Language

English

Publication Date

5-7-2026

Journal

Molecular Cell

DOI

10.1016/j.molcel.2026.03.029

PMID

42019497

PMCID

PMC13120737

PubMedCentral® Posted Date

4-28-2026

PubMedCentral® Full Text Version

Author MSS

Abstract

Identifying tertiary structures and protein binding sites in RNA molecules remains a key challenge in RNA biology. We describe multi-site dimethyl sulfate (DMS)-mutational profiling (MaP) (msDMS-MaP), a strategy that enables simultaneous measurement of RNA secondary, tertiary, and quaternary structures via a single DMS chemical probing experiment. Optimized reverse transcription decodes typically invisible DMS N7-methylguanine (N7-G) modifications via a tautomer-induced mutational signature concurrent with N1 and N3 modifications. We show that N7-G reactivity reports on higher-order RNA structures, revealing key functional motifs such as pseudoknots and protein binding sites. Using msDMS-MaP, we find that E. coli ribosomal RNAs encode numerous independently folding tertiary structures that coincide with binding sites for primary assembly proteins. We further apply msDMS-MaP to define the quaternary structural ensemble of the 7SK small nuclear ribonucleoprotein particle (snRNP), revealing that each of the three 7SK structural isoforms possesses distinct protein binding profiles in cells. msDMS-MaP represents a broadly applicable strategy for enhanced RNA functional motif discovery and characterization.

Keywords

Nucleic Acid Conformation, Binding Sites, Sulfuric Acid Esters, Escherichia coli, Protein Binding, RNA-Binding Proteins, RNA, Bacterial, Models, Molecular, RNA, Ribosomal, Mutation, RNA Methylation, Escherichia coli Proteins, RNA structure, RNA folding, RNA tertiary structure, structure modeling, RNA binding proteins, RNP, RNA motif discovery, 7SK, ribosome assembly

Published Open-Access

yes

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