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TATA binding protein associated factor 3 (TAF3) interacts with p53 and inhibits its function
BACKGROUND: The tumour suppressor protein p53 is a sequence specific DNA-binding transcription regulator, which exerts its versatile roles in genome protection and apoptosis by affecting the expression of a large number of genes. In an attempt to obtain a better understanding of the mechanisms by wh...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2441632/ https://www.ncbi.nlm.nih.gov/pubmed/18549481 http://dx.doi.org/10.1186/1471-2199-9-57 |
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author | Bereczki, Orsolya Ujfaludi, Zsuzsanna Pardi, Norbert Nagy, Zita Tora, Laszlo Boros, Imre M Balint, Eva |
author_facet | Bereczki, Orsolya Ujfaludi, Zsuzsanna Pardi, Norbert Nagy, Zita Tora, Laszlo Boros, Imre M Balint, Eva |
author_sort | Bereczki, Orsolya |
collection | PubMed |
description | BACKGROUND: The tumour suppressor protein p53 is a sequence specific DNA-binding transcription regulator, which exerts its versatile roles in genome protection and apoptosis by affecting the expression of a large number of genes. In an attempt to obtain a better understanding of the mechanisms by which p53 transcription function is regulated, we studied p53 interactions. RESULTS: We identified BIP2 (Bric-à-brac interacting protein 2), the fly homolog of TAF3, a histone fold and a plant homeodomain containing subunit of TFIID, as an interacting partner of Drosophila melanogaster p53 (Dmp53). We detected physical interaction between the C terminus of Dmp53 and the central region of TAF3 both in yeast two hybrid assays and in vitro. Interestingly, DmTAF3 can also interact with human p53, and mammalian TAF3 can bind to both Dmp53 and human p53. This evolutionarily conserved interaction is functionally significant, since elevated TAF3 expression severely and selectively inhibits transcription activation by p53 in human cell lines, and it decreases the level of the p53 protein as well. CONCLUSION: We identified TAF3 as an evolutionarily conserved negative regulator of p53 transcription activation function. |
format | Text |
id | pubmed-2441632 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-24416322008-06-28 TATA binding protein associated factor 3 (TAF3) interacts with p53 and inhibits its function Bereczki, Orsolya Ujfaludi, Zsuzsanna Pardi, Norbert Nagy, Zita Tora, Laszlo Boros, Imre M Balint, Eva BMC Mol Biol Research Article BACKGROUND: The tumour suppressor protein p53 is a sequence specific DNA-binding transcription regulator, which exerts its versatile roles in genome protection and apoptosis by affecting the expression of a large number of genes. In an attempt to obtain a better understanding of the mechanisms by which p53 transcription function is regulated, we studied p53 interactions. RESULTS: We identified BIP2 (Bric-à-brac interacting protein 2), the fly homolog of TAF3, a histone fold and a plant homeodomain containing subunit of TFIID, as an interacting partner of Drosophila melanogaster p53 (Dmp53). We detected physical interaction between the C terminus of Dmp53 and the central region of TAF3 both in yeast two hybrid assays and in vitro. Interestingly, DmTAF3 can also interact with human p53, and mammalian TAF3 can bind to both Dmp53 and human p53. This evolutionarily conserved interaction is functionally significant, since elevated TAF3 expression severely and selectively inhibits transcription activation by p53 in human cell lines, and it decreases the level of the p53 protein as well. CONCLUSION: We identified TAF3 as an evolutionarily conserved negative regulator of p53 transcription activation function. BioMed Central 2008-06-12 /pmc/articles/PMC2441632/ /pubmed/18549481 http://dx.doi.org/10.1186/1471-2199-9-57 Text en Copyright © 2008 Bereczki et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Bereczki, Orsolya Ujfaludi, Zsuzsanna Pardi, Norbert Nagy, Zita Tora, Laszlo Boros, Imre M Balint, Eva TATA binding protein associated factor 3 (TAF3) interacts with p53 and inhibits its function |
title | TATA binding protein associated factor 3 (TAF3) interacts with p53 and inhibits its function |
title_full | TATA binding protein associated factor 3 (TAF3) interacts with p53 and inhibits its function |
title_fullStr | TATA binding protein associated factor 3 (TAF3) interacts with p53 and inhibits its function |
title_full_unstemmed | TATA binding protein associated factor 3 (TAF3) interacts with p53 and inhibits its function |
title_short | TATA binding protein associated factor 3 (TAF3) interacts with p53 and inhibits its function |
title_sort | tata binding protein associated factor 3 (taf3) interacts with p53 and inhibits its function |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2441632/ https://www.ncbi.nlm.nih.gov/pubmed/18549481 http://dx.doi.org/10.1186/1471-2199-9-57 |
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