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Biogeographic patterns in the chromosomal distribution of a satellite DNA in the banded tetra Astyanax fasciatus (Teleostei: Characiformes)

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Abstract

The As-51 satellite DNA is a transposon-like sequence formerly described for arthropods and physically identifiable by fluorescent in situ hybridization. In the present work, we describe the occurrence of this sequence, as well the C-banding and karyotype composition, in populations of the group Astyanax fasciatus from Mogi-Guaçu (Araras-SP), Paranapanema (Angatuba and Pilar do Sul-SP), Ribeira de Iguape (Sete Barras-SP) and Tietê (Indaiatuba and Salesópolis-SP) river basins. The specimens from Sete Barras (10 M + 20SM + 12ST + 6A) and Araras (8 M + 22SM + 12ST + 6A) have 2n = 48 chromosomes. The samples from Angatuba, Pilar do Sul and Indaiatuba presented 2n = 46 chromosomes (12 M + 20SM + 10ST + 4A). The individuals collected in Salesópolis showed three cytotypes, bearing 2n = 46 (12 M + 20SM + 10ST + 4A), 2n = 48 (8 M + 22SM + 12ST + 6A) and 2n = 50 (8 M + 16SM + 14ST + 12A). C-banding revealed large heterochromatic blocks at terminal chromosomal regions in all populations and/or cytotypes. All analyzed populations have conspicuous blocks carrying the As-51 satellite DNA, although the number of chromosomes bearing this repetitive sequence was variable among them. Such differences were not related to the diploid number of individuals, but rather to a biogeographic pattern. Aspects of the karyotype evolution and distribution of this sequence in distinct populations are discussed.

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References

  • Ab’Saber, N. A. (1957). O problema das conexões antigas e da separação da drenagem do Paraíba e Tietê. Boletim Paulista de Geografia, 26, 38–49.

    Google Scholar 

  • Abel, L. D. S., Mantovani, M., & Moreira-Filho, O. (2006). Chromosomal distribution of the As-51 satellite DNA in two species complexes of the genus Astyanax (Pisces, Characidae). Genetics and Molecular Biology, 29, 448–452.

    Article  Google Scholar 

  • Almeida, F. F. M., & Carneiro, C. D. R. (1998). Origem e evolução da Serra do Mar. Revista Brasileira de Geociências, 28, 135–150.

    Google Scholar 

  • Bizerril, C. R. S. F. (1994). Análise taxonômica e biogeográfica da ictiofauna de água doce do leste brasileiro. Acta Biologica Leopoldensia, 16, 51–80.

    Google Scholar 

  • Castro, R. M. C. (1999). Evolução da ictiofauna de riachos sul-americanos: padrões gerais e possíveis processos causais. In E. P. Caramashi, R. Mazzoni, & P. R. Peres-Neto (Eds.), Ecologia de Peixes de Riachos. Rio de Janeiro: PPGE-UFRJ.

    Google Scholar 

  • Centofante, L., Bertollo, L. A. C., Justi, A. J., & Moreira-Filho, O. (2003). Correlation of chromosomal and morphologic characters in two Astyanax species (Teleostei: Characidae). Ichthyological Exploration of Freshwaters, 14, 361–368.

    Google Scholar 

  • Fernandes, C. A., & Martins-Santos, I. C. (2004). Cytogenetic studies in two populations of Astyanax altiparanae (Pisces, Characiformes). Hereditas, 141, 328–332.

    Article  PubMed  Google Scholar 

  • Gold, J. R., Li, C., Shipley, N. S., & Powers, P. K. (1990). Improved methods for working with fish chromosomes with a review of metaphase chromosome banding. Journal of Fish Biology, 37, 563–575.

    Article  Google Scholar 

  • Gross, M. C., Schneider, C. E., Matiello, M. C. A., Leite, M. L., Bertollo, L. A. C., & Artoni, R. F. (2004). Population structure, fluctuating asymmetry and genetic variability in an endemic and highly isolated Astyanax fish Population (Characidae). Genetics and Molecular Biology, 27, 529–535.

    Article  Google Scholar 

  • Jin, S. N., & Toledo, V. (1975). Citogenética de Astyanax fasciatus e Astyanax bimaculatus (Characidae, Tetragonopterinae). Ciência e Cultura, 27, 1122–1124.

    Google Scholar 

  • Justi, A.J. (1993). Caracterização cariotípica de populações de Astyanax fasciatus (Cuvier, 1819), Pisces, Characidae, em três bacias hidrográficas. MSc Thesis, Federal University of São Carlos.

