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Mitogenome Announcement

The complete chloroplast genome sequence of Rhus potaninii

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Pages 2425-2426 | Received 14 May 2020, Accepted 24 May 2020, Published online: 11 Jun 2020

Abstract

We reported the complete chloroplast genome sequences of Rhus potaninii which was characterized by de novo assembly with Illumina sequencing data. The size of R. potaninii complete chloroplast genome is 159,620 bp in length and includes a large single copy region of 87,722 bp, a small single copy region of 18,948 bp, and a pair of inverted repeats of 26,475 bp. Its GC content is 37.9%. A total of 133 genes were predicted, including 86 protein-coding genes, 8 rRNA genes, 37 tRNA genes, and 2 pseudogenes. Maximum-likelihood (ML) phylogenetic tree indicates that R. potaninii is sister to R. chinensis.

The deciduous tree Rhus potaninii is 5–8 m tall. It grows on the hill or mountain forests at an altitude of 900–2500 m. The R. potaninii belongs to Anacardiaceae family of Sapindales order. The Galla chinensis, induced by infection with Gallnut Aphid on R. chinensis, R. potaninii, and R. punjabensis, is a traditional Chinese medicine (National Pharmacopoeia Committee Citation2010). It is known to have analgesic and anti-inflammatory effects (Sun et al. Citation2018). In recent years, Galla chinensis has attracted the attention of drug researchers at home and abroad because of its unique advantages such as strong pharmacological effect, extensive sources, and strong selectivity (Karimi-Khouzani et al. Citation2017). Although there are many pharmacology related research of it, there are few researches on its genome. Therefore, our research provides a basis for the study of the coevolution of Gallnut Aphid and host tree and the further study on phylogenetic evolution of R. potaninii.

Fresh leaves of R. potaninii were collected from Danfeng County, Shaanxi Province (33°36′33.52″N, 110°14′04.89″E). The specimen was saved in Herbarium of Institute of Medicinal Plant Development (voucher: Pan0101). Its total genomic DNA was extracted using QIAGEN DNeasy Plant Mini Kit and the whole genome was sequenced on Illumina Hiseq 2000 platform. Using SOAPdenovo 2 (Luo et al. Citation2012) and SSPACE (Boetzer et al. Citation2011) to assemble clean data into a complete chloroplast genome.

The total length of chloroplast genome of R. potaninii was 159,620 bp (Genbank accession number: MT230556) with 37.9% GC content. The genome consists of four distinct parts, including a large single copy region of 87,722 bp, a small single copy region of 18,948 bp, and a pair of inverted repeats of 26,475 bp. In the genome, 86 protein-coding genes, 8 rRNA genes, and 2 pseudogenes were identified by CPGAVAS (Liu et al. Citation2012), DOGMA (http://dogma.ccbb.utexas.edu/) (Wyman et al. Citation2004) and BLAST search (Cui et al. Citation2019), and 37 tRNA genes were annotated by tRNAscan-SE (Schattner et al. Citation2005).

Phylogenetic analysis of the complete chloroplast genome sequence of R. potaninii and 10 species was performed through a maximum likelihood (ML) analyses with 1000 bootstrap replicates (), 10 species of which belonging to Sapindales order. The ML tree showed that R. potaninii was sister to R. chinensis with 100% support value, belonging to the Anacardiaceae family.

Figure 1. Phylogenetic tree of Rhus potaninii and 10 species in order Sapindales using maximum likelihood (ML) analyses based on complete chloroplast genome sequences. The numbers at nodes of phylogenetic tree show the bootstrap support values.

Figure 1. Phylogenetic tree of Rhus potaninii and 10 species in order Sapindales using maximum likelihood (ML) analyses based on complete chloroplast genome sequences. The numbers at nodes of phylogenetic tree show the bootstrap support values.

Disclosure statement

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

Data availability statement

The data that support the findings of this study are openly available in NCBI at https://www.ncbi.nlm.nih.gov/nuccore/MT230556, accession number MT230556.

Additional information

Funding

This work was supported by the CAMS Innovation Fund for Medical Sciences(CIFMS) under Grant [Project No.: 2016—12 M—2—003]; and National Science & Technology Fundamental Resources Investigation Program of China under Grant [Project No.: 2018FY100700].

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