Skip to main content
Log in

Metaphase and meiotic chromosomes, synaptonemal complexes (SC) of the lizard Zootoca vivipara

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

Abstract

Somatic mitotic and meiotic chromosomes at the pachytene and at the metaphase I of the males of the viviparous lizard, Zootoca vivipara (Lichtenstein, 1823), from northwestern Russia, belonging to the Russian form of Z. v. vivipara, are examined. The spreading of synaptonemal complexes (SC) of their chromosomes are obtained and analyzed for the first time. Eighteen SC are observed, including SC of the Z1Z1 (pairs 5 or 6) and the Z2Z2 (pair 13) sex chromosomes. Characteristics of SC are compared with the number and the shape of bivalents and with those of the karyotype structure. In the studied Russian form of Z. v. vivipara, the length ratios of bivalents correlate with that of mitotic chromosomes (2n = 36); however, some specificity in the morphology of SC of the Z1Z1 sex chromosomes is reported in this article.

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. Kupriyanova, L., About possible ways of evolution of lizard karyotype, Tr. Zool. Inst. Akad. Nauk USSR, 1986, vol. 157, pp. 86–101.

    Google Scholar 

  2. Kupriyanova, L., Cytogenetic studies in lacertid lizards, in Cytogenetics of Amphibians and Reptiles, Olmo, E., Ed., Basel: Birkhauser, 1990, pp. 242–245.

    Google Scholar 

  3. Dresser, M. and Moses, M., Synaptonemal complex karyotyping in spermatocytes of the Chinese hamster (Cricetulus griscus): 4. Light and electron microscopy of synapsis and nucleolar development by silver staining, Chromosoma, 1980, vol. 76, pp. 1–22.

    Article  CAS  PubMed  Google Scholar 

  4. Bogdanov, Yu.F. and Kolomiets, O.L., Karyotyping based on synaptonemal systems and the use of this method in cytogenetics, Genetika (Moscow), 1985, vol. 21, no. 5, pp. 793–802.

    Google Scholar 

  5. Safronova, L.D., Kolomiets, O.L., Bogdanov, Yu.F., et al., The association between synaptonemal complexes of genital and autosomal bivalents in tx/ty male mice as a possible cause of sterility, Genetika (Moscow), 1988, vol. 24, no. 7, pp. 1187–1198.

    CAS  Google Scholar 

  6. Wallace, B. and Wallace, H., Synaptonemal complex karyotype of zebrafish, Heredity, 2003, vol. 90, pp. 136–140.

    Article  CAS  PubMed  Google Scholar 

  7. Safronova, L.D. and Krysanov, E.Yu., Synaptonemal complex of two fish species of the genus Nothobranchius (Cyprinodontidae), Russ. J. Genet., 2015, vol. 51, no. 10, pp. 1036–1039.

    Article  CAS  Google Scholar 

  8. Reed, K.M., Sites, J.W., and Greenbaum, I.F., Synapsis, recombination, and meiotic segregation in the mesquite lizard, Sceloporus grammicus complex: 1. Pericentric inversion heteromorphism of the F5 cytotype, Cytogenet. Cell Genet., 1992, vol. 61, pp. 40–45. doi 10.1159/000133366

    CAS  PubMed  Google Scholar 

  9. Lutes, A., Neaves, W.B., Baumann, D.P., Wiegräbe, W., and Baumann, P., Sister chromosome pairing maintains heterozygosity in parthenogenetic lizards, Nature, 2010, vol. 464, no. 7286, pp. 283–286.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Chevalier, M., Dufaure, J.P., and Leche, P., Cytogenetic study of several species of Lacerta (Lacertidae,Reptilia) with particular reference to sex chromosomes, Genetica, 1979, vol. 50, pp. 11–18.

    Article  Google Scholar 

  11. Odierna, G., Kupriyanova, L., Capriglione, T., and Olmo, E., Further data on sex chromosomes of Lacertidae and a hypothesis on their evolutionary trend, Amphibia–Reptilia, 1993, vol. 14, pp. 1–11.

    Google Scholar 

  12. Odierna, G., Aprea, G., Capriglione, T., Arribas, O., Kupriyanova, L., and Olmo, E., Progressive differentiation of the W sex-chromosome between oviparous and viviparous populations of Zootoca vivipara (Reptilia,Laceridae), Ital. J. Zool., 1998, vol. 65, pp. 295–302.

    Article  Google Scholar 

  13. Kupriyanova, L., Kuksin, A., and Odierna, G., Karyotype,chromosome structure,reproductive modalities of three Southern Eurasian populations of the common lacertid lizard, Zootoca vivipara (Jacquin, 1787), Acta Herpetol., 2008, no. 3(2), pp. 99–106.

    Google Scholar 

  14. Ashley, T., G-band position effects on meiotic synapsis and crossing over, Genetics, 1988, vol. 118, pp. 307–317.

    CAS  PubMed  PubMed Central  Google Scholar 

  15. Srikulnath, K., Matsubara, K., Uno, Y., Nishida, C., Olsson, M., and Matsuda, Y., Identification of the linkage group of the Z sex chromosomes of the sand lizard (Lacerta agilis, Lacertidae) and elucidation of karyotype evolution in lacertid lizards, Chromosoma, 2014, vol. 123, pp. 563–575.

    Article  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to L. D. Safronova.

Additional information

Original Russian Text © L.D. Safronova, L.A. Kupriyanova, 2016, published in Genetika, 2016, Vol. 52, No. 11, pp. 1311–1317.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Safronova, L.D., Kupriyanova, L.A. Metaphase and meiotic chromosomes, synaptonemal complexes (SC) of the lizard Zootoca vivipara . Russ J Genet 52, 1186–1191 (2016). https://doi.org/10.1134/S1022795416110120

Download citation

  • Received:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S1022795416110120

Keywords

Navigation