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Mitogenome Announcement

Characterization of the complete chloroplast genome of the Chinese Kadsura vine Kadsura longipedunculata (Schisandraceae)

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Pages 476-477 | Received 11 Jul 2018, Accepted 29 Jul 2018, Published online: 23 Jan 2019

Abstract

Kadsura (Schisandraceae) comprises ca. 16 species and widely distributes in eastern Asia. Many species in the genus were used as important medicinal plants in China and other Asian countries. In present study, we described the first Kadsura chloroplast genome, Kadsura longipedunculata, based on illumine pair-end sequencing data. The complete plastome length is 145,346 bp long with a large single copy, a small single copy, and two inverted repeat regions of length 94,947, 17,752, and 16,323 bp, respectively. A total of 118 genes were identified, including 75 protein-coding gens, 8 rRNA genes, and 34 tRNA genes. Eighteen plastome accessions from Austrobaileyales, Nymphaeales, and Magnoliales were selected to assess the phylogenetic placement of genus.

The genus Kadsura includes 16 species of scandent and twining woody vines with relatively primitive morphological characters placed in a basal angiosperm family, Schisandraceae (Austrobaileyales). Many species in the genus were used as important medicinal plants in China and other Asian countries (Zhang et al. Citation2015). Previous molecular phylogenetic study has shown that both Kadsura and its sister genus Schisandra are not monophyletic (Liu et al. Citation2006; Zhang et al. Citation2015). Kadsura longipedunculata, the Chinese Kadsura vine, is a widely used medicinal plant native to eastern China (Mulyaningsih et al. Citation2010). In this study, we assembled and characterized the complete plastome of K. longipedunculata. It is the first complete plastome reported in this genus, and will provide potential genetic resources for elucidating possible evolutionary relationships between Kadsura and Schisandra in Schisandraceae.

The plant sample collected from Xuansheng, Anhui, China (Voucher No. WH1803007255, deposited at Zhejiang Sci-Tech University). Total genomic DNA was extracted from fresh leaves of K. longipedunculata individual using DNA Plantzol Reagent (Invitrogen, Carlsbad, USA), according to the manufacturer’s instructions. Whole plastome sequences were generated using Illumina HiSeq 2500 platform (Illumina Inc., San Diego, CA, USA). In total, ca. 18.1 million high-quality clean reads (150 bp PE read length) were generated with adaptors trimmed. The CLC de novo assembler (CLC Bio, Aarhus, Denmark), BLAST, GeSeq (Tillich et al. Citation2017), and tRNAscan-SE v1.3.1 were used to align, assemble, and annotate the plastome (Schattner et al. Citation2005).

The full length of K. longipedunculata chloroplast genome (GenBank acession MH550622) was 145,346 bp and consist of a large single copy region (LSC with 94,947 bp), a small single copy region (SSC with 17,752 bp), and a pair of inverted repeat regions (IRs) of 16,323 bp. The overall GC content of the K. longipedunculata cp genome was 39.7% and the GC content in the LSC, SSC, and IR regions are 38.6%, 35%, and 45.6%, respectively. A total of 118 genes were contained in the cp genome (75 protein-coding genes, 8 rRNA genes, and 34 tRNA genes). Twelve genes had two copies, which included 2 PCG genes (ndhb, rps7), 6 tRNA genes (trnI-CAU, trnI-GAU, trnL-CAA, trnN-GUU, trnR-ACG, and trnV-GAC), and all 4 rRNA species (rrn4.5, rrn5, rrn16 and rrn23). Among the protein-coding genes, two genes (clpP and ycf3) contained two introns, and other seven genes (atpF, ndhA, ndhB, rpl2, rpoC1, rps16) had one intron each.

For conducting its phylogenetic relationships with present reported complete chloroplast genomes, eighteen chloroplast genomes sequences from the order of Austrobaileyales, Nymphaeales, and Magnoliales were selected (). All of genomes were fully aligned with MAFFT v7.3 (Katoh and Standley Citation2013), and the maximum-likelihood (ML) inference was performed using GTR model with support for branches evaluated by 1000 bootstrap replicates with RAxML v.8.2.1 (Stamatakis Citation2014) on the CIPRES cluster service (Miller et al. Citation2010). We hope the complete plastome of K. longipedunculata will provide a valuable resource for further genetic conservation, phylogenomic, and evolution studies in the genus and family.

Figure 1. RAxML phylogeny of Kadsura based on 18 complete cp genomes (Bootstrap values were showed above each node, and a “*” indicates 100% statistical support value).

Figure 1. RAxML phylogeny of Kadsura based on 18 complete cp genomes (Bootstrap values were showed above each node, and a “*” indicates 100% statistical support value).

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

This work was supported by the National Natural Science Foundation of China [31600183, 31400194], Zhejiang Provincial Public Welfare Technology and Application Research Project [2017C32044], and Science Foundation of Zhejiang Sci-Tech University [grant No. 14042010-Y, 15042170-Y], 521 Distinguished Young Scientist Foundation of Zhejiang Sci-Tech University [grant No. 11610132521509], and Basic Work Project of Ministry of Science and Technology [grant no. 2015FY110200]

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