8urn:lsid:arphahub.com:pub:A71ED5FC-60ED-5DA3-AC8E-F6D2BB5B3573urn:lsid:zoobank.org:pub:C8FA3ADA-5585-4F26-9215-A520EE683979Comparative CytogeneticsCCG1993-07711993-078XPensoft Publishers10.3897/CompCytogen.v10i4.95079507Research ArticleAnimaliaCallichthyidaeChordataOsteichthyesPiscesSiluriformesGeneticsKaryosystematicsBrazilAn uncommon co-localization of rDNA 5S with major rDNA clusters in Callichthyidae (Siluriformes): a report case in Corydorascarlae Nijssen & Isbrücker, 1983da RochaRafael Henrique1BaumgärtnerLucas2PaizLeonardo Marcel23MargaridoVladimir Pavan23FernandesCarlos Alexandre4fxande@gmail.comGubianiÉder André1Universidade Estadual do Oeste do Paraná, Centro de Engenharias e Ciências Exatas, 85903-000 Toledo, Paraná, BrazilUniversidade Estadual do Oeste do Paraná, Centro de Ciências Biológicas e da Saúde, 85819-110 Cascavel, Paraná, BrazilUniversidade Estadual de Maringá, Centro de Ciências Biológicas, 87020-900 Maringá, Paraná, BrazilUniversidade Estadual de Mato Grosso do Sul, Unidade Universitária de Mundo Novo, 79980-000 Mundo Novo, Mato Grosso do Sul, Brazil
Corresponding author: Carlos Alexandre Fernandes (fxande@gmail.com)
Academic editor: N. Bogutskaya
201618112016104603613FFD37542-FFE4-FFB6-FFE6-FFC5FFC63B40CBDEBC52-CB24-47A9-B7E3-62ED285BB9B211390381006201612102016Rafael Henrique da Rocha, Lucas Baumgätner, Leonardo Marcel Paiz, Vladimir Pavan Margarido, Carlos Alexandre Fernandes, Eder Andre GubianiThis is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.http://zoobank.org/CBDEBC52-CB24-47A9-B7E3-62ED285BB9B2
Corydoras Lacepède, 1803 is the most specious genus of Corydoradinae subfamily and many of its species are still unknown in relation to molecular cytogenetic markers. However, the diploid number and karyotypic formula were recorded for many species of this group. In current study, we provided the first cytogenetic information of Corydorascarlae Nijssen & Isbrücker, 1983, an endemic fish species from Iguassu River basin, Paraná State, Brazil. The individuals were collected in Florido River, a tributary of Iguassu River and analysed with respect to diploid number, heterochromatin distribution pattern, Ag-NORs and mapping of 5S and 18S ribosomal genes. The karyotype of this species comprises 46 chromosomes arranged in 22m+22sm+2st. The heterochromatin is distributed in centromeric and pericentromeric positions in most of the chromosomes, and also associated with NORs. The Ag-NORs were detected in the terminal position on the long arm of the metacentric pair 6. The double-FISH technique showed that 5S rDNA and 18S rDNA were co-localized in the terminal portion on the long arm of the metacentric pair 6. This condition of co-localization of ribosomal genes in C.carlae seems to represent a marker for this species.
Rocha RH, Baumgärtner L, Paiz LM, Margarido VP, Fernandes CA, Gubiani ÉA (2016) An uncommon co-localization of rDNA 5S with major rDNA clusters in Callichthyidae (Siluriformes): a report case in Corydoras carlae Nijssen & Isbrücker, 1983. Comparative Cytogenetics 10(4): 603–613. doi: 10.3897/CompCytogen.v10i4.9507
Introduction
In higher eukaryotes, rDNA is organized into two distinct gene classes: major class (45S rDNA), which contains the genes that code for the 18S, 5.8S and 28S rRNAs, and the minor class (5S rDNA), which contains the genes that code for 5S rRNA. Fish species have been analyzed for 5S and 18S rDNA location in chromosomes using
fluorescent in situ hybridization
(FISH). The major rDNA sequences detected by FISH always coincided with
silver-stained NORs
(Ag-NORs) location, although in species with multiple Ag-NORs the number of markings was usually smaller than the regions detected by the DNA probes.
