Format

Send to

Choose Destination
Genetics. 2015 Feb;199(2):475-85. doi: 10.1534/genetics.114.169797. Epub 2014 Dec 17.

Autophagy competes for a common phosphatidylethanolamine pool with major cellular PE-consuming pathways in Saccharomyces cerevisiae.

Author information

1
Department of Biology, Institute of Biochemistry, ETH Zurich, 8093 Zürich, Switzerland.
2
Department of Biochemistry, University of Geneva, 1211 Geneva 4, Switzerland.
3
Department of Cell Biology, Center for Molecular Medicine, University Medical Center Utrecht, Heidelberglaan 100, 3584 CX Utrecht, The Netherlands.
4
Institute for Genetics, University of Cologne, Zülpicherstrasse 47a, D-50674 Cologne, Germany.
5
Department of Biology, Institute of Biochemistry, ETH Zurich, 8093 Zürich, Switzerland Department for Biochemistry and Cell Biology, Max F. Perutz Laboratories, University of Vienna, A-1030 Vienna, Austria.
6
Department of Biology, Institute of Biochemistry, ETH Zurich, 8093 Zürich, Switzerland matthias.peter@bc.biol.ethz.ch.

Abstract

Autophagy is a highly regulated pathway that selectively degrades cellular constituents such as protein aggregates and excessive or damaged organelles. This transport route is characterized by engulfment of the targeted cargo by autophagosomes. The formation of these double-membrane vesicles requires the covalent conjugation of the ubiquitin-like protein Atg8 to phosphatidylethanolamine (PE). However, the origin of PE and the regulation of lipid flux required for autophagy remain poorly understood. Using a genetic screen, we found that the temperature-sensitive growth and intracellular membrane organization defects of mcd4-174 and mcd4-P301L mutants are suppressed by deletion of essential autophagy genes such as ATG1 or ATG7. MCD4 encodes an ethanolamine phosphate transferase that uses PE as a precursor for an essential step in the synthesis of the glycosylphosphatidylinositol (GPI) anchor used to link a subset of plasma membrane proteins to lipid bilayers. Similar to the deletion of CHO2, a gene encoding the enzyme converting PE to phosphatidylcholine (PC), deletion of ATG7 was able to restore lipidation and plasma membrane localization of the GPI-anchored protein Gas1 and normal organization of intracellular membranes. Conversely, overexpression of Cho2 was lethal in mcd4-174 cells grown at restrictive temperature. Quantitative lipid analysis revealed that PE levels are substantially reduced in the mcd4-174 mutant but can be restored by deletion of ATG7 or CHO2. Taken together, these data suggest that autophagy competes for a common PE pool with major cellular PE-consuming pathways such as the GPI anchor and PC synthesis, highlighting the possible interplay between these pathways and the existence of signals that may coordinate PE flux.

KEYWORDS:

Atg8; GPI anchor; Mcd4; autophagy; phospholipids

PMID:
25519895
PMCID:
PMC4317655
DOI:
10.1534/genetics.114.169797
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for HighWire Icon for PubMed Central
Loading ...
Support Center