Control of basal autophagy rate by vacuolar peduncle

PLoS One. 2019 Feb 8;14(2):e0209759. doi: 10.1371/journal.pone.0209759. eCollection 2019.

Bourouis M1, Mondin M1, Dussert A2, Leopold P2.

Author information

1. Université Côte d’Azur, Centre National de la Recherche Scientifique, Institut de Biologie Valrose, Nice-France.
2. Université Côte d’Azur, Institut national de la santé et de la recherche médicale, Institut de Biologie Valrose, Nice -France.


Basal autophagy is as a compressive catabolic mechanism engaged in the breakdown of damaged macromolecules and organelles leading to the recycling of elementary nutrients. Thought essential to cellular refreshing, little is known about the origin of a constitutional rate of basal autophagy. Here, we found that loss of Drosophila vacuolar peduncle (vap), a presumed GAP enzyme, is associated with enhanced basal autophagy rate and physiological alterations resulting in a wasteful cell energy balance, a hallmark of overactive autophagy. By contrast, starvation-induced autophagy was disrupted in vap mutant conditions, leading to a block of maturation into autolysosomes. This phenotype stem for exacerbated biogenesis of PI(3)P-dependent endomembranes, including autophagosome membranes and ectopic fusions of vesicles. These findings shed new light on the neurodegenerative phenotype found associated to mutant vap adult brains in a former study. A partner of Vap, Sprint (Spri), acting as an endocytic GEF for Rab5, had the converse effect of leading to a reduction in PI(3)P-dependent endomembrane formation in mutants. Spri was conditional to normal basal autophagy and instrumental to the starvation-sensitivity phenotype specific of vap. Rab5 activity itself was essential for PI(3)P and for pre-autophagosome structures formation. We propose that Vap/Spri complexes promote a cell surface-derived flow of endocytic Rab5-containing vesicles, the traffic of which is crucial for the implementation of a basal autophagy rate.

PMID: 30735514
DOI: 10.1371/journal.pone.0209759