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Mammalian hybrid pre-autophagosomal structure HyPAS generates autophagosomes.

Authors :
Kumar, Suresh
Kumar, Suresh
Javed, Ruheena
Mudd, Michal
Pallikkuth, Sandeep
Lidke, Keith A
Jain, Ashish
Tangavelou, Karthikeyan
Gudmundsson, Sigurdur Runar
Ye, Chunyan
Rusten, Tor Erik
Anonsen, Jan Haug
Lystad, Alf Håkon
Claude-Taupin, Aurore
Simonsen, Anne
Salemi, Michelle
Phinney, Brett
Li, Jing
Guo, Lian-Wang
Bradfute, Steven B
Timmins, Graham S
Eskelinen, Eeva-Liisa
Deretic, Vojo
Kumar, Suresh
Kumar, Suresh
Javed, Ruheena
Mudd, Michal
Pallikkuth, Sandeep
Lidke, Keith A
Jain, Ashish
Tangavelou, Karthikeyan
Gudmundsson, Sigurdur Runar
Ye, Chunyan
Rusten, Tor Erik
Anonsen, Jan Haug
Lystad, Alf Håkon
Claude-Taupin, Aurore
Simonsen, Anne
Salemi, Michelle
Phinney, Brett
Li, Jing
Guo, Lian-Wang
Bradfute, Steven B
Timmins, Graham S
Eskelinen, Eeva-Liisa
Deretic, Vojo
Source :
Cell; vol 184, iss 24, 5950-5969.e22; 0092-8674
Publication Year :
2021

Abstract

The biogenesis of mammalian autophagosomes remains to be fully defined. Here, we used cellular and in vitro membrane fusion analyses to show that autophagosomes are formed from a hitherto unappreciated hybrid membrane compartment. The autophagic precursors emerge through fusion of FIP200 vesicles, derived from the cis-Golgi, with endosomally derived ATG16L1 membranes to generate a hybrid pre-autophagosomal structure, HyPAS. A previously unrecognized apparatus defined here controls HyPAS biogenesis and mammalian autophagosomal precursor membranes. HyPAS can be modulated by pharmacological agents whereas its formation is inhibited upon severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection or by expression of SARS-CoV-2 nsp6. These findings reveal the origin of mammalian autophagosomal membranes, which emerge via convergence of secretory and endosomal pathways, and show that this process is targeted by microbial factors such as coronaviral membrane-modulating proteins.

Details

Database :
OAIster
Journal :
Cell; vol 184, iss 24, 5950-5969.e22; 0092-8674
Notes :
application/pdf, Cell vol 184, iss 24, 5950-5969.e22 0092-8674
Publication Type :
Electronic Resource
Accession number :
edsoai.on1391591484
Document Type :
Electronic Resource