Krug R M, Ueda M, Palese P
J Virol. 1975 Oct;16(4):790-6. doi: 10.1128/JVI.16.4.790-796.1975.
Influenza WSN virus temperature-sensitive (ts) mutants were examined for defects in viral complementary RNA (cRNA) synthesis. The synthesis of viral cRNA was determined by hybridizing RNA from infected cells to radiolabeled virion RNA of known specific activity. Mutants in complementation groups I and III synthesized little, or no, cRNA at the nonpermissive temperature (39.5 C). When cells infected by these mutants were incubated for 5 h at the permissive temperature (33 C) and were then shifted to 39.5 C, net synthesis of cRNA ceased. This strongly suggests that mutants in these two complementation groups possess a ts defect in the transciptase complex. Mutants in group II and group V synthesize reduced amounts of cRNA at 39.5 C. In contrast to the group I and group III mutants, cRNA synthesis in cells infected by a group II or a group V mutant continues after a shift-up. This indicated that these mutants do not possess a ts transcriptase complex and that these mutants are most probably defective in some step in the amplification of cRNA synthesis. As will be discussed, the most likely defect in these mutants is in the synthesis of virion-type RNA. These results suggest that there are two influenza viral gene functions required for transcription and most likely two additional gene functions required for RNA replication.
对流感WSN病毒温度敏感(ts)突变体进行了病毒互补RNA(cRNA)合成缺陷检测。通过将感染细胞的RNA与已知比活性的放射性标记病毒粒子RNA杂交来确定病毒cRNA的合成。互补组I和III中的突变体在非允许温度(39.5℃)下合成很少或不合成cRNA。当被这些突变体感染的细胞在允许温度(33℃)下孵育5小时,然后转移到39.5℃时,cRNA的净合成停止。这有力地表明这两个互补组中的突变体在转录酶复合物中存在ts缺陷。II组和V组中的突变体在39.5℃下合成的cRNA量减少。与I组和III组突变体不同,II组或V组突变体感染的细胞在温度升高后cRNA合成仍在继续。这表明这些突变体不具有ts转录酶复合物,并且这些突变体很可能在cRNA合成扩增的某个步骤中存在缺陷。如将讨论的,这些突变体最可能的缺陷在于病毒粒子型RNA的合成。这些结果表明转录需要两种流感病毒基因功能,RNA复制很可能还需要另外两种基因功能。