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Rapid Communication

The complete chloroplast genome sequences of two ornamental Epimedium species (Berberidaceae)

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Pages 878-880 | Received 20 Oct 2021, Accepted 20 Mar 2022, Published online: 26 May 2022

Abstract

Both Epimedium sutchuenense Franch. 1894 and E. fargesii Franch. 1894 are perennial herbs with excellent ornamental values due to their showy flowers. However, little molecular research has been done on these species. Here, the complete chloroplast (cp) genome of E. sutchuenense and E. fargesii was analyzed and reported. The cp genome sizes of E. sutchuenense and E. fargesii were 157, 263 and 157, 133 bp, respectively. Both the two cp genomes contained a pair of inverted repeat regions (IRs) (25,782 and 25,796 bp), separated by the small single-copy (SSC) region (17,106 and 17,071 bp) and a large single-copy (LSC) region (88,593 and 88,470 bp). A total of 113 unique genes were annotated in each of the two cp genomes, including 79 protein-coding genes, 30 tRNA genes, and four rRNA genes. Phylogenetic analysis supported a close relationship between E. sutchuenense and E. wushanense, while E. fargesii had no clear clustering branch.

1. Background

Epimedium L., the largest genus of Berberidaceae, is a perennial herb discontinuously distributed in eastern Asia and the Mediterranean regions (Stearn Citation2002; Ying et al. Citation2011). The genus contains approximately 68 species/taxa, among which 58 species were distributed in China (Xu et al. Citation2020). It was noted that 27 Chinese Epimedium species were listed in the Red List of China Higher Plants (Qin et al. Citation2017). Some Epimedium species are of outstanding ornamental values (Probst Citation1998; Ren et al. Citation2008; Avent Citation2010). One of such species, E. sutchuenense Franch. 1894 is an excellent ornamental groundcover plant because of its rapidly growing rhizomes and attractive foliage and flowers. The species is mainly distributed in Sichuan, Hubei, Shaanxi provinces, and Chongqing city of China (Stearn Citation2002; Ying et al. Citation2011). Another species, E. fargesii Franch. 1894 is endemic to mountainous areas of Chongqing City, Sichuan, and Hubei Provinces (Stearn Citation2002; Ying et al. Citation2011; Xu et al. Citation2020). Due to its excellent ornamental values, the plant has been over-exploited and endangered (Qin et al. Citation2017).

Epimedium is one of the most taxonomically difficult representatives of Berberidaceae. Although the complete chloroplast (cp) genomes of same species have been presented recently (Liu et al. Citation2021a, Citation2021b), more molecular evidences are indispensable for further investigation of Epimedium. In this study, the sampling sites of the current two species were at a distance of about 40 km from those of the two published ones. Given the complex terrains of mountains, the distances would cause the genetic differences within the same species. Meanwhile, the phylogenetic tree with more species would more accurately explain the evolutionary status of the two species. Here, the complete cp genome of E. sutchuenense and E. fargesii was sequenced, and the phylogenetic relationship within Epimedium was analyzed. The baseline information would be beneficial to the conservation of the horticultural germplasm resources.

2. Methods

An individual of E. sutchuenense was collected from Shennongjia Forest District, Hubei Province, China (latitude 31.4734, longitude 110.3910); the sample of E. fargesii was collected from Chengkou County, Chongqing, China (latitude 31.8391, longitude 108.6277). The specimens of the two species were deposited at the Herbaria of Jiangxi University of Chinese Medicine (JXCM) (https://www.jxutcm.edu.cn/, Yanqin Xu, [email protected]) under the voucher numbers Y. Q. Xu and S. Y. Tian 2021006 and Y. Q. Xu and S. X. Liu 2016024, respectively.

Genome DNA was isolated from 0.5 g fresh leaves using the CTAB method (Doyle and Doyle Citation1987). The purified DNA was used to build a sequencing library with the Illumina NovaSeq 6000 platform. The complete cp genomes of two species were assembled using GetOrgnelle v1.71 (Jin et al. Citation2020). The resultant genomes were annotated by the genome annotator GeSeq (Tillich et al. Citation2017) with E. wushanense (NC_044891) as the reference, and the results were manually adjusted by Geneious (Kearse et al. Citation2012). The complete annotation cp genomes were deposited in GenBank with accession numbers MZ645926 (E. sutchuenense) and MZ603801 (E. fargesii).

