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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/66830
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dc.contributor.authorChew, Joyce S. K.-
dc.contributor.authorOliveira, Claudio-
dc.contributor.authorWright, Jonathan M.-
dc.contributor.authorDobson, Melanie J.-
dc.date.accessioned2014-05-27T11:20:25Z-
dc.date.accessioned2016-10-25T18:17:40Z-
dc.date.available2014-05-27T11:20:25Z-
dc.date.available2016-10-25T18:17:40Z-
dc.date.issued2002-03-01-
dc.identifierhttp://dx.doi.org/10.1007/s00412-002-0187-3-
dc.identifier.citationChromosoma, v. 111, n. 1, p. 45-52, 2002.-
dc.identifier.issn0009-5915-
dc.identifier.urihttp://hdl.handle.net/11449/66830-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/66830-
dc.description.abstractThe majority of chromosomes in Oreochromis niloticus, as with most fish karyotyped to date, cannot be individually identified owing to their small size. As a first step in establishing a physical map for this important aquaculture species of tilapia we have analyzed the location of the vertebrate telomeric repeat sequence, (TTAGGG)n, in O. niloticus. Southern blot hybridization analysis and a Bal31 sensitivity assay confirm that the vertebrate telomeric repeat is indeed present at O. niloticus chromosomal ends with repeat tracts extending for 4-10 kb on chromosomal ends in erythrocytes. Fluorescent in situ hybridization revealed that (TTAGGG)n is found not only at telomeres, but also at two interstitial loci on chromosome 1. These data support the hypothesis that chromosome 1, which is significantly larger than all the other chromosomes in the karyotype, was produced by the fusion of three chromosomes and explain the overall reduction of chromosomal number from the ancestral teleost karyotype of 2n=48 to 2n=44 observed in tilapia.en
dc.format.extent45-52-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectanimal cell-
dc.subjectanimal experiment-
dc.subjectaquaculture-
dc.subjectchromosome 1-
dc.subjectchromosome analysis-
dc.subjectcontrolled study-
dc.subjecterythrocyte-
dc.subjectfemale-
dc.subjectfluorescence in situ hybridization-
dc.subjectgene sequence-
dc.subjectkaryotype-
dc.subjectmale-
dc.subjectnonhuman-
dc.subjectoreochromis niloticus-
dc.subjectSouthern blotting-
dc.subjectteleost-
dc.subjecttelomere-
dc.subjectTilapia-
dc.subjectvertebrate-
dc.subjectanimal-
dc.subjectgenetics-
dc.subjectkaryotyping-
dc.subjectmetabolism-
dc.subjectnucleotide repeat-
dc.subjectpulsed field gel electrophoresis-
dc.subjectAnimalia-
dc.subjectCichlidae-
dc.subjectOreochromis niloticus-
dc.subjectTeleostei-
dc.subjectVertebrata-
dc.subjectdeoxyribonuclease-
dc.subjectDNA-
dc.subjectexonuclease Bal 31-
dc.subjectAnimals-
dc.subjectBlotting, Southern-
dc.subjectElectrophoresis, Gel, Pulsed-Field-
dc.subjectEndodeoxyribonucleases-
dc.subjectFemale-
dc.subjectIn Situ Hybridization, Fluorescence-
dc.subjectKaryotyping-
dc.subjectMale-
dc.subjectRepetitive Sequences, Nucleic Acid-
dc.subjectTelomere-
dc.titleMolecular and cytogenetic analysis of the telomeric (TTAGGG)n repetitive sequences in the Nile tilapia, Oreochromis niloticus (Teleostei: Cichlidae)en
dc.typeoutro-
dc.contributor.institutionDalhousie University-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartment of Biochemistry and Molecular Biology Dalhousie University, Halifax, NS B3H 4H7-
dc.description.affiliationDepartment of Biology Dalhousie University, Halifax, NS B3H 4J1-
dc.description.affiliationDepartamento de Morfologia Instituto de Biociências UNESP, Botucatu, São Paulo-
dc.description.affiliationUnespDepartamento de Morfologia Instituto de Biociências UNESP, Botucatu, São Paulo-
dc.identifier.doi10.1007/s00412-002-0187-3-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofChromosoma-
dc.identifier.scopus2-s2.0-0036491982-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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