733
Views
14
CrossRef citations to date
0
Altmetric
Mitogenome Announcement

The second complete chloroplast genome sequence of the Viburnum erosum (Adoxaceae) showed a low level of intra-species variations

, , ORCID Icon, , ORCID Icon, ORCID Icon & ORCID Icon show all
Pages 271-272 | Received 11 Nov 2019, Accepted 23 Nov 2019, Published online: 13 Dec 2019

Abstract

We presented the second complete chloroplast genome of the plant. The length of chloroplast genome is 158,587 bp, consisting of four subregions: 87,050 bp of LSC and 18,503 bp of SSC regions separated by a pair of 26,517 bp IR regions. It includes 129 genes (84 protein-coding genes, 8 rRNAs, and 37 tRNAs). A low-level of molecular variation within Viburnum erosum was found with 16 SNPs and 49 indels. The phylogenetic tree shows that the two accessions of V. erosum are clustered with Viburnum japonicum with no resolution between the species, suggesting that chloroplast genome in these species evolve slowly.

Viburnum erosum Thunb. is a common species in East Asia, characterized by having extrafloral nectaries on the abaxial surface of leaves and stipules in Adoxaceae (Choi and Oh Citation2019). As V. erosum is widely distributed from southern China, Taiwan, and Korea to Japan the species may be a model system to examine a geographical structure across the regions within the species. To evaluate the level of molecular variation at the genomic level within the species, we determined the second complete chloroplast genome sequence.

Plant sample of V. erosum was collected on Mt. Samsungsan (35°46′16.78′′N, 128°47′43.72′′E) in Gyeongsan-si, Gyeongsangbuk-do, Korea (voucher in the herbarium of Daejeon University (TUT); Oh KBVE_01). Molecular methods for DNA extraction, genome sequencing, and de novo assembly were done by the method described in Park, Choi, et al. (Citation2019). Genome annotation was based on V. erosum chloroplast genome (MN218778; Park, Choi, et al. Citation2019) using Geneious R11 v11.0.5 (Biomatters Ltd, Auckland, New Zealand).

The chloroplast genome of V. erosum (GenBank accession number is MN641480) is 158,587 bp with four subregions: 87,050 bp of large single-copy (LSC), 18,503 bp of small single-copy (SSC) regions, and 26,517 bp of a pair of inverted repeats (IRs). It contains 129 genes (84 protein-coding genes, 8 rRNAs, and 37 tRNAs); 18 genes (7 protein-coding genes, 4 rRNAs, and 7 tRNAs) are duplicated in the IR regions. The overall GC-ratio of V. erosum was 38.1% and those in the LSC, SSC, and IR regions were 36.4, 32.0, and 43.0%, respectively.

Based on the alignment of two V. erosum genomes conducted by MAFFT 7.388, (Katoh and Standley Citation2013), 16 single nucleotide polymorphisms (SNPs) and 49 insertions and deletions (INDELs) were identified. There is one non-synonymous substitution in ndhL and ycf1, respectively, and one synonymous change in psbB. The remaining 13 SNPs are located in the non-coding regions. This low level of sequence variation is similar to intra-species variations of Cucumis melo (Zhu et al. Citation2016), Chenopodium quinoa (Maughan et al. Citation2019), Coffea arabica (Park, Kim, et al. Citation2019), Artemisia fukudo (Min et al. Citation2019), and Dysphania pumilio (Park and Kim Citation2019). Interestingly, numbers of SNPs and INDELs between V. erosum (Park, Choi, et al. Citation2019) and V. japonicum (Cho et al. Citation2018) are 18 and 36 (), which is lower than those between two V. erosum accessions and between Salix koriyanagi and Salix gracilistyla (Xi et al. Citation2019).

Figure 1. (A) Pairwise comparison of two V. erosum and V. japonicum. (B) A maximum-likelihood tree of based on Adoxaceae nine complete chloroplast genomes: Viburnum erosum (MN641480 in this study and MN218778), Viburnum japonicum (MH036493), Viburnum betulifolium (NC_037951), Viburnum utile (NC_032296), Adoxa moschatellina (NC_034792), Sambucus williamsii (NC_033878), Sinadoxa corydalifolia (NC_032040), and Tetradoxa omeiensis (NC_034793). The numbers above branches indicate bootstrap support values of maximum-likelihood and neighbor-joining phylogenetic trees. Numbers of single nucleotide polymorphisms (SNPs) and insertions and deletions (INDELs) between each pair are indicated along the branch.

