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The p53–Mdm2 interaction and the E3 ligase activity of Mdm2/Mdm4 are conserved from lampreys to humans
The extant jawless vertebrates, represented by lampreys and hagfish, are the oldest group of vertebrates and provide an interesting genomic evolutionary pivot point between invertebrates and jawed vertebrates. Through genome analysis of one of these jawless vertebrates, the Japanese lamprey (Lethent...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743058/ https://www.ncbi.nlm.nih.gov/pubmed/26798135 http://dx.doi.org/10.1101/gad.274118.115 |
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author | Coffill, Cynthia R. Lee, Alison P. Siau, Jia Wei Chee, Sharon M. Joseph, Thomas L. Tan, Yaw Sing Madhumalar, Arumugam Tay, Boon-Hui Brenner, Sydney Verma, Chandra S. Ghadessy, Farid J. Venkatesh, Byrappa Lane, David P. |
author_facet | Coffill, Cynthia R. Lee, Alison P. Siau, Jia Wei Chee, Sharon M. Joseph, Thomas L. Tan, Yaw Sing Madhumalar, Arumugam Tay, Boon-Hui Brenner, Sydney Verma, Chandra S. Ghadessy, Farid J. Venkatesh, Byrappa Lane, David P. |
author_sort | Coffill, Cynthia R. |
collection | PubMed |
description | The extant jawless vertebrates, represented by lampreys and hagfish, are the oldest group of vertebrates and provide an interesting genomic evolutionary pivot point between invertebrates and jawed vertebrates. Through genome analysis of one of these jawless vertebrates, the Japanese lamprey (Lethenteron japonicum), we identified all three members of the important p53 transcription factor family—Tp53, Tp63, and Tp73—as well as the Mdm2 and Mdm4 genes. These genes and their products are significant cellular regulators in human cancer, and further examination of their roles in this most distant vertebrate relative sheds light on their origin and coevolution. Their important role in response to DNA damage has been highlighted by the discovery of multiple copies of the Tp53 gene in elephants. Expression of lamprey p53, Mdm2, and Mdm4 proteins in mammalian cells reveals that the p53–Mdm2 interaction and the Mdm2/Mdm4 E3 ligase activity existed in the common ancestor of vertebrates and have been conserved for >500 million years of vertebrate evolution. Lamprey Mdm2 degrades human p53 with great efficiency, but this interaction is not blocked by currently available small molecule inhibitors of the human HDM2 protein, suggesting utility of lamprey Mdm2 in the study of the human p53 signaling pathway. |
format | Online Article Text |
id | pubmed-4743058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-47430582016-02-17 The p53–Mdm2 interaction and the E3 ligase activity of Mdm2/Mdm4 are conserved from lampreys to humans Coffill, Cynthia R. Lee, Alison P. Siau, Jia Wei Chee, Sharon M. Joseph, Thomas L. Tan, Yaw Sing Madhumalar, Arumugam Tay, Boon-Hui Brenner, Sydney Verma, Chandra S. Ghadessy, Farid J. Venkatesh, Byrappa Lane, David P. Genes Dev Research Paper The extant jawless vertebrates, represented by lampreys and hagfish, are the oldest group of vertebrates and provide an interesting genomic evolutionary pivot point between invertebrates and jawed vertebrates. Through genome analysis of one of these jawless vertebrates, the Japanese lamprey (Lethenteron japonicum), we identified all three members of the important p53 transcription factor family—Tp53, Tp63, and Tp73—as well as the Mdm2 and Mdm4 genes. These genes and their products are significant cellular regulators in human cancer, and further examination of their roles in this most distant vertebrate relative sheds light on their origin and coevolution. Their important role in response to DNA damage has been highlighted by the discovery of multiple copies of the Tp53 gene in elephants. Expression of lamprey p53, Mdm2, and Mdm4 proteins in mammalian cells reveals that the p53–Mdm2 interaction and the Mdm2/Mdm4 E3 ligase activity existed in the common ancestor of vertebrates and have been conserved for >500 million years of vertebrate evolution. Lamprey Mdm2 degrades human p53 with great efficiency, but this interaction is not blocked by currently available small molecule inhibitors of the human HDM2 protein, suggesting utility of lamprey Mdm2 in the study of the human p53 signaling pathway. Cold Spring Harbor Laboratory Press 2016-02-01 /pmc/articles/PMC4743058/ /pubmed/26798135 http://dx.doi.org/10.1101/gad.274118.115 Text en © 2016 Coffill et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article, published in Genes & Development, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Research Paper Coffill, Cynthia R. Lee, Alison P. Siau, Jia Wei Chee, Sharon M. Joseph, Thomas L. Tan, Yaw Sing Madhumalar, Arumugam Tay, Boon-Hui Brenner, Sydney Verma, Chandra S. Ghadessy, Farid J. Venkatesh, Byrappa Lane, David P. The p53–Mdm2 interaction and the E3 ligase activity of Mdm2/Mdm4 are conserved from lampreys to humans |
title | The p53–Mdm2 interaction and the E3 ligase activity of Mdm2/Mdm4 are conserved from lampreys to humans |
title_full | The p53–Mdm2 interaction and the E3 ligase activity of Mdm2/Mdm4 are conserved from lampreys to humans |
title_fullStr | The p53–Mdm2 interaction and the E3 ligase activity of Mdm2/Mdm4 are conserved from lampreys to humans |
title_full_unstemmed | The p53–Mdm2 interaction and the E3 ligase activity of Mdm2/Mdm4 are conserved from lampreys to humans |
title_short | The p53–Mdm2 interaction and the E3 ligase activity of Mdm2/Mdm4 are conserved from lampreys to humans |
title_sort | p53–mdm2 interaction and the e3 ligase activity of mdm2/mdm4 are conserved from lampreys to humans |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743058/ https://www.ncbi.nlm.nih.gov/pubmed/26798135 http://dx.doi.org/10.1101/gad.274118.115 |
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