Eulalio Ana, Mano Miguel
Institute for Molecular Infection Biology (IMIB), University of Würzburg, Würzburg, Germany.
International Centre for Genetic Engineering and Biotechnology (ICGEB), Trieste, Italy UC-BIOTECH, Center for Neuroscience and Cell Biology (CNC), University of Coimbra, Coimbra, Portugal
J Biomol Screen. 2015 Sep;20(8):1003-17. doi: 10.1177/1087057115578837. Epub 2015 Mar 30.
MicroRNAs (miRNAs) are a class of genome-encoded small RNAs that post-transcriptionally regulate gene expression by repressing target transcripts containing partially or fully complementary binding sites.Despite their relatively low number, miRNAs have been shown to directly regulate a large fraction of the transcriptome. In agreement with their pervasive role in the regulation of eukaryotic gene expression, miRNAs have been implicated in virtually all biological processes, including different pathologies.The use of screening technologies to systematically analyze miRNA function in cell-based assays offers a unique opportunity to gain new insights into complex biological and disease-relevant processes. Given the low complexity of the miRNome and the similarities to small interfering RNA (siRNA) screening experimental approaches, phenotypic screening using genome-wide libraries of miRNA mimics or inhibitors is not, per se, technically challenging. The identification of miRNA targets and, more importantly, the characterization of their mechanisms of action through the identification of the key targets underlying observed phenotypes remain the major challenges of this approach.This article provides an overview of cell-based screenings for miRNA function that were performed in different biological contexts. The advantages and limitations of computational and experimental approaches commonly used to identify miRNA targets are also discussed.
微小RNA(miRNA)是一类由基因组编码的小RNA,它们通过抑制含有部分或完全互补结合位点的靶转录本来在转录后调节基因表达。尽管miRNA数量相对较少,但已证明它们能直接调节很大一部分转录组。与它们在真核基因表达调控中的普遍作用一致,miRNA几乎涉及所有生物学过程,包括不同的病理过程。利用筛选技术在基于细胞的实验中系统分析miRNA功能,为深入了解复杂的生物学和疾病相关过程提供了独特的机会。鉴于miRNA组的低复杂性以及与小干扰RNA(siRNA)筛选实验方法的相似性,使用miRNA模拟物或抑制剂的全基因组文库进行表型筛选本身在技术上并不具有挑战性。鉴定miRNA靶标,更重要的是,通过鉴定观察到的表型背后的关键靶标来表征其作用机制,仍然是这种方法的主要挑战。本文概述了在不同生物学背景下针对miRNA功能进行的基于细胞的筛选。还讨论了常用于鉴定miRNA靶标的计算和实验方法的优缺点。