Shan Ge, Li Yujing, Zhang Junliang, Li Wendi, Szulwach Keith E, Duan Ranhui, Faghihi Mohammad A, Khalil Ahmad M, Lu Lianghua, Paroo Zain, Chan Anthony W S, Shi Zhangjie, Liu Qinghua, Wahlestedt Claes, He Chuan, Jin Peng
Department of Human Genetics, Emory University School of Medicine, 615 Michael St, Atlanta, Georgia 30322, USA.
Nat Biotechnol. 2008 Aug;26(8):933-40. doi: 10.1038/nbt.1481. Epub 2008 Jul 20.
Small interfering RNAs (siRNAs) and microRNAs (miRNAs) are sequence-specific post-transcriptional regulators of gene expression. Although major components of the RNA interference (RNAi) pathway have been identified, regulatory mechanisms for this pathway remain largely unknown. Here we demonstrate that the RNAi pathway can be modulated intracellularly by small molecules. We have developed a cell-based assay to monitor the activity of the RNAi pathway and find that the small-molecule enoxacin (Penetrex) enhances siRNA-mediated mRNA degradation and promotes the biogenesis of endogenous miRNAs. We show that this RNAi-enhancing activity depends on the trans-activation-responsive region RNA-binding protein. Our results provide a proof-of-principle demonstration that small molecules can be used to modulate the activity of the RNAi pathway. RNAi enhancers may be useful in the development of research tools and therapeutics.
小分子干扰RNA(siRNA)和微小RNA(miRNA)是基因表达的序列特异性转录后调节因子。尽管RNA干扰(RNAi)途径的主要成分已被确定,但该途径的调节机制仍 largely未知。在这里,我们证明RNAi途径可以被小分子在细胞内调节。我们开发了一种基于细胞的检测方法来监测RNAi途径的活性,发现小分子依诺沙星(Penetrex)增强了siRNA介导的mRNA降解并促进了内源性miRNA的生物合成。我们表明这种RNAi增强活性依赖于反式激活应答区域RNA结合蛋白。我们的结果提供了一个原理证明,即小分子可用于调节RNAi途径的活性。RNAi增强剂可能在研究工具和治疗方法的开发中有用。