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Neotropical Ichthyology

Print version ISSN 1679-6225On-line version ISSN 1982-0224

Neotrop. ichthyol. vol.12 no.4 Porto Alegre Oct./Dec. 2014  Epub Jan 09, 2015 


Molecular and cytogenetic analyses of cryptic species within the Synbranchus marmoratus Bloch, 1795 (Synbranchiformes: Synbranchidae) grouping: species delimitations, karyotypic evolution and intraspecific diversification

Ricardo Utsunomia 1  

José C. Pansonato-Alves 1  

Guilherme J. Costa-Silva 1  

Fernando F. Mendonça 2  

Priscilla C. Scacchetti 1  

Claudio Oliveira 1  

Fausto Foresti 1  

1Departamento de Morfologia, Instituto de Biociências, Universidade Estadual Paulista. Distrito de Rubião Junior, s/n, 18618-970 Botucatu, SP, Brazil. (RU) (corresponding author);;;;;

2Departamento de Ciências do Mar, Instituto do Mar, Universidade Federal de São Paulo. Av. Almirante Saldanha da Gama, 89, 11030-400 Santos, SP, Brazil.


The fish species Synbranchus marmoratus has been reported to exist as a species complex due to high intraspecific karyotypic variability in spite of the difficulty or impossibility to distinguish them using morphological traits alone. The goal of this work was to use cytogenetic and molecular methods to determine the species delimitations and understand the karyoevolution ofS. marmoratus using samples collected from distinct Brazilian localities. Among the analyzed specimens, a large degree of cytogenetic variation related to diploid numbers and karyotype structure was observed, with karyotypes showing 2n=42, 44 and 46 chromosomes. In addition, using sequences of three mitochondrial genes, the phylogenetic relationships between every sample with a known karyotype were determined, which revealed significant nucleotide divergence among the karyomorphs. Also, the analyses indicate that chromosomal rearrangements occurred independently within the distinct lineages of S. marmoratus complex, which resulted in the appearance of distinct karyotypic variants in a non-linear fashion related to diploid numbers and in the appearance of similar non-homologous chromosomes. Finally, the integration of both molecular cytogenetic and phylogenetic approaches allowed the determination of specific chromosomes possibly involved in rearrangements and a better understanding about the evolutionary processes involved in the differentiation ofSynbranchus genus.

Key words: Chromosomal diversity; Fish cytogenetics; karyotype evolution; Repetitive DNA; Species complex


A espécie de peixe Synbranchus marmoratus tem sido reportada como um complexo de espécies devido à elevada variabilidade cariotípica intraespecífica a despeito da dificuldade ou impossibilidade de distingui-las usando apenas caracteres morfológicos. O objetivo deste trabalho foi utilizar métodos citogenéticos e moleculares para determinar a delimitação das espécies e compreender a carioevolução de S. marmoratus utilizando amostras coletadas em distintas localidades brasileiras. Dentre os espécimes analisados, um alto grau de variação citogenética relativo aos números diploides e estrutura cariotípica foi observado, com cariótipos mostrando 2n=42, 44 e 46 cromossomos. Adicionalmente, utilizando sequências de três genes mitocondriais, as relações filogenéticas entre cada amostra com cariótipo conhecido foram determinadas, revelando uma divergência nucleotídica significativa entre os cariomorfos. Além disso, as análises indicam que rearranjos cromossômicos ocorreram independentemente nas distintas linhagens do complexo S. marmoratus, o que resultou no aparecimento de distintas variantes cariotípicas de forma não linear em relação aos números diploides e no surgimento de cromossomos similares e não homólogos. Finalmente, a integração de uma abordagem citogenética molecular e filogenética permitiu a determinação de cromossomos específicos que, possivelmente, estão envolvidos em rearranjos e um melhor entendimento sobre os processos evolutivos envolvidos na diferenciação do gênero Synbranchus.


