Grimson Andrew, Farh Kyle Kai-How, Johnston Wendy K, Garrett-Engele Philip, Lim Lee P, Bartel David P
Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Mol Cell. 2007 Jul 6;27(1):91-105. doi: 10.1016/j.molcel.2007.06.017.
Mammalian microRNAs (miRNAs) pair to 3'UTRs of mRNAs to direct their posttranscriptional repression. Important for target recognition are approximately 7 nt sites that match the seed region of the miRNA. However, these seed matches are not always sufficient for repression, indicating that other characteristics help specify targeting. By combining computational and experimental approaches, we uncovered five general features of site context that boost site efficacy: AU-rich nucleotide composition near the site, proximity to sites for coexpressed miRNAs (which leads to cooperative action), proximity to residues pairing to miRNA nucleotides 13-16, positioning within the 3'UTR at least 15 nt from the stop codon, and positioning away from the center of long UTRs. A model combining these context determinants quantitatively predicts site performance both for exogenously added miRNAs and for endogenous miRNA-message interactions. Because it predicts site efficacy without recourse to evolutionary conservation, the model also identifies effective nonconserved sites and siRNA off-targets.
哺乳动物微小RNA(miRNA)与mRNA的3'非翻译区(3'UTR)配对,以指导其转录后抑制。对靶标识别很重要的是与miRNA种子区域匹配的约7个核苷酸位点。然而,这些种子匹配并不总是足以实现抑制,这表明其他特征有助于确定靶向作用。通过结合计算和实验方法,我们发现了增强位点效力的位点上下文的五个一般特征:位点附近富含AU的核苷酸组成、与共表达miRNA的位点接近(这导致协同作用)、与miRNA核苷酸13 - 16配对的残基接近、在3'UTR内距离终止密码子至少15个核苷酸的位置以及远离长UTR中心的位置。结合这些上下文决定因素的模型定量预测了外源添加的miRNA以及内源性miRNA - 信使RNA相互作用的位点性能。因为该模型在不依赖进化保守性的情况下预测位点效力,所以它还能识别有效的非保守位点和小干扰RNA(siRNA)脱靶位点。