Skip to main content
Log in

Variation of Mini- and Microsatellite DNA Markers in Populations of Parthenogenetic Rock Lizard Darevskia rostombekovi

  • Published:
Russian Journal of Genetics Aims and scope Submit manuscript

Abstract

Variation and clonal diversity in populations of the parthenogenetic rock lizard Darevskia rostombekovi was examined by means of multilocus DNA fingerprinting using mini- and microsatellite DNA markers M13, (GATA)4, and (TCC)50). The animals examined were shown to exhibit a clonally inherited, species-specific pattern of DNA markers (fingerprint profile) that is different from the species-specific patterns of parthenogenetic species D. dahli, D. armenica, and D. unisexualis. The mean intraspecific similarity indexS was 0.950 (0.003) for a sample of 19 animals from three isolated populations of North Armenia. This significantly differed from the estimate of this parameter for a sample of 21 animals including two individuals from mountainous, relict population from the vicinity of the Sevan Lake, which was equal to 0.875 (0.001). A comparison of DNA fingerprints showed differences between 21 individuals attaining 79 DNA fragments of 1801 mini- and microsatellite markers included in the analysis. The results obtained show that intraspecific variation in D. rostombekovi is higher than that in the previously studied parthenogenetic species D. dahli (S = 0.962) andD. unisexualis (S= 0.950) (P< 0.001). Taking into account that D. rostombekovi is considered monoclonal on the basis of allozyme data, the problem of clonal variability is discussed with regard to the evidence on nuclear DNA markers. It is suggested that the hybrid karyotype of D. rostombekovi, which is more unstable than that of D. dahli and D. unisexualis, generates a series of chromosomal rearrangements (mutations). This may lead to the appearance of a geographically isolated chromosomal race (clone) in the population inhabiting the southeastern coast of the Sevan Lake.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

REFERENCES

  1. Arribas, O.J., Phylogeny and Relationships of the Mountain Lizards of Europe and Near East (Archaeolacerta Merttens, 1921, sensulato) and Their Relationships Among the Eurasian Lacertid Lizards, Rus. J. Herpetol., 1999, vol. 6, no. 1, pp. 1-22.

    Google Scholar 

  2. Turner, B.J., Elder, J.F., Laughlin, T.H., and Davis, W.P., Genetic Variation in Clonal Vertebrates Detected by Simple Sequence DNA Fingerprinting, Proc. Natl. Acad. Sci. USA, 1990, vol. 87, pp. 5653-5657.

    Google Scholar 

  3. Umino, T., Arai, K., Maeda, K., et al., Natural Clones Detected by Multilocus DNA Fingerprinting in Gynogenetic Triploid Ginbuna Carassius langsdorfii in the Kurose River, Hiroshima, Fish Sci., 1997, vol. 63, pp. 147-148.

    Google Scholar 

  4. Elder, J.F. and Schlosser, I., Jr., Extreme Clonal Uniformity of Proxinus eos/neogaeus Gynogens (Pisces: Cyprinidae) among Variable Habitants in Northern Minnesota Beaver Ponds, Proc. Natl. Acad. Sci. USA, 1995, vol. 92, pp. 5001-5005.

    Google Scholar 

  5. Schartl, M., Schlupp, I., Schartl, A., et al., On the Stability of Dispensable Constituents of the Eukaryotic Genome: Stability of Coding Sequences Versus Truly Hypervariable Sequences in a Clonal Vertebrate, the Amazon Molly, Poecilia formosa, Proc. Natl. Acad. Sci. USA, 1991, vol. 88, pp. 8759-8763.

    Google Scholar 

  6. Kan, N.G., Petrosyan, V.G., Martirosyan, I.A., et al., DNA Fingerprinting in the Parthenogenetic Lizard Species Lacerta dahli: Detection of Genome Polymorphism of Mini-and Microsatellite Loci, Mol. Biol. (Moscow), 1998, vol. 32, no. 5, pp. 805-812.

    Google Scholar 

  7. Ryskov, A.P., Kan, N.G., Martirosyan, I.A., et al., Enhanced Variation of the (TCC)n Microsatellite Loci in Populations of the Parthenogenetic Lizard Species Lacerta unisexualis Darevsky, Genetika (Moscow), 2000, vol. 36, no. 11, pp. 1501-1506.

    Google Scholar 

  8. Tokarskaya, O.N., Kan, N.G., Petrosyan, V.G., et al., Variation of the GATA Microsatellite DNAs in Populations of the Parthenogenetic Lizard Species Lacerta unisexualis Darevsky, Genetika (Moscow), 2000, vol. 36, no. 5, pp. 693-698.

    Google Scholar 

  9. Tokarskaya, O.N., Kan, N.G., Petrosyan, V.G., et al., Genetic Variation in Parthenogenetic Caucasian Rock Lizards of the Genus Lacerta (L. dahli, L. armeniaca, L. unisexualis) Analyzed by DNA Fingerprinting, Mol. Genet. Genomics, 2001, vol. 265, pp. 812-819.

