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9G74

Mouse mitochondrial DNA polymerase gamma ternary complex in replication conformer

Summary for 9G74
Entry DOI10.2210/pdb9g74/pdb
Related9G75 9G77
EMDB information51109
DescriptorDNA polymerase subunit gamma-1, DNA polymerase subunit gamma-2, DNA (primer strand), ... (6 entities in total)
Functional Keywordsmitochondrial dna polymerase, transferase
Biological sourceMus musculus (house mouse)
More
Total number of polymer chains5
Total formula weight257085.51
Authors
Valenzuela, S.,Falkenberg, M. (deposition date: 2024-07-19, release date: 2025-06-04)
Primary citationCorra, S.,Zuppardo, A.,Valenzuela, S.,Jenninger, L.,Cerutti, R.,Sillamaa, S.,Hoberg, E.,Johansson, K.A.S.,Rovsnik, U.,Volta, S.,Silva-Pinheiro, P.,Davis, H.,Trifunovic, A.,Minczuk, M.,Gustafsson, C.M.,Suomalainen, A.,Zeviani, M.,Macao, B.,Zhu, X.,Falkenberg, M.,Viscomi, C.
Modelling POLG mutations in mice unravels a critical role of POL gamma Beta in regulating phenotypic severity.
Nat Commun, 16:4782-4782, 2025
Cited by
PubMed Abstract: DNA polymerase γ (POLγ), responsible for mitochondrial DNA replication, consists of a catalytic POLγA subunit and two accessory POLγB subunits. Mutations in POLG, which encodes POLγA, lead to various mitochondrial diseases. We investigated the most common POLG mutations (A467T, W748S, G848S, Y955C) by characterizing human and mouse POLγ variants. Our data reveal that these mutations significantly impair POLγ activities, with mouse variants exhibiting milder defects. Cryogenic electron microscopy highlighted structural differences between human and mouse POLγ, particularly in the POLγB subunit, which may explain the higher activity of mouse POLγ and the reduced severity of mutations in mice. We further generated a panel of mouse models mirroring common human POLG mutations, providing crucial insights into the pathogenesis of POLG-related disorders and establishing robust models for therapeutic development. Our findings emphasize the importance of POLγB in modulating the severity of POLG mutations.
PubMed: 40404629
DOI: 10.1038/s41467-025-60059-y
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.75 Å)
Structure validation

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