Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia, Canada.
Institut de Chimie Moléculaire, ICMUB CNRS UMR 6302, UBFC, Dijon, France.
Nat Protoc. 2022 Mar;17(3):870-889. doi: 10.1038/s41596-021-00671-6. Epub 2022 Feb 9.
Guanine-rich RNAs can fold into four-stranded structures, termed G-quadruplexes (G4-RNAs), and participate in a wide range of biological processes. Here we describe in detail a G4-RNA-specific precipitation (G4RP) protocol, which enables the transcriptomic profiling of G4-RNAs. The G4RP protocol consists of a chemical cross-linking step, followed by affinity capture with a G4-specific probe, BioTASQ. G4RP can be coupled with sequencing to capture a comprehensive global snapshot of folded G4-RNAs. This method can also be used to profile induced changes (i.e., through G4 ligand treatments) within the G4-RNA transcriptome. The entire protocol can be completed in 1-2 weeks and can be scaled up or down depending on the specific experimental goals. In addition to the protocol details, we also provide here a guide for optimization in different laboratory setups.
富含鸟嘌呤的 RNA 可以折叠成四链结构,称为 G-四链体 (G4-RNA),并参与广泛的生物学过程。在这里,我们详细描述了一种 G4-RNA 特异性沉淀 (G4RP) 方案,该方案可实现 G4-RNA 的转录组分析。G4RP 方案包括化学交联步骤,然后用 G4 特异性探针 BioTASQ 进行亲和捕获。G4RP 可以与测序相结合,以捕获折叠 G4-RNA 的全面全局快照。该方法还可用于分析 G4-RNA 转录本中的诱导变化(例如,通过 G4 配体处理)。整个方案可以在 1-2 周内完成,并可根据具体的实验目标进行扩展或缩小。除了协议细节外,我们还在此处提供了不同实验室设置下优化的指南。