Sood V D, Beattie T L, Collins R A
Department of Molecular and Medical Genetics, University of Toronto, 1 King's College Circle, Toronto, Ontario, M5S 1A8, Canada.
J Mol Biol. 1998 Oct 2;282(4):741-50. doi: 10.1006/jmbi.1998.2049.
We have used ethylation protection experiments and modification interference using phosphorothioate nucleosides to identify phosphate groups involved in the magnesium-dependent tertiary structure and function of the VS ribozyme, a small, self-cleaving RNA. Phosphorothioate interference-rescue experiments in the presence of the thiophilic manganese ion implicate four phosphate groups in direct metal ion binding. Phosphorothioate substitution also creates a new manganese binding site that increases the cis cleavage rate of the ribozyme, possibly by disrupting an inhibitory structure. Interpreting these data in the context of a recently developed structural model shows that almost all of the important phosphate groups are located in the central core of the ribozyme. The model suggests roles for certain phosphate groups in particular steps of RNA folding and identifies a candidate region for the active site of the ribozyme.
我们利用乙基化保护实验以及使用硫代磷酸核苷进行的修饰干扰,来鉴定参与小型自我切割RNA——VS核酶的镁依赖性三级结构和功能的磷酸基团。在亲硫锰离子存在的情况下进行的硫代磷酸酯干扰拯救实验表明,有四个磷酸基团参与直接的金属离子结合。硫代磷酸酯取代还会产生一个新的锰结合位点,可能通过破坏一种抑制性结构来提高核酶的顺式切割速率。在最近开发的结构模型背景下解读这些数据表明,几乎所有重要的磷酸基团都位于核酶的中央核心区域。该模型揭示了某些磷酸基团在RNA折叠特定步骤中的作用,并确定了核酶活性位点的一个候选区域。