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A design principle underlying the paradoxical roles of E3 ubiquitin ligases
E3 ubiquitin ligases are important cellular components that determine the specificity of proteolysis in the ubiquitin-proteasome system. However, an increasing number of studies have indicated that E3 ubiquitin ligases also participate in transcription. Intrigued by the apparently paradoxical functi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381699/ https://www.ncbi.nlm.nih.gov/pubmed/24994517 http://dx.doi.org/10.1038/srep05573 |
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author | Lee, Daewon Kim, Minjin Cho, Kwang-Hyun |
author_facet | Lee, Daewon Kim, Minjin Cho, Kwang-Hyun |
author_sort | Lee, Daewon |
collection | PubMed |
description | E3 ubiquitin ligases are important cellular components that determine the specificity of proteolysis in the ubiquitin-proteasome system. However, an increasing number of studies have indicated that E3 ubiquitin ligases also participate in transcription. Intrigued by the apparently paradoxical functions of E3 ubiquitin ligases in both proteolysis and transcriptional activation, we investigated the underlying design principles using mathematical modeling. We found that the antagonistic functions integrated in E3 ubiquitin ligases can prevent any undesirable sustained activation of downstream genes when E3 ubiquitin ligases are destabilized by unexpected perturbations. Interestingly, this design principle of the system is similar to the operational principle of a safety interlock device in engineering systems, which prevents a system from abnormal operation unless stability is guaranteed. |
format | Online Article Text |
id | pubmed-5381699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53816992017-04-11 A design principle underlying the paradoxical roles of E3 ubiquitin ligases Lee, Daewon Kim, Minjin Cho, Kwang-Hyun Sci Rep Article E3 ubiquitin ligases are important cellular components that determine the specificity of proteolysis in the ubiquitin-proteasome system. However, an increasing number of studies have indicated that E3 ubiquitin ligases also participate in transcription. Intrigued by the apparently paradoxical functions of E3 ubiquitin ligases in both proteolysis and transcriptional activation, we investigated the underlying design principles using mathematical modeling. We found that the antagonistic functions integrated in E3 ubiquitin ligases can prevent any undesirable sustained activation of downstream genes when E3 ubiquitin ligases are destabilized by unexpected perturbations. Interestingly, this design principle of the system is similar to the operational principle of a safety interlock device in engineering systems, which prevents a system from abnormal operation unless stability is guaranteed. Nature Publishing Group 2014-07-04 /pmc/articles/PMC5381699/ /pubmed/24994517 http://dx.doi.org/10.1038/srep05573 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Article Lee, Daewon Kim, Minjin Cho, Kwang-Hyun A design principle underlying the paradoxical roles of E3 ubiquitin ligases |
title | A design principle underlying the paradoxical roles of E3 ubiquitin ligases |
title_full | A design principle underlying the paradoxical roles of E3 ubiquitin ligases |
title_fullStr | A design principle underlying the paradoxical roles of E3 ubiquitin ligases |
title_full_unstemmed | A design principle underlying the paradoxical roles of E3 ubiquitin ligases |
title_short | A design principle underlying the paradoxical roles of E3 ubiquitin ligases |
title_sort | design principle underlying the paradoxical roles of e3 ubiquitin ligases |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381699/ https://www.ncbi.nlm.nih.gov/pubmed/24994517 http://dx.doi.org/10.1038/srep05573 |
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