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p53, p63 and p73 in the wonderland of S. cerevisiae
Since its discovery in 1979, p53 has been on the forefront of cancer research. It is considered a master gene of cancer suppression and is found mutated in around 50% of all human tumors. In addition, the progressive identification of p53-related transcription factors p63 and p73 as well as their mu...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593689/ https://www.ncbi.nlm.nih.gov/pubmed/28915717 http://dx.doi.org/10.18632/oncotarget.18506 |
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author | Billant, Olivier Blondel, Marc Voisset, Cécile |
author_facet | Billant, Olivier Blondel, Marc Voisset, Cécile |
author_sort | Billant, Olivier |
collection | PubMed |
description | Since its discovery in 1979, p53 has been on the forefront of cancer research. It is considered a master gene of cancer suppression and is found mutated in around 50% of all human tumors. In addition, the progressive identification of p53-related transcription factors p63 and p73 as well as their multiple isoforms have added further layers of complexity to an already dense network. Among the numerous models used to unravel the p53 family mysteries, S. cerevisiae has been particularly useful. This seemingly naive model allows the expression of a functional human p53 and thus the assessment of p53 intrinsic transcriptional activity. The aim of this article is to review the various contributions that the budding yeast has made to the understanding of p53, p63 and p73 biology and to envision new possible directions for yeast-based assays in the field of cancer as well as other p53-family-related diseases. |
format | Online Article Text |
id | pubmed-5593689 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-55936892017-09-14 p53, p63 and p73 in the wonderland of S. cerevisiae Billant, Olivier Blondel, Marc Voisset, Cécile Oncotarget Review Since its discovery in 1979, p53 has been on the forefront of cancer research. It is considered a master gene of cancer suppression and is found mutated in around 50% of all human tumors. In addition, the progressive identification of p53-related transcription factors p63 and p73 as well as their multiple isoforms have added further layers of complexity to an already dense network. Among the numerous models used to unravel the p53 family mysteries, S. cerevisiae has been particularly useful. This seemingly naive model allows the expression of a functional human p53 and thus the assessment of p53 intrinsic transcriptional activity. The aim of this article is to review the various contributions that the budding yeast has made to the understanding of p53, p63 and p73 biology and to envision new possible directions for yeast-based assays in the field of cancer as well as other p53-family-related diseases. Impact Journals LLC 2017-06-16 /pmc/articles/PMC5593689/ /pubmed/28915717 http://dx.doi.org/10.18632/oncotarget.18506 Text en Copyright: © 2017 Billant et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Review Billant, Olivier Blondel, Marc Voisset, Cécile p53, p63 and p73 in the wonderland of S. cerevisiae |
title | p53, p63 and p73 in the wonderland of S. cerevisiae |
title_full | p53, p63 and p73 in the wonderland of S. cerevisiae |
title_fullStr | p53, p63 and p73 in the wonderland of S. cerevisiae |
title_full_unstemmed | p53, p63 and p73 in the wonderland of S. cerevisiae |
title_short | p53, p63 and p73 in the wonderland of S. cerevisiae |
title_sort | p53, p63 and p73 in the wonderland of s. cerevisiae |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593689/ https://www.ncbi.nlm.nih.gov/pubmed/28915717 http://dx.doi.org/10.18632/oncotarget.18506 |
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