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揭示细胞通路调控中微小RNA介导的冗余原理。

Unveiling the principle of microRNA-mediated redundancy in cellular pathway regulation.

作者信息

Fischer Simon, Handrick René, Aschrafi Armaz, Otte Kerstin

机构信息

a Institute of Applied Biotechnology; University of Applied Sciences Biberach ; Biberach , Germany.

出版信息

RNA Biol. 2015;12(3):238-47. doi: 10.1080/15476286.2015.1017238.

Abstract

Understanding the multifaceted nature of microRNA (miRNA) function in mammalian cells is still a challenge. Commonly accepted principles of cooperativity and multiplicity of miRNA function imply that individual mRNAs can be targeted by several miRNAs whereas a single miRNA may concomitantly regulate a subset of different genes. However, there is a paucity of information whether multiple miRNAs regulate critical cellular events and thereby acting redundantly. To gain insight into this notion, we conducted an unbiased high-content miRNA screen by individually introducing 1139 miRNA mimics into Chinese hamster ovary (CHO) cells. We discovered that 66% of all miRNAs significantly impacted on proliferation, protein expression, apoptosis and necrosis. In summary, we provide evidence for a substantial degree of redundancy among miRNAs to maintain cellular homeostasis.

摘要

了解微小RNA(miRNA)在哺乳动物细胞中的多方面功能仍然是一项挑战。miRNA功能协同性和多重性的普遍接受原则表明,单个mRNA可能被多种miRNA靶向,而单个miRNA可能同时调节不同基因的一个子集。然而,关于多种miRNA是否调节关键细胞事件并因此发挥冗余作用的信息却很少。为了深入了解这一概念,我们通过将1139种miRNA模拟物分别导入中国仓鼠卵巢(CHO)细胞,进行了一项无偏倚的高内涵miRNA筛选。我们发现,所有miRNA中有66%对细胞增殖、蛋白质表达、细胞凋亡和坏死有显著影响。总之,我们提供了证据表明miRNA之间存在很大程度的冗余以维持细胞稳态。

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