    Google Scholar 

  10. Darevsky, I.S., Kupriyanova, L.A., and Uzzell, T., Parthenogenesis in Reptiles, Biology of the Reptilia, New York: Wiley, 1985, vol. 15, pp. 412-526.

    Google Scholar 

  11. Moritz, C., Uzzell, T., Spolsky, C., et al., The Maternal Ancestry and Approximate Age of Parthenogenetic Species of Caucasian Rock Lizards (Lacerta: Lacertidae), Genetica (The Hague), 1992, vol. 87, pp. 53-62.

    Google Scholar 

  12. MacCulloch, R.D., Murphy, R.W., Kupriyanova, L.A., et al., Clonal Variation in the Parthenogenetic Rock Lizard Lacerta armeniaca, Genome, 1995, vol. 38, pp. 1057-1060.

    Google Scholar 

  13. Murphy, R.W., Darevsky, I.S., MacCulloch, R.D., et al., Old Age, Multiple Formations or Genetic Plasticity? Clonal Diversity in the Uniparental Caucasian Rock Lizard, Lacerta dahli, Genetica (The Hague), 1997, vol. 101, pp. 125-130.

    Google Scholar 

  14. Fu, J., MacCulloch, R.D., Murphy, R.W., et al., The Par-thenogenetic Rock Lizard Lacerta unisexualis: An Example of Limited Genetic Polymorphism, J. Mol. Evol., 1998, vol. 46, pp. 127-130.

    Google Scholar 

  15. MacCuloch, R.D., Murphy, R.W., Kupriyanova, L.A., and Darevsky, I.S., The Caucasian Rock Lizard Lacerta rostombekovi: A Monoclonal Parthenogenetic Vertebrate, Biochem. Syst. Ecol., 1997, vol. 25, no. 1, pp. 33-37.

    Google Scholar 

  16. Mathew, C.G.P., The Isolation of High-Molecular-Weight Eukaryotic DNA, Methods in Molecular Biology, Walker, J.M., Ed., New York: Humana, 1984, vol. 2, pp. 31-34.

    Google Scholar 

  17. Petrosyan, V.G., Development of Methods to Assess the Dynamics of Abundance and Optimal Density in Large Phytophagous Mammals, in Monitoring bioraznoo-braziya (The Monitoring of Biodiversity), Moscow: Nauka, 1997, pp. 105-114.

    Google Scholar 

  18. Duran, B.S. and Odell, P.L., Cluster Analysis: A Survey, Berlin: Springer-Verlag, 1974, p. 128.

    Google Scholar 

  19. Dawley, R.M., An Introduction to Unisexual Vertebrates, Evolution and Ecology of Unisexual Vertebrates, Dawley, R.M. and Bogart, J.P., Eds., Albany, NY: Bull. N. Y. State Mus., 1989, vol. 466, pp. 1-18.

    Google Scholar 

  20. Parker, E.D., Phenotypic Consequences of Parthenogenesis in Cnemidophorus Lizards: I. Variability in Parthenogenetic and Sexual Populations, Evolution, 1979, vol. 33, pp. 1150-1166.

    Google Scholar 

  21. Cole, C.J., Dessauer, H.C., and Barrowclough, G.F., Hybrid Origin of a Unisexual Species of Whiptail Lizard, Cnemidophorus neomexicanus, in Western North America: New Evidence and a Review, Am. Mus. Novitat., 1988, vol. 2905, pp. 1-38.

    Google Scholar 

  22. Moritz, C., Donnelan, S., Adams, M., and Baverstock, P.R., The Origin and Evolution of Parthenogenesis in Heteronotia binoei (Gekkonidae): Extensive Genotypic Diversity among Parthenogens, Evolution, 1989, vol. 43, pp. 994-1003.

    Google Scholar 

  23. Donnellan, S.C. and Moritz, C., Genetic Diversity of Bisexual and Parthenogenetic Populations of the Tropical Gecko Nactus pelagicus (Lacertilia: Gekkonidae), Herpetologica, 1995, vol. 51, pp. 140-154.

    Google Scholar 

  24. Parker, E.D. and Selanger, R.K., The Organization of Genetic Diversity in the Parthenogenetic Lizard Cnemidophorus tesselatus, Genetics, 1976, vol. 38, pp. 1186-1193.

    Google Scholar 

  25. Fu, J., MacCulloch, R.D., Murphy, R.W., and Darevsky, I.S., Clonal Variation in the Caucasian Rock Lizard Lacerta armeniaca and Its Origin, Amphibia-Reptilia, 2000, vol. 21, no. 1, pp. 83-89.