Cryptic species are defined as two or more morphologically indistinguishable species that are incapable of interbreeding (Bickfordet al., 2007). Such species likely arise through interespecific reproductive isolation, which can be caused by pre-zygotic means, such as gametic incompatibility and/or ecological isolation (Miyatake et al., 1999; Landry et al., 2003), or by post-zygotic means, such as hybrid inviability and/or sexual selection against hybrids (Orr, 1995; Nooret al., 2001; Presgraves et al., 2002). Generally, these types of speciation events occur in organisms with little or no motility, making certain plants (Presgraves et al., 2002), insects (Campbell et al., 1994), fungi (Theodoroet al., 2008), small mammals (Green et al., 1980), amphibians (Kozak et al., 2006) and fishes (Moreira-Filho & Bertollo, 1991) suitable model organisms for studying this phenomenon. Although morphological differences between cryptic species are minimal, other traits can be used to detect these species complexes, including behaviour (Crossley, 1986), karyotype structure (Moreira-Filho & Bertollo, 1991; Dobigny et al., 2002; Amaro et al., 2012) and protein (Nakamoto et al., 1986; Fong & Garthwaite, 1994) and DNA (Kazan et al., 1993; Hebert et al., 2004) sequences.

Neotropical fishes are excellent models for studying cryptic species, as they are distributed widely across continents and have a propensity to form endemic and isolated populations, often culminating in allopatric differentiation (Lundberg et al., 1998; Ribeiro, 2006). In addition, natural or unnatural random events, such as headwater capture or changes in watercourses, can lead to secondary contacts between previously separated species (Blanco et al., 2009; Peres et al., 2009), providing ideal scenarios to study novel species complexes. Indeed, such complexes have already been studied in a variety of fish orders, including Characiformes, Synbranchiformes, and Gymnotiformes (Moreira-Filho & Bertollo, 1991; Torres et al., 2005; Milhomemet al., 2008).

Fishes belonging to the genus Synbranchus (Synbranchiformes, Synbranchidae) are currently divided into three recognized species: (1)S. madeirae Rosen & Rumney, 1972, which is restricted to the Madeira River basin; (2) S. lampreia Favorito, Zanata & Assumpção, 2005, which is restricted to Marajó Island; and (3) S. marmoratusBloch, 1795, which is widely distributed throughout South and Central America (Rosen & Rumney, 1972). AlthoughS. marmoratus specimens appear to belong to a single taxonomic group, some populations may display an extensive karyotype diversity, with diploid numbers ranging from 42 to 46 chromosomes; furthermore, variations in chromosome morphology as well as in the distribution of constitutive heterochromatin and rDNA genes have also been observed (Foresti et al., 1992; Melilo et al., 1996; Sanchez & Fenocchio, 1996; Torres et al., 2005). Although distinguishing the intraspecific S. marmoratus groups is relatively easy with cytogenetic tools, distinguishing between these groups based solely on morphology is often impossible (Rosen & Rumney, 1972), making the identification of new species difficult. Furthermore, one must say that karyotypic structural analyses are limited in their utility; for example, whereas these analyses can identify chromosomal diversity and suggest possible rearrangements leading to this diversity, the chronological order in which such events occurred and the evolutionary relationships among the karyomorphs cannot be directly determined.

Considering the wide distribution of S. marmoratusthroughout the waters of South and Central America, the purpose of this study was to characterize the karyotypes of distinct groups within this species and determine whether divergent species exist within the current S. marmoratusgrouping, to analyze the relationships between the sampled taxa and to investigate the history of chromosomal rearrangements in this species as a whole.

Material and Methods

A total of 75 S. marmoratus specimens were collected from distinct Brazilian localities (Fig. 1, Table 1) and analyzed in the present study. The specimens were identified as previously reported (Rosen & Greenwood, 1976). Following analysis, the fish were fixed in 10% formalin, stored in 70% ethanol and deposited in the fish collection of the Laboratório de Biologia e Genética de Peixes - UNESP, Botucatu, São Paulo, Brazil. Voucher information is shown in Table 1. Two specimens of Ophisternon aenigmaticum Rosen & Greenwood, 1976, basal sister species ofSynbranchus (Miya et al., 2003), from Isla Margarita, Venezuela were included as out-groups for the molecular analyses.

Fig. 1. A map showing the Synbranchus marmoratus specimen collection sites. Numbers indicate the sample locality, whereas symbols represent the karyomorphs found at each locality. 

Table 1. Specimens of Synbranchus marmoratus analysed. N, Number of samples; LBP, deposit number at the fish collection of the Laboratório de Biologia e Genética de Peixes, Instituto de Biociências de Botucatu, UNESP. 

