Evidence map›Paper›PMID 26966258›Full record

ArticleGenetics2016

Mitonuclear Epistasis for Development Time and Its Modification by Diet in Drosophila.

Jim A Mossman, Leann M Biancani, Chen-Tseh Zhu, David M Rand

Abstract read
In one paragraph

Article in Genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing 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

61 citing papers in PubMed.

  1. Pervasive effects ofbioRxiv : the preprint server for biology · 2026
    Article
  2. OutbredbioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
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  9. The role of mitochondria in sex- and age-specific gene expression in a species without sex chromosomes.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Mitochondrial Genome Diversity across the Subphylum Saccharomycotina.bioRxiv : the preprint server for biology · 2023
    Article
  16. Review
  17. Article
  18. Mitochondrial effects on fertility and longevity inProceedings. Biological sciences · 2022
    Article
  19. Genomic Signatures of Mitonuclear Coevolution in Mammals.Molecular biology and evolution · 2022
    Article
  20. Article

1 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

4 authors.

Jim A MossmanDepartment of Ecology and Evolutionary Biology, Brown University, Providence, Rhode Island 02912 David_Rand@brown.edu.
Leann M BiancaniDepartment of Ecology and Evolutionary Biology, Brown University, Providence, Rhode Island 02912.
Chen-Tseh ZhuDepartment of Ecology and Evolutionary Biology, Brown University, Providence, Rhode Island 02912.
David M RandDepartment of Ecology and Evolutionary Biology, Brown University, Providence, Rhode Island 02912 David_Rand@brown.edu.

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

Mitochondrial (mtDNA) and nuclear genes have to operate in a coordinated manner to maintain organismal function, and the regulation of this homeostasis presents a substantial source of potential epistatic (G × G) interactions. How these interactions shape the fitness landscape is poorly understood. Here we developed a novel mitonuclear epistasis model, using selected strains of the Drosophila Genetic Reference Panel (DGRP) and mitochondrial genomes from within Drosophila melanogaster and D. simulans to test the hypothesis that mtDNA × nDNA interactions influence fitness. In total we built 72 genotypes (12 nuclear backgrounds × 6 mtDNA haplotypes, with 3 from each species) to dissect the relationship between genotype and phenotype. Each genotype was assayed on four food environments. We found considerable variation in several phenotypes, including development time and egg-to-adult viability, and this variation was partitioned into genetic (G), environmental (E), and higher-order (G × G, G × E, and G × G × E) components. Food type had a significant impact on development time and also modified mitonuclear epistases, evidencing a broad spectrum of G × G × E across these genotypes. Nuclear background effects were substantial, followed by mtDNA effects and their G × G interaction. The species of mtDNA haplotype had negligible effects on phenotypic variation and there was no evidence that mtDNA variation has different effects on male and female fitness traits. Our results demonstrate that mitonuclear epistases are context dependent, suggesting the selective pressure acting on mitonuclear genotypes may vary with food environment in a genotype-specific manner.

Indexed as

DietEpistasis, GeneticGenome, MitochondrialAnimalsDrosophila melanogasterFemaleGene-Environment InteractionGenetic FitnessMaleModels, Geneticdevelopment timeDGRPepistasisfitnessgenotype-by-environment interactionmitonuclearMtDNA

Identifiers

PMID26966258
PMCPMC4858792

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.