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Mitogenome Announcement

The complete chloroplast genome sequence of the medicinal plant, Dracocephalum rupestre (Lamiaceae)

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Pages 229-232 | Received 07 Nov 2022, Accepted 20 Jan 2023, Published online: 02 Feb 2023

Abstract

Dracocephalum rupestre (tribe Mentheae; Lamiaceae) is a perennial herb from Korea and China with high ornamental and medicinal value. Here, we report its complete chloroplast genome to provide insight into the phylogenetic relationships of Dracocephalum. The genome is 151,230 bp long, with two inverted repeat regions (25,643 bp each) that separate a large single-copy region (82,536 bp) and a small single-copy region (17,408 bp). It contains 133 genes that encode 88 proteins, eight rRNAs, and 37 tRNAs. The maximum-likelihood phylogenetic analysis strongly supported Dracocephalum monophyly, showing that the genus forms a sister group with the subtribe Menthinae in the tribe Mentheae.

Introduction

The perennial herb Dracocephalum rupestre (Hance 1869) belongs to the economically important tribe Mentheae (Lamiaceae). Distributed throughout northern China and Korea (Ren et al. Citation2008; Drew and Sytsma Citation2012; Kim et al. Citation2021), D. rupestre has large, fragrant purple-blue flowers that are used for ornamentation (Li and Hedge Citation1994) and consumed as a tea in Hebei and Shanxi provinces (also known as Maojian tea; Gao et al. Citation2022). In addition, the herb is an ingredient in traditional Chinese medicine with documented pharmacological benefits, including antioxidant and antitumor activity, as well as liver protection. It is mainly used to treat damp heat, headache, fever, jaundice, and liver toxicity (Esmaeili et al. Citation2014; Zhu et al. Citation2018; Gao et al. Citation2022).

Despite their considerable economic value, little is known about the genetic information of D. rupestre. Moreover, the plants are rare in Korea and listed as protected species by the Korea Forest Service (Korea National Arboretum Citation2008). Populations of Korean D. rupestre are restricted to small areas at the southern limit of their geographical distribution (Song et al. Citation2016; Kim et al. Citation2018). Here, we report the complete chloroplast genome of D. rupestre and examine its phylogenetic position within the tribe Mentheae. The chloroplast genome provides basic genetic data for future phylogenetic and conservation studies.

Materials and methods

Fresh leaves of D. rupestre were collected from Mt. Deokhang, Gangwon-do, South Korea (37°19′24.13″N, 129°0′17.26ʺE; ) and dried with silica gel. The voucher specimen (BDNA-SB-20401) was stored in Baekdudaegan National Arboretum (KBA; [email protected]). Total genomic DNA was extracted from dried leaves using a DNeasy Plant Mini Kit (Qiagen, Seoul, South Korea). The DNA library was constructed with the MGIEasy DNA Library Prep Kit (MGI Technology, Shenzhen, China) and sequenced on the MGISEQ-2000 platform (LAS, Seoul, Korea) following manufacturer protocol. Sequencing generated 75,374,386 raw pair-end reads (150 bp) that were then assembled in NOVOPlasty 4.1 (Dierckxsens et al. Citation2017). The selected seed sequence was D. moldavica matK (Yao et al. Citation2020; NC_057509). Next, 7,315,587 reads were mapped in Geneious Prime 2022.2.2 (Kearse et al. Citation2012) to check the assembled plastome, yielding a coverage of 9802× (Figure S1). The plastome was also annotated in Geneious and manually corrected for start and stop codons, as well as for intron/exon boundaries. The complete chloroplast sequence of D. rupestre was deposited in GenBank of the National Center for Biotechnology Information (NCBI, accession number OP526971).

Figure 1. The morphological characteristics of Dracocephalum rupestre. D. rupestre is a perennial, 20–30 cm tall. Stems ascending, unbranched, pubescent; leaf blade cordiform or reinform, crenate, white villous; corolla purple-blue, pubescent. The photo was taken by Dr. Tae-Im Heo in Mt. Deokhang, South Korea, June 2022, without any copyright issues.

