Vps13 is required for the packaging of the ER into autophagosomes during ER-phagy.


Journal

Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876

Informations de publication

Date de publication:
04 08 2020
Historique:
pubmed: 22 7 2020
medline: 2 10 2020
entrez: 22 7 2020
Statut: ppublish

Résumé

Endoplasmic reticulum (ER) macroautophagy (hereafter called ER-phagy) uses autophagy receptors to selectively degrade ER domains in response to starvation or the accumulation of aggregation-prone proteins. Autophagy receptors package the ER into autophagosomes by binding to the ubiquitin-like yeast protein Atg8 (LC3 in mammals), which is needed for autophagosome formation. In budding yeast, cortical and cytoplasmic ER-phagy requires the autophagy receptor Atg40. While different ER autophagy receptors have been identified, little is known about other components of the ER-phagy machinery. In an effort to identify these components, we screened the genome-wide library of viable yeast deletion mutants for defects in the degradation of cortical ER following treatment with rapamycin, a drug that mimics starvation. Among the mutants we identified was

Identifiants

pubmed: 32690699
pii: 2008923117
doi: 10.1073/pnas.2008923117
pmc: PMC7414049
doi:

Substances chimiques

Saccharomyces cerevisiae Proteins 0
VPS13 protein, S cerevisiae 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

18530-18539

Subventions

Organisme : NIGMS NIH HHS
ID : R35 GM131681
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM115422
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM035370
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM114111
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM082861
Pays : United States

Déclaration de conflit d'intérêts

The authors declare no competing interest.

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Auteurs

Shuliang Chen (S)

Department of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA 92093-0668.

Muriel Mari (M)

Department of Biomedical Sciences of Cells and Systems, University of Groningen, University Medical Center Groningen, 9713 AV Groningen, The Netherlands.

Smriti Parashar (S)

Department of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA 92093-0668.

Dongmei Liu (D)

Department of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA 92093-0668.

Yixian Cui (Y)

Department of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA 92093-0668.

Fulvio Reggiori (F)

Department of Biomedical Sciences of Cells and Systems, University of Groningen, University Medical Center Groningen, 9713 AV Groningen, The Netherlands.

Peter J Novick (PJ)

Department of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA 92093-0668; pnovick@ucsd.edu sfnovick@ucsd.edu.

Susan Ferro-Novick (S)

Department of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA 92093-0668; pnovick@ucsd.edu sfnovick@ucsd.edu.

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