Lai M M, Chao Y C, Chang M F, Lin J H, Gust I
Dept. of Microbiology, Univ. of So. Calif., Sch. of Med., Los Angeles 90033.
Prog Clin Biol Res. 1991;364:283-92.
We have sequenced an HDV RNA from an acute delta hepatitis patient from the Nauru Islands. By comparison with other HDV sequences previously reported, we have identified three conserved regions: the first one is the sequence around the catalytic cleavage site for genomic-sense RNA; the second is the corresponding site for the antigenomic sense RNA; and the third is the sequence encoding the middle domain of the hepatitis delta antigen. We have shown that the middle domain of the delta antigen can bind specifically to the HDV RNA. This binding was demonstrated both in vitro and in the purified virion. It was suggested that this RNA-protein interaction is important for HDV RNA replication. We also suggest that the conserved sequences provide ideal primers for use in polymerase chain reaction (PCR) in clinical diagnosis of HDV infections. We recommend the use of nucleotides 870-900 and 690-720 (Makino et al., 1987a) as primers for routine screening.
我们对来自瑙鲁群岛一名急性丁型肝炎患者的丁型肝炎病毒(HDV)RNA进行了测序。通过与先前报道的其他HDV序列比较,我们确定了三个保守区域:第一个是基因组正义RNA催化切割位点周围的序列;第二个是反基因组正义RNA的相应位点;第三个是编码丁型肝炎抗原中间结构域的序列。我们已经表明,丁型肝炎抗原的中间结构域可以特异性结合HDV RNA。这种结合在体外和纯化的病毒粒子中均得到证实。有人提出,这种RNA-蛋白质相互作用对HDV RNA复制很重要。我们还认为,这些保守序列为聚合酶链反应(PCR)用于HDV感染的临床诊断提供了理想的引物。我们建议使用核苷酸870 - 900和690 - 720(牧木等人,1987a)作为常规筛查的引物。