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Structure Dynamics and Branch Migration of a DNA Holliday Junction: A Single-Molecule Fluorescence and Modeling Study

机译:DNA霍利迪结的结构动力学和分支迁移:单分子荧光和建模研究

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摘要

The Holliday junction (HJ) is a central intermediate of various genetic processes, including homologous and site-specific DNA recombination and DNA replication. Elucidating the structure and dynamics of HJs provides the basis for understanding the molecular mechanisms of these genetic processes. Our previous single-molecule fluorescence studies led to a model according to which branch migration is a stepwise process consisting of consecutive migration and folding steps. These data led us to the conclusion that one hop can be more than 1 basepair (bp); moreover, we hypothesized that continuous runs over the entire sequence homology (5 bp) can occur. Direct measurements of the dependence of the fluorescence resonance energy transfer (FRET) value on the donor-acceptor (D-A) distance are required to justify this model and are the major goal of this article. To accomplish this goal, we performed single-molecule FRET experiments with a set of six immobile HJ molecules with varying numbers of bps between fluorescent dyes placed on opposite arms. The designs were made in such a way that the distances between the donor and acceptor were equal to the distances between the dyes formed upon 1-bp migration hops of a HJ having 10-bp homology. Using these designs, we confirmed our previous hypothesis that the migration of the junction can be measured with bp accuracy. Moreover, the FRET values determined for each acceptor-donor separation corresponded very well to the values for the steps on the FRET time trajectories, suggesting that each step corresponds to the migration of the branch at a defined depth. We used the dependence of the FRET value on the D-A distance to measure directly the size for each step on the FRET time trajectories. These data showed that one hop is not necessarily 1 bp. The junction is able to migrate over several bps, detected as one hop and confirming our model. The D-A distances extracted from the FRET properties of the immobile junctions formed the basis for modeling the HJ structures. The composite data fit a partially opened, side-by-side model with adjacent double-helical arms slightly kinked at the four-way junction and the junction as a whole adopting a global X-shaped form that mimics the coaxially stacked-X structure implicated in previous solution studies.
机译:霍利迪交界处(HJ)是各种遗传过程的中心中间体,包括同源和位点特异性的DNA重组和DNA复制。阐明HJ的结构和动力学为理解这些遗传过程的分子机制提供了基础。我们以前的单分子荧光研究得出了一个模型,根据该模型,分支迁移是一个由连续迁移和折叠步骤组成的逐步过程。这些数据使我们得出这样的结论,即一跳可以超过1个碱基对(bp)。此外,我们假设在整个序列同源性(5 bp)处可能发生连续运行。需要直接测量荧光共振能量转移(FRET)值对供体-受体(D-A)距离的依赖性,以证明该模型的正确性,这是本文的主要目标。为了实现此目标,我们用一组六个固定的HJ分子进行了单分子FRET实验,这些分子在相对臂上放置的荧光染料之间具有不同的bps数量。以这样的方式进行设计:供体和受体之间的距离等于具有10bp同源性的HJ的1bp迁移跃点上形成的染料之间的距离。使用这些设计,我们证实了我们先前的假设,即可以bp精度测量结的迁移。此外,为每个受体-供体分离确定的FRET值与FRET时间轨迹上的阶跃值非常吻合,表明每个阶跃对应于在定义深度的分支迁移。我们使用FRET值对D-A距离的依赖性来直接测量FRET时间轨迹上每一步的大小。这些数据表明一跳不一定是1 bp。该结点能够迁移几个bps,被检测为一跳并证实了我们的模型。从不动结的FRET特性中提取的D-A距离构成了对HJ结构建模的基础。复合数据适合部分打开的并排模型,相邻的双螺旋臂在四向交叉点处稍微扭结,并且该交叉点整体上采用整体X形形式,模仿了所涉及的同轴堆叠X结构在以前的解决方案研究中。

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