    Google Scholar 

  26. Turner, B.J., Elder, J.F., Jr., Laughlin, T.F., et al., Extreme Clonal Diversity and Divergence in Populations of a Selfing Hermaphroditic Fish, Proc. Natl. Acad. Sci. USA, 1992, vol. 89, pp. 10-643-10-647.

    Google Scholar 

  27. Wyman, A. and White, R., A Highly Polymorphic Locus in Human DNA, Proc. Natl. Acad. Sci. USA, 1980, vol. 77, pp. 6754-6758.

    Google Scholar 

  28. White, R. and Laluel, G.-M., Chromosome Mapping with the Help of DNA Markers, in V mire nauki (In Scientific World), Moscow: Mir, 1988, vol. 4, pp. 6-15.

    Google Scholar 

  29. Jeffreys, A.J., Royle, N.J., Wilson, V., and Wong, Z., Spontaneous Mutation Rates to New Length Alleles at Tandem-Repetitive Hypervariable Loci in Human DNA, Nature, 1988, vol. 322, pp. 278-281.

    Google Scholar 

  30. Jeffreys, A.J., Allen, M.J., Armour, J.A., et al., Mutation Processes at Human Minisatellites, Electrophoresis (Weinheim, Fed. Repub. Ger.), 1995, vol. 16, pp. 1577-1585.

    Google Scholar 

  31. Vergnaud, G., Mariat, D., Apiou, F., et al., The Use of Synthetic Tandem Repeats to Isolate New VNTR Loci: Cloning of a Human Hypermutable Sequence, Genomics, 1991, vol. 11, pp. 135-144.

    Google Scholar 

  32. Suzuki, S., Mitani, K., Kuwabara, K., et al., Two Mouse Hypervariable Minisatellites: Chromosomal Location and Simultaneous Mutation, J. Biochem., 1993, vol. 114, pp. 135-144.

    Google Scholar 

  33. Djian, P., Evolution of Simple Repeats in DNA and Their Relation to Human Disease, Cell (Cambridge, Mass.), 1998, vol. 94, pp. 155-160.

    Google Scholar 

  34. Ionov, Y., Peinado, M.A., Malkhosyan, S., et al., Ubiquitous Somatic Mutations in Simple Repeated Sequences Revealed a New Mechanism for Colonic Carcinogenesis, Nature, 1993, vol. 363, pp. 558-561.

    Google Scholar 

  35. Palsboll, P.J., Berube, M., and Jorgensen, H., Multiple Levels of Single-Strand Slippage at Cetacean Tri-and Tetranucleotide Repeat Microsatellite Loci, Genetics, 1999, vol. 151, pp. 285-296.

    Google Scholar 

  36. Wells, R.D., Molecular Basis of Genetic Instability of Triplet Repeats, J. Biol. Chem., 1996, vol. 271, no. 6, pp. 2875-2878.

    Google Scholar 

  37. Kan, N.G., Martirosyan, I.A., Darevskii, I.A., et al., DNA Fingerprinting of Parthenogenetic Lizard Families of the Genus Lacerta: Detection of Genetically Unstable Loci, Mol. Biol. (Moscow), 2000, vol. 3, no. 5, pp. 834-838.

    Google Scholar 

  38. Kupriyanova, L.A., Genetic Diversity of Hybrid Unisexual Species and Forms of the Genus Lacerta (Lacertidae, Reptilia): Possible Cytogenetic Mechanisms, Cytogenetics of Meiosis in Natural Polyploid Forms, Tsitologiya, 1999, vol. 41, no. 12, pp. 1038-1047.

    Google Scholar 

  39. Kupriyanova, L.A., Several Cytogenetic Regularities of Reticulous Speciation in Unisexual Lizard Species (Reptilia, Lacertidae) and Other Vertebrate Groups, Tsitologiya, 1997, vol. 39, no. 2, pp. 1089-1108.

    Google Scholar 

  40. Weber, J.L. and Wong, C., Mutation of Human Short Tandem Repeats, Hum. Mol. Genet., 1993, vol. 2, pp. 1123-1128.

    Google Scholar 

  41. Ayala, F. and Kaiger, D., Gene Mutations, in Sovremennaya genetika (Modern Genetics), Moscow: Mir, 1988, vol. 3, p. 19.

    Google Scholar 

  42. Sclartl, M., Nanda, I., Schlupp, I., et al., Incorporation of Subgenomic Amounts of DNA as Compensation for Mutational Load in a Gynogenetic Fish, Nature, 1995, vol. 373, pp. 67-68.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Martirosyan, I.A., Ryskov, A.P., Petrosyan, V.G. et al. Variation of Mini- and Microsatellite DNA Markers in Populations of Parthenogenetic Rock Lizard Darevskia rostombekovi. Russian Journal of Genetics 38, 691–698 (2002). https://doi.org/10.1023/A:1016000219576

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1016000219576

Keywords

Navigation