Abstracts
Karyotype and other chromosomal markers as revealed by C-banding and silver (Ag) impregnation in two Astyanax bockmanni populations (Barra Seca Stream and Campo Novo River) were examined. The diploid chromosome number 2n = 50 and nearly identical karyotypes were documented. C-banding revealed heterochromatic blocks on the terminal regions of some chromosomes, with high frequencies of polymorphisms. The Ag-impregnation showed that the nucleolus organizer regions (NORs) varied in number, location and organization. Astyanax bockmanni revealed chromosome characteristics similar those of the species complex "A. scabripinnis". Mechanisms that may be responsible for the high degree of polymorphism are discussed.
Fish cytogenetics; Chromosomal rearrangements; Karyotype differentiation
Cariótipo e outros marcadores cromossômicos revelados pelo bandamento C e impregnação da prata (Ag) em duas populações de Astyanax bockmanni (córrego Barra Seca e rio Campo Novo) foram examinados. O número cromossômico diploide 2n = 50 e cariótipo quase idênticos são documentados. Bandamento C revelou blocos heterocromáticos na região terminal de alguns cromossomos, com um elevado nível de polimorfismos. A impregnação da prata mostrou variabilidade do número, posição e organização para as regiões organizadoras de nucléolo (RONs). Astyanax bockmanni revelou características cromossômicas similares ao complexo "A. scabripinnis" e os mecanismos responsáveis pelo alto nível do polimorfismo foram discutidos.
Departamento de Ciências Biológicas, Faculdade de Ciências, Universidade Estadual Paulista (UNESP), Campus de Bauru. 17033-360 Bauru, SP, Brazil. diogo@fc.unesp.br, fpforesti@fc.unesp.br
ABSTRACT
Karyotype and other chromosomal markers as revealed by C-banding and silver (Ag) impregnation in two Astyanax bockmanni populations (Barra Seca Stream and Campo Novo River) were examined. The diploid chromosome number 2n = 50 and nearly identical karyotypes were documented. C-banding revealed heterochromatic blocks on the terminal regions of some chromosomes, with high frequencies of polymorphisms. The Ag-impregnation showed that the nucleolus organizer regions (NORs) varied in number, location and organization. Astyanax bockmanni revealed chromosome characteristics similar those of the species complex "A. scabripinnis". Mechanisms that may be responsible for the high degree of polymorphism are discussed.
Key words: Fish cytogenetics, Chromosomal rearrangements, Karyotype differentiation.
RESUMO
Cariótipo e outros marcadores cromossômicos revelados pelo bandamento C e impregnação da prata (Ag) em duas populações de Astyanax bockmanni (córrego Barra Seca e rio Campo Novo) foram examinados. O número cromossômico diploide 2n = 50 e cariótipo quase idênticos são documentados. Bandamento C revelou blocos heterocromáticos na região terminal de alguns cromossomos, com um elevado nível de polimorfismos. A impregnação da prata mostrou variabilidade do número, posição e organização para as regiões organizadoras de nucléolo (RONs). Astyanax bockmanni revelou características cromossômicas similares ao complexo "A. scabripinnis" e os mecanismos responsáveis pelo alto nível do polimorfismo foram discutidos.
Introduction
The family Characidae, order Characiformes, is one of the most numerous and diverse families of freshwater fishes in South America (Nelson, 2006), consisting of approximately 597 recognized species (Buckup et al., 2007). The genus Astyanax, a speciose group of Neotropical characids, comprises about 86 valid species (Lima et al., 2003) that occur in diverse habitats within freshwater drainages from the southern United States to central Argentina.
According to Mirande (2009), the nominal species currently assigned to Astyanax represent a non-monophyletic assemblage. Consequently, cytogenetic studies have been valuable for better systematic analysis of Astyanax, especially for species that need more than morphological criteria for their characterization. An example is Astyanax scabripinnis, which was first characterized as a "species complex" by Moreira-Filho & Bertollo (1991) based on chromosomal and morphological characters. It currently contains 15 valid species (Bertaco & Lucena, 2006).
Astyanax bockmanni is broadly distributed in tributaries from the upper Paraná River system of central, southeastern, and southern Brazil (Vari & Castro, 2007). According to these authors, even though the lack of a comprehensive treatment of the Astyanax species complicates the diagnosis of A. bockmanni from all congeners, this species can be distinguished from its congeners by a combination of diagnostic characters that allow the elimination of A. bockmanni from the complex "A. scabripinnis" (Eigenmann, 1921; Bertaco & Lucena, 2006).
