The Role of ATG9 Vesicles in Autophagosome Biogenesis
[Display omitted] •ATG9 is a conserved transmembrane scramblase, which is important for macroautophagy.•ATG9 resides in trans-Golgi derived vesicles, of which some traffic to the site of autophagosome biogenesis.•ATG9 vesicles can serve as platforms for the assembly of the autophagy machinery.•ATG9...
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Veröffentlicht in: | Journal of molecular biology 2024-08, Vol.436 (15), p.168489, Article 168489 |
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Sprache: | eng |
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•ATG9 is a conserved transmembrane scramblase, which is important for macroautophagy.•ATG9 resides in trans-Golgi derived vesicles, of which some traffic to the site of autophagosome biogenesis.•ATG9 vesicles can serve as platforms for the assembly of the autophagy machinery.•ATG9 vesicles may form seeds for autophagosomes by establishing contact sites with the endoplasmic reticulum.
Autophagy mediates the degradation and recycling of cellular material in the lysosomal system. Dysfunctional autophagy is associated with a plethora of diseases including uncontrolled infections, cancer and neurodegeneration. In macroautophagy (hereafter autophagy) this material is encapsulated in double membrane vesicles, the autophagosomes, which form upon induction of autophagy. The precursors to autophagosomes, referred to as phagophores, first appear as small flattened membrane cisternae, which gradually enclose the cargo material as they grow. The assembly of phagophores during autophagy initiation has been a major subject of investigation over the past decades. A special focus has been ATG9, the only conserved transmembrane protein among the core machinery. The majority of ATG9 localizes to small Golgi-derived vesicles. Here we review the recent advances and breakthroughs regarding our understanding of how ATG9 and the vesicles it resides in serve to assemble the autophagy machinery and to establish membrane contact sites for autophagosome biogenesis. We also highlight open questions in the field that need to be addressed in the years to come. |
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ISSN: | 0022-2836 1089-8638 1089-8638 |
DOI: | 10.1016/j.jmb.2024.168489 |