European Molecular Biology Laboratory, Structural and Computational Biology, Heidelberg, Germany.
Leibniz University Hannover, Centre for Biomolecular Drug Research, Hannover, Germany.
Elife. 2020 Mar 23;9:e50027. doi: 10.7554/eLife.50027.
2'-O-rRNA methylation, which is essential in eukaryotes and archaea, is catalysed by the Box C/D RNP complex in an RNA-guided manner. Despite the conservation of the methylation sites, the abundance of site-specific modifications shows variability across species and tissues, suggesting that rRNA methylation may provide a means of controlling gene expression. As all Box C/D RNPs are thought to adopt a similar structure, it remains unclear how the methylation efficiency is regulated. Here, we provide the first structural evidence that, in the context of the Box C/D RNP, the affinity of the catalytic module fibrillarin for the substrate-guide helix is dependent on the RNA sequence outside the methylation site, thus providing a mechanism by which both the substrate and guide RNA sequences determine the degree of methylation. To reach this result, we develop an iterative structure-calculation protocol that exploits the power of integrative structural biology to characterize conformational ensembles.
2'-O-rRNA 甲基化在真核生物和古菌中是必不可少的,它由 Box C/D RNP 复合物以 RNA 指导的方式催化。尽管甲基化位点具有保守性,但特定位置的修饰丰度在不同物种和组织中表现出可变性,这表明 rRNA 甲基化可能提供了一种控制基因表达的手段。由于所有 Box C/D RNP 都被认为采用类似的结构,因此仍不清楚甲基化效率是如何调节的。在这里,我们提供了第一个结构证据,即在 Box C/D RNP 的背景下,催化模块核仁小 RNA 蛋白 F 的亲和力对底物指导螺旋的依赖性取决于甲基化位点之外的 RNA 序列,从而提供了一种机制,其中底物和指导 RNA 序列决定了甲基化的程度。为了得出这个结果,我们开发了一种迭代的结构计算方案,利用综合结构生物学的力量来描述构象集合。