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Differentiation of wild accessions within the Panax bipinnatifidus complex using newly developed polymorphic microsatellite markers

Published online by Cambridge University Press:  07 October 2024

Jie Song
Affiliation:
Department of Economic Plants and Biotechnology, Yunnan Key Laboratory for Wild Plant Resources, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China College of Life Sciences, University of Chinese Academy of Science, Beijing 100049, China
Yujuan Zhao
Affiliation:
Department of Economic Plants and Biotechnology, Yunnan Key Laboratory for Wild Plant Resources, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China
Xun Gong
Affiliation:
Department of Economic Plants and Biotechnology, Yunnan Key Laboratory for Wild Plant Resources, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China
Yuezhi Pan*
Affiliation:
Department of Economic Plants and Biotechnology, Yunnan Key Laboratory for Wild Plant Resources, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China
*
Corresponding author: Yuezhi Pan; Email: panyuezhi@mail.kib.ac.cn

Abstract

Panax L., renowned as ginseng genus, is a famous medicinal group of family Araliaceae. Within this genus, the taxa of Panax bipinnatifidus complex are mainly distributed in Himalayas and Hengduan Mountain areas. Due to the complex evolutionary history and short-term rapid radiation, the relationships among species within the complex have not been clearly resolved, and the taxa identification is difficult due to the intermediate morphological traits. This study aimed to use the available restriction-site associated DNA sequence data from 29 individuals of P. bipinnatifidus complex to mine high-polymorphic simple sequence repeat (SSR) markers, with the goal of evaluating their utility in taxa identification. Eleven polymorphic SSR loci were ultimately selected and validated through polymerase chain reactions amplifying across 63 individuals of P. bipinnatifidus complex and 13 individuals of three outgroup species. The subsequent genetic diversity analysis uncovered 76 alleles in total, ranging from 5 to 15 per locus. Observed heterozygosity spanned 0.241–0.512, while expected heterozygosity ranged between 0.345 and 0.644. The genetic kinship analysis revealed a sister relationship between Panax zingiberensis and Panax vietnamensis. The analysis result also supported the classification of samples from Hunan and Hubei provinces into a single genetic unit within the P. bipinnatifidus complex. These newly developed SSR markers will facilitate the identification of wild ginseng plants.

Type
Short Communication
Copyright
Copyright © The Author(s), 2024. Published by Cambridge University Press on behalf of National Institute of Agricultural Botany

