Martín A C, López R, García P
Departamento de Microbiología Molecular, Centro de Investigaciones Biológicas, CSIC, Madrid, Spain.
Virology. 1995 Aug 1;211(1):21-32. doi: 10.1006/viro.1995.1375.
Cp-1 is a small virulent bacteriophage infecting Streptococcus pneumoniae. It has a linear, double-stranded genome of about 19 kb that replicates by a protein-priming mechanism. We have determined the nucleotide sequence of the leftmost 4780 bp of the DNA of this bacteriophage; computer analysis revealed that this fragment contains seven open reading frames (ORFs) which could encode polypeptides containing more than 50 amino acids. The ORFs are clustered in two groups separated by noncoding intergenic regions. Two of these ORFs code for the terminal protein and a specific DNA polymerase that participate in the replication of the DNA. The predicted amino acid sequence of the terminal protein shows significant similarity with the terminal protein of Bacillus subtilis phage phi 29, and Cp-1 DNA polymerase is homologous to the subgroup of eukaryotic-type DNA polymerases that use a protein as a primer. Combined Northern blots and primer extension experiments have allowed us to map the 5' initiation sites of left early transcripts. These studies revealed that transcripts elongate from left to right and identified the left early promoters.
Cp-1是一种感染肺炎链球菌的毒性小噬菌体。它有一个约19 kb的线性双链基因组,通过蛋白质引发机制进行复制。我们已经确定了该噬菌体DNA最左端4780 bp的核苷酸序列;计算机分析表明,该片段包含7个开放阅读框(ORF),它们可编码含50多个氨基酸的多肽。这些开放阅读框聚集成两组,由非编码基因间隔区隔开。其中两个开放阅读框编码参与DNA复制的末端蛋白和一种特定的DNA聚合酶。预测的末端蛋白氨基酸序列与枯草芽孢杆菌噬菌体phi 29的末端蛋白有显著相似性,并且Cp-1 DNA聚合酶与以蛋白质为引物的真核生物型DNA聚合酶亚组同源。结合Northern印迹和引物延伸实验,我们得以绘制左侧早期转录本的5'起始位点图谱。这些研究表明转录本从左向右延伸,并确定了左侧早期启动子。