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THE CHLOROPLAST GENOME OF SALVIA: GENOMIC CHARACTERIZATION AND PHYLOGENETIC ANALYSIS

机译:丹参的叶绿体基因组:基因组特征和系统发育分析

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摘要

Premise of research. Previous studies based on plastid fragments and/or nuclear ribosomal DNA have had limited success resolving relationships within the genus Salvia. This study evaluates the efficacy of complete plastome sequences for phylogenetic inference within Salvia, using the recently established Salvia subg. Glutinaria as a case study. We use these plastomes to identify hypervariable and simple sequence repeat (SSR) regions for future studies within Salvia. Methodology. In order to produce a phylogenetic backbone for Salvia, we sequenced and assembled complete plastomes for six species of Salvia. These plastomes were combined with 11 plastomes (10 species) of Salvia from GenBank for analyses. This sampling represented seven of the 10 subgenera of Salvia. Genome features of these plastomes were analyzed, and hypervariable regions, SSRs, and longer repeats were identified. Phylogenetic relationships of 16 Salvia species were investigated using maximum likelihood and Bayesian methods based on four different data sets. Pivotal results. All of the 17 Salvia plastomes displayed a typical quadripartite structure, and 114 different genes were identified in each accession. In addition, a total of 18 hypervariable regions and 626 SSRs were identified. The monophyly of Salvia and Salvia subg. Glutinaria was supported in our phylogenetic analyses. Conclusions. Complete plastome sequences are promising for phylogenetic reconstruction of Salvia and likely other clades within Lamiaceae. In addition, we identified 18 hypervariable regions that should be useful as plastid phylogenetic markers for phylogenetic inferences within the genus and potentially as bar code markers for identifying different species of Salvia. The extended analysis of SSRs will be helpful for future population genetics studies and in elucidating the genetic diversity of Salvia and its relatives.
机译:研究的前提。以前基于塑体片段和/或核核糖体DNA的研究已经有限地成功解决了丹参内的关系。该研究评估了丹参内的完全塑料序列的疗效,使用最近建立的Salvia Subg。谷氨酸作为案例研究。我们使用这些塑料来确定丹参内的未来研究的高变和简单的序列重复(SSR)地区。方法。为了制作丹参的系统发育骨架,我们测序并组装了六种丹参的完整塑料。将这些塑料与来自Genbank的11种唾液中的塑料(10种)组合出来分析。这种抽样代表了Salvia的10个亚因素中的七个。分析了这些塑料的基因组特征,鉴定了高变区域,SSR和更长的重复。基于四种不同数据集的最大可能性和贝叶斯方法研究了16种丹参的系统发育关系。关染术。所有17种丹参血浆显示出典型的Quadriparte结构,并在每次加入中鉴定了114种不同的基因。此外,还确定了总共18个高变区域和626个SSR。丹参和萨尔维亚Subg的一定。在我们的系统发育分析中都支持谷氨酸。结论。完全的塑料序列是对丹参的系统发育重建以及LamiCeae中的其他片状的含义。此外,我们鉴定了18个高变区域,其应该是在属中的系统发育推断的体积系统发育标志物,并且可能是用于鉴定不同种类的丹参的条形码标记。 SSRS的扩展分析将有助于未来人口遗传学研究,并阐明丹参的遗传多样性及其亲属。

著录项

  • 来源
    《International journal of plant sciences》 |2020年第8期|812-830|共19页
  • 作者单位

    Key Laboratory for Plant Diversity and Biogeography of East Asia Kunming Institute of Botany Chinese Academy of Sciences Kunming Yunnan 650201 China University of Chinese Academy of Sciences Beijing 100049 China;

    Department of Biology University of Nebraska-Kearney Kearney Nebraska 68849 USA;

    Key Laboratory for Plant Diversity and Biogeography of East Asia Kunming Institute of Botany Chinese Academy of Sciences Kunming Yunnan 650201 China;

    College of Life Sciences Guizhou University Guiyang Guizhou 550025 China;

    Research Centre of Ecological Sciences College of Agronomy Jiangxi Agricultural University Nanchang 330045 China;

    Key Laboratory for Plant Diversity and Biogeography of East Asia Kunming Institute of Botany Chinese Academy of Sciences Kunming Yunnan 650201 China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Lamiaceae; Mentheae; Nepetoideae; Salviinae; ycf1;

    机译:Lamiaceae;芯合;Nepeetaea;Salviina;YCF1;
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