Structure-function defects of human mitochondrial DNA polymerase in autosomal dominant progressive external ophthalmoplegia

Maria A. Graziewicz, Matthew J. Longley, Rachelle J. Bienstock, Massimo Zeviani, William C. Copeland

Research output: Contribution to journalArticle


Progressive external ophthalmoplegia (PEO) is a mitochondrial disorder associated with mutations in the POLG gene encoding the mitochondrial DNA polymerase (pol γ). Four autosomal dominant mutations that cause PEO encode the amino acid substitutions G923D, R943H, Y955C and A957S in the polymerase domain of pol γ. A homology model of the pol γ catalytic domain in complex with DNA was developed to investigate the effects of these mutations. Two mutations causing the most severe disease phenotype, Y955C and R943H, change residues that directly interact with the incoming dNTP. Polymerase mutants exhibit 0.03-30% wild-type polymerase activity and a 2- to 35-fold decrease in nucleotide selectivity in vitro. The reduced selectivity and catalytic efficiency of the autosomal dominant PEO mutants predict in vivo dysfunction, and the extent of biochemical defects correlates with the clinical severity of the disease.

Original languageEnglish
Pages (from-to)770-776
Number of pages7
JournalNature Structural and Molecular Biology
Issue number8
Publication statusPublished - Aug 2004


ASJC Scopus subject areas

  • Structural Biology
  • Molecular Biology

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