Weiss B, Goran D, Cancedda R, Schlesinger S
J Virol. 1974 Nov;14(5):1189-98. doi: 10.1128/JVI.14.5.1189-1198.1974.
BHK cells infected with defective-interfering passages of Sindbis virus accumulate a species of RNA (20S) that is about half the molecular weight of the major viral mRNA (26S). We have performed competitive hybridization experiments with these species of RNA and have established that 20S RNA contains approximately 50% of the nucleotide sequences present in 26S RNA. Our further studies, however, demonstrate that 20S RNA is unable to carry out the messenger function of 26S RNA. We found very little of the defective RNA associated with polysomes in vivo. In addition, it was unable to stimulate protein synthesis in vitro under conditions in which 26S RNA was translated. We have also examined viral RNA synthesis in BHK cells infected with standard or defective-interfering passages of Sindbis virus. This comparison suggests that defective partioles do not synthesize a functional replicase.
用辛德毕斯病毒缺陷干扰传代株感染的BHK细胞积累了一种RNA(20S),其分子量约为主要病毒mRNA(26S)的一半。我们用这些RNA种类进行了竞争性杂交实验,并确定20S RNA含有26S RNA中约50%的核苷酸序列。然而,我们的进一步研究表明,20S RNA无法执行26S RNA的信使功能。我们发现在体内很少有缺陷RNA与多核糖体相关。此外,在26S RNA被翻译的条件下,它在体外无法刺激蛋白质合成。我们还检测了用辛德毕斯病毒标准传代株或缺陷干扰传代株感染的BHK细胞中的病毒RNA合成。这种比较表明,缺陷颗粒不合成功能性复制酶。