Skip to main content
Mitochondrial DNA. Part B, Resources logoLink to Mitochondrial DNA. Part B, Resources
. 2019 Oct 21;4(2):3673–3674. doi: 10.1080/23802359.2019.1678436

The complete chloroplast genome of Primula bulleyana, a popular ornamental species

Xiong Chen a, Li Zhang a, Wenqing Li b, Yuan Huang a,, Zhikun Wu c,
PMCID: PMC7707575  PMID: 33366137

Abstract

Primula bulleyana is a popular ornamental species, with high commercial values. Here, we reported the first chloroplast genome of P. bulleyana. The complete chloroplast genome is 150978 bp, containing a large single-copy (LSC) region of 82873 bp, a small single-copy (SSC) region of 17,741 bp, and a pair of inverted repeats (IRs) regions of 25,182 bp. In total, there are 142 genes, 92 protein-coding genes, 8 rRNA genes, and 38 tRNA genes are annotated in the whole cp genome, including 119 unique genes, 82 unique CDSs, 29 unique tRNAs, and 4 unique rRNAs. The overall GC content of the cp genome is 37.1%. The phylogenetic tree shows that close relationships among P. bulleyana and Primula stenodonta.

Keywords: Complete chloroplast genome, Primula bulleyana, ornamental species


Primula bulleyana Forrest is a beautiful species of flowering herbs perennial in the family Primulaceae, native to southwest Sichuan and northwest Yunnan (Lijiang) of China (Hu and Kelso 1996). The species is one of the plants with ornamental value and it has been popular garden plants and crossing parent strain since first introduced by Forrest in 1906. In garden hybrids, P. bulleyana is usually as the mother to hybridize with Primula beesiana, and the hybrids tending to be yellow or orange (Richards 1993, 2003). In this study, we reported the first chloroplast genome of P. bulleyana for understanding its systematics and provide scientific basis for the breeding hybrid of P. bulleyana resource in the garden.

The fresh leaves of P. bulleyana were collected from Yulong Snow Mountain (Lijiang, Yunnan, China). The voucher specimens (WZK140521) of P. bulleyana were deposit at the Herbarium of Yunnan Normal University. Total genomic DNA was extracted using a modified CTAB method (Porebski et al. 1997) and then fragmented and applied to establish short-insert libraries (300 bp), and then the paired-end library was sequenced using Illumina Hiseq X Ten sequencer. The clean data (ca. 36.5 million) were obtained after the removal of low-quality reads and adapter sequences and then were assembled via the programme NOVOPlasty version 2.7.2 (https://github.com/ndierckx/NOVOPlasty)(Dierckxsens et al. 2016), with complete chloroplast genome of its close relative Primula poissonii as reference (GenBank accession No. KF753634). The assembled chloroplast genome was annotated and adjusted manually using Geneious version 8 (Biomatters Ltd., Auckland, New Zealand) software (Kearse et al. 2012).

The complete chloroplast genome of P. bulleyana is 150978 bp in length with an overall GC content of 37.1% (GenBank accession MN428416). The assembled genome containing a large single-copy (LSC) region of 82873 bp, a small single-copy (SSC) region of 17,741 bp, and a pair of inverted repeats (IRs) regions of 25,182 bp. In total, there are 142 genes, 92 protein-coding genes, 8 rRNA genes, and 38 tRNA genes are annotated in the whole cp genome, including 119 unique genes, 82 unique CDSs, 29 unique tRNAs, and 4 unique rRNAs.

Phylogenetic position of P. bulleyana was analysed using the maximum likelihood (ML) method. The relative 13 Primulaceae species with complete chloroplast genomes were downloaded from Genbank. The whole chloroplast genome sequence of these species were aligned by the MAFFT (Katoh and Standley 2013); The ML tree was constructed using IQ_TREE 1.6.2 (Nguyen et al. 2015) and performed base on TVM + F+R2 model according to Bayesian information criterion using ModelFinder (Kalyaanamoorthy et al. 2017); ultrafast bootstrap (UFBoot) was used to teste branch supports (Hoang et al. 2018) and SH-like approximate likelihood ratio test (SHAlrt) (Guindon et al. 2010) with 10,000 bootstrap replicates. The phylogenetic tree showed that P. bulleyana and Primula stenodonta formed a monophyletic clade with 100% bootstrap value and sister to P. chrysochlora and P. poissonii (Figure 1). The complete chloroplast genome of P. bulleyana will provide a genome resource for the breeding of horticultural varieties of Primose as well as for the phylogenetic studies of Primulaceae.

Figure 1.

Figure 1.

ML phylogenetic tree of P. bulleyana and 13 Primulaceae species based on chloroplast complete genome, branch supports values were reported as SH-aLRT/UFBoot, green solid dot denotes supports values of 100/100.

Disclosure statement

No potential conflict of interest was reported by the authors.

References

  1. Dierckxsens N, Mardulyn P, Smits G. 2016. Novoplasty: de novo assembly of organelle genomes from whole genome data. Nucleic Acids Res. 45:e18. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Guindon S, Dufayard J, Lefort V, Anisimova M, Hordijk W, Gascuel O. 2010. New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of phyml 3.0. Syst Biol. 59:307–321. [DOI] [PubMed] [Google Scholar]
  3. Hoang DT, Chernomor O, Von Haeseler A, Minh BQ, Vinh LS. 2018. Ufboot2: improving the ultrafast bootstrap approximation. Mol Biol Evol. 35:518–522. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Hu Q, Kelso S. 1996. Primulaceae In: Wu CY, Raven PH, eidtors. Flora of China. Beijing and St Louis, China: Science Press and Missouri Botanical Garden. [Google Scholar]
  5. Kalyaanamoorthy S, Minh BQ, Wong TKF, Von Haeseler A, Jermiin LS. 2017. Modelfinder: fast model selection for accurate phylogenetic estimates. Nat Methods. 14:587–589. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Katoh K, Standley DM. 2013. Mafft multiple sequence alignment software version 7: improvements in performance and usability. Mol Biol Evol. 30:772–780. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. 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. 28:1647–1649. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Nguyen L, Schmidt HA, Von Haeseler A, Minh BQ. 2015. Iq-tree: a fast and effective stochastic algorithm for estimating maximum likelihood phylogenies. Mol Biol Evol. 32:268–274. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Porebski S, Bailey LG, Baum BR. 1997. Modification of a ctab DNA extraction protocol for plants containing high polysaccharide and polyphenol components. Plant Mol Biol Rep. 15:8–15. [Google Scholar]
  10. Richards J. 1993. Primula. 1st ed London: Batsford; p. 28–201. [Google Scholar]
  11. Richards J. 2003. Primula. 2st ed London: Batsford; p. 36–153. [Google Scholar]

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

RESOURCES