Structural basis for intrinsic strand displacement activity of mitochondrial DNA polymerase

被引:0
作者
Nayak, Ashok R. [1 ]
Sokolova, Viktoriia [1 ]
Sillamaa, Sirelin [2 ]
Herbine, Karl [1 ]
Sedman, Juhan [2 ]
Temiakov, Dmitry [1 ]
机构
[1] Thomas Jefferson Univ, Dept Biochem & Mol Biol, 1020 Locust St, Philadelphia, PA 19107 USA
[2] Univ Tartu, Inst Mol & Cell Biol, Riia 23, Tartu, Estonia
基金
美国国家卫生研究院;
关键词
CRYO-EM; CRYSTAL-STRUCTURES; PROCESSIVITY; PREVENTION; MECHANISM; FRAGMENT; SUBUNIT;
D O I
10.1038/s41467-025-57594-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 gamma 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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页数:13
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