p53 transactivation and the impact of mutations, cofactors and small molecules using a simplified yeast-based screening system.

<h4>Background</h4>The p53 tumor suppressor, which is altered in most cancers, is a sequence-specific transcription factor that is able to modulate the expression of many target genes and influence a variety of cellular pathways. Inactivation of the p53 pathway in cancer frequently occur...

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Main Authors: Virginia Andreotti, Yari Ciribilli, Paola Monti, Alessandra Bisio, Mattia Lion, Jennifer Jordan, Gilberto Fronza, Paola Menichini, Michael A Resnick, Alberto Inga
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0020643&type=printable
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author Virginia Andreotti
Yari Ciribilli
Paola Monti
Alessandra Bisio
Mattia Lion
Jennifer Jordan
Gilberto Fronza
Paola Menichini
Michael A Resnick
Alberto Inga
author_facet Virginia Andreotti
Yari Ciribilli
Paola Monti
Alessandra Bisio
Mattia Lion
Jennifer Jordan
Gilberto Fronza
Paola Menichini
Michael A Resnick
Alberto Inga
author_sort Virginia Andreotti
collection DOAJ
description <h4>Background</h4>The p53 tumor suppressor, which is altered in most cancers, is a sequence-specific transcription factor that is able to modulate the expression of many target genes and influence a variety of cellular pathways. Inactivation of the p53 pathway in cancer frequently occurs through the expression of mutant p53 protein. In tumors that retain wild type p53, the pathway can be altered by upstream modulators, particularly the p53 negative regulators MDM2 and MDM4.<h4>Methodology/principal findings</h4>Given the many factors that might influence p53 function, including expression levels, mutations, cofactor proteins and small molecules, we expanded our previously described yeast-based system to provide the opportunity for efficient investigation of their individual and combined impacts in a miniaturized format. The system integrates i) variable expression of p53 proteins under the finely tunable GAL1,10 promoter, ii) single copy, chromosomally located p53-responsive and control luminescence reporters, iii) enhanced chemical uptake using modified ABC-transporters, iv) small-volume formats for treatment and dual-luciferase assays, and v) opportunities to co-express p53 with other cofactor proteins. This robust system can distinguish different levels of expression of WT and mutant p53 as well as interactions with MDM2 or 53BP1.<h4>Conclusions/significance</h4>We found that the small molecules Nutlin and RITA could both relieve the MDM2-dependent inhibition of WT p53 transactivation function, while only RITA could impact p53/53BP1 functional interactions. PRIMA-1 was ineffective in modifying the transactivation capacity of WT p53 and missense p53 mutations. This dual-luciferase assay can, therefore, provide a high-throughput assessment tool for investigating a matrix of factors that can influence the p53 network, including the effectiveness of newly developed small molecules, on WT and tumor-associated p53 mutants as well as interacting proteins.
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publishDate 2011-01-01
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spelling doaj-art-2b8a025dfb6a4609b60f93c77cb8b8e62025-08-20T03:46:54ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0166e2064310.1371/journal.pone.0020643p53 transactivation and the impact of mutations, cofactors and small molecules using a simplified yeast-based screening system.Virginia AndreottiYari CiribilliPaola MontiAlessandra BisioMattia LionJennifer JordanGilberto FronzaPaola MenichiniMichael A ResnickAlberto Inga<h4>Background</h4>The p53 tumor suppressor, which is altered in most cancers, is a sequence-specific transcription factor that is able to modulate the expression of many target genes and influence a variety of cellular pathways. Inactivation of the p53 pathway in cancer frequently occurs through the expression of mutant p53 protein. In tumors that retain wild type p53, the pathway can be altered by upstream modulators, particularly the p53 negative regulators MDM2 and MDM4.<h4>Methodology/principal findings</h4>Given the many factors that might influence p53 function, including expression levels, mutations, cofactor proteins and small molecules, we expanded our previously described yeast-based system to provide the opportunity for efficient investigation of their individual and combined impacts in a miniaturized format. The system integrates i) variable expression of p53 proteins under the finely tunable GAL1,10 promoter, ii) single copy, chromosomally located p53-responsive and control luminescence reporters, iii) enhanced chemical uptake using modified ABC-transporters, iv) small-volume formats for treatment and dual-luciferase assays, and v) opportunities to co-express p53 with other cofactor proteins. This robust system can distinguish different levels of expression of WT and mutant p53 as well as interactions with MDM2 or 53BP1.<h4>Conclusions/significance</h4>We found that the small molecules Nutlin and RITA could both relieve the MDM2-dependent inhibition of WT p53 transactivation function, while only RITA could impact p53/53BP1 functional interactions. PRIMA-1 was ineffective in modifying the transactivation capacity of WT p53 and missense p53 mutations. This dual-luciferase assay can, therefore, provide a high-throughput assessment tool for investigating a matrix of factors that can influence the p53 network, including the effectiveness of newly developed small molecules, on WT and tumor-associated p53 mutants as well as interacting proteins.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0020643&type=printable
spellingShingle Virginia Andreotti
Yari Ciribilli
Paola Monti
Alessandra Bisio
Mattia Lion
Jennifer Jordan
Gilberto Fronza
Paola Menichini
Michael A Resnick
Alberto Inga
p53 transactivation and the impact of mutations, cofactors and small molecules using a simplified yeast-based screening system.
PLoS ONE
title p53 transactivation and the impact of mutations, cofactors and small molecules using a simplified yeast-based screening system.
title_full p53 transactivation and the impact of mutations, cofactors and small molecules using a simplified yeast-based screening system.
title_fullStr p53 transactivation and the impact of mutations, cofactors and small molecules using a simplified yeast-based screening system.
title_full_unstemmed p53 transactivation and the impact of mutations, cofactors and small molecules using a simplified yeast-based screening system.
title_short p53 transactivation and the impact of mutations, cofactors and small molecules using a simplified yeast-based screening system.
title_sort p53 transactivation and the impact of mutations cofactors and small molecules using a simplified yeast based screening system
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0020643&type=printable
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