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首页> 外文期刊>Journal of Molecular Evolution >Gene Conversion and the Evolution of Euryarchaeal Chaperonins: A Maximum Likelihood-Based Method for Detecting Conflicting Phylogenetic Signals
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Gene Conversion and the Evolution of Euryarchaeal Chaperonins: A Maximum Likelihood-Based Method for Detecting Conflicting Phylogenetic Signals

机译:基因转换和Euryarchaeal伴侣蛋白的进化:基于最大似然的方法来检测冲突的系统发生信号。

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摘要

Recombination is well known as a complicating factor in the interpretation of molecular phylogenies. Here we describe a maximum likelihood sliding window method based on a likelihood ratio test for scanning DNA sequence alignments for regions of incongruent phylogenetic signals, such as those influenced by recombination. Using this method, we identify several instances of gene conversion between paralogous chaperonin genes in euryarchaeote Archaea, many of which are not detected by two other widely used methods. In the Thermococcus/Pyrococcus lineage, where a gene duplication producing a and b paralogues predates the divergence of Thermococcus strains KS-1 and KS-8, gene conversion has homogenized portions of the a and b genes in KS-8 since the divergence of these two strains. A region near the 3′ end of the a and b paralogues in the methanogen Methanobacterium thermoautotrophicum also appears to have undergone gene conversion. We apply the method to two additional test data sets, the argF gene of Neisseria and a set of actin paralogues in maize, and show that it successfully identifies all the recombinant regions that were previously detected with other methods. Our approach is relatively insensitive to the presence of divergent sequences in the alignment, making it ideal for detecting recombination between both closely and distantly related genes.
机译:重组是解释分子系统发育的复杂因素。在这里,我们描述了一种基于似然比测试的最大似然滑动窗方法,用于扫描DNA序列比对的不一致的系统发生信号区域,例如受重组影响的区域。使用这种方法,我们确定了古生古生物中的近亲伴侣蛋白基因之间的几种基因转化实例,其中许多没有被其他两种广泛使用的方法检测到。在嗜热球菌/热球菌谱系中,产生a和b旁系同源物的基因重复早于嗜热球菌菌株KS-1和KS-8的差异,基因转化已使KS-8中a和b基因的部分同质化,因为这些差异两个菌株。产甲烷甲烷菌嗜热自养甲烷甲烷菌a和b旁系同源物3'端附近的区域似乎也已经历了基因转化。我们将该方法应用于两个附加的测试数据集,即奈瑟氏球菌的argF基因和玉米中的一组肌动蛋白旁系同源物,并表明该方法成功地鉴定了先前用其他方法检测到的所有重组区域。我们的方法对比对中差异序列的存在相对不敏感,因此非常适合检测紧密和远距离相关基因之间的重组。

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