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Genet. Mol. Biol. vol.31 no.1 suppl.0 São Paulo 2008
Susana Suely Rodrigues MilhomemI; Augusto Cesar Paes de SouzaI; Aline Lira do NascimentoI; Jaime Ribeiro Carvalho Jr.III; Eliana FeldbergII; Julio Cesar PieczarkaI; Cleusa Yoshiko NagamachiI
IDepartamento de Genética, Universidade Federal do Pará, Belém, Pará, Brazil
IIInstituto Nacional de Pesquisas da Amazônia, Manaus, AM, Brazil
IIICentro Jovem de Aquaculturismo, Belém, Pará, Brazil
We studied the karyotypes of Hassar cf. orestis and an undescribed Hassar species from the Jarí River and Opsodoras ternetzi, H. orestis and Platydoras cf. costatus from the Xingú River, all with 2n = 58. Constitutive heterochromatin is located in the centromere in most metacentric pairs; in some chromosomes this banding is not present, or it is located on the whole chromosome arm or in the distal regions. The NOR is located on a single biarmed pair at a distal region of the short arm in H. cf. orestis, H. orestis and P. cf. costatus at a distal region of the long arm in O. ternetzi and at a proximal region of the long arm in the Hassar species. In all species (except for Hassar sp.) the CMA3 analysis revealed a rich GC region coincident with the NOR. Probably inversions occurred in the NOR chromosome during the chromosomal differentiation of the Doradidae species here described.
Key words: chromosomes, Amazon, biodiversity, Siluriformes, banding, fluorochromes.
The species of the Doradidae family are usually known as thorny catfishes. They are distributed throughout all the main river systems in the American continent (Higushi, 1992). In South America, these fishes can be found in a large range of freshwaters habitats, between the parallels 10° N and 35° S. Approximately 80 species are described from the Orinoco, Essequibo, Putumayo, Napo, UcayaliMarañon, Amazonas and its tributaries (Negro, Madeira and Xingú), TocantinsAraguaia and ParaguayParaná River systems. Some endemic species can be found in the São FranciscoVelhas River system in central eastern Brazil with two primitive forms limited to the Jequitinhonha and Paraguaçu River system (Higushi, 1992; de Pinna, 1998).
The fishes from this family have a size range from three centimeters to one meter. They are easily identified by the series of bony plates on each side of the body, where each plate has a curved torn of different size, depending on the species. Some have additional plates among the dorsal and adipose fins, or even covering most of the body. They are omnivorous fishes (Ferreira et al., 1998) and are also called talking catfishes because they are able to make sounds by movements of the pectoral spine or as vibrations produced by the swim bladder (Nelson, 1994).
Based on the cladistic methodology applied for osteological traits, Higuchi (1992) divided this family of 70 species into 33 genera, where three were new. Nelson (1994) reports that the family Doradidae has around of 35 genera with 90 species. Sabaj and Ferraris Jr. (2003) recognized 72 valid species in 30 genera. Following this review, Moyer et al. (2004) provide a genuslevel phylogeny for doradids based on mitochondrial (12S and 16S rRNA) and nuclear (elongation factor1 alpha EF1a) gene sequences, as well as a reevaluation of published morphological data. This phylogeny differs in some aspects from the one proposed by Higuchi (1992).
Few species have their karyotypes studied (Fenocchio et al., 1993; Venere, 1998; Eler et al., 2007). These data show that, even with few species cytogenetically studied in this family, a large variation among the karyotypes is evident, especially in chromosomes morphology (Table 1). In the present paper we describe the karyotypes of Hassar cf. orestis, Hassar sp., Hassar orestis Burgess, 1989, Opsodoras ternetzi Eigenmann, 1925 and Platydoras cf. costatus Linnaeus, 1758 aiming to contribute to their taxonomic classification and a better understanding of their chromosomal evolution.
