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Cul3-KLHL20 ubiquitin ligase: physiological functions, stress responses, and disease implications
Cullin-RING ubiquitin ligases are the largest Ubiquitin ligase family in eukaryotes and are multi-protein complexes. In these complexes, the Cullin protein serves as a scaffold to connect two functional modules of the ligases, the catalytic subunit and substrate-binding subunit. KLHL20 is a substrat...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818519/ https://www.ncbi.nlm.nih.gov/pubmed/27042198 http://dx.doi.org/10.1186/s13008-016-0017-2 |
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author | Chen, Hsin-Yi Liu, Chin-Chih Chen, Ruey-Hwa |
author_facet | Chen, Hsin-Yi Liu, Chin-Chih Chen, Ruey-Hwa |
author_sort | Chen, Hsin-Yi |
collection | PubMed |
description | Cullin-RING ubiquitin ligases are the largest Ubiquitin ligase family in eukaryotes and are multi-protein complexes. In these complexes, the Cullin protein serves as a scaffold to connect two functional modules of the ligases, the catalytic subunit and substrate-binding subunit. KLHL20 is a substrate-binding subunit of Cullin3 (Cul3) ubiquitin ligase. Recent studies have identified a number of substrates of KLHL20-based ubiquitin ligase. Through ubiquitination of these substrates, KLHL20 elicits diverse cellular functions, some of which are associated with human diseases. Furthermore, the functions, subcellular localizations, and expression of KLHL20 are regulated by several physiological and stressed signals, which allow KLHL20 to preferentially act on certain substrates to response to these signals. Here, we provide a summary of the functions and regulations of KLHL20 in several physiological processes and stress responses and its disease implications. |
format | Online Article Text |
id | pubmed-4818519 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48185192016-04-03 Cul3-KLHL20 ubiquitin ligase: physiological functions, stress responses, and disease implications Chen, Hsin-Yi Liu, Chin-Chih Chen, Ruey-Hwa Cell Div Review Cullin-RING ubiquitin ligases are the largest Ubiquitin ligase family in eukaryotes and are multi-protein complexes. In these complexes, the Cullin protein serves as a scaffold to connect two functional modules of the ligases, the catalytic subunit and substrate-binding subunit. KLHL20 is a substrate-binding subunit of Cullin3 (Cul3) ubiquitin ligase. Recent studies have identified a number of substrates of KLHL20-based ubiquitin ligase. Through ubiquitination of these substrates, KLHL20 elicits diverse cellular functions, some of which are associated with human diseases. Furthermore, the functions, subcellular localizations, and expression of KLHL20 are regulated by several physiological and stressed signals, which allow KLHL20 to preferentially act on certain substrates to response to these signals. Here, we provide a summary of the functions and regulations of KLHL20 in several physiological processes and stress responses and its disease implications. BioMed Central 2016-04-01 /pmc/articles/PMC4818519/ /pubmed/27042198 http://dx.doi.org/10.1186/s13008-016-0017-2 Text en © Chen et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Chen, Hsin-Yi Liu, Chin-Chih Chen, Ruey-Hwa Cul3-KLHL20 ubiquitin ligase: physiological functions, stress responses, and disease implications |
title | Cul3-KLHL20 ubiquitin ligase: physiological functions, stress responses, and disease implications |
title_full | Cul3-KLHL20 ubiquitin ligase: physiological functions, stress responses, and disease implications |
title_fullStr | Cul3-KLHL20 ubiquitin ligase: physiological functions, stress responses, and disease implications |
title_full_unstemmed | Cul3-KLHL20 ubiquitin ligase: physiological functions, stress responses, and disease implications |
title_short | Cul3-KLHL20 ubiquitin ligase: physiological functions, stress responses, and disease implications |
title_sort | cul3-klhl20 ubiquitin ligase: physiological functions, stress responses, and disease implications |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818519/ https://www.ncbi.nlm.nih.gov/pubmed/27042198 http://dx.doi.org/10.1186/s13008-016-0017-2 |
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