Yin F H, Lockart R Z
J Virol. 1968 Jul;2(7):728-37. doi: 10.1128/JVI.2.7.728-737.1968.
Temperature-sensitive mutants of Sindbis virus, which synthesize viral ribonucleic acid (RNA) but not mature virus at the nonpermissible temperature, were selected for the study of viral maturation. Of these, three mutants which complement each other genetically were used. Two major proteins, the nucleocapsid and membrane proteins, located, respectively, in the viral nucleoid and membrane, were found in intact virions. In cells infected with wild-type Sindbis virus, four distinct types of viral RNA with sedimentation coefficients of 40S, 26S, 20S, and 15S were detected in constant distribution. The 20S RNA was ribonuclease-resistant, whereas the other types were ribonuclease-sensitive. The 40S RNA, identical to that obtained from the virion, was found associated with nucleocapsid protein as a subviral particle, which was assumed to be the nucleoid. Viral materials from cells infected with the mutants under nonpermissive conditions were compared with those from cells infected with wild-type virus, in terms of (i) the distribution of the different types of RNA, (ii) the association of infectious viral RNA into subviral particles, and (iii) the ability of infected cells to hemadsorb goose erythrocytes. According to these criteria, each of the three mutants demonstrated different maturation defects. Defective nucleocapsid proteins and membrane proteins may each account for one of the above mutants. The thrid mutant may have defects in a minor structural protein or possibly a maturation protein which is involved in the assembly of Sindbis virus.
选择辛德毕斯病毒的温度敏感突变体来研究病毒成熟过程,这些突变体在非允许温度下能合成病毒核糖核酸(RNA)但不能合成成熟病毒。其中,选用了三个在遗传上相互互补的突变体。在完整的病毒粒子中发现了两种主要蛋白质,即分别位于病毒核衣壳和包膜中的核衣壳蛋白和膜蛋白。在感染野生型辛德毕斯病毒的细胞中,检测到四种沉降系数分别为40S、26S、20S和15S的不同类型病毒RNA,其分布恒定。20S RNA对核糖核酸酶有抗性,而其他类型对核糖核酸酶敏感。40S RNA与从病毒粒子中获得的相同,被发现与核衣壳蛋白结合形成亚病毒颗粒,该颗粒被认为是核衣壳。将在非允许条件下感染突变体的细胞中的病毒物质与感染野生型病毒的细胞中的病毒物质在以下方面进行比较:(i)不同类型RNA的分布;(ii)感染性病毒RNA与亚病毒颗粒的结合;(iii)感染细胞吸附鹅红细胞的能力。根据这些标准,三个突变体中的每一个都表现出不同的成熟缺陷。有缺陷的核衣壳蛋白和膜蛋白可能分别是上述其中一个突变体的原因。第三个突变体可能在一种次要结构蛋白或可能在参与辛德毕斯病毒组装的成熟蛋白方面存在缺陷。