Evidence map›Paper›PMID 28085251›Full record

ArticleACS chemical biology2017

Differential Ability of Five DNA Glycosylases to Recognize and Repair Damage on Nucleosomal DNA.

Eric D Olmon, Sarah Delaney

Open access · greenAbstract read
In one paragraph

Article in ACS chemical biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

45 citing papers in PubMed, 64 citations in OpenAlex.

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  18. Generation of Recombinant Nucleosomes Containing Site-Specific DNA Damage.Methods in molecular biology (Clifton, N.J.) · 2023
    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

2 authors at 1 institution in 1 country.

Eric D OlmonDepartment of Chemistry, Brown University , Providence, Rhode Island 02912, United States.ORCID 0000-0001-5742-3854
Sarah DelaneyDepartment of Chemistry, Brown University , Providence, Rhode Island 02912, United States.ORCID 0000-0002-8366-3808
Brown University · US

Funding

Resource for Biocomputing Visualization and InformaticsP41GM103311 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FERRIN, THOMAS E · 2012 to 2017
$8.2M
Inflammation as a Mediator of Dynamic DNA MutationsR01ES019296 · NIEHS · BROWN UNIVERSITY · PI DELANEY, SARAH · 2010 to 2014
$2.2M
Examining the Kinetics of Base Excision Repair in the Context of ChromatinF32CA183573 · NCI · BROWN UNIVERSITY · PI OLMON, ERIC DANIEL · 2014 to 2016
$148k
NCI NIH HHS F32 CA183573NIEHS NIH HHS R01 ES019296NIGMS NIH HHS P41 GM103311
6 · The paper itself

Abstract

Damage to genomic DNA leads to mutagenesis and disease. Repair of single base damage is initiated by DNA glycosylases, the first enzymes in the base excision repair pathway. Although eukaryotic packaging of chromosomal DNA in nucleosomes is known to decrease DNA glycosylase efficiency, the impact on individual glycosylases is unclear. Here, we present a model system in which we examine the repair of site-specific base damage in well-characterized nucleosome core particles by five different DNA glycosylases. We find that DNA glycosylase efficiency on nucleosome substrates depends not only on the geometric orientation of the damaged base but also on its identity, as well as on the size, structure, and mechanism of the glycosylase. We show via molecular modeling that inhibition of glycosylase activity is largely due to steric obstruction by the nucleosome core.

Indexed as

DNA DamageDNA RepairDNA GlycosylasesHumansNucleosomesDNA GlycosylasesNucleosomes

Identifiers

PMID28085251
PMCPMC6557264
OpenAlexW2578182948

What OpenQuestion holds

Textmetadata
LicenceTDM
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.