Reifenberg K, Wilts H, Löhler J, Nusser P, Hanano R, Guidotti L G, Chisari F V, Schlicht H J
Laboratory Animal Research Unit, University of Ulm, 89081 Ulm, Germany.
J Virol. 1999 Dec;73(12):10399-405. doi: 10.1128/JVI.73.12.10399-10405.1999.
The function of the X protein in the life cycle of mammalian hepadnaviruses is unclear. Based on tissue culture experiments it has been suggested that this protein represents a transcriptional transactivator which might be essential for the expression of the viral core gene. Here we have examined whether the activity of the human hepatitis B virus (HBV) core gene in vivo depends on X coexpression. To this end we compared core gene expression between four lineages of transgenic mice carrying the HBV core gene in cis arrangement with the X gene (cex lineage) and six lineages containing a modified construct in which the start codon of the X gene had been deleted (ce lineage). Whereas all cex lineages consistently exhibited a high-level hepatic core gene expression, the liver-specific core gene expression pattern of the ce lineages was heterogenous with four lineages virtually not expressing the core gene. This defect was due to a strongly reduced transcription since no core mRNA could be detected by Northern blotting. To test whether core gene expression could be restored by providing an intact X gene in trans, we crossbred mice of two lines which expressed no core mRNA or core protein with transgenic mice expressing the X-gene product under the transcriptional regulation of the liver-specific major-urinary-protein promoter/enhancer (MUP-X mice). The introduction of the MUP-X transgene induced core mRNA expression and core protein biosynthesis in the livers of the double-transgenic mice. This demonstrates that the X-gene product has the capacity to transactivate HBV core gene expression in vivo.
X蛋白在哺乳动物嗜肝DNA病毒生命周期中的功能尚不清楚。基于组织培养实验,有人提出该蛋白是一种转录反式激活因子,可能对病毒核心基因的表达至关重要。在此,我们研究了人类乙型肝炎病毒(HBV)核心基因在体内的活性是否依赖于X基因的共表达。为此,我们比较了四个携带顺式排列的HBV核心基因与X基因的转基因小鼠品系(cex品系)和六个含有修饰构建体(其中X基因的起始密码子已被删除)的品系(ce品系)之间的核心基因表达。所有cex品系均持续表现出高水平的肝脏核心基因表达,而ce品系的肝脏特异性核心基因表达模式则是异质性的,其中四个品系几乎不表达核心基因。这种缺陷是由于转录大幅减少,因为通过Northern印迹法无法检测到核心mRNA。为了测试通过反式提供完整的X基因是否可以恢复核心基因表达,我们将两个不表达核心mRNA或核心蛋白的品系的小鼠与在肝脏特异性主要尿蛋白启动子/增强子(MUP-X小鼠)的转录调控下表达X基因产物的转基因小鼠进行杂交。MUP-X转基因的引入诱导了双转基因小鼠肝脏中核心mRNA表达和核心蛋白生物合成。这表明X基因产物具有在体内反式激活HBV核心基因表达的能力。