Evidence map›Paper›PMID 30445650›Full record

ArticleNucleic acids research2019

NMR solution structure of an asymmetric intermolecular leaped V-shape G-quadruplex: selective recognition of the d(G2NG3NG4) sequence motif by a short linear G-rich DNA probe.

Chanjuan Wan, Wenqiang Fu, Haitao Jing, Na Zhang

Abstract read
In one paragraph

Article in Nucleic acids research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Sugar Puckering Drives G-Quadruplex Refolding: Implications for V-Shaped Loops.Chemistry (Weinheim an der Bergstrasse, Germany) · 2020
    Article
  9. Article
  10. Review
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Chanjuan WanHigh Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei 230031, China.
Wenqiang FuHigh Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei 230031, China.
Haitao JingHigh Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei 230031, China.
Na ZhangHigh Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei 230031, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aside from classical loops among G-quadruplexes, the unique leaped V-shape scaffold spans over three G-tetrads, without any intervening residues. This scaffold enables a sharp reversal of two adjacent strand directions and simultaneously participates in forming the G-tetrad core. These features make this scaffold itself distinctive and thus an essentially more accessible target. As an alternative to the conventional antisense method using a complementary chain, forming an intermolecular G-quadruplex from two different oligomers, in which the longer one as the target is captured by a short G-rich fragment, could be helpful for recognizing G-rich sequences and structural motifs. However, such an intermolecular leaped V-shape G-quadruplex consisting of DNA oligomers of quite different lengths has not been evaluated. Here, we present the first nuclear magnetic resonance (NMR) study of an asymmetric intermolecular leaped V-shape G-quadruplex assembled between an Oxytricha nova telomeric sequence d(G2T4G4T4G4) and a single G-tract fragment d(TG4A). Furthermore, we explored the selectivity of this short fragment as a potential probe, examined the kinetic discrimination for probing a specific mutant, and proposed the key sequence motif d(G2NG3NG4) essential for building the leaped V-shape G-quadruplexes.

Indexed as

G-QuadruplexesNucleic Acid ConformationBase SequenceDNADNA ProbesKineticsMagnetic Resonance SpectroscopySolutionsTelomereDNADNA ProbesSolutions

Identifiers

PMID30445650
PMCPMC6379650

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