| Literature DB >> 32202498 |
Andrea Graziadei1,2, Frank Gabel3,4, John Kirkpatrick2,5, Teresa Carlomagno2,5.
Abstract
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.Entities:
Keywords: Box C/D RNP; NMR; SAS; biochemistry; chemical biology; conformational equilibrium; integrative structural biology; molecular biophysics; rRNA methylation; structural biology
Year: 2020 PMID: 32202498 PMCID: PMC7089733 DOI: 10.7554/eLife.50027
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140