Establishment of rapid and non-invasive protocols to identify b-carrying individuals of psalidodon paranae

dc.contributor.authorGoes, Caio Augusto Gomes [UNESP]
dc.contributor.authorDe Andrade Silva, Duílio Mazzoni Zerbinato [UNESP]
dc.contributor.authorUtsunomia, Ricardo
dc.contributor.authorYasui, George Shigueki
dc.contributor.authorArtoni, Roberto Ferreira
dc.contributor.authorForesti, Fausto [UNESP]
dc.contributor.authorPorto-Foresti, Fábio [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionICBS
dc.contributor.institutionCentro nacional de Pesquisa e Conservação da Biota Aquática Continental (CEPTA-ICMBIO)
dc.contributor.institutionUniversidade Estadual de Ponta Grossa (UEPG)
dc.date.accessioned2021-06-25T11:14:11Z
dc.date.available2021-06-25T11:14:11Z
dc.date.issued2021-01-01
dc.description.abstractSupernumerary, or B, chromosomes are present in several eukaryotes, including characid fish of the genus Psalidodon. Notably, Psalidodon paranae carries the most studied B chromosome variant, a macro-B chromosome. The origin of this element was determined to be an isochromosome; however, data regarding its inheritance remain unavailable due to methodological barriers such as the lack of an efficient, non-invasive, and rapid protocol for identifying B-carrying individuals that would enable the design of efficient crossing experiments. Thus, in this study, we primarily aimed was to develop two non-invasive and fast (approximately 2 h) methods to identify the presence of B chromosomes in live specimens of P. paranae based on satellite DNA (satDNA) sequences known to be present in this element. The methods include fluorescence in situ hybridization in interphase nuclei and relative gene quantification of satDNAs using quantitative polymerase chain reaction. Our results reveal the efficiency of quickfluorescence in situ hybridization and quantitative polymerase chain reaction for identifying B-carrying individuals using the proposed satDNA sequences and open up new possibilities to study B chromosomes.en
dc.description.affiliationUniversidade Estadual Paulista “Júlio de Mesquita Filho” (UNESP) Faculdade de Ciências
dc.description.affiliationUniversidade Estadual Paulista “Júlio de Mesquita Filho” (UNESP) Instituto de Biociências
dc.description.affiliationUniversidade Federal Rural do Rio de Janeiro Instituto de Ciências Biológicas e da Saúde ICBS
dc.description.affiliationCentro nacional de Pesquisa e Conservação da Biota Aquática Continental (CEPTA-ICMBIO)
dc.description.affiliationUniversidade Estadual de Ponta Grossa Setor de Ciências Biológicas e da Saúde
dc.description.affiliationUnespUniversidade Estadual Paulista “Júlio de Mesquita Filho” (UNESP) Faculdade de Ciências
dc.description.affiliationUnespUniversidade Estadual Paulista “Júlio de Mesquita Filho” (UNESP) Instituto de Biociências
dc.identifierhttp://dx.doi.org/10.1590/1678-4685-gmb-2020-0003
dc.identifier.citationGenetics and Molecular Biology, v. 44, n. 2, 2021.
dc.identifier.doi10.1590/1678-4685-gmb-2020-0003
dc.identifier.fileS1415-47572021000300202.pdf
dc.identifier.issn1678-4685
dc.identifier.issn1415-4757
dc.identifier.scieloS1415-47572021000300202
dc.identifier.scopus2-s2.0-85103627239
dc.identifier.urihttp://hdl.handle.net/11449/208561
dc.language.isoeng
dc.relation.ispartofGenetics and Molecular Biology
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectB chromosomes
dc.subjectNeotropical fishes
dc.subjectPsalidodon
dc.subjectQPCR
dc.subjectSatellite DNA
dc.titleEstablishment of rapid and non-invasive protocols to identify b-carrying individuals of psalidodon paranaeen
dc.typeArtigo
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Biociências, Botucatupt
unesp.departmentCiências Biológicas - FCpt
unesp.departmentMorfologia - IBBpt

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