Study of deep intronic sequence exonization in a Japanese neonate with a mitochondrial trifunctional protein deficiency

Mol Genet Metab. 2008 Sep-Oct;95(1-2):46-51. doi: 10.1016/j.ymgme.2008.06.013. Epub 2008 Aug 9.

Abstract

Mitochondrial trifunctional protein (MTP) comprises heterooctamer alpha4beta4 and a deficiency in this protein causes a mitochondrial long-chain beta-oxidation defect. Here, we describe the molecular basis of an MTPbeta-subunit deficiency in a Japanese neonate. Mutation screening at the genomic level including all exons and exon-intron boundaries identified a novel c.1136A>G (H346R) mutation in exon 13 of the maternal allele, but none in the paternal allele. Analysis by RT-PCR identified paternal-specific 106- and 56-bp intronic insertions between exons 7 and 8, which introduced premature terminations. This intronic exonization was caused by a deep intronic mutation in intron 7 on the paternal allele that generates a cryptic splice donor site. This is the first report of a deep intronic mutation in MTP deficiency.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asian People / genetics
  • Cells, Cultured
  • Codon, Nonsense
  • Exons
  • Fatal Outcome
  • Fibroblasts / metabolism
  • Humans
  • Infant, Newborn
  • Introns*
  • Lipid Metabolism, Inborn Errors / enzymology
  • Lipid Metabolism, Inborn Errors / genetics*
  • Mitochondrial Trifunctional Protein
  • Multienzyme Complexes / deficiency
  • Multienzyme Complexes / genetics*
  • Mutagenesis, Insertional*
  • Mutation, Missense
  • RNA Splice Sites

Substances

  • Codon, Nonsense
  • Multienzyme Complexes
  • RNA Splice Sites
  • Mitochondrial Trifunctional Protein