Karyotype analysis of seven species of the tribe lophiohylini (Hylinae, Hylidae, Anura), with conventional and molecular cytogenetic techniques

Detalhes bibliográficos
Autor(a) principal: Gruber, Simone Lilian [UNESP]
Data de Publicação: 2012
Outros Autores: Haddad, Célio Fernando Baptista [UNESP], Kasahara, Sanae [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.3897/CompCytogen.v6i4.3945
http://hdl.handle.net/11449/73894
Resumo: Few species of the tribe Lophiohylini have been karyotyped so far, and earlier analyses were performed mainly with standard staining. Based on the analysis of seven species with use of routine banding and molecular cytogenetic techniques, the karyotypes were compared and the cytogenetic data were evaluated in the light of the current phylogenies. A karyotype with 2n = 24 and NOR in the chromosome 10 detected by Ag-impregnation and FISH with an rDNA probe was shared by Aparasphenodon bokermanni Miranda-Ribeiro, 1920, Itapotihyla langsdorffii (Duméril and Bibron, 1841), Trachycephalus sp., T. mesophaeus (Hensel, 1867), and T. typhonius (Linnaeus, 1758). Phyllodytes edelmoi Peixoto, Caramaschi et Freire, 2003 and P. luteolus (Wied-Neuwied, 1824) had reduced the diploid number from 2n = 24 to 2n = 22 with one of the small-sized pairs clearly missing, and NOR in the large chromosome 2, but the karyotypes were distinct regarding the morphology of chromosome pairs 4 and 6. Based on the cytogenetic and phylogenetic data, it was presumed that the chromosome evolution occurred from an ancestral type with 2n = 24, in which a small chromosome had been translocated to one or more unidentified chromosomes. Whichever hypothesis is more probable, other rearrangements should have occurred later, to explain the karyotype differences between the two species of Phyllodytes Wagler, 1830. The majority of the species presented a small amount of centromeric C-banded heterochromatin and these regions were GC-rich. The FISH technique using a telomeric probe identified the chromosome ends and possibly (TTAGGG)n-like sequences in the repetitive DNA out of the telomeres in I. langsdorffii and P. edelmoi. The data herein obtained represent an important contribution for characterizing the karyotype variability within the tribe Lophiohylini scarcely analysed so far. © Simone Lilian Gruber et al.
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spelling Karyotype analysis of seven species of the tribe lophiohylini (Hylinae, Hylidae, Anura), with conventional and molecular cytogenetic techniquesAg-NORAmphibian cytogeneticsC-bandingFluorochrome stainingrDNA probeTelomeric probeFew species of the tribe Lophiohylini have been karyotyped so far, and earlier analyses were performed mainly with standard staining. Based on the analysis of seven species with use of routine banding and molecular cytogenetic techniques, the karyotypes were compared and the cytogenetic data were evaluated in the light of the current phylogenies. A karyotype with 2n = 24 and NOR in the chromosome 10 detected by Ag-impregnation and FISH with an rDNA probe was shared by Aparasphenodon bokermanni Miranda-Ribeiro, 1920, Itapotihyla langsdorffii (Duméril and Bibron, 1841), Trachycephalus sp., T. mesophaeus (Hensel, 1867), and T. typhonius (Linnaeus, 1758). Phyllodytes edelmoi Peixoto, Caramaschi et Freire, 2003 and P. luteolus (Wied-Neuwied, 1824) had reduced the diploid number from 2n = 24 to 2n = 22 with one of the small-sized pairs clearly missing, and NOR in the large chromosome 2, but the karyotypes were distinct regarding the morphology of chromosome pairs 4 and 6. Based on the cytogenetic and phylogenetic data, it was presumed that the chromosome evolution occurred from an ancestral type with 2n = 24, in which a small chromosome had been translocated to one or more unidentified chromosomes. Whichever hypothesis is more probable, other rearrangements should have occurred later, to explain the karyotype differences between the two species of Phyllodytes Wagler, 1830. The majority of the species presented a small amount of centromeric C-banded heterochromatin and these regions were GC-rich. The FISH technique using a telomeric probe identified the chromosome ends and possibly (TTAGGG)n-like sequences in the repetitive DNA out of the telomeres in I. langsdorffii and P. edelmoi. The data herein obtained represent an important contribution for characterizing the karyotype variability within the tribe Lophiohylini scarcely analysed so far. © Simone Lilian Gruber et al.UNESP, Universidade Estadual Paulista Instituto de Biociências Departamento de Biologia, Av. 24A, 1515, 13506-900 Rio Claro, SPUNESP, Universidade Estadual Paulista Instituto de Biociências Departamento de Zoologia, Av. 24A, 1515, 13506-900 Rio Claro, SPUNESP, Universidade Estadual Paulista Instituto de Biociências Departamento de Biologia, Av. 24A, 1515, 13506-900 Rio Claro, SPUNESP, Universidade Estadual Paulista Instituto de Biociências Departamento de Zoologia, Av. 24A, 1515, 13506-900 Rio Claro, SPUniversidade Estadual Paulista (Unesp)Gruber, Simone Lilian [UNESP]Haddad, Célio Fernando Baptista [UNESP]Kasahara, Sanae [UNESP]2014-05-27T11:27:20Z2014-05-27T11:27:20Z2012-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article409-423application/pdfhttp://dx.doi.org/10.3897/CompCytogen.v6i4.3945Comparative Cytogenetics, v. 6, n. 4, p. 409-423, 2012.1993-07711993-078Xhttp://hdl.handle.net/11449/7389410.3897/CompCytogen.v6i4.39452-s2.0-848752617802-s2.0-84875261780.pdf04580773990587628422327495725206Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengComparative Cytogenetics1.3190,431info:eu-repo/semantics/openAccess2024-01-27T06:55:20Zoai:repositorio.unesp.br:11449/73894Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-06T00:04:50.962235Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Karyotype analysis of seven species of the tribe lophiohylini (Hylinae, Hylidae, Anura), with conventional and molecular cytogenetic techniques
