Evidence map›Paper›PMID 22496853›Full record

ArticlePloS one2012

Genome-wide association analysis of oxidative stress resistance in Drosophila melanogaster.

Allison L Weber, George F Khan, Michael M Magwire, Crystal L Tabor, Trudy F C Mackay, Robert R H Anholt

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
10.0field-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

83 citing papers in PubMed, 153 citations in OpenAlex.

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  19. Exercise-induced changes in climbing performance.Royal Society open science · 2021
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23 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

6 authors at 1 institution in 1 country.

Allison L WeberDepartment of Genetics, North Carolina State University, Raleigh, North Carolina, United States of America. allisonwebergenetics@gmail.com
George F Khan
Michael M Magwire
Crystal L Tabor
Trudy F C Mackay
Robert R H Anholt
North Carolina State University · US

Funding

QUANTITATIVE TRAIT LOCI IN DROSOPHILAR01GM045146 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI ANHOLT, ROBERT R. H, MACKAY, TRUDY F. · 1991 to 2012
$5.1M
Oxidative stress and neurogenetic networks in DrosophilaRC1ES018255 · NIEHS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI ANHOLT, ROBERT R. H · 2009 to 2010
$716k
Systems Genetics of Oxidative Stress Resistance in DrosophilaF32GM089010 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI WEBER, ALLISON LYNN · 2009 to 2011
$151k
NIEHS NIH HHS 5RC1ES018255NIEHS NIH HHS RC1 ES018255NIGMS NIH HHS F32 GM089010NIGMS NIH HHS GM045146NIGMS NIH HHS R01 GM045146
6 · The paper itself

Abstract

backgroundAerobic organisms are susceptible to damage by reactive oxygen species. Oxidative stress resistance is a quantitative trait with population variation attributable to the interplay between genetic and environmental factors. Drosophila melanogaster provides an ideal system to study the genetics of variation for resistance to oxidative stress. METHODS AND

findingsWe used 167 wild-derived inbred lines of the Drosophila Genetic Reference Panel for a genome-wide association study of acute oxidative stress resistance to two oxidizing agents, paraquat and menadione sodium bisulfite. We found significant genetic variation for both stressors. Single nucleotide polymorphisms (SNPs) associated with variation in oxidative stress resistance were often sex-specific and agent-dependent, with a small subset common for both sexes or treatments. Associated SNPs had moderately large effects, with an inverse relationship between effect size and allele frequency. Linear models with up to 12 SNPs explained 67-79% and 56-66% of the phenotypic variance for resistance to paraquat and menadione sodium bisulfite, respectively. Many genes implicated were novel with no known role in oxidative stress resistance. Bioinformatics analyses revealed a cellular network comprising DNA metabolism and neuronal development, consistent with targets of oxidative stress-inducing agents. We confirmed associations of seven candidate genes associated with natural variation in oxidative stress resistance through mutational analysis.

conclusionsWe identified novel candidate genes associated with variation in resistance to oxidative stress that have context-dependent effects. These results form the basis for future translational studies to identify oxidative stress susceptibility/resistance genes that are evolutionary conserved and might play a role in human disease.

Indexed as

Genome-Wide Association StudyAnimalsDNADrosophila melanogasterFemaleHerbicidesMaleNeurogenesisOxidative StressParaquatPolymorphism, Single NucleotideQuantitative Trait LociVitamin K 3VitaminsDNAHerbicidesParaquatVitamin K 3Vitamins

Identifiers

PMID22496853
PMCPMC3319608
OpenAlexW1977409932

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.