Evidence map›Paper›PMID 19151371›Full record

ArticleNucleic acids research2009

Influence of flanking sequence context on the conformational flexibility of aminofluorene-modified dG adduct in dA mismatch DNA duplexes.

Nidhi Jain, Srinivasarao Meneni, Vipin Jain, Bongsup P Cho

Abstract read
In one paragraph

Article in Nucleic acids research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

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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

4 authors.

Nidhi JainDepartment of Biomedical and Pharmaceutical Sciences, College of Pharmacy, University of Rhode Island, Kingston, RI 02881, USA.
Srinivasarao Meneni
Vipin Jain
Bongsup P Cho

Funding

Training CoreP20GM103430 · NIGMS · UNIVERSITY OF RHODE ISLAND · PI Bongsup P Cho · 2012 to 2026
$63.6M
UNDERGRADUATE RESEARCH AND SEMINARSP20RR016457 · NCRR · UNIVERSITY OF RHODE ISLAND · PI MARSTON, MARCIA · 2001 to 2011
$35.5M
Sequence Effects of Arylamine-DNA Adducts: Repair and ReplicationR01CA098296 · NCI · UNIVERSITY OF RHODE ISLAND · PI CHO, BONGSUP P · 2003 to 2013
$2.6M
Sequence Effects of Arylamine-DNA Adducts: Repair and ReplicationR56CA098296 · NCI · UNIVERSITY OF RHODE ISLAND · PI CHO, BONGSUP P · 2008 to 2008
$300k
NCI NIH HHS CA098296NCI NIH HHS R01 CA098296NCI NIH HHS R56 CA098296NCRR NIH HHS P20 RR-16457
6 · The paper itself

Abstract

When positioned opposite to a dA in a DNA duplex, the prototype arylamine-DNA adduct [N-(2'-deoxyguanosin-yl)-7-fluoro-2-aminofluorene (FAF)] adopts the so-called 'wedge' (W) conformation, in which the carcinogen resides in the minor groove of the duplex. All 16 FAF-modified 12-mer NG*N/NAN dA mismatch duplexes (G* = FAF, N = G, A, C, T) exhibited strongly positive induced circular dichroism in the 290-360 nm range (ICD(290-360 nm)), which supports the W conformation. The ICD(290-360 nm) intensities were the greatest for duplexes with a 3'-flanking T. The AG*N duplex series showed little adduct-induced destabilization. An exception was the AG*T duplex, which displayed two well-resolved signals in the (19)F NMR spectra. This was presumably due to a strong lesion-destabilizing effect of the 3'-T. The flanking T effect was substantiated further by findings with the TG*T duplex, which exhibited greater lesion flexibility and nucleotide excision repair recognition. Adduct conformational heterogeneity decreased in order of TG*T > AG*T > CG*T > AG*A > AG*G > AG*C. The dramatic flanking T effect on W-conformeric duplexes is consistent with the strong dependence of the ICD(290-360) on both temperature and salt concentration and could be extended to the arylamine food mutagens that are biologically relevant in humans.

Indexed as

Base Pair MismatchBase SequenceCircular DichroismDeoxyadenosinesDeoxyguanosineDNA AdductsFluorenesNuclear Magnetic Resonance, BiomolecularNucleic Acid ConformationSodium ChlorideTemperatureDeoxyadenosinesDeoxyguanosineDNA AdductsFluorenesN-(2'-deoxyguanosinyl)-7-fluoro-2-aminofluoreneSodium Chloride

Identifiers

PMID19151371
PMCPMC2655675

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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.