Department of Biology, Center for RNA Biology, University of Rochester, Rochester, NY, USA.
Methods Mol Biol. 2021;2298:197-216. doi: 10.1007/978-1-0716-1374-0_13.
The post-transcriptional modification of tRNAs at the wobble position plays a critical role in proper mRNA decoding and efficient protein synthesis. In particular, certain wobble uridines in eukaryotes are converted to 5-methoxycarbonylmethyl-2-thiouridine (mcm5s2U). The mcm5s2U modification modulates decoding during translation by increasing the stringency of the wobble uridine to base pair with its canonical nucleotide partner, thereby restricting decoding to its cognate codon. Here, we outline a technique to monitor wobble uridine status in mcm5s2U-containing tRNAs using the gamma-toxin endonuclease from the yeast Kluyveromyces lactis that naturally cleaves tRNAs containing the mcm5s2U modification. This technique is coupled to Northern blotting or reverse transcription-PCR to enable rapid and sensitive detection of changes in mcm5s2U modification state.
tRNA 在 wobble 位置的转录后修饰在正确的 mRNA 解码和高效的蛋白质合成中起着关键作用。特别是,真核生物中某些 wobble 尿嘧啶被转化为 5-甲氧基羰基甲基-2-硫代尿嘧啶(mcm5s2U)。mcm5s2U 修饰通过增加 wobble 尿嘧啶与其规范核苷酸伙伴碱基配对的严格性来调节翻译过程中的解码,从而将解码限制在其同源密码子上。在这里,我们概述了一种使用来自酵母 Kluyveromyces lactis 的γ-毒素内切核酸酶监测含有 mcm5s2U 的 tRNA 中 wobble 尿嘧啶状态的技术,该内切核酸酶天然切割含有 mcm5s2U 修饰的 tRNA。该技术与 Northern 印迹或反转录-PCR 相结合,可快速灵敏地检测 mcm5s2U 修饰状态的变化。