The chloroplast genome structure and gene content are highly conserved among land plants, providing valuable information for the studies of taxonomy and plant evolution. Viburnum odoratissimum is a well-known evergreen shrub widely distributed in Asia. It possesses excellent medicinal properties used as traditional medicine for menstrual, stomach, and kidney cramps. In this study, the complete chloroplast genome (cpDNA) of V. odoratissimum is reported and compared with five close Viburnum species and an outgroup. The cpDNA of V. odoratissimum is 158,744 bp in length and contains 130 genes with 17 genes duplicated in the inverted repeat region. The gene content, gene organization and GC content in V. odoratissimum are highly similar to other Viburnum species. A total of 270 tandem repeats is found in these plastomes, most of which are distributed in intergenic space. Differences in the location of the IR/SC boundaries reflect expansions and contractions of IR regions in all species studied. Phylogenetic analysis based on complete chloroplast genomes and the combination of barcodes indicates a sister relationship between V. odoratissimum and V. brachybotryum. Furthermore, a comparative cpDNA analysis identifies three DNA regions (trnC-petN-psbM, trnH-psbA, ndhC-trnV) containing high divergence among seven studied species that could be used as potential phylogenetic markers in taxonomic studies.
Published in | Plant (Volume 9, Issue 2) |
DOI | 10.11648/j.plant.20210902.12 |
Page(s) | 28-35 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
Copyright |
Copyright © The Author(s), 2021. Published by Science Publishing Group |
Adoxaceae, Barcodes, Phylogenetic Relationship, Viburnum odoratissimum
[1] | Donoghue, M. J., Baldwin, B. G., Li, J. and Winkworth, R. C. (2004) Viburnum Phylogeny Based on Chloroplast TrnK Intron and Nuclear Ribosomal ITS DNA Sequences. Systematic Botany, 29, 188–198. https://doi.org/10.1600/036364404772974095. |
[2] | Killip, E. P. and Smith, A. C. (1929) The Genus Viburnum in Northwestern South America. Bulletin of the Torrey Botanical Club, 56, 265. https://doi.org/10.2307/2480649. |
[3] | The Angiosperm Phylogeny Group. (2016) An Update of the Angiosperm Phylogeny Group Classification for the Orders and Families of Flowering Plants: APG IV. Botanical Journal of the Linnean Society, 181, 1–20. https://doi.org/10.1111/boj.12385. |
[4] | Ge, Y.-C., Zhang, H.-J., Lei, J.-X. and Wang, K.-W. (2018) Chemical Constituents of Viburnum Odoratissimum and Their Cytotoxic Activities. Chemistry of Natural Compounds, 54, 600–602. https://doi.org/10.1007/s10600-018-2422-z. |
[5] | Velioglu, Y. S., Ekici, L. and Poyrazoglu, E. S. (2006) Phenolic Composition of European Cranberrybush (Viburnum Opulus L.) Berries and Astringency Removal of Its Commercial Juice. International Journal of Food Science & Technology, 41, 1011–1015. https://doi.org/10.1111/j.1365-2621.2006.01142.x. |
[6] | Wang, L.-Q., Chen, Y.-G., Xu, J.-J., Liu, Y., Li, X.-M. and Zhao, Y. (2008) Compounds from Viburnum Species and Their Biological Activities. Chemistry & Biodiversity, 5, 1879–1899. https://doi.org/10.1002/cbdv.200890175. |
[7] | Bock, K., Jensen, S. R., Nielsen, B. J. and Norn, V. (1978) Iridoid Allosides from Viburnum Opulus. Phytochemistry, 17, 753–757. https://doi.org/10.1016/S0031-9422(00)94220-1. |
[8] | Nguyen, T. T., Truong, B. N., Doan Thi Mai, H., Litaudon, M., Nguyen, V. H., Do Thi, T., Chau, V. M. and Pham, V. C. (2017) Cytotoxic Dammarane-Type Triterpenoids from the Leaves of Viburnum Sambucinum. Bioorganic & Medicinal Chemistry Letters, 27, 1665–1669. https://doi.org/10.1016/j.bmcl.2017.03.014. |
