2016
DOI: 10.1371/journal.pone.0153008
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The Use of DNA Barcoding on Recently Diverged Species in the Genus Gentiana (Gentianaceae) in China

Abstract: DNA barcoding of plants poses particular challenges, especially in differentiating, recently diverged taxa. The genus Gentiana (Gentianaceae) is a species-rich plant group which rapidly radiated in the Himalaya-Hengduan Mountains in China. In this study, we tested the core plant barcode (rbcL + matK) and three promising complementary barcodes (trnH-psbA, ITS and ITS2) in 30 Gentiana species across 6 sections using three methods (the genetic distance-based method, Best Close Match and tree-based method). rbcL h… Show more

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Cited by 35 publications
(30 citation statements)
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“…This high resolution was also found in previous research (e.g., Li et al, 2011; Liu et al, 2016; Wirta et al, 2016), for example, in Rhododendron (Yan et al, 2015), Venus Slipper (Guo et al, 2016) and in Rosewood (Hartvig et al, 2015). These previous results showed that the ITS marker performed well as a single barcode for species identification, although the ITS marker was considered to have drawbacks, including incomplete lineage sorting and homogeneous concerted evolution (Liu et al, 2011, 2016; Wang et al, 2011; Wirta et al, 2016). However, in a recent study, Li et al (2011) found that the nuclear ITS barcode had high species discrimination power, and they proposed that it should be incorporated into the core barcode marker for land plants.…”
Section: Discussionsupporting
confidence: 86%
See 1 more Smart Citation
“…This high resolution was also found in previous research (e.g., Li et al, 2011; Liu et al, 2016; Wirta et al, 2016), for example, in Rhododendron (Yan et al, 2015), Venus Slipper (Guo et al, 2016) and in Rosewood (Hartvig et al, 2015). These previous results showed that the ITS marker performed well as a single barcode for species identification, although the ITS marker was considered to have drawbacks, including incomplete lineage sorting and homogeneous concerted evolution (Liu et al, 2011, 2016; Wang et al, 2011; Wirta et al, 2016). However, in a recent study, Li et al (2011) found that the nuclear ITS barcode had high species discrimination power, and they proposed that it should be incorporated into the core barcode marker for land plants.…”
Section: Discussionsupporting
confidence: 86%
“…Thus, the ITS fragment has a larger effective population size than the chloroplast DNA regions, which makes the ITS marker is not easily quicker to complete lineage sorting than the cpDNA markers (Wachowiak et al, 2011). However, the nuclear ITS marker showed a higher evolutionary rate and higher inter-species differentiation than the chloroplast regions, and the nuclear ITS region in plants comprises multiple (reiterated) copies and usually undergoes concerted evolution (Alvarez and Wendel, 2003; Liu et al, 2016). During this process, different copies become homogenized to the same sequence type (becoming almost identical types) as a result of mechanisms such as high-frequency unequal crossing over or gene conversion (Alvarez and Wendel, 2003; Hartvig et al, 2015; Wirta et al, 2016).…”
Section: Discussionmentioning
confidence: 99%
“…In contrast, many studies have considered only M. azedarach as an accepted species (Dassanayake 1995;Ahmed et al 2012;Dharmalingam et al 2014;Lake 2015). The existing complexity of whether M. azedarach and M. dubia are the same or different species can be D r a f t resolved using DNA barcoding, which was reported to be efficient in species differentiation and identification of cryptic species (Ragupathy et al 2009;Liu et al 2016).…”
Section: Despite Its Multipurpose Values and Importance Species Levementioning
confidence: 99%
“…To understand the mechanisms that facilitate these processes, we however need to resolve the phylogenetic relationships between closely related species. This task is usually difficult to achieve with traditional genetic markers (e.g., rbcL, matK, ITS), especially for genera that harbor high species richness and experience hybridization during their evolution, such as Primula L. (Guggisberg, Mansion, & Conti, 2009;Schmidt-Lebuhn, de Vos, Keller, & Conti, 2012) and Gentiana L. (Liu, Yan, & Ge, 2016). This problem may be overcome by using many thousands of DNA markers (e.g., Pante et al, 2015;Wagner et al, 2013), for example, using recently developed next-generation sequencing methods such as restriction site associated DNA (RAD) sequencing (Baird et al, 2008).…”
Section: Introductionmentioning
confidence: 99%