Human Molecular Genetics Advance Access published online on February 16, 2009
Human Molecular Genetics, doi:10.1093/hmg/ddp074
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In vitro supplementation with dAMP/dGMP leads to partial restoration of mtDNA levels in mitochondrial depletion syndromes
1 Friedrich-Baur-Institute, Department of Neurology, Ludwig-Maximilians-University of Munich, Germany 2 Medical Genetic Center, Munich, Germany 3 Institute of Human Genetics, University of Newcastle upon Tyne, UK 4 Mitochondrial Research Group, University of Newcastle upon Tyne, UK
* Address correspondence to: Rita Horvath MD, Mitochondrial Research Group, University of Newcastle upon Tyne, UK Phone: +44 191 222 5982, Fax: +44 191 222 8553, Email: Rita.Horvath{at}ncl.ac.uk
Received December 17, 2008; Revised January 25, 2009; Accepted February 11, 2009
Mitochondrial DNA depletion syndrome (MDS), a frequent cause of childhood (hepato)encephalomyopathies, is defined as a reduction of mitochondrial DNA copy number related to nuclear DNA. It was previously shown that mtDNA depletion can be prevented by dAMP/dGMP supplementation in deoxyguanosine kinase-deficient fibroblasts. We investigated myotubes of patients diagnosed with mtDNA depletion carrying pathogenic mutations in DGUOK, POLG1 (Alpers syndrome) and TYMP. Differentiating myotubes of all patients and controls were supplemented with different doses of dAMP/dGMP or dAMP/dGMP/dCMP in TYMP deficiency, and analysed for mtDNA/nDNA ratio and for cytochrome c oxidase (COX) activity. Serum deprivation and myotube formation triggered a decrease in mtDNA copy number in DGUOK or POLG1 deficient myotubes, but not in TYMP deficiency and healthy controls. Supplementation with dAMP/dGMP lead to a significant and reproducible rescue of mtDNA depletion in DGUOK deficiency. POLG1 deficient myotubes also showed a mild, not significant increase in mtDNA copy number. MtDNA depletion did not result in deficient COX staining in DGUOK and POLG1 deficient myotubes. Treatment with ethidium bromide resulted in very severe depletion and absence of COX staining in all cell types, and no recovery was observed after supplementation with dAMP/dGMP.
We show that supplementation with dAMP/dGMP increases mtDNA copy number significantly in DGUOK deficient myotubes and, leads to a mild, non-significant improvement of mtDNA depletion in POLG1 deficiency. No adverse effect on mtDNA copy number was observed on high dose supplementation in vitro. Further studies are needed to determine possible therapeutic implications of dAMP/dGMP supplementation for DGUOK deficiency in vivo.
Disclosure: The authors report no conflicts of interest.