Several species of the genus Astyanax have already been studied genetically, primarily cytogenetically (e.g., Moreira-Filho & Bertollo, 1991; Artoni et al., 2006; Hashimoto et al., 2008; Vicari et al., 2008a). The first cytogenetic study of A. bockmanni was carried out by Kavalco et al. (2009) who described the karyotypes of two populations originating from the Paranapanema River basin. The karyotype of this species differs from other Astyanax species such as A. scabripinnis and A. fasciatus for which intensive chromosomal polymorphism was reported (Moreira-Filho & Bertollo, 1991; Abel et al., 2006; Artoni et al., 2006).
In the present paper, karyotypes and other chromosomal characteristics of specimens from two populations of Astyanax bockmanni from the same hydrographic basin (Barra Seca Stream and Campo Novo River) were studied to characterize the variations in heterochromatin revealed by C-banding and the phenotypes of the nucleolus organizer region (NOR) revealed by Ag-staining.
Material and Methods
Two Astyanax bockmanni populations were examined: 12 specimens (5 females and 7 males) collected from the Campo Novo River and 13 specimens (4 females, 3 males and 6 sex undefined individuals) from the Barra Seca Stream. Both sources belong to the Tietê River basin, São Paulo State, Brazil. The fishes were identified according to Vari & Castro (2007), and the voucher specimens were stored in the fish collection from the Laboratório de Genética de Peixes, UNESP, Bauru, SP, Brazil.
Chromosomal preparations were obtained from gill and kidney tissues using the technique described by Foresti et al. (1993). Silver staining followed the technique of Howell & Black (1980), and C-banding was performed according to Sumner (1972). Chromosomal morphology was determined by arm ratio as proposed by Levan et al. (1964), and the chromosomes were classified as metacentric (m), submetacentric (sm), subtelocentric (st), and acrocentric (a).
Results
The same diploid chromosome number, 2n = 50, was found for specimens examined from both populations. The karyotypes of specimens from the Barra Seca Stream and the Campo Novo River populations were composed of 6m+14sm+14st+16a chromosomes, with a fundamental number (FN) of 84 (Fig. 1). Moreover, a pericentric inversion for the chromosomal pair No. 20 was detected in one individual from the Barra Seca Stream and was confirmed by C-banding (Fig. 2). No karyotype difference related to sex, and no B chromosomes were observed.
Constitutive heterochromatin patterns revealed by C-banding showed heterochromatic blocks in the pericentromeric regions of most chromosomes and bands in the terminal regions of some chromosomes. Among the individuals of both populations, these positive terminal signals showed a high frequency of polymorphism (Fig. 3).
The Ag-impregnation revealed a high inter- and intra-individual variability for the NOR phenotypes in karyotypes of individuals from both populations, ranging from 1 to 8 terminal Ag-positive sites in several chromosomes. These polymorphisms were not only related to the number but also to the location of ribosomal cistrons because these sites were distributed on the long or short arm of several chromosomes. Sequential Ag-NOR staining and C-banding demonstrated that some NORs were C-band positive (Fig. 4).
Discussion
The diploid chromosome number of 2n = 50 described in the present study is in accordance with data previously reported for other populations of Astyanax bockmanni (Kavalco et al., 2009). Therefore, our results indicate a stable 2n for A. bockmanni in contrast to the species complexes A. fasciatus and A. scabripinnis that show variable diploid chromosome numbers in different individuals, some of which live in sympatry (Moreira-Filho & Bertollo, 1991; Artoni et al., 2006).
Except for the invariable 2n, the karyotypes of specimens from the populations we studied and those analyzed by Kavalco et al. (2009) showed few differences. These differences were primarily in the number of m, sm and st chromosomes. Such divergence can be responsible for the allopatric differentiation that occurs in some Astyanax species restricted to small tributaries and streams (Vicari et al., 2008b), and probably is due to the occurrence of non-Robertsonian chromosomal rearrangements such as centromeric shifts (Fig. 2), or extensive heterochromatin polymorphism, or both (Fig. 3).
Chromosome rearrangements due to inversions have been described in some fish groups (Centofante et al., 2002; Jorge & Moreira-Filho, 2004), with some cases involving the NOR-bearing chromosomes (Porto-Foresti et al., 2004; Mariotto et al., 2009). Based on experimental crosses of farmed stocks of the salmonid Oncorhynchus mykiss, Porto-Foresti et al. (2004) suggested that a particular combination of chromosomes with inversions might be lethal in rainbow trout. For natural populations of neotropical fish, there are few descriptions of the biological effects related to this kind of chromosome polymorphism. A pericentric inversion of the first karyotype pair was detected in Serrasalmus spilopleura but without the structural homozygote (Centofante et al., 2002). Although this may be due to a sampling bias, such a situation seems to be comparable to our results where the homozygotes for the chromosomes with inversions were not found, suggesting that homozygosity might be a lethal genotype similar to the situation in O. mykiss (Porto-Foresti et al., 2004). Moreover, according to Mariotto et al. (2009), in the species Ancistrus cuiabae it would be possible to correlate differential fitness with distinct frequencies of cytotypes bearing chromosome inversions.
