Abstract

MotivationRNA molecules can undergo complex structural dynamics, especially during transcription, which influence their biological functions. Recently developed high-throughput chemical probing experiments that study RNA cotranscriptional folding generate nucleotide-resolution ‘reactivities’ for each length of a growing nascent RNA that reflect structural dynamics. However, the manual annotation and qualitative interpretation of reactivity across these large datasets can be nuanced, laborious, and difficult for new practitioners. We developed a quantitative and systematic approach to automatically detect RNA folding events from these datasets to reduce human bias/error, standardize event discovery and generate hypotheses about RNA folding trajectories for further analysis and experimental validation.ResultsDetection of Unknown Events with Tunable Thresholds (DUETT) identifies RNA structural transitions in cotranscriptional RNA chemical probing datasets. DUETT employs a feedback control-inspired method and a linear regression approach and relies on interpretable and independently tunable parameter thresholds to match qualitative user expectations with quantitatively identified folding events. We validate the approach by identifying known RNA structural transitions within the cotranscriptional folding pathways of the Escherichia coli signal recognition particle RNA and the Bacillus cereus crcB fluoride riboswitch. We identify previously overlooked features of these datasets such as heightened reactivity patterns in the signal recognition particle RNA about 12 nt lengths before base-pair rearrangement. We then apply a sensitivity analysis to identify tradeoffs when choosing parameter thresholds. Finally, we show that DUETT is tunable across a wide range of contexts, enabling flexible application to study broad classes of RNA folding mechanisms.Availability and implementation https://github.com/BagheriLab/DUETT.Supplementary information Supplementary data are available at Bioinformatics online.

Highlights

  • RNA molecules play diverse functional roles ranging from catalysis of splicing and peptide bond formation, regulation of mRNA processing and gene expression, and molecular scaffolding and localization (Sharp, 2009; Cech and Steitz, 2014)

  • We present a framework for detecting events in cotranscriptional SHAPE-Seq datasets termed Detection of Unknown Events with Tunable Thresholds (DUETT)

  • We validated DUETT by identifying known cotranscriptional structural events that occur in the folding pathways of two RNA molecules: the E. coli. signal recognition particle (SRP) RNA and the B. cereus. fluoride riboswitch (Watters, Strobel, et al, 2016; Batey et al, 2000; Wong et al, 2007)

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Summary

Introduction

RNA molecules play diverse functional roles ranging from catalysis of splicing and peptide bond formation, regulation of mRNA processing and gene expression, and molecular scaffolding and localization (Sharp, 2009; Cech and Steitz, 2014). These functions are in turn mediated by RNA structures that form in complex cellular environments. There has been great interest in developing both computational and experimental approaches to uncover RNA cotranscriptional folding pathways and their implications for cellular RNA function

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