Alonso J C, Lüder G, Stiege A C, Chai S, Weise F, Trautner T A
Centro Nacional de Biotecnologia, CSIC, Campus Universidad Autónoma de Madrid, Cantoblanco, Spain.
Gene. 1997 Dec 19;204(1-2):201-12. doi: 10.1016/s0378-1119(97)00547-7.
The complete nucleotide sequence of the B. subtilis bacteriophage SPP1 is described. The genome is 44,007 bp in size and has a base composition of 43.7% dG + dC. Only 32.2 kb are essential for phage amplification under laboratory conditions. Transcription using only the 'heavy strand' is asymmetric. Eighty-one orfs organized in five early and four late operons were identified. Experiments have shown that 25 orfs are essential. Of the remaining orfs, functions could be predicted for the products of five of the orfs on the basis of comparison of the deduced amino acid sequence to known proteins. Intergenic regions include most of the 5 PE and the 4 PL promoters. Transcripts are polycistronic. Transcription from the PE promoters is mediated by host RP, whereas recognition of the PL promoters requires an additional unidentified phage-encoded product. Translation of mRNA transcribed from most of the orfs seems to be initiated independently, each from its own ribosomal binding and initiation site, although a few cases of coupled translation have been reported. The organization of SPP1 genes involved in the replication, DNA packaging and phage assembly proteins resembles the organization of genes of equivalent regions of different E. coli double-stranded DNA phages. Absence of aa sequence similarity between analogous proteins of different phages suggested that the conserved gene organization is representative of a primordial bacteriophage.
本文描述了枯草芽孢杆菌噬菌体SPP1的完整核苷酸序列。该基因组大小为44,007 bp,碱基组成为43.7%的dG + dC。在实验室条件下,只有32.2 kb对于噬菌体扩增是必需的。仅使用“重链”的转录是不对称的。鉴定出了81个开放阅读框(orf),它们被组织成5个早期操纵子和4个晚期操纵子。实验表明,25个orf是必需的。在其余的orf中,基于推导的氨基酸序列与已知蛋白质的比较,可以预测其中5个orf产物的功能。基因间区域包括大部分的5个PE启动子和4个PL启动子。转录本是多顺反子的。来自PE启动子的转录由宿主RP介导,而PL启动子的识别需要一种额外的未鉴定的噬菌体编码产物。从大多数orf转录的mRNA的翻译似乎是独立起始的,各自从其自身的核糖体结合和起始位点开始,尽管已经报道了少数偶联翻译的情况。参与复制、DNA包装和噬菌体组装蛋白的SPP1基因的组织类似于不同大肠杆菌双链DNA噬菌体等效区域的基因组织。不同噬菌体类似蛋白之间缺乏氨基酸序列相似性表明,保守的基因组织代表了一种原始噬菌体。