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The Uneven Rate of the Molecular Evolution of Gene Sequences of DNA-Dependent RNA Polymerase I of the Genus Lamium L

机译:属L属DNA依赖的RNA聚合酶I基因序列的分子进化的不均匀速率

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摘要

RNA polymerase type I (plastid-encoded polymerase, PEP) is one of the key chloroplast enzymes. However, the rpo genes that encode its subunits (rpoA, rpoB, rpoC1 and rpoC2) are relatively rapidly evolving sequences. The aim of this study was to investigate the rate of the molecular evolution of rpo genes and to evaluate them as phylogenetic markers on the example of the genus Lamium L. (Lamiaceae). The analyzed genes were shown to differ in the level of variation, rate of intragenic mutations, phylogenetic informativeness, and in the impact of these mutations on the properties of encoded peptides. Destabilizing effects of the positive pressure were observed in all genes examined coding for PEP enzyme. We have demonstrated the relationship between mutations fixed by positive selection and the separation of phylogenetic lines within the genus Lamium. The study showed also that the rpo genes were reliable phylogenetic markers, useful in the reconstruction of interconnections of species belonging to the same genus. Of the four tested genes, the most promising phylogenetic marker was rpoA gene, while the least useful gene appeared to be rpoC1.
机译:I型RNA聚合酶(质体编码聚合酶,PEP)是关键的叶绿体酶之一。但是,编码其亚基(rpoA,rpoB,rpoC1和rpoC2)的rpo基因是相对快速进化的序列。这项研究的目的是调查rpo基因的分子进化速率,并以Lamium L.(Lamiaceae)属为例子,评估它们作为系统发育标记。结果表明,所分析的基因在变异水平,基因内突变率,系统发育信息以及这些突变对编码肽的性质的影响方面存在差异。在检查的所有编码PEP酶的基因中均观察到正压的不稳定作用。我们已经证明了由正选择固定的突变与Lamium属内系统发生系的分离之间的关系。该研究还表明,rpo基因是可靠的系统发育标记,可用于重建属于同一属的物种的互连。在这四个测试基因中,最有前途的系统发育标记是rpoA基因,而最不有用的基因似乎是rpoC1。

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