Evidence map›Paper›PMID 28110272›Full record

ArticleMolecular biology and evolution2017

Mitonuclear Interactions Mediate Transcriptional Responses to Hypoxia in Drosophila.

Jim A Mossman, Jennifer G Tross, Nick A Jourjine, Nan Li, Zhijin Wu, David M Rand

Open access · hybridAbstract read
In one paragraph

Article in Molecular biology and evolution, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

32 citing papers in PubMed, 52 citations in OpenAlex.

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  16. Review
  17. Mapping and editing animal mitochondrial genomes: can we overcome the challenges?Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Review
  18. Mitonuclear conflict and cooperation govern the integration of genotypes, phenotypes and environments.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Article
  19. Sex-specific effects of mitochondrial haplotype on metabolic rate inPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Article
  20. Impact of mitonuclear interactions on life-history responses to diet.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    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 3 institutions in 1 country.

Jim A MossmanDepartment of Ecology and Evolutionary Biology, Box G, Brown University, Providence, RI.
Jennifer G TrossDepartment of Ecology and Evolutionary Biology, Box G, Brown University, Providence, RI.
Nick A JourjineDepartment of Ecology and Evolutionary Biology, Box G, Brown University, Providence, RI.
Nan LiDepartment of Biostatistics, Brown University, Providence, RI.
Zhijin WuDepartment of Biostatistics, Brown University, Providence, RI.
David M RandDepartment of Ecology and Evolutionary Biology, Box G, Brown University, Providence, RI.
Brown University · USHarvard–MIT Division of Health Sciences and Technology · USUniversity of California, Berkeley · US

Funding

Nuclear-Mitochondrial Fitness Interactions in DrosophilaR01GM067862 · NIGMS · BROWN UNIVERSITY · PI RAND, DAVID M · 2004 to 2020
$5.1M
Mitochondrial Genetics of Aging in DrosophilaR01AG027849 · NIA · BROWN UNIVERSITY · PI RAND, DAVID M · 2009 to 2013
$1.5M
NIA NIH HHS R01 AG027849NIGMS NIH HHS R01 GM067862
6 · The paper itself

Abstract

Among the major challenges in quantitative genetics and personalized medicine is to understand how gene × gene interactions (G × G: epistasis) and gene × environment interactions (G × E) underlie phenotypic variation. Here, we use the intimate relationship between mitochondria and oxygen availability to dissect the roles of nuclear DNA (nDNA) variation, mitochondrial DNA (mtDNA) variation, hypoxia, and their interactions on gene expression in Drosophila melanogaster. Mitochondria provide an important evolutionary and medical context for understanding G × G and G × E given their central role in integrating cellular signals. We hypothesized that hypoxia would alter mitonuclear communication and gene expression patterns. We show that first order nDNA, mtDNA, and hypoxia effects vary between the sexes, along with mitonuclear epistasis and G × G × E effects. Females were generally more sensitive to genetic and environmental perturbation. While dozens to hundreds of genes are altered by hypoxia in individual genotypes, we found very little overlap among mitonuclear genotypes for genes that were significantly differentially expressed as a consequence of hypoxia; excluding the gene hairy. Oxidative phosphorylation genes were among the most influenced by hypoxia and mtDNA, and exposure to hypoxia increased the signature of mtDNA effects, suggesting retrograde signaling between mtDNA and nDNA. We identified nDNA-encoded genes in the electron transport chain (succinate dehydrogenase) that exhibit female-specific mtDNA effects. Our findings have important implications for personalized medicine, the sex-specific nature of mitonuclear communication, and gene × gene coevolution under variable or changing environments.

Indexed as

AnimalsBiological EvolutionCell NucleusDNA, MitochondrialDrosophila melanogasterEpistasis, GeneticFemaleGene Expression RegulationGenotypeHaplotypesHypoxiaMaleMitochondriaPolymorphism, GeneticTranscriptional ActivationTranscriptomeDNA, MitochondrialDrosophilaEepistasisG ×hypoxiamitonuclearmtDNAtranscriptome

Identifiers

PMID28110272
PMCPMC6095086
OpenAlexW2551467169

What OpenQuestion holds

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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.