Spatial control of avidity regulates initiation and progression of selective autophagy

Nat Commun. 2021 Dec 10;12(1):7194. doi: 10.1038/s41467-021-27420-3.

Abstract

Autophagosomes form at the endoplasmic reticulum in mammals, and between the vacuole and the endoplasmic reticulum in yeast. However, the roles of these sites and the mechanisms regulating autophagosome formation are incompletely understood. Vac8 is required for autophagy and recruits the Atg1 kinase complex to the vacuole. Here we show that Vac8 acts as a central hub to nucleate the phagophore assembly site at the vacuolar membrane during selective autophagy. Vac8 directly recruits the cargo complex via the Atg11 scaffold. In addition, Vac8 recruits the phosphatidylinositol 3-kinase complex independently of autophagy. Cargo-dependent clustering and Vac8-dependent sequestering of these early autophagy factors, along with local Atg1 activation, promote phagophore assembly site assembly at the vacuole. Importantly, ectopic Vac8 redirects autophagosome formation to the nuclear membrane, indicating that the vacuolar membrane is not specifically required. We propose that multiple avidity-driven interactions drive the initiation and progression of selective autophagy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagosomes / metabolism*
  • Autophagy-Related Proteins
  • Endopeptidases
  • Humans
  • Macroautophagy*
  • Membrane Proteins
  • Nuclear Envelope / metabolism
  • Protein Kinases
  • Saccharomyces cerevisiae / metabolism
  • Saccharomyces cerevisiae Proteins
  • Vacuoles / metabolism*
  • Vesicular Transport Proteins / metabolism
  • Yeasts

Substances

  • Autophagy-Related Proteins
  • Membrane Proteins
  • Saccharomyces cerevisiae Proteins
  • VAC8 protein, S cerevisiae
  • Vesicular Transport Proteins
  • Protein Kinases
  • ATG1 protein, S cerevisiae
  • ATG21 protein, S cerevisiae
  • Endopeptidases