DUETT quantitatively identifies known and novel events in nascent RNA structural dynamics from chemical probing data.
Journal
Bioinformatics (Oxford, England)
ISSN: 1367-4811
Titre abrégé: Bioinformatics
Pays: England
ID NLM: 9808944
Informations de publication
Date de publication:
15 12 2019
15 12 2019
Historique:
received:
27
11
2018
revised:
29
04
2019
accepted:
19
07
2019
pubmed:
8
8
2019
medline:
1
7
2020
entrez:
8
8
2019
Statut:
ppublish
Résumé
RNA 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. Detection 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. https://github.com/BagheriLab/DUETT. Supplementary data are available at Bioinformatics online.
Identifiants
pubmed: 31389563
pii: 5544638
doi: 10.1093/bioinformatics/btz449
pmc: PMC6954663
doi:
Substances chimiques
Riboswitch
0
RNA
63231-63-0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
5103-5112Subventions
Organisme : NIGMS NIH HHS
ID : DP2 GM110838
Pays : United States
Organisme : NCI NIH HHS
ID : U54 CA199091
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM083937
Pays : United States
Informations de copyright
© The Author(s) 2019. Published by Oxford University Press.
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