Different effects of Atg2 and Atg18 mutations on Atg8a and Atg9 trafficking during starvation in Drosophila

Research output: Contribution to journalArticle

Abstract

The Atg2-Atg18 complex acts in parallel to Atg8 and regulates Atg9 recycling from phagophore assembly site (PAS) during autophagy in yeast. Here we show that in Drosophila, both Atg9 and Atg18 are required for Atg8a puncta formation, unlike Atg2. Selective autophagic degradation of ubiquitinated proteins is mediated by Ref(2)P/p62. The transmembrane protein Atg9 accumulates on refractory to Sigma P (Ref(2)P) aggregates in Atg7, Atg8a and Atg2 mutants. No accumulation of Atg9 is seen on Ref(2)P in cells lacking Atg18 or Vps34 lipid kinase function, while the Atg1 complex subunit FIP200 is recruited. The simultaneous interaction of Atg18 with both Atg9 and Ref(2)P raises the possibility that Atg18 may facilitate selective degradation of ubiquitinated protein aggregates by autophagy.

Details

Authors
External organisations
  • Eötvös Loránd University
Research areas and keywords

Keywords

  • Animals, Autophagy, Autophagy-Related Proteins, Carrier Proteins, Drosophila, Drosophila Proteins, Membrane Proteins, Mutation, Protein Transport, Proteolysis, Starvation, Ubiquitinated Proteins, Journal Article, Research Support, Non-U.S. Gov't
Original languageEnglish
Pages (from-to)408-13
Number of pages6
JournalFEBS Letters
Volume588
Issue number3
Publication statusPublished - 2014 Jan 31
Publication categoryResearch
Peer-reviewedYes
Externally publishedYes