Evidence map›Paper›PMID 38262701›Full record

ArticleG3 (Bethesda, Md.)2024

Gene expression variation underlying tissue-specific responses to copper stress in Drosophila melanogaster.

Elizabeth R Everman, Stuart J Macdonald

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.5field-weighted citation impact, top 13% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Natural variation suggests candidate genes underlying Caenorhabditis elegans susceptibility to diverse toxicants.Toxicological sciences : an official journal of the Society of Toxicology · 2026
    Article
  2. Natural variation suggests candidate genes underlyingbioRxiv : the preprint server for biology · 2025
    Article
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 1 country.

Elizabeth R EvermanSchool of Biological Sciences, The University of Oklahoma, 730 Van Vleet Oval, Norman, OK 73019, USA.ORCID 0000-0002-3190-4171
Stuart J MacdonaldMolecular Biosciences, University of Kansas, 1200 Sunnyside Ave, Lawrence, KS 66045, USA.ORCID 0000-0002-9421-002X
University of Kansas · USUniversity of Oklahoma · US

Funding

Mentoring CoreP20GM103418 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI Douglas E Wright · 2012 to 2026
$63.0M
Synthetic Chemical Biology CoreP30GM145499 · NIGMS · UNIVERSITY OF KANSAS LAWRENCE · PI Susan M Lunte · 2022 to 2026
$6.9M
A Resource for the Genetic Dissection of Complex TraitsR01OD034064 · OD · UNIVERSITY OF KANSAS LAWRENCE · PI ANTHONY Douglas LONG, Stuart John Macdonald · 2023 to 2026
$2.4M
Toxicogenomics of metal response in genetically-variable DrosophilapopulationsR01ES029922 · NIEHS · UNIVERSITY OF KANSAS LAWRENCE · PI MACDONALD, STUART JOHN · 2019 to 2021
$682k
Linking genomic, physiological, and behavioral responses using a Drosophila model of heavy metal stressK99ES033257 · NIEHS · UNIVERSITY OF KANSAS LAWRENCE · PI EVERMAN, ELIZABETH · 2021 to 2022
$180k
Genetic dissection and characterization of variation in copper resistance in Drosophila melanogasterF32GM133111 · NIGMS · UNIVERSITY OF KANSAS LAWRENCE · PI EVERMAN, ELIZABETH · 2019 to 2020
$127k
NIEHS NIH HHS K99 ES033257NIEHS NIH HHS R01 ES029922NIGMS NIH HHS F32 GM133111NIGMS NIH HHS P20 GM103418NIGMS NIH HHS P30 GM145499NIH HHS P30 GM145499NIH HHS R01 OD034064
6 · The paper itself

Abstract

Copper is one of a handful of biologically necessary heavy metals that is also a common environmental pollutant. Under normal conditions, copper ions are required for many key physiological processes. However, in excess, copper results in cell and tissue damage ranging in severity from temporary injury to permanent neurological damage. Because of its biological relevance, and because many conserved copper-responsive genes respond to nonessential heavy metal pollutants, copper resistance in Drosophila melanogaster is a useful model system with which to investigate the genetic control of the heavy metal stress response. Because heavy metal toxicity has the potential to differently impact specific tissues, we genetically characterized the control of the gene expression response to copper stress in a tissue-specific manner in this study. We assessed the copper stress response in head and gut tissue of 96 inbred strains from the Drosophila Synthetic Population Resource using a combination of differential expression analysis and expression quantitative trait locus mapping. Differential expression analysis revealed clear patterns of tissue-specific expression. Tissue and treatment specific responses to copper stress were also detected using expression quantitative trait locus mapping. Expression quantitative trait locus associated with MtnA, Mdr49, Mdr50, and Sod3 exhibited both genotype-by-tissue and genotype-by-treatment effects on gene expression under copper stress, illuminating tissue- and treatment-specific patterns of gene expression control. Together, our data build a nuanced description of the roles and interactions between allelic and expression variation in copper-responsive genes, provide valuable insight into the genomic architecture of susceptibility to metal toxicity, and highlight candidate genes for future functional characterization.

Indexed as

Drosophila melanogasterMetals, HeavyAnimalsCopperDrosophilaGene ExpressionGene Expression RegulationCopperMetals, HeavyDSPReQTL mappinggene expressionheavy metals

Identifiers

PMID38262701
PMCPMC11021028
OpenAlexW4391151470

What OpenQuestion 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 OpenQuestion graph.