Takeda N, Miyamura K, Takegami T, Yamazaki S
Central Virus Diagnostic Laboratory, National Institute of Health, Tokyo, Japan.
Virus Genes. 1989 Aug;2(4):347-55. doi: 10.1007/BF00684042.
The temperature-sensitive phenotype of enterovirus 70 (EV70) was examined by use of an in-vitro RNA replication system derived from a membrane fraction (crude replication complex, CRC) of EV70-infected HeLa cells. This system was capable of synthesizing the nucleotidyl proteins VPg-pU and VPg-pUpU. Formation of these nucleotidyl proteins was completely abolished when the in-vitro reaction was performed at the nonpermissive temperature for virus replication. Considering our previous observation that the defective stage of the temperature-sensitive growth of EV70 resides in the initiation step of RNA transcription in vivo, it is most likely that the lack of uridylylation of VPg at the restricted temperature in vitro is directly involved in the temperature-sensitive defect of virus growth in vivo.
利用从肠道病毒70型(EV70)感染的HeLa细胞的膜组分(粗复制复合体,CRC)衍生的体外RNA复制系统,检测了EV70的温度敏感表型。该系统能够合成核苷酸蛋白VPg-pU和VPg-pUpU。当在病毒复制的非允许温度下进行体外反应时,这些核苷酸蛋白的形成完全被消除。鉴于我们之前的观察结果,即EV70温度敏感生长的缺陷阶段存在于体内RNA转录的起始步骤中,很可能在体外受限温度下VPg缺乏尿苷酸化直接参与了病毒在体内生长的温度敏感缺陷。