Evidence map›Paper›PMID 35017489›Full record

ArticleNature communications2022

An anionic ligand snap-locks a long-range interaction in a magnesium-folded riboswitch.

Rajeev Yadav, Julia R Widom, Adrien Chauvier, Nils G Walter

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.6field-weighted citation impact, top 6% of its field
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

25 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. RNA folding kinetics control riboswitch sensitivity in vivo.bioRxiv : the preprint server for biology · 2024
    Article
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

4 authors at 2 institutions in 1 country.

Rajeev YadavSingle Molecule Analysis Group, Department of Chemistry and Center for RNA Biomedicine, University of Michigan, Ann Arbor, MI, 48109, USA.ORCID http://orcid.org/0000-0002-9652-3388
Julia R WidomSingle Molecule Analysis Group, Department of Chemistry and Center for RNA Biomedicine, University of Michigan, Ann Arbor, MI, 48109, USA.ORCID http://orcid.org/0000-0002-6357-2749
Adrien ChauvierSingle Molecule Analysis Group, Department of Chemistry and Center for RNA Biomedicine, University of Michigan, Ann Arbor, MI, 48109, USA.ORCID http://orcid.org/0000-0003-4473-6194
Nils G WalterSingle Molecule Analysis Group, Department of Chemistry and Center for RNA Biomedicine, University of Michigan, Ann Arbor, MI, 48109, USA. nwalter@umich.edu.ORCID http://orcid.org/0000-0002-7301-1275
University of Michigan · USUniversity of Oregon · US

Funding

The RNA nanomachines of the gene expression machinery dissected at the single molecule levelR35GM131922 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NILS G WALTER · 2019 to 2026
$6.9M
Cotranscriptional folding of single riboswitchesR01GM118524 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WALTER, NILS G · 2016 to 2018
$911k
Novel Tools to Investigate Local and Global RNA Conformations in the SpliceosomeR00GM120457 · NIGMS · UNIVERSITY OF OREGON · PI WIDOM, JULIA REED · 2019 to 2021
$747k
Novel tools to investigate local and global RNA conformations in the spliceosomeK99GM120457 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WIDOM, JULIA REED · 2016 to 2017
$180k
NIGMS NIH HHS K99 GM120457NIGMS NIH HHS R00 GM120457NIGMS NIH HHS R01 GM118524NIGMS NIH HHS R35 GM131922
6 · The paper itself

Abstract

The archetypical transcriptional crcB fluoride riboswitch from Bacillus cereus is an intricately structured non-coding RNA element enhancing gene expression in response to toxic levels of fluoride. Here, we used single molecule FRET to uncover three dynamically interconverting conformations appearing along the transcription process: two distinct undocked states and one pseudoknotted docked state. We find that the fluoride anion specifically snap-locks the magnesium-induced, dynamically docked state. The long-range, nesting, single base pair A40-U48 acts as the main linchpin, rather than the multiple base pairs comprising the pseudoknot. We observe that the proximally paused RNA polymerase further fine-tunes the free energy to promote riboswitch docking. Finally, we show that fluoride binding at short transcript lengths is an early step toward partitioning folding into the docked conformation. These results reveal how the anionic fluoride ion cooperates with the magnesium-associated RNA to govern regulation of downstream genes needed for fluoride detoxification of the cell.

Indexed as

RiboswitchBacillus cereusBase PairingDNA-Directed RNA PolymerasesFluoridesGene Expression Regulation, BacterialMagnesiumMolecular Docking SimulationNucleic Acid ConformationProtein BindingRNA, BacterialRNA, MessengerThermodynamicsDNA-Directed RNA PolymerasesFluoridesMagnesiumRiboswitchRNA, BacterialRNA, Messenger

Identifiers

PMID35017489
PMCPMC8752731
OpenAlexW4225811392

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.