Adenovirus E1B oncoprotein tethers a transcriptional repression domain to p53.
- 1 January 1994
- journal article
- Published by Cold Spring Harbor Laboratory in Genes & Development
- Vol. 8 (2), 190-202
- https://doi.org/10.1101/gad.8.2.190
Abstract
Many DNA tumor viruses express a protein that inhibits transcriptional activation by the tumor-suppressing transcription factor p53. We report that adenovirus E1B 55K represses p53-mediated activation by a mechanism not described previously. E1B 55K binds p53 without displacing it from its DNA-binding site. A fusion of E1B 55K to the GAL4 DNA-binding domain represses transcription from a variety of promoters with engineered upstream GAL4-binding sites. Mutations within E1B 55K that interfere with its transforming activity and its ability to inhibit p53-mediated trans-activation also interfere with transcriptional repression by the GAL4-55K fusion. These results demonstrate that E1B 55K functions as a direct transcriptional repressor that is targeted to p53-responsive genes by binding to p53.Keywords
This publication has 51 references indexed in Scilit:
- New eukaryotic transcriptional repressersNature, 1993
- Oncoprotein MDM2 conceals the activation domain of tumour suppressor p53Nature, 1993
- p53 is required for radiation-induced apoptosis in mouse thymocytesNature, 1993
- A death in the life of p53Nature, 1993
- Wild-type p53 restores cell cycle control and inhibits gene amplification in cells with mutant p53 allelesCell, 1992
- Altered cell cycle arrest and gene amplification potential accompany loss of wild-type p53Cell, 1992
- p53, guardian of the genomeNature, 1992
- The mdm-2 oncogene product forms a complex with the p53 protein and inhibits p53-mediated transactivationCell, 1992
- The p53 tumour suppressor geneNature, 1991
- Negative effect of the transcriptional activator GAL4Nature, 1988