MRC Laboratory of Molecular Biology, Cambridge, UK.
MRC Laboratory of Molecular Biology, Cambridge, UK.
Methods. 2017 Aug 15;126:95-104. doi: 10.1016/j.ymeth.2017.06.009. Epub 2017 Jun 13.
Poly(A) tails are found at the 3' end of almost every eukaryotic mRNA and are important for the stability of mRNAs and their translation into proteins. Thus, removal of the poly(A) tail, a process called deadenylation, is critical for regulation of gene expression. Most deadenylation enzymes are components of large multi-protein complexes. Here, we describe an in vitro deadenylation assay developed to study the exonucleolytic activities of the multi-protein Ccr4-Not and Pan2-Pan3 complexes. We discuss how this assay can be used with short synthetic RNAs, as well as longer RNA substrates generated using in vitro transcription. Importantly, quantitation of the reactions allows detailed analyses of deadenylation in the presence and absence of accessory factors, leading to new insights into targeted mRNA decay.
多聚(A)尾存在于几乎所有真核生物 mRNA 的 3' 端,对于 mRNA 的稳定性及其翻译成蛋白质至关重要。因此,多聚(A)尾的去除过程,即脱腺苷酸化,对于基因表达的调控至关重要。大多数脱腺苷酸化酶是大型多蛋白复合物的组成部分。在这里,我们描述了一种体外脱腺苷酸化测定法,用于研究多蛋白 Ccr4-Not 和 Pan2-Pan3 复合物的外切核酸酶活性。我们讨论了如何使用短的合成 RNA 以及使用体外转录生成的较长 RNA 底物来使用该测定法。重要的是,反应的定量分析可以在存在和不存在辅助因子的情况下详细分析脱腺苷酸化,从而深入了解靶向 mRNA 降解。