Interactions of the transcription factors MIBP1 and RFX1 with the EP element of the hepatitis B virus enhancer

被引:15
作者
Blake, M
Niklinski, J
Zajac-Kaye, M
机构
[1] NIH, BIOL CHEM LAB, BETHESDA, MD 20892 USA
[2] SCH MED, DEPT THORAC SURG, BIALYSTOK, POLAND
关键词
D O I
10.1128/JVI.70.9.6060-6066.1996
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:6060 / 6066
页数:7
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