Buckwold V E, Chen M, Ou J H
Department of Molecular Microbiology and Immunology, University of Southern California, School of Medicine, Los Angeles 90033, USA.
Virology. 1997 Jan 20;227(2):515-8. doi: 10.1006/viro.1996.8360.
The negative regulatory element (NRE) of the hepatitis B virus (HBV) core promoter contains three subregions which act synergistically to suppress core promoter activity. One of these subregions, NRE gamma, is active in both HeLa cervical carcinoma cells and Huh7 hepatoma cells and was found to be bound by a protein factor present in both cell types. Here we show that the transcription factor RFX1 can bind to NRE gamma and transactivate the core promoter through this site. Mutations which abrogated the gene-suppressive activity of NRE gamma prevented RFX1 from binding to NRE gamma. In addition, RFX1 can bind simultaneously, most likely as a heterodimer, with the transcription factor MIBP1 to NRE gamma. In the absence of a cloned MIBP1 gene for further studies, we hypothesize that RFX1 acts with MIBP1 to negatively regulate the core promoter activity through the NRE gamma site. The ability of RFX1 to transactivate the core promoter raises the possibility that RFX1 may play a dual role in regulating HBV gene expression.
乙型肝炎病毒(HBV)核心启动子的负调控元件(NRE)包含三个协同作用以抑制核心启动子活性的亚区域。其中一个亚区域,即NREγ,在HeLa宫颈癌细胞和Huh7肝癌细胞中均有活性,并且发现这两种细胞类型中都存在一种能与之结合的蛋白质因子。在此我们表明,转录因子RFX1可与NREγ结合,并通过该位点反式激活核心启动子。消除NREγ基因抑制活性的突变会阻止RFX1与NREγ结合。此外,RFX1很可能以异二聚体形式与转录因子MIBP1同时结合到NREγ上。由于缺乏用于进一步研究的克隆MIBP1基因,我们推测RFX1与MIBP1共同作用,通过NREγ位点负调控核心启动子活性。RFX1反式激活核心启动子的能力增加了RFX1可能在调节HBV基因表达中发挥双重作用的可能性。