The most common condition in the karyotype of different fish groups is the positioning of ribosomal genes in different chromosome pairs (Galetti Jr. and Martins 2004). However, syntenic localization of the major rDNA clusters and the 5S sites were observed for the first time in the genus Corydoras Lacepède, 1803 (present study) and Callichthyscallichthys (Linnaeus, 1758) (Konerat et al. 2014), the other integrant of the family Callichthyidae. In Loricariidae, Kronichthyslacerta (Nichols, 1919), Isbrueckerichthysduseni (Miranda Ribeiro, 1907), Parotocinclusmaculicauda (Steindachner, 1877) and Trichomycterus sp. (Ziemniczak et al. 2012) also presented syntenic localization of ribosomal genes. Thus, the mapping of ribosomal genes has added important information about the chromosomal diversification in Corydoras, as in other groups of Siluriformes.
Callichthyidae is a family of the order Siluriformes widely distributed in Neotropical region, which has 215 valid species, divided in two subfamilies, Callichthyinae with 17 valid species and Corydoradinae with 198 valid species (Eschmeyer and Fong 2016). Corydoras is the most specious and cytogenetically studied genus of Corydoradinae, demonstrating different diploid numbers, which may vary from 2n = 40 chromosomes in C.nattereri Steindachner, 1876 (Oliveira et al. 1990, 1993) to 2n = 134 chromosomes in C.aeneus (Gill, 1858) (Turner et al. 1992).
Considering aspects related to number and morphology of chromosomes, as well as analysis of DNA content, Oliveira et al. (1992) and Shimabukuro-Dias et al. (2004) proposed the existence of five groups of species in Corydoras. However, the vast majority of studies in Corydoras is restricted to conventional analysis and little is known about location of the different types of rDNA, only in C.paleatus (Jenyns, 1842) and C.ehrhardti Steindachner, 1910 for 18S rDNA (Artoni et al. 2006) and C.britskii (Nijssen & Isbrücker, 1983) for 18S and 5S rDNA (Takagui et al. 2014), making essential the development of studies with this approach to better understand the relationships between species of Corydoras.
Thus, the current paper presents the first cytogenetic description of Corydorascarlae, focusing on karyotype characterization, heterochromatin distribution pattern and location of 5S and 18S rDNA sites. Besides the new data for the species, this study also reveal for the first time the co-localization of 5S and major rDNA in Callichthyidae.
Materials and methods
Ten individuals (four females and six males) of Corydorascarlae were sampled in the Florido River (26°00'32.60"S; 53°25'50.70"W), Paraná State, Brazil. A sub-tributary of left margin of Lower Iguassu River that flows into Capanema River, which flows immediately above of the Iguassu falls (Fig. 1). Voucher specimens were deposited in the fish collection of the
Núcleo de Pesquisas em Limnologia Ictiologia e Aquicultura
(NUPELIA), Universidade Estadual de Maringá, Paraná, Brazil, as Corydorascarlae (NUP 17885).
6D22D44B-397B-55E4-9005-DF4AE3F881BB
Localization of Florido River from the Iguassu River basin, where Corydorascarlae individuals were captured. Red triangle indicates the sampled point.
https://binary.pensoft.net/fig/111571
This study was carried out in strict accordance with the recommendations of the Guide for the Care and Use of Laboratory Animals, approved by the Committee on the Ethics of Animal Experiments of the Universidade Estadual do Oeste do Paraná (License Number: Protocol 13/09 – CEEAAP/Unioeste). Before the evisceration process, the individuals were anesthetized by an overdose of clove oil (Griffiths 2000). Metaphase chromosomes were obtained from anterior kidney cells using the air-drying technique (Bertollo et al. 1978). Analysis of the C-positive heterochromatin (C-bands) followed the basic procedure of Sumner (1972), with some minor adaptations (Lui et al. 2012). The NORs were detected by means of silver nitrate staining (Ag-NORs), according to Howell and Black (1980). The chromosomes were classified as
metacentric
(m),
submetacentric
(sm), and
subtelocentric
(st) according to their arm ratio (Levan et al. 1964). For the determination of the
fundamental number
(FN), or number of chromosome arms, the m, sm and st chromosomes were considered as bearing two arms and the acrocentric chromosomes only one arm.
