Molecular Genetic Characterization of Maple Syrup Urine Disease in European Families

Abstract

Maple syrup urine disease results from defects in the branched chain α-ketoacid dehydrogenase complex. Cells from seven German, three Turkish, and two Italian families including five consanguineous matings were analyzed for the causative mutations. Enzyme assays were used to confirm the initial clinical diagnosis of all probands. Immunoblots of mitochondrial proteins from these probands revealed reduced expression of the E1 α and β proteins of the complex. Previous studies showed that interaction of α and β was necessary to stabilize both proteins so that defects in either protein can result in decreased presence of both. The E1α Y393N mutation common in the Mennonite population that results in diminished amounts of both α and β proteins was not the cause of the reduction in these European patients.