[9] | Sagdic, O., Aksoy, A. and Ozkan, G. (2006) Evaluation of the Antibacterial and Antioxidant Potentials of Cranberry (Gilaburu, Viburnum Opulus L.) Fruit Extract. Acta Alimentaria, Akadémiai Kiadó, 35, 487–492. https://doi.org/10.1556/AAlim.35.2006.4.12. |
[10] | Wang, L.-X., Fang, Y.-D., Zhang, R.-H., Ren, F.-C., Zhang, X.-J., Wang, F. and Xiao, W.-L. (2018) Hispanane-Type Diterpenoid and Secoiridoid Glucosides from Viburnum Cylindricum. Chemistry & Biodiversity, 15, e1700418. https://doi.org/10.1002/cbdv.201700418. |
[11] | Donoghue, M. J. (1983) A Preliminary Analysis of Phylogenetic Relationships in Viburnum (Caprifoliaceae s.1.). Systematic Botany, American Society of Plant Taxonomists, 8, 45–58. https://doi.org/10.2307/2418562. |
[12] | Winkworth, R. C. and Donoghue, M. J. (2004) Viburnum Phylogeny: Evidence from the Duplicated Nuclear Gene GBSSI. Molecular Phylogenetics and Evolution, 33, 109–126. https://doi.org/10.1016/j.ympev.2004.05.006. |
[13] | Choi, Y. G., Youm, J. W., Lim, C. E. and Oh, S. H. (2018) Phylogenetic Analysis of Viburnum (Adoxaceae) in Korea Using DNA Sequences. Korean Journal of Plant Taxonomy, 48, 206–217. https://doi.org/10.11110/kjpt.2018.48.3.206. |
[14] | Clement, W. L. and Donoghue, M. J. (2012) Barcoding Success as a Function of Phylogenetic Relatedness in Viburnum, a Clade of Woody Angiosperms. BMC Evolutionary Biology, 12, 73. https://doi.org/10.1186/1471-2148-12-73. |
[15] | Soltis, D., Soltis, P., Endress, P., Chase, M. W., Manchester, S., Judd, W., Majure, L. and Mavrodiev, E. (2018) Phylogeny and Evolution of the Angiosperms: Revised and Updated Edition. University of Chicago Press. |
[16] | Huo, Y., Gao, L., Liu, B., Yang, Y., Kong, S., Sun, Y., Yang, Y. and Wu, X. (2019) Complete Chloroplast Genome Sequences of Four Allium Species: Comparative and Phylogenetic Analyses. Scientific Reports, 9, 1–14. https://doi.org/10.1038/s41598-019-48708-x. |
[17] | Sahu, S. K., Thangaraj, M. and Kathiresan, K. (2012) DNA Extraction Protocol for Plants with High Levels of Secondary Metabolites and Polysaccharides without Using Liquid Nitrogen and Phenol. ISRN Molecular Biology, 2012. https://doi.org/10.5402/2012/205049. |
[18] | Li, H. and Durbin, R. (2009) Fast and Accurate Short Read Alignment with Burrows–Wheeler Transform. Bioinformatics, 25, 1754–1760. https://doi.org/10.1093/bioinformatics/btp324. |
[19] | Koren, S., Walenz, B. P., Berlin, K., Miller, J. R., Bergman, N. H. and Phillippy, A. M. (2017) Canu: Scalable and Accurate Long-Read Assembly via Adaptive k-Mer Weighting and Repeat Separation. Genome Research, 27, 722–736. https://doi.org/10.1101/gr.215087.116. |
[20] | Tillich, M., Lehwark, P., Pellizzer, T., Ulbricht-Jones, E. S., Fischer, A., Bock, R. and Greiner, S. (2017) GeSeq – Versatile and Accurate Annotation of Organelle Genomes. Nucleic Acids Research, 45, W6–W11. https://doi.org/10.1093/nar/gkx391. |
[21] | Greiner, S., Lehwark, P. and Bock, R. (2019) OrganellarGenomeDRAW (OGDRAW) Version 1.3.1: Expanded Toolkit for the Graphical Visualization of Organellar Genomes. Nucleic Acids Research, 47, W59–W64. https://doi.org/10.1093/nar/gkz238. |
[22] | Benson, G. (1999) Tandem Repeats Finder: A Program to Analyze DNA Sequences. Nucleic Acids Research, 27, 573–580. https://doi.org/10.1093/nar/27.2.573. |
[23] | Beier, S., Thiel, T., Münch, T., Scholz, U. and Mascher, M. (2017) MISA-Web: A Web Server for Microsatellite Prediction. Bioinformatics, Oxford Academic, 33, 2583–2585. https://doi.org/10.1093/bioinformatics/btx198. |
[24] | Frazer, K. A., Pachter, L., Poliakov, A., Rubin, E. M. and Dubchak, I. (2004) VISTA: Computational Tools for Comparative Genomics. Nucleic Acids Research, 32, W273–W279. https://doi.org/10.1093/nar/gkh458. |
