MPC2 variants disrupt mitochondrial pyruvate metabolism and cause an early-onset mitochondriopathy
Claire Pujol, Lebigot Elise, Gaignard Pauline, Wai Timothy, Slama Abdelhamid · FENS Forum 2024
Pyruvate is an essential metabolite produced by glycolysis in the cytosol and must be transported across the inner mitochondrial membrane into the mitochondrial matrix, where it is oxidized to fuel mitochondrial respiration. Pyruvate import is performed by the mitochondrial pyruvate carrier (MPC), a hetero-oligomeric complex composed by interdependent subunits MPC1 and MPC2. Pathogenic variants in the MPC1 gene disrupt mitochondrial pyruvate uptake and oxidation and cause autosomal-recessive early-onset neurological dysfunction in humans. The present work describes the first pathogenic variant
ePoster · Neuroscience