ESCRT machinery mediates selective microautophagy of endoplasmic reticulum in yeast

Autor: Julia Schessner, Michael Knop, Takuma Tsuji, Dimitrios Papagiannidis, Toyoshi Fujimoto, Katharina Schaeff, Peter W. Bircham, Jasmin A. Schäfer, Oliver Pajonk, Giulia Ruffini, Sebastian Schuck, Charlotta Funaya
Jazyk: angličtina
Rok vydání: 2020
Předmět:
ESCRT machinery
yeast
Endoplasmic Reticulum
SACCHAROMYCES-CEREVISIAE
0302 clinical medicine
Homeostasis
Membrane & Intracellular Transport
0303 health sciences
biology
MEMBRANE-PROTEINS
General Neuroscience
PROLIFERATION
Nuclear Proteins
Articles
Endoplasmic Reticulum Stress
Cell biology
endoplasmic reticulum
Phosphatase complex
AUTOPHAGY
TURNOVER
Autophagy & Cell Death
Life Sciences & Biomedicine
Biochemistry & Molecular Biology
microautophagy
Saccharomyces cerevisiae Proteins
Saccharomyces cerevisiae
BIOGENESIS
General Biochemistry
Genetics and Molecular Biology

Article
ER-PHAGY
03 medical and health sciences
TOMOGRAPHY
Organelle
Microautophagy
Molecular Biology
030304 developmental biology
Science & Technology
General Immunology and Microbiology
RECEPTOR
Endosomal Sorting Complexes Required for Transport
Endoplasmic reticulum
Autophagy
Membrane Proteins
Cell Biology
Intracellular Membranes
biology.organism_classification
Membrane protein
030217 neurology & neurosurgery
Biogenesis
SYSTEM
Zdroj: EMBO Journal
The EMBO Journal
Popis: ER‐phagy, the selective autophagy of endoplasmic reticulum (ER), safeguards organelle homeostasis by eliminating misfolded proteins and regulating ER size. ER‐phagy can occur by macroautophagic and microautophagic mechanisms. While dedicated machinery for macro‐ER‐phagy has been discovered, the molecules and mechanisms mediating micro‐ER‐phagy remain unknown. Here, we first show that micro‐ER‐phagy in yeast involves the conversion of stacked cisternal ER into multilamellar ER whorls during microautophagic uptake into lysosomes. Second, we identify the conserved Nem1‐Spo7 phosphatase complex and the ESCRT machinery as key components for micro‐ER‐phagy. Third, we demonstrate that macro‐ and micro‐ER‐phagy are parallel pathways with distinct molecular requirements. Finally, we provide evidence that the ESCRT machinery directly functions in scission of the lysosomal membrane to complete the microautophagic uptake of ER. These findings establish a framework for a mechanistic understanding of micro‐ER‐phagy and, thus, a comprehensive appreciation of the role of autophagy in ER homeostasis.
Micro‐ER‐phagy requires the Nem1‐Spo7 phosphatase complex and ESCRT proteins for membrane scission during uptake of multilamellar ER whorls into the lysosome.
Databáze: OpenAIRE