Evidence map›Paper›PMID 30277522›Full record

ArticleNucleic acids research2018

NMR structure of a G-quadruplex formed by four d(G4C2) repeats: insights into structural polymorphism.

Jasna Brcic, Janez Plavec

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

39 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
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  7. G-Quadruplex Structures Formed by Human Telomere andInternational journal of molecular sciences · 2025
    Review
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  15. Development of MnInternational journal of molecular sciences · 2023
    Article
  16. G-quadruplex formation at humanBiochemistry and biophysics reports · 2023
    Article
  17. G-Quadruplexes Formation by theMolecules (Basel, Switzerland) · 2023
    Article
  18. Article
  19. Hidden Information Revealed Using the Orthogonal System of Nucleic Acids.International journal of molecular sciences · 2022
    Article
  20. 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

2 authors at 2 institutions in 1 country.

Jasna BrcicSlovenian NMR Center, National Institute of Chemistry, Ljubljana SI-1000, Slovenia.
Janez PlavecSlovenian NMR Center, National Institute of Chemistry, Ljubljana SI-1000, Slovenia.
National Institute of Chemistry · SIUniversity of Ljubljana · SI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Most frequent genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD), is a largely increased number of d(G4C2)n•(G2C4)n repeats located in the non-coding region of C9orf72 gene. Non-canonical structures, including G-quadruplexes, formed within expanded repeats have been proposed to drive repeat expansion and pathogenesis of ALS and FTD. Oligonucleotide d[(G4C2)3G4], which represents the shortest oligonucleotide model of d(G4C2) repeats with the ability to form a unimolecular G-quadruplex, forms two major G-quadruplex structures in addition to several minor species which coexist in solution with K+ ions. Herein, we used solution-state NMR to determine the high-resolution structure of one of the major G-quadruplex species adopted by d[(G4C2)3G4]. Structural characterization of the G-quadruplex named AQU was facilitated by a single substitution of dG with 8Br-dG at position 21 and revealed an antiparallel fold composed of four G-quartets and three lateral C-C loops. The G-quadruplex exhibits high thermal stability and is favored kinetically and under slightly acidic conditions. An unusual structural element distinct from a C-quartet is observed in the structure. Two C•C base pairs are stacked on the nearby G-quartet and are involved in a dynamic equilibrium between symmetric N3-amino and carbonyl-amino geometries and protonated C+•C state.

Indexed as

G-QuadruplexesBase PairingC9orf72 ProteinDeoxyguanosineGuanineHumansMagnetic Resonance SpectroscopyModels, MolecularNucleic Acid ConformationPolymorphism, GeneticRepetitive Sequences, Nucleic Acid8-bromo-2'-deoxyguanosineC9orf72 ProteinC9orf72 protein, humanDeoxyguanosineGuanine

Identifiers

PMID30277522
PMCPMC6265483
OpenAlexW2895009915

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.