ArticleMolecular ecology2025
Reduced Parallel Gene Expression Evolution With Increasing Genetic Divergence-A Hallmark of Polygenic Adaptation.
Article in Molecular ecology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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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.
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Who cites it
2 citing papers in PubMed.
- Parallel adaptation to geothermally-warmed habitats due to common structural variation and functional developmental pathways.Nature communications · 2026Article
- Identifying the Degree of Gene Reuse During Repeated Adaptation.Molecular ecology · 2025Review
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Authors and funding
6 authors.
Funding
Abstract
Parallel evolution, the repeated evolution of similar traits in independent lineages, is a topic of considerable interest in evolutionary biology. Although previous studies have focused on the parallelism of phenotypic traits and their underlying genetic basis, the extent of parallelism at the level of gene expression across different levels of genetic divergence is not yet fully understood. This study investigates the evolution of gene expression in replicate Drosophila populations exposed to the same novel environment at three divergence levels: within a population, between populations and between species. We show that adaptive gene expression changes are more heterogeneous with increasing genetic divergence between the compared groups. This finding suggests that the adaptive architecture-comprising factors such as allele frequencies and the effect size of contributing loci-becomes more distinct with increasing divergence. As a result, this leads to a reduction in parallel gene expression evolution. This result implies that redundancy is a crucial factor in both genetic selection responses and gene expression evolution. Hence, our findings are consistent with the omnigenic model, which posits that selection acts on higher-order phenotypes. This work contributes to our understanding of phenotypic evolution and the complex interplay between genomic and molecular responses.
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