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I260Q DNA polymerase beta highlights precatalytic conformational rearrangements critical for fidelity

机译:I260Q DNA聚合酶β突出突出致力于保真性关键的预结容重排

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DNA polymerase beta (pol beta) fills single nucleotide gaps in DNA during base excision repair and non-homologous end-joining. Pol beta must select the correct nucleotide from among a pool of four nucleotides with similar structures and properties in order to maintain genomic stability during DNA repair. Here, we use a combination of X-ray crystallography, fluorescence resonance energy transfer and nuclear magnetic resonance to show that pol beta's ability to access the appropriate conformations both before and upon binding to nucleotide substrates is integral to its fidelity. Importantly, we also demonstrate that the inability of the I260Q mutator variant of pol beta to properly navigate this conformational landscape results in error-prone DNA synthesis. Our work reveals that precatalytic conformational rearrangements themselves are an important underlying mechanism of substrate selection by DNA pol beta.
机译:DNA聚合酶β(POLβ)在基础切除修复和非同源终端接合期间填充DNA中的单核苷酸间隙。 Polβ必须从具有相似结构和性质的四个核苷酸的池中选择正确的核苷酸,以便在DNA修复期间保持基因组稳定性。 这里,我们使用X射线晶体学,荧光共振能量转移和核磁共振的组合,表明POLβ在与核苷酸底物结合之前和结合核苷酸底物之前获得适当构象的能力是一体的。 重要的是,我们还表明,POLβ的I260Q突变变体无法正确导航的这种构型景观导致易于易于的DNA合成。 我们的工作表明,预催化构象重排本身是DNAPolβ的基材选择的重要潜在机制。

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