title Karyotype analysis of seven species of the tribe lophiohylini (Hylinae, Hylidae, Anura), with conventional and molecular cytogenetic techniques
spellingShingle Karyotype analysis of seven species of the tribe lophiohylini (Hylinae, Hylidae, Anura), with conventional and molecular cytogenetic techniques
Gruber, Simone Lilian [UNESP]
Ag-NOR
Amphibian cytogenetics
C-banding
Fluorochrome staining
rDNA probe
Telomeric probe
title_short Karyotype analysis of seven species of the tribe lophiohylini (Hylinae, Hylidae, Anura), with conventional and molecular cytogenetic techniques
title_full Karyotype analysis of seven species of the tribe lophiohylini (Hylinae, Hylidae, Anura), with conventional and molecular cytogenetic techniques
title_fullStr Karyotype analysis of seven species of the tribe lophiohylini (Hylinae, Hylidae, Anura), with conventional and molecular cytogenetic techniques
title_full_unstemmed Karyotype analysis of seven species of the tribe lophiohylini (Hylinae, Hylidae, Anura), with conventional and molecular cytogenetic techniques
title_sort Karyotype analysis of seven species of the tribe lophiohylini (Hylinae, Hylidae, Anura), with conventional and molecular cytogenetic techniques
author Gruber, Simone Lilian [UNESP]
author_facet Gruber, Simone Lilian [UNESP]
Haddad, Célio Fernando Baptista [UNESP]
Kasahara, Sanae [UNESP]
author_role author
author2 Haddad, Célio Fernando Baptista [UNESP]
Kasahara, Sanae [UNESP]
author2_role author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Gruber, Simone Lilian [UNESP]
Haddad, Célio Fernando Baptista [UNESP]
Kasahara, Sanae [UNESP]
dc.subject.por.fl_str_mv Ag-NOR
Amphibian cytogenetics
C-banding
Fluorochrome staining
rDNA probe
Telomeric probe
topic Ag-NOR
Amphibian cytogenetics
C-banding
Fluorochrome staining
rDNA probe
Telomeric probe
description Few species of the tribe Lophiohylini have been karyotyped so far, and earlier analyses were performed mainly with standard staining. Based on the analysis of seven species with use of routine banding and molecular cytogenetic techniques, the karyotypes were compared and the cytogenetic data were evaluated in the light of the current phylogenies. A karyotype with 2n = 24 and NOR in the chromosome 10 detected by Ag-impregnation and FISH with an rDNA probe was shared by Aparasphenodon bokermanni Miranda-Ribeiro, 1920, Itapotihyla langsdorffii (Duméril and Bibron, 1841), Trachycephalus sp., T. mesophaeus (Hensel, 1867), and T. typhonius (Linnaeus, 1758). Phyllodytes edelmoi Peixoto, Caramaschi et Freire, 2003 and P. luteolus (Wied-Neuwied, 1824) had reduced the diploid number from 2n = 24 to 2n = 22 with one of the small-sized pairs clearly missing, and NOR in the large chromosome 2, but the karyotypes were distinct regarding the morphology of chromosome pairs 4 and 6. Based on the cytogenetic and phylogenetic data, it was presumed that the chromosome evolution occurred from an ancestral type with 2n = 24, in which a small chromosome had been translocated to one or more unidentified chromosomes. Whichever hypothesis is more probable, other rearrangements should have occurred later, to explain the karyotype differences between the two species of Phyllodytes Wagler, 1830. The majority of the species presented a small amount of centromeric C-banded heterochromatin and these regions were GC-rich. The FISH technique using a telomeric probe identified the chromosome ends and possibly (TTAGGG)n-like sequences in the repetitive DNA out of the telomeres in I. langsdorffii and P. edelmoi. The data herein obtained represent an important contribution for characterizing the karyotype variability within the tribe Lophiohylini scarcely analysed so far. © Simone Lilian Gruber et al.
publishDate 2012
dc.date.none.fl_str_mv 2012-12-01
2014-05-27T11:27:20Z
2014-05-27T11:27:20Z
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 http://dx.doi.org/10.3897/CompCytogen.v6i4.3945
Comparative Cytogenetics, v. 6, n. 4, p. 409-423, 2012.
1993-0771
1993-078X
http://hdl.handle.net/11449/73894
10.3897/CompCytogen.v6i4.3945
2-s2.0-84875261780
2-s2.0-84875261780.pdf
0458077399058762
8422327495725206
url http://dx.doi.org/10.3897/CompCytogen.v6i4.3945
http://hdl.handle.net/11449/73894
identifier_str_mv Comparative Cytogenetics, v. 6, n. 4, p. 409-423, 2012.
1993-0771
1993-078X
10.3897/CompCytogen.v6i4.3945
2-s2.0-84875261780
2-s2.0-84875261780.pdf
0458077399058762
8422327495725206
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Comparative Cytogenetics
1.319
0,431
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 409-423
application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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