline
Guimarães, Rodrigo
Mari, Muriel
Papinski, Daniel
Rieter, Ester
Geerts, Willie J.
Hardenberg, Ralph
Kraft, Claudine
Ungermann, Christian
Reggiori, Fulvio

DOI
10.1083/jcb.201710116
URN
urn:nbn:de:bsz:25-freidok-1487498
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
14.08.2025, 10:49 MESZ

Datenpartner

Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.

Beteiligte

Entstanden

  • 2019

Ähnliche Objekte (12)