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Rapid detection of BRCA1 mutations by the protein truncation test.
Hogervorst, F B; Cornelis, R S; Bout, M; van Vliet, M; Oosterwijk, J C; Olmer, R; Bakker, B; Klijn, J G; Vasen, H F; Meijers-Heijboer, H.
Afiliação
  • Hogervorst FB; MGC-Department of Human Genetics, University of Leiden, The Netherlands.
Nat Genet ; 10(2): 208-12, 1995 Jun.
Article em En | MEDLINE | ID: mdl-7663517
ABSTRACT
More than 75% of the reported mutations in the hereditary breast and ovarian cancer gene, BRCA1, result in truncated proteins. We have used the protein truncation test (PTT) to screen for mutations in exon 11, which encodes 61% of BRCA1. In 45 patients from breast and/or ovarian cancer families we found six novel mutations two single nucleotide insertions, three small deletions (1-5 bp) and a nonsense mutation identified two unrelated families. Furthermore, we were able to amplify the remaining coding region by RT-PCR using lymphocyte RNA. Combined with PTT, we detected aberrantly spliced products affecting exons 5 and 6 in one of two BRCA1-linked families examined. The protein truncation test promises to become a valuable technique in detecting BRCA1 mutations.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Fatores de Transcrição / Neoplasias da Mama / Mutação / Proteínas de Neoplasias Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Middle aged Idioma: En Revista: Nat Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 1995 Tipo de documento: Article País de afiliação: Holanda
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Fatores de Transcrição / Neoplasias da Mama / Mutação / Proteínas de Neoplasias Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Middle aged Idioma: En Revista: Nat Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 1995 Tipo de documento: Article País de afiliação: Holanda