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Torque measurements reveal sequence-specific cooperative transitions in supercoiled DNA

机译:扭矩测量揭示了超螺旋DNA中序列特异性的协同转变

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摘要

B-DNA becomes unstable under superhelical stress and is able to adopt a wide range of alternative conformations including strand-separated DNA and Z-DNA. Localized sequence-dependent structural transitions are important for the regulation of biological processes such as DNA replication and transcription. To directly probe the effect of sequence on structural transitions driven by torque, we have measured the torsional response of a panel of DNA sequences using single molecule assays that employ nanosphere rotational probes to achieve high torque resolution. The responses of Z-forming d(pGpC)n sequences match our predictions based on a theoretical treatment of cooperative transitions in helical polymers. “Bubble” templates containing 50–100 bp mismatch regions show cooperative structural transitions similar to B-DNA, although less torque is required to disrupt strand–strand interactions. Our mechanical measurements, including direct characterization of the torsional rigidity of strand-separated DNA, establish a framework for quantitative predictions of the complex torsional response of arbitrary sequences in their biological context.
机译:B-DNA在超螺旋应力作用下变得不稳定,并能够采用多种替代构象,包括链分离的DNA和Z-DNA。依赖于序列的局部结构转变对于调节生物过程(例如DNA复制和转录)很重要。为了直接探测序列对由扭矩驱动的结构转变的影响,我们已经使用单分子测定法测量了一组DNA序列的扭转响应,该分子采用纳米球旋转探针来实现高转矩分辨率。 Z形成d(pGpC)n序列的响应与我们对基于螺旋聚合物中协同转变的理论处理的预测相符。包含50–100 bp错配区域的“气泡”模板显示出类似于B-DNA的协同结构转变,尽管破坏链间相互作用所需的扭矩较小。我们的机械测量,包括对链分离DNA的扭转刚度的直接表征,为定量预测在其生物学背景下任意序列的复杂扭转响应建立了框架。

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