Laboratory of Virology, Institute of Microbial Chemistry (BIKAKEN), Tokyo, Japan.
Department of Bacteriology, Faculty of Medical Sciences, Kyushu University, Fukuoka, Japan.
Virology. 2019 May;531:126-140. doi: 10.1016/j.virol.2019.03.004. Epub 2019 Mar 7.
The influenza A virus genome consists of eight single-stranded negative-sense RNA segments. The noncoding regions located at the 3'- and 5'- ends of each segment are necessary for genome packaging, and the terminal coding regions are required to precisely bundle the eight segments. However, the nucleotide residues important for genome bundling are not defined. Here, we introduced premature termination codons in the hemagglutinin (HA) or matrix protein 2 (M2) gene and constructed virus libraries containing random sequences in the terminal coding regions. Using these virus libraries, we identified nucleotide residues involved in efficient virus propagation. Viral genome packaging was impaired in viruses that contained single mutations at these identified residues. Furthermore, these single mutations altered the local structure of the viral ribonucleoprotein complex. Our results show that specific nucleotide residues in the viral protein coding region are involved in forming the precise structure of the viral ribonucleoprotein complex.
甲型流感病毒基因组由八个单链负义 RNA 片段组成。每个片段 3' 和 5' 末端的非编码区对于基因组包装是必需的,而末端编码区则需要精确地将这八个片段捆绑在一起。然而,对于基因组捆绑至关重要的核苷酸残基尚未确定。在这里,我们在血凝素(HA)或基质蛋白 2(M2)基因中引入了过早终止密码子,并构建了在末端编码区含有随机序列的病毒文库。使用这些病毒文库,我们鉴定了参与病毒高效增殖的核苷酸残基。在这些鉴定出的残基处只有单个突变的病毒中,病毒基因组包装受到了损害。此外,这些单个突变改变了病毒核糖核蛋白复合物的局部结构。我们的结果表明,病毒蛋白编码区中的特定核苷酸残基参与形成病毒核糖核蛋白复合物的精确结构。