The p53–Mdm2 interaction and the E3 ligase activity of Mdm2/Mdm4 are conserved from lampreys to humans

  1. David P. Lane1
  1. 1p53 Laboratory (p53Lab), Agency for Science, Technology, and Research (A*STAR), Singapore 138648;
  2. 2Institute of Molecular and Cellular Biology, A*STAR, Singapore 138673;
  3. 3Bioinformatics Institute, A*STAR, Singapore 138671;
  4. 4National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi 110067, India;
  5. 5Okinawa Institute of Science and Technology Graduate University, Onna-son, Okinawa 904-0495, Japan;
  6. 6School of Biological Sciences, Nanyang Technological University, Singapore 637551;
  7. 7Department of Biological Sciences, National University of Singapore, Singapore 117543;
  8. 8Department of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228
  1. Corresponding authors: dplane{at}p53lab.a-star.edu.sg, mcbbv{at}imcb.a-star.edu.sg
  1. 9 These authors contributed equally to this work.

Abstract

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.

Keywords

Footnotes

  • Supplemental material is available for this article.

  • Article published online ahead of print. Article and publication date are online at http://www.genesdev.org/cgi/doi/10.1101/gad.274118.115.

  • Freely available online through the Genes & Development Open Access option.

  • Received October 28, 2015.
  • Accepted December 14, 2015.

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/.

| Table of Contents
OPEN ACCESS ARTICLE

Life Science Alliance