Uppala Jagadeesh Kumar, Dey Madhusudan
Department of Biological Sciences, University of Wisconsin-Milwaukee, Milwaukee, WI, USA.
Methods Mol Biol. 2022;2378:101-110. doi: 10.1007/978-1-0716-1732-8_7.
HAC1 mRNA remains translationally repressed in the cytoplasm of the budding yeast Saccharomyces cerevisiae. Under conditions of cellular stress, a dual kinase RNase IRE1 (Inositol Requiring Enzyme-1) cleaves out an intervening sequence from the HAC1 mRNA. Cleaved mRNAs are then ligated by tRNA ligase, thus generating a spliced mRNA that translates an active transcription factor. This unconventional splicing of HAC1 mRNA in the cytoplasm is a molecular marker for various cellular stresses including oxidative stress and endoplasmic reticulum (ER) stress. This article describes a PCR-based protocol to detect the HAC1 mRNA splicing.
HAC1信使核糖核酸(mRNA)在出芽酵母酿酒酵母的细胞质中保持翻译抑制状态。在细胞应激条件下,双激酶核糖核酸酶IRE1(肌醇需要酶-1)从HAC1 mRNA中切割出一个间隔序列。然后,切割后的mRNA由转运RNA连接酶连接,从而产生一个可翻译活性转录因子的剪接mRNA。HAC1 mRNA在细胞质中的这种非常规剪接是包括氧化应激和内质网(ER)应激在内的各种细胞应激的分子标记。本文描述了一种基于聚合酶链反应(PCR)的方法来检测HAC1 mRNA剪接。