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Genetic diversity across natural populations of Dendrobium officinale, the endangered medicinal herb endemic to China, revealed by ISSR and RAPD markers

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Abstract

Dendrobium officinale is a rare and endangered herb with special habitats and endemic to China. Genetic diversity was examined within and among nine natural populations using inter-simple sequence repeat (ISSR) and random amplified polymorphic (RAPD) for conservation. Both molecular markers revealed a high percentage (>89%) of polymorphic bands and ISSR markers detected more diversity than RAPD markers. Analysis of molecular variance (AMOVA) revealed that 78.84% (ISSR) and 78.88% (RAPD) of variability was partitioned among individuals within populations. This genetic structure was probably due to severe genetic drift resulting from habitat fragmentation and human overexploitation since 1950s. Moreover, there is a lack of significant association between genetic and geographic distances (r = 0.276; p > 0.05) in the populations of D. officinale. From the conservation point of view, populations GL, GS and GSD with higher genetic diversity should be protected firstly to maintain the species potential for evolutionary change and population YG with lower diversity but representing a novel evolutionary unit should also be paid more attention to during D. officinale conservation practice.

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References

  1. Shrestha, M.K., Golan-Goldhirsh, A., and Ward, D., Population Genetic Structure and the Conservation of Isolated Populations of Acacia raddeana in the Negev Desert, Biol. Conserv., 2002, vol. 108, no. 1, pp. 119–127.

    Article  Google Scholar 

  2. Hogbin, P.M., Ayre, D.J., and Whelan, R.J., Genetic Variation and Reproductive Success of Road Verge Populations of the Rare Shrub Grevillea barklyana (Proteaceae), Heredity, 1998, vol. 80, pp. 180–186.

    Article  Google Scholar 

  3. Jian, S.G., Zhong, Y., Liu, N., et al., Genetic Variation in the Endangered Endemic Species Cycas fairylakea (Cycadaceae) in China and Implications for Conservation, Biodivers. Conserv., 2006, vol. 15, no. 5, pp. 1681–1694.

    Article  Google Scholar 

  4. Zawko, G., Krauss, S.L., Dixon, K.W., and Sivasithamparam, K., Conservation Genetics of the Rare and Endangered Leucopogon obtectus (Ericaceae), Mol. Ecol., 2001, vol. 10, pp. 2389–2396.

    Article  PubMed  CAS  Google Scholar 

  5. Premoli, A.C., Kitzberger, T., and Veblen, T.T., Conservation Genetics of the Endangered Conifer Fitzroya cupressoides in Chile and Argentina, Conserv. Genet., 2000, vol. 1, no. 1, pp. 57–66.

    Article  CAS  Google Scholar 

  6. The Pharmacopoeia Commission of PRC: Pharmacopoeia of the People’s Republic of China, Beijing: Chemical Industry Press, 2000.

  7. Ding, X.Y., Xu, L.S., Wang, Z.T., et al., Authentication of Stems of Dendrobium officinale by rDNA ITS Region Sequences, Planta Med., 2002, vol. 68, no. 2, pp. 191–192.

    Article  PubMed  CAS  Google Scholar 

  8. Fu, L.G., Chinese Plant Red Book, Bejing: Science Press, 1992.

    Google Scholar 

  9. Kochieva, E.Z., Ryzhova, N.N., Legkobit, M.P., and Khadeeva, N.V., RAPD and ISSR Analyses of Species and Populations of the Genus Stachys, Russ. J. Genet., 2006, vol. 42, no. 7, pp. 887–892.

    Article  CAS  Google Scholar 

  10. Ge, X.J., Yu, Y., Zhao, N.X., et al., Genetic Variation in the Endangered Inner Mongolia Endemic Shrub Tetraena mongolica Maxim. (Zygophyllaceae), Biol. Conserv., 2003, vol. 111, no. 3, pp. 427–434.

    Article  Google Scholar 

  11. Williams, J.G.K., Kubelik, A.R., Livak, K.J., et al., DNA Polymorphisms Amplified by Arbitrary Primers are Useful as Genetic Markers, Nucleic Acids Res., 1990, vol. 18, no. 22, pp. 6531–6535.

    Article  PubMed  CAS  Google Scholar 

  12. Artyukova, E.V., Kozyreko, M.M., Koren, O.G., et al., RAPD and Allozyme Analysis of Genetic Diversity in Panax ginseng C.A. Meyer and P. quinquefolius L., Russ. J. Genet., 2004, vol. 40, no. 2, pp. 239–247.

    Article  Google Scholar 

  13. Wang, J.L., Zhao, N.X., Gai, Y.B., et al., RAPD Analysis of Genetic Diversity and Population Genetic Structure of Stipa krylovii Reshov. in Inner Mongolia Steppe, Russ. J. Genet., 2006, vol. 42, no. 5, pp. 468–475.

    Article  CAS  Google Scholar 

  14. Yeh, F.C., Yang, R.C., and Boyle, T., POPGENE. Microsoft Windows-Based Freeware for Population Genetic Analysis: Release 1.31, Edmonton: Univ. Alberta, 1999.

