The phenotypes of ATG9, ATG16 and ATG9/16 knock-out mutants imply autophagy-dependent and -independent functions. Issue 4 (April 2015)

• Record Type: Journal Article
• Authors: Xiong, Qiuhong; Ünal, Can; Matthias, Jan; Steinert, Michael; Eichinger, Ludwig
• Is Part Of: Open biology. Volume 5:Issue 4(2015)
• Publication Date: 2015-04
• Subjects: Dictyostelium -- autophagy -- development -- phagocytosis -- proteasome -- protein aggregate; Biology -- Periodicals; 570
• DOI: 10.1098/rsob.150008
• Languages: English
• ISSNs: 2046-2441

Abstract

Abstract : Macroautophagy is a highly conserved intracellular bulk degradation system of all eukaryotic cells. It is governed by a large number of autophagy proteins (ATGs) and is crucial for many cellular processes. Here, we describe the phenotypes of Dictyostelium discoideum ATG16 − and ATG9 − /16 − cells and compare them to the previously reported ATG9 − mutant. ATG16 deficiency caused an increase in the expression of several core autophagy genes, among them atg9 and the two atg8 paralogues. The single and double ATG9 and ATG16 knock-out mutants had complex phenotypes and displayed severe and comparable defects in pinocytosis and phagocytosis. Uptake of Legionella pneumophila was reduced. In addition, ATG9 − and ATG16 − cells had dramatic defects in autophagy, development and proteasomal activity which were much more severe in the ATG9 − /16 − double mutant. Mutant cells showed an increase in poly-ubiquitinated proteins and contained large ubiquitin-positive protein aggregates which partially co-localized with ATG16-GFP in ATG9 − /16 − cells. The more severe autophagic, developmental and proteasomal phenotypes of ATG9 − /16 − cells imply that ATG9 and ATG16 probably function in parallel in autophagy and have in addition autophagy-independent functions in further cellular processes.