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Methionine Restriction Impairs Degradation of a Protein that Aberrantly Engages the Endoplasmic Reticulum Translocon

Proteins that persistently engage endoplasmic reticulum (ER) translocons are degraded by multiple translocon quality control (TQC) mechanisms. In Saccharomyces cerevisiae , the model translocon-associated protein Deg1 -Sec62 is subject to ER-associated degradation (ERAD) by the Hrd1 ubiquitin ligase...

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Autores principales: Runnebohm, Avery M., Indovina, Christopher J., Turk, Samantha M., Bailey, Connor G., Orchard, Cade J., Wade, Lauren, Overton, Danielle L., Snow, Brian J., Rubenstein, Eric M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Caltech Library 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10667923/
https://www.ncbi.nlm.nih.gov/pubmed/38021175
http://dx.doi.org/10.17912/micropub.biology.001021
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author Runnebohm, Avery M.
Indovina, Christopher J.
Turk, Samantha M.
Bailey, Connor G.
Orchard, Cade J.
Wade, Lauren
Overton, Danielle L.
Snow, Brian J.
Rubenstein, Eric M.
author_facet Runnebohm, Avery M.
Indovina, Christopher J.
Turk, Samantha M.
Bailey, Connor G.
Orchard, Cade J.
Wade, Lauren
Overton, Danielle L.
Snow, Brian J.
Rubenstein, Eric M.
author_sort Runnebohm, Avery M.
collection PubMed
description Proteins that persistently engage endoplasmic reticulum (ER) translocons are degraded by multiple translocon quality control (TQC) mechanisms. In Saccharomyces cerevisiae , the model translocon-associated protein Deg1 -Sec62 is subject to ER-associated degradation (ERAD) by the Hrd1 ubiquitin ligase and, to a lesser extent, proteolysis mediated by the Ste24 protease. In a recent screen, we identified nine methionine-biosynthetic genes as candidate TQC regulators. Here, we found methionine restriction impairs Hrd1-independent Deg1 -Sec62 degradation. Beyond revealing methionine as a novel regulator of TQC, our results urge caution when working with laboratory yeast strains with auxotrophic mutations, often presumed not to influence cellular processes under investigation.
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spelling pubmed-106679232023-11-09 Methionine Restriction Impairs Degradation of a Protein that Aberrantly Engages the Endoplasmic Reticulum Translocon Runnebohm, Avery M. Indovina, Christopher J. Turk, Samantha M. Bailey, Connor G. Orchard, Cade J. Wade, Lauren Overton, Danielle L. Snow, Brian J. Rubenstein, Eric M. MicroPubl Biol New Finding Proteins that persistently engage endoplasmic reticulum (ER) translocons are degraded by multiple translocon quality control (TQC) mechanisms. In Saccharomyces cerevisiae , the model translocon-associated protein Deg1 -Sec62 is subject to ER-associated degradation (ERAD) by the Hrd1 ubiquitin ligase and, to a lesser extent, proteolysis mediated by the Ste24 protease. In a recent screen, we identified nine methionine-biosynthetic genes as candidate TQC regulators. Here, we found methionine restriction impairs Hrd1-independent Deg1 -Sec62 degradation. Beyond revealing methionine as a novel regulator of TQC, our results urge caution when working with laboratory yeast strains with auxotrophic mutations, often presumed not to influence cellular processes under investigation. Caltech Library 2023-11-09 /pmc/articles/PMC10667923/ /pubmed/38021175 http://dx.doi.org/10.17912/micropub.biology.001021 Text en Copyright: © 2023 by the authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle New Finding
Runnebohm, Avery M.
Indovina, Christopher J.
Turk, Samantha M.
Bailey, Connor G.
Orchard, Cade J.
Wade, Lauren
Overton, Danielle L.
Snow, Brian J.
Rubenstein, Eric M.
Methionine Restriction Impairs Degradation of a Protein that Aberrantly Engages the Endoplasmic Reticulum Translocon
title Methionine Restriction Impairs Degradation of a Protein that Aberrantly Engages the Endoplasmic Reticulum Translocon
title_full Methionine Restriction Impairs Degradation of a Protein that Aberrantly Engages the Endoplasmic Reticulum Translocon
title_fullStr Methionine Restriction Impairs Degradation of a Protein that Aberrantly Engages the Endoplasmic Reticulum Translocon
title_full_unstemmed Methionine Restriction Impairs Degradation of a Protein that Aberrantly Engages the Endoplasmic Reticulum Translocon
title_short Methionine Restriction Impairs Degradation of a Protein that Aberrantly Engages the Endoplasmic Reticulum Translocon
title_sort methionine restriction impairs degradation of a protein that aberrantly engages the endoplasmic reticulum translocon
topic New Finding
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10667923/
https://www.ncbi.nlm.nih.gov/pubmed/38021175
http://dx.doi.org/10.17912/micropub.biology.001021
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