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Mitogenome Announcement

The complete chloroplast genome sequence of Potentilla tanacetifolia Willd. ex Schltdl.

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Pages 478-479 | Received 20 Oct 2020, Accepted 02 Jan 2021, Published online: 09 Feb 2021

Abstract

Potentilla tanacetifolia Willd. ex Schltdl. is a perennial herb in China, which has high ecological and economic values. Its complete chloroplast genome was reported in this study for the first time. The whole chloroplast genome was 157, 051 base pairs in length with 129 genes, including 84 protein-coding genes, 37 tRNAs, and 8 rRNAs. In addition, phylogenetic analysis showed a sister relationship between P. tanacetifolia and P. chinensis.

Potentilla tanacetifolia Willd. ex Schltdl. is a perennial herb as a member of the Potentilla belonged to the family Rosaceae and widely distributed in China, which has persisted largely in an undomesticated state that is highly resistant to different environmental stresses (Li et al. Citation2019). P. tanacetifolia has high ecological and economic values, that seedlings of P. tanacetifolia in spring is one of important fodder plant. Furthermore, P. tanacetifolia is usually regarded as an indicator plant for community succession because of its sensitivity to the environment change and grazing (Li et al. Citation2011). It makes that P. tanacetifolia represents an excellent model for understanding how different evolutionary forces have sculpted the variation patterns in the genome during the process of population differentiation and ecological speciation, because P. tanacetifolia has wide geographic distribution, and adaptability to different environments. In the present research, we characterized the whole chloroplast genome of P. tanacetifolia and comprehended more about genetic information of this species, which can contribute to the understanding population genetics studies of P. tanacetifolia.

The fresh leaves of P. tanacetifolia were collected from Duolun County (42°02′N, 116°17′E, 1324 m asl), Inner Mongolia Autonomous Region of China. The leaf samples were silica-dried and taken to the laboratory until DNA extraction. The voucher specimen (HF2019002) was laid in the Herbarium of Xi’an Botanical Garden of Shaanxi Province, China. The total genomic DNA was isolated according to a modified CTAB method (Doyle and Doyle Citation1987). Total genome DNA of P. tanacetifolia was sequenced by Illumina Hiseq 2500 Sequencing System (Illumina, Hayward, CA) to construct the shotgun library. The qualified clean reads were assembled by NOVOPlasty (Dierckxsens et al. Citation2017), with P. stolonifera (NC_044418) as a reference. The low-quality sequences were filtered out using CLC Genomics Workbench v8.0 (CLC Bio, Aarhus, Denmark). The complete chloroplast genome of P. tanacetifolia was annotated by Geneious ver. 10.1 (http://www.geneious.com, Kearse et al. Citation2012) and online program Chloroplast Genome Annotation, Visualization, Analysis, and GenBank Submission (CPGAVAS) (Institute of Medicinal Plant development, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China) (Zuo et al. Citation2017). Finally, the validated complete chloroplast genome of P. tanacetifolia was deposited in Genbank (Accession number MW125592).

The complete chloroplast genome of P. tanacetifolia was 157, 051 bp in length, containing a large single-copy region (LSC) of 86, 147 bp, a small single-copy region (SSC) of 18, 883 bp, and two inverted repeat (IR) regions of 26, 010 bp. The overall GC content is 36.8%. The genome contains 129 complete genes, including 84 protein-coding genes, 37 tRNA genes and 8 rRNA genes.

To identify the phylogenetic position of P. tanacetifolia, 8 complete chloroplast genomes sequence of Potentilla were obtained from NCBI GenBank, and Agrimonia pilosa and Sanguisorba officinalis was used as out-group for phylogenetic analysis. The 11 chloroplast genome sequences were aligned with MAFFT (Katoh and Standley Citation2013) and then the maximum likelihood (ML) tree was constructed by RAxML (Stamatakis Citation2014). The results confirmed that P. tanacetifolia was clustered with P. chinensis ().

Figure 1. Maximum likelihood (ML) analysis of P. tanacetifolia and other related species based on the complete chloroplast genome sequence. Genbank accession numbers: P. freyniana (NC_041210), P. stolonifera (NC_044418), P. freyniana var. chejuensis (MK472813), P. stolonifera var. quelpaertensis (MK229189), P. chinensis (MN871983), P. indica (NC_041178), P. hebiichigo (NC_041199), P. centigrana (NC_041209), Agrimonia pilosa (NC_050051), and Sanguisorba officinalis (NC_044694).

Figure 1. Maximum likelihood (ML) analysis of P. tanacetifolia and other related species based on the complete chloroplast genome sequence. Genbank accession numbers: P. freyniana (NC_041210), P. stolonifera (NC_044418), P. freyniana var. chejuensis (MK472813), P. stolonifera var. quelpaertensis (MK229189), P. chinensis (MN871983), P. indica (NC_041178), P. hebiichigo (NC_041199), P. centigrana (NC_041209), Agrimonia pilosa (NC_050051), and Sanguisorba officinalis (NC_044694).

Disclosure statement

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

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] under the accession no. MW125592. The associated BioProject, SRA, and Bio-Sample numbers are PRJNA678424, SRR13062013, and SAMN16796184 respectively.

Additional information

Funding

This work was supported by the Scientific Research Program of Shaanxi Province under Grant [2019JQ-436]; Scientific Research Program of Xi’an City under Grant [2019112913CXSF007SF017, 20NYYF0003]; Science and Technology Program of the Shaanxi Academy of Sciences under Grant [2021K-18, 2016K-16].

References

  • Dierckxsens N, Mardulyn P, Smits G. 2017. NOVOPlasty: de novo assembly of organelle genomes from whole genome data. Nucleic Acids Res. 45(4):e18.
  • Doyle JJ, Doyle JL. 1987. A rapid DNA isolation procedure for small quantities of fresh leaf tissue. Phytochem Bull. 19:11–15.
  • Katoh K, Standley DM. 2013. MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Mol Biol Evol. 30(4):772–780.
  • 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.
  • Li Y, Hou L, Song B, Wan S, Sun X, Li L. 2019. Seasonal distribution of increased precipitation in maternal environments influences offspring performance of Potentilla tanacetifolia in a temperate steppe ecosystem. J Plant Ecol. 12(4):742–750.
  • Li Y, Yang H, Xia J, Zhang W, Wan S, Li L. 2011. Effects of increased nitrogen deposition and precipitation on seed and seedling production of Potentilla tanacetifolia in a temperate steppe ecosystem. PLoS One. 6(12):e28601.
  • Stamatakis A. 2014. RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinformatics. 30(9):1312–1313.
  • Zuo LH, Shang AQ, Zhang S, Yu XY, Ren YC, Yang MS, Wang JM. 2017. The first complete chloroplast genome sequences of Ulmus species by de novo sequencing: Genome comparative and taxonomic position analysis. PLoS One. 12(2):e0171264.