The localization of the 5S and 18S rDNA sites in the chromosomes was performed using the fluorescence in situ hybridization (FISH) method (Pinkel et al. 1986) with modifications (Margarido and Moreira-Filho 2008), with probes obtained from the fish species Leporinuselongatus Valenciennes, 1850 (Martins and Galetti Jr 1999) and Prochilodusargenteus Spix & Agassiz, 1829 (Hatanaka and Galetti Jr 2004), respectively. The probes were labelled through nick translation, with digoxigenin-11-dUTP (5S rDNA) and biotin-16-dUTP (18S rDNA) (Roche). Detection and amplification of the hybridization signal were made using avidin-FITC and anti-avidin biotin (Sigma) for probes labelled with biotin, and anti-digoxigenin rhodamine (Roche) for probes labelled with digoxigenin. Slides were counterstained with DAPI (50 µg/mL) and analysed in epifluorescence microscope (Olympus BX61). The images were captured using the software DP controller (Media Cybernetics).
Results
Corydorascarlae presented a modal diploid number of 46 chromosomes in males and females, and the karyotype contained 22 metacentric, 22 submetacentric and 2 subtelocentric chromosomes (22m+22sm+2st), yielding a FN of 92 in both sexes (Fig. 2a). The Ag-NORs was detected in the terminal position on the long arm of metacentric pair 6 (Box Fig. 2a). Positive C-band heterochromatins were detected in the centromeric and pericentromeric regions of nine and eight pairs, respectively, and coincident with the ribosomal sites (Fig. 2b). The double-FISH technique showed 5S rDNA cluster appears interspersed with 18S cistrons in the terminal portion of the long arm of pair 6 (Fig. 2c). Thus, featuring synteny and co-location of ribosomal genes in C.carlae. The ideogram summarizes all markers on chromosomes of C.carlae (Fig. 3).
9513C6B6-08AD-57E2-BF4C-D1EB7E6D1665
Karyotypes of Corydorascarlae stained with a Giemsa b C-banded and c after double FISH with 5S rDNA probes (red) and 18S rDNA (green). The NORs bearing chromosomes (pair 6) are boxed. Bar = 10 µm.
Ideogram of Corydorascarlae, showing the heterochromatin, Ag-NORs, 18S and 5S rDNA distribution pattern.
https://binary.pensoft.net/fig/111573Discussion
Cytogenetic studies have classified the species of the genus Corydoras into five groups according to their karyotype composition (Oliveira et al. 1992, Shimabukuro-Dias et al. 2004). Corydorascarlae has been included in group 4 (2n = 40-52 chromosomes, with many metacentric and submetacentric chromosomes). Considering our results, three species of this group occurring in the Iguassu River basin were cytogenetically analyzed: C.carlae (2n=46, 22m+22sm+2st), collected in the Lower Iguassu River; C.paleatus (2n=44, 20m+24sm) collected in the Upper Iguassu River (Oliveira et al. 1993), and C.paleatus and C.ehrhardti (2n=44, 18m+26sm), collected in the Upper Tibagi River (Artoni et al. 2006).
Individuals of C.carlae analyzed here probably do not co-occur with C.paleatus from Upper Iguassu River, since the lower portion is characterized by numerous waterfalls which gave rise to several reservoirs (Baumgartner et al. 2012). Therefore, the geographic isolation of C.carlae may have facilitated the establishment of this numerical and structural karyotypic variation, as also observed in different populations of Glanidiumribeiroi Haseman, 1911 along the Iguassu River basin (Lui et al. 2015). Thus, the lack of gene flow among Corydoras species in the Iguassu River basin could favor different changes in each sample, supposedly resulting in speciation.
