--Atg9 interactions via its transmembrane domains are required for phagophore expansion during autophagy

Autophagy. 2023 May;19(5):1459-1478. doi: 10.1080/15548627.2022.2136340. Epub 2022 Nov 10.

Abstract

During macroautophagy/autophagy, precursor cisterna known as phagophores expand and sequester portions of the cytoplasm and/or organelles, and subsequently close resulting in double-membrane transport vesicles called autophagosomes. Autophagosomes fuse with lysosomes/vacuoles to allow the degradation and recycling of their cargoes. We previously showed that sequential binding of yeast Atg2 and Atg18 to Atg9, the only conserved transmembrane protein in autophagy, at the extremities of the phagophore mediates the establishment of membrane contact sites between the phagophore and the endoplasmic reticulum. As the Atg2-Atg18 complex transfers lipids between adjacent membranes in vitro, it has been postulated that this activity and the scramblase activity of the trimers formed by Atg9 are required for the phagophore expansion. Here, we present evidence that Atg9 indeed promotes Atg2-Atg18 complex-mediated lipid transfer in vitro, although this is not the only requirement for its function in vivo. In particular, we show that Atg9 function is dramatically compromised by a F627A mutation within the conserved interface between the transmembrane domains of the Atg9 monomers. Although Atg9F627A self-interacts and binds to the Atg2-Atg18 complex, the F627A mutation blocks the phagophore expansion and thus autophagy progression. This phenotype is conserved because the corresponding human ATG9A mutant severely impairs autophagy as well. Importantly, Atg9F627A has identical scramblase activity in vitro like Atg9, and as with the wild-type protein enhances Atg2-Atg18-mediated lipid transfer. Collectively, our data reveal that interactions of Atg9 trimers via their transmembrane segments play a key role in phagophore expansion beyond Atg9's role as a lipid scramblase.Abbreviations: BafA1: bafilomycin A1; Cvt: cytoplasm-to-vacuole targeting; Cryo-EM: cryo-electron microscopy; ER: endoplasmic reticulum; GFP: green fluorescent protein; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; MCS: membrane contact site; NBD-PE: N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)-1,2-dihexadecanoyl-sn-glycero-3-phosphoethanolamine; PAS: phagophore assembly site; PE: phosphatidylethanolamine; prApe1: precursor Ape1; PtdIns3P: phosphatidylinositol-3-phosphate; SLB: supported lipid bilayer; SUV: small unilamellar vesicle; TMD: transmembrane domain; WT: wild type.

Keywords: Autophagosome; lipid transfer; membrane contact site; phagophore; scramblase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autophagosomes* / metabolism
  • Autophagy / genetics
  • Autophagy-Related Proteins / metabolism
  • Cryoelectron Microscopy
  • Endoplasmic Reticulum / metabolism
  • Humans
  • Lipids
  • Membrane Proteins / metabolism
  • Saccharomyces cerevisiae / metabolism
  • Saccharomyces cerevisiae Proteins* / metabolism

Substances

  • Autophagy-Related Proteins
  • Saccharomyces cerevisiae Proteins
  • Lipids
  • ATG2 protein, S cerevisiae
  • ATG9 protein, S cerevisiae
  • Membrane Proteins

Grants and funding

This work was supported by the Horizon 2020 [Marie Skłodowska Curie ETN (765912)]; Novo Nordisk Foundation [0066384]; ZonMW Top [91217002]; Deutsche Forschungsgemeinschaft; [SFB 944, P26] [UN111/13-1]; Open Competition ENW-KLEIN [OCENW.KLEIN.118].