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Inositol Requiring Enzyme (IRE), a multiplayer in sensing endoplasmic reticulum stress

The endoplasmic reticulum (ER) can sense a wide variety of external and internal perturbations and responds by mounting stress coping responses, such as the unfolded protein response (UPR). The UPR is composed of three stress sensors, namely IRE1α, PERK, and ATF6 that are activated to re-establish E...

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Detalles Bibliográficos
Autores principales: Zhou, Zhixin, Wang, Qian, Michalak, Marek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8765250/
https://www.ncbi.nlm.nih.gov/pubmed/35059134
http://dx.doi.org/10.1080/19768354.2021.2020901
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author Zhou, Zhixin
Wang, Qian
Michalak, Marek
author_facet Zhou, Zhixin
Wang, Qian
Michalak, Marek
author_sort Zhou, Zhixin
collection PubMed
description The endoplasmic reticulum (ER) can sense a wide variety of external and internal perturbations and responds by mounting stress coping responses, such as the unfolded protein response (UPR). The UPR is composed of three stress sensors, namely IRE1α, PERK, and ATF6 that are activated to re-establish ER homeostasis. IRE1α represents the most ancient branch of the UPR affecting many cellular processes in plant and animal cells. IRE1α is a type I transmembrane protein with kinase/nuclease activities in response to ER stress. Both the ER luminal and cytosolic IRE1α interactomes have been identified revealing a multifunctional role of the ER stress sensor. IRE1α is also associated with organellar membrane contacts to promote rapid communication between intracellular organelles under stress conditions.
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spelling pubmed-87652502022-01-19 Inositol Requiring Enzyme (IRE), a multiplayer in sensing endoplasmic reticulum stress Zhou, Zhixin Wang, Qian Michalak, Marek Anim Cells Syst (Seoul) Articles The endoplasmic reticulum (ER) can sense a wide variety of external and internal perturbations and responds by mounting stress coping responses, such as the unfolded protein response (UPR). The UPR is composed of three stress sensors, namely IRE1α, PERK, and ATF6 that are activated to re-establish ER homeostasis. IRE1α represents the most ancient branch of the UPR affecting many cellular processes in plant and animal cells. IRE1α is a type I transmembrane protein with kinase/nuclease activities in response to ER stress. Both the ER luminal and cytosolic IRE1α interactomes have been identified revealing a multifunctional role of the ER stress sensor. IRE1α is also associated with organellar membrane contacts to promote rapid communication between intracellular organelles under stress conditions. Taylor & Francis 2022-01-10 /pmc/articles/PMC8765250/ /pubmed/35059134 http://dx.doi.org/10.1080/19768354.2021.2020901 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Zhou, Zhixin
Wang, Qian
Michalak, Marek
Inositol Requiring Enzyme (IRE), a multiplayer in sensing endoplasmic reticulum stress
title Inositol Requiring Enzyme (IRE), a multiplayer in sensing endoplasmic reticulum stress
title_full Inositol Requiring Enzyme (IRE), a multiplayer in sensing endoplasmic reticulum stress
title_fullStr Inositol Requiring Enzyme (IRE), a multiplayer in sensing endoplasmic reticulum stress
title_full_unstemmed Inositol Requiring Enzyme (IRE), a multiplayer in sensing endoplasmic reticulum stress
title_short Inositol Requiring Enzyme (IRE), a multiplayer in sensing endoplasmic reticulum stress
title_sort inositol requiring enzyme (ire), a multiplayer in sensing endoplasmic reticulum stress
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8765250/
https://www.ncbi.nlm.nih.gov/pubmed/35059134
http://dx.doi.org/10.1080/19768354.2021.2020901
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