Evidence map›Paper›PMID 37986223›Full record

ArticleNucleic acids research2024

A sodium/potassium switch for G4-prone G/C-rich sequences.

Yu Luo, Martina Lenarčič Živković, Jiawei Wang, Jan Ryneš, Silvie Foldynová-Trantírková, Lukáš Trantírek, Daniela Verga, Jean-Louis Mergny

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.0field-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

14 citing papers in PubMed, 26 citations in OpenAlex.

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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

8 authors at 2 institutions in 3 countries.

Yu LuoLaboratoire d'Optique et Biosciences, Ecole Polytechnique, CNRS, Inserm, Institut Polytechnique de Paris, 91128 Palaiseau, France.
Martina Lenarčič ŽivkovićCentral European Institute of Technology, Masaryk University, 625 00 Brno, Czech Republic.
Jiawei WangLaboratoire d'Optique et Biosciences, Ecole Polytechnique, CNRS, Inserm, Institut Polytechnique de Paris, 91128 Palaiseau, France.
Jan RynešCentral European Institute of Technology, Masaryk University, 625 00 Brno, Czech Republic.
Silvie Foldynová-TrantírkováCentral European Institute of Technology, Masaryk University, 625 00 Brno, Czech Republic.
Lukáš TrantírekCentral European Institute of Technology, Masaryk University, 625 00 Brno, Czech Republic.ORCID 0000-0001-5948-4837
Daniela VergaCNRS UMR9187, INSERM U1196, Université Paris-Saclay, F-91405 Orsay, France.ORCID 0000-0002-7555-6033
Jean-Louis MergnyLaboratoire d'Optique et Biosciences, Ecole Polytechnique, CNRS, Inserm, Institut Polytechnique de Paris, 91128 Palaiseau, France.ORCID 0000-0003-3043-8401
Central European Institute of Technology · CZCentre National de la Recherche Scientifique · FR

Funding

ANR G4Access ANR-20-CE12-0023Chinese Scholarship Council fellowships 201906340018Czech Science Foundation GX19-26041XEuropean Union-Next Generation EUINCa G4AccessInsermMEYS CR LM2023050 Czech-BioImagingNational Institute for Cancer Research LX22NPO5102
6 · The paper itself

Abstract

Metal ions are essential components for the survival of living organisms. For most species, intracellular and extracellular ionic conditions differ significantly. As G-quadruplexes (G4s) are ion-dependent structures, changes in the [Na+]/[K+] ratio may affect the folding of genomic G4s. More than 11000 putative G4 sequences in the human genome (hg19) contain at least two runs of three continuous cytosines, and these mixed G/C-rich sequences may form a quadruplex or a competing hairpin structure based on G-C base pairing. In this study, we examine how the [Na+]/[K+] ratio influences the structures of G/C-rich sequences. The natural G4 structure with a 9-nt long central loop, CEBwt, was chosen as a model sequence, and the loop bases were gradually replaced by cytosines. The series of CEB mutations revealed that the presence of cytosines in G4 loops does not prevent G4 folding or decrease G4 stability but increases the probability of forming a competing structure, either a hairpin or an intermolecular duplex. Slow conversion to the quadruplex in vitro (in a potassium-rich buffer) and cells was demonstrated by NMR. 'Shape-shifting' sequences may respond to [Na+]/[K+] changes with delayed kinetics.

Indexed as

G-QuadruplexesPotassiumSodiumHumansMagnetic Resonance SpectroscopyMutationPotassiumSodium

Identifiers

PMID37986223
PMCPMC10783510
OpenAlexW4388870084

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.