Centric fusions behind the karyotype evolution of neotropical nannostomus pencilfishes (Characiforme, Lebiasinidae): First insights from a molecular cytogenetic perspective

Detalhes bibliográficos
Autor(a) principal: Sember, Alexandr
Data de Publicação: 2020
Outros Autores: Oliveira, Ezequiel Aguiar de, Ráb, Petr, Bertollo, Luiz Antônio Carlos, Freitas, Natália Lourenço de, Viana, Patrik Ferreira, Yano, Cassia Fernanda, Hatanaka, Terumi, Marinho, Manoela Maria Ferreira, Moraes, Renata Luiza Rosa de, Feldberg, Eliana, Cioffi, Marcelo de Bello
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional do INPA
Texto Completo: https://repositorio.inpa.gov.br/handle/1/15477
Resumo: Lebiasinidae is a Neotropical freshwater family widely distributed throughout South and Central America. Due to their often very small body size, Lebiasinidae species are cytogenetically challenging and hence largely underexplored. However, the available but limited karyotype data already suggested a high interspecific variability in the diploid chromosome number (2n), which is pronounced in the speciose genus Nannostomus, a popular taxon in ornamental fish trade due to its remarkable body coloration. Aiming to more deeply examine the karyotype diversification in Nannostomus, we combined conventional cytogenetics (Giemsa-staining and C-banding) with the chromosomal mapping of tandemly repeated 5S and 18S rDNA clusters and with interspecific comparative genomic hybridization (CGH) to investigate genomes of four representative Nannostomus species: N. beckfordi, N. eques, N. marginatus, and N. unifasciatus. Our data showed a remarkable variability in 2n, ranging from 2n = 22 in N. unifasciatus (karyotype composed exclusively of metacentrics/submetacentrics) to 2n = 44 in N. beckfordi (karyotype composed entirely of acrocentrics). On the other hand, patterns of 18S and 5S rDNA distribution in the analyzed karyotypes remained rather conservative, with only two 18S and two to four 5S rDNA sites. In view of the mostly unchanged number of chromosome arms (FN = 44) in all but one species (N. eques; FN = 36), and with respect to the current phylogenetic hypothesis, we propose Robertsonian translocations to be a significant contributor to the karyotype differentiation in (at least herein studied) Nannostomus species. Interspecific comparative genome hybridization (CGH) using whole genomic DNAs mapped against the chromosome background of N. beckfordi found a moderate divergence in the repetitive DNA content among the species’ genomes. Collectively, our data suggest that the karyotype differentiation in Nannostomus has been largely driven by major structural rearrangements, accompanied by only low to moderate dynamics of repetitive DNA at the sub-chromosomal level. Possible mechanisms and factors behind the elevated tolerance to such a rate of karyotype change in Nannostomus are discussed. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.
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spelling Sember, AlexandrOliveira, Ezequiel Aguiar deRáb, PetrBertollo, Luiz Antônio CarlosFreitas, Natália Lourenço deViana, Patrik FerreiraYano, Cassia FernandaHatanaka, TerumiMarinho, Manoela Maria FerreiraMoraes, Renata Luiza Rosa deFeldberg, ElianaCioffi, Marcelo de Bello2020-05-14T15:32:09Z2020-05-14T15:32:09Z2020https://repositorio.inpa.gov.br/handle/1/1547710.3390/genes11010091Lebiasinidae is a Neotropical freshwater family widely distributed throughout South and Central America. Due to their often very small body size, Lebiasinidae species are cytogenetically challenging and hence largely underexplored. However, the available but limited karyotype data already suggested a high interspecific variability in the diploid chromosome number (2n), which is pronounced in the speciose genus Nannostomus, a popular taxon in ornamental fish trade due to its remarkable body coloration. Aiming to more deeply examine the karyotype diversification in Nannostomus, we combined conventional cytogenetics (Giemsa-staining and C-banding) with the chromosomal mapping of tandemly repeated 5S and 18S rDNA clusters and with interspecific comparative genomic hybridization (CGH) to investigate genomes of four representative Nannostomus species: N. beckfordi, N. eques, N. marginatus, and N. unifasciatus. Our data showed a remarkable variability in 2n, ranging from 2n = 22 in N. unifasciatus (karyotype composed exclusively of metacentrics/submetacentrics) to 2n = 44 in N. beckfordi (karyotype composed entirely of acrocentrics). On the other hand, patterns of 18S and 5S rDNA distribution in the analyzed karyotypes remained rather conservative, with only two 18S and two to four 5S rDNA sites. In view of the mostly unchanged number of chromosome arms (FN = 44) in all but one species (N. eques; FN = 36), and with respect to the current phylogenetic hypothesis, we