Oxidative damage diminishes mitochondrial DNA polymerase replication fidelity

Andrew P. Anderson, Xuemei Luo, William Russell, Y. Whitney Yin

Research output: Contribution to journalArticle

4 Scopus citations

Abstract

Mitochondrial DNA (mtDNA) resides in a high ROS environment and suffers more mutations than its nuclear counterpart. Increasing evidence suggests that mtDNA mutations are not the results of direct oxidative damage, rather are caused, at least in part, by DNA replication errors. To understand how the mtDNA replicase, Pol γ, can give rise to elevated mutations, we studied the effect of oxidation of Pol γon replication errors. Pol γis a high fidelity polymerase with polymerase (pol) and proofreading exonuclease (exo) activities. We show that Pol γexo domain is far more sensitive to oxidation than pol; under oxidative conditions, exonuclease activity therefore declines more rapidly than polymerase. The oxidized Pol γbecomes editing-deficient, displaying a 20-fold elevated mutations than the unoxidized enzyme. Mass spectrometry analysis reveals that Pol γexo domain is a hotspot for oxidation. The oxidized exo residues increase the net negative charge around the active site that should reduce the affinity to mismatched primer/template DNA. Our results suggest that the oxidative stress induced high mutation frequency on mtDNA can be indirectly caused by oxidation of the mitochondrial replicase.

Original languageEnglish (US)
Pages (from-to)817-829
Number of pages13
JournalNucleic acids research
Volume48
Issue number2
DOIs
StatePublished - Jan 24 2020

ASJC Scopus subject areas

  • Genetics

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