Co-transcriptional folding orchestrates sequential multi-effector sensing by a glycine tandem riboswitch
Year: 2026
Type: article
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.
Source: Nature Communications
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $6,990
Awards: Unveiling Functionally Critical, Ephemeral RNA (un)folding States with Magnetic Tape Head Tweezers, G2243884602, Michigan Predoctoral Training in Genetics, Kinetic modeling of the CRISPR-Cas9 genome editing system, G524597515, Michigan Predoctoral Training in Genetics, G7075470626, New methods for computational modeling of RNA structures, Center for Structural Biology of HIV RNA, Mechanisms of cotranscriptional RNA structure formation
OpenAlex ID: W7128915182
