Structural basis for intrinsic strand displacement activity of mitochondrial DNA polymerase

Members of the Pol A family of DNA polymerases, found across all domains of life, utilize various strategies for DNA strand separation during replication. In higher eukaryotes, mitochondrial DNA polymerase γ relies on the replicative helicase TWINKLE, whereas the yeast ortholog, Mip1, can unwind DNA independently. Using Mip1 as a model, we present a series of high-resolution cryo-EM structures that capture the process of DNA strand displacement. Our data reveal previously unidentified structural elements that facilitate the unwinding of the downstream DNA duplex. Yeast cells harboring Mip1 variants defective in strand displacement exhibit impaired oxidative phosphorylation and loss of mtDNA, corroborating the structural observations. This study provides a molecular basis for the intrinsic strand displacement activity of Mip1 and illuminates the distinct unwinding mechanisms utilized by Pol A family DNA polymerases.

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Publication Details

Journal
Nature Communications
Published
2025-03-11
DOI
https://doi.org/10.1038/s41467-025-57594-z
Citations
1
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
0.81
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article

Structural basis for intrinsic strand displacement activity of mitochondrial DNA polymerase

Dmitry Temiakov, Sirelin Sillamaa, Karl Herbine, Ashok R. Nayak et al.
1 citations
Nature Communications
RNA and protein synthesis mechanisms
0.81
article

Structural basis for intrinsic strand displacement activity of mitochondrial DNA polymerase

Dmitry Temiakov, Sirelin Sillamaa, Karl Herbine, Ashok R. Nayak, V. E. Sokolova, Juhan Sedman
article en
1 citations

Abstract

Members of the Pol A family of DNA polymerases, found across all domains of life, utilize various strategies for DNA strand separation during replication. In higher eukaryotes, mitochondrial DNA polymerase γ relies on the replicative helicase TWINKLE, whereas the yeast ortholog, Mip1, can unwind DNA independently. Using Mip1 as a model, we present a series of high-resolution cryo-EM structures that capture the process of DNA strand displacement. Our data reveal previously unidentified structural elements that facilitate the unwinding of the downstream DNA duplex. Yeast cells harboring Mip1 variants defective in strand displacement exhibit impaired oxidative phosphorylation and loss of mtDNA, corroborating the structural observations. This study provides a molecular basis for the intrinsic strand displacement activity of Mip1 and illuminates the distinct unwinding mechanisms utilized by Pol A family DNA polymerases.

Nature CommunicationsVol. 16(1)
Thomas Jefferson University (US), Jefferson Institute (US), University of Tartu (EE), Philadelphia University (US)
Openalex Percentile: Top 30%
RNA and protein synthesis mechanisms
0.81
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