Martín A C, López R, García P
Consejo Superior de Investigaciones Científicas, Madrid, Spain.
J Virol. 1996 Jun;70(6):3678-87. doi: 10.1128/JVI.70.6.3678-3687.1996.
Cp-1, a bacteriophage infecting Streptococcus pneumoniae, has a linear double-stranded DNA genome, with a terminal protein covalently linked to its 5' ends, that replicates by the protein-priming mechanism. We describe here the complete DNA sequence and transcriptional map of the Cp-1 genome. These analyses have led to the firm assignment of 10 genes and the localization of 19 additional open reading frames in the 19,345-bp Cp-1 DNA. Striking similarities and differences between some of these proteins and those of the Bacillus subtilis phage phi 29, a system that also replicates its DNA by the protein-priming mechanism, have been revealed. The genes coding for structural proteins and assembly factors are located in the central part of the Cp-1 genome. Several proteins corresponding to the predicted gene products were identified by in vitro and in vivo expression of the cloned genes. Mature major head protein from the virion particles results from hydrolysis of the primary gene product at the His-49 residue, whereas the phage gene is expressed in Escherichia coli without modification. We have also identified two open reading frames coding for proteins that show high degrees of similarity to the N- and C-terminal regions, respectively, of the single tail protein identified in phi 29. Sequencing and primer extension analysis suggest transcription of a small RNA showing a secondary structure similar to that of the prohead RNA required for the ATP-dependent packaging of phi 29 DNA. On the basis of its temporal expression, transcription of the Cp-1 genome takes place in two stages, early and late. Combined Northern (RNA) blot and primer extension experiments allowed us to map the 5' initiation sites of the transcripts, and we found that only three genes were transcribed from right to left. These analyses reveal that there are also noticeable differences between Cp-l and phi 29 in transcriptional organization. Considered together, the observations reported here provide new tangible evidence on phylogenetic relationships between B. subtilis and S. pneumoniae.
Cp-1是一种感染肺炎链球菌的噬菌体,具有线性双链DNA基因组,其5'端共价连接有末端蛋白,通过蛋白质引发机制进行复制。我们在此描述了Cp-1基因组的完整DNA序列和转录图谱。这些分析确定了10个基因,并在19345 bp的Cp-1 DNA中定位了另外19个开放阅读框。已揭示出其中一些蛋白质与枯草芽孢杆菌噬菌体phi 29的蛋白质之间存在显著的相似性和差异,phi 29也是通过蛋白质引发机制复制其DNA的系统。编码结构蛋白和装配因子的基因位于Cp-1基因组的中部。通过克隆基因的体外和体内表达鉴定了几种与预测基因产物相对应的蛋白质。病毒粒子中的成熟主要头部蛋白是由初级基因产物在His-49残基处水解产生的,而噬菌体基因在大肠杆菌中未经修饰就得以表达。我们还鉴定了两个开放阅读框,它们编码的蛋白质分别与phi 29中鉴定的单尾蛋白的N端和C端区域具有高度相似性。测序和引物延伸分析表明,一种小RNA的转录产物具有与phi 29 DNA的ATP依赖性包装所需的原头部RNA相似的二级结构。根据其时间表达,Cp-1基因组的转录分早期和晚期两个阶段进行。结合Northern(RNA)印迹和引物延伸实验,我们绘制了转录本的5'起始位点图谱,发现只有三个基因是从右向左转录的。这些分析表明,Cp-1和phi 29在转录组织上也存在明显差异。综合考虑,本文报道的观察结果为枯草芽孢杆菌和肺炎链球菌之间的系统发育关系提供了新的确凿证据。