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The Roles of the Ubiquitin–Proteasome System in the Endoplasmic Reticulum Stress Pathway

The endoplasmic reticulum (ER) is a highly dynamic organelle in eukaryotic cells, which is essential for synthesis, processing, sorting of protein and lipid metabolism. However, the cells activate a defense mechanism called endoplasmic reticulum stress (ER stress) response and initiate unfolded prot...

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Detalles Bibliográficos
Autores principales: Qu, Junyan, Zou, Tingting, Lin, Zhenghong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913544/
https://www.ncbi.nlm.nih.gov/pubmed/33546413
http://dx.doi.org/10.3390/ijms22041526
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author Qu, Junyan
Zou, Tingting
Lin, Zhenghong
author_facet Qu, Junyan
Zou, Tingting
Lin, Zhenghong
author_sort Qu, Junyan
collection PubMed
description The endoplasmic reticulum (ER) is a highly dynamic organelle in eukaryotic cells, which is essential for synthesis, processing, sorting of protein and lipid metabolism. However, the cells activate a defense mechanism called endoplasmic reticulum stress (ER stress) response and initiate unfolded protein response (UPR) as the unfolded proteins exceed the folding capacity of the ER due to the environmental influences or increased protein synthesis. ER stress can mediate many cellular processes, including autophagy, apoptosis and senescence. The ubiquitin-proteasome system (UPS) is involved in the degradation of more than 80% of proteins in the cells. Today, increasing numbers of studies have shown that the two important components of UPS, E3 ubiquitin ligases and deubiquitinases (DUBs), are tightly related to ER stress. In this review, we summarized the regulation of the E3 ubiquitin ligases and DUBs in ER stress.
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spelling pubmed-79135442021-02-28 The Roles of the Ubiquitin–Proteasome System in the Endoplasmic Reticulum Stress Pathway Qu, Junyan Zou, Tingting Lin, Zhenghong Int J Mol Sci Review The endoplasmic reticulum (ER) is a highly dynamic organelle in eukaryotic cells, which is essential for synthesis, processing, sorting of protein and lipid metabolism. However, the cells activate a defense mechanism called endoplasmic reticulum stress (ER stress) response and initiate unfolded protein response (UPR) as the unfolded proteins exceed the folding capacity of the ER due to the environmental influences or increased protein synthesis. ER stress can mediate many cellular processes, including autophagy, apoptosis and senescence. The ubiquitin-proteasome system (UPS) is involved in the degradation of more than 80% of proteins in the cells. Today, increasing numbers of studies have shown that the two important components of UPS, E3 ubiquitin ligases and deubiquitinases (DUBs), are tightly related to ER stress. In this review, we summarized the regulation of the E3 ubiquitin ligases and DUBs in ER stress. MDPI 2021-02-03 /pmc/articles/PMC7913544/ /pubmed/33546413 http://dx.doi.org/10.3390/ijms22041526 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Qu, Junyan
Zou, Tingting
Lin, Zhenghong
The Roles of the Ubiquitin–Proteasome System in the Endoplasmic Reticulum Stress Pathway
title The Roles of the Ubiquitin–Proteasome System in the Endoplasmic Reticulum Stress Pathway
title_full The Roles of the Ubiquitin–Proteasome System in the Endoplasmic Reticulum Stress Pathway
title_fullStr The Roles of the Ubiquitin–Proteasome System in the Endoplasmic Reticulum Stress Pathway
title_full_unstemmed The Roles of the Ubiquitin–Proteasome System in the Endoplasmic Reticulum Stress Pathway
title_short The Roles of the Ubiquitin–Proteasome System in the Endoplasmic Reticulum Stress Pathway
title_sort roles of the ubiquitin–proteasome system in the endoplasmic reticulum stress pathway
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913544/
https://www.ncbi.nlm.nih.gov/pubmed/33546413
http://dx.doi.org/10.3390/ijms22041526
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