Journal article
Direct interaction of the hepatitis B virus HBx protein with p53 leads to inhibition by HBx of p53 response element-directed transactivation
Abstract
Hepatitis B virus is a major risk factor in human hepatocellular carcinomas. We have used protein affinity chromatography to show that the 17-kDa hepatitis B virus gene product, HBx, binds directly to the human tumor suppressor gene product, p53. Interaction of HBx with p53 did not prevent p53 from specifically binding DNA. Instead, HBx enhanced p53's oligomerization state on a DNA oligonucleotide containing a p53 response element. Optimal …
Authors
Truant R; Antunovic J; Greenblatt J; Prives C; Cromlish JA
Journal
Journal of Virology, Vol. 69, No. 3, pp. 1851–1859
Publisher
American Society for Microbiology
Publication Date
March 1995
DOI
10.1128/jvi.69.3.1851-1859.1995
ISSN
0022-538X
Associated Experts
Fields of Research (FoR)
Sustainable Development Goals (SDG)
Medical Subject Headings (MeSH)
Base SequenceGene Expression Regulation, ViralHepatitis B virusMacromolecular SubstancesMolecular Sequence DataOligodeoxyribonucleotidesProtein BindingRegulatory Sequences, Nucleic AcidTrans-ActivatorsTranscription, GeneticTranscriptional ActivationTumor Suppressor Protein p53Viral Regulatory and Accessory Proteins