Hashimoto H, Nomoto A, Watanabe K, Mori T, Takezawa T, Aizawa C, Takegami T, Hiramatsu K
Department of Virology, Kitasato Institute, Tokyo, Japan.
Virus Genes. 1988 Jun;1(3):305-17. doi: 10.1007/BF00572709.
The genomic RNA of the Japanese encephalitis virus (JEV) Beijing-1 strain was reversely transcribed and the synthesized cDNA was molecularly cloned. Six continuous cDNA clones that cover the entire virus genome were established and sequenced to determine the complete nucleotide sequence of the JEV RNA. The precise genomic size was estimated as 10,965 bases long. With flanking 95 bases at the 5' and 583 bases at the 3' non-coding regions, one long open reading frame (ORF) was revealed encoding a virus polyprotein with 3,429 amino acid residues. Because of sequence homologies observed between JEV and other flaviviruses, the genome organization of JEV appears to be identical with other flaviviruses. Genetic variation detected among flavivirus genomes is consistent with the established serological relatedness between JEV and other members of flaviviruses. The secondary structure of the JEV genome is deduced and discussed concerning its involvement in genome replication.
对日本脑炎病毒(JEV)北京-1株的基因组RNA进行逆转录,并对合成的cDNA进行分子克隆。建立了六个覆盖整个病毒基因组的连续cDNA克隆并进行测序,以确定JEV RNA的完整核苷酸序列。精确的基因组大小估计为10965个碱基长。在5'端有95个侧翼碱基,3'非编码区有583个碱基,揭示了一个长开放阅读框(ORF),编码一个含有3429个氨基酸残基的病毒多蛋白。由于JEV与其他黄病毒之间存在序列同源性,JEV的基因组结构似乎与其他黄病毒相同。在黄病毒基因组中检测到的遗传变异与JEV和黄病毒其他成员之间已确定的血清学相关性一致。推导并讨论了JEV基因组的二级结构及其在基因组复制中的作用。