Skip to main content
Mitochondrial DNA. Part B, Resources logoLink to Mitochondrial DNA. Part B, Resources
. 2021 Mar 24;6(3):1186–1188. doi: 10.1080/23802359.2021.1902413

The complete chloroplast genome of Phlomoides younghushandii (Lamiaceae), a traditional Tibetan medicinal herb

Dao-Zhang Min a, Fei Zhao b, Qiong Zhang b, Bo Li a,
PMCID: PMC7995819  PMID: 33796781

Abstract

The species Phlomoides younghushandii is a medicinal herb mainly distributed in southwest China. The first complete plastid genome sequence of P. younghushandii reported here was 151,747 bp long, with the large single copy (LSC) region of 83,181 bp, the small single copy (SSC) region of 17,372 bp and two inverted repeats (IRa and IRb) of 25,597 bp. The plastome contained 114 genes, including 80 protein-coding genes, four encoding rRNAs, and 30 encoding tRNAs. The overall GC content was 38.5%. Phylogenetic analysis of Lamiaceae based on a whole plastome matrix suggested that Phlomoides is closely related to the genus Phlomis as members of subfamily Lamioideae.

Keywords: Chinese herbal medicine, Lamiodide, Phlomideae, Phlomoides, plastome


As currently defined (Scheen et al. 2010; Bendiksby et al. 2011; Salmaki et al. 2012), Phlomideae consists of two genera, Phlomis L. (50–90 spp.) and Phlomoides Moench (150–170 spp.). The latter genus is highly diverse in the Iranian highlands, Central Asia, and China (Khosroshahi and Salmaki 2019; Zhao et al. 2019). Phlomoides younghushandii (S.M. Mukerjee) Kamelin & Makhm. is a perennial herb, widely distributed in the Qinghai–Tibet Plateau (QTP), and is commonly used in traditional Chinese medicine (TCM) to treat colds, sore ulceration, bronchitis, and other diseases (Peng 2017).

Young leaves of P. younghushandii were freshly collected in Langkazi County, Xizang, China (90°24′33.61″E, 29°06′10.72″N) and dried immediately in silica gel. A voucher specimen was deposited in the Herbarium of Kunming Institute of Botany, Chinese Academy of Sciences (Herbarium Code: KUN, URL: http://kun.kingdonia.org/, contact Prof. Zhu-Liang Yang via fungi@mail.kib.ac.cn) under the voucher number Chen et al. EM1033. Total genomic DNA was isolated using the CTAB method (Doyle and Doyle 1987) and fragmented into ca. 300 bp size by transposome tagmentation using the Nextera XT kit. A paired-end library was constructed according to the manufacture’s protocol (NEBNext® Ultra IIDNA Library Prep Kit) and sequenced on the Illumina HiSeq 2000 using the 150 PE kit (BGI-Shenzhen, Guangdong, China).

Illumina paired-end sequencing produced 13,640,496 raw reads for the P. younghushandii. The high-quality clean reads were carried out using Fast QC toolkit (Andrews 2010) with the parameter set as Q ≥ 25. De novo assembly was conducted with the GetOrganelle pipeline (https://github.com/Kinggerm/GetOrganelle, Jin et al. 2020) under the optimal k-mer 105, and the resulting plastome was annotated in Geneious version 11.0.3 (Kearse et al. 2012) using the previously published Phlomoides betonicoides (Diels) Kamelin & Makhm plastome as reference (Zhao et al. 2019). The annotated plastid genome sequence was deposited on GenBank with accession number MW405448.

The whole plastid genome of P. younghushandii was 151,747 bp, with a large single-copy (LSC) region (83,181 bp), a small single-copy (SSC) region (17,372 bp), and a pair of inverted repeats (IRa and IRb: 25,597 bp). The annotated genome comprised 114 genes, including 80 protein-coding genes, four ribosomal RNA genes (rrn16, rrn23, rrn4.5, and rrn5), and 30 transfer RNA genes.

Eighteen genes were duplicated in the IR regions, including seven protein-coding genes (ndhB, rpl2, rpl23, rps12, rps7, ycf2, and ycf15), four ribosomal RNA genes (rrn16, rrn23, rrn4.5, and rrn5), and seven transfer RNA genes (trnA-UGC, trnI-CAU, trnI-GAU, trnL-CAA, trnN-GUU, trnR-ACG, and trnV-GAC). The overall GC content of P. younghushandii plastid genome is 38.5% (LSC, 36.7%; SSC, 32.6%; IRs, 43.4%).

