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A Dynamic Search Process Underlies MicroRNA Targeting

机译:动态搜索过程是MicroRNA靶向的基础

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Argonaute proteins play a central role in mediating post-transcriptional gene regulation by microRNAs (miRNAs). Argonautes use the nucleotide sequences in miRNAs as guides for identifying target messenger RNAs for repression. Here, we used single-molecule FRET to directly visualize how human Argonaute-2 (Ago2) searches for and identifies target sites in RNAs complementary to its miRNA guide. Our results suggest that Ago2 initially scans for target sites with complementarity to nucleotides 2-4 of the miRNA. This initial transient interaction propagates into a stable association when target complementarity extends to nucleotides 2-8. This stepwise recognition process is coupled to lateral diffusion of Ago2 along the target RNA, which promotes the target search by enhancing the retention of Ago2 on the RNA. The combined results reveal the mechanisms that Argonaute likely uses to efficiently identify miRNA target sites within the vast and dynamic agglomeration of RNA molecules in the living cell.
机译:Argonaute蛋白在通过microRNA(miRNA)介导转录后基因调控中起着核心作用。 Argonautes使用miRNA中的核苷酸序列作为指导,以鉴定用于抑制的目标信使RNA。在这里,我们使用单分子FRET直接可视化人类Argonaute-2(Ago2)如何搜索和识别与其miRNA指南互补的RNA中的靶位点。我们的结果表明,Ago2最初会扫描与miRNA核苷酸2-4互补的目标位点。当靶标互补性延伸至核苷酸2-8时,该初始瞬时相互作用传播为稳定的缔合。该逐步识别过程与Ago2沿着靶RNA的侧向扩散相耦合,这通过增强Ago2在RNA上的保留来促进靶标搜索。合并的结果揭示了Argonaute可能用来有效识别活细胞中庞大而动态的RNA分子团聚中miRNA靶位点的机制。

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