Locality River Basin Karyomorph (N) Map Coordinates LBP
Cerrito – RS Laguna dos Patos C(3) 1 31°52’31 S – 52°48’58 W 11356
Guaíra – PR Upper rio Paraná B(20) 2 24°04’13 S – 54°12’08 W 11364
Bataguassu - MS Upper rio Paraná A(3) 3 21°38’49 S – 52°17’52 W 11355
Igaraçu do Tietê – SP Rio Tietê A(13) / E(2) 4 22°34’43 S – 48°27’48 W 17518/17519
Pirassununga – SP Rio Grande A(11) / D(2) / E(5) 5 21°55’41 S – 47°22’85 W 17512/17513/17514
Icém – SP Rio Grande A(6) / D(3) 6 20°20’13 S – 49°07’56 W 17515/17516
Cáceres - MT Rio Paraguai A(5) 7 16°02’29 S – 57°40’52 W 11357
Rio Branco - AC Rio Amazonas C(5) 8 57°54’94 S – 67°44’41 W 17520

Cell suspensions and chromosome banding. Fish were anaesthetized with a benzoncaine solution before being sacrificed for cytogenetic analyses. Mitotic chromosomes were obtained from cell suspensions of anterior kidney tissue using standard methods (Foresti et al., 1981). In addition to Giemsa staining, chromosomes were analyzed using a C-banding procedure to visualize constitutive heterochromatin (Sumner, 1972) and Ag-NOR staining to detect active nucleolar regions (Howell & Black, 1980).

Fluorescence in situ hybridization (FISH) was performed using the method described by Pinkel et al., (1986). Ribosomal 5S and 18S probes, isolated from the genome ofS. marmoratus (karyomorph B) were labeled during secondary PCR by incorporating the nucleotide biotin-16-dUTP (Roche Applied Science) (5S rDNA) and digoxigenin-11-dUTP (Roche Applied Science) (18S rDNA) and the detection of hybridization signals was obtained with avidin-FITC and anti-digoxigenin-rhodamine, respectively. Chromosomes were counterstained with DAPI (4', 6-diamidino-2-phenylindole, Vector Laboratories).

Chromosomal morphology was determined as described previously (Levan et al., 1964), and samples were classified as metacentric (m), submetacentric (sm), subtelocentric (st) or acrocentric (a).

Molecular analyses. For the molecular analyses, 42 samples were selected to represent all known karyomorphs from every sampled locality, and DNA was extracted using the Wizard Genomic DNA Purification Kit (Promega, Heidelberg, Germany), as suggested by the manufacturer. Partial sequences from the mitochondrial genes COI, CytB, and 16S were obtained for each sample using the primers described by Ward et al. (2005), Kocheret al. (1989) and Palumbi (1996) The PCR products were purified using ExoSap-IT (USB Corporation, Cleveland, OH, USA), according to the manufacturer's instruction, and the fragments were sequenced using an ABI Prism 3110 DNA sequencer (Applied Biosystems, Foster City, CA, USA) and the Big DyeTM Terminator v 3.1 Cycle Sequencing Ready Reaction Kit (Applied Biosystems, Foster City, CA, USA). The sequences were aligned using the software program BioEdit, version 7.0.9 (Hall, 1999), and deposited in the GenBank database under the accession numbers KC880197-KC880242 (COI), KC880243-KC880288 (CytB) and KC880289-KC880334 (16S).

For the phylogenetic analyses, the gene sequences were aligned using the MUSCLE algorithm (Edgar, 2004) and concatenated into a single matrix, which was separated into seven partitions: one for the noncoding 16S gene and six corresponding to each of the three codon reading frames for the two protein-coding genes CytB and COI. A matrix saturation test was conducted using the DAMBE software program, version 5.1.1, as described previously (Xia et al., 2003). A search for the best model of nucleotide evolution for each partition was performed using Modeltest, version 3.6 (Posada & Crandall, 1998). The phylogenetic analysis based on Maximum Likelihood (ML) was performed using the RaxML-HPC2 tool on XSEDE (Stamatakis et al., 2008). A bootstrap test using 1,000 pseudo-replicates (Felsenstein, 1985) was used as a statistical test of phylogeny.

Ethics statement. Samples were collected in accordance with Brazilian environmental protection legislation (collection permission MMA/IBAMA/SISBIO - number 3245), and the procedures for collection, maintenance and analysis of the fish were performed in compliance with the Brazilian College of Animal Experimentation (COBEA) and was approved (protocol 503) by the BIOSCIENCE INSTITUTE/UNESP ETHICS COMMITTEE ON USE OF ANIMALS (CEUA).


