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PhiSiGns: an online tool to identify signature genes in phages and design PCR primers for examining phage diversity

机译:PhiSiGns:一种在线工具,可识别噬菌体中的签名基因并设计PCR引物以检查噬菌体多样性

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Background Phages (viruses that infect bacteria) have gained significant attention because of their abundance, diversity and important ecological roles. However, the lack of a universal gene shared by all phages presents a challenge for phage identification and characterization, especially in environmental samples where it is difficult to culture phage-host systems. Homologous conserved genes (or "signature genes") present in groups of closely-related phages can be used to explore phage diversity and define evolutionary relationships amongst these phages. Bioinformatic approaches are needed to identify candidate signature genes and design PCR primers to amplify those genes from environmental samples; however, there is currently no existing computational tool that biologists can use for this purpose. Results Here we present PhiSiGns, a web-based and standalone application that performs a pairwise comparison of each gene present in user-selected phage genomes, identifies signature genes, generates alignments of these genes, and designs potential PCR primer pairs. PhiSiGns is available at ( http://www.phantome.org/phisigns/ webcite ; http://phisigns.sourceforge.net/ webcite ) with a link to the source code. Here we describe the specifications of PhiSiGns and demonstrate its application with a case study. Conclusions PhiSiGns provides phage biologists with a user-friendly tool to identify signature genes and design PCR primers to amplify related genes from uncultured phages in environmental samples. This bioinformatics tool will facilitate the development of novel signature genes for use as molecular markers in studies of phage diversity, phylogeny, and evolution.
机译:背景噬菌体(感染细菌的病毒)由于其丰富,多样和重要的生态作用而受到了广泛的关注。然而,缺乏所有噬菌体共有的通用基因对噬菌体的鉴定和表征提出了挑战,特别是在难以培养噬菌体宿主系统的环境样品中。存在于密切相关的噬菌体组中的同源保守基因(或“特征基因”)可用于探索噬菌体多样性并定义这些噬菌体之间的进化关系。需要生物信息学方法来鉴定候选特征基因并设计PCR引物,以从环境样品中扩增这些基因。但是,目前没有生物学家可用于此目的的现有计算工具。结果在这里,我们介绍了PhiSiGns,这是一个基于Web的独立应用程序,可以对用户选择的噬菌体基因组中存在的每个基因进行成对比较,鉴定特征基因,生成这些基因的比对并设计潜在的PCR引物对。可在(http://www.phantome.org/phisigns/ webcite; http://phisigns.sourceforge.net/ webcite)上找到PhiSiGns,并提供源代码的链接。在这里,我们描述了PhiSiGns的规格,并通过案例研究证明了其应用。结论PhiSiGns为噬菌体生物学家提供了一种用户友好的工具,可用于识别特征基因并设计PCR引物,以扩增环境样品中未经培养的噬菌体的相关基因。这种生物信息学工具将促进新型特征基因的开发,以用作噬菌体多样性,系统发育和进化研究的分子标记。

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