Meijer W J, Horcajadas J A, Salas M
Centro de Biología Molecular Severo Ochoa, Universidad Autónoma, Canto Blanco, 28049 Madrid, Spain.
Microbiol Mol Biol Rev. 2001 Jun;65(2):261-87 ; second page, table of contents. doi: 10.1128/MMBR.65.2.261-287.2001.
Continuous research spanning more than three decades has made the Bacillus bacteriophage phi29 a paradigm for several molecular mechanisms of general biological processes, such as DNA replication, regulation of transcription, phage morphogenesis, and phage DNA packaging. The genome of bacteriophage phi29 consists of a linear double-stranded DNA (dsDNA), which has a terminal protein (TP) covalently linked to its 5' ends. Initiation of DNA replication, carried out by a protein-primed mechanism, has been studied in detail and is considered to be a model system for the protein-primed DNA replication that is also used by most other linear genomes with a TP linked to their DNA ends, such as other phages, linear plasmids, and adenoviruses. In addition to a continuing progress in unraveling the initiation of DNA replication mechanism and the role of various proteins involved in this process, major advances have been made during the last few years, especially in our understanding of transcription regulation, the head-tail connector protein, and DNA packaging. Recent progress in all these topics is reviewed. In addition to phi29, the genomes of several other Bacillus phages consist of a linear dsDNA with a TP molecule attached to their 5' ends. These phi29-like phages can be divided into three groups. The first group includes, in addition to phi29, phages PZA, phi15, and BS32. The second group comprises B103, Nf, and M2Y, and the third group contains GA-1 as its sole member. Whereas the DNA sequences of the complete genomes of phi29 (group I) and B103 (group II) are known, only parts of the genome of GA-1 (group III) were sequenced. We have determined the complete DNA sequence of the GA-1 genome, which allowed analysis of differences and homologies between the three groups of phi29-like phages, which is included in this review.
持续超过三十年的研究使芽孢杆菌噬菌体phi29成为一般生物学过程中多种分子机制的范例,如DNA复制、转录调控、噬菌体形态发生和噬菌体DNA包装。噬菌体phi29的基因组由线性双链DNA(dsDNA)组成,其5'端共价连接有一个末端蛋白(TP)。由蛋白质引发机制进行的DNA复制起始已得到详细研究,被认为是蛋白质引发DNA复制的模型系统,大多数其他DNA末端连接有TP的线性基因组(如其他噬菌体、线性质粒和腺病毒)也使用该系统。除了在揭示DNA复制起始机制以及参与该过程的各种蛋白质的作用方面不断取得进展外,过去几年还取得了重大进展,特别是在我们对转录调控、头尾连接蛋白和DNA包装的理解方面。本文综述了所有这些主题的最新进展。除了phi29外,其他几种芽孢杆菌噬菌体的基因组也由5'端连接有TP分子的线性dsDNA组成。这些phi29样噬菌体可分为三组。第一组除phi29外,还包括噬菌体PZA、phi15和BS32。第二组包括B103、Nf和M2Y,第三组仅包含GA-1。虽然phi29(第一组)和B103(第二组)的完整基因组DNA序列已知,但GA-1(第三组)的基因组仅测序了部分。我们已经确定了GA-1基因组的完整DNA序列,这使得对三组phi29样噬菌体之间的差异和同源性进行分析成为可能,本文对此进行了阐述。