The number and position of NORs in Corydoras species are quite variable and almost all information pertaining to the characterization of NORs in this species is based on silver nitrate impregnation (Table 1). These data show that most species have simple NORs located in the terminal position, as in the case of C.carlae. However, not all species have this pattern, as in the case of C.simulatus Weitzman & Nijssen, 1970 with interstitial NORs (Oliveira et al. 1992), as well as C.britskii (Takagui et al. 2014), C.simulatus, Corydoras sp. Galheiro river, C.flaveolus Ihering, 1911 and C.metae Eigenmann, 1914 (Oliveira et al. 1992), which exhibits a systems of multiple NORs. According to Oliveira and Gosztonyi (2000), the condition of simple Ag-NORs in terminal location is the possible basal condition for Siluriformes. Thus, C.carlae and other species presenting simple Ag-NORs in terminal location seem to maintain this basal condition.
Ag-NORs, major and minor ribosomal genes sites distribution in Callichthyidae. The 45S and 5S columns report the number of chromosomes bearing the cistrons and its location.
Family Callichthyidae
Locality
2n
Ag-NOR
45S
5S
Note
References
Subfamily Corydoradinae
Corydorascarlae
Florido River/Paraná State, Brazil
46
simple
2, q terminal
2, q terminal
Synteny, Co-localization
Present study
Corydorasbritskii
Miranda River/ Mato Grosso do Sul State, Brazil
90
multiple
3, p terminal
2 p, interstitial
Non-Synteny
Takagui et al. (2014)
Corydoraspaleatus
Tibagi River/Paraná State, Brazil
44
simple
3, q terminal
-------
---------
Artoni et al. (2006)
Corydorasehrhardti
Tibagi River/Paraná State, Brazil
44
simple
2, q terminal
-------
---------
Artoni et al. (2006)
Corydorassodalis
from aquarium
74
simple
---------
---------
---------
Shimabukuro-Dias et al. 2004
Corydorasarcuatus
Tabatinga River/frontier Brazil and Peru
46
simple
---------
---------
---------
Oliveira et al. 1992
Corydorastrilineatus
Caripi River/Pará State, Brazil
46
simple
---------
---------
---------
Oliveira et al. 1992
Corydorasschwartzi
Negro River/Amazonas State, Brazil
46
simple
---------
---------
---------
Oliveira et al. 1992
Corydorascf.simulatus
Colombia
62
simple
---------
---------
---------
Oliveira et al. 1992
Corydoras sp. Caripi River
Caripi River/Pará State, Brazil
60
simple
---------
---------
---------
Oliveira et al. 1992
Corydorasreticulatus
Negro River/Amazonas State, Brazil
74
simple
---------
---------
---------
Oliveira et al. 1992
Corydorasaff.punctatus Negro River
Negro River/Amazonas State, Brazil
102
simple
---------
---------
---------
Oliveira et al. 1992
Corydorassimulatus
Colombia
62
multiple
---------
---------
---------
Oliveira et al. 1992
Corydoras sp. Galheiro River
Galheiro River/Minas Gerais State, Brazil
84
multiple
---------
---------
---------
Oliveira et al. 1992
Corydorasflaveolus
Alambari River/São Paulo State, Brazil
58
multiple
---------
---------
---------
Oliveira et al. 1992
Corydorasmetae
Colombia
92
multiple
---------
---------
---------
Oliveira et al. 1992
Subfamily Callichthyinae
Hoplosternumlittorale
Contas River/Bahia State, Brazil
60
simple
2, p terminal
4, p terminal
Non-Synteny
Almeida et al. (2012)
Callichthyscallichthys
Paraná River/Paraná State, Brazil
56
simple
2-3, p terminal e interstitial
7-9, p interstitial and terminal
Synteny, Adjacent regions
Konerat et al. (2014)
Hoplosternumlittorale
Coastal River/São Paulo State Brazil
60
simple
2, p terminal
4 p terminal
Non-Synteny
Pazza et al. (2005)
Callichthyscallichthys
Contas River/Bahia State, Brazil
54
multiple
7, p terminal, 5, q terminal, 1 p interstitial
8-12, p interstitial and terminal
Non-Synteny
Almeida et al. (2013)
Lepthoplosternumpectorale
Paraná River/Paraná State, Brazil
64
multiple
10, p terminal; 2, q terminal
6, p terminal
Non-Synteny
Konerat et al. (2014)
Despite exhibiting wide variation on the diploid number, chromosome morphology and location of NORs, Corydoras species share a heterochromatin distribution pattern very similar, preferably centromeric and pericentomeric, and in most cases, associated to NORs. In C.carlae, this pattern was also observed, with heterochromatic blocks also displayed in many chromosomes. Corydorasbritskii from Miranda River also showed large amount of pericentromeric heterochromatin, but with terminal heterochromatic blocks (Takagui et al. 2014), which were not observed in this study.
