Peroxisomal bifunctional enzyme deficiency.
Authors:
- W W ChenWCW W Chen
- C J HarrisCHC J Harris
- G HoeflerG Hoefler
- S HoeflerSHS Hoefler
- D C BlakeDBD C Blake
- A BalfeABA Balfe
- R I KelleyRKR I Kelley
- A B MoserAMA B Moser
- M E BeardMBM E Beard
Open Access
- 1 March 1989
- journal article
- research article
- Published by American Society for Clinical Investigation in Journal of Clinical Investigation
- Vol. 83 (3) , 771-777
Abstract
Peroxisomal function was evaluated in a male infant with clinical features of neonatal adrenoleukodystrophy. Very long chain fatty acid levels were elevated in both plasma and fibroblasts, and beta-oxidation of very long chain fatty acids in cultured fibroblasts was significantly impaired. Although the level of the bile acid intermediate trihydroxycoprostanoic acid was slightly elevated in plasma, phytanic acid and L-pipecolic acid levels were normal, as was plasmalogen synthesis in cultured fibroblasts. The latter three parameters distinguish this case from classical neonatal adrenoleukodystrophy. In addition, electron microscopy and catalase subcellular distribution studies revealed that, in contrast to neonatal adrenoleukodystrophy, peroxisomes were present in the patient's tissues. Immunoblot studies of peroxisomal beta-oxidation enzymes revealed that the bifunctional enzyme (enoyl-CoA hydratase/3-hydroxyacyl-CoA dehydrogenase) was deficient in postmortem liver samples, whereas acyl-CoA oxidase and the mature form of beta-ketothiolase were present. Density gradient centrifugation of fibroblast homogenates confirmed that intact peroxisomes were present. Immunoblots of fibroblasts peroxisomal fractions showed that they contained acyl-CoA oxidase and beta-ketothiolase, but bifunctional enzyme was not detected. Northern analysis, however, revealed that mRNA coding for the bifunctional enzyme was present in the patient's fibroblasts. These results indicate that the primary biochemical defect in this patient is a deficiency of peroxisomal bifunctional enzyme. It is of interest that the phenotype of this patient resembled neonatal adrenoleukodystrophy and would not have been distinguished from this disorder by clinical study alone.Keywords
This publication has 40 references indexed in Scilit:
- Biochemical abnormalities in rhizomelic chondrodysplasia punctataThe Journal of Pediatrics, 1988
- Peroxisomes in infantile phytanic acid storage disease: a cytochemical study of skin fibroblastsJournal of Inherited Metabolic Disease, 1986
- Pseudo-Zellweger syndrome: Deficiencies in several peroxisomal oxidative activitiesThe Journal of Pediatrics, 1986
- Infantile Refsum's disease: Biochemical findings suggesting multiple peroxisomal dysfunctionJournal of Inherited Metabolic Disease, 1985
- Deficiency of Enzymes Catalyzing the Biosynthesis of Glycerol-Ether Lipids in Zellweger SyndromeNew England Journal of Medicine, 1984
- The Cerebrohepatorenal (Zellweger) SyndromeNew England Journal of Medicine, 1984
- The cerebrohepatorenal syndrome of Zellweger, morphologic and metabolic aspectsAmerican Journal of Medical Genetics, 1983
- Infantile phytanic acid storage disease, a possible variant of Refsum's disease: Three cases, including ultrastructural studies of the liverJournal of Inherited Metabolic Disease, 1982
- A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye BindingAnalytical Biochemistry, 1976
- Cerebro-hepato-renal syndrome of ZellwegerThe Journal of Pediatrics, 1975