Study of a Bethlem myopathy pedigree resulted from a novel mutation of COL6A3 gene / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 698-702, 2014.
Article
em Zh
| WPRIM
| ID: wpr-291700
Biblioteca responsável:
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To determine the molecular etiology for a muscular dystrophy pedigree with target region sequencing platform using hereditary myopathy capture array.</p><p><b>METHODS</b>Specific gene testing was performed based on the clinical diagnosis. Since no pathogenic mutation was found, target region sequencing with hereditary myopathy capture array combined with Sanger sequencing and bioinformatics analysis were employed in turn. PolyPhen and NCBI were used to evaluate the pathogenicity of identified mutation and conservation of the gene.</p><p><b>RESULTS</b>Target region sequencing indicated the proband has carried a heterozygous c.3353 A>C mutation of COL6A3 gene, which was confirmed by Sanger-sequencing in 4 affected individuals from the family. The same mutation was not detected in healthy members of the pedigree. Bioinformatics analysis suggested that the mutation has caused a highly pathogenic amino acid substitution from Histidine to Proline. The affected patients featured normal intelligence with mild myogenic damage by muscle biopsy, slightly increased serum creatine kinase and slow disease progression, which was consistent with Bethlem myopathy.</p><p><b>CONCLUSION</b>Target region sequencing is an effective and efficient method for genetic testing. The heterozygous c.3353A>C mutation in exon 8 of the COL6A3 gene probably underlies the Bethlem myopathy with autosomal dominant inheritance.</p>
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Índice:
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Assunto principal:
Linhagem
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Dados de Sequência Molecular
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Sequência de Bases
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Éxons
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Sequência de Aminoácidos
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Contratura
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Substituição de Aminoácidos
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Mutação de Sentido Incorreto
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Colágeno Tipo VI
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Genética
Limite:
Adult
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Female
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Humans
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Male
Idioma:
Zh
Revista:
Chinese Journal of Medical Genetics
Ano de publicação:
2014
Tipo de documento:
Article