Supplementation studies with dAMP/dGMP in primary cultures of human myoblasts and myotubes of patients with mitochondrial DNA depletion caused by mutations in the DGUOK and POLG1…

Mitochondrial DNA depletion syndrome (MDS), a frequent cause of severe childhood (hepato)encephalomyopathies, is defined as a reduction of mitochondrial DNA copy number related to nuclear DNA in different tissues which leads to insufficient synthesis of respiratory chain complexes. MDS is responsible for approximately 30–40% of combined RC deficiencies in children. Mutations of eight nuclear genes (DGUOK, POLG1, MVP17. ECGF1, TK2, SUCLA2, SUCLG1 and RRM2B), all involved in the synthesis or maintenance of mitochondrial nucleotide pools, were identified in approximately 40% of all MDS cases implying further geneti…