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Identification of the most informative regions of the mitochondrial genome for phylogenetic and coalescent analyses

机译:鉴定线粒体基因组信息最丰富的区域,以进行系统发育和合并分析

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Analysis of complete mitochondrial genome sequences is becoming increasingly common in genetic studies. The availability of full,genome datasets enables an analysis of the information content distributed throughout the mitochondrial genome in order to optimize the research design of future evolutionary studies. The goal of our study was to identify informative regions of the human mitochondrial genome using two criteria: (1) accurate reconstruction of a phylogeny and (2) consistent estimates of time to most recent common ancestor (TMRCA). We created two series of datasets by deleting individual genes of varied length and by deleting 10 equal-size fragments throughout the coding region. Phylogenies were statistically compared to the full-coding-region tree, while coalescent methods were used to estimate the TMRCA and associated credible intervals. Individual fragments important for maintaining a phylogeny similar to the full-coding-region tree encompassed bp 577-2122 and 11,399-16,023, including all or part of 12S rRNA, 16S rRNA, ND4, ND5, ND6, and cytb. The control region only tree was the most poorly resolved with the majority of the tree manifest as an unresolved polytomy. Coalescent estimates of TMRCA were less sensitive to removal of any particular fragment(s) than reconstruction of a consistent phylogeny. Overall, we discovered that half the genome, i.e., bp 3669-11 398, could be removed with no significant change in the phylogeny (P-AU = 0.077) while still maintaining overlap of TMRCA 95% credible intervals. Thus, sequencing a contiguous fragment from bp 11,399 through the control region to bp 3668 would create a dataset that optimizes the information necessary for phylogenctic and coalescent analyses and also takes advantage of the wealth of data already available on the control region. (c) 2007 Elsevier Inc. All riLyhts reserved.
机译:完整的线粒体基因组序列分析在遗传研究中变得越来越普遍。完整的基因组数据集的可用性可以分析整个线粒体基因组中分布的信息内容,从而优化未来进化研究的研究设计。我们研究的目的是使用两个标准来鉴定人类线粒体基因组的信息区域:(1)系统发育的准确重建和(2)到最新共同祖先(TMRCA)的时间的一致估计。我们通过删除不同长度的单个基因并在整个编码区删除10个等长片段来创建两个数据集系列。系统发生率与全编码区域树进行了统计比较,而合并方法则用于估计TMRCA和相关的可信区间。对于维持与完整编码区树相似的系统发育重要的单个片段包括577-2122和11,399-16,023 bp,包括12S rRNA,16S rRNA,ND4,ND5,ND6和cytb的全部或部分。仅对照区域的树是分解最差的树,大多数树表现为未分解的多角体。与重建一致的系统发育相比,TMRCA的合并估计对删除任何特定片段的敏感性较低。总体而言,我们发现可以删除一半的基因组,即bp 3669-11398,而系统发育没有明显变化(P-AU = 0.077),同时仍保持95%可信区间的TMRCA重叠。因此,将一个连续片段从第11399个碱基对通过控制区域测序到第3668个碱基将创建一个数据集,该数据集可优化系统发育分析和合并分析所需的信息,并且还利用了控制区域中已有的大量数据。 (c)2007 Elsevier Inc.保留所有权利。

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