We analyzed fishes of the family Doradidae, from Rivers Jarí (PA) and Xingú (PA). From Jarí River (S = 03° 18' 14,9" and W = 52° 03' 29,3") three females and two males of the Hassar cf. orestis species were analyzed as well as three females of the species Hassar sp. From Xingú River (S = 02° 37' 44,3" and W = 51° 57' 06,4"), three females and two males of the Opsodoras ternetzi species were analyzed as well as one male and one female of the species Hassar orestis. Also from this River (S = 03° 50' 46,6" and W = 52° 29' 22,3") four females of the species Platydoras cf. costatus were analyzed. Voucher specimens were deposited in the fish collection of the Museu Paraense Emilio Goeldi in Belém, Pará, Brazil: Hassar orestis (MPEG 12463) and Opsodoras ternetzi (MPEG 12464), both from Xingú River. The other specimens here described remain uncatalogued.
Mitotic chromosome preparations were obtained from kidney cells using the airdrying technique of Bertollo et al. (1978). Cbanding (Sumner, 1972), AgNOR staining (Howell and Black, 1980) and Chromomycin A3 (CMA3) banding (Schweizer, 1980) were applied. Chromosome morphology was determined on the basis of arm ratio as proposed by Guerra (1986), and chromosomes were classified as metacentrics (M), submetacentrics (SM), subtelocentrics (ST) and acrocentrics (A).
The five species here studied have 2n = 58 chromosomes. Hassar cf. orestis (Figure 1a) and Hassar sp. (Figure 1b) have 32M+18SM+8ST and FN = 116 Opsodoras ternetzi (Figure 1c) has 44M+12SM+2A and FN = 114, Hassar orestis (Figure 1d) has 32M+20SM+6ST and FN = 116, and Platydoras cf. costatus (Figure 1e) has 26M+16SM+4ST+12A and FN = 104. None of these species has shown any sex chromosome heteromorphism.
Single AgNORs were observed in all species. In Hassar cf. orestis (Figure 1a) from Jarí River, and in Hassar orestis (Figure 1d) and Platydoras cf. costatus (Figure 1e) from Xingú River the NOR is located at a distal position of the short arm, while in Hassar sp. (Figure 1b) it is at interstitial position of the long arm and in Opsodoras ternetzi (Figure 1c) it locates to a distal position of the long arm on submetacentric chromosomes.
Constitutive heterochromatin could be found in the centromeric region of most of metacentric chromosomes, showing a faint banding pattern in all the species here studied. It was possible also to find heterochromatic blocks in the short arms of Hassar orestis (Figure 2d) and Opsodoras ternetzi (Figure 2c). CMA3 banding in the species Hassar cf. orestis (Figure 2a), Opsodoras ternetzi (Figure 2c), Hassar orestis (Figure 2d) and Platydoras cf. costatus (Figure 2e) showed regions rich in GC base pairs coincident with the NOR location. Unfortunately, it was not possible to do this banding in Hassar sp.
Table 1 summarizes the karyotype data obtained in the present study and those available in the literature. When we compare the results here obtained with the ones described by Venere (1998) we can note that there is good agreement on the diploid number in the genus Hassar, except for a small difference in the fundamental number of Hassar oresti, because the karyotype described by that author has one acrocentric pair which is not present in the karyotype here described. The species Opsodoras ternetzi here described also has the same diploid number, however, the karyotype is different from the species Opsodoras sp. (Venere, 1998) because it does not have sex chromosome heteromorphism or acrocentric pairs.
The family Doradidae has around of 80 species (de Pinna, 1998), from which 14 were already karyotyped and most have 2n = 58. Probably this is the modal diploid number of this family, the same diploid number which is also considered ancestral for Siluriformes (Oliveira et al., 1988). Eler et al. (2007) described the karyotype of Wertheimeria maculata, which according to Higushi (1992) is a sister taxon of all Doradidae. This species has 2n = 58 (24M+14SM+8ST+12A), supportig the hypothesis that this diploid number is plesiomorphic for the Doradidae.
The Cbanding pattern was similar for the entire group, with a heterochromatic faint pattern. Fenocchio and Bertollo (1992) noted that it is very difficult to obtain good Cbanding in Pimelodidae, a family phylogenetically related to Doradidae. This can best be explained by the peculiar traits of the chromatin of these fishes rather than by the absence of heterochromatic regions.