propose Robertsonian translocations to be a significant contributor to the karyotype differentiation in (at least herein studied) Nannostomus species. Interspecific comparative genome hybridization (CGH) using whole genomic DNAs mapped against the chromosome background of N. beckfordi found a moderate divergence in the repetitive DNA content among the species’ genomes. Collectively, our data suggest that the karyotype differentiation in Nannostomus has been largely driven by major structural rearrangements, accompanied by only low to moderate dynamics of repetitive DNA at the sub-chromosomal level. Possible mechanisms and factors behind the elevated tolerance to such a rate of karyotype change in Nannostomus are discussed. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.Volume 11, Número 1Attribution-NonCommercial-NoDerivs 3.0 Brazilhttp://creativecommons.org/licenses/by-nc-nd/3.0/br/info:eu-repo/semantics/openAccessDna 18sDna 5sGenomic DnaAcrocentric ChromosomeAnimals ExperimentAnimals TissueBrasilC BandingCharaciformesChromosomal MappingChromosome NumberChromosome RearrangementComparative Genomic HybridizationCytogeneticsFemaleIn Situ Hybridization, FluorescenceGene ClusterGene FusionGenetic VariabilityGenomeGiemsa StainInterspecific HybridizationKaryotype EvolutionMaleNannostomusNannostomus BeckfordiNannostomus EquesNannostomus MarginatusNannostomus UnifasciatusNeotropicsNonhumanPhylogenyRobertsonian Chromosome TranslocationWhole Genome SequencingCentric fusions behind the karyotype evolution of neotropical nannostomus pencilfishes (Characiforme, Lebiasinidae): First insights from a molecular cytogenetic perspectiveinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleGenesengreponame:Repositório Institucional do INPAinstname:Instituto Nacional de Pesquisas da Amazônia (INPA)instacron:INPAORIGINALartigo-inpa.pdfartigo-inpa.pdfapplication/pdf2344757https://repositorio.inpa.gov.br/bitstream/1/15477/1/artigo-inpa.pdf4ed8c8f25046b28bb9b5736985b827a7MD511/154772020-05-14 11:42:26.763oai:repositorio:1/15477Repositório de PublicaçõesPUBhttps://repositorio.inpa.gov.br/oai/requestopendoar:2020-05-14T15:42:26Repositório Institucional do INPA - Instituto Nacional de Pesquisas da Amazônia (INPA)false
dc.title.en.fl_str_mv Centric fusions behind the karyotype evolution of neotropical nannostomus pencilfishes (Characiforme, Lebiasinidae): First insights from a molecular cytogenetic perspective
title Centric fusions behind the karyotype evolution of neotropical nannostomus pencilfishes (Characiforme, Lebiasinidae): First insights from a molecular cytogenetic perspective
spellingShingle Centric fusions behind the karyotype evolution of neotropical nannostomus pencilfishes (Characiforme, Lebiasinidae): First insights from a molecular cytogenetic perspective
Sember, Alexandr
Dna 18s
Dna 5s
Genomic Dna
Acrocentric Chromosome
Animals Experiment
Animals Tissue
Brasil
C Banding
Characiformes
Chromosomal Mapping
Chromosome Number
Chromosome Rearrangement
Comparative Genomic Hybridization
Cytogenetics
Female
In Situ Hybridization, Fluorescence
Gene Cluster
Gene Fusion
Genetic Variability
Genome
Giemsa Stain
Interspecific Hybridization
Karyotype Evolution
Male
Nannostomus
Nannostomus Beckfordi
Nannostomus Eques
Nannostomus Marginatus
Nannostomus Unifasciatus
Neotropics
Nonhuman
Phylogeny
Robertsonian Chromosome Translocation
Whole Genome Sequencing
title_short Centric fusions behind the karyotype evolution of neotropical nannostomus pencilfishes (Characiforme, Lebiasinidae): First insights from a molecular cytogenetic perspective
title_full Centric fusions behind the karyotype evolution of neotropical nannostomus pencilfishes (Characiforme, Lebiasinidae): First insights from a molecular cytogenetic perspective
title_fullStr Centric fusions behind the karyotype evolution of neotropical nannostomus pencilfishes (Characiforme, Lebiasinidae): First insights from a molecular cytogenetic perspective
title_full_unstemmed Centric fusions behind the karyotype evolution of neotropical nannostomus pencilfishes (Characiforme, Lebiasinidae): First insights from a molecular cytogenetic perspective
title_sort Centric fusions behind the karyotype evolution of neotropical nannostomus pencilfishes (Characiforme, Lebiasinidae): First insights from a molecular cytogenetic perspective
author Sember, Alexandr
author_facet Sember, Alexandr
Oliveira, Ezequiel Aguiar de
Ráb, Petr
Bertollo, Luiz Antônio Carlos
Freitas, Natália Lourenço de
Viana, Patrik Ferreira
Yano, Cassia Fernanda
Hatanaka, Terumi
Marinho, Manoela Maria Ferreira
Moraes, Renata Luiza Rosa de
Feldberg, Eliana
Cioffi, Marcelo de Bello
author_role author
author2 Oliveira, Ezequiel Aguiar de
Ráb, Petr
Bertollo, Luiz Antônio Carlos
Freitas, Natália Lourenço de
Viana, Patrik Ferreira
Yano, Cassia Fernanda
Hatanaka, Terumi
Marinho, Manoela Maria Ferreira
