Nickless Andrew, You Zhongsheng
Department of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO, USA.
Methods Mol Biol. 2018;1720:213-224. doi: 10.1007/978-1-4939-7540-2_16.
The nonsense-mediated mRNA decay (NMD) pathway degrades aberrant transcripts containing premature translation termination codons (PTCs) and also regulates the levels of many normal mRNAs containing NMD-inducing features. The activity of this pathway varies considerably in different cell types and can change in response to developmental and environmental cues. Modulating NMD activity represents a potential therapeutic avenue for certain genetic disorders and cancers. Simple reporter systems capable of faithfully assessing NMD activity in mammalian cells greatly facilitate both basic and translational research on NMD. Here we describe a simple and effective method for assaying NMD specifically and quickly in live mammalian cells using a multicolored bioluminescence-based reporter system. This reporter can be transiently or stably introduced into cultured cells as well as animals, and NMD activity can be accurately assessed by bioluminescence imaging, western blot, or RT-qPCR.
无义介导的mRNA降解(NMD)途径可降解含有过早翻译终止密码子(PTC)的异常转录本,还可调节许多含有NMD诱导特征的正常mRNA的水平。该途径的活性在不同细胞类型中差异很大,并可响应发育和环境信号而发生变化。调节NMD活性是某些遗传疾病和癌症的潜在治疗途径。能够在哺乳动物细胞中忠实地评估NMD活性的简单报告系统极大地促进了对NMD的基础研究和转化研究。在此,我们描述了一种使用基于多色生物发光的报告系统在活的哺乳动物细胞中特异性、快速地检测NMD的简单有效方法。该报告基因可瞬时或稳定地导入培养细胞以及动物体内,通过生物发光成像、蛋白质免疫印迹或逆转录定量聚合酶链反应(RT-qPCR)可准确评估NMD活性。