A patient with a deficient voltage-dependent anion channel (VDAC) is reported, presenting clinically with psychomotor retardation and minor dysmorphic features. Biochemical studies on muscle mitochondria showed impaired rates of pyruvate oxidation and ATP production; however, no specific deficient activity of one of the mitochondrial enzymes was involved. Western blotting experiments indicated an almost complete VDAC deficiency in skeletal muscle. The only moderately decreased VDAC content in the patient's fibroblasts might indicate that VDAC is expressed in a tissue-specific manner. The deficiency is likely caused by a mutation in the HVDAC1 gene or by a disturbed posttranslational modification. This is the first described deficiency of a component of the outer mitochondrial membrane associated with the pyruvate oxidation pathway. Defects in this membrane should be considered as a possible cause of otherwise unexplained mitochondrial disorders.
|Titolo:||Deficiency of the voltage-dependent anion channel: A novel cause of mitochondriopathy|
|Data di pubblicazione:||1996|
|Citazione:||Deficiency of the voltage-dependent anion channel: A novel cause of mitochondriopathy / Huizing M; Ruitenbeek W; Thinnes FP; De Pinto V; Wendel U; Trijbels FJM; Smit LME; terLaak HJ; VanDenHeuvel LP. - In: PEDIATRIC RESEARCH. - ISSN 0031-3998. - 39:5(1996), pp. 760-765.|
|Appare nelle tipologie:||1.1 Articolo in rivista|