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OTUD5 Regulates p53 Stability by Deubiquitinating p53
BACKGROUND: The p53 tumour suppressor protein is a transcription factor that prevents oncogenic progression by activating the expression of apoptosis and cell-cycle arrest genes in stressed cells. The stability of p53 is tightly regulated by ubiquitin-dependent degradation, driven mainly by its nega...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3797110/ https://www.ncbi.nlm.nih.gov/pubmed/24143256 http://dx.doi.org/10.1371/journal.pone.0077682 |
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author | Luo, Judong Lu, Zhonghua Lu, Xujing Chen, Ling Cao, Jianping Zhang, Shuyu Ling, Yang Zhou, Xifa |
author_facet | Luo, Judong Lu, Zhonghua Lu, Xujing Chen, Ling Cao, Jianping Zhang, Shuyu Ling, Yang Zhou, Xifa |
author_sort | Luo, Judong |
collection | PubMed |
description | BACKGROUND: The p53 tumour suppressor protein is a transcription factor that prevents oncogenic progression by activating the expression of apoptosis and cell-cycle arrest genes in stressed cells. The stability of p53 is tightly regulated by ubiquitin-dependent degradation, driven mainly by its negative regulators ubiquitin ligase MDM2. PRINCIPAL FINDINGS: In this study, we have identified OTUD5 as a DUB that interacts with and deubiquitinates p53. OTUD5 forms a direct complex with p53 and controls level of ubiquitination. The function of OTUD5 is required to allow the rapid activation of p53-dependent transcription and a p53-dependent apoptosis in response to DNA damage stress. CONCLUSIONS: As a novel deubiquitinating enzyme for p53, OTUD5 is required for the stabilization and the activation of a p53 response. |
format | Online Article Text |
id | pubmed-3797110 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37971102013-10-18 OTUD5 Regulates p53 Stability by Deubiquitinating p53 Luo, Judong Lu, Zhonghua Lu, Xujing Chen, Ling Cao, Jianping Zhang, Shuyu Ling, Yang Zhou, Xifa PLoS One Research Article BACKGROUND: The p53 tumour suppressor protein is a transcription factor that prevents oncogenic progression by activating the expression of apoptosis and cell-cycle arrest genes in stressed cells. The stability of p53 is tightly regulated by ubiquitin-dependent degradation, driven mainly by its negative regulators ubiquitin ligase MDM2. PRINCIPAL FINDINGS: In this study, we have identified OTUD5 as a DUB that interacts with and deubiquitinates p53. OTUD5 forms a direct complex with p53 and controls level of ubiquitination. The function of OTUD5 is required to allow the rapid activation of p53-dependent transcription and a p53-dependent apoptosis in response to DNA damage stress. CONCLUSIONS: As a novel deubiquitinating enzyme for p53, OTUD5 is required for the stabilization and the activation of a p53 response. Public Library of Science 2013-10-15 /pmc/articles/PMC3797110/ /pubmed/24143256 http://dx.doi.org/10.1371/journal.pone.0077682 Text en © 2013 Luo et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Luo, Judong Lu, Zhonghua Lu, Xujing Chen, Ling Cao, Jianping Zhang, Shuyu Ling, Yang Zhou, Xifa OTUD5 Regulates p53 Stability by Deubiquitinating p53 |
title | OTUD5 Regulates p53 Stability by Deubiquitinating p53 |
title_full | OTUD5 Regulates p53 Stability by Deubiquitinating p53 |
title_fullStr | OTUD5 Regulates p53 Stability by Deubiquitinating p53 |
title_full_unstemmed | OTUD5 Regulates p53 Stability by Deubiquitinating p53 |
title_short | OTUD5 Regulates p53 Stability by Deubiquitinating p53 |
title_sort | otud5 regulates p53 stability by deubiquitinating p53 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3797110/ https://www.ncbi.nlm.nih.gov/pubmed/24143256 http://dx.doi.org/10.1371/journal.pone.0077682 |
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