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首页> 外文期刊>BMC Evolutionary Biology >A practical approach to phylogenomics: the phylogeny of ray-finned fish (Actinopterygii) as a case study
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A practical approach to phylogenomics: the phylogeny of ray-finned fish (Actinopterygii) as a case study

机译:系统发育组学的实用方法:以鳍鳍鱼(Actinopterygii)为系统的案例研究

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Background Molecular systematics occupies one of the central stages in biology in the genomic era, ushered in by unprecedented progress in DNA technology. The inference of organismal phylogeny is now based on many independent genetic loci, a widely accepted approach to assemble the tree of life. Surprisingly, this approach is hindered by lack of appropriate nuclear gene markers for many taxonomic groups especially at high taxonomic level, partially due to the lack of tools for efficiently developing new phylogenetic makers. We report here a genome-comparison strategy to identifying nuclear gene markers for phylogenetic inference and apply it to the ray-finned fishes – the largest vertebrate clade in need of phylogenetic resolution. Results A total of 154 candidate molecular markers – relatively well conserved, putatively single-copy gene fragments with long, uninterrupted exons – were obtained by comparing whole genome sequences of two model organisms, Danio rerio and Takifugu rubripes. Experimental tests of 15 of these (randomly picked) markers on 36 taxa (representing two-thirds of the ray-finned fish orders) demonstrate the feasibility of amplifying by PCR and directly sequencing most of these candidates from whole genomic DNA in a vast diversity of fish species. Preliminary phylogenetic analyses of sequence data obtained for 14 taxa and 10 markers (total of 7,872 bp for each species) are encouraging, suggesting that the markers obtained will make significant contributions to future fish phylogenetic studies. Conclusion We present a practical approach that systematically compares whole genome sequences to identify single-copy nuclear gene markers for inferring phylogeny. Our method is an improvement over traditional approaches (e.g., manually picking genes for testing) because it uses genomic information and automates the process to identify large numbers of candidate makers. This approach is shown here to be successful for fishes, but also could be applied to other groups of organisms for which two or more complete genome sequences exist, which has important implications for assembling the tree of life.
机译:背景技术分子系统学是基因组学时代生物学的主要阶段之一,DNA技术的空前发展迎来了它。现在,根据许多独立的遗传基因座来推断生物的系统发育,这是组装生命树的一种广泛接受的方法。出人意料的是,由于许多生物分类学群体缺乏适当的核基因标记,特别是在高生物分类学水平上,这种方法受到了阻碍,部分原因是缺乏有效开发新的系统发育基因的工具。我们在这里报告了一种基因组比较策略,以鉴定用于系统发育推断的核基因标记,并将其应用于射线鳍鱼类–需要系统发育解析的最大脊椎动物进化枝。结果通过比较两种模式生物丹尼奥里奥和塔基福格红豆的全基因组序列,总共获得了154个候选分子标记-相对保守的,假定的单拷贝基因片段,外显子长且不间断。对36个类群(代表有鳍的鱼类订单的三分之二)中的15个(随机挑选的)标记物进行的实验测试表明,可以通过PCR扩增并直接从整个基因组DNA中以多种多样的形式直接对大多数候选基因进行测序的可行性鱼种。对14个分类单元和10个标记(每个物种总计7,872 bp)获得的序列数据进行初步的系统发育分析令人鼓舞,这表明所获得的标记将为未来鱼类系统发育研究做出重要贡献。结论我们提供了一种实用的方法,可以系统地比较整个基因组序列,以鉴定用于推断系统发育的单拷贝核基因标记。我们的方法是对传统方法的改进(例如,手动挑选基因进行测试),因为它使用基因组信息并自动执行流程以识别大量候选基因。此处显示了这种方法对鱼类是成功的,但也可以应用于存在两个或多个完整基因组序列的其他生物体,这对于组装生命树具有重要意义。

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