Cytogenetic analyses. Conventional Giemsa staining revealed the existence of five distinct groups, which could be described using the following karyotypic formulae (Figs. 2a-f): 2n=42 (4m + 12st + 26a), referred to as karyomorph A; 2n=42 (6m + 10sm + 30a), referred to as karyomorph B; 2n=44 (4m + 10st + 30a), referred to as karyomorph C; 2n=46 (6m + 10st + 30a), referred to as karyomorph D; and 2n=46 (4m + 10st + 32a), referred to as karyomorph E. Each karyomorph showed a distinct distribution among the collection sites, with sympatric karyomorphs being found at Igaraçu do Tietê (karyomorphs A and E), Pirassununga (karyomorphs A, D and E) and Icém (karyomorphs A and D). Information concerning each karyomorph and the localities in which specimens were collected is summarized in Table 1.

Fig. 2. Karyotypes of Synbranchus marmoratus after FISH with 5S (green) and 18S (red) rDNA, and metaphase plates after silver staining and C-banding of Karyomorph A (a, g, m), B (b, h, n), C-Cerrito (c, i, o), C-Rio Branco (d, j, p), D (e, k, q) and E (f, l, r). The interindividual polymorphisms of 18S rDNA distribution are highlighted as "variation" in the karyotypes. The arrows indicate the Ag-NOR bearing sites chromosomes and the positive C-banding in these chromosomes. Bar = 10 mm. 

Ag-NORs were revealed at the terminal position in the 15th pair of chromosomes in karyomorph A, in the 15th pair in karyomorph B, in the 15th pair and in one of the homologues of pair 9 in karyomorph C, in the 2nd pair in karyomorph D and in the 3rd pair in karyomorph E (Figs. 2g-l). Furthermore, interstitial heterochromatic blocks associated with the active NOR sites were detected (Figs. 2m-r).

The C-banding technique revealed centromeric constitutive heterochromatin, as well as some interstitial blocks on particular chromosome pairs, such as in pair 2 of karyomorphs A and B and pair 3 of karyomorphs B, C and E (Figs. 2m-r; Supplementary file 1). These characteristics allowed us to infer certain chromosomal homologies between the different karyomorphs, which are represented in the ideogram in Fig. 3 constructed using organized karyotypes (Supplementary file 1).

Fig. 3. Representative ideograms of the analyzed karyomorphs of Synbranchus marmoratus showing the heterochromatic blocks, as determined by C-banding, and hybridization patterns of ribosomal sites. 

FISH experiments with 5S rDNA probes revealed that all of the analyzed samples had only two clusters of the 5S ribosomal gene in the interstitial position of a homologous acrocentric chromosomal pair (Figs. 2a-f), except samples of karyomorph C collected at Rio Branco, which presented an additional 5S rDNA-bearing pair (Fig. 2d). In contrast, the 18S rDNA probes revealed distinct hybridization patterns between the karyomorphs. In addition, the hybridizations demonstrated intrapopulational variability at the 18S rDNA sequences, revealing that these populations are polymorphic in the number and chromosomal distribution of these sites. Remarkably, each karyomorph had two constant chromosomal clusters present in all individuals, which corresponded to the Ag-NOR-bearing pairs: pair 15 (karyomorph A), pair 15 (karyomorph B), pair 15 (karyomorph C-Cerrito), pair 3 (karyomorph C-Rio Branco), pair 2 (karyomorph D) and pair 3 (karyomorph E) (Figs. 2a-f).

Molecular analyses. Molecular data consisted of 2,150 nucleotides, of which 414 were polymorphic sites and 389 parsimony informative. The matrix saturation test indicated that there are not saturations in the genes. Appropriate evolutionary models for the genes were investigated in Modeltest 3.6 (Posada & Crandall, 1998) and the best fit-model to each partition was GTR+I (16S), TrNef+I (Codon 1 COI), F81 (Codon 2 COI), GTR (Codon 3 COI), TrN+I (Codon 1 CytB), TrN+I (Codon 2 CytB), HKY+I (Codon 3 CytB).

Phylogenetic analysis yielded the dendrogram shown in Fig. 4, which provided significant statistical support for each node. Furthermore, the analysis revealed complex biogeographical relationships, with certain localities bearing only single karyomorphs and other localities showing different karyomorphs living in sympatry. In addition, it was also shown that karyomorphs with the same diploid number do not necessarily constitute monophyletic groups. Also, the analyses provided evidence for the existence of two main clades within S. marmoratus (I and II), one of which can be further subdivided into four subclades (IA, IB, IC and ID). Thus, subclades IA, IB and IC contain specimens sharing the same karyomorph (A); subclade IB is composed of specimens belonging to different karyomorphs (A and B); subclade ID is composed solely of karyomorph D specimens; and clade II is composed by specimens belonging to karyomorphs C and E (Fig. 4).

