Evidence map›Paper›PMID 17626043›Full record

ArticleNucleic acids research2007

Structure of the Hybrid-2 type intramolecular human telomeric G-quadruplex in K+ solution: insights into structure polymorphism of the human telomeric sequence.

Jixun Dai, Megan Carver, Chandanamali Punchihewa, Roger A Jones, Danzhou Yang

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 229 papers.

0numbers the graph read from it
0cells of the map it votes in
229citing papers in PubMed
11.4field-weighted citation impact, top 1% 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

229 citing papers in PubMed, 549 citations in OpenAlex.

  1. Unraveling G-Quadruplex and i-Motif Coexistence Within a Double-Stranded DNA.Angewandte Chemie (International ed. in English) · 2026
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  14. G-Quadruplex Structures Formed by Human Telomere andInternational journal of molecular sciences · 2025
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169 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 1 country.

Jixun DaiCollege of Pharmacy, The University of Arizona, 1703 E. Mabel St, Tucson, AZ 85721, USA.
Megan Carver
Chandanamali Punchihewa
Roger A Jones
Danzhou Yang
University of Arizona · USRutgers, The State University of New Jersey · US

Funding

DNA TOPOISOMERASE I TARGET INTERACTIONS OF CAMPTOTHECINSK01CA083886 · NCI · UNIVERSITY OF KENTUCKY · PI YANG, DANZHOU · 2000 to 2004
$691k
Acquisition of a Bruker 600MHz NMR SpectrometerS10RR016659 · NCRR · UNIVERSITY OF ARIZONA · PI YANG, DANZHOU · 2002 to 2002
$393k
NCI NIH HHS 1K01CA83886NCI NIH HHS K01 CA083886NCRR NIH HHS 1S10 RR16659
6 · The paper itself

Abstract

Formation of the G-quadruplex in the human telomeric sequence can inhibit the activity of telomerase, thus the intramolecular telomeric G-quadruplexes have been considered as an attractive anticancer target. Information of intramolecular telomeric G-quadruplex structures formed under physiological conditions is important for structure-based drug design. Here, we report the first structure of the major intramolecular G-quadruplex formed in a native, non-modified human telomeric sequence in K(+) solution. This is a hybrid-type mixed parallel/antiparallel-G-stranded G-quadruplex, one end of which is covered by a novel T:A:T triple capping structure. This structure (Hybrid-2) and the previously reported Hybrid-1 structure differ in their loop arrangements, strand orientations and capping structures. The distinct capping structures appear to be crucial for the favored formation of the specific hybrid-type intramolecular telomeric G-quadruplexes, and may provide specific binding sites for drug targeting. Our study also shows that while the hybrid-type G-quadruplexes appear to be the major conformations in K(+) solution, human telomeric sequences are always in equilibrium between Hybrid-1 and Hybrid-2 structures, which is largely determined by the 3'-flanking sequence. Furthermore, both hybrid-type G-quadruplexes suggest a straightforward means for multimer formation with effective packing in the human telomeric sequence and provide important implications for drug targeting of G-quadruplexes in human telomeres.

Indexed as

Models, MolecularBase SequenceDNADNA Mutational AnalysisG-QuadruplexesGuanineHumansNuclear Magnetic Resonance, BiomolecularNucleic Acid ConformationPotassiumProtonsSolutionsTelomereDNAGuaninePotassiumProtonsSolutions

Identifiers

PMID17626043
PMCPMC1976458
OpenAlexW1978685619

What OpenQuestion holds

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LicenceCC BY-NC
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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.