Abstract
This study was the first report about complete chloroplast genome of Pertya phylicoides (Asteraceae: Pertyeae), a critically shurby plant. The complete chloroplast genome of Pertya phylicoides was 153,379 bp in length and a typical circular structure, which comprises a pair of inverted repeat (IR) region of 25,191 bp divided by a large single-copy (LSC) region of 84,535 bp and a small single-copy (SSC) region of 18,462 bp. The general GC content was 37.6% in the whole sequence, whereas corresponding values of 35.6%, 31.2%, and 43.1% in the LSC, SSC, and IR regions, respectively. The whole genome contained 113 unique genes, including 79 protein-coding genes, 4 ribosomal RNA genes, and 30 tRNA genes. The phylogenetic hypotheses obtained based on the analyses of 21 cp genomes indicates Pertya phylicoides was supported as a sister group to the tribe Carduoideae.
Keywords: Asteraceae, Pertya phylicoides, chloroplast genome, endemic species
The Pertya Sch. Bip. is the shrub genus (17 species) mainly distributed in China (16 endemic species), with a few species in adjacent Japan, Thailand, Pakistan, and Afghanistan (Gao et al. 2011). The shrub Pertya phylicoides Jeffrey is a Chinese endemic species distributed in the dry valleys of Xizang, Yunnan, and Sichuan province. It also has ecological value. So far, the complete chloroplast genome of Pertya phylicoides has not yet been published. A good knowledge of genomic information of this species would contribute to the formulation of protection strategy and the study of genome diversity and species diversity. In this study, we assembled and characterized its complete chloroplast genome (Gen-Bank accession no. MN935435) from Illumina sequencing data.
Fresh leaves of Pertya phylicoides were collected from Muli, Sichuan Province, China, and deposited in the Herbarium of Sichuan Normal University, SCNU (specimen no.: Z.X. Fu 4038). High-quality total genomic DNA was extracted from ca. 6 cm2 sections of the silica-dried leaf using improved Tiangen Plant Genomic DNA Kits, then 4 μl RNAseA and 20 μl Proteinase K were added after incubation (65 °C). Total DNA was directly constructed using short-insert of 150 bp length libraries and sequenced on the Illumina Genome Analyzer (Hiseq 2000) according to the manufacturer’s protocol (Illumina, San Diego, CA, USA) by ORI-GENE, Beijing. Generally, more than 6 Gb of data were obtained for complete cp genome of P. phylicoides. Data were de novo assembled in CLC Genomic Workbench v11 (CLC Bio, Aarhus, Denmark) and the consensus were sequenced in Geneious R11.1.5 (Biomatters Ltd., Auckland, New Zealand) with the referenced chloroplast genome sequence of Saussurea polylepis (Accession: MF695711). The chloroplast genome was annotated using a web-based annotation program GeSeq (https://chlorobox.mpimp-golm.mpg.de/geseq.html), edited manually, and imaging was done with OGDraw v1.2 (Lohse et al. 2013). The complete chloroplast genome of P. phylicoides was 153,379 bp (GenBank Accession No. MN935435) in length with a typical circular structure, comprising a pair of inverted repeat (IR) of 25,191 bp divided by a large single-copy (LSC) region of 84,535 bp and a small single-copy (SSC) region of 18,462 bp. The general GC content was 37.6% in the whole sequence, with corresponding values of 35.6%, 31.2%, and 43.1% in the LSC, SSC, and IR regions, respectively. The whole genome contained 113 unique genes, including 79 protein-coding genes, 4 ribosomal RNA genes, and 30 tRNA genes.
To construct the phylogenetic tree, all of the cp genome sequences were aligned in MAFFT (Katoh and Standley 2013). A maximum likelihood analysis based on the GTRGAMMA model was performed with RaxML v7.2.8 on the CIPRES (Stamatakis et al. 2008; Miller et al. 2010) using 1000 bootstrap replicates with Kalopanax septemlobus (Thunb.) Koidz. (Araliaceae) and Anthriscus cerefolium (L.) Hoffm (Umbelliferae) as the outgroup. Based on limited materials, the phylogenetic hypotheses obtained with the analyses of 21 cp genomes indicates P. phylicoides was supported as a sister group to the tribe Carduoideae (Bootstrap support = 100, Figure 1). The complete plastome sequence of P. phylicoides will provide a useful resource for the conservation genetics of this species as well as for the phylogenetic studies for Asteraceae.
Figure 1.
The best Maximum likelihood (ML) phylogram inferred from 21 chloroplast genomes in Asteraceae (bootstrap value are indicated on the branches).
Funding Statement
This work was financially supported by the Special Research Project of National Tradition Chinese Medicine Industy, the Fourth National Survey on Chinese Material Medica Resources [GZY-KJS-2018-004], Sichuan Science and Technology Research Projects of Traditional Chinese Medicine [No. 2018PC005] and the Philosophy and Social Science Key Research Base Project of Sichuan Province, Sichuan Nationalities and Mountain Economy Development Research Center [No. SDJJ1907].
Disclosure statement
No potential conflict of interest was reported by the author(s).
References
- Gao TG, Freire SE, Hind D. 2011. Ainsliaea, Pertya and Myripnois. In: Wu ZY, Raven PH, Hong DY editor. Flora of China. Beijing: Science Press; St. Louis: Missouri Botanical Garden Press; p. 20–21. 15–32. [Google Scholar]
- Katoh K, Standley DM. 2013. MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Mol Biol Evol. 30(4):772–780. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lohse M, Drechsel O, Kahlau S, Bock R. 2013. Organellar Genome DRAW—a suite of tools for generating physical maps of plastid and mitochondrial genomes and visualizing expression data sets. Nucl Acids Res. 41:575–581. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miller MA, Pfeiffer W, Schwartz T. 2010. Creating the CIPRES science gateway for inference of large phylogenetic trees. Proceedings of the gateway computing environments workshop (GCE). New Orleans(LA): IEEE; p. 1–8. [Google Scholar]
- Stamatakis A, Hoover P, Rougemont J. 2008. A rapid bootstrap algorithm for the RAxML Web servers. Syst Biol. 57(5):758–771. [DOI] [PubMed] [Google Scholar]

