Ori A, Atzmony D, Haviv I, Shaul Y
Department of Molecular Genetics and Virology, Weizmann Institute of Science, Rehovot, Israel.
Virology. 1994 Nov 1;204(2):600-8. doi: 10.1006/viro.1994.1574.
The hepatitis B virus enhancer plays an important role in transcription regulation of the viral genes in a liver-specific manner. In animal models a homologous element seems to be involved in activation of cellular oncogenes and tumorigenesis. Previously, the enhancer was divided into several functional domains, whereby each one seemed to be required for optimal transcription activity. To gain more information on the mode of action of these elements and their role in viral genome, we mutagenized the individual enhancer elements and analyzed their functions in three different experimental systems. All show that the NF1b motif of the enhancer plays a central role, with the most dramatic results obtained from the cell-free in vitro transcription assay. Furthermore, an intact viral genome mutated at the NF1b site is a poor template for the synthesis of the 3.5-kb pregenomic RNA. These data are rather unexpected, given the ubiquitous appearance of this factor. On the other hand, our findings are in agreement with a large number of recently reported cases in which NF1 seems to determine tissue-specific expression of a wide range of cellular and viral promoters.
乙肝病毒增强子以肝脏特异性方式在病毒基因的转录调控中发挥重要作用。在动物模型中,一个同源元件似乎参与细胞癌基因的激活和肿瘤发生。以前,增强子被分为几个功能域,每个功能域似乎都是最佳转录活性所必需的。为了获得更多关于这些元件的作用方式及其在病毒基因组中作用的信息,我们对各个增强子元件进行了诱变,并在三种不同的实验系统中分析了它们的功能。所有结果表明,增强子的NF1b基序起着核心作用,无细胞体外转录试验得到的结果最为显著。此外,在NF1b位点发生突变的完整病毒基因组是合成3.5kb前基因组RNA的不良模板。鉴于该因子普遍存在,这些数据相当出人意料。另一方面,我们的发现与最近大量报道的案例一致,其中NF1似乎决定了广泛的细胞和病毒启动子的组织特异性表达。