Back to Search
Start Over
ATG9 promotes autophagosome formation through interaction with LC3.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2025 Feb 02; Vol. 747, pp. 151254. Date of Electronic Publication: 2024 Dec 27. - Publication Year :
- 2025
-
Abstract
- The autophagosome is a double-membrane organelle that executes macroautophagy. Previous studies have shown that the autophagosome formation is driven by autophagy-related genes, among which ATG9 is the only conserved transmembrane protein and has been shown to play a critical role in the autophagosome formation. However, how ATG9 binds to the growing autophagosome membrane has remained uncertain. Herein, we report that ATG9 binds to LC3, an essential membrane component of the autophagosome, thereby allowing ATG9 to incorporate into the autophagosome membrane. Mechanistically, we show that ATG9 interacts with LC3 through its UIM motives, which bind to the UDS site of LC3. Interrupting such UIM-UDS interaction abolishes the autophagosome association of ATG9 and suppresses the autophagosome formation. Collectively, our findings reveal a novel mechanism regulating autophagosome biogenesis and suggest that the interaction of ATG9 with LC3 is critical for ATG9 binding to the growing autophagosome membrane.<br />Competing Interests: Declaration of Competing interest The authors have no interests to declare.<br /> (Copyright © 2024 Elsevier Inc. All rights reserved.)
- Subjects :
- Humans
Protein Binding
Membrane Proteins metabolism
Membrane Proteins genetics
HEK293 Cells
HeLa Cells
Vesicular Transport Proteins
Microtubule-Associated Proteins metabolism
Microtubule-Associated Proteins genetics
Autophagy-Related Proteins metabolism
Autophagy-Related Proteins genetics
Autophagosomes metabolism
Autophagy
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2104
- Volume :
- 747
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 39787789
- Full Text :
- https://doi.org/10.1016/j.bbrc.2024.151254