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枯草芽孢杆菌噬菌体φ29发育过程中的基因表达。I. 脱氧核糖核酸-核糖核酸竞争杂交法分析病毒特异性转录

Gene expression during the development of Bacillus subtilis bacteriophage phi 29. I. Analysis of viral-specific transcription by deoxyribonucleic acid-ribonucleic acid competition hybridization.

作者信息

Loskutoff D J, Pène J J, Andrews D P

出版信息

J Virol. 1973 Jan;11(1):78-86. doi: 10.1128/JVI.11.1.78-86.1973.

Abstract

The ribonucleic acid (RNA) specified by bacteriophage phi29 was analyzed to determine its composition at various times in the viral lytic cycle. Although viral-specific RNA was detected immediately after infection, a large increase in the rate was observed at 10 min when DNA synthesis began. phi29 was found to resemble other viruses in that gene expression occurred in two stages which could be defined temporally as "early" and "late." Early RNA appeared before the onset of viral deoxyribonucleic acid (DNA) replication and accounted for approximately 40% of the viral genetic potential. This RNA was also present late in the infectious cycle because of the slow turnover rate of phi29-specific RNA (approximately 10 min half-life) and the continued synthesis of much early viral RNA throughout infection. Late RNA was first detected at approximately the same time as viral DNA replication, although late transcription was not dependent upon DNA synthesis. This RNA was only partially displaced by early RNA in the appropriate competition experiments, suggesting that it contained sequences not present in the early class. Expression of viral genes was sensitive to rifamycin throughout the lytic cycle, the sensitivity resulting from a dependence upon the rifamycin phenotype of the host RNA polymerase.

摘要

对噬菌体φ29所指定的核糖核酸(RNA)进行了分析,以确定其在病毒裂解周期不同时间的组成。尽管在感染后立即检测到病毒特异性RNA,但在DNA合成开始的10分钟时观察到其合成速率大幅增加。发现φ29与其他病毒相似,即基因表达分两个阶段进行,从时间上可定义为“早期”和“晚期”。早期RNA在病毒脱氧核糖核酸(DNA)复制开始之前出现,约占病毒遗传潜能的40%。由于φ29特异性RNA的周转速度较慢(半衰期约为10分钟)且在整个感染过程中早期病毒RNA持续合成,这种RNA在感染后期也存在。晚期RNA最早在与病毒DNA复制大致相同的时间被检测到,尽管晚期转录不依赖于DNA合成。在适当的竞争实验中,这种RNA仅被早期RNA部分取代,这表明它包含早期类别中不存在的序列。在整个裂解周期中,病毒基因的表达对利福平敏感,这种敏感性源于对宿主RNA聚合酶利福平表型的依赖性。

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