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Genetics and Molecular Biology

Print version ISSN 1415-4757On-line version ISSN 1678-4685

Genet. Mol. Biol. vol.32 no.1 São Paulo  2009  Epub Jan 23, 2009

http://dx.doi.org/10.1590/S1415-47572009005000017 

ANIMAL GENETICS
RESEARCH ARTICLE

 

Chromosomal location of 18S and 5S rDNA sites in Triportheus fish species (Characiformes, Characidae)

 

 

Débora DinizI; Alejandro LaudicinaII; Luiz Antonio Carlos BertolloI

IDepartamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos, SP, Brazil
IICentro Nacional de Energia Atômica, Buenos Aires, Argentina

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ABSTRACT

The location of 18S and 5S rDNA sites was determined in eight species and populations of the fish genus Triportheus by using fluorescent in situ hybridization (FISH). The males and females of all species had 2n = 52 chromosomes and a ZZ/ZW sex chromosome system. A single 18S rDNA site that was roughly equivalent to an Ag-NOR was detected on the short arms of a submetacentric pair in nearly all species, and up to two additional sites were also observed in some species. In addition, another 18S rDNA cluster was identified in a distal region on the long arms of the W chromosome; this finding corroborated previous evidence that this cluster would be a shared feature amongst Triportheus species. In T. angulatus, a heterozygotic paracentric inversion involving the short arms of one homolog of a metacentric pair was associated with NORs. The 5S rDNA sites were located on the short arms of a single submetacentric chromosomal pair, close to the centromeres, except in T. auritus, which had up to ten 5S rDNA sites. The 18S and 5S rDNA sites were co-localized and adjacent on the short arms of a chromosomal pair in two populations of T. nematurus. Although all Triportheus species have a similar karyotypic macrostructure, the results of this work show that in some species ribosomal genes may serve as species-specific markers when used in conjunction with other putatively synapomorphic features.

Key words: chromosomal markers, fish cytogenetics, NOR, ribosomal genes.


 

 

Introduction

The advent of fluorescent in situ hybridization (FISH) has made it possible to map specific DNA sequences in plants and animals. In fish, the location of ribosomal genes (45S and 5S rDNA) has been widely used to characterize species and populations and/or to establish evolutionary relationships. Two important features have contributed to the widespread use of FISH with ribosomal DNA probes, namely, the organization of rRNA genes that consist of multiple repeats and the presence of highly conserved nucleotide sequences that are very similar among eukaryotes in general.

Fish of the genus Triportheus, popularly known as "sardinhas de água doce", "sardela" or "sardinha facão", have a widespread distribution throughout South America, ranging from Colombia to Uruguay. These fish, which may reach 20-24 cm in length, are an important source of food in certain regions of Brazil such as the Amazon. In a recent review of the genus, Malabarba (2004) considered 16 valid species, with some of the names being regarded as synonyms whereas other new species were described. Among the nomenclatural changes introduced in this revision, it was included T. elongatus as synonymous of T. auritus, T. flavus as synonymous of T. angulatus and T. paranensis as synonymous of T. nematurus. This updated nomenclature was used in the present report, concerning the species now investigated as well as other species previously analyzed.

The first cytogenetic studies of Triportheus were done by Falcão (Falcão JN, PhD thesis, University of São Paulo, Brazil, 1988) who analyzed the species T. albus, T. culter, T. auritus, T. angulatus and T. cf. signatus, followed by reports for T. guentheri, T. cf. auritus and distinct populations of T. nematurus (Bertollo and Cavallaro, 1992; Sánchez and Jorge, 1999; Artoni et al., 2001; Artoni and Bertollo, 2002; Diniz et al., 2008) and T. venezuelensis (Nirchio et al., 2007). All of these species and populations share a common diploid number, 2n = 52, and a very similar karyotypic macrostructure composed mainly of meta/submetacentric chromosomes and a ZZ/ZW sex chromosome system. The Z chromosome is the largest in the karyotype, whereas the morphology and size of the W chromosome are characteristic of each species, but always smaller than the Z element and nearly entirely heterochromatic (Falcão, op. cit.; Bertollo and Cavallaro, 1992; Sánchez and Jorge, 1999; Artoni et al., 2001; Artoni and Bertollo, 2002; Nirchio et al., 2007).

Active Ag-NORs in this fish group are usually located on the short arms of a submetacentric pair with secondary constrictions, and probably represent the main nucleolar organizer sites in Triportheus, although the size of the chromosomes involved may vary among species. In most species, single Ag-NORs are the common pattern, although variation in the number of these sites has been observed (Falcão, op. cit.; Artoni and Bertollo, 2002). T. venezuelensis, e.g., shows marked NOR polymorphism, with up to four Ag-NORs and seven 18S rDNA sites (Nirchio et al., 2007). An extra 18S rDNA site has also been reported at a terminal position on long arms of the W chromosome in T. nematurus, T. cf. auritus and T. guentheri (Artoni and Bertollo, 2002), and on the Z chromosome (Nirchio et al., 2007). In contrast, there is no information on the chromosomal location of 5S ribosomal sites in Triportheus species.

