Chang M F, Chen C H, Lin S L, Chen C J, Chang S C
Institute of Biochemistry, College of Medicine, National Taiwan University, Taipei, Republic of China.
J Virol. 1995 Apr;69(4):2508-14. doi: 10.1128/JVI.69.4.2508-2514.1995.
The functions of delta antigens (HDAgs) in the morphogenesis of hepatitis delta virus (HDV) have been studied previously. The C terminus of large HDAg has been shown to complex with the small surface antigen (HBsAg) of helper hepatitis B virus, whereas the assembly of small HDAg requires interaction with the N terminus of large HDAg (M.-F. Chang, C.-J. Chen, and S. C. Chang, J. Virol. 68:646-653, 1994). To further examine the molecular mechanisms by which HDAgs are involved in the assembly of HDV RNA, we have cotransfected Huh-7 cells with plasmids representing a longer than unit-length HDV and the small HBsAg cDNAs. We found that HDAg mRNA could be generated from an endogenous promoter within the HDV cDNA that was translated into large HDAg. Large HDAg is capable of complexing with monomeric HDV genomic RNA to form ribonucleoprotein particles (RNPs) and is capable of forming enveloped HDV-like particles in the presence of small HBsAg without undergoing HDV replication. In addition, the middle region from amino acid residues 89 to 145 of large HDAg is required for assembly of the RNPs but is dispensable for assembly of the enveloped particles. RNA assembly is also demonstrated with small HDAg when it is cotransfected with a packaging-defective large HDAg mutant and small HBsAg. Leu-115 within the putative helix-loop-helix structure of the small HDAg is important for the replication of HDV but is not essential for RNA assembly, suggesting that conformational requirements of small HDAg for replication and assembly of viral RNA may be different. Further studies indicate that a 312-nucleotide linear HDV RNA from one end of the HDV and structure is sufficient to form RNP complexes competent for assembly of virus-like particles with large HDAg and small HBsAg.
此前已对δ抗原(HDAgs)在丁型肝炎病毒(HDV)形态发生中的功能进行了研究。已表明大HDAg的C末端与辅助乙型肝炎病毒的小表面抗原(HBsAg)形成复合物,而小HDAg的组装需要与大HDAg的N末端相互作用(M.-F. 张、C.-J. 陈和S. C. 张,《病毒学杂志》68:646 - 653,1994年)。为了进一步研究HDAgs参与HDV RNA组装的分子机制,我们用代表比单位长度更长的HDV的质粒和小HBsAg cDNA共转染Huh - 7细胞。我们发现HDAg mRNA可从HDV cDNA内的一个内源性启动子产生,并被翻译成大HDAg。大HDAg能够与单体HDV基因组RNA形成复合物以形成核糖核蛋白颗粒(RNPs),并且在存在小HBsAg的情况下能够形成包膜样HDV颗粒,而无需经历HDV复制。此外,大HDAg氨基酸残基89至145的中间区域是RNPs组装所必需的,但对于包膜颗粒的组装是可有可无的。当小HDAg与包装缺陷型大HDAg突变体和小HBsAg共转染时,也证明了RNA组装。小HDAg假定的螺旋 - 环 - 螺旋结构内的Leu - 115对HDV的复制很重要,但对RNA组装不是必需的,这表明小HDAg对病毒RNA复制和组装的构象要求可能不同。进一步的研究表明,来自HDV一端的312个核苷酸的线性HDV RNA及其结构足以形成能够与大HDAg和小HBsAg组装病毒样颗粒的RNP复合物。