Co-transcriptional folding orchestrates sequential multi-1 effector sensing by a glycine tandem riboswitch

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Authors: Rosa A. Romero, Adrien Chauvier, Serena S. Teh, Vincent A. Reed, Sicheng Zhang, Courtney E. Szyjka, Shi‐Jie Chen, Eric J. Strobel, Nils G. Walter
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Abstract

Riboswitches are non-coding RNA motifs that regulate gene expression in response to ligand binding. The glycine tandem riboswitch (GTR) contains two glycine aptamers that interact extensively, driving conformational changes in the downstream expression platform to control gene expression. Despite extensive studies, the role of glycine and RNA folding pathways in co-transcriptional regulation remains unclear. Here, we integrate single-molecule kinetic analysis, co-transcriptional RNA structure probing, and modeling to reveal that the GTR processes multiple molecular inputs sequentially, guided by polymerase pausing. Our findings elucidate its stepwise 5’-to-3’ folding pathway and demonstrate how sequential glycine binding to each aptamer, K+ binding to a kink-turn, non-native folding intermediates, inter-aptamer docking driving binding site pre-organization, and modulation by transcription factor NusA collectively orchestrate co-transcriptional gene regulation. These results support a model wherein glycine binding cooperativity arises through non-equilibrium mechanisms, not a classical concerted model.

Fields of Study & Subjects

RNA and protein synthesis mechanisms RNA Research and Splicing Bacterial Genetics and Biotechnology

Publication details

Journal / source
University of Michigan Library
Publication date
9 January 2026
Language
EN
Document type
Dataset