In this study, we examined the chromosomal locations of the 18S and 5S rDNA sites of several Triportheus species and populations, and assessed the usefulness of these sites as possible chromosomal markers within and among species.

 

Material and Methods

Specimens

Eight species and populations of Triportheus from distinct hydrographic basins in Brazil and Argentina were analyzed (Figure 1): T. trifurcatus (Rio Araguaia, MT - 9 males and 5 females), T. guentheri (Rio São Francisco, MG - 1 male and 5 females), T. cf. signatus (Rio Piranha-açu, Lago Itans, RN - 9 males and 13 females), T. albus (Rio Negro, AM - 3 females), T. auritus (Rio Negro, AM - 7 males and 1 female), T. angulatus (Rio Negro, AM - 2 females), T. nematurus (Rio Piracicaba, SP - 23 males and 17 females), T. nematurus (Rio Paraná, Corrientes, Argentina - 13 males and 3 females).

 

 

Chromosomal preparation

Mitotic chromosomes were obtained from anterior kidney cells. After killing the specimens, fragments of renal tissue were placed into 10 mL of RPMI culture medium and the cells were dissociated and processed according to Foresti et al. (1993).

Fluorescent in situ hybridization (FISH)

The chromosomal preparations were processed for fluorescent in situ hybridization (FISH), as described by Pinkel et al. (1986), using 18S (Hatanaka and Galetti Jr., 2004) and 5S (Martins and Galetti Jr., 1999) rDNA probes. The probes were labeled by nick translation (BioNick Labeling System – Invitrogen), according to the manufacturer's instructions. Double FISH was done in T. nematurus to simultaneously identify 18S and 5S rDNA clusters. The stained chromosomes were analyzed by epifluorescence microscopy with an Olympus BX50 microscope and the metaphase images were captured digitally using the software CoolSNAP-pro (Media Cybernetics).

 

Results

All of the species had the previously reported karyotypic features, i.e., the same diploid number (2n = 52) and a similar chromosomal macrostructure consisting of meta/submetacentric chromosomes. The occurrence of a ZZ/ZW sex chromosome system was also confirmed, with the Z chromosome being the largest metacentric element in the karyotype while the W chromosome had a distinct morphology and size that varied according to the species; this chromosome was invariably smaller than the Z chromosome.

In T. trifurcatus and T. auritus, only males gave good results in FISH. In the remaining species, the results were sufficiently good to allow the location of the 18S and 5S rDNA sites in both sexes.

 

18S rDNA FISH

In T. guentheri, T. cf. signatus, T. albus and T. nematurus, the males and females showed two hybridization signals on the short arms of a submetacentric pair, and the females also had 18S rDNA sites at a terminal position on the long arms of the W chromosome (Figures 2b-d and 4a,c). Four positive sites were identified in T. trifurcatus and T. auritus and occupied the short arms of two submetacentric pairs (Figures 2a, e). In T. angulatus, in which only females were studied, hybridization signals were observed on five chromosomes: in two cases they were located on the short arms of a metacentric pair, in another two cases they were located on the long arms of a meta-submetacentric pair (these two sites were probably homologous despite their slight difference in size) and in one case the site was located at a distal position on the long arm of the W chromosome (Figure 2f).

 



 

 



 

 


 

5S rDNA FISH

Only one pair of chromosomes bore 5S rDNA in T. trifurcatus, T. guentheri, T. cf. signatus, T. albus, T. angulatus and T. nematurus. Although identification of the chromosomal morphology was not possible in some preparations, the 5S rDNA sites were always located on the short arms of submetacentric chromosomes, either close to centromeres or to the telomeric region (Figures 3a-d, f and 4). The only exception to this pattern was T. auritus, which had ten 5S rDNA sites with a similar location relative to the other species (Figure 3e). In both populations of T. nematurus, the 18S and 5S ribosomal genes showed adjacent co-localization on the short arms of a submetacentric chromosomal pair, as shown by sequential hybridization (Figures 4a, b) and double-labeling FISH experiments (Figure 4c). The 5S rDNA sites were located closer to centromeres than the adjacent 18S sites (Figure 4c).

 

Discussion

At least two 18S rDNA sites were observed on the short arms of a submetacentric pair in virtually all of the species analyzed here. This chromosomal pair apparently corresponded to the Ag-NOR-bearing pair previously reported for Triportheus species (Falcão, op. cit.; Bertollo and Cavallaro, 1992; Artoni and Bertollo, 2002; Diniz et al., 2008), showing a similar position between the silver nitrate-stained sites and the 18S hybridization signals. Two additional sites were found in T. trifurcatus and T. auritus at a similar location, but in another submetacentric pair. In T. guentheri, a second chromosomal pair bearing Ag-NORs was reported by Bertollo and Cavallaro (1992), but it was not detected by FISH (Artoni and Bertollo, 2002; present study). Triportheus angulatus also had four 18S rDNA sites located on two metacentric and two submetacentric chromosomes, in agreement with previous Ag-NOR data (Falcão, op. cit.). In this case, a putative paracentric inversion involving NORs may have occurred in one homologue of the metacentric pair, resulting in the subdivision of major DNA cistrons into interstitial and terminal sites on this chromosome (Figure 2f, detail).

