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Rapid Communication

The complete plastid genome sequence of Vaccinium japonicum (Ericales: Ericaceae), a deciduous broad-leaved shrub endemic to East Asia

, , , , &
Pages 1926-1928 | Received 30 Mar 2021, Accepted 23 May 2021, Published online: 07 Jun 2021

Abstract

We here sequenced the complete plastid genome (plastome) of Vaccinium japonicum (Ericaceae), a deciduous broad-leaved shrub endemic to East Asia. This species has considerable practical economic value. The plastome of V. japonicum is assembled as a single contig (187,213 bp). A large single copy (104,637 bp) and a small single copy (3,000 bp) of the genome are separated by a pair of inverted repeats (39,788 bp). The genome consists of 135 genes, which include 88 protein coding, eight ribosomal RNA, and 39 transfer RNA genes. The plastome of V. japonicum is similar to that of Vaccinium macrocarpon in gene content and order. Our phylogenetic analysis revealed the phylogenetic position of V. japonicum in a highly supported clade of the genus Vaccinium together with other four congeners, V. bracteatum, V. vitis-idaea, V. uliginosum and V. macrocarpon.

Vaccinium L., the largest genus within the blueberry tribe (Vaccinieae Rchb.) in the family Ericaceae, consists of approximately 450 species that are widely distributed globally (Vander Kloet and Dickinson Citation2009; Kim et al. Citation2020). Owing to the economic, agricultural, and medical importance, several plastid genomes (plastomes) of this genus have been sequenced (Fajardo et al. Citation2013). Moreover, several studies have provided evidence for powerful phylogenetic utilities and, particularly, noteworthy evolutionary evidence for early-diverging Vaccinium (Kim et al. Citation2019; Kim et al. Citation2020). Nonetheless, there is limited understanding of the evolution of species of the genus Vaccinium, especially with regard to the East Asian species.

Vaccinium japonicum Miq. is a deciduous broad-leaved shrub belonging to the section Oxycoccoides and is widely distributed in the warm-temperate regions of East Asia, including China, Korea (Jeju Island), and Japan. The main characteristics of this species include corolla divided nearly to the base and margin strongly revolute, and morphologically indistinct from Vaccinium erythrocarpum Michx. distributed in North America. For these reasons, V. japonicum is sometimes treated as a subspecies of V. erythrocarpum (Vander Kloet and Bohm Citation1991; Tamada Citation2004), which still under taxonomic controversy. Vaccinium japonicum consists of three varieties: V. japonicum var. japonicum is restricted to Korea (Jeju Island; Lee Citation2003; Kong et al. Citation2014) and Japan (Yamazaki Citation1993), V. japonicum var. sinicum (Nakai) Rehder to China (Ruizheng and Stevens Citation2005), and V. japonicum var. lasiostemon Hayata to Taiwan (Boufford et al. Citation2003). The complete plastome sequence of V. japonicum var. japonicum can provide crucial clues regarding the evolutionary process of the genus, and solve taxonomic controversies of inter/intra species within the section Oxycoccoides. We here sequenced and characterized a complete plastome from V. japonicum endemic to East Asia.

Vaccinium japonicum samples were collected from Jeju Island, South Korea (33°17′59.3ʺN, 126°35′02.7ʺE). The voucher specimen (Lee. 2007016) was stored in the Korea National Arboretum ([email protected]). The total genomic DNA was sequenced on MGI-seq 2000 platform (LAS, Seoul, Korea) following manufacturer’s protocols. It generated 57,912,004 raw reads (150 bp paired-end). The plastome was assembled using NOVOPlasty 4.1 (Dierckxsens et al. Citation2017), with the V. macrocarpon rbcL gene sequence (Fajardo et al. Citation2013; JQ757046) as the seed. The assembled plastome was checked using Geneious 10.2.3 (Kearse et al. Citation2012) by mapping 590,424 reads, resulting in a coverage of 150x. The annotation was separately performed using Geneious and was manually corrected for the start and stop codons as well as for the intron/exon boundaries. The annotated plastome sequence was deposited in GenBank (accession number: MW006668). To construct the phylogenetic tree, plastomes of 13 species from the NCBI database were downloaded. The alignments were performed using MAFFT (Katoh and Toh Citation2010). The maximum likelihood (ML) analysis was performed with RAxML v.8.0 (Stamatakis, Citation2014) using default parameters and 1000 bootstrap replicates. For the RAxML tree, the general time-reversible (GTR) model of nucleotide substitution was used with the Gamma model of rate heterogeneity.

The V. japonicum plastome is 187,213 bp long, with two inverted repeat (IR) regions (39,788 bp each) that separate a large single copy (LSC) region (104,637 bp) and a small single copy (SSC) region (3000 bp). The genome has a pair of enlarged IR regions and an extremely shortened SSC region, which contains only a single gene—ndhF. In total, 135 genes, which include 88 protein-coding, eight ribosomal RNA, and 39 transfer RNA genes, were annotated. The GC content in overall, LSC, SSC, IR regions are 36.7%, 35.7%, 29.3%, and 38.4%, respectively. The most similar plastome, compared to V. japonicum (187,213 bp) in gene content and order, is V. macrocarpon (176,045 bp), despite the length difference.

The ML tree shows that all five Vaccinium species, V. bracteatum, V. vitis-idaea, V. uliginosum, V. macrocarpon and V. japonicum, are a monophyletic group with a 100% bootstrap value (). This suggests that the complete plastome sequenced in this study is a valuable input to the genomic resources of Ericaceae and can be utilized in future evolutionary studies.

Figure 1. Maximum-likelihood phylogenetic tree constructed with RAxML using complete plastomes of the 14 species of Ericales. Numbers above the nodes indicate bootstrap values with 1000 replicates.

Figure 1. Maximum-likelihood phylogenetic tree constructed with RAxML using complete plastomes of the 14 species of Ericales. Numbers above the nodes indicate bootstrap values with 1000 replicates.

Disclosure statement

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

Data availability statement

The genome sequence data that support the findings of this study are openly available in GenBank of NCBI at [https://www.ncbi.nlm.nih.gov] (https://www.ncbi.nlm.nih.gov/) under the accession no. MW006668. The associated Sequence Read Archive (SRA) number is PRJNA681995.

Additional information

Funding

This study was supported by the research project of the Korea National Arboretum [KNA-1-1-18, 15-3].

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