  • Kantek, D. L. Z., Vicari, M. R., Peres, W. A. M., Cestari, M. M., Artoni, R. F., Bertollo, L. A. C., et al. (2009). Chromosomal location and distribution of As51 satellite DNA in five species of the genus Astyanax (Teleostei, Characidae, Incertae sedis). Journal of Fish Biology, 75, 408–421.

    Article  PubMed  CAS  Google Scholar 

  • Kavalco, K. F., & Almeida-Toledo, L. F. (2007). Molecular cytogenetics of blind mexican tetra and comments on the karyotypic characteristics of genus Astyanax (Teleostei, Characidae). Zebrafish, 4, 103–111.

    Article  PubMed  CAS  Google Scholar 

  • Kavalco, K. F., & Moreira-Filho, O. (2003). Cytogenetical analyses in four species of the genus Astyanax (Pisces, Characidae) from Paraíba do Sul river basin. Caryologia, 56, 453–461.

    Article  Google Scholar 

  • Kavalco, K. F., Pazza, R., Bertollo, L. A. C., & Moreira-Filho, O. (2007). Satellite DNA sites of four species of the genus Astyanax (Teleostei, Characiformes). Genetics and Molecular Biology, 30, 329–335.

    Article  Google Scholar 

  • Kavalco, K. F., Brandão, K. O., Pazza, R., & Almeida-Toledo, L. F. (2009). Astyanax hastatus Myers, 1928 (Teleostei, Characidae): a new species complex within the genus Astyanax? Genetics and Molecular Biology, 32, 477–483.

    Article  PubMed  Google Scholar 

  • Kavalco, K. F., Pazza, R., & Almeida-Toledo, L. F. (2009). Astyanax bockmanni Vari and Castro, 2007: an ambiguous karyotype in the Astyanax genus. Genetica, 136, 135–139.

    Article  PubMed  Google Scholar 

  • Kavalco, K. F., Pazza, R., & Almeida-Toledo, L. F. (2010). Molecular cytogenetics of Astyanax ribeirae (Teleostei, Characidae), an endemic characin of the Atlantic rainforest. The Nucleus, 53, 51–54.

    Article  Google Scholar 

  • Kavalco, K.F., Brandão, K.O., Garcia, C., Pazza, R., & Almeida-Toledo, L.F. (2011). Comparative cytogenetics and molecular phylogeography in the group Astyanax altiparanae - Astyanax aff. bimaculatus (Teleostei, Characidae). Cytogenetic and Genome Research, 134(2), 108-119. doi:10.1159/000325539.

  • Levan, A., Fredga, K., & Sandberg, A. A. (1964). Nomenclature for centromeric position on chromosomes. Hereditas, 52, 201–220.

    Article  Google Scholar 

  • Mantovani, M., Abel, L. D. S., Mestriner, C. A., & Moreira-Filho, O. (2000). Accentuated polymorphism of heterochromatin and nucleolar organizer regions in Astyanax scabripinnis (Pisces, Characidae): tools for understanding karyotypic evolution. Genetica, 109, 161–168.

    Article  PubMed  CAS  Google Scholar 

  • Mantovani, M., Abel, L. D. S., & Moreira-Filho, O. (2004). Evidence of the differentiated structural arrangement of constitutive heterochromatin between two populations of Astyanax scabripinnis (Pisces, Characidae). Genetics and Molecular Biology, 27, 536–542.

    Article  CAS  Google Scholar 

  • Melo, F. A. G. (2001). Revisão taxonômica das espécies do gênero Astyanax Baird e Girard, 1854 (Teleostei: Characiformes: Characidae) da região da Serra dos Órgãos, Rio de Janeiro. Arquivos do Museu Nacional, 59, 1–46.

    Google Scholar 

  • Mestriner, C. A., Galetti, P. M., Jr., Valentini, S. R., Ruiz, I. R. G., Abel, L. D. S., Moreira-Filho, O., et al. (2000). Structural and functional evidence that a B chromosome in the characid fish Astyanax scabripinnis is an isochromosome. Heredity, 85, 1–9.

    Article  PubMed  CAS  Google Scholar 

  • Moreira-Filho, O., & Bertollo, L. A. C. (1991). Astyanax scabripinnis (Pisces, Characidae): a species complex. Genetics and Molecular Biology, 14, 331–357.

