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Mitogenome Announcement

The complete chloroplast genome of candidate new species from Rosa rugosa in Korea (Rosaceae)

ORCID Icon, ORCID Icon, , , & ORCID Icon
Pages 2433-2435 | Received 29 May 2019, Accepted 22 Jun 2019, Published online: 12 Jul 2019

Abstract

Complete chloroplast genome of candidate new species from Rosa rugosa, named as Rosa angusta, is 156,989 bp long and has four subregions: 86,227 bp of large single copy (LSC) and 18,816 bp of small single copy (SSC) regions are separated by 25,793 bp of inverted repeat (IR) regions including 130 genes (85 protein-coding genes, eight rRNAs, and 37 tRNAs). The overall GC content of this chloroplast genome is 37.2% and in the LSC, SSC, and IR regions are 35.2%, 31.1%, and 42.8%, respectively. Phylogenetic trees show that R. angusta is close to R. rugosa with enough number of sequence variations.

Genus Rosa belonging to family Rosaceae consists of around 200 species distributed in the temperate and subtropical regions of the Northern hemisphere (Rehder Citation1949) and its taxonomic treatment is complicated due to highly diverged characteristics (Wissemann and Ritz Citation2005). In 2013, Mr. Suhwan Nam, one of the authors, found a small population of Rosa rugosa in Hakampo beach of Taean-gun in Chungcheongnam-do, presenting that leaflets are elliptic and petals are not overlapped; while those of R. rugosa are widely elliptic and petals are overlapped (). We suspected that this population is a candidate new species, named as Rosa angusta. To decipher its genetic background, its chloroplast genome was completed.

Figure 1. (A) Picture of Rosa augsta flower, (B) Picture of Rosa rugosa flower, (C) Neighbor joining (bootstrap repeat is 10,000) and maximum likelihood (bootstrap repeat is 1,000) phylogenetic trees of ten Rosa chloroplast genomes and three outgroup species: Rosa angusta (MK947051 in this study), Rosa rugosa (MK986659), Rosa praelucens (NC_037492), Rosa roxburghii (NC_032038), Rosa banksiae (NC_042194), Rosa chinensis var. spontanea (NC_038102), Rosa odorata var. gigantea (KF753637), Rosa multiflora (NC_039989 and MG727863), Rosa maximowicziana (NC_040960), and three outgroup species: Potentilla freyniana (NC_041210), Rubus crataegifolius (NC_039704), and Prunus persica (NC_014697). Phylogenetic tree was drawn based on neighbor joining tree. The numbers above branches indicate bootstrap support values of maximum likelihood and neighbor joining phylogenetic tree, respectively.

Figure 1. (A) Picture of Rosa augsta flower, (B) Picture of Rosa rugosa flower, (C) Neighbor joining (bootstrap repeat is 10,000) and maximum likelihood (bootstrap repeat is 1,000) phylogenetic trees of ten Rosa chloroplast genomes and three outgroup species: Rosa angusta (MK947051 in this study), Rosa rugosa (MK986659), Rosa praelucens (NC_037492), Rosa roxburghii (NC_032038), Rosa banksiae (NC_042194), Rosa chinensis var. spontanea (NC_038102), Rosa odorata var. gigantea (KF753637), Rosa multiflora (NC_039989 and MG727863), Rosa maximowicziana (NC_040960), and three outgroup species: Potentilla freyniana (NC_041210), Rubus crataegifolius (NC_039704), and Prunus persica (NC_014697). Phylogenetic tree was drawn based on neighbor joining tree. The numbers above branches indicate bootstrap support values of maximum likelihood and neighbor joining phylogenetic tree, respectively.

Its total DNA isolated from Hagampo coast, Wonbuk-myeon, Taean-gun, Chungcheongnam-do, Republic of Korea, was extracted from fresh leaves using a DNeasy Plant Mini Kit (QIAGEN, Hilden, Germany). Voucher was deposited in InfoBoss Cyber Herbarium (IN; IB-90006). Genome was sequenced using HiSeqX at Macrogen Inc., Korea, and de novo assembly and confirmation were performed by Velvet 1.2.10 (Zerbino and Birney Citation2008), SOAPGapCloser 1.12 (Zhao et al. Citation2011), BWA 0.7.17 (Li Citation2013), and SAMtools 1.9 (Li et al. Citation2009). Geneious R11 11.0.5 (Biomatters Ltd., Auckland, New Zealand) was used for annotation based on Rosa praelucens chloroplast (NC_037492; Jian et al. Citation2018).

Chloroplast genome of R. angusta (Genbank accession is MK947051) is 156,989 bp long (GC ratio is 37.2%) and has four subregions: 86,227 bp of large single copy (35.2%) and 18,816 bp of small single copy (SSC; 31.1%) regions are separated by 25,793 bp of inverted repeat (IR; 42.8%). It contains 130 genes (85 protein-coding genes, eight rRNAs, and 37 tRNAs); 17 genes (seven protein-coding gene, four rRNAs, and six tRNAs) are duplicated in IR regions.

Based on raw reads of R. rugosa (SRR1660458), chloroplast genome (Genbank accession is MK986659) was reconstructed. Pair-wise alignment between R. rugosa and R. angusta chloroplast genomes was conducted under the Plant Chloroplast Database (PCD; Park et al., in preparation), resulting 40 single nucleotide polymorphisms and 224 insertions and deletions. They present enough differences between two neighbor species supported by various researches showing less number of intraspecies variations on chloroplast genomes (Kim et al. Citation2019; Min et al. Citation2019; Park and Kim Citation2019; Park, Kim, Kwon, et al. Citation2019; Park, Kim, Lee Citation2019; Park, Kim, Xi Citation2019; Park, Kim, Xi, Heo Citation2019; Park, Kim, Xi, Nho, et al. Citation2019; Park et al. Citation2019b, Citation2019a; Park, Xi, et al. Citation2019).

Ten Rosa chloroplast genomes including that of R. angusta, and three outgroup chloroplast genomes were used for constructing neighbor joining (bootstrap repeat is 10,000) and maximum likelihood (bootstrap repeat is 1,000) phylogenic trees using MEGA X (Kumar et al. Citation2018) after aligning whole chloroplast genomes by MAFFT 7.388 (Katoh and Standley Citation2013) with fixing SSC directions of Rosa maximowicziana and Rosa multiflora (Jeon and Kim Citation2019). Phylogenetic trees show that R. augusta is similar to R. rugosa with reasonable number of sequence varaitions (). Chloroplast genome of candidate new species (Heo et al. Citation2019; Kim et al. Citation2019; Oh et al. Citation2019) can provide additional evidence to clarify its taxonomical position which is similar to the cases (Heo et al. Citation2019; Oh et al. Citation2019).

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

This work was supported by InfoBoss Research Grant [IBB-0005].

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