Matthias-Schleiden-Institut für Genetik, Bioinformatik und Molekulare Botanik, AG Bakteriengenetik, Friedrich-Schiller-Universität Jena, Jena, Germany.
Methods Mol Biol. 2024;2741:145-174. doi: 10.1007/978-1-0716-3565-0_8.
So far, in Bacillus subtilis, only four trans-encoded and 11 cis-encoded sRNAs and their targets have been investigated in detail, the majority of them in our group (rev. in 1, 2). Here, we describe in vitro methods for the analysis of sRNA/mRNA interactions. All these methods have been either elaborated or significantly improved in our group and successfully applied to characterize a number of sRNA/target mRNA systems in Bacillus subtilis for which we provide examples from our own work. The in vitro methods comprise the synthesis and purification of labeled and unlabeled RNA, the analysis of sRNA/mRNA interactions in electrophoretic mobility shift assays (EMSAs) including the calculation of their apparent binding rate constants (k) and equilibrium dissociation constants (Kd), the localization of minimal regulatory regions of an sRNA, the determination of the secondary structures of both interacting RNAs and their complex as well as the analysis of RNA chaperones that may promote the sRNA/mRNA interaction.
到目前为止,枯草芽孢杆菌中仅有 4 个反式编码和 11 个顺式编码的 sRNA 及其靶标被详细研究过,其中大多数是在我们组(综述 1、2)。在这里,我们描述了用于分析 sRNA/mRNA 相互作用的体外方法。我们组对所有这些方法都进行了阐述或显著改进,并成功应用于鉴定枯草芽孢杆菌中许多 sRNA/靶标 mRNA 系统,我们提供了一些来自我们自己工作的例子。体外方法包括标记和未标记 RNA 的合成和纯化、电泳迁移率变动分析(EMSA)中 sRNA/mRNA 相互作用的分析,包括它们的表观结合率常数(k)和平衡解离常数(Kd)的计算、sRNA 最小调节区域的定位、相互作用的 RNA 及其复合物的二级结构的测定以及可能促进 sRNA/mRNA 相互作用的 RNA 伴侣的分析。