Carter T H, Ginsberg H S
J Virol. 1976 Apr;18(1):156-66. doi: 10.1128/JVI.18.1.156-166.1976.
DNA hybridization was used to study the synthesis of viral RNA in two DNA-minus, temperature-sensitive mutants of type 5 adenovirus (H5ts125 and H5ts149) belonging to two different, non-overlapping complementation groups. Hybridization competition analysis showed that both mutants transcribed all early gene sequences at the restrictive temperature (41 C). In mutant-infected cells at 41 C, the rate of viral transcription was similar to the rate of early RNA synthesis in wild-type virus infection and was dependent on the multiplicity of infection; little or no late transcription was detected. The shutoff of class I early RNA transcription was shown to be a late function during wild-type virus infection and did not occur at 41 C in mutant-infected cells. When mutant-infected cells were incubated at the permissive temperature (32 C) for 25 h and then shifted to 41 C, the rate of viral DNA synthesis decreased rapidly for H5ts125 and slowly for H5ts149. However, the rate of viral transcription remained unchanged in H5ts125-infected cells for at least 3 h after the temperature shift; although the synthesis of viral DNA had stopped by this time, the synthesis of late viral RNA sequences continued.
DNA杂交技术被用于研究属于两个不同且不重叠互补组的5型腺病毒的两个DNA缺失型温度敏感突变体(H5ts125和H5ts149)中病毒RNA的合成。杂交竞争分析表明,在限制温度(41℃)下,这两个突变体均转录所有早期基因序列。在41℃下感染突变体的细胞中,病毒转录速率与野生型病毒感染时早期RNA合成速率相似,且依赖于感染复数;几乎检测不到晚期转录。I类早期RNA转录的关闭被证明是野生型病毒感染期间的晚期功能,在41℃下感染突变体的细胞中不会发生。当感染突变体的细胞在允许温度(32℃)下孵育25小时,然后转移到41℃时,H5ts125的病毒DNA合成速率迅速下降,H5ts149的则缓慢下降。然而,在温度转移后至少3小时内,H5ts125感染的细胞中病毒转录速率保持不变;尽管此时病毒DNA合成已经停止,但晚期病毒RNA序列的合成仍在继续。