When looking at Hassar wilderi and Opsodoras sp. which were already analyzed using CMA3 banding (Venere, 1998), we can conclude that this GC base pairs specific fluorochrome is useful for visualizing the NOR in fishes. According to Pendás et al. (1993), the positive correlation between NOR and CMA3 banding occurs because the rRNA genes from NOR region are interspersed by DNA sequences which are rich in GC base pairs.
The single NOR in the distal position of a short arm in the species Hassar cf. orestis from Jarí River, Hassar orestis and Platydoras cf. costatus from Xingú River is similar to the one described for Hassar wilderi, Leptodoras acipenserinus, Opsodoras sp. and Rhynodoras sp. (Venere, 1998), and also for Pseudodoras niger and Rhynodoras d'orbignyi (Fenocchio et al. 1993). In Hassar sp. from Jarí, the NOR is similar to the one in Trachydoras paraguaiensis (Fenocchio et al. 1993) since both are located in an interstitial region in the long arm of a submetacentric pair. In Opsodoras ternetzi from Xingú the NOR is located at the distal region of the long arm of a submetacentric chromosome pair same as in Hassar orestis (Venere, 1998).
The results here obtained for the species Hassar orestis from Jarí and Xingú Rivers show that the NOR is located in the distal region of the short arm. One chromosome pair with heterochromatic blocks in the short arms in Hassar orestis (Figure 2d) from Xingú River is probably the NOR bearer chromosome, showing a more evident secondary constriction in one copy of the pair which seems to be a speciesspecific marker. Venere (1998) studied the same species from Araguaia River and found the NOR in the distal region of the long arm. These results are important since they show the possibility of using the NOR as a population marker.
If one accepts that the analyzed NOR bearer chromosomes in the genus Hassar are homologous, potential paracentric and/or pericentric inversions could have played a role in the karyotypic evolution of these species, moving the NOR to different places of the chromosomes. According to AlmeidaToledo (1998), NOR position changes can be an important marker for karyotypic differences among populations or species of fishes. The NOR size polymorphisms are very frequent in fishes and can be found also in mammals and other vertebrates and seems to be a general trait of NORs. This size polymorphism was observed in all the species here studied. Concerning the Opsodoras ternetzi we observed a difference in NOR position when compared with the Opsodoras sp. (Venere, 1998). In the first one the staining occurred in the distal region of the long arm of a metacentric pair, while in the latter the staining was in the distal region of the short arm of a subtelocentric pair. Apart from this, the modal number is conserved as in other species of this group, but the chromosome formulae and the fundamental numbers change with respect to M+SM+ST+A, suggesting that inversions can be involved not only in the NOR bearers but also in the differentiation of other chromosomal pairs.
According to Lundberg and Friel (2004), Auchenipteridae is the family that is most closely related to Doradidae. Souza et al. (2001) described the karyotypes of four species of this family, where three species have a single NOR located in a distal portion of a short arm, like Hassar cf. orestis from Jarí River, Hassar orestis and Platydoras cf. costatus from Xingú River here presented, as well as Hassar wilderi, Leptodoras acipenserinus, Opsodoras sp. and Rhynodoras sp. (Venere, 1998) and Pseudodoras niger and Rhynodoras d'orbignyi (Fenocchio et al., 1993). The ancestral location of NORs may be in the distal portion of a short arm, since it is found in species from both Doradidae and Auchenipteridae. Cytogenetic research on other species of this family should help to define the phylogenetic relationships within this group, as well as the understanding of the chromosomal evolutionary mechanisms that acted in the chromosomal differentiation of these species.
This work was supported by: SECTAMFUNTEC, IBAMA, CNPq, CAPES, UFPA/PROPESP/PROINT and INPA.
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Send correspondence to:
Cleusa Yoshiko Nagamachi
Departamento de Genética
Universidade Federal do Pará
Campus do Guamá
Av. Augusto Corrêa, sn., CCB, 3° andar
66075900 Belém, PA, Brazil
Accepted: August 28, 2006; Received: June 8, 2007.
Associate Editor: Fausto Foresti
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