A maximum-likelihood (ML) phylogenetic tree was constructed based on the 19 published complete cp genomes of Epimedium, with Vancouveria hexandra as an out-group. The ML tree was computed by PhyML v.3.0 (Stéphane et al. Citation2010) under the best model (F81) evaluated by Jmodeltest (Darriba et al. Citation2012).

3. Results

The lengths of the complete cp genomes of E. sutchuenense and E. fargesii were 157,263 and 157,133 bp, respectively. Both the two cp genomes exhibited typical quadripartite structures, including two inverted repeat regions (IRs), one large single-copy (LSC) region, and one small single-copy (SSC) region. For E. sutchuenense, the lengths of the IR, LSC, and SSC regions were 25,782 bp, 88,593 bp, and 17,106 bp, respectively; for E. fargesii, the lengths of the corresponding regions were 25,796 bp, 88,470 bp, and 17,071 bp, respectively. Both the two cp genomes showed overall GC content of 38.78%. The GC contents of E. sutchuenense were 37.37, 32.77, and 43.20% in the LSC, SSC, and IR regions, respectively, while these of E. fargesii were 37.38, 32.74, and 43.18%, respectively. Each of the two cp genomes was comprised of 113 unique genes, including 79 protein-coding genes, 30 tRNA genes, and four rRNA genes. Among them, 19 genes were duplicated, including seven protein-coding genes, eight tRNA genes, and four rRNA genes.

The phylogenetic analysis showed a close relationship between E. sutchuenense and E. wushanense, although the two species belong to different series with distinct morphological traits (). The similar phylogenetic pattern was also reported in recent studies within the genus Epimedium (Huang et al. Citation2020; Guo et al. Citation2021). Contrastingly, E. fargesii had no clear cluster with other species of Epimedium, which might be associated with the short history of speciation of the species (Zhang et al. Citation2007; De Smet et al. Citation2012; Guo et al. Citation2021).

Figure 1. The maximum-likelihood (ML) phylogenetic tree based on 19 complete chloroplast genomes, with Vancouveria hexandra as an out-group. Numbers at the right of nodes are bootstrap support values (≥50).

Figure 1. The maximum-likelihood (ML) phylogenetic tree based on 19 complete chloroplast genomes, with Vancouveria hexandra as an out-group. Numbers at the right of nodes are bootstrap support values (≥50).

Ethical approval

The collecting of all samples in this study followed the Regulations on the Protection of Wild Plants of the People's Republic of China.

Author contributions

YX and HH contributed the design of the study; ST, QT, and XP performed the sample collection and experiments; ZZ, FL, and XP performed analysis and interpretation of the data. YX, QT, ZZ, and HH were involved in the drafting of the manuscript. YX supervised. YX and HH revised the manuscript critically for intellectual content. All authors were involved in the final approval of the version to be published. All authors agree to be accountable for all aspects of the work.

Disclosure statement

No potential conflict of interest was reported by the authors.

Data availability statement

The genome sequence data that support the findings of this study are openly available in GenBank of NCBI at https://www.ncbi.nlm.nih.gov/, reference numbers MZ645926 (E. sutchuenense) and MZ603801 (E. fargesii). The associated BioProject, SRA, and Bio-Sample numbers of E. sutchuenense are PRJNA771213, SRR16348881, and SAMN22256841, respectively, and these of E. fargesii are PRJNA771209, SRR16350057, and SAMN22256802, respectively.

Additional information

Funding

This work was supported by the National Natural Science Foundation of China [82060684]; Jiangxi University of Traditional Chinese Medicine 1050 Young Talents Project [5141900107]; and Young and Middle-Aged Talents Training Program of Traditional Chinese Medicine of Jiangxi Province [2020-2].

