Skip to main content
Mitochondrial DNA. Part B, Resources logoLink to Mitochondrial DNA. Part B, Resources
. 2019 Nov 22;4(2):4220–4222. doi: 10.1080/23802359.2019.1693933

The complete chloroplast genome sequence of the threatened Cypripedium calceolus (Orchidaceae)

Li-Jie Zhang a,*, Rui Ding b,*, Wei-Wei Meng c, Hua-Lei Hu c, Xu-Hui Chen c,, Hai-Hong Wu d,
PMCID: PMC7707734  PMID: 33366391

Abstract

The complete chloroplast genome of Cypripedium calceolus, a rare species in the family Orchidaceae was reported in this study. The genome size is 175,122 bp in length, and contains four sub-regions: 97,486 bp of large single copy (LSC) and 22,260 bp of small copy (SSC) regions, separated by 27,688 bp of inverted repeat (IR) regions. A total of 133 genes were annotated, including 87 protein-coding genes, 38 tRNA genes and 8 rRNA genes. The GC content of this cp genome is 34.36%. Phylogenetic analysis revealed a close relationship between C. calceolus with C. japonicum and C. formosanum. This is the first complete cp genome for C. calceolus that would be useful for conservation and phylogenetic studies of this species.

Keywords: Chloroplast genome, Cypripedium calceolus, rare orchid, conservation


Cypripedium (Cypripedioideae, Orchidaceae) is a remarkable genus with highly ornamental value because of their showy flowers. Cypripedium calceolus is a terrestrial orchid in this genus and naturally distributed in northeast China, Japan, North Korea and Europe (Lang et al. 1999). However, due to habitat destruction and ruthless collection for horticultural purposes (Minasiewicz et al. 2018; Fay 2018), the range of C. calceolus is declining rapidly in recent years. As a result, C. calecolus is now regarded as a least concern species according to the IUCN (Rankou and Bilz 2014), and is listed among the level-I state protected wild plants by the Chinese Central Government. In this study, we assembled and characterized the complete chloroplast (cp) genome of C. calecolus for the first time which will contribute to development of conservation strategy for this rare orchid species. The annotated cp genome sequence was submitted to GenBank under the accession number of MN602053.

The plant material of C. calecolus was collected from Longgang mountain (N41°58′09″, E125°08′56″), Liaoning, northeast China. The specimen was stored with the archival number of ORCHID_CYP_CAL_01 at College of Forestry of Shenyang Agricultural University. Total genomic DNA was extracted and sequenced on the Illumina Miseq sequencing platform by Shanghai Personal Biotechnology Co. Ltd, China. A reference-guided assembly was used to reconstruct the cp genome, with C. japonicum (KJ625630) as the reference. The complete genome was manually annotated by comparing with the cp genomes of Cypripedium species (Kim et al. 2014; Luo et al. 2014; Lin et al. 2015).

The cp genome of C. calecolus is 175,122 bp in length and has a typical circular structure including a large single-copy (LSC) region of 97,486 bp and a small single-copy (SSC) region of 22,260 bp, which is separated by a pair of inverted repeat (IR) regions of 27,688 bp. The overall GC content is 34.36% and in the LSC, SSC, and IR regions are 31.57%, 26.13%, and 42.58%, respectively. A total of 133 genes were successfully annotated, including 87 protein-coding genes, 38 tRNA genes and 8 rRNA genes. Seven protein-coding, eight tRNA, and all four rRNA genes were duplicated in IR regions. In total, 22 intron-containing genes were annotated, with 4 genes having two introns and the rests having one intron.

To study the phylogenetic position of C. calecolus within the Orchidaceae family, the published cp genomes of 46 species from this family were selected for analysis. The complete genomes were downloaded from the NCBI GenBank database and were aligned using HomBlocks (Bi et al. 2018) with the Gblocks method (Talavera and Castresana 2007). Phylogenetic analysis was performed by maximum-likelihood analysis with MEGA 7.0 (Kumar et al. 2016). The topology of the phylogenetic tree corroborates the current taxonomy of the family Orchidaceae at the subfamily level (Cameron et al. 1999), and C. calecolus is closely related to the congeneric C. japonicum and C. formosanum. The complete cp genome information provided data useful for conservation works on C. calecolus as well as for phylogenetic studies within Orchidaceae.

Disclosure statement

The authors declare no competing financial interest. The authors alone are responsible for the content and writing of the paper.

Figure 1.

Figure 1.

Phylogenetic raltionship of 47 orchids species built by maximum-likelihood method based on complete chloroplast genomes, with Oryza genus As the outgroup. The branch support was determined by computing 1000 non-parametric bootstrap replicates.

References

  1. Bi GQ, Mao YX, Xing QK, Cao M. 2018. HomBlocks: A multiple-alignment construction pipeline for organelle phylogenomics based on locally collinear block searching. Genomics. 110(1):18–22. [DOI] [PubMed] [Google Scholar]
  2. Cameron KM, Chase MW, Whitten WM, Kores PJ, Jarrell DC, Albert VA, Yukawa T, Hills HG, Goldman DH. 1999. A phylogenetic analysis of the Orchidaceae: evidence from rbcL nucleotide sequences. Am J Bot. 86(2):208–224. [PubMed] [Google Scholar]
  3. Fay MF. 2018. Orchid conservation: how can we meet the challenges in the twenty-first century? Bot Stud. 59(1):16. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Kim JS, Kim HT, Kim JH. 2014. The largest plastid genome of Monocots: a novel genome type containing AT residue repeats in the slipper orchid Cypripedium japonicum. Plant Mol Biol Rep. 33(5):1–11. [Google Scholar]
  5. Kumar S, Stecher G, Tamura K. 2016. MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol. 33(7):1870–1874. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Lang KY, Chen XQ, Zhu GH. 1999. Flora reipublicae popularis sinicae Vol. 17 Beijing (China): Science Press, p. 34. [Google Scholar]
  7. Lin CS, Chen JJW, Huang YT, Chan MT, Daniell H, Chang WJ, Hsu CT, Liao DC, Wu FH, Lin SY, et al. 2015. The location and translocation of ndh genes of chloroplast origin in the Orchidaceae family. Sci Rep. 5(1):9040. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Luo J, Hou BW, Niu ZT, Liu W, Xue QY, Ding XY. 2014. Comparative chloroplast genomes of photosynthetic orchids: insights into evolution of the Orchidaceae and development of molecular markers for phylogenetic applications. PLoS One. 9(6):e99016. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Minasiewicz J, Znaniecka JM, Górniak M, Kawiński A. 2018. Spatial genetic structure of an endangered orchid Cypripedium calceolus (Orchidaceae) at a regional scale: limited gene flow in a fragmented landscape. Conserv Genet. 19(6):1449–1460. [Google Scholar]
  10. Rankou H, Bilz M. 2014. Cypripedium calceolus. The IUCN Red List of Threatened Species. e.T162021A43316125. [Google Scholar]
  11. Talavera G, Castresana J. 2007. Improvement of phylogenies after removing divergent and ambiguously aligned blocks from protein sequence alignments. Syst Biol. 56(4):564–577. [DOI] [PubMed] [Google Scholar]

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

RESOURCES