Contribuição citogenética à análise da biodiversidade em Astyanax fasciatus (Pisces, Characidae).

• Autor(a) principal: Pazza, Rubens
• Data de Publicação: 2005
• Tipo de documento: Tese
• Idioma: por
• Título da fonte: Repositório Institucional da UFSCAR
• Texto Completo: https://repositorio.ufscar.br/handle/ufscar/5426
• topic: Citogenética; Mogi-Guaçu, Rio (MG e SP); Marcador molecular; Astyanax fasciatus; Variabilidade genética; CIENCIAS BIOLOGICAS::GENETICA::GENETICA ANIMAL

Astyanax fasciatus is characterized as a cytogenetically diverse species. Sympatric and syntopic occurrence of distinct cytotypes corroborates the hypothesis that A. fasciatus might represent a species complex sharing a common denomination. In this work, specimens from three collection sites along Mogi-Guaçu River, on Southeastern Brazil, were examined: (1) close to headwaters (Ouro Fino MG), (2) in the mean river portion (Cachoeira de Emas, Pirassununga SP, characterized by the presence of a dam) and (3) close to river mouth at Pardo river (Barrinha SP). Two karyotypes bearing perfectly paired chromosomes, named standard cytotypes, were identified; one of them with 2n=46 and another one with 2n=48 chromosomes. The cytotype 2n = 48 was found in all collection sites, whereas the cytotype 2n = 46 was restricted to Barrinha and Cachoeira de Emas. In this latter locality, the cytotype 2n=46 was predominant, but variant karyotypical forms were also reported, bearing 2n=45 and 47 chromosomes, besides a structural variant with 2n=46. A variant with 2n=47 chromosomes was also found in Ouro Fino. The Ag-NORs and 18S and 5S rDNA sites showed a conserved distribution among cytotypes, as well as the constitutive heterochromatin, preferentially located at terminal region on the long arms of submetacentric, subtelocentric and acrocentric chromosomes and terminal region on short arms of a submetacentric pair. This latter region showed to be GC-rich after chromomycin A3 staining and it corresponds to the location of a Nucleolar Organizer Region. Sites bearing the satellite DNA As51 were detected at terminal region on the long arms of several chromosomes, distributed over 4 submetacentric pairs, 3 subtelocentric pairs and one acrocentric pair in the standard cytotype 2n=46, and over 3 submetacentric pairs, 4 subtelocentric pairs and one acrocentric pair in the standard cytotype 2n=48. The variant karyotypical forms also presented other chromosomes bearing such satellite DNA, remarkably at a large metacentric chromosome bearing a terminal site on the long arms (found in two variant karyotypes), two subtelocentric pairs bearing additional interstitial site (found in one variant karyotype), and one submetacentric pair bearing a subterminal site on the long arms (found in one variant karyotype). Data based on RAPD (Random Amplified Polymorphic DNA) were poorly informative to analyze the reported diversity, indicating a high number of migrants per generation among cytotypes. On the other hand, data from ISSR (Inter-Simple Sequence Repeats) showed a low structuring, mainly between two standard cytotypes from Barrinha, where a Nm value of 0,4301 was observed, with a genetic identity of 0,6862 and genetic distance of 0,3765. The values of genetic distance (0,3219) and genetic identity (0,7248) between cytotypes with 2n=48 from Barrinha and Ouro Fino also evidenced a slight differentiation, indicating that the dam at Cachoeiras de Emas is probably a barrier to gene flow among populations located upstream and downstream the dam. The obtained results with molecular markers do not discard the possibility of inbreeding among the cytotypes of A. fasciatus, as a source of the diversity found. Hypothetically, the standard cytotype with 2n=48 might be the resident form at Mogi- Guaçu River, while the cytotype with 2n=46 would represent an invasive form, showing recent divergence. Although the variant karyotypes present a karyotypical structure similar to the cytotype with 2n=46, there are evidences that chromosomes typical from the cytotype with 2n=48 have been incorporated, suggesting that such variants may be derived from viable crossings among standard cytotypes, and/or their offsprings, which share some homologies, as demonstrated by chromosomal markers. The presence of a higher number of As-51 sites in some variants reinforces their inbreeding origin. The As-51 sites, which showed to be specific for some variant forms, might be originated by complementary chromosomal rearrangements, propitious to new locations of this satellite DNA on karyotypes.