Li Yong-Fang, Sunkar Ramanjulu
Department of Biochemistry and Molecular Biology, Oklahoma State University, Stillwater, OK, USA.
Methods Mol Biol. 2013;956:119-29. doi: 10.1007/978-1-62703-194-3_10.
Small RNAs (microRNAs and other classes of endogenous small interfering RNAs) play important roles in a wide variety of biological processes. However, integration of small RNAs in diverse biological networks relies on the confirmation of their RNA targets. In plants, miRNAs negatively regulate mRNA targets by guiding a cleavage in the complementary site that leaves a 3' polyadenylated RNA possessing monophosphate at its 5' end. This chapter describes a detailed step-by-step protocol for cloning such sliced 3' products in order to identify small RNA targets. Using this protocol, we have identified more than 150 small RNA targets in rice; some are conserved and others are non-conserved targets for rice small RNAs.
小RNA(微小RNA和其他种类的内源性小干扰RNA)在多种生物学过程中发挥着重要作用。然而,小RNA在不同生物网络中的整合依赖于对其RNA靶标的确认。在植物中,微小RNA通过引导互补位点的切割来负调控mRNA靶标,切割后会产生一个3'多聚腺苷酸化的RNA,其5'端带有单磷酸。本章描述了一个详细的逐步方案,用于克隆此类切割后的3'产物,以鉴定小RNA靶标。使用该方案,我们已经在水稻中鉴定出150多个小RNA靶标;其中一些是保守靶标,另一些是水稻小RNA的非保守靶标。