Abstract

BackgroundMicroRNAs (miRNAs) are small, non-coding RNAs that are important regulators of gene expression, and play major roles in plant development and their response to the environment. Root extracts from Panax notoginseng contain triterpene saponins as their principal bioactive constituent, and demonstrate medicinal properties. To investigate the novel and conserved miRNAs in P. notoginseng, three small RNA libraries constructed from 1-, 2-, and 3-year-old roots in which root saponin levels vary underwent high-throughput sequencing.MethodsP. notoginseng roots, purified from 1-, 2-, and 3-year-old roots, were extracted for RNA, respectively. Three small libraries were constructed and subjected to next generation sequencing.ResultsSequencing of the three libraries generated 67,217,124 clean reads from P. notoginseng roots. A total of 316 conserved miRNAs (belonging to 67 miRNA families and one unclassified family) and 52 novel miRNAs were identified. MIR156 and MIR166 were the largest miRNA families, while miR156i and miR156g showed the highest abundance of miRNA species. Potential miRNA target genes were predicted and annotated using Cluster of Orthologous Groups, Gene Ontology, and Kyoto Encyclopedia of Genes and Genomes. Comparing these miRNAs between root samples revealed 33 that were differentially expressed between 2- and 1-year-old roots (8 increased, 25 decreased), 27 differentially expressed between 3- and 1-year-old roots (7 increased, 20 decreased), and 29 differentially expressed between 3- and 2-year-old roots (8 increased, 21 decreased). Two significantly differentially expressed miRNAs and four miRNAs predicted to target genes involved in the terpenoid backbone biosynthesis pathway were selected and validated by quantitative reverse transcription PCR. Furthermore, the expression patterns of these six miRNAs were analyzed in P. notoginseng roots, stems, and leaves at different developmental stages.ConclusionsThis study identified a large number of P. notoginseng miRNAs and their target genes, functional annotations, and gene expression patterns. It provides the first known miRNA profiles of the P. notoginseng root development cycle.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-015-2010-6) contains supplementary material, which is available to authorized users.

Highlights

  • MicroRNAs are small, non-coding RNAs that are important regulators of gene expression, and play major roles in plant development and their response to the environment

  • The levels of P. notoginseng saponins ginsenoside Rg1, ginsenoside Rb1, and notoginsenoside R1 were highest in the roots, with a large increase observed in saponin content between 1-year-old (1y) and 2-year-old (2y) roots

  • QRT-PCR validation and analysis of six miRNAs in P. notoginseng To validate the data obtained from high-throughput sequencing, two significantly differentially expressed miRNAs and four miRNAs predicted to target genes involved in the terpenoid backbone biosynthesis pathway were selected and their expression levels quantified using stem–loop qRT-PCR (Fig. 4)

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Summary

Introduction

MicroRNAs (miRNAs) are small, non-coding RNAs that are important regulators of gene expression, and play major roles in plant development and their response to the environment. Root extracts from Panax notoginseng contain triterpene saponins as their principal bioactive constituent, and demonstrate medicinal properties. The root of Panax notoginseng (Burk.) F. H. Chen, known as Radix Notoginseng or Sanchi, is a well-known traditional Chinese medicine belonging to the genus Panax and family Araliaceae. The principal bioactive constituents of the herb are triterpene saponins, which are dammarane-type glycosides [3,4,5]. More than 60 variant dammarane-type saponins have been isolated and identified from P. notoginseng. The oleanane-type saponin ginsenoside Ro has not been isolated from this species, it exists in other major Panax plants such as P. ginseng and P. quinquefolius [7]. The P. notoginseng saponins (PNS) mainly contain ginsenoside Rg1, ginsenoside Rb1, and notoginsenoside R1 according to the Chinese Pharmacopoeia (2010 Edition). PNS content and composition differs between tissues and plant age, with the highest PNS levels found in roots [6]

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