Analysis of mutant DNA polymerase γ in patients with mitochondrial DNA depletion

Jan Willem Taanman, Shamima Rahman, Alistair T. Pagnamenta, Andrew A.M. Morris, Maria Bitner-Glindzicz, Nicole I. Wolf, James V. Leonard, Peter T. Clayton, Anthony H.V. Schapira

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We studied six unrelated children with depletion of mitochondrial DNA (mtDNA). They presented with Leigh syndrome, infantile hepatocerebral mtDNA depletion syndrome, or Alpers-Huttenlocher syndrome. Several genes have been implicated in mtDNA depletion. Screening of candidate genes indicated that all six patients were compound heterozygous for missense mutations in the gene for the catalytic subunit of DNA polymerase γ (POLG). Three of the identified mutations, c.3328C>T (p.H1110Y), c.3401A>G (p.H1134R), and c.3406G>A (p.E1136K), have not been reported earlier. To investigate the functional consequences of the mutations, we carried out a series of biochemical assays in cultured fibroblasts. These studies revealed that fibroblast cultures from the patients with infantile hepatocerebral mtDNA depletion syndrome progressively lost their mtDNA during culturing, whereas fibroblast cultures from patients presenting with Leigh syndrome or Alpers-Huttenlocher syndrome had reduced but stable levels of mtDNA. DNA polymerase γ activity was below the normal range in all patient cultures, except for one; however, this culture showed low levels of the heterodimeric enzyme and poor DNA polymerase γ processivity. Parental fibroblast cultures had normal catalytic efficiency of DNA polymerase γ, consistent with the observation that all carriers are asymptomatic. Thus, we report the first patient with Leigh syndrome caused by POLG mutations. The cell culture experiments established the pathogenicity of the identified POLG mutations and helped to define the molecular mechanisms responsible for mtDNA depletion in the patients' tissues. The assays may facilitate the identification of those patients in whom screening for POLG mutations would be most appropriate.

Original languageEnglish
Pages (from-to)248-254
Number of pages7
JournalHuman mutation
Issue number2
Publication statusPublished - Feb 2009


  • Alpers-Huttenlocher syndrome
  • DNA polymerase γ
  • Leigh syndrome
  • Mitochondrial DNA
  • Mitochondrial DNA depletion syndrome
  • POLG
  • mtDNA

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