The exonuclease activity of DNA polymerase gamma is required for ligation 
during mitochondrial DNA replication

Macao, B.; Uhler, J. P.; Siibak, T.; Zhu, X.; Shi, Y.; Sheng, W.; Olsson, M.; Stewart, J. B.; Gustafsson, C. M.; Falkenberg, M.

doi:10.1038/ncomms8303

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Journal Article

The exonuclease activity of DNA polymerase gamma is required for ligation during mitochondrial DNA replication

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Stewart, J. B.
Stewart – Mitochondrial Mutations and Genome Co-evolution, Research Groups, Max Planck Institute for Biology of Ageing, Max Planck Society;

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http://www.ncbi.nlm.nih.gov/pubmed/26095671
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Citation

Macao, B., Uhler, J. P., Siibak, T., Zhu, X., Shi, Y., Sheng, W., et al. (2015). The exonuclease activity of DNA polymerase gamma is required for ligation during mitochondrial DNA replication. Nat Commun, 6, 7303. doi:10.1038/ncomms8303.

Cite as: https://hdl.handle.net/21.11116/0000-000B-816F-7

Abstract

Mitochondrial DNA (mtDNA) polymerase gamma (POLgamma) harbours a 3'-5' exonuclease proofreading activity. Here we demonstrate that this activity is required for the creation of ligatable ends during mtDNA replication. Exonuclease-deficient POLgamma fails to pause on reaching a downstream 5'-end. Instead, the enzyme continues to polymerize into double-stranded DNA, creating an unligatable 5'-flap. Disease-associated mutations can both increase and decrease exonuclease activity and consequently impair DNA ligation. In mice, inactivation of the exonuclease activity causes an increase in mtDNA mutations and premature ageing phenotypes. These mutator mice also contain high levels of truncated, linear fragments of mtDNA. We demonstrate that the formation of these fragments is due to impaired ligation, causing nicks near the origin of heavy-strand DNA replication. In the subsequent round of replication, the nicks lead to double-strand breaks and linear fragment formation.