Molecular analysis of a human liver mitochondrial ornithine transcarbamylase deficiency

J Inherit Metab Dis. 1991;14(1):29-36. doi: 10.1007/BF01804385.

Abstract

The liver of a young girl which had been successfully transplanted was investigated at the ornithine transcarbamylase (OTC, EC 2.1.3.3) gene expression level. Northern blot hybridization using a human OTC cDNA probe showed a greater than 80% decrease in specific OTC mRNA although having the same molecular size as a normal control. OTC polypeptide was simultaneously synthesized with a normal molecular size but at a low level (20%) as shown by immunoblotting. The OTC enzyme from the deficient liver exhibited very little catalytic activity (7.2% as compared to the normal subject). These results may support several explanations of this disease such as mutation of the OTC gene promoter leading to a low transcriptional activity or mutation of the encoding sequence which results in a modified translation product but with a normal size. mRNA instability may also occur.

Publication types

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

MeSH terms

  • Blotting, Northern
  • Catalysis
  • Child, Preschool
  • Cloning, Molecular
  • DNA / metabolism
  • Female
  • Humans
  • Mitochondria, Liver / enzymology*
  • Nucleic Acid Hybridization
  • Ornithine Carbamoyltransferase / analysis
  • Ornithine Carbamoyltransferase / metabolism
  • Ornithine Carbamoyltransferase Deficiency Disease*
  • Peptides / analysis
  • Peptides / chemistry
  • RNA / analysis
  • RNA, Messenger / metabolism

Substances

  • Peptides
  • RNA, Messenger
  • RNA
  • DNA
  • Ornithine Carbamoyltransferase