Evidence map›Paper›PMID 38366792›Full record

ArticleNucleic acids research2024

Site-specific incorporation of a fluorescent nucleobase analog enhances i-motif stability and allows monitoring of i-motif folding inside cells.

Bartomeu Mir, Israel Serrano-Chacón, Pedro Medina, Veronica Macaluso, Montserrat Terrazas, Albert Gandioso, Miguel Garavís, Modesto Orozco, Núria Escaja, Carlos González

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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Non-G Base Tetrads.Molecules (Basel, Switzerland) · 2022
    Review
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

10 authors at 3 institutions in 1 country.

Bartomeu MirInstituto de Química Física 'Blas Cabrera'. CSIC. Serrano 119. 28006 Madrid. Spain.
Israel Serrano-ChacónInstituto de Química Física 'Blas Cabrera'. CSIC. Serrano 119. 28006 Madrid. Spain.
Pedro MedinaInstitute for Research in Biomedicine (IRB Barcelona). The Barcelona Institute of Science and Technology (BIST). 08028 Barcelona. Spain.
Veronica MacalusoInstitute for Research in Biomedicine (IRB Barcelona). The Barcelona Institute of Science and Technology (BIST). 08028 Barcelona. Spain.
Montserrat TerrazasInstitute for Research in Biomedicine (IRB Barcelona). The Barcelona Institute of Science and Technology (BIST). 08028 Barcelona. Spain.
Albert GandiosoInstitute for Research in Biomedicine (IRB Barcelona). The Barcelona Institute of Science and Technology (BIST). 08028 Barcelona. Spain.
Miguel GaravísInstituto de Química Física 'Blas Cabrera'. CSIC. Serrano 119. 28006 Madrid. Spain.
Modesto OrozcoInstitute for Research in Biomedicine (IRB Barcelona). The Barcelona Institute of Science and Technology (BIST). 08028 Barcelona. Spain.
Núria EscajaInorganic and Organic Chemistry Department. Organic Chemistry Section and IBUB. University of Barcelona, Martí i Franquès 1-11, 08028 Barcelona. Spain.
Carlos GonzálezInstituto de Química Física 'Blas Cabrera'. CSIC. Serrano 119. 28006 Madrid. Spain.ORCID 0000-0001-8796-1282
Institute for Research in Biomedicine · ESInstituto de Química Física Blas Cabrera · ESUniversitat de Barcelona · ES

Funding

BioExcel-3. Centre of Excellence for Computational Biomolecular Research 823830Catalan SGRCenter of Excellence for HPC H2020 European CommissionCSICERFD Operative Programme for Catalunya, the Catalan Government AGAUR SGR2017-134Fondo Europeo de Desarrollo RegionalInstituto de Salud Carlos III ISCIII PT 17/0009/0007Ministerio de Ciencia e Innovación PID2020-116620GB-I00
6 · The paper itself

Abstract

The i-motif is an intriguing non-canonical DNA structure, whose role in the cell is still controversial. Development of methods to study i-motif formation under physiological conditions in living cells is necessary to study its potential biological functions. The cytosine analog 1,3-diaza-2-oxophenoxazine (tCO) is a fluorescent nucleobase able to form either hemiprotonated base pairs with cytosine residues, or neutral base pairs with guanines. We show here that when tCO is incorporated in the proximity of a G:C:G:C minor groove tetrad, it induces a strong thermal and pH stabilization, resulting in i-motifs with Tm of 39ºC at neutral pH. The structural determination by NMR methods reveals that the enhanced stability is due to a large stacking interaction between the guanines of the tetrad with the tCO nucleobase, which forms a tCO:C+ in the folded structure at unusually-high pHs, leading to an increased quenching in its fluorescence at neutral conditions. This quenching is much lower when tCO is base-paired to guanines and totally disappears when the oligonucleotide is unfolded. By taking profit of this property, we have been able to monitor i-motif folding in cells.

Indexed as

CytosineDNABase PairingFluorescenceHeLa CellsHumansNucleic Acid ConformationOxazines1,3-diaza-2-oxophenoxazineCytosineDNAOxazines

Identifiers

PMID38366792
PMCPMC11014255
OpenAlexW4391897566

What OpenQuestion holds

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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.