Abstract

DNA barcoding is expected to be one of the most promising tools in biological taxonomy. However, there have been no agreements on which core barcode should be used in plants, especially in species-rich genera with wide geographical distributions. To evaluate their discriminatory power in large genera, four of the most widely used DNA barcodes, including three plastid regions (matK, rbcL, trnH-psbA) and nuclear internal transcribed spacer (nrITS), were tested in seven species-rich genera (Ficus, Pedicularis, Rhodiola, Rhododendron,Viburnum, Dendrobium and Lysimachia) and a moderate size genus, Codonopsis. All of the sequences from the aforementioned seven large genera were downloaded from NCBI. The related barcodes for Codonopsis were newly generated in this study. Genetics distances, DNA barcoding gaps and phylogenetic trees of the four single barcodes and their combinations were calculated and compared in the seven genera. As for single barcode, nrITS has the most variable sites, the clearest intra- and inter-specific divergences and the highest discrimination rates in the seven genera. Among the combinations of barcodes, ITS+matK performed better than all the single barcodes in most cases and even the three- and four-loci combinations in the seven genera. Therefore, we recommend ITS+matK as the core barcodes for large plant genera.

Highlights

  • DNA barcoding, the use of a short gene sequence from a standardized region of the genome as a tool for species identification, provides new tools for use in biological taxonomy [1,2,3,4,5]

  • DNA barcoding in Codonopsis and large plant genera functions in TaxonDNA were applied to calculate the accuracy of the barcode regions for species identification

  • Among the four single barcodes in Ficus, the trnH-psbA matrix showed the shortest length for the aligned sequences, and ITS provided the highest percentage of variable sites (38.63%) and the highest percentage of informative sites (32.64%), with rbcL having the lowest percentages of variable and informative sites (1.79% and 1.30%, respectively)

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Summary

Introduction

DNA barcoding, the use of a short gene sequence from a standardized region of the genome as a tool for species identification, provides new tools for use in biological taxonomy [1,2,3,4,5]. It has shown promise in providing a practical, standardized, species-level identification tool that can be used for taxonomic research, population genetics [6], phylogenetics [7], biodiversity assessment [8], and ecological studies [9,10,11]. An ideal DNA barcode should be variable enough to PLOS ONE | DOI:10.1371/journal.pone.0170286 February 9, 2017

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