Figure 1. The morphological characteristics of Dracocephalum rupestre. D. rupestre is a perennial, 20–30 cm tall. Stems ascending, unbranched, pubescent; leaf blade cordiform or reinform, crenate, white villous; corolla purple-blue, pubescent. The photo was taken by Dr. Tae-Im Heo in Mt. Deokhang, South Korea, June 2022, without any copyright issues.

For phylogenetic analysis, the complete chloroplast genome sequences of 12 species in Mentheae were downloaded from NCBI (Dracocephalum: six species, Schizonepeta, Nepeta, Mentha, Prunella, Lycopus, and Salvia: one species each). The outgroup was Lavandula angistifolia (tribe Lavanduleae). Sequences were aligned in MAFFT (Katoh and Toh Citation2010). Maximum likelihood (ML) analysis was performed in RAxML v.8.0 (Stamatakis Citation2014) using default parameters and 1,000 bootstrap replicates. For the RAxML tree, the general time-reversible model of nucleotide substitution was used along with the GTR gamma model of rate heterogeneity.

Results and discussion

The complete chloroplast genome of D. rupestre is 151,230 bp and comprises a large single-copy (LSC) region of 82,536 bp, two inverted repeat (IR) regions of 25,643 bp, and a small single-copy (SSC) region of 17,408 bp (). We annotated 133 genes, including 88 protein-coding genes (PCGs), eight ribosomal RNA genes (rRNAs), and 37 transfer RNA genes (tRNAs). Of these, 17 were duplicated in IR regions, including six PCGs (ndhB, rpl2, rpl23, rps7, ycf15, and ycf2), four rRNAs (4.5S, 5S, 16S, and 23S rRNA), and seven tRNAs (trnA-UGC, trnI-CAU, trnI-GAU, trnL-CAA, trnN-GUU, trnR-ACG, and trnV-GAC). Respectively, rps19 and ycf1 were located at the borders of IR/LSC and IR/SSC. Fifteen genes (trnK-UUU, rps16, trnG-UCC, atpF, rpoC1, trnL-UAA, trnV-UAC, petB, petD, rpl16, rpl2, ndhB, trnI-GAU, trnA-UGC, and ndhA) contained one intron, whereas clpP and ycf3 contained two introns. rps12 is also a trans-spliced gene (Figure S2). Overall GC content of chloroplast DNA was 37.8%, while CG content in the LSC, SSC, and IR regions were 35.9%, 31.7%, and 43.0%, respectively. Gene content and order are similar to those of D. tanguticum and D. heterophyllum (Yao et al. Citation2020; Fu et al. Citation2022).

Figure 2. Schematic map of overall features of the chloroplast genome of Dracocephalum rupestre. The circular map of the chloroplast genome was generated using CPGview (Liu et al. Citation2023). The map contains seven circles. From the center going outward, the first circle shows the distributed repeats connected with red (the forward direction) and green (the reverse direction) arcs. The next circle shows the tandem repeats marked with short bars. The third circle shows the microsatellite sequences as short bars. The fourth circle shows the size of the LSC and SSC. The fifth circle shows the IRA and IRB. The sixth circle shows the GC contents along the plastome. The seventh circle shows the genes having different colors based on their functional groups.

Figure 2. Schematic map of overall features of the chloroplast genome of Dracocephalum rupestre. The circular map of the chloroplast genome was generated using CPGview (Liu et al. Citation2023). The map contains seven circles. From the center going outward, the first circle shows the distributed repeats connected with red (the forward direction) and green (the reverse direction) arcs. The next circle shows the tandem repeats marked with short bars. The third circle shows the microsatellite sequences as short bars. The fourth circle shows the size of the LSC and SSC. The fifth circle shows the IRA and IRB. The sixth circle shows the GC contents along the plastome. The seventh circle shows the genes having different colors based on their functional groups.

