Smith M C, Burns R N, Wilson S E, Gregory M A
Institute of Genetics, University of Nottingham, Queen's Medical Centre, Nottingham NG7 2UH, UK.
Nucleic Acids Res. 1999 May 15;27(10):2145-55. doi: 10.1093/nar/27.10.2145.
The completed genome sequence of the temperate Streptomyces phage straight phiC31 is reported. straight phiC31 contains genes that are related by sequence similarities to several other dsDNA phages infecting many diverse bacterial hosts, including Escherichia, Arthrobacter, Mycobacterium, Rhodobacter, Staphylococcus, Bacillus, Streptococcus, Lactobacillus and Lactococcus. These observations provide further evidence that dsDNA phages from diverse bacterial hosts are related and have had access to a common genetic pool. Analysis of the late genes was particularly informative. The sequences of the head assembly proteins (portal, head protease and major capsid) were conserved between straight phiC31, coliphage HK97, staphylococcal phage straight phiPVL, two Rhodobacter capsulatus prophages and two Mycobacterium tuberculosis prophages. These phages and prophages (where non-defective) from evolutionarily diverse hosts are, therefore, likely to share a common head assembly mechanism i.e. that of HK97. The organisation of the tail genes in straight phiC31 is highly reminiscent of tail regions from other phage genomes. The unusual organisation of the putative lysis genes in straight phiC31 is discussed, and speculations are made as to the roles of some inessential early gene products. Similarities between certain phage gene products and eukaryotic dsDNA virus proteins were noted, in particular, the primase/helicases and the terminases (large subunits). Furthermore, the complete sequence clarifies the overall transcription map of the phage during lytic growth and the positions of elements involved in the maintenance of lysogeny.
报道了温和型链霉菌噬菌体直phiC31的完整基因组序列。直phiC31包含一些基因,这些基因与其他几种感染多种不同细菌宿主(包括大肠杆菌、节杆菌、分枝杆菌、红杆菌、葡萄球菌、芽孢杆菌、链球菌、乳酸杆菌和乳球菌)的双链DNA噬菌体在序列上具有相似性。这些观察结果进一步证明,来自不同细菌宿主的双链DNA噬菌体是相关的,并且能够获取共同的基因库。对晚期基因的分析特别有意义。直phiC31、大肠杆菌噬菌体HK97、葡萄球菌噬菌体直phiPVL、两种红杆菌前噬菌体和两种结核分枝杆菌前噬菌体的头部组装蛋白(门户蛋白、头部蛋白酶和主要衣壳蛋白)序列是保守的。因此,这些来自进化上不同宿主的噬菌体和前噬菌体(无缺陷时)可能共享一种共同的头部组装机制,即HK97的机制。直phiC31中尾部基因的组织与其他噬菌体基因组的尾部区域高度相似。讨论了直phiC31中假定的裂解基因的异常组织,并对一些非必需早期基因产物的作用进行了推测。注意到某些噬菌体基因产物与真核双链DNA病毒蛋白之间的相似性,特别是引发酶/解旋酶和末端酶(大亚基)。此外,完整序列阐明了噬菌体在裂解生长期间的整体转录图谱以及参与溶原性维持的元件的位置。