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Anatomy of Mdm2 and Mdm4 in evolution
Mouse double minute (Mdm) genes span an evolutionary timeframe from the ancient eukaryotic placozoa Trichoplax adhaerens to Homo sapiens, implying a significant and possibly conserved cellular role throughout history. Maintenance of DNA integrity and response to DNA damage involve many key regulator...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372010/ https://www.ncbi.nlm.nih.gov/pubmed/28077607 http://dx.doi.org/10.1093/jmcb/mjx002 |
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author | Tan, Ban Xiong Liew, Hoe Peng Chua, Joy S. Ghadessy, Farid J. Tan, Yaw Sing Lane, David P. Coffill, Cynthia R. |
author_facet | Tan, Ban Xiong Liew, Hoe Peng Chua, Joy S. Ghadessy, Farid J. Tan, Yaw Sing Lane, David P. Coffill, Cynthia R. |
author_sort | Tan, Ban Xiong |
collection | PubMed |
description | Mouse double minute (Mdm) genes span an evolutionary timeframe from the ancient eukaryotic placozoa Trichoplax adhaerens to Homo sapiens, implying a significant and possibly conserved cellular role throughout history. Maintenance of DNA integrity and response to DNA damage involve many key regulatory pathways, including precise control over the tumour suppressor protein p53. In most vertebrates, degradation of p53 through proteasomal targeting is primarily mediated by heterodimers of Mdm2 and the Mdm2-related protein Mdm4 (also known as MdmX). Both Mdm2 and Mdm4 have p53-binding regions, acidic domains, zinc fingers, and C-terminal RING domains that are conserved throughout evolution. Vertebrates typically have both Mdm2 and Mdm4 genes, while analyses of sequenced genomes of invertebrate species have identified single Mdm genes, suggesting that a duplication event occurred prior to emergence of jawless vertebrates about 550–440 million years ago. The functional relationship between Mdm and p53 in T. adhaerens, an organism that has existed for 1 billion years, implies that these two proteins have evolved together to maintain a conserved and regulated function. |
format | Online Article Text |
id | pubmed-6372010 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63720102019-02-21 Anatomy of Mdm2 and Mdm4 in evolution Tan, Ban Xiong Liew, Hoe Peng Chua, Joy S. Ghadessy, Farid J. Tan, Yaw Sing Lane, David P. Coffill, Cynthia R. J Mol Cell Biol Invited Review Mouse double minute (Mdm) genes span an evolutionary timeframe from the ancient eukaryotic placozoa Trichoplax adhaerens to Homo sapiens, implying a significant and possibly conserved cellular role throughout history. Maintenance of DNA integrity and response to DNA damage involve many key regulatory pathways, including precise control over the tumour suppressor protein p53. In most vertebrates, degradation of p53 through proteasomal targeting is primarily mediated by heterodimers of Mdm2 and the Mdm2-related protein Mdm4 (also known as MdmX). Both Mdm2 and Mdm4 have p53-binding regions, acidic domains, zinc fingers, and C-terminal RING domains that are conserved throughout evolution. Vertebrates typically have both Mdm2 and Mdm4 genes, while analyses of sequenced genomes of invertebrate species have identified single Mdm genes, suggesting that a duplication event occurred prior to emergence of jawless vertebrates about 550–440 million years ago. The functional relationship between Mdm and p53 in T. adhaerens, an organism that has existed for 1 billion years, implies that these two proteins have evolved together to maintain a conserved and regulated function. Oxford University Press 2017-02 2017-02-07 /pmc/articles/PMC6372010/ /pubmed/28077607 http://dx.doi.org/10.1093/jmcb/mjx002 Text en © The Author (2017). Published by Oxford University Press on behalf of Journal of Molecular Cell Biology, IBCB, SIBS, CAS. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Invited Review Tan, Ban Xiong Liew, Hoe Peng Chua, Joy S. Ghadessy, Farid J. Tan, Yaw Sing Lane, David P. Coffill, Cynthia R. Anatomy of Mdm2 and Mdm4 in evolution |
title | Anatomy of Mdm2 and Mdm4 in evolution |
title_full | Anatomy of Mdm2 and Mdm4 in evolution |
title_fullStr | Anatomy of Mdm2 and Mdm4 in evolution |
title_full_unstemmed | Anatomy of Mdm2 and Mdm4 in evolution |
title_short | Anatomy of Mdm2 and Mdm4 in evolution |
title_sort | anatomy of mdm2 and mdm4 in evolution |
topic | Invited Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372010/ https://www.ncbi.nlm.nih.gov/pubmed/28077607 http://dx.doi.org/10.1093/jmcb/mjx002 |
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