Evidence map›Paper›PMID 42152678›Full record

ArticleNucleic acids research2026

Topological rules and anomalies in intramolecular G-quadruplex folding: a comprehensive study.

Anton Granzhan, Liliane Mouawad

Abstract read
In one paragraph

Article in Nucleic acids research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Anton GranzhanLaboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques (LCBPT), CNRS UMR8601, Université Paris Cité, Paris 75006, France.ORCID 0000-0002-0424-0461
Liliane MouawadChemistry and Modeling for the Biology of Cancer, CNRS UMR9187, INSERM U1196, Institut Curie, PSL Research University, Université Paris-Saclay, Orsay 91400, France.ORCID 0000-0002-7155-9712

Funding

Institut Curie
6 · The paper itself

Abstract

G-quadruplexes (G4s) make knots in DNA and RNA. One-block G4s can adopt eight different topologies, yet their folding rules are not precisely known. A systematic study of 353 intramolecular G4s enabled us to establish certain characteristics that rule their topology. In the absence of restraints imposed by a ligand or modified guanosines, when two loops are one nucleotide-long (nt), the topology is parallel, regardless of the third loop length. When loops 1 and 3 are 2-nt long, loop 2 length (L2) determines the G4 topology: parallel for L2 = 1, parallel or antiparallel-chair for L2 = 2, antiparallel-chair for L2 = 3, and antiparallel-basket for L2 = 4-5 nts. Diagonal loops require at least 4 nts; the only three structures with a diagonal loop of 3 nts present multiple anomalies. Only three topologies can accommodate a diagonal loop; the other five cannot. This shows the importance of distinguishing between the eight different topologies. We explain why parallel and hybrid topologies form preferentially three-tetrad G4s, while antiparallel topologies form preferentially two-tetrad G4s. We also explain why bulges between the G4 stem and the hairpin loop in quadruplex-duplex hybrids are sometimes needed. These findings clarify G4 folding principles and topological restraints.

Indexed as

DNAG-QuadruplexesModels, MolecularNucleic Acid ConformationRNADNARNA

Identifiers

PMID42152678
PMCPMC13183678

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.