Your browser doesn't support javascript.
loading
Genomic Investigation of Balanced Chromosomal Rearrangements in Patients with Abnormal Phenotypes.
Simioni, Milena; Artiguenave, François; Meyer, Vincent; Sgardioli, Ilária C; Viguetti-Campos, Nilma L; Lopes Monlleó, Isabella; Maciel-Guerra, Andréa T; Steiner, Carlos E; Gil-da-Silva-Lopes, Vera L.
Afiliação
  • Simioni M; Department of Medical Genetics, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.
  • Artiguenave F; Centre National de Génotypage, Evry, France.
  • Meyer V; Centre National de Génotypage, Evry, France.
  • Sgardioli IC; Department of Medical Genetics, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.
  • Viguetti-Campos NL; Department of Medical Genetics, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.
  • Lopes Monlleó I; Clinical Genetics Service, Faculty of Medicine, University Hospital, Federal University of Alagoas (UFAL), Maceió, Brazil.
  • Maciel-Guerra AT; Department of Medical Genetics, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.
  • Steiner CE; Department of Medical Genetics, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.
  • Gil-da-Silva-Lopes VL; Department of Medical Genetics, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.
Mol Syndromol ; 8(4): 187-194, 2017 Jun.
Article em En | MEDLINE | ID: mdl-28690484
Balanced chromosomal rearrangements (BCR) are associated with abnormal phenotypes in approximately 6% of balanced translocations and 9.4% of balanced inversions. Abnormal phenotypes can be caused by disruption of genes at the breakpoints, deletions, or positional effects. Conventional cytogenetic techniques have a limited resolution and do not enable a thorough genetic investigation. Molecular techniques applied to BCR carriers can contribute to the characterization of this type of chromosomal rearrangement and to the phenotype-genotype correlation. Fifteen individuals among 35 with abnormal phenotypes and BCR were selected for further investigation by molecular techniques. Chromosomal rearrangements involved 11 reciprocal translocations, 3 inversions, and 1 balanced insertion. Array genomic hybridization (AGH) was performed and genomic imbalances were detected in 20% of the cases, 1 at a rearrangement breakpoint and 2 further breakpoints in other chromosomes. Alterations were further confirmed by FISH and associated with the phenotype of the carriers. In the analyzed cases not showing genomic imbalances by AGH, next-generation sequencing (NGS), using whole genome libraries, prepared following the Illumina TruSeq DNA PCR-Free protocol (Illumina®) and then sequenced on an Illumina HiSEQ 2000 as 150-bp paired-end reads, was done. The NGS results suggested breakpoints in 7 cases that were similar or near those estimated by karyotyping. The genes overlapping 6 breakpoint regions were analyzed. Follow-up of BCR carriers would improve the knowledge about these chromosomal rearrangements and their consequences.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Mol Syndromol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Brasil

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Mol Syndromol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Brasil