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miRNA 海绵:吸收 miRNA 以调节基因表达。

miRNA sponges: soaking up miRNAs for regulation of gene expression.

机构信息

Department of Biomedicine, Aarhus University, Aarhus C, Denmark.

出版信息

Wiley Interdiscip Rev RNA. 2014 May-Jun;5(3):317-33. doi: 10.1002/wrna.1213. Epub 2013 Dec 23.

Abstract

MicroRNAs (miRNAs) are small regulatory RNAs that act in an entangled web of interactions with target mRNAs to shape the cellular protein landscape by post-transcriptional control of mRNA decay and translation. miRNAs are themselves subject to numerous regulatory mechanisms that adjust their prevalence and activity. Emerging evidence suggests that miRNAs are themselves targeted by regulatory RNA species, and the identification of several classes of noncoding RNA molecules carrying miRNA binding sites has added a new intricate dimension to miRNA regulation. Such miRNA 'sponges' bind miRNAs and competitively sequester them from their natural targets. Endogenous miRNA sponges, also termed competing endogenous RNAs (ceRNAs), act to buffer the activity of miRNAs on physiologically relevant targets. This class of sponges includes endogenously transcribed pseudogenes, long noncoding RNAs, and recently discovered circular RNAs and may act in large complex networks in conjunction with miRNAs to regulate the output of protein. With the growing demand of regulating miRNA activity for experimental purposes and potential future clinical use, naturally occurring miRNA sponges are providing inspiration for engineering of gene vector-encoded sponges as potent inhibitors of miRNA activity. Combined with potent and versatile vector technologies, expression of custom-designed sponges provides new means of managing miRNAs and soaking up miRNAs for therapeutic regulation of gene expression.

摘要

微小 RNA(miRNA)是一种小型调节 RNA,通过与靶 mRNA 的相互作用形成复杂的网络,对 mRNA 的降解和翻译进行转录后调控,从而影响细胞内的蛋白质景观。miRNA 本身受到多种调节机制的调控,这些机制可以调节其丰度和活性。新出现的证据表明,miRNA 本身也是调节 RNA 物种的靶标,并且已经鉴定出几类携带 miRNA 结合位点的非编码 RNA 分子,这为 miRNA 调节增加了一个新的复杂维度。这种 miRNA“海绵”可以结合 miRNA,并与它们的天然靶标竞争结合。内源性 miRNA 海绵,也称为竞争内源性 RNA(ceRNA),可以缓冲 miRNA 在生理相关靶标上的活性。这类海绵包括内源性转录的假基因、长非编码 RNA,以及最近发现的环状 RNA,它们可能与 miRNA 一起在大的复杂网络中发挥作用,调节蛋白质的表达。由于对 miRNA 活性进行实验调节和未来潜在临床应用的需求不断增长,天然存在的 miRNA 海绵为工程设计基因载体编码的海绵作为 miRNA 活性的有效抑制剂提供了灵感。结合强大且多功能的载体技术,定制设计的海绵的表达为 miRNA 的管理和吸收提供了新的手段,以实现基因表达的治疗性调节。

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