Ueda K, Wei Y, Ganem D
Department of Microbiology and Immunology, Howard Medical Institute, University of California Medical Center, San Francisco, California 94143, USA.
J Virol. 1996 Jul;70(7):4714-23. doi: 10.1128/JVI.70.7.4714-4723.1996.
Woodchuck hepatitis virus (WHV) efficiently induces hepatocellular carcinoma in chronically infected hosts. A key step in hepatocarcinogenesis by WHV is insertional activation of the cellular N-myc gene by integrated viral DNA. WHV enhancer II (En II) is the major cis-acting element involved in this activation. Here we characterize this viral enhancer element and define the cellular factors involved in its activity. WHV En II activity is strongly liver specific and maps to an 88-nucleotide DNA segment (nucleotides 1772 to 1859) located 5' to the pregenomic RNA start site. Genetic analyses and electrophoretic mobility shift assays indicate that the enhancer contains three subregions important to its activity. The core elements of the enhancer are recognition sites for the liver-enriched factors HNF1 and HNF4; together, these signals account for the bulk of En II activity as well as its strong liver specificity. Multimerization of either recognition site produced strong activity even in the absence of other En II sequences. 5' to these elements is a binding site for the ubiquitous Oct-1 transcription factor, which further augments enhancer activity ca. twofold.
土拨鼠肝炎病毒(WHV)能在慢性感染宿主中高效诱发肝细胞癌。WHV致癌的关键步骤是整合的病毒DNA对细胞N-myc基因的插入激活。WHV增强子II(En II)是参与此激活过程的主要顺式作用元件。在此,我们对该病毒增强子元件进行了表征,并确定了涉及其活性的细胞因子。WHV En II活性具有很强的肝脏特异性,定位于位于前基因组RNA起始位点5'端的一个88个核苷酸的DNA片段(核苷酸1772至1859)。遗传分析和电泳迁移率变动分析表明,该增强子包含对其活性重要的三个亚区域。增强子的核心元件是肝脏富集因子HNF1和HNF4的识别位点;这些信号共同构成了En II活性的大部分以及其强大的肝脏特异性。即使在没有其他En II序列的情况下,任一识别位点的多聚化也会产生很强的活性。在这些元件的5'端是普遍存在的Oct-1转录因子的结合位点,它可使增强子活性进一步增强约两倍。