Brown Jessica A, Steitz Joan A
Department of Molecular Biophysics and Biochemistry, Howard Hughes Medical Institute, Yale University School of Medicine, 295 Congress Avenue, New Haven, CT, 06536, USA.
Methods Mol Biol. 2016;1428:77-92. doi: 10.1007/978-1-4939-3625-0_5.
The intronless β-globin reporter, whose mRNA is intrinsically unstable due to the lack of introns, is a useful tool to study RNA stability elements in a heterologous transcript. Insertion of a stability element leads to the accumulation of intronless β-globin mRNA that can be visualized by conventional Northern blot analyses. In this chapter, we explain how to perform the β-globin reporter assay using the ENE (expression and nuclear retention element), a triple-helix-forming RNA stability element that protects reporter mRNA from 3'- 5' decay. A list of considerations is included for the use of ENEs as a tool to stabilize other RNAs. In this chapter, we provide a brief description of how to insert an ENE sequence into the 3'-untranslated region of an intronless β-globin reporter plasmid using basic cloning technology. Then, we provide a detailed protocol for quantitative measurements of steady-state levels of β-globin mRNA. This entails the transient transfection of mammalian cells with β-globin reporter plasmids, isolation of total cellular RNA, and detection of reporter mRNA via Northern blot. This methodology can be applied for the study of any nuclear RNA stability element using the intronless β-globin reporter.
无内含子β-珠蛋白报告基因,其mRNA由于缺乏内含子而本质上不稳定,是研究异源转录本中RNA稳定性元件的有用工具。插入一个稳定性元件会导致无内含子β-珠蛋白mRNA的积累,这可以通过传统的Northern印迹分析来可视化。在本章中,我们将解释如何使用ENE(表达和核保留元件)进行β-珠蛋白报告基因检测,ENE是一种形成三链螺旋的RNA稳定性元件,可保护报告基因mRNA免受3'-5'降解。还列出了将ENE用作稳定其他RNA的工具时的注意事项。在本章中,我们简要描述了如何使用基本克隆技术将ENE序列插入无内含子β-珠蛋白报告基因质粒的3'-非翻译区。然后,我们提供了一个详细的方案,用于定量测量β-珠蛋白mRNA的稳态水平。这需要用β-珠蛋白报告基因质粒瞬时转染哺乳动物细胞,分离总细胞RNA,并通过Northern印迹检测报告基因mRNA。这种方法可用于使用无内含子β-珠蛋白报告基因研究任何核RNA稳定性元件。