Blake M, Niklinski J, Zajac-Kaye M
Laboratory of Biological Chemistry, National Cancer Institute, Bethesda, Maryland 20892, USA.
J Virol. 1996 Sep;70(9):6060-6. doi: 10.1128/JVI.70.9.6060-6066.1996.
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.
我们先前证明,MIBP1和RFX1多肽在体内相互作用形成复合物,该复合物可结合c-myc基因中的MIF-1元件以及主要组织相容性复合体II类X盒识别序列。我们现在发现,乙肝病毒增强子I内的关键调控序列EP元件也与MIBP1和RFX1相关。使用针对寡核苷酸纯化的MIBP1或源自主要组织相容性复合体II类启动子结合蛋白RFX1的肽的多克隆抗血清,我们发现MIBP1和RFX1均存在于EP位点的DNA-蛋白质复合物中。此外,虽然EP元件可与几个相邻元件协同作用以反式激活乙肝病毒表达,但我们证明单独的EP位点可独立于位置和方向抑制猿猴病毒40启动子的转录,提示其在肝癌细胞中的沉默子功能。