    Google Scholar 

  • Moreira-Filho, O., & Buckup, P. A. (2005). A poorly known case of watershed transposition between the São Francisco and upper Paraná river basins. Neotropical Ichthyology, 3, 449–452.

    Article  Google Scholar 

  • Morelli, S., Bertollo, L. A. C., Foresti, F., Moreira-Filho, O., & Toledo-Filho, S. A. (1983). Cytogenetic considerations on the genus Astyanax (Pisces, Characidae). I. Karyotypic variability. Caryologia, 36, 235–244.

    Google Scholar 

  • Paiva, M. P. (1982). As grandes represas do Brasil. Brasília: Editerra.

    Google Scholar 

  • Pazza, R., Kavalco, K. F., & Bertollo, L. A. C. (2006). Chromosome polymorphism in Astyanax fasciatus (Teleostei, Characidae). 1 - Karyotypic analysis, Ag-NORs and mapping of the 18 S and 5 S ribosomal genes in sympatric karyotypes and their possible hybrid forms. Cytogenetic and Genome Research, 112, 313–319.

    Article  PubMed  CAS  Google Scholar 

  • Pazza, R., Kavalco, K. F., Prioli, S. M. A. P., Prioli, A. J., & Bertollo, L. A. C. (2007). Chromosome polymorphism in Astyanax fasciatus (Teleostei, Characidae). 3 – Analysis of the RAPD and ISSR molecular markers. Biochemical Systematics and Ecology, 35, 841–851.

    Article  Google Scholar 

  • Pazza, R., Kavalco, K. F., & Bertollo, L. A. C. (2008). Chromosome polymorphism in Astyanax fasciatus (Teleostei, Characidae). 2 - Gene mapping of satellite DNA. Cytogenetic and Genome Research, 122, 61–66.

    Article  PubMed  CAS  Google Scholar 

  • Pazza, R., Kavalco, S. A. F., Penteado, P. R., Kavalco, K. F., & Almeida-Toledo, L. F. (2008). The species complex Astyanax fasciatus Cuvier, 1819 (Teleostei, Characiformes): a multidisciplinary approach. Journal of Fish Biology, 72, 2002–2010.

    Article  Google Scholar 

  • Peres, W. A. M., Buckup, P. A., Kantek, D. L. Z., Bertollo, L. A. C., & Moreira-Filho, O. (2009). Chromosomal evidence of downstream dispersal of Astyanax fasciatus (Characiforems, Characidae) associated with river shed interconnection. Genetica, 137, 305–311.

    Article  PubMed  Google Scholar 

  • Pinkel, D., Straume, T., & Gray, J. W. (1986). Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization. Proceedings of National Academy of Science, 83, 2934–2938.

    Article  CAS  Google Scholar 

  • Ribeiro, A. C. (2006). Tectonic history and the biogeography of the freshwater fishes from the coastal drainages of eastern Brazil: an example of faunal evolution associated with a divergent continental margin. Neotropical Ichthyology, 4, 225–246.

    Article  Google Scholar 

  • Strecker, U., Faundez, W. H., & Wilkens, H. (2004). Phylogeography of surface and cave Astyanax (Teleostei) from Central and North America based on cytochrome b sequence data. Molecular Phylogenetics and Evolution, 33, 469–481.

    Article  PubMed  CAS  Google Scholar 

  • Sumner, A. T. (1972). A simple technique for demonstrating centromeric heterocromatin. Experimental Cell Research, 75, 304–306.

    Article  PubMed  CAS  Google Scholar 

  • Vicari, M. R., Artoni, R. F., Moreira-Filho, O. & Bertollo, L. A. C. (2008). Colocalization of repetitive DNAs and silencing of major rRNA genes. A case report of the fish Astyanax janeiroensis. Cytogenetic and Genome Research, 122, 67–72. doi:10.1159/000151318.

    Google Scholar 

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Acknowledgments

The authors wish to thank Malabarba LR and Bertaco V, for the taxonomical identification; Lopes CE for helping with the samples; Smarzaro RS for helping with the GIS software; and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) and Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) for the financial support.

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Correspondence to Karine Frehner Kavalco.

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Kavalco, K.F., Pazza, R., de Oliveira Brandão, K. et al. Biogeographic patterns in the chromosomal distribution of a satellite DNA in the banded tetra Astyanax fasciatus (Teleostei: Characiformes). Org Divers Evol 13, 67–76 (2013). https://doi.org/10.1007/s13127-012-0100-8

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