The distribution of constitutive heterochromatin patterns observed in the present study was similar to those described for karyotypes of different A. scabripinnis populations (Souza et al., 1996; Mantovani et al., 2000), with considerable heterochromatin variability on the distal regions of several chromosomes. These heterochromatic regions demonstrated a great inter-individual polymorphism, in contrast to the specimens studied by Kavalco et al. (2009) that did not possess such patterns.
Currently, several hypotheses have been proposed to explain the extensive polymorphism in the heterochromatin distribution in A. scabripinnis chromosomes, and our data corroborate some of them. Souza et al. (1996) suggested that the model proposed by Schweizer & Loidl (1987), specifically the linear orientation of the anaphase opposite pole-directed centromeres during mitotic interphase, would permit heterochromatin transfers among sites equidistant from the centromeres of non-homologous chromosomes. According to Mantovani et al. (2000), heterochromatinization of euchromatic regions (King, 1980), unequal crossing-over (Smith, 1976), or amplification, accumulation and deletion (John, 1988), can also be responsible for the high polymorphism in heterochromatin. Moreover, we cannot disregard the possible mechanism of genome invasion by transposable elements (Tafalla et al., 2006; Slotkin & Martienssen, 2007).
Great variation in heterochromatic regions in the genomes of other Astyanax species has also been reported, and different groups have been revealed by the composition or structural organization of these regions (Souza et al., 1996; Mantovani et al., 2004; Abel et al., 2006). In some cases, such as A. janeiroensis and A. scabripinnis, there is still heterochromatin/rDNA (ribosomal DNA) association (Mestriner et al., 2000; Vicari et al., 2008a). In these studies, a satellite DNA (As51) isolated from A scabripinnis (Mestriner et al., 2000) was used as the probe for in situ hybridization (FISH) to analyze the different heterochromatin classes in these species and NOR silencing in A. janeiroensis.
On the other hand, in A. bockmanni a different situation was reported (Kavalco et al., 2009). According to the authors, in FISH experiments the As51 satellite DNA probe did not hybridize to any genome region of this species. However, the absence of As51 satellite DNA in the genome of those individuals can be explained by the lack of major heterochromatic regions. Therefore, the analyses of other populations, using FISH with the As51 probe, will be necessary for better conclusions. In some populations with individuals showing a high degree of polymorphism of heterochromatin, as in the present study, the As51 DNA might hybridize to the genome of some of the specimens. Such a situation is found for the complex A. scabripinnis, which reveals populations with individuals bearing the As51 repetitive DNA on the chromosomes, as well as populations without the As51 satellite and major heterochromatic blocks (Abel et al., 2006).
Two structural classes of differently organized NORs were observed in the genomes of A. bockmanni individuals. Some active NORs were arranged in heterochromatic regions and some were not associated with heterochromatin (Fig. 4); apparently neither showed interference or divergence in their expression.
The NOR polymorphism observed in karyotypes of specimens from both populations has been a common characteristic among several Astyanax species (Ferro et al., 2001; Vicari et al., 2008a; Kavalco et al., 2009). This variation should be related to the NOR expression because the silver nitrate detects only active NORs (Howell, 1977; Jordan, 1987). The inter-individual polymorphism can also be explained by simple translocation events or, according to Schweizer & Loidl (1987), by terminal regions exchanging genetic material due to their proximity within the interphase nucleus, promoted by chromosome ordering according to Rabl's model.
In conclusion, our data revealed a high degree of chromosome polymorphism in A. bockmanni. The populations from the Tietê River basin might be a good model to use for analyzing karyotype differentiation in this species. However, it is not possible to infer that karyotype variations of these populations have a direct relation to a speciation process or that this group constitutes a species complex. Despite our data indicating a chromosomal similarity to the species complex "A. scabripinnis", this latter group is very well studied and represents a taxon with historical inertia. In contrast, A. bockmanni was only recently described and may represent a truly valid taxon, with some degree of karyotype variation. This uncertainty shows that extensive studies of other populations are needed to better understand the karyotype diversification of this group.
Acknowledgements
The authors would like to thank Fernando C. P. D´Agosta and Ricardo M. C. Castro for the taxonomical identification. This work was supported by grants from Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq).
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Accepted September 8, 2010
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Chromosome polymorphism of heterochromatin and nucleolar regions in two populations of the fish Astyanax bockmanni (Teleostei: Characiformes)
Publication Dates
-
Publication in this collection
06 Jan 2011 -
Date of issue
2010
History
-
Received
08 Sept 2010 -
Accepted
16 Dec 2010