Please use this identifier to cite or link to this item: http://dspace.mediu.edu.my:8181/xmlui/handle/123456789/3447
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dc.creatorANUNCIAÇÃO CARLOS EDUARDO-
dc.creatorASTOLFI-FILHO SPARTACO-
dc.date2000-
dc.date.accessioned2013-05-30T01:56:38Z-
dc.date.available2013-05-30T01:56:38Z-
dc.date.issued2013-05-30-
dc.identifierhttp://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-204X2000001000012-
dc.identifierhttp://www.doaj.org/doaj?func=openurl&genre=article&issn=0100204X&date=2000&volume=35&issue=10&spage=2007-
dc.identifier.urihttp://koha.mediu.edu.my:8181/jspui/handle/123456789/3447-
dc.descriptionGC-rich molecular minisatellite probes isolated from the human genome have presented a poor ability for individualization in horses. In this study new DNA sequences were isolated which could be used in paternity tests in horses. Genomic DNA from "Mangalarga-Marchador" horses was treated with restriction enzymes that preferentially digest non-repetitive sequences, so preserving the structure where mini and microsatellites are located. Four clones (S01, S05, S07 and S09) selected from a genomic library screened with a (TG)n oligonucleotide showed similar hybridization profiles generating bands of DNA-fingerprinting type. Using these probes the individualization power obtained was 10-8, which is 10(5)fold higher than that obtained with M13, another GC-rich type probe. All clones were efficient in parentage detection in crossbreedings and presented a 27 bp consensus sequence, GTTTCATTTATTATTCTTTGGAAGAAA, which was repeated 12, 18, 11 and 21 times in clones S01, S05, S07 and S09, respectively.-
dc.publisherEmpresa Brasileira de Pesquisa Agropecuária (Embrapa)-
dc.sourcePesquisa Agropecuária Brasileira-
dc.subjectbreeding methods-
dc.subjectmolecular cloning-
dc.subjectprogeny testing-
dc.subjecthorses-
dc.subjectidentification-
dc.subjectgenetic polymorphism-
dc.titlePaternity test in "Mangalarga-Marchador" equines by DNA-fingerprinting-
Appears in Collections:Agriculture and Food Sciences

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