Trujillo M A, Letovsky J, Maguire H F, Lopez-Cabrera M, Siddiqui A
Department of Microbiology and Immunology, University of Colorado Medical School, Denver 80262.
Proc Natl Acad Sci U S A. 1991 May 1;88(9):3797-801. doi: 10.1073/pnas.88.9.3797.
The liver-specific enhancer I of the human hepatitis B virus contains several regions of DNA-protein interaction. Located within this element are also the domains of a promoter controlling the synthesis of the X open reading frame. Functional domains of the enhancer I and the X gene promoter were identified using DNase I protection analysis, deletion mutagenesis, and cell transfections. A unique liver-specific interaction was identified within this element whose binding site includes a direct sequence repeat, 5'-AGTAAACAGTA-3'. The factor(s) binding to this sequence motif was purified by oligonucleotide-affinity chromatography. Binding of this factor appears to play a key role in determining the overall enhancer function. Additionally, the interaction of several purified factors is presented. Cotransfection of liver cells with expression vectors encoding transcriptional factors resulted in trans-activation of the promoter/enhancer function. Based on the results of genetic analysis a model outlining the functional domains of the enhancer/promoter region is presented.
人类乙型肝炎病毒的肝脏特异性增强子I包含几个DNA-蛋白质相互作用区域。在该元件内还存在一个控制X开放阅读框合成的启动子结构域。使用DNA酶I保护分析、缺失诱变和细胞转染鉴定了增强子I和X基因启动子的功能结构域。在该元件内鉴定出一种独特的肝脏特异性相互作用,其结合位点包括一个直接序列重复,5'-AGTAAACAGTA-3'。通过寡核苷酸亲和色谱法纯化了与该序列基序结合的因子。该因子的结合似乎在决定整体增强子功能中起关键作用。此外,还展示了几种纯化因子的相互作用。将肝细胞与编码转录因子的表达载体共转染导致启动子/增强子功能的反式激活。基于遗传分析结果,提出了一个概述增强子/启动子区域功能结构域的模型。