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Physiological ER stress caused by amylase production induces regulated Ire1-dependent mRNA decay in Aspergillus oryzae
Regulated Ire1-dependent decay (RIDD) is a feedback mechanism in which the endoribonuclease Ire1 cleaves endoplasmic reticulum (ER)-localized mRNAs encoding secretory and membrane proteins in eukaryotic cells under ER stress. RIDD is artificially induced by chemicals that generate ER stress; however...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10551036/ https://www.ncbi.nlm.nih.gov/pubmed/37794162 http://dx.doi.org/10.1038/s42003-023-05386-w |
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author | Tanaka, Mizuki Zhang, Silai Sato, Shun Yokota, Jun-ichi Sugiyama, Yuko Kawarasaki, Yasuaki Yamagata, Youhei Gomi, Katsuya Shintani, Takahiro |
author_facet | Tanaka, Mizuki Zhang, Silai Sato, Shun Yokota, Jun-ichi Sugiyama, Yuko Kawarasaki, Yasuaki Yamagata, Youhei Gomi, Katsuya Shintani, Takahiro |
author_sort | Tanaka, Mizuki |
collection | PubMed |
description | Regulated Ire1-dependent decay (RIDD) is a feedback mechanism in which the endoribonuclease Ire1 cleaves endoplasmic reticulum (ER)-localized mRNAs encoding secretory and membrane proteins in eukaryotic cells under ER stress. RIDD is artificially induced by chemicals that generate ER stress; however, its importance under physiological conditions remains unclear. Here, we demonstrate the occurrence of RIDD in filamentous fungus using Aspergillus oryzae as a model, which secretes copious amounts of amylases. α-Amylase mRNA was rapidly degraded by IreA, an Ire1 ortholog, depending on its ER-associated translation when mycelia were treated with dithiothreitol, an ER-stress inducer. The mRNA encoding maltose permease MalP, a prerequisite for the induction of amylolytic genes, was also identified as an RIDD target. Importantly, RIDD of malP mRNA is triggered by inducing amylase production without any artificial ER stress inducer. Our data provide the evidence that RIDD occurs in eukaryotic microorganisms under physiological ER stress. |
format | Online Article Text |
id | pubmed-10551036 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105510362023-10-06 Physiological ER stress caused by amylase production induces regulated Ire1-dependent mRNA decay in Aspergillus oryzae Tanaka, Mizuki Zhang, Silai Sato, Shun Yokota, Jun-ichi Sugiyama, Yuko Kawarasaki, Yasuaki Yamagata, Youhei Gomi, Katsuya Shintani, Takahiro Commun Biol Article Regulated Ire1-dependent decay (RIDD) is a feedback mechanism in which the endoribonuclease Ire1 cleaves endoplasmic reticulum (ER)-localized mRNAs encoding secretory and membrane proteins in eukaryotic cells under ER stress. RIDD is artificially induced by chemicals that generate ER stress; however, its importance under physiological conditions remains unclear. Here, we demonstrate the occurrence of RIDD in filamentous fungus using Aspergillus oryzae as a model, which secretes copious amounts of amylases. α-Amylase mRNA was rapidly degraded by IreA, an Ire1 ortholog, depending on its ER-associated translation when mycelia were treated with dithiothreitol, an ER-stress inducer. The mRNA encoding maltose permease MalP, a prerequisite for the induction of amylolytic genes, was also identified as an RIDD target. Importantly, RIDD of malP mRNA is triggered by inducing amylase production without any artificial ER stress inducer. Our data provide the evidence that RIDD occurs in eukaryotic microorganisms under physiological ER stress. Nature Publishing Group UK 2023-10-04 /pmc/articles/PMC10551036/ /pubmed/37794162 http://dx.doi.org/10.1038/s42003-023-05386-w Text en © The Author(s) 2023 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 Tanaka, Mizuki Zhang, Silai Sato, Shun Yokota, Jun-ichi Sugiyama, Yuko Kawarasaki, Yasuaki Yamagata, Youhei Gomi, Katsuya Shintani, Takahiro Physiological ER stress caused by amylase production induces regulated Ire1-dependent mRNA decay in Aspergillus oryzae |
title | Physiological ER stress caused by amylase production induces regulated Ire1-dependent mRNA decay in Aspergillus oryzae |
title_full | Physiological ER stress caused by amylase production induces regulated Ire1-dependent mRNA decay in Aspergillus oryzae |
title_fullStr | Physiological ER stress caused by amylase production induces regulated Ire1-dependent mRNA decay in Aspergillus oryzae |
title_full_unstemmed | Physiological ER stress caused by amylase production induces regulated Ire1-dependent mRNA decay in Aspergillus oryzae |
title_short | Physiological ER stress caused by amylase production induces regulated Ire1-dependent mRNA decay in Aspergillus oryzae |
title_sort | physiological er stress caused by amylase production induces regulated ire1-dependent mrna decay in aspergillus oryzae |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10551036/ https://www.ncbi.nlm.nih.gov/pubmed/37794162 http://dx.doi.org/10.1038/s42003-023-05386-w |
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