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Helix‐7 in Argonaute2 shapes the microRNA seed region for rapid target recognition

机译:Argonaute2中的Helix‐7形成了microRNA种子区域可快速识别靶标

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摘要

Argonaute proteins use microRNAs (miRNAs) to identify mRNAs targeted for post‐transcriptional repression. Biochemical assays have demonstrated that Argonaute functions by modulating the binding properties of its miRNA guide so that pairing to the seed region is exquisitely fast and accurate. However, the mechanisms used by Argonaute to reshape the binding properties of its small RNA guide remain poorly understood. Here, we identify a structural element, α‐helix‐7, in human Argonaute2 (Ago2) that is required for speed and fidelity in binding target RNAs. Biochemical, structural, and single‐molecule data indicate that helix‐7 acts as a molecular wedge that pivots to enforce rapid making and breaking of miRNA:target base pairs in the 3′ half of the seed region. These activities allow Ago2 to rapidly dismiss off‐targets and dynamically search for seed‐matched sites at a rate approaching the limit of diffusion.
机译:Argonaute蛋白使用microRNA(miRNA)来识别靶向转录后阻遏的mRNA。生化分析表明,Argonaute通过调节其miRNA向导的结合特性起作用,从而与种子区域的配对非常快速和准确。然而,人们对Argonaute用来重塑其小RNA向导的结合特性的机制了解甚少。在这里,我们确定了人类Argonaute2(Ago2)中的结构元件α-螺旋-7,这是结合靶RNA的速度和保真度所必需的。生化,结构和单分子数据表明,helix-7充当分子楔形物,可在种子区域的3'一半内枢转以强制快速制造和破坏miRNA:靶碱基对。这些活动使Ago2可以迅速驱散目标,并以接近扩散极限的速率动态搜索种子匹配的位点。

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