Evidence map›Paper›PMID 29322505›Full record

ArticleBiopolymers2018

Impact of bistrand abasic sites and proximate orientation on DNA global structure and duplex energetics.

Conceição A Minetti, Jeffrey Y Sun, Daniel P Jacobs, Inkoo Kang, David P Remeta, Kenneth J Breslauer

Open access · hybridAbstract read
In one paragraph

Article in Biopolymers, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

13 citing papers in PubMed, 16 citations in OpenAlex.

  1. Disruption of energetic and dynamic base pairing cooperativity in DNA duplexes by an abasic site.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. The Relevance of G-Quadruplexes for DNA Repair.International journal of molecular sciences · 2021
    Review
  8. Endogenous oxidized DNA bases and APE1 regulate the formation of G-quadruplex structures in the genome.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

6 authors at 1 institution in 1 country.

Conceição A MinettiDepartment of Chemistry and Chemical Biology, Rutgers - The State University of New Jersey, Piscataway, New Jersey.ORCID http://orcid.org/0000-0002-9682-2898
Jeffrey Y SunDepartment of Chemistry and Chemical Biology, Rutgers - The State University of New Jersey, Piscataway, New Jersey.
Daniel P JacobsDepartment of Chemistry and Chemical Biology, Rutgers - The State University of New Jersey, Piscataway, New Jersey.
Inkoo KangDepartment of Chemistry and Chemical Biology, Rutgers - The State University of New Jersey, Piscataway, New Jersey.
David P RemetaDepartment of Chemistry and Chemical Biology, Rutgers - The State University of New Jersey, Piscataway, New Jersey.ORCID http://orcid.org/0000-0002-4142-0904
Kenneth J BreslauerDepartment of Chemistry and Chemical Biology, Rutgers - The State University of New Jersey, Piscataway, New Jersey.
Rutgers, The State University of New Jersey · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bistrand lesions embedded within a single helical turn of tridecameric deoxyoligonucleotide duplexes represent a model system for exploring the impact of clustered lesions that occur in vivo and pose a significant challenge to cellular repair machineries. Such investigations are essential for understanding the forces that dictate lesion-induced mutagenesis, carcinogenesis, and cytotoxicity within a context that mimics local helical perturbations caused by an ionizing radiation event. This study characterizes the structural and energy profiles of DNA duplexes harboring synthetic abasic sites (tetrahydrofuran, F) as models of clustered bistrand abasic (AP) lesions. The standard tridecameric dGCGTACCCATGCG·dCGCATGGGTACGC duplex is employed to investigate the energetic impact of single and bistrand AP sites by strategically replacing one or two bases within the central CCC/GGG triplet. Our combined analysis of temperature-dependent UV and circular dichroism (CD) profiles reveals that the proximity and relative orientation of AP sites within bistrand-damaged duplexes imparts a significant thermodynamic impact. Specifically, 3'-staggered lesions (CCF/GFG) exert a greater destabilizing effect when compared with their 5'-counterpart (FCC/GFG). Moreover, a duplex harboring the central bistrand AP lesion (CFC/GFG) is moderately destabilized yet exhibits distinct properties relative to both the 3' and 5'-orientations. Collectively, our energetic data are consistent with structural studies on bistrand AP-duplexes of similar sequence in which a 3'-staggered lesion exerts the greatest perturbation, a finding that provides significant insight regarding the impact of orientation on lesion repair processing efficiency.

Indexed as

Models, MolecularNucleic Acid ConformationDNAThermodynamicsDNAbistrand abasic sitesclustered lesionsDNA damagethermodynamic stability

Identifiers

PMID29322505
PMCPMC6175389
OpenAlexW2783958036

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.