Abstract
The X gene product of the human hepatitis B virus (HBx), a major factor responsible for hepatitis and hepatocellular carcinoma, modulates transactivation by a variety of transcription factors. Herein, expression of the phosphoenolpyruvate carboxykinase (PEPCK) gene was found to be regulated transcriptionally by HBx through two distinct promoter regions. The cAMP response element (CRE)-1 site within the proximal promoter region mediated the HBx-induced transactivation of the PEPCK gene through C/EBPα and ATF-2. A retinoid X receptor (RXR) response element within the distal promoter region also contributed to the HBx-induced transactivation. Consistent with these results, HBx directly interacted with RXR, and the interaction interfaces were localized to the transactivation domain of HBx and the ligand binding domain of RXR. (C) 2000 Federation of European Biochemical Societies.
Original language | English (US) |
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Pages (from-to) | 114-118 |
Number of pages | 5 |
Journal | FEBS Letters |
Volume | 483 |
Issue number | 2-3 |
DOIs | |
State | Published - Oct 20 2000 |
Externally published | Yes |
Keywords
- ATF-2
- Hepatitis B virus X protein
- Phosphoenolpyruvate carboxykinase
- Retinoid X receptor
- Transactivation
ASJC Scopus subject areas
- Biophysics
- Structural Biology
- Biochemistry
- Molecular Biology
- Genetics
- Cell Biology