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Patterns and Relative Rates of Nucleotide and Insertion/Deletion Evolution at Six Chloroplast Intergenic Regions in New World Species of the Lecythidaceae

机译:Lecythidaceae新世界物种6个叶绿体基因间区核苷酸和插入/缺失进化的模式和相对速率

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Insertions and deletions (indels) in chloroplast noncoding regions are common genetic markers to estimate population structure and gene flow, although relatively little is known about indel evolution among recently diverged lineages such as within plant families. Because indel events tend to occur nonrandomly along DNA sequences, recurrent mutations may generate homoplasy for indel haplotypes. This is a potential problem for population studies, because indel haplotypes may be shared among populations after recurrent mutation as well as gene flow. Furthermore, indel haplotypes may differ in fitness and therefore be subject to natural selection detectable as rate heterogeneity among lineages. Such selection could contribute to the spatial patterning of cpDNA haplotypes, greatly complicating the interpretation of cpDNA population structure. This study examined both nucleotide and indel cpDNA variation and divergence at six noncoding regions (psbB-psbH, atpB-rbcL, trnL-trnH, rpl20-5'rps12, trnS-trnG, and trnH-psbA) in 16 individuals from eight species in the Lecythidaceae and a Sapotaceae outgroup. We described patterns of cpDNA changes, assessed the level of indelhomoplasy, and tested for rate heterogeneity among lineages and regions. Although regression analysis of branch lengths suggested some degree of indel homoplasy among the most divergent lineages, there was little evidence for indel homoplasy within the Lecythidaceae. Likelihood ratio tests applied to the entire phylogenetic tree revealed a consistent pattern rejecting a molecular clock. Tajima's 1D and 2D tests revealed two taxa with consistent rate heterogeneity, one showing relatively more and one relatively fewer changes than other taxa. In general, nucleotide changes showed more evidence of rate heterogeneity than did indel changes. The rate of evolution was highly variable among the six cpDNA regions examined, with trnS-trnG and trnH-psbA regions showing as much as 10 and 15 divergence within the Lecythidaceae. Deviations from rate homogeneity in the two taxa were constant across cpDNA regions, consistent with lineage-specific rates of evolution rather than cpDNA region-specific natural selection. There is no evidence that indels are more likely than nucleotide changes to experience homoplasy within the Lecythidaceae. These results support a neutral interpretation of cpDNA indel and nucleotide variation in population studies within species such as Corythophora alta.
机译:叶绿体非编码区的插入和缺失(插入缺失)是估计种群结构和基因流的常见遗传标记,尽管对最近分化的谱系(例如植物科内)的插入缺失进化知之甚少。由于插入缺失事件往往沿 DNA 序列非随机发生,因此复发突变可能会产生插入缺失单倍型的同质性。这是种群研究的一个潜在问题,因为插入缺失单倍型可能在复发突变和基因流动后在种群之间共享。此外,插入缺失单倍型的适应度可能不同,因此受到自然选择的影响,可检测为谱系之间的率异质性。这种选择可能有助于cpDNA单倍型的空间模式化,使cpDNA群体结构的解释变得非常复杂。本研究检查了来自Lecythidaceae和Sapotaceae外群的16个物种的16个个体的6个非编码区(psbB-psbH、atpB-rbcL、trnL-trnH、rpl20-5'rps12、trnS-trnG和trnH-psbA)的核苷酸和插入缺失cpDNA变异和分歧。我们描述了cpDNA变化的模式,评估了不去齐型的水平,并测试了谱系和区域之间的速率异质性。尽管对分支长度的回归分析表明,在最不同的谱系中存在一定程度的插入缺失同质性,但几乎没有证据表明 Lecythidaceae 内插入缺失同质性。应用于整个系统发育树的似然比测试揭示了拒绝分子钟的一致模式。Tajima的1D和2D测试揭示了两个具有一致率异质性的分类群,一个显示出相对更多的变化,一个相对少于其他分类群的变化。一般来说,核苷酸变化比插入缺失变化显示出更多的速率异质性证据。在所研究的六个cpDNA区域中,进化速率变化很大,其中trnS-trnG和trnH-psbA区域在Lecythidaceae中显示出高达10%和15%的差异。两个分类群中速率同质性的偏差在cpDNA区域是恒定的,与谱系特异性的进化速率一致,而不是与cpDNA区域特异性的自然选择一致。没有证据表明插入缺失比核苷酸变化更有可能在Lecythidaceae内经历同质性。这些结果支持了 Corythophora alta 等物种内种群研究中对 cpDNA 插入缺失和核苷酸变异的中性解释。

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