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Genotype by environment interaction for gene expression in Drosophila melanogaster
Wen Huang1,2, Mary Anna Carbone3,4, Richard F Lyman3,5
1Program in Genetics, Department of Biological Sciences, W. M. Keck Center for Behavioral Biology, North Carolina State University, Raleigh, NC, 27695-7614, USA. huangw53@msu.edu.
Nature Communications
|October 29, 2020
Summary
Environmental changes significantly alter gene expression genetics in fruit flies. Stabilizing selection on gene expression promotes the robustness of genetic networks despite environmental plasticity.
Area of Science:
- Genomics
- Evolutionary Biology
- Molecular Biology
Background:
- Understanding how genetic factors influence phenotypic responses to environmental changes is crucial.
- Gene expression variation is a key component of phenotypic plasticity.
- The genetic architecture of gene expression can be influenced by environmental conditions.
Purpose of the Study:
- To investigate how the genetic architecture of gene expression regulation changes in response to different temperatures.
- To identify the genetic basis of environmentally plastic gene expression in Drosophila melanogaster.
Main Methods:
- Utilized whole-genome quantitative gene expression analysis in fully sequenced inbred Drosophila melanogaster strains.
- Compared gene expression patterns between flies reared at 25°C and 18°C.
- Analyzed genotype-by-environment interactions and expression quantitative trait loci (eQTLs).
Main Results:
- A significant portion of the transcriptome showed genotype-by-environment interaction, indicating plastic genetic architecture.
- Genetic variance in gene expression generally increased at 18°C compared to 25°C.
- Environment-specific eQTLs were enriched for transcription factor binding sites, and co-expression networks remained conserved across temperatures.
Conclusions:
- Gene expression exhibits environmentally plastic genetic architecture, with temperature influencing genetic variance.
- Despite plasticity, gene co-expression networks are robust, likely due to stabilizing selection on highly connected genes.
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