Cormack D V, Chow C T, Holloway A F
Can J Microbiol. 1976 Sep;22(9):1357-63. doi: 10.1139/m76-199.
The RNA polymerase in cells infected with three group I mutants of vesicular stomatitis virus has been examined. Mouse L cells were incubated at the permissive temperature (30 degrees C) for a few hours after infection to allow the development of secondary transcription. The temperature dependence of the secondary transcription system was determined from the incorporation of labelled uridine, in the presence of cycloheximide, at 30 and at 38 degrees C, the later temperature being non-permissive for viral replication. In cells infected with mutants W14, W28, and G11 at a low multiplicity (20 PFU/cells) secondary transcriptase activity was markedly temperature-sensitive after 3 and 5 h of infection at 30 degrees C. At a high multiplicity of infection (1000 PFU/cell) cells infected with W28 showed considerable RNA synthesis at 38 degrees C after 3 h at 30 degrees C. RNA synthesis was also observed in W28-infected cells in which protein synthesis was allowed to continue after the shift from 30 to 38 degrees C. In the latter two cases the RNA synthesized contained 12-18S species but little or no 30S mRNA.
已对感染水疱性口炎病毒三种I组突变体的细胞中的RNA聚合酶进行了检测。感染后,将小鼠L细胞在允许温度(30℃)下孵育数小时,以使二级转录得以发展。在存在环己酰亚胺的情况下,通过在30℃和38℃下掺入标记的尿苷来确定二级转录系统的温度依赖性,后一温度对病毒复制而言是不允许的。在以低感染复数(20个蚀斑形成单位/细胞)感染突变体W14、W28和G11的细胞中,在30℃感染3小时和5小时后,二级转录酶活性明显对温度敏感。在高感染复数(1000个蚀斑形成单位/细胞)下,感染W28的细胞在30℃ 3小时后于38℃显示出可观的RNA合成。在从30℃转移到38℃后允许蛋白质合成继续进行的W28感染细胞中也观察到了RNA合成。在后两种情况下,合成的RNA包含12 - 18S种类,但几乎没有或没有30S mRNA。