Evidence map›Paper›PMID 22372563›Full record

ArticleJournal of the American Chemical Society2012

Tertiary DNA structure in the single-stranded hTERT promoter fragment unfolds and refolds by parallel pathways via cooperative or sequential events.

Zhongbo Yu, Vanessa Gaerig, Yunxi Cui, HyunJin Kang, Vijay Gokhale, Yuan Zhao, Laurence H Hurley, Hanbin Mao

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2012. 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
3.6field-weighted citation impact, top 6% 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, 82 citations in OpenAlex.

  1. Review
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  13. G-quadruplex structural variations in human genome associated with single-nucleotide variations and their impact on gene activity.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  14. Article
  15. Article
  16. Duplex formation in a G-quadruplex bulge.Nucleic acids research · 2020
    Article
  17. Duplex DNA Is Weakened in Nanoconfinement.Journal of the American Chemical Society · 2020
    Article
  18. Article
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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

8 authors at 3 institutions in 1 country.

Zhongbo YuDepartment of Chemistry and Biochemistry and School of Biomedical Sciences, Kent State University, Kent, Ohio 44242, United States.
Vanessa Gaerig
Yunxi Cui
HyunJin Kang
Vijay Gokhale
Yuan Zhao
Laurence H Hurley
Hanbin Mao
Kent State University · USUniversity of Arizona · USBIO5 Institute

Funding

Establishing a molecular system for drug targeting of transcriptional controlR01GM085585 · NIGMS · UNIVERSITY OF ARIZONA · PI HURLEY, LAURENCE H. · 2008 to 2011
$1.5M
Effect of G-rich Higher Order Structures on Insulin Linked Polymorphism RegionR15DK081191 · NIDDK · KENT STATE UNIVERSITY · PI MAO, HANBIN · 2008 to 2010
$262k
NIDDK NIH HHS DK081191-01NIDDK NIH HHS R15 DK081191NIGMS NIH HHS GM085585NIGMS NIH HHS R01 GM085585
6 · The paper itself

Abstract

The discovery of G-quadruplexes and other DNA secondary elements has increased the structural diversity of DNA well beyond the ubiquitous double helix. However, it remains to be determined whether tertiary interactions can take place in a DNA complex that contains more than one secondary structure. Using a new data analysis strategy that exploits the hysteresis region between the mechanical unfolding and refolding traces obtained by a laser-tweezers instrument, we now provide the first convincing kinetic and thermodynamic evidence that a higher order interaction takes place between a hairpin and a G-quadruplex in a single-stranded DNA fragment that is found in the promoter region of human telomerase. During the hierarchical unfolding or refolding of the DNA complex, a 15-nucleotide hairpin serves as a common species among three intermediates. Moreover, either a mutant that prevents this hairpin formation or the addition of a DNA fragment complementary to the hairpin destroys the cooperative kinetic events by removing the tertiary interaction mediated by the hairpin. The coexistence of the sequential and the cooperative refolding events provides direct evidence for a unifying kinetic partition mechanism previously observed only in large proteins and complex RNA structures. Not only does this result rationalize the current controversial observations for the long-range interaction in complex single-stranded DNA structures, but also this unexpected complexity in a promoter element provides additional justification for the biological function of these structures in cells.

Indexed as

Promoter Regions, GeneticDNAHumansKineticsNucleic Acid ConformationProtein FoldingTelomeraseThermodynamicsDNATelomeraseTERT protein, human

Identifiers

PMID22372563
PMCPMC3336359
OpenAlexW2318033929

What OpenQuestion holds

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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.