Institute of Organic Chemistry and Center for Molecular Biosciences Innsbruck CMBI, Leopold-Franzens University, Innrain 80-82, Innsbruck 6020, Austria.
Division for Biomedical Physics, Medical University of Innsbruck, Müllerstraße 44, Innsbruck 6020, Austria.
Nucleic Acids Res. 2018 Aug 21;46(14):6983-6995. doi: 10.1093/nar/gky555.
Self-cleaving ribozymes are biologically relevant RNA molecules which catalyze site-specific cleavage of the phosphodiester backbone. Gathering knowledge of their three-dimensional structures is critical toward an in-depth understanding of their function and chemical mechanism. Equally important is collecting information on the folding process and the inherent dynamics of a ribozyme fold. Over the past years, Selective-2'-Hydroxyl Acylation analyzed by Primer Extension (SHAPE) turned out to be a significant tool to probe secondary and tertiary interactions of diverse RNA species at the single nucleotide level under varying environmental conditions. Small self-cleaving ribozymes, however, have not been investigated by this method so far. Here, we describe SHAPE probing of pre-catalytic folds of the recently discovered ribozyme classes twister, twister-sister (TS), pistol and hatchet. The study has implications on Mg2+-dependent folding and reveals potentially dynamic residues of these ribozymes that are otherwise difficult to identify. For twister, TS and pistol ribozymes the new findings are discussed in the light of their crystal structures, and in case of twister also with respect to a smFRET folding analysis. For the hatchet ribozyme where an atomic resolution structure is not yet available, the SHAPE data challenge the proposed secondary structure model and point at selected residues and putative long-distance interactions that appear crucial for structure formation and cleavage activity.
自我切割核酶是具有生物学相关性的 RNA 分子,能够催化磷酸二酯骨架的特异性切割。收集有关其三维结构的知识对于深入了解其功能和化学机制至关重要。同样重要的是收集有关折叠过程和核酶折叠固有动力学的信息。在过去的几年中,通过引物延伸分析的选择性 2'-羟基酰化(SHAPE)已成为一种重要的工具,可以在不同的环境条件下探测各种 RNA 物种的二级和三级相互作用,达到单核苷酸水平。然而,这种方法尚未用于研究小型自我切割核酶。在这里,我们描述了对最近发现的核酶类 twist er、twister-sister(TS)、pistol 和 hatchet 的催化前折叠进行 SHAPE 探测。该研究对 Mg2+依赖性折叠具有重要意义,并揭示了这些核酶中潜在的动态残基,否则这些残基很难识别。对于 twist er、TS 和 pistol 核酶,新发现的结果根据它们的晶体结构进行了讨论,对于 twist er 核酶,还考虑了 smFRET 折叠分析的结果。对于尚未获得原子分辨率结构的 hatchet 核酶,SHAPE 数据对提出的二级结构模型提出了挑战,并指出了一些关键的残基和潜在的长距离相互作用,这些残基和相互作用对于结构形成和切割活性至关重要。