Maximum-likelihood (ML) phylogenetic analysis was conducted using RAxML version 8.1.11 (Stamatakis 2014) as implemented on the Cyberinfrastructure for Phylogenetic Research (CIPRES) Science Gateway (http://www.phylo.org/, Miller et al. 2010), employing the GTR + G model with 1000 bootstrap iterations (-#j-N). Other parameters used the default settings. Phylogenetic analysis based on 80 protein-coding genes of 38 representative plastomes within the family Lamiaceae further confirmed that Phlomoides is a member of the subfamily Lamioideae (Figure 1).

Figure 1.

Figure 1.

Maximum likelihood (ML) tree of Lamiaceae inferred from 80 protein-coding genes of 25 plastomes (including the outgroup Lancea hirsuta). Bootstrap support values are indicated on branches.

Funding Statement

This work was supported by National Natural Science Foundation of China [No. 31900181, 31872648] and the Natural Science Foundation of Yunnan Province [202001AS070016].

Disclosure statement

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

Data availability statement

The 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. MW405448, and the raw sequenced reads was submitted to the Sequence Read Archive (SRA) database under the Bioproject number PRJNA687635.

References

  1. Andrews S. 2010. Fast QC: a quality control tool for high throughput sequence data. v. 0.10.0. Available from: http://www.bioinformatics.babraham.ac.uk/projects/fastqc/
  2. Bendiksby M, Thorbek L, Scheen AC, Lindqvist C, Ryding O.. 2011. An updated phylogeny and classification of Lamiaceae subfamily Lamioideae. Taxon. 60(2):471–484. [Google Scholar]
  3. Doyle JJ, Doyle J.. 1987. A rapid DNA isolation procedure for small quantities of fresh leaf tissue. Phytochem Bull. 19:11–15. [Google Scholar]
  4. Jin JJ, Yu WB, Yang JB, Song Y, dePamphilis CW, Yi TS, Li DZ.. 2020. Get organelle: a fast and versatile toolkit for accurate de novo assembly of organelle genomes. Genome Biol. 21(1):241. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. 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. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Khosroshahi EE, Salmaki Y.. 2019. Evolution of trichome types and its systematic significance in the genus Phlomoides (Lamioideae, Lamiaceae). Nord J Bot. 37:02132. [Google Scholar]
  7. Miller MA, Pfeiffer W, Schwartz T.. 2010. Creating the CIPRES science gateway for inference of large phylogenetic trees. Gateway Computing Environments Workshop (GCE), 2010. Piscataway (NJ): IEEE. [Google Scholar]
  8. Peng H. 2017. Medicinal Flora of China. Vol. 9. Beijing, China: Peking University Medical Press. [Google Scholar]
  9. Salmaki Y, Zarre S, Ryding O, Lindqvist C, Scheunert A, Bräuchler C, Heubl G.. 2012. Phylogeny of the tribe Phlomideae (Lamioideae: Lamiaceae) with special focus on Eremostachys and Phlomoides: new insights from nuclear and chloroplast sequences. Taxon. 61(1):161–179. [Google Scholar]
  10. Scheen AC, Bendiksbe M, Ryding O, Mathiesen C, Albert VA, Lindqvist C.. 2010. Molecular phylognenetics, character evolution, and suprageneric classification of Lamioideae (Lamiaceae). Ann Missouri Bot Gard. 97:121–217. [Google Scholar]
  11. Stamatakis A. 2014. RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinformatics. 30(9):1312–1313. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Zhao Y, Turdimatovich TO, Xiang CL.. 2019. The complete chloroplast genome of Phlomoides betonicoides (Lamiaceae), a traditional Tibetan medicinal herb. Mitochondrial DNA B Resour. 5(1):75–76. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The 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. MW405448, and the raw sequenced reads was submitted to the Sequence Read Archive (SRA) database under the Bioproject number PRJNA687635.


Articles from Mitochondrial DNA. Part B, Resources are provided here courtesy of Taylor & Francis

RESOURCES