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ER-associated RNA silencing promotes ER quality control
The endoplasmic reticulum (ER) coordinates mRNA translation and processing of secreted and endomembrane proteins. ER-associated degradation (ERAD) prevents the accumulation of misfolded proteins in the ER, but the physiological regulation of this process remains poorly characterized. Here, in a gene...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729107/ https://www.ncbi.nlm.nih.gov/pubmed/36471127 http://dx.doi.org/10.1038/s41556-022-01025-4 |
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author | Efstathiou, Sotirios Ottens, Franziska Schütter, Lena-Sophie Ravanelli, Sonia Charmpilas, Nikolaos Gutschmidt, Aljona Le Pen, Jérémie Gehring, Niels H. Miska, Eric A. Bouças, Jorge Hoppe, Thorsten |
author_facet | Efstathiou, Sotirios Ottens, Franziska Schütter, Lena-Sophie Ravanelli, Sonia Charmpilas, Nikolaos Gutschmidt, Aljona Le Pen, Jérémie Gehring, Niels H. Miska, Eric A. Bouças, Jorge Hoppe, Thorsten |
author_sort | Efstathiou, Sotirios |
collection | PubMed |
description | The endoplasmic reticulum (ER) coordinates mRNA translation and processing of secreted and endomembrane proteins. ER-associated degradation (ERAD) prevents the accumulation of misfolded proteins in the ER, but the physiological regulation of this process remains poorly characterized. Here, in a genetic screen using an ERAD model substrate in Caenorhabditis elegans, we identified an anti-viral RNA interference pathway, referred to as ER-associated RNA silencing (ERAS), which acts together with ERAD to preserve ER homeostasis and function. Induced by ER stress, ERAS is mediated by the Argonaute protein RDE-1/AGO2, is conserved in mammals and promotes ER-associated RNA turnover. ERAS and ERAD are complementary, as simultaneous inactivation of both quality-control pathways leads to increased ER stress, reduced protein quality control and impaired intestinal integrity. Collectively, our findings indicate that ER homeostasis and organismal health are protected by synergistic functions of ERAS and ERAD. |
format | Online Article Text |
id | pubmed-9729107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97291072022-12-09 ER-associated RNA silencing promotes ER quality control Efstathiou, Sotirios Ottens, Franziska Schütter, Lena-Sophie Ravanelli, Sonia Charmpilas, Nikolaos Gutschmidt, Aljona Le Pen, Jérémie Gehring, Niels H. Miska, Eric A. Bouças, Jorge Hoppe, Thorsten Nat Cell Biol Article The endoplasmic reticulum (ER) coordinates mRNA translation and processing of secreted and endomembrane proteins. ER-associated degradation (ERAD) prevents the accumulation of misfolded proteins in the ER, but the physiological regulation of this process remains poorly characterized. Here, in a genetic screen using an ERAD model substrate in Caenorhabditis elegans, we identified an anti-viral RNA interference pathway, referred to as ER-associated RNA silencing (ERAS), which acts together with ERAD to preserve ER homeostasis and function. Induced by ER stress, ERAS is mediated by the Argonaute protein RDE-1/AGO2, is conserved in mammals and promotes ER-associated RNA turnover. ERAS and ERAD are complementary, as simultaneous inactivation of both quality-control pathways leads to increased ER stress, reduced protein quality control and impaired intestinal integrity. Collectively, our findings indicate that ER homeostasis and organismal health are protected by synergistic functions of ERAS and ERAD. Nature Publishing Group UK 2022-12-05 2022 /pmc/articles/PMC9729107/ /pubmed/36471127 http://dx.doi.org/10.1038/s41556-022-01025-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Efstathiou, Sotirios Ottens, Franziska Schütter, Lena-Sophie Ravanelli, Sonia Charmpilas, Nikolaos Gutschmidt, Aljona Le Pen, Jérémie Gehring, Niels H. Miska, Eric A. Bouças, Jorge Hoppe, Thorsten ER-associated RNA silencing promotes ER quality control |
title | ER-associated RNA silencing promotes ER quality control |
title_full | ER-associated RNA silencing promotes ER quality control |
title_fullStr | ER-associated RNA silencing promotes ER quality control |
title_full_unstemmed | ER-associated RNA silencing promotes ER quality control |
title_short | ER-associated RNA silencing promotes ER quality control |
title_sort | er-associated rna silencing promotes er quality control |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729107/ https://www.ncbi.nlm.nih.gov/pubmed/36471127 http://dx.doi.org/10.1038/s41556-022-01025-4 |
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