Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
RNA Biol. 2011 Nov-Dec;8(6):1115-23. doi: 10.4161/rna.8.6.17626.
MicroRNA (miRNA) genes produce three major RNA products; primary (pri-), precursor (pre-), and mature miRNAs. Each product includes sequences complementary to cognate targets, thus they all can in principle interact with the targets. In a recent study we showed that pri-miRNAs play a direct role in target recognition and repression in the absence of functional mature miRNAs. Here we examined the functional contribution of pri-miRNAs in target regulation when full-length functional miRNAs are present. We found that pri-let-7 loop nucleotides control the production of the 5' end of mature miRNAs and modulate the activity of the miRNA gene. This insight enabled us to modulate biogenesis of functional mature miRNAs and dissect the causal relationships between mature miRNA biogenesis and target repression. We demonstrate that both pri- and mature miRNAs can contribute to target repression and that their contributions can be distinguished by the differences between the pri- and mature miRNAs' sensitivity to bind to the first seed nucleotide. Our results demonstrate that the regulatory information encoded in the pri-/pre-miRNA loop nucleotides controls the activities of pri-miRNAs and mature let-7 by influencing pri-miRNA and target complex formation and the fidelity of mature miRNA seed generation.
微小 RNA(miRNA)基因产生三种主要的 RNA 产物;初级(pri-)、前体(pre-)和成熟 miRNA。每个产物都包含与同源靶标互补的序列,因此它们原则上都可以与靶标相互作用。在最近的一项研究中,我们表明 pri-miRNA 在缺乏功能性成熟 miRNA 的情况下直接参与靶标识别和抑制。在这里,当存在全长功能性 miRNA 时,我们研究了 pri-miRNA 在靶标调控中的功能贡献。我们发现 pri-let-7 环核苷酸控制成熟 miRNA 的 5' 端的产生,并调节 miRNA 基因的活性。这一见解使我们能够调节功能性成熟 miRNA 的生物发生,并剖析成熟 miRNA 生物发生和靶标抑制之间的因果关系。我们证明,pri- 和成熟 miRNA 都可以有助于靶标抑制,并且它们的贡献可以通过 pri- 和成熟 miRNA 对结合第一个种子核苷酸的敏感性之间的差异来区分。我们的结果表明,pri-/pre-miRNA 环核苷酸中的调节信息通过影响 pri-miRNA 和靶标复合物的形成以及成熟 miRNA 种子生成的保真度来控制 pri-miRNA 和成熟 let-7 的活性。