Moraes, Renata Luiza Rosa de
Feldberg, Eliana
Cioffi, Marcelo de Bello
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Sember, Alexandr
Oliveira, Ezequiel Aguiar de
Ráb, Petr
Bertollo, Luiz Antônio Carlos
Freitas, Natália Lourenço de
Viana, Patrik Ferreira
Yano, Cassia Fernanda
Hatanaka, Terumi
Marinho, Manoela Maria Ferreira
Moraes, Renata Luiza Rosa de
Feldberg, Eliana
Cioffi, Marcelo de Bello
dc.subject.eng.fl_str_mv Dna 18s
Dna 5s
Genomic Dna
Acrocentric Chromosome
Animals Experiment
Animals Tissue
Brasil
C Banding
Characiformes
Chromosomal Mapping
Chromosome Number
Chromosome Rearrangement
Comparative Genomic Hybridization
Cytogenetics
Female
In Situ Hybridization, Fluorescence
Gene Cluster
Gene Fusion
Genetic Variability
Genome
Giemsa Stain
Interspecific Hybridization
Karyotype Evolution
Male
Nannostomus
Nannostomus Beckfordi
Nannostomus Eques
Nannostomus Marginatus
Nannostomus Unifasciatus
Neotropics
Nonhuman
Phylogeny
Robertsonian Chromosome Translocation
Whole Genome Sequencing
topic Dna 18s
Dna 5s
Genomic Dna
Acrocentric Chromosome
Animals Experiment
Animals Tissue
Brasil
C Banding
Characiformes
Chromosomal Mapping
Chromosome Number
Chromosome Rearrangement
Comparative Genomic Hybridization
Cytogenetics
Female
In Situ Hybridization, Fluorescence
Gene Cluster
Gene Fusion
Genetic Variability
Genome
Giemsa Stain
Interspecific Hybridization
Karyotype Evolution
Male
Nannostomus
Nannostomus Beckfordi
Nannostomus Eques
Nannostomus Marginatus
Nannostomus Unifasciatus
Neotropics
Nonhuman
Phylogeny
Robertsonian Chromosome Translocation
Whole Genome Sequencing
description Lebiasinidae is a Neotropical freshwater family widely distributed throughout South and Central America. Due to their often very small body size, Lebiasinidae species are cytogenetically challenging and hence largely underexplored. However, the available but limited karyotype data already suggested a high interspecific variability in the diploid chromosome number (2n), which is pronounced in the speciose genus Nannostomus, a popular taxon in ornamental fish trade due to its remarkable body coloration. Aiming to more deeply examine the karyotype diversification in Nannostomus, we combined conventional cytogenetics (Giemsa-staining and C-banding) with the chromosomal mapping of tandemly repeated 5S and 18S rDNA clusters and with interspecific comparative genomic hybridization (CGH) to investigate genomes of four representative Nannostomus species: N. beckfordi, N. eques, N. marginatus, and N. unifasciatus. Our data showed a remarkable variability in 2n, ranging from 2n = 22 in N. unifasciatus (karyotype composed exclusively of metacentrics/submetacentrics) to 2n = 44 in N. beckfordi (karyotype composed entirely of acrocentrics). On the other hand, patterns of 18S and 5S rDNA distribution in the analyzed karyotypes remained rather conservative, with only two 18S and two to four 5S rDNA sites. In view of the mostly unchanged number of chromosome arms (FN = 44) in all but one species (N. eques; FN = 36), and with respect to the current phylogenetic hypothesis, we propose Robertsonian translocations to be a significant contributor to the karyotype differentiation in (at least herein studied) Nannostomus species. Interspecific comparative genome hybridization (CGH) using whole genomic DNAs mapped against the chromosome background of N. beckfordi found a moderate divergence in the repetitive DNA content among the species’ genomes. Collectively, our data suggest that the karyotype differentiation in Nannostomus has been largely driven by major structural rearrangements, accompanied by only low to moderate dynamics of repetitive DNA at the sub-chromosomal level. Possible mechanisms and factors behind the elevated tolerance to such a rate of karyotype change in Nannostomus are discussed. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.
publishDate 2020
dc.date.accessioned.fl_str_mv 2020-05-14T15:32:09Z
dc.date.available.fl_str_mv 2020-05-14T15:32:09Z
dc.date.issued.fl_str_mv 2020
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://repositorio.inpa.gov.br/handle/1/15477
dc.identifier.doi.none.fl_str_mv 10.3390/genes11010091
url https://repositorio.inpa.gov.br/handle/1/15477
identifier_str_mv 10.3390/genes11010091
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.pt_BR.fl_str_mv Volume 11, Número 1
dc.rights.driver.fl_str_mv Attribution-NonCommercial-NoDerivs 3.0 Brazil
http://creativecommons.org/licenses/by-nc-nd/3.0/br/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Attribution-NonCommercial-NoDerivs 3.0 Brazil
http://creativecommons.org/licenses/by-nc-nd/3.0/br/
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Genes
publisher.none.fl_str_mv Genes
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institution INPA
reponame_str Repositório Institucional do INPA
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