Ashok R. Nayak, Viktoriia Sokolova, Sirelin Sillamaa, Karl Herbine, Juhan Sedman, Dmitry Temiakov
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引用次数: 0
摘要
Pol A DNA聚合酶家族的成员遍布生命的所有领域,在复制过程中利用各种策略进行DNA链分离。在高等真核生物中,线粒体DNA聚合酶γ依赖于复制解旋酶TWINKLE,而酵母同源物Mip1可以独立解开DNA。以Mip1为模型,我们展示了一系列高分辨率的低温电镜结构,可以捕捉DNA链位移的过程。我们的数据揭示了以前未知的结构元素,促进下游DNA双链的解绕。携带Mip1变异链位移缺陷的酵母细胞表现出氧化磷酸化受损和mtDNA丢失,证实了结构观察。该研究为Mip1的固有链位移活性提供了分子基础,并阐明了Pol a家族DNA聚合酶所利用的独特解绕机制。
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.
期刊介绍:
Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.