    Google Scholar 

  15. Nei, M., Analysis of Gene Diversity in Subdivided Populations, Proc. Natl. Acad. Sci. USA, 1973, vol. 70, no. 12, pp. 3321–3323.

    Article  PubMed  CAS  Google Scholar 

  16. Nei, M., Genetic Distance between Populations, Am. Naturalist, 1972, vol. 106, no. 949, pp. 283–292.

    Article  Google Scholar 

  17. Lewontin, R.C., The Apportionment of Human Diversity, Evol. Biol., 1972, vol. 6, pp. 381–398.

    Google Scholar 

  18. Wright, S., Evolution and Genetics of Populations: Variability within and among Natural Populations, Chicago: Univ. Chicago Press, 1978, vol. 4.

    Google Scholar 

  19. Excoffier, L., Smouse, P., and Quattro, J., Analysis of Molecular Variance Inferred from Metric Distances among DNA Haplotypes: Application to Human Mitochondrial DNA Restriction Data, Genetics, 1992, vol. 131, no. 2, pp. 479–491.

    PubMed  CAS  Google Scholar 

  20. Miller, M.P., AMOVA-PREP: A Program for the Preparation of AMOVA Input Files from Dominant-Marker Raw Data, Release 1.01, Flagstaff: Northern Arizona Univ., 1998.

    Google Scholar 

  21. Rohlf, F.J., NTSYS-Pc, Numerical Taxonomy and Multivariate Analysis System: Version 2.1, New York: Exeter Software, 2000.

    Google Scholar 

  22. Slatkin, M. and Hudson, R.R., Pairwise Comparisons of Mitochondrial DNA Sequences in Stable and Exponentially Growing Populations, Genetics, 1991, vol. 129, no. 2, pp. 555–562.

    PubMed  CAS  Google Scholar 

  23. Schneider, S., Roessli, D., and Excoffier, L., ARLEQUIN, Version 2.000: A Software for Population Genetics Data Analysis, Geneva: Univ. Geneva, 2000.

    Google Scholar 

  24. Tajima, F., Statistical Method for Testing the Neutral Mutation Hypothesis by DNA Polymorphism, Genetics, 1989, vol. 123, no. 3, pp. 585–595.

    PubMed  CAS  Google Scholar 

  25. Fu, Y.X., Statistical Tests of Neutrality of Mutations against Population Growth, Hitchhiking and Background Selection, Genetics, 1997, vol. 147, no. 2, pp. 915–925.

    PubMed  CAS  Google Scholar 

  26. Li, Y.Y., Chen, X.Y., Zhang, X., et al., Genetic Differences between Wild and Artificial Populations of Metasequoia glyptostroboides: Implications for Species Recovery, Conserv. Biol., 2005, vol. 19, no. 1, pp. 224–231.

    Article  Google Scholar 

  27. Maguire, T.L. and Sedgley, M., Genetic Diversity in Banksia and Dryandra (Proteaceae) with Emphasis on Banksia cuneata, a Rare and Endangered Species, Heredity, 1997, vol. 79, no. 4, pp. 394–401.

    Article  CAS  Google Scholar 

  28. Fischer, M., Husi, R., Prati, D., et al., RAPD Variation among and within Small and Large Populations of the Rare Clonal Plant Ranunculus reptans (Ranunculaceae), Am. J. Botany, 2000, vol. 87, no. 8, pp. 1128–1137.

    Article  Google Scholar 

  29. Real, L.A., Ecological Genetics, Princeton: Princeton Univ. Press, 1994.

    Google Scholar 

  30. Zhang, M., Xia, H.X., Zhu, L.Q., and Zhang, Y.J., Research Progress of Dendrobium Tissue Culture, China J. Chinese Materia. Medic., 2000, vol. 25, no. 6, pp. 323–326.

    CAS  Google Scholar 

  31. Marshall, D.R. and Brown, A.H.D., Optimum Sampling Strategies, Genetic Conservation, Crop Genetic Resource for Today and Tomorrow, Frankel, O.H., and Hawkes, J.G., Eds., Cambrige: Cambrige Univ. Press, 1975, pp. 53–80.

    Google Scholar 

  32. Goodman, D., The Demography of Chance Extinction, Viable Population for Conservation, Soule, M.E., Ed., Cambrigde: Cambrige Univ. Press, 1987, pp. 11–34.

    Google Scholar 

  33. Waser, N.M., Population Structure, Optimal Outbreeding, and Assortative Mating in Angiosperms, The Natural History of Inbreeding and Outbreeding: Theoretical and Empirical Perspectives, Thornhill, N.W, Ed., Chicago: Univ. of Chicago, 1993, pp. 173–199.

    Google Scholar 

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Correspondence to G. Ding.

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Published in Russian in Genetika, 2009, Vol. 45, No. 3, pp. 375–382.

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Ding, G., Li, X., Ding, X. et al. Genetic diversity across natural populations of Dendrobium officinale, the endangered medicinal herb endemic to China, revealed by ISSR and RAPD markers. Russ J Genet 45, 327–334 (2009). https://doi.org/10.1134/S1022795409030119

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  • DOI: https://doi.org/10.1134/S1022795409030119

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