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Double-stranded RNA bending by AU-tract sequences

机译:由Au-tract序列双链RNA弯曲

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摘要

Sequence-dependent structural deformations of the DNA double helix (dsDNA) have been extensively studied, where adenine tracts (A-tracts) provide a striking example for global bending in the molecule. However, in contrast to dsDNA, sequence-dependent structural features of dsRNA have received little attention. In this work, we demonstrate that the nucleotide sequence can induce a bend in a canonical Watson-Crick base-paired dsRNA helix. Using all-atom molecular dynamics simulations, we identified a sequence motif consisting of alternating adenines and uracils, or AU-tracts, that strongly bend the RNA double-helix. This finding was experimentally validated using atomic force microscopy imaging of dsRNA molecules designed to display macroscopic curvature via repetitions of phased AU-tract motifs. At the atomic level, this novel phenomenon originates from a localized compression of the dsRNA major groove and a large propeller twist at the position of the AU-tract. Moreover, the magnitude of the bending can be modulated by changing the length of the AU-tract. Altogether, our results demonstrate the possibility of modifying the dsRNA curvature by means of its nucleotide sequence, which may be exploited in the emerging field of RNA nanotechnology and might also constitute a natural mechanism for proteins to achieve recognition of specific dsRNA sequences.
机译:已经广泛研究了DNA双螺旋(DSDNA)的序列依赖性结构变形,其中腺嘌呤串(A-散)提供了分子中全球弯曲的引人注目的例子。然而,与DSDNA相反,DSRNA的序列依赖性结构特征几乎没有注意。在这项工作中,我们证明核苷酸序列可以在规范沃特森 - 克里克基碱基配对的DSRNA螺旋中诱导弯曲。使用全原子分子动力学模拟,我们鉴定了一种由交替的腺嘌呤和尿嘧啶或尿布,或肛门菌,强烈地弯曲RNA双螺旋的序列基序。使用设计用于显示宏观曲率的DsRNA分子的原子力显微镜成像进行了实验验证的,该发现通过重复分阶段的Au-Tract基序显示宏观曲率。在原子水平,这种新颖现象来自DSRNA主沟的局部压缩和在Au-arct的位置处的大型螺旋桨扭曲。此外,可以通过改变Au-aract的长度来调节弯曲的大小。完全,我们的结果证明了通过其核苷酸序列来修饰DSRNA曲率的可能性,其可以在RNA纳米技术的新出现领域中被利用,并且还可以构成蛋白质的自然机制,以实现特定的DSRNA序列的识别。

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