[25] | Thompson, J. D., Gibson, T. J., Plewniak, F., Jeanmougin, F. and Higgins, D. G. (1997) The CLUSTAL_X Windows Interface: Flexible Strategies for Multiple Sequence Alignment Aided by Quality Analysis Tools. Nucleic Acids Research, 25, 4876–4882. |
[26] | Rozas, J., Ferrer-Mata, A., Sánchez-DelBarrio, J. C., Guirao-Rico, S., Librado, P., Ramos-Onsins, S. E. and Sánchez-Gracia, A. (2017) DnaSP 6: DNA Sequence Polymorphism Analysis of Large Data Sets. Molecular Biology and Evolution, 34, 3299–3302. https://doi.org/10.1093/molbev/msx248. |
[27] | Li, W., Yang, W. and Wang, X.-J. (2013) Pseudogenes: Pseudo or Real Functional Elements? Journal of Genetics and Genomics, 40, 171–177. https://doi.org/10.1016/j.jgg.2013.03.003. |
[28] | Li, X., Tan, W., Sun, J., Du, J., Zheng, C., Tian, X., Zheng, M., Xiang, B. and Wang, Y. (2019) Comparison of Four Complete Chloroplast Genomes of Medicinal and Ornamental Meconopsis Species: Genome Organization and Species Discrimination. Scientific Reports, 9. https://doi.org/10.1038/s41598-019-47008-8. |
[29] | Powell, W., Morgante, M., McDevitt, R., Vendramin, G. G. and Rafalski, J. A. (1995) Polymorphic Simple Sequence Repeat Regions in Chloroplast Genomes: Applications to the Population Genetics of Pines. Proceedings of the National Academy of Sciences, 92, 7759–7763. https://doi.org/10.1073/pnas.92.17.7759. |
[30] | Chen, S., Yao, H., Han, J., Liu, C., Song, J., Shi, L., Zhu, Y., Ma, X., Gao, T., Pang, X., Luo, K., Li, Y., Li, X., Jia, X., Lin, Y. and Leon, C. (2010) Validation of the ITS2 Region as a Novel DNA Barcode for Identifying Medicinal Plant Species. PLOS ONE, Public Library of Science, 5, e8613. https://doi.org/10.1371/journal.pone.0008613. |
[31] | Ford, C. S., Ayres, K. L., Toomey, N., Haider, N., Van Alphen Stahl, J., Kelly, L. J., Wikström, N., Hollingsworth, P. M., Duff, R. J., Hoot, S. B., Cowan, R. S., Chase, M. W. and Wilkinson, M. J. (2009) Selection of Candidate Coding DNA Barcoding Regions for Use on Land Plants. Botanical Journal of the Linnean Society, Oxford Academic, 159, 1–11. https://doi.org/10.1111/j.1095-8339.2008.00938.x. |
[32] | Johnson, M. and Trott, T. (2017) DNA Barcoding of Quercus Falcata, Quercus Palustris, Quercus Rubra, and Their Hybrids Using RbcL, MatK, and Ycf1. 26. |
[33] | Kress, W. J. and Erickson, D. L. (2007) A Two-Locus Global DNA Barcode for Land Plants: The Coding RbcL Gene Complements the Non-Coding TrnH-PsbA Spacer Region. PLOS ONE, Public Library of Science, 2, e508. https://doi.org/10.1371/journal.pone.0000508. |
[34] | Shneyer, V. S. and Rodionov, A. V. (2019) Plant DNA Barcodes. Biology Bulletin Reviews, 9, 295–300. https://doi.org/10.1134/S207908641904008X. |
APA Style
Le Thi Yen, Joonho Park. (2021). The Complete Chloroplast Genome Sequence of Viburnum odoratissimum and Phylogenetic Relationship with Other Close Species in the Adoxaceae Family. Plant, 9(2), 28-35. https://doi.org/10.11648/j.plant.20210902.12
ACS Style
Le Thi Yen; Joonho Park. The Complete Chloroplast Genome Sequence of Viburnum odoratissimum and Phylogenetic Relationship with Other Close Species in the Adoxaceae Family. Plant. 2021, 9(2), 28-35. doi: 10.11648/j.plant.20210902.12
AMA Style
Le Thi Yen, Joonho Park. The Complete Chloroplast Genome Sequence of Viburnum odoratissimum and Phylogenetic Relationship with Other Close Species in the Adoxaceae Family. Plant. 2021;9(2):28-35. doi: 10.11648/j.plant.20210902.12
