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Genet Mol Res. 2016 Jul 14;15(2). doi: 10.4238/gmr.15028258.

Splicing mutation of a gene within the Duchenne muscular dystrophy family.

Author information

1
Provincial Medical College, Fujian Medical University, Fujian University of Traditional Chinese Medicine, Fuzhou, China.
2
Department of Traditional Chinese Medicine, Fujian Provincial Hospital, Fuzhou, China.
3
School of Clinical Medicine, Capital Medical University, Beijing, China.

Abstract

The aim of this study was to identify the mutation site and phenotype of the Duchenne muscular dystrophy (DMD) gene in a DMD family. The DMD gene is by far the largest known gene in humans. Up to 34% of the point mutations reported to date affect splice sites of the DMD gene. However, no hotspot mutation has been reported. Capture sequencing of second-generation exons was used to investigate the DMD gene in a proband. Sanger sequencing was performed for mutation scanning in eight family members. Scale-invariant feature transform and PolyPhen were applied to predict the functional impact of protein mutations. A hemizygous splicing mutation IVS44ds +1G-A (c.6438 +1G>A) that induces abnormal splicing variants during late transcription and produces abnormal proteins was located in intron 44. Four missense mutations (p.Arg2937Gln, p.Asp882Gly, p.Lys2366Gln, and p.Arg1745His) that are known multiple-polymorphic sites were found in the coding region of the DMD gene. A heterozygous c.6438+1G>A mutation was detected on the X chromosome of the proband's mother and maternal grandmother.

PMID:
27421007
DOI:
10.4238/gmr.15028258
[Indexed for MEDLINE]
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