Fig. 4. A dendrogram representing the relationship between the sampled Synbranchus marmoratus specimens based on the mitochondrial 16S, COI and Cyt B genes. The colors represent each of the characterized karyomorphs, and the groups (IA, IB, IC, ID and II) used as references are shown on the right side. Bootstrap support (>50%) are given above the branches. Diploid numbers of the samples are given along the branches. 2n=46* Diploid number of Ophisternon aenigmaticum (Nirchio et al., 2011). 


Morphological differences between species in the Synbranchiformes order are commonly used in systematic and biogeographical studies (Rosen & Rumney, 1972; Rosen & Greenwood, 1976; Favorito et al., 2005). However, many morphological traits can be subtle or ambiguous, which often makes it difficult to recognize and describe new species. Therefore, it is necessary to increase the number of tools and characteristics available for differentiating species from this group (Nakamoto et al., 1986; Foresti et al., 1992; Melilo et al., 1996; Sanchez & Fenocchio, 1996; Perdices et al., 2005; Torres et al., 2005; Nirchio et al., 2011; Carvalho et al., 2012). In the present study, several karyomorphs of S. marmoratus collected in distinct Brazilian river basins were described. From these, sympatric karyomorphs were sampled in three distinct localities and the lack of reports of hybrids reinforces the hypothesis that exists as a species complex, which point the need of a deep taxonomic review in this group.

The phylogenetic analyses evidenced the existence of five distinct groups (clades IA, IB, IC, ID and II) within S. marmoratus. However, these results suggest that such grouping do not correspond to the five described karyomorphs reciprocally, indicating that not every karyomorph correspond to a unique species (e.g., karyomorph C), nor a single species is represented by one karyomorph (e.g., karyomorphs A and B). Therefore we propose the existence of, at least, five species withinS. marmoratus complex. Thus, karyomorphs D and E represent one species each; karyomorph C is split in two species; and karyomorph A and B represent one single species in initial stages of differentiation.

Although more detailed information concerning the geographic distribution ofS. marmoratus specimens is needed, acquiring such data is often problematic; for example, these species are widely used as fisheries bait, which can result in the widespread accidental introduction of these organisms into new environments. As a consequence of fish transposition, the specimens from karyomorph A sampled at Cáceres (Paraguay River basin) should be noted, as this karyomorph is positioned between two distinct branches of the dendrogram that includes specimens from the Parana River basin (Icém and Igaraçu do Tietê) (Fig. 4). Considering that many recreational fishermen frequent the Cáceres region, it is possible that these animals originated as bait fish from the Paraná River. Therefore, sample transposition events can be very harmful and make biogeographical and historical studies in this group difficult.

The debate concerning the relationship between chromosomal rearrangements and speciation has been long and controversial (Trickett & Butlin, 1994; Rieseberg, 2001; Noor et al., 2005; Hoffman & Rieseberg, 2008; Faria & Navarro, 2010). Although the data presented here are not strong enough to determine whether chromosomal alterations were the cause or consequence of speciation in Synbranchus, it was possible to demonstrate that within subclade IB, two distinct karyomorphs (A and B) from nearby localities constitute the same haplotype and constitute a monophyletic group (Fig. 4). Namely, karyomorph B contained a small pair of metacentric chromosomes, whereas karyomorph A lacked these chromosomes, a difference which most likely arose after the occurrence of a pericentric inversion in a submetacentric chromosome in karyomorph A (Fig. 3). Although small metacentric chromosomes can be observed in all other karyomorphs (with the exception of karyomorph A), the phylogenetic tree highlighted that this specific chromosome pair present in karyomorph B likely arose independently from the small metacentric chromosomes observed in the other samples, since this is a more parsimonious hypothesis than one claiming a common origin for these chromosomes at the base of the Synbranchus lineage with a more recent loss of these chromosomes in all karyomorph A lineages.

The occurrence of species with distinct diploid numbers in Synbranchidae reveals that fusion/fission rearrangements are fundamental mechanisms in the karyoevolution of this group (Torres et al., 2005; Carvalho et al., 2012). Hypotheses concerning the primitive diploid number inSynbranchus have already been proposed, but lead to opposite predictions (Melilo et al., 1996; Torres et al., 2005). Herein, based on the karyotypic information plotted on a phylogenetic tree of S. marmoratus an alternative hypothesis concerning chromosomal differentiation patterns inSynbranchus can be suggested.