Figure 1. (A) Pairwise comparison of two V. erosum and V. japonicum. (B) A maximum-likelihood tree of based on Adoxaceae nine complete chloroplast genomes: Viburnum erosum (MN641480 in this study and MN218778), Viburnum japonicum (MH036493), Viburnum betulifolium (NC_037951), Viburnum utile (NC_032296), Adoxa moschatellina (NC_034792), Sambucus williamsii (NC_033878), Sinadoxa corydalifolia (NC_032040), and Tetradoxa omeiensis (NC_034793). The numbers above branches indicate bootstrap support values of maximum-likelihood and neighbor-joining phylogenetic trees. Numbers of single nucleotide polymorphisms (SNPs) and insertions and deletions (INDELs) between each pair are indicated along the branch.

Complete chloroplast genomes from nine chloroplast genomes of Adoxaceae and one outgroup species, Dipsacus japonicus (NC_039668), were included in the phylogenetic analysis using the neighbor-joining and maximum-likelihood methods. Sequence alignment and phylogenetic trees were constructed by using MEGA X (Kumar et al. Citation2018) with 10,000 and 1000 bootstrap repeats, respectively.

The phylogenetic tree shows that the two accessions of V. erosum are clustered with V. japonicum with no resolution between the species (. The phylogenetic tree shows that the chloroplast genomes of the two species are highly conserved, suggesting that the chloroplast genome in these species evolve slowly or the two species originated from their common ancestor very recently.

Disclosure statement

No potential conflict of interest was reported by the authors.

Correction Statement

This article has been republished with minor changes. These changes do not impact the academic content of the article.

Additional information

Funding

This study was supported by research grants from the National Institute of Biological Resources of Korea [NIBR201803201 and NIBR201905201].

References

  • Cho WB, Han EK, Choi HJ, Lee JH. 2018. The complete chloroplast genome sequence of Viburnum japonicum (Adoxaceae), an evergreen broad-leaved shrub. Mitochondrial DNA Part B. 3(1):458–459.
  • Choi YG, Oh S-H. 2019. A comparative morphological study of Viburnum (Adoxaceae) in Korea. Korean J Pl Taxon. 49(2):107–117.
  • Katoh K, Standley DM. 2013. MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Mol Biol Evol. 30(4):772–780.
  • Kumar S, Stecher G, Li M, Knyaz C, Tamura K. 2018. MEGA X: Molecular Evolutionary Genetics Analysis across computing platforms. Mol Biol Evol. 35(6):1547–1549.
  • Maughan PJ, Chaney L, Lightfoot DJ, Cox BJ, Tester M, Jellen EN, Jarvis DE. 2019. Mitochondrial and chloroplast genomes provide insights into the evolutionary origins of quinoa (Chenopodium quinoa Willd.). Sci Rep. 9(1):185.
  • Min J, Park J, Kim Y, Kwon W. 2019. The complete chloroplast genome of Artemisia fukudo Makino (Asteraceae): providing insight of intraspecies variations. Mitochondrial DNA Part B. 4(1):1510–1512.
  • Park J, Choi YG, Yun N, Xi H, Min J, Kim Y, Oh SH. 2019. The complete chloroplast genome sequence of Viburnum erosum (Adoxaceae). Mitochondrial DNA Part B. 4(2):3278–3279.
  • Park J, Kim Y. 2019. The second complete chloroplast genome of Dysphania pumilio (R. Br.) mosyakin & clemants (Amranthaceae): intraspecies variation of invasive weeds. Mitochondrial DNA Part B. 4(1):1428–1429.
  • Park J, Kim Y, Xi H, Heo K-I. 2019. The complete chloroplast genome of ornamental coffee tree, Coffea arabica L.(Rubiaceae). Mitochondrial DNA Part B. 4(1):1059–1060.
  • Xi H, Park J, Kim Y. 2019. The complete chloroplast genome sequence of rose-gold pussy willow, Salix gracilistyla Miq.(Salicaceae). Mitochondrial DNA Part B. 4(2):2118–2120.
  • Zhu Q, Gao P, Liu S, Amanullah S, Luan F. 2016. Comparative analysis of single nucleotide polymorphisms in the nuclear, chloroplast, and mitochondrial genomes in identification of phylogenetic association among seven melon (Cucumis melo L.) cultivars. Breed Sci. 66(5):711–719.