References

  • Avent T. 2010. An overview of Epimedium. Plantsman. 9:878–17.
  • Darriba D, Taboada GL, Doallo R, Posada D. 2012. jModelTest 2: more models, new heuristics and parallel computing. Nat Methods. 9(8):772–772.
  • De Smet Y, Goetghebeur P, Wanke S, Asselman P, Samain MS. 2012. Additional evidence for recent divergence of Chinese Epimedium (Berberidaceae) derived from AFLP, chloroplast and nuclear data supplemented with characterization of leaflet pubescence. Plant Ecol Evol. 145(1):73–87.
  • Doyle JJ, Doyle JL. 1987. A rapid DNA isolation procedure for small quantities of fresh leaf tissue. Phytochem Bull. 19:11–15.
  • Guo MY, Pang XH, Xu YQ, Jiang WJ, Liao BS, Yu JS, Xu J, Song JY, Chen SL. 2021. Plastid genome data provide new insights into the phylogeny and evolution of the genus Epimedium. J Adv Res. 36:175–185.
  • Huang RQ, Liang Q, Wang Y, Yang TJ, Zhang YJ. 2020. The complete chloroplast genome of Epimedium pubescens Maxim. (Berberidaceae), a traditional Chinese medicine herb. Mitochondrial DNA B Resour. 5(3):2042–2044.
  • Jin JJ, Yu WB, Yang JB, Song Y, dePamphilis CW, Yi TS, Li DZ. 2020. GetOrganelle: a fast and versatile toolkit for accurate de novo assembly of organelle genomes. Genome Biol. 21(1):241.
  • Kearse M, Moir R, Wilson A, Stones-Havas S, Cheung M, Sturrock S, Buxton S, Cooper A, Markowitz S, Duran C, et al. 2012. Geneious Basic: an integrated and extendable desktop software platform for the organization and analysis of sequence data. Bioinformatics. 28(12):1647–1649.
  • Liu X, Zhang Y, Zhang C, Xu C, Qin W, Shen G, Guo B. 2021a. The complete chloroplast genome of Epimedium sutchuenense Franch. (Berberidaceae). Mitochondrial DNA B Resour. 6(11):3289–3291.
  • Liu X, Zhang Y, Zhang C, Xu C, Qin W, Shen G, Guo B. 2021b. The complete chloroplast genome of Epimedium fargesii Franch. (Berberidaceae), a rare plant species endemic to China . Mitochondrial DNA B Resour. 6(11):3286–3288.
  • Probst D. 1998. Garden elegance. Amer Nurseryman. 187(5):34–40.
  • Qin HN, Yang Y, Dong SY, He Q, Jia Y, Zhao LN, Yu SX, Liu HY, Liu B, Yan YH, et al. 2017. Threatened species list of China’s higher plants. Biodivers Sci. 25(7):696–744.
  • Ren L, Dai SL, Wang Y. 2008. The germplasm resources of Epimedium in China and its application in landscape architecture. J Wuhan Bot Res. 26:644–649.
  • Stearn WT. 2002. The genus Epimedium and other herbaceous Berberidaceae. Portland: Timber Press; p. 27–34.
  • Stéphane G, Francois DJ, Vincent L, Maria A, Wim H, Olivier G. 2010. New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of PhyML 3.0. Syst Biol. 59:307–321.
  • Tillich M, Lehwark P, Pellizzer T, Ulbricht-Jones ES, Fischer A, Bock R, Greiner S. 2017. GeSeq- versatile and accurate annotation of organelle genomes. Nucleic Acids Res. 45(W1):W6–W11.
  • Xu YQ, Jiang Y, Huang H, Li RE, Li FQ, Liu Y, Huang XF. 2020. Taxonomic study of Epimedium L.: status, issues and prospect. Guihaia. 40(5):601–617.
  • Ying TS, Boufford DE, Brach AR. 2011. Epimedium L. In: Wu ZY, Raven PH, Hong DY, editors. Flora of China. Vol. 19. Beijing; St. Louis: Science Press; Missouri Botanical Garden Press; p. 787–799.
  • Zhang ML, Uhink CH, Kadereit JW. 2007. Phylogeny and biogeography of Epimedium/Vancouveria (Berberidaceae): Western North American–East Asian disjunctions, the origin of European mountain plant taxa, and East Asian species diversity. Syst Bot. 32(1):81–92.