@article{10.11648/j.plant.20210902.12, author = {Le Thi Yen and Joonho Park}, title = {The Complete Chloroplast Genome Sequence of Viburnum odoratissimum and Phylogenetic Relationship with Other Close Species in the Adoxaceae Family}, journal = {Plant}, volume = {9}, number = {2}, pages = {28-35}, doi = {10.11648/j.plant.20210902.12}, url = {https://doi.org/10.11648/j.plant.20210902.12}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.plant.20210902.12}, abstract = {The chloroplast genome structure and gene content are highly conserved among land plants, providing valuable information for the studies of taxonomy and plant evolution. Viburnum odoratissimum is a well-known evergreen shrub widely distributed in Asia. It possesses excellent medicinal properties used as traditional medicine for menstrual, stomach, and kidney cramps. In this study, the complete chloroplast genome (cpDNA) of V. odoratissimum is reported and compared with five close Viburnum species and an outgroup. The cpDNA of V. odoratissimum is 158,744 bp in length and contains 130 genes with 17 genes duplicated in the inverted repeat region. The gene content, gene organization and GC content in V. odoratissimum are highly similar to other Viburnum species. A total of 270 tandem repeats is found in these plastomes, most of which are distributed in intergenic space. Differences in the location of the IR/SC boundaries reflect expansions and contractions of IR regions in all species studied. Phylogenetic analysis based on complete chloroplast genomes and the combination of barcodes indicates a sister relationship between V. odoratissimum and V. brachybotryum. Furthermore, a comparative cpDNA analysis identifies three DNA regions (trnC-petN-psbM, trnH-psbA, ndhC-trnV) containing high divergence among seven studied species that could be used as potential phylogenetic markers in taxonomic studies.}, year = {2021} }
TY - JOUR T1 - The Complete Chloroplast Genome Sequence of Viburnum odoratissimum and Phylogenetic Relationship with Other Close Species in the Adoxaceae Family AU - Le Thi Yen AU - Joonho Park Y1 - 2021/05/08 PY - 2021 N1 - https://doi.org/10.11648/j.plant.20210902.12 DO - 10.11648/j.plant.20210902.12 T2 - Plant JF - Plant JO - Plant SP - 28 EP - 35 PB - Science Publishing Group SN - 2331-0677 UR - https://doi.org/10.11648/j.plant.20210902.12 AB - The chloroplast genome structure and gene content are highly conserved among land plants, providing valuable information for the studies of taxonomy and plant evolution. Viburnum odoratissimum is a well-known evergreen shrub widely distributed in Asia. It possesses excellent medicinal properties used as traditional medicine for menstrual, stomach, and kidney cramps. In this study, the complete chloroplast genome (cpDNA) of V. odoratissimum is reported and compared with five close Viburnum species and an outgroup. The cpDNA of V. odoratissimum is 158,744 bp in length and contains 130 genes with 17 genes duplicated in the inverted repeat region. The gene content, gene organization and GC content in V. odoratissimum are highly similar to other Viburnum species. A total of 270 tandem repeats is found in these plastomes, most of which are distributed in intergenic space. Differences in the location of the IR/SC boundaries reflect expansions and contractions of IR regions in all species studied. Phylogenetic analysis based on complete chloroplast genomes and the combination of barcodes indicates a sister relationship between V. odoratissimum and V. brachybotryum. Furthermore, a comparative cpDNA analysis identifies three DNA regions (trnC-petN-psbM, trnH-psbA, ndhC-trnV) containing high divergence among seven studied species that could be used as potential phylogenetic markers in taxonomic studies. VL - 9 IS - 2 ER -