Hostname: page-component-cd9895bd7-jn8rn Total loading time: 0 Render date: 2024-12-27T15:31:34.246Z Has data issue: false hasContentIssue false

Genetic characterization of novel polymorphic microsatellite markers for Epilobium nankotaizanense (Onagraceae), an endemic and threatened herb in Taiwan

Published online by Cambridge University Press:  26 April 2021

Yu-Wei Tseng
Affiliation:
Graduate Institute of Bioresources, Pingtung University of Science and Technology, Pingtung, Taiwan
Chi-Chun Huang
Affiliation:
Taiwan Endemic Species Research Institute, Nantou, Taiwan
Chih-Chiang Wang
Affiliation:
Department of Forestry, Pingtung University of Science and Technology, Pingtung, Taiwan
Chiuan-Yu Li
Affiliation:
Graduate Institute of Bioresources, Pingtung University of Science and Technology, Pingtung, Taiwan Taiwan Endemic Species Research Institute, Nantou, Taiwan
Kuo-Hsiang Hung*
Affiliation:
Graduate Institute of Bioresources, Pingtung University of Science and Technology, Pingtung, Taiwan
*
*Corresponding author. E-mail: [email protected]

Abstract

Epilobium belongs to the family Onagraceae, which consists of approximately 200 species distributed worldwide, and some species have been used as medicinal plants. Epilobium nankotaizanense is an endemic and endangered herb that grows in the high mountains in Taiwan at an elevation of more than 3300 m. Alpine herbs are severely threatened by climate change, which leads to a reduction in their habitats and population sizes. However, only a few studies have addressed genetic diversity and population genetics. In the present study, we developed a new set of microsatellite markers for E. nankotaizanense using high-throughput genome sequencing data. Twenty polymorphic microsatellite markers were developed and tested on 30 individuals collected from three natural populations. These loci were successfully amplified, and polymorphisms were observed in E. nankotaizanense. The number of alleles per locus (A) ranged from 2.000 to 3.000, and the observed (Ho) and expected (He) heterozygosities ranged from 0.000 to 0.929 and from 0.034 to 0.631, respectively. The developed polymorphic microsatellite markers will be useful in future conservation genetic studies of E. nankotaizanense as well as for developing an effective conservation strategy for this species and facilitating germplasm collections and sustainable utilization of other Epilobium species.

Type
Short Communication
Copyright
Copyright © The Author(s), 2021. Published by Cambridge University Press on behalf of NIAB

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Footnotes

*

These authors contributed equally to this work.

References

Chen, CL (1997) The population genetics study of Epilobium nankotaizanensis. Master thesis, National Taiwan Normal University, Taiwan.Google Scholar
Da Maia, LC, Palmieri, DA, de Souza, VQ, Kopp, MM, de Carvalho, FI and Costa de Oliveira, A (2008) SSR locator: tool for simple sequence repeat discovery integrated with primer design and PCR simulation. International Journal of Plant Genomics 2008: 412696.CrossRefGoogle ScholarPubMed
Doyle, JJ and Doyle, JL (1987) A rapid DNA isolation procedure for small quantities of fresh leaf tissue. Phytochemical Bulletin 19: 1115.Google Scholar
Editorial Committee of the Red List of Taiwan Plants (2017) The Red List of Vascular Plants of Taiwan, 2017. Endemic Species Research Institute, Forestry Bureau, Council of Agriculture, Executive Yuan and Taiwan Society of Plant Systematics.Google Scholar
Granica, S, Piwowarski, JP, Czerwinska, ME and Kiss, AK (2014) Phytochemistry, pharmacology and traditional uses of different Epilobium species (Onagraceae): a review. Journal of Ethnopharmacology 156: 316346.CrossRefGoogle ScholarPubMed
Huang, CC, Hsu, TW, Wang, HV, Liu, ZH, Chen, YY, Chiu, CT, Huang, CL, Hung, KH and Chiang, TY (2016) Multilocus analyses reveal postglacial demographic shrinkage of Juniperus morrisonicola (Cupressaceae), a dominant alpine species in Taiwan. PLoS ONE 11: e0161713.CrossRefGoogle Scholar
Kadam, P, Patil, M and Yadav, KA (2018) Review on phytopharmacopial potential of Epilobium angustifolium. Pharmacognosy Journal 10: 10761078.CrossRefGoogle Scholar
Keating, RC, Hoch, PC and Raven, PH (1982) Perennation in Epilobium (Onagraceae) and its relation to classification and ecology. Systematic Botany 7: 379404.CrossRefGoogle Scholar
Liu, K and Muse, SV (2005) Powermarker: an integrated analysis environment for genetic marker analysis. Bioinformatics (Oxford, England) 21: 21282129.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 (Oxford, England) 28: 25372539.CrossRefGoogle ScholarPubMed
Raven, PH (1988) Onagraceae as a model of plant evolution. In: Gottlieb, LD and Jain, SK (eds.) Plant Evolutionary Biology. New York: Chapman and Hall, pp. 85107.CrossRefGoogle Scholar
Raymond, M and Rousset, F (1995) GENEPOP (version-1.2): population genetics software for exact tests and ecumenicism. Journal of Heredity 86: 248249.CrossRefGoogle Scholar
Schierenbeck, KA (2017) Population-level genetic variation and climate change in a biodiversity hotspot. Annals of Botany 119: 215228.CrossRefGoogle Scholar
Untergrasser, A, Cutcutache, I, Koressaar, T, Ye, J, Faircloth, BC, Remm, M and Rozen, SG (2012) Primer3 – new capabilities and interfaces. Nucleic Acids Research 40: e115.CrossRefGoogle Scholar
Supplementary material: File

Tseng et al. supplementary material

Tseng et al. supplementary material

Download Tseng et al. supplementary material(File)
File 16.7 KB