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References

Catchen, J, Hohenlohe, PA, Bassham, S, Amores, A and Cresko, WA (2013) Stacks: an analysis tool set for population genomics. Molecular Ecology 22, 31243140.CrossRefGoogle ScholarPubMed
Choi, HI, Kim, NH, Kim, JH, Choi, BS, Ahn, IO, Lee, JS and Yang, TJ (2011) Development of reproducible EST-derived SSR markers and assessment of genetic diversity in Panax ginseng cultivars and related species. Journal of Ginseng Research 35, 399412.CrossRefGoogle ScholarPubMed
Doyle, J (1991) DNA protocols for plants–CTAB total DNA isolation. In Hewitt, GM and Johnston, A (eds), Molecular Techniques in Taxonomy. Berlin: Springer-Verlag, pp. 283293.CrossRefGoogle Scholar
Felsenstein, J (2005) PHYLIP (Phylogeny Inference Package) Version 3.6. Distributed by the Author. Seattle: Department of Genome Sciences, University of Washington.Google Scholar
Hauser, SS, Athrey, G and Leberg, PL (2021) Waste not, want not: microsatellites remain an economical and informative technology for conservation genetics. Ecology and Evolution 11, 1580015814.CrossRefGoogle Scholar
Jang, W, Jang, Y, Kim, NH, Waminal, NE, Kim, YC, Lee, JW and Yang, TJ (2020) Genetic diversity among cultivated and wild Panax ginseng populations revealed by high-resolution microsatellite markers. Journal of Ginseng Research 44, 637643.CrossRefGoogle ScholarPubMed
Ji, YH, Liu, CK, Yang, ZY, Yang, LF, He, ZS, Wang, HC, Yang, JB and Yi, TS (2019) Testing and using complete plastomes and ribosomal DNA sequences as the next generation DNA barcodes in Panax (Araliaceae). Molecular Ecology Resources 19, 13331345.CrossRefGoogle Scholar
Jiang, P, Shi, FX, Li, YL, Liu, B and Li, LF (2016) Development of highly transferable microsatellites for Panax ginseng (Araliaceae) using whole-genome data. Applications in Plant Sciences 4, 1600075.CrossRefGoogle ScholarPubMed
Kalia, RK, Rai, MK, Kalia, S, Singh, R and Dhawan, AK (2011) Microsatellite markers: an overview of the recent progress in plants. Euphytica 177, 309334.CrossRefGoogle Scholar
Lee, C and Wen, J (2004) Phylogeny of Panax using chloroplast trnC-trnD intergenic region and the utility of trnC-trnD in interspecific studies of plants. Molecular Phylogenetics and Evolution 31, 894903.CrossRefGoogle ScholarPubMed
Liu, K and Muse, SV (2005) PowerMarker: an integrated analysis environment for genetic marker analysis. Bioinformatics 21, 21282129.CrossRefGoogle ScholarPubMed
Meglécz, E, Pech, N, Gilles, A, Dubut, V, Hingamp, P, Trilles, A, Grenier, R and Martin, JF (2014) QDD version 3.1: a user-friendly computer program for microsatellite selection and primer design revisited: experimental validation of variables determining genotyping success rate. Molecular Ecology Resources 14, 13021313.CrossRefGoogle ScholarPubMed
Peakall, R and Smouse, PE (2012) GenALEx 6.5: genetic analysis in Excel. Population genetic software for teaching and research – an update. Bioinformatics 28, 25372539.CrossRefGoogle ScholarPubMed
Shi, FX, Li, MR, Li, YL, Jiang, P, Zhang, C, Pan, YZ, Liu, B, Xiao, HX and Li, LF (2015) The impacts of polyploidy, geographic and ecological isolations on the diversification of Panax (Araliaceae). BMC Plant Biology 15, 297.CrossRefGoogle ScholarPubMed
Su, L, Zhang, Y, Yang, Y, Qu, Y, Cui, X, Ge, F and Liu, D (2023) Development of SSR markers on the basis of the Panax notoginseng transcriptome for agronomic and biochemical trait association analyses. Journal of Applied Research on Medicinal and Aromatic Plants 34, 100475.CrossRefGoogle Scholar
Untergasser, A, Cutcutache, I, Koressaar, T, Ye, J, Faircloth, BC, Remm, M and Rozen, SG (2012) Primer3-new capabilities and interfaces. Nucleic Acids Research 40, e115e115.CrossRefGoogle ScholarPubMed
Varshney, RK, Graner, A and Sorrells, ME (2005) Genic microsatellite markers in plants: features and applications. Trends in Biotechnology 23, 4855.CrossRefGoogle ScholarPubMed
Vu, DD, Shah, SNM, Pham, MP, Bui, VT, Nguyen, MT and Nguyen, TPT (2020) De novo assembly and transcriptome characterization of an endemic species of Vietnam, Panax vietnamensis Ha et Grushv., including the development of EST-SSR markers for population genetics. BMC Plant Biology 20, 358.CrossRefGoogle Scholar
Wen, J, Zhang, JQ, Nie, ZL, Zhong, Y and Sun, H (2014) Evolutionary diversifications of plants on the Qinghai-Tibetan Plateau. Frontiers in genetics 5, 4.CrossRefGoogle ScholarPubMed
Wen, J and Zimmer, EA (1996) Phylogeny and biogeography of Panax L (the ginseng genus, Araliaceae): inferences from ITS sequences of nuclear ribosomal DNA. Molecular Phylogenetics and Evolution 6, 167177.CrossRefGoogle ScholarPubMed
Yang, Z, Li, X, Yang, L, Peng, S, Song, W, Lin, Y, Xiang, G, Li, Y, Ye, S, Ma, C, Miao, J, Zhang, G, Chen, W, Yang, S and Dong, Y (2023) Comparative genomics reveals the diversification of triterpenoid biosynthesis and origin of ocotillol-type triterpenes in Panax. Plant Communication 4, 100591.CrossRefGoogle ScholarPubMed
Zhou, MM, Yang, GQ, Sun, GL, Guo, ZH, Gong, X and Pan, YZ (2020) Resolving complicated relationships of the Panax bipinnatifidus complex in southwestern China by RAD-seq data. Molecular Phylogenetics and Evolution 149, 106851.CrossRefGoogle ScholarPubMed
Zuo, YJ, Chen, ZJ, Kondo, K, Funamoto, T, Wen, J and Zhou, SL (2011) DNA barcoding of Panax species. Planta Medica 77, 182187.CrossRefGoogle ScholarPubMed
Zuo, YJ, Wen, J, Ma, JS and Zhou, SL (2015) Evolutionary radiation of the Panax bipinnatifidus species complex (Araliaceae) in the Sino–Himalayan region of eastern Asia as inferred from AFLP analysis. Journal of Systematics and Evolution 53, 210220.CrossRefGoogle Scholar
Zuo, YJ, Wen, J and Zhou, SL (2017) Intercontinental and intracontinental biogeography of the eastern Asian–Eastern North American disjunct Panax (the ginseng genus, Araliaceae), emphasizing its diversification processes in eastern Asia. Molecular Phylogenetics and Evolution 117, 6074.CrossRefGoogle ScholarPubMed
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