Branched chain acyltransferase absence due to an Alu-based genomic deletion allele and an exon skipping allele in a compound heterozygote proband expressing maple syrup urine disease

W. Joseph Herring, Martha McKean, Nicolas Dracopoli, Dean J. Danner

Research output: Contribution to journalArticle

Abstract

Branched chain α-ketoacid dehydrogenase assembles around a core of the acyltransferase components on the matrix side of the mitochondrial inner membrane. Autosomal recessive mutations in humans are known to decrease the function of this complex resulting in the clinical phenotype of maple syrup urine disease. Within this wide group of mutations are a subset which result in the antigenic absence of the acyltransferase protein of the complex. Here we describe two mutations in a compound heterozygote proband which result in this acyltransferase-negative phenotype. The mutant allele inherited from the father lacks 15-20 kilobases of genomic DNA resulting from a recombinational event between an intronic Alu sequence and coding sequence in the terminal exon. The mother's mutant allele contains a single base substitution in the -1 position of the 5′ splice junction following exon 8. This G1002 → A transition results in exon skipping producing two different mRNAs. The first lacks only exon 8 while the second lacks exons 8-10. All mRNAs for the acyltransferase found in cells from the proband have the potential to produce proteins ranging in size from 251-395 amino acids, the largest being 26 amino acid short of a full-length acyltransferase. The potential of these transcripts to produce protein is of interest since the patient is clinically responsive to pharmacologic treatment with thiamin, showing a higher tolerance to protein in the diet. The mechanism for this thiamin response remains to be explained.

Original languageEnglish (US)
Pages (from-to)236-242
Number of pages7
JournalBiochimica et Biophysica Acta - Molecular Basis of Disease
Volume1138
Issue number3
DOIs
StatePublished - Mar 20 1992
Externally publishedYes

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Maple Syrup Urine Disease
Acyltransferases
Heterozygote
Exons
Alleles
Thiamine
Mutation
3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide)
Phenotype
Amino Acids
Messenger RNA
Proteins
Mitochondrial Membranes
Fathers
Mothers
dihydrolipoamide acyltransferase
Diet
DNA

Keywords

  • Branched chain acyltrasnferase
  • Exon skipping
  • Gene deletion
  • Maple syrup urine disease

ASJC Scopus subject areas

  • Molecular Medicine
  • Molecular Biology

Cite this

Branched chain acyltransferase absence due to an Alu-based genomic deletion allele and an exon skipping allele in a compound heterozygote proband expressing maple syrup urine disease. / Herring, W. Joseph; McKean, Martha; Dracopoli, Nicolas; Danner, Dean J.

In: Biochimica et Biophysica Acta - Molecular Basis of Disease, Vol. 1138, No. 3, 20.03.1992, p. 236-242.

Research output: Contribution to journalArticle

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