Although the deduction of an ancestral karyomorph was not possible, our phylogenetic analyses support the hypothesis that homoplastic cytogenetic events occurred inS. marmoratus and are related to the origins of the karyomorphs showing 2n=44 (karyomorph C-Rio Branco and karyomorph C-Cerrito) and 2n=46 (karyomorphs D and E) chromosomes. Therefore, a chromosome fusion event could have led to the karyomorph showing 2n=44 chromosomes, with a subsequent reversion event (via chromosome fission) returning the diploid number to 2n=46 (karyomorph E); another hypothesis states that both karyomorph C samples (2n=44) could have originated in parallel by independent fusion events. Despite the absence of a clear evolutionary pathway, one should note that one of these homoplasies did occur. In this way, we hypothesize that independent and potentially bidirectional rearrangements, such as fusion and fission events, were responsible for the appearance of distinct diploid numbers and karyotype arrangements observed in this species complex.

Variations related to NORs have already been detected in Synbranchusand indicate that microstructural rearrangements occur frequently and contribute to the karyotypic differentiation of these fish (Foresti et al., 1992; Melillo et al., 1996; Sanchez & Fenocchio, 1996; Carvalho et al., 2012). Herein, an extensive intrapopulational polymorphism of 18S rDNA sites in several karyomorphs was detected and seems to be related to the association of these sequences with transposable elements or with their telomeric position, which would facilitate the transference of this material during interphase (Forestiet al., 1981; Mantovani et al., 2005). Furthermore, these polymorphic differences have also been detected in other Synbranchus species (Carvalho et al., 2012), suggesting that this is a common characteristic in this group of organisms. Thus, 18S rDNA dispersion was likely already present before the diversification of these species/karyomorphs. Moreover, intrapopulational polymorphism would be potentiated by gametic combination and therefore contribute to the diversification of these sites.

Remarkably, from all analyzed individuals, only one pair of 18S rDNA-bearing chromosomes was constant, in contrast to the occurrence of several random variants. In most cases, Ag-NORs were located in these constant pairs; this finding is likely a consequence of an epigenetic phenomenon that controls the effective dosage of rRNA genes, such as nucleolar dominance (Pikaard, 2000; Hashimoto et al., 2009). An interesting feature observed here is the co-localization of heterochromatic blocks with the active NORs, unlike the other 18S rDNA variants. Thus, the mechanism responsible for this situation may be related to the associated heterochromatin that is likely located in the intergenic spacers of 45S rDNA.

Finally, the identification of specific marker chromosomes in certain karyomorphs, which could be tracked by unique morphologies, banding characteristics or repetitive DNAs distribution patterns, could be informative with respect to the genomic rearrangements that occurred during the evolutionary history ofSynbranchus and help understand the phylogenetic relationships between the karyomorphs. Thus, karyomorphs A and B share the exclusive second metacentric pair containing one interstitial heterochromatic block within the long arm and the first submetacentric pair containing two interstitial heterochromatic blocks within the long arm. Besides that, both had the same constant 18S rDNA sites-bearing chromosomes (pair 15). Marker chromosomes also confirm the proximity between karyomorphs C and E, which share the first subtelocentric pair containing one interstitial heterochromatic block within the long arm. Moreover, karyomorph C (Rio Branco) and E have constant sites of 18S rDNA in this same pair. However, the presence of similar chromosomes in distinct lineages can be misleading; for example, a small metacentric pair was identified in karyomorphs B, C, D, and E, although the origin of this pair in karyomorph B was independent of the others. Besides, the detection of an additional 5S rDNA-bearing acrocentric pair observed in individuals belonging to karyomorph C-Rio Branco and some 18S rDNA chromosomal variants of karyomorphs C-Cerrito and E, that evidence sinteny between both ribosomal sites also casts doubt on the real homology of the 5S rDNA-bearing chromosomes in all karyomorphs. Therefore, the nature of the homology between these specific chromosomes remains unclear, and it highlights the importance of phylogenetic and/or chromosome painting analyses to reduce possible misinterpretations of karyoevolution in organisms.


This study was supported by Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP), Coordenadoria de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq). The authors would like to thank D. T. Hashimoto, G. T. Rocha and M. R. Vicari for their substantial contributions to the manuscript.

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Received: March 24, 2014; Accepted: September 04, 2014

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