The mapping of 18S rDNA and 5S rDNA are scarce in Callichthyidae, being known only for some species (Table 1). Concerning the genus Corydoras, C.carlae exhibited only one chromosome pair bearing 18S rDNA sites, as well as C.ehrhardti (Artoni et al. 2006), confirming the system of simple NORs evidenced by silver impregnation for both species. FISH with rDNA probes has helped detect the presence of inactive NORs, as in the case of C.paleatus (Artoni et al. 2006), which presented multiple NORs sites after 18S-FISH, while the silver impregnation had detected only simple NORs. Thus, studies with 18S-FISH can be useful for better evaluating the pattern distribution of the NORs in Corydoras.
In Corydoras, data on the location and number of 5S rDNA cistrons had only been described for C.britskii, for which was detected interstitially in a pair of subtelocentric chromosomes (Takagui et al. 2014). In C.carlae, the 5S rDNA was displayed at terminal position on the long arm of the metacentric pair 6. The presence of one chromosome pair bearing 5S rDNA is a common feature in different families of Siluriformes (Swarça et al. 2009), although multiple loci of 5S rDNA have been observed in Callichthyinae (Table 1). Inter– and intra–individual numerical and position variations of 5S rDNA cistrons have been observed in Callichthyidae and seem to represent a species-specific marker.
Furthermore, 5S rDNA cluster appears interspersed with 18S cistrons, featuring synteny and co-location of ribosomal genes in C.carlae. The synteny is an unusual feature in fish, and such condition could influence an unwanted translocation of 5S sequences within 45S clusters, which could probably occur if these clusters were maintained linked in the same chromosome area (Martins and Galetti Jr 1999). This may explain why most vertebrates have these sequences on different chromosomes. Interestingly, all the possible syntenic conditions have been found in fishes, both sets of genes in distinct and disjoint chromosomal regions, as observed in Parodonnasus Kner, 1859 cited as Parodontortuosus (Vicente et al. 2001) and Astyanaxparanae Eigenmann, 1914 cited as Astyanaxscabripinnis (Mantovani et al. 2005), or in adjacent regions, as in Triportheusnematurus (Kner, 1858) (Diniz et al. 2009), Mugilincilis Hancock, 1830 (Hett et al. 2011), Kronichthyslacerta, Isbrueckerichthysduseni, Parotocinclusmaculicauda, Trichomycterus sp. (Ziemniczak et al. 2012) and Callichthyscallichthys (Konerat et al. 2014), or the 5S rDNA interspersed along the clusters of 45S rDNA (co-localization), as in Astyanaxaltiparanae Garutti & Britski, 2000, Astyanaxlacustris (Lütken, 1875), Astyanaxfasciatus (Cuvier, 1819), Astyanaxschubarti Britski, 1964 and Astyanaxparanae cited as Astyanaxscabripinnis (Almeida-Toledo et al. 2002), Soleasenegalensis Kaup, 1858 (Cross et al. 2006), Bryconamericus cf. iheringii (Piscor et al. 2013) and Corydorascarlae (present study).
Despite little studies about mapping of rDNA genes in Callichthyidae, the majority of the species share the condition of non-synteny between the 5S rDNA and 45S rDNA. Therefore, this condition of co-localization of ribosomal genes in C.carlae seems to represent a marker for this species.
Acknowledgments
The authors thank the Ineo/Gerpel, specially Poliana, Guido, Angélica and Werike by assistance in sample collection. The authors are also grateful to Dr. Weferson Júnio da Graça and MSc. Luiz Tencatt for taxonomic identification of the specimens. We would also like to express our gratitude to Brazilian agency Fundação Araucária for scholarship to first author.
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