Obert S, Zachmann-Brand B, Deindl E, Tucker W, Bartenschlager R, Schaller H
Zentrum für Molekulare Biologie Heidelberg (ZMBH), Universität Heidelberg, Germany.
EMBO J. 1996 May 15;15(10):2565-74.
According to the current model of hepadnavirus gene expression, the viral envelope proteins are produced from unspliced subgenomic RNAs, in contrast to the retroviral mechanism, where the subgenomic env RNA is generated by RNA splicing. We now describe and characterize a novel duck hepatitis B virus RNA species which is derived from the RNA pregenome by loss of a 1.15 kb intron. This RNA (termed spliced L RNA) codes for the large surface protein (L protein), as does the previously described unspliced mRNA (the preS RNA); however, it differs in 5' leader sequence and promoter control. Mutational analysis indicates that the spliced L RNA is functionally important for virus replication in infected hepatocytes and ducks, but not for virus formation from transfected DNA genomes. This suggests that the newly discovered second pathway for L protein synthesis plays a distinct role in an early step in the viral life cycle.
根据目前嗜肝DNA病毒基因表达模型,病毒包膜蛋白由未剪接的亚基因组RNA产生,这与逆转录病毒机制相反,在逆转录病毒机制中,亚基因组env RNA是通过RNA剪接产生的。我们现在描述并鉴定了一种新型鸭乙型肝炎病毒RNA种类,它是由RNA前基因组缺失一个1.15 kb内含子衍生而来的。这种RNA(称为剪接L RNA)与先前描述的未剪接mRNA(前S RNA)一样,编码大表面蛋白(L蛋白);然而,它在5'前导序列和启动子控制方面有所不同。突变分析表明,剪接L RNA对感染的肝细胞和鸭中的病毒复制功能重要,但对转染DNA基因组形成病毒不重要。这表明新发现的L蛋白合成的第二条途径在病毒生命周期的早期步骤中发挥着独特作用。