The ML phylogenetic tree showed that D. rupestre is closely related to D. psammophilum, and all seven Dracocephalum species are a monophyletic group with a 100% bootstrap value (). Subtribe Nepetinae (comprising Dracocephalum, Schizonepeta, and Nepeta) forms a sister clade to subtribe Menthinae.

Figure 3. A phylogenetic tree (RAxML) was established based on concatenated sequences of 75 common protein-coding genes in 14 complete chloroplast genomes of the family Lamiaceae. The sequences used for tree construction are as follows: Salvia miltiorrhiza (JX312195; Qian et al. Citation2013), Lycopus europaeus (OM617843), Prunella vulgaris (MZ636547), Mentha longifolia (KU956042; Vining et al. Citation2017), Dracocephalum rupestre (OP526971), D. psammophilum (MZ750980), D. palmatum (KU958581), D. moldavica (MT457747; Yao et al. Citation2020), D. heterophyllum (MW970109; Zhang et al. Citation2021), D. tanguticum (MT457746; Yao et al. Citation2020), D. taliense (MT473756; Zhao et al. Citation2021), Schizonepeta tenuifolia (MW900176), Nepeta stewartiana (MT733874; Wu et al. Citation2021), Lavandula angustifolia (KT948988). The numbers above the nodes indicate bootstrap values with 1,000 replicates.

Figure 3. A phylogenetic tree (RAxML) was established based on concatenated sequences of 75 common protein-coding genes in 14 complete chloroplast genomes of the family Lamiaceae. The sequences used for tree construction are as follows: Salvia miltiorrhiza (JX312195; Qian et al. Citation2013), Lycopus europaeus (OM617843), Prunella vulgaris (MZ636547), Mentha longifolia (KU956042; Vining et al. Citation2017), Dracocephalum rupestre (OP526971), D. psammophilum (MZ750980), D. palmatum (KU958581), D. moldavica (MT457747; Yao et al. Citation2020), D. heterophyllum (MW970109; Zhang et al. Citation2021), D. tanguticum (MT457746; Yao et al. Citation2020), D. taliense (MT473756; Zhao et al. Citation2021), Schizonepeta tenuifolia (MW900176), Nepeta stewartiana (MT733874; Wu et al. Citation2021), Lavandula angustifolia (KT948988). The numbers above the nodes indicate bootstrap values with 1,000 replicates.

In conclusion, this study sequenced the complete chloroplast genome of D. rupestre, providing a valuable genetic source for conservation studies. Additionally, the novel phylogenetic data can be used in future evolutionary studies of Lamiaceae.

Author contributions

JH Lee and TI Heo conceived and designed the experiments. TI Heo contributed to the resource sampling and species identification. AG and JW Park conducted laboratory works. EK Han performed the data analysis and wrote the manuscript. JH Lee revised and approved the final version of the paper. All authors have reviewed and approved the manuscript. All authors agree to be accountable for all aspects of the work.

Ethical approval

The study species used in this research were collected for ex situ conservation at the Baekdudaegan National Arboretum (BDNA), the forest biological resources management institution, and individuals were not collected from protected areas. Therefore, this study does not need ethical approval or permissions to collect the sample. All procedures conducted to produce and publish this article were conducted in compliance with the regulations of the Baekdudaegan National Arboretum.

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Disclosure statement

No potential conflict of interest was reported by the author(s).

Data availability statement

Data from this study are available in the NCBI GenBank at https://www.ncbi.nlm.nih.gov (accession number OP526971). The associated BioProject, SRA, and Bio-Sample numbers are PRJNA883819, SRS15224747, and SAMN30996907, respectively.

Additional information

Funding

This study was supported by a research grant from the Baekdudaegan National Arboretum [KIAM-2022-KS-OB-02-01-02].

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