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Snapshot of the Genome of the Pseudo-T-Even Bacteriophage RB49

机译:伪T均噬菌体RB49基因组快照

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RB49 is a virulent bacteriophage that infects Escherichia coli. Its virion morphology is indistinguishable from the well-known T-even phage T4, but DNA hybridization indicated that it was phylogenetically distant from T4 and thus it was classified as a pseudo-T-even phage. To further characterize RB49, we randomly sequenced small fragments corresponding to about 20% of the ≈170-kb genome. Most of these nucleotide sequences lacked sufficient homology to T4 to be detected in an NCBI BlastN analysis. However, when translated, about 70% of them encoded proteins with homology to T4 proteins. Among these sequences were the numerous components of the virion and the phage DNA replication apparatus. Mapping the RB49 genes revealed that many of them had the same relative order found in the T4 genome. The complete nucleotide sequence was determined for the two regions of RB49 genome that contain most of the genes involved in DNA replication. This sequencing revealed that RB49 has homologues of all the essential T4 replication genes, but, as expected, their sequences diverged considerably from their T4 homologues. Many of the nonessential T4 genes are absent from RB49 and have been replaced by unknown sequences. The intergenic sequences of RB49 are less conserved than the coding sequences, and in at least some cases, RB49 has evolved alternative regulatory strategies. For example, an analysis of transcription in RB49 revealed a simpler pattern of regulation than in T4, with only two, rather than three, classes of temporally controlled promoters. These results indicate that RB49 and T4 have diverged substantially from their last common ancestor. The different T4-type phages appear to contain a set of common genes that can be exploited differently, by means of plasticity in the regulatory sequences and the precise choice of a large group of facultative genes.
机译:RB49是一种可感染大肠杆菌的强力噬菌体。其病毒体形态与众所周知的T-even噬菌体T4没有区别,但是DNA杂交表明它与T4在系统发育上相距遥远,因此被分类为假T-even噬菌体。为了进一步表征RB49,我们随机测序了约≈170-kb基因组约20%的小片段。这些核苷酸序列中的大多数缺乏与T4足够的同源性,无法在NCBI BlastN分析中检测到。但是,当翻译时,其中约70%编码的蛋白与T4蛋白具有同源性。在这些序列中是病毒体和噬菌体DNA复制装置的众多组成部分。绘制RB49基因的图谱表明,它们中的许多具有在T4基因组中发现的相同相对顺序。确定了RB49基因组的两个区域的完整核苷酸序列,其中包含与DNA复制有关的大多数基因。该测序表明RB49具有所有必需的T4复制基因的同源物,但是,正如所期望的,它们的序列与它们的T4同源物有很大的差异。 RB49不存在许多非必需的T4基因,并已被未知序列取代。 RB49的基因间序列比编码序列保守性低,并且在至少某些情况下,RB49已发展出替代的调控策略。例如,对RB49中转录的分析显示,其调节模式比T4中更简单,只有两类而非三类暂时控制的启动子。这些结果表明,RB49和T4与他们的上一个共同祖先有很大的出入。不同的T4型噬菌体似乎包含一组共同的基因,可以通过调节序列的可塑性和一大批兼性基因的精确选择来不同地利用它们。

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