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Mitogenome Announcement

The complete chloroplast genome sequence of Dendrobium wangliangii (Orchidaceae)

ORCID Icon, &
Pages 3495-3497 | Received 03 Aug 2020, Accepted 04 Sep 2020, Published online: 07 Oct 2020

Abstract

Dendrobium wangliangii is a rare orchid species with extremely small populations, endemic to China. In this study, the complete chloroplast (cp) genome sequence and the genome features of D. wangliangii were analyzed. The whole cp genome sequence of D. wangliangii is 160,052 including a large single-copy region (LSC, 87,525 bp), a small single-copy region (SSC, 18,373 bp), and a pair of repeat regions (IRs, 27,077 bp, each). The contents of four bases in cpDNA were A (30.9%), C (18.9%), G (18.3%) and T (31.9%), respectively. The total content of GC is 37.1%. The cp genome contains 129 genes, consisting of 124 unique genes (78 protein-coding genes, 38 tRNAs, and 8 rRNAs). Phylogenetic analysis showed that D. wangliangii nested with other Dendrobium spp. and was closely related to D. ellipsophyllum, D. wattii and D. longicornu.

Dendrobium is one of the largest genera in the orchid family. It consists of approximately 1500 species, mainly distributed in tropical and subtropical regions of the world (Pridgeon et al. Citation2014). Seventy-eight species of this genus in 14 sections were recorded in China (Zhu et al. Citation2009). However, molecular phylogenies of the combination of partial chloroplast marks and ITS-rDNA are not always consistent to morphological sections (Xiang et al. Citation2016). Additional molecular marks such as complete chloroplast genome sequences are needed for phylogenetic and evolutionary analyses.

Dendrobium wangliangii was discovered as a new species in section Dendrobium in 2008 (Hu et al. Citation2008). Dendrobium wangliangii is distributed in specific habitats with narrow distributions, e.g. the Jinshajiang dry-hot valley in Luquan County, Kunming, Yunnan Province (Wang et al. Citation2019), and the populations are extremely small. Given the special features of morphology and the nature of drought tolerance, phylogenetic position of D. wangliangii is unknown. In this study, a complete chloroplast genome (cp genome) sequence of D. wangliangii was characterized and analyzed for its phylogenetic position.

The leave samples of D. wangliangii was collected in Fumin County, Yunnan, China (25°20′19″N, 102° 27′26″E). Total genomic DNA from leaf was extracted using Tiangen DNA kit (TIANGEN, China), and sequenced by the Illumina Hiseq 2500 sequencing platform (Illumina, CA, USA) at Personal Biotechnology Co., Ltd (Shanghai, China). The DNA of D. wangliangii sample was preserved in Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences with collection number JSJSH17122018-1. The sequence data were de novo assembled to a complete and circular cp genome using GetOrganelle (Jin et al. 2020). Gene annotation was accomplished using GeSeq with default sets (Tillich et al. Citation2017), and manually checked in Geneious Primer 2020 (Kearse et al. Citation2012). Sequences of Coding regions (CDS) and rRNAs were extracted, aligned and concatenated in Geneious Primer 2020.

The whole cp genome sequence of D. wangliangii (GenBank accession no. MT798588) is totally 160,052 bp in length, in which the contents of four bases in cpDNA were A (30.9%), C (18.9%), G (18.3%) and T (31.9%), respectively. The total content of GC is 37.1%. The structure of cp genome includes a large single-copy region (LSC, 87,525 bp), a small single-copy region (SSC, 18,373 bp), and a pair of inverted repeat regions (IRs, 27,077 bp, each). Typical code ATG was used as the initiator codon and typical code TAA as the terminator codon in all the 78 protein-coding genes. The gene order and features of the D. wangliangii are consistent with congener species in Dendrobium (Niu, Xue et al. Citation2017; Niu, Zhu, et al. Citation2017).

To further investigate its phylogenetic position, the complete chloroplast genomes from 22 species of subfamily Epidendroideae, e.g. 16 Dendrobium species, three Bulbophyllum species and three Cymbidium species, and two species of Paphiopedilum from subfamily Cypripedioideae as outgroup, were selected to reconstruct the phylogenetic tree. The best-fit model GTR + F+R2 using the Akaike information criterion (AIC) was applied to read the best model to construct maximum likelihood (ML) trees using IQ-TREE 1.6 (Lam-Tung et al. Citation2015). Phylogenetic analysis showed that D. wangliangii nested in Dendrobium clade () and was closely related to D. ellipsophyllum, D. wattii and D. longicornu. This newly reported chloroplast genome of D. wangliangii provides important genomic information for Dendrobium species phylogenetic and evolutionary analyses.

Figure 1. Phylogenetic analysis of Dendrobium wangliangii using maximum likelihood of 69 protein-coding genes and four rRNA genes from 16 species from the genus Dendrobium, two species of Paphiopedilum as outgroup. The support values were indicated on the branch node or right side of node; and each tip was labeled by species name and GenBank accession no. The phylogenetic position of the species D. wangliangii was shown in gray box.

Figure 1. Phylogenetic analysis of Dendrobium wangliangii using maximum likelihood of 69 protein-coding genes and four rRNA genes from 16 species from the genus Dendrobium, two species of Paphiopedilum as outgroup. The support values were indicated on the branch node or right side of node; and each tip was labeled by species name and GenBank accession no. The phylogenetic position of the species D. wangliangii was shown in gray box.

Acknowledgments

The authors thank Dr. Wen-Bin Yu for help in software applications and Ms. Bi-Ying Yue for lab assistance during DNA extraction. We are also grateful to Mrs. Xiao-Yun Wang from the Wild Orchid conservation Center of Yunnan Fengchunfang Biotechnology Company for providing sample materials.

Disclosure statement

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

Data availability statement

The data that support the analyses and results of Dendrobium wangliangii in this paper are available in GenBank with accession no. MT798588 (https://www.ncbi.nlm.nih.gov/). Raw sequencing reads was deposited in SRA with BioProject accession: PRJNA659161. (https://www.ncbi.nlm.nih.gov/Traces/study/?acc=PRJNA659161).

Additional information

Funding

This study was funded by the National Key R & D Program of China under grants [No. 2017YFC0505204] and the National Natural Science Foundation of China [grant No. 31870183].

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