Sevostyanova Anastasiya, Djordjevic Marko, Kuznedelov Konstantin, Naryshkina Tatyana, Gelfand Mikhail S, Severinov Konstantin, Minakhin Leonid
Institute of Molecular Genetics, Russian Academy of Sciences, Moscow 123182, Russia.
J Mol Biol. 2007 Feb 16;366(2):420-35. doi: 10.1016/j.jmb.2006.11.050. Epub 2006 Nov 18.
Regulation of gene expression of lytic bacteriophage varphiYS40 that infects the thermophilic bacterium Thermus thermophilus was investigated and three temporal classes of phage genes, early, middle, and late, were revealed. varphiYS40 does not encode a (RNAP) and must rely on host RNAP for transcription of its genes. Bioinformatic analysis using a model of Thermus promoters predicted 43 putative sigma(A)-dependent -10/-35 class phage promoters. A randomly chosen subset of those promoters was shown to be functional in vivo and in vitro and to belong to the early temporal class. Macroarray analysis, primer extension, and bioinformatic predictions identified 36 viral middle and late promoters. These promoters have a single common consensus element, which resembles host sigma(A) RNAP holoenzyme -10 promoter consensus element sequence. The mechanism responsible for the temporal control of the three classes of promoters remains unknown, since host sigma(A) RNAP holoenzyme purified from either infected or uninfected cells efficiently transcribed all varphiYS40 promoters in vitro. Interestingly, our data showed that during infection, there is a significant increase and decrease of transcript amounts of host translation initiation factors IF2 and IF3, respectively. This finding, together with the fact that most middle and late varphiYS40 transcripts were found to be leaderless, suggests that the shift to late viral gene expression may also occur at the level of mRNA translation.
对感染嗜热栖热菌的烈性噬菌体φYS40的基因表达调控进行了研究,发现了噬菌体基因的三个时序类别,即早期、中期和晚期。φYS40不编码(RNA聚合酶),其基因转录必须依赖宿主RNA聚合酶。利用栖热菌启动子模型进行的生物信息学分析预测了43个假定的依赖σ(A)的-10/-35类噬菌体启动子。随机选择的这些启动子的一个子集在体内和体外均显示具有功能,且属于早期时序类别。宏阵列分析、引物延伸和生物信息学预测确定了36个病毒中期和晚期启动子。这些启动子有一个单一的共同共有元件,类似于宿主σ(A) RNA聚合酶全酶-10启动子共有元件序列。由于从感染或未感染细胞中纯化的宿主σ(A) RNA聚合酶全酶在体外能有效转录所有φYS40启动子,因此三类启动子时序控制的机制仍不清楚。有趣的是,我们的数据表明,在感染期间,宿主翻译起始因子IF2和IF3的转录本量分别有显著增加和减少。这一发现,连同大多数φYS40中期和晚期转录本无前导序列这一事实,表明向病毒晚期基因表达的转变也可能发生在mRNA翻译水平。