Evidence map›Paper›PMID 33104789›Full record

ArticleNucleic acids research2020

2'-O-Methylation can increase the abundance and lifetime of alternative RNA conformational states.

Hala Abou Assi, Atul K Rangadurai, Honglue Shi, Bei Liu, Mary C Clay, Kevin Erharter, Christoph Kreutz, Christopher L Holley, Hashim M Al-Hashimi

Abstract read
In one paragraph

Article in Nucleic acids research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

84 citing papers in PubMed.

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  20. Genome-wide profiling of RNA 2'-bioRxiv : the preprint server for biology · 2025
    Article

24 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Hala Abou AssiDepartment of Biochemistry, Duke University School of Medicine, Durham, NC 27710, USA.
Atul K RangaduraiDepartment of Biochemistry, Duke University School of Medicine, Durham, NC 27710, USA.
Honglue ShiDepartment of Chemistry, Duke University, Durham, NC 27708, USA.
Bei LiuDepartment of Biochemistry, Duke University School of Medicine, Durham, NC 27710, USA.
Mary C ClayDepartment of Biochemistry, Duke University School of Medicine, Durham, NC 27710, USA.
Kevin ErharterInstitute of Organic Chemistry and Center for Molecular Biosciences Innsbruck (CMBI), University of Innsbruck, 6020 Innsbruck, Austria.
Christoph KreutzInstitute of Organic Chemistry and Center for Molecular Biosciences Innsbruck (CMBI), University of Innsbruck, 6020 Innsbruck, Austria.
Christopher L HolleyDepartment of Medicine, Duke University School of Medicine, Durham, NC 27710, USA.
Hashim M Al-HashimiDepartment of Biochemistry, Duke University School of Medicine, Durham, NC 27710, USA.

Funding

The Center for HIV RNA Studies (CRNA)U54GM103297 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TELESNITSKY, ALICE · 2017 to 2018
$10.2M
MULTIDISCIPLINARY HEART &VASCULAR DISEASEST32HL007101 · NHLBI · DUKE UNIVERSITY · PI FREEDMAN, NEIL J. · 1985 to 2020
$9.8M
Fundamental Studies of RNA Conformational ThermodynamicsR01GM132899 · NIGMS · STANFORD UNIVERSITY · PI AL-HASHIMI, HASHIM M, HERSCHLAG, DANIEL · 2019 to 2022
$2.7M
Austrian Science Fund FWF P 32773NHLBI NIH HHS T32 HL007101NIGMS NIH HHS R01 GM132899NIGMS NIH HHS U54 GM103297
6 · The paper itself

Abstract

2'-O-Methyl (Nm) is a highly abundant post-transcriptional RNA modification that plays important biological roles through mechanisms that are not entirely understood. There is evidence that Nm can alter the biological activities of RNAs by biasing the ribose sugar pucker equilibrium toward the C3'-endo conformation formed in canonical duplexes. However, little is known about how Nm might more broadly alter the dynamic ensembles of flexible RNAs containing bulges and internal loops. Here, using NMR and the HIV-1 transactivation response (TAR) element as a model system, we show that Nm preferentially stabilizes alternative secondary structures in which the Nm-modified nucleotides are paired, increasing both the abundance and lifetime of low-populated short-lived excited states by up to 10-fold. The extent of stabilization increased with number of Nm modifications and was also dependent on Mg2+. Through phi-value analysis, the Nm modification also provided rare insights into the structure of the transition state for conformational exchange. Our results suggest that Nm could alter the biological activities of Nm-modified RNAs by modulating their secondary structural ensembles as well as establish the utility of Nm as a tool for the discovery and characterization of RNA excited state conformations.

Indexed as

HIV Long Terminal RepeatRNA Processing, Post-TranscriptionalBase PairingCations, DivalentDensity Functional TheoryHIV-1MagnesiumMagnetic Resonance SpectroscopyMethylationNucleic Acid ConformationRNA StabilityRNA, ViralThermodynamicsCations, DivalentMagnesiumRNA, Viral

Identifiers

PMID33104789
PMCPMC7708057

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.