Triportheus has been regarded as a karyotypically conserved fish group, based on the identical diploid number (2n = 52), similar chromosomal macrostructure and presence of a ZZ/ZW sex chromosome system in the different species. However, as shown here, this conservativeness was not applicable to nucleolus organizer regions (NORs), which varied in number, position and chromosomal location among species. In this sense, T. venezuelensis was also notable for the extensive polymorphism of its Ag-NORs and/or 18S rDNA sites (Nirchio et al., 2007).

Another interesting chromosomal feature in Triportheus is the occurrence of 18S rDNA sites on the long arms of the W chromosome. This particularity has previously been reported for T. guentheri, T. nematurus (two populations) and T. cf. auritus (Artoni and Bertollo, 2002). As shown here, this feature was also found in another population of T. nematurus, as well as in T. cf. signatus, T. albus, T. angulatus and in a review of data for T. guentheri. These findings suggest that the presence of NORs on the W chromosome could be another characteristic shared by Triportheus species. However, in T. venezuelensis, 18S rDNA sites were unexpectedly located on the Z chromosome instead of the W chromosome (Nirchio et al., 2007). This unusual occurrence may reflect an ancestral location of rDNA sites at equivalent regions in the Z and W chromosomes of Triportheus. Presumably the 18S rDNA site was eliminated from the Z chromosome of some species, while in others this site remained unchanged, although not always active.

In agreement with this hypothesis, T. guentheri showed sporadic Ag-NORs in the telomeric region of the long arms of Z chromosomes (Bertollo and Cavallaro, 1992), although this has not been confirmed by FISH (Artoni and Bertollo, 2002). According to Nirchio et al. (2007), the lack of detection of some NOR sites by FISH may reflect a reduced number of gene copies in these regions, while the corresponding Ag-NOR sites may be identified after high transcriptional gene activity. The current evidence supports the hypothesis that the NORs detected on the W chromosomes of Triportheus probably represent a plesiomorphic condition in this genus that most likely predates differentiation of the sex chromosome system (Artoni and Bertollo, 2002).

In all of the species studied, the 5S ribosomal genes were detected on the short arms of a single submetacentric chromosomal pair, close to centromeres. The only exception to this pattern was T. auritus, which had up to ten positive signals in distinct chromosomal pairs, which could be a genetic marker for this taxon. Another interesting case with a high number of 5S rDNA sites was found in Centropyge aurantonotus (order Percifomes), a marine reef-associated species, where up to 18 sites could be identified in the karyotype. In this case, it was suggested the probable occurrence of pseudogenes in the species' genome (Affonso and Galetti Jr., 2005).

In general, the 18S and 5S rDNA sites are located on different chromosome pairs in distinct biological groups, and this feature is also the most commonly reported situation among fish (Martins and Galetti Jr, 1999, 2000, 2001). Ribosomal cistrons consist of different multigene families composed of hundreds to thousands of copies organized in tandemly arrayed repeats. According to Dover (1986), mechanisms such as gene conversion and unequal crossovers often occur within these gene arrangements during evolution. In this context, the location of 45S and 5S rDNA sites on different chromosomes and at different positions would prevent some unfavorable rearrangements such as the translocation of 18S rDNA segments into 5S rDNA sequences and vice versa. Thus, the results for T. nematurus, where occurs an adjacent co-localization of 18S and 5S rDNA sites on the short arms of a single chromosomal pair, represent an unusually feature. However, it is still possible that this feature might be shared by other Triportheus species since 18S and 5S rDNA sites were detected on the short arms of similar chromosomes. Unfortunately, sequential hybridization or double FISH was not done in species other than T. nematurus. Further studies could help to establish whether this feature is a synapomorphy for this group or corresponds to a unique chromosomal marker for T. nematurus.

 

Acknowledgments

The authors thank Dr. Maria Muhlmann-Diaz of the Molecular Cytogenetics Laboratory at the National Center of Atomic Energy (Buenos Aires, Argentina), for allowing us to use her laboratory for some of our experiments, and Celeste Mutuko Nakayama, Wagner Franco Molina, Lilian Cristina Jorge, Paulo César Venere and Issakar Lima Souza for providing the samples. We also thank Dr. Maria Claudia S. L. Malabarba (Museum of Sciences and Tecnology, PUCRS, Porto Alegre, RS) for help in identifying the specimens. This work was supported by Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq).

 

References

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Send correspondence to:
Luiz Antonio Carlos Bertollo
Departamento de Genética e Evolução, Universidade Federal de São Carlos
Caixa Postal 676
13565-905 São Carlos, SP, Brazil
E-mail: bertollo@power.ufscar.br

Received: January 25, 2008; Accepted: June 17, 2008.

 

 

Associate Editor: Fausto Foresti

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