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Functions of MDMX in the Modulation of the p53-Response
The MDM family proteins MDM2 and MDMX are two critical regulators of the p53 tumor suppressor protein. Expression of both proteins is necessary for allowing the embryonal development by keeping the activity of p53 in check. Upon stresses that need to activate p53 to perform its function as guardian...
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3085504/ https://www.ncbi.nlm.nih.gov/pubmed/21541195 http://dx.doi.org/10.1155/2011/876173 |
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author | Lenos, Kristiaan Jochemsen, Aart G. |
author_facet | Lenos, Kristiaan Jochemsen, Aart G. |
author_sort | Lenos, Kristiaan |
collection | PubMed |
description | The MDM family proteins MDM2 and MDMX are two critical regulators of the p53 tumor suppressor protein. Expression of both proteins is necessary for allowing the embryonal development by keeping the activity of p53 in check. Upon stresses that need to activate p53 to perform its function as guardian of the genome, p53 has to be liberated from these two inhibitors. In this review, we will discuss the various mechanisms by which MDMX protein levels are downregulated upon various types of stress, including posttranslational modifications of the MDMX protein and the regulation of mdmx mRNA expression, including alternative splicing. In addition, the putative function(s) of the described MDMX splice variants, particularly in tumor development, will be discussed. Lastly, in contrast to common belief, we have recently shown the existence of a p53-MDMX feedback loop, which is important for dampening the p53-response at later phases after genotoxic stress. |
format | Text |
id | pubmed-3085504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-30855042011-05-03 Functions of MDMX in the Modulation of the p53-Response Lenos, Kristiaan Jochemsen, Aart G. J Biomed Biotechnol Review Article The MDM family proteins MDM2 and MDMX are two critical regulators of the p53 tumor suppressor protein. Expression of both proteins is necessary for allowing the embryonal development by keeping the activity of p53 in check. Upon stresses that need to activate p53 to perform its function as guardian of the genome, p53 has to be liberated from these two inhibitors. In this review, we will discuss the various mechanisms by which MDMX protein levels are downregulated upon various types of stress, including posttranslational modifications of the MDMX protein and the regulation of mdmx mRNA expression, including alternative splicing. In addition, the putative function(s) of the described MDMX splice variants, particularly in tumor development, will be discussed. Lastly, in contrast to common belief, we have recently shown the existence of a p53-MDMX feedback loop, which is important for dampening the p53-response at later phases after genotoxic stress. Hindawi Publishing Corporation 2011 2011-03-22 /pmc/articles/PMC3085504/ /pubmed/21541195 http://dx.doi.org/10.1155/2011/876173 Text en Copyright © 2011 K. Lenos and A. G. Jochemsen. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Lenos, Kristiaan Jochemsen, Aart G. Functions of MDMX in the Modulation of the p53-Response |
title | Functions of MDMX in the Modulation of the p53-Response |
title_full | Functions of MDMX in the Modulation of the p53-Response |
title_fullStr | Functions of MDMX in the Modulation of the p53-Response |
title_full_unstemmed | Functions of MDMX in the Modulation of the p53-Response |
title_short | Functions of MDMX in the Modulation of the p53-Response |
title_sort | functions of mdmx in the modulation of the p53-response |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3085504/ https://www.ncbi.nlm.nih.gov/pubmed/21541195 http://dx.doi.org/10.1155/2011/876173 |
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