Previous Article | Next Article ![]()
J. Virol., 09 1996, 6060-6066, Vol 70, No. 9
M Blake, J Niklinski and M Zajac-Kaye
We previously demonstrated that MIBP1 and RFX1 polypeptides associate in
vivo to form a complex that binds to the MIF-1 element in the c-myc gene
and the major histocompatibility complex class II X-box recognition
sequence. We now show that the EP element, a key regulatory sequence within
hepatitis B virus enhancer I, also associates with MIBP1 and RFX1. Using
polyclonal antisera directed against either oligonucleotide-purified MIBP1
or a peptide derived from the major histocompatibility complex class II
promoter-binding protein RFX1, we showed that MIBP1 and RFX1 are both
present in the DNA-protein complexes at the EP site. In addition, while the
EP element can act cooperatively with several adjacent elements to
transactivate hepatitis B virus expression, we demonstrated that the EP
site alone can repress transcription of simian virus 40 promoter in a
position- and orientation-independent manner, suggesting a silencer
function in hepatocarcinoma cells.
Copyright © 1996, American Society for Microbiology
Interactions of the transcription factors MIBP1 and RFX1 with the EP element of the hepatitis B virus enhancer
Laboratory of Biological Chemistry, National Cancer Institute, Bethesda, Maryland 20892, USA.
This article has been cited by other articles:
| J. Bacteriol. | Mol. Cell. Biol. | Microbiol. Mol. Biol. Rev. |
|---|
| Clin. Vaccine Immunol. | ALL ASM JOURNALS |
|---|