Medizinische Universität Graz - Research portal

Logo MUG Resarch Portal

Selected Publication:

van Grunsven, EG; van Berkel, E; Mooijer, PA; Watkins, PA; Moser, HW; Suzuki, Y; Jiang, LL; Hashimoto, T; Hoefler, G; Adamski, J; Wanders, RJ.
Peroxisomal bifunctional protein deficiency revisited: resolution of its true enzymatic and molecular basis.
Am J Hum Genet. 1999; 64(1):99-107 Doi: 10.1086/302180 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG Google Scholar

 

Co-authors Med Uni Graz
Höfler Gerald
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
In the past few years, many patients have been described who have a defect of unknown origin in the peroxisomal beta-oxidation pathway. Complementation analysis has been done by various groups to establish the extent of the genetic heterogeneity among the patients. These studies were based on the use of two established cell lines, one with a deficiency of acyl-CoA oxidase and one with a deficiency of l-bifunctional protein (l-BP), and they showed that most patients belong to the l-BP-deficient group. However, molecular analysis of the cDNA encoding l-BP in patients failed to show any mutations. The recent identification of a new d-specific bifunctional protein (d-BP) prompted us to reinvestigate the original patient with presumed l-BP deficiency. In a collaborative effort, we have now found that the true defect in this patient is at the level of the d-BP and not at the level of the l-BP. Our results suggest that most, if not all, patients whose condition has been diagnosed as l-BP are, in fact, d-BP deficient. We tested this hypothesis in nine patients whose condition was diagnosed as l-BP deficiency on the basis of complementation analysis and found clear-cut mutations in the d-BP cDNA from all patients.
Find related publications in this database (using NLM MeSH Indexing)
17-Hydroxysteroid Dehydrogenases -
3-Hydroxyacyl CoA Dehydrogenases - deficiency
Cells, Cultured - deficiency
DNA Mutational Analysis - deficiency
Enoyl-CoA Hydratase - deficiency
Fatty Acids - metabolism
Fibroblasts - enzymology
Fluorescent Antibody Technique - enzymology
Humans - enzymology
Hydro-Lyases - deficiency
Isomerism - deficiency
Multienzyme Complexes - deficiency
Oxidation-Reduction - deficiency

© Med Uni GrazImprint