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The mechanism of linear ubiquitination in regulating cell death and correlative diseases

Linear ubiquitination is a specific post-translational modification in which ubiquitin is linked through M1 residue to form multiple types of polyubiquitin chains on substrates in order to regulate cellular processes. LUBAC comprised by HOIP, HOIL-1L, and SHARPIN as a sole E3 ligase catalyzes the ge...

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Autores principales: Gao, Liyuan, Zhang, Wei, Shi, Xiao hui, Chang, Xiaoyan, Han, Yi, Liu, Chundi, Jiang, Zhitao, Yang, Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562472/
https://www.ncbi.nlm.nih.gov/pubmed/37813853
http://dx.doi.org/10.1038/s41419-023-06183-3
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author Gao, Liyuan
Zhang, Wei
Shi, Xiao hui
Chang, Xiaoyan
Han, Yi
Liu, Chundi
Jiang, Zhitao
Yang, Xiang
author_facet Gao, Liyuan
Zhang, Wei
Shi, Xiao hui
Chang, Xiaoyan
Han, Yi
Liu, Chundi
Jiang, Zhitao
Yang, Xiang
author_sort Gao, Liyuan
collection PubMed
description Linear ubiquitination is a specific post-translational modification in which ubiquitin is linked through M1 residue to form multiple types of polyubiquitin chains on substrates in order to regulate cellular processes. LUBAC comprised by HOIP, HOIL-1L, and SHARPIN as a sole E3 ligase catalyzes the generation of linear ubiquitin chains, and it is simultaneously adjusted by deubiquitinases such as OTULIN and CYLD. Several studies have shown that gene mutation of linear ubiquitination in mice accompanied by different modalities of cell death would develop relative diseases. Cell death is a fundamental physiological process and responsible for embryonic development, organ maintenance, and immunity response. Therefore, it is worth speculating that linear ubiquitin mediated signaling pathway would participate in different diseases. The relative literature search was done from core collection of electronic databases such as Web of Science, PubMed, and Google Scholar using keywords about main regulators of linear ubiquitination pathway. Here, we summarize the regulatory mechanism of linear ubiquitination on cellular signaling pathway in cells with apoptosis, necroptosis, autophagy, pyroptosis, and ferroptosis. Intervening generation of linear ubiquitin chains in relative signaling pathway to regulate cell death might provide novel therapeutic insights for various human diseases.
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spelling pubmed-105624722023-10-11 The mechanism of linear ubiquitination in regulating cell death and correlative diseases Gao, Liyuan Zhang, Wei Shi, Xiao hui Chang, Xiaoyan Han, Yi Liu, Chundi Jiang, Zhitao Yang, Xiang Cell Death Dis Review Article Linear ubiquitination is a specific post-translational modification in which ubiquitin is linked through M1 residue to form multiple types of polyubiquitin chains on substrates in order to regulate cellular processes. LUBAC comprised by HOIP, HOIL-1L, and SHARPIN as a sole E3 ligase catalyzes the generation of linear ubiquitin chains, and it is simultaneously adjusted by deubiquitinases such as OTULIN and CYLD. Several studies have shown that gene mutation of linear ubiquitination in mice accompanied by different modalities of cell death would develop relative diseases. Cell death is a fundamental physiological process and responsible for embryonic development, organ maintenance, and immunity response. Therefore, it is worth speculating that linear ubiquitin mediated signaling pathway would participate in different diseases. The relative literature search was done from core collection of electronic databases such as Web of Science, PubMed, and Google Scholar using keywords about main regulators of linear ubiquitination pathway. Here, we summarize the regulatory mechanism of linear ubiquitination on cellular signaling pathway in cells with apoptosis, necroptosis, autophagy, pyroptosis, and ferroptosis. Intervening generation of linear ubiquitin chains in relative signaling pathway to regulate cell death might provide novel therapeutic insights for various human diseases. Nature Publishing Group UK 2023-10-10 /pmc/articles/PMC10562472/ /pubmed/37813853 http://dx.doi.org/10.1038/s41419-023-06183-3 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 Review Article
Gao, Liyuan
Zhang, Wei
Shi, Xiao hui
Chang, Xiaoyan
Han, Yi
Liu, Chundi
Jiang, Zhitao
Yang, Xiang
The mechanism of linear ubiquitination in regulating cell death and correlative diseases
title The mechanism of linear ubiquitination in regulating cell death and correlative diseases
title_full The mechanism of linear ubiquitination in regulating cell death and correlative diseases
title_fullStr The mechanism of linear ubiquitination in regulating cell death and correlative diseases
title_full_unstemmed The mechanism of linear ubiquitination in regulating cell death and correlative diseases
title_short The mechanism of linear ubiquitination in regulating cell death and correlative diseases
title_sort mechanism of linear ubiquitination in regulating cell death and correlative diseases
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562472/
https://www.ncbi.nlm.nih.gov/pubmed/37813853
http://dx.doi.org/10.1038/s41419-023-06183-3
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