ArticleProceedings of the National Academy of Sciences of the United States of America2022
Genetic architecture of dispersal and local adaptation drives accelerating range expansions.
Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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5 citing papers in PubMed, 17 citations in OpenAlex.
- Selection for Molecularly Complementary Modules (MCMs) Drives the Origins and Evolution of Pleiofunctional, Epistatic Interactomes (PEIs).Life (Basel, Switzerland) · 2026Review
- Dispersal evolution can only rescue a limited set of species from climate change.Proceedings. Biological sciences · 2025Article
- Spatially VaryingEvolutionary applications · 2024Article
- Evolutionary ecology of dispersal in biodiverse spatially structured systems: what is old and what is new?Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024Review
- Gene loss during a transition to multicellularity.Scientific reports · 2023Article
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Authors and funding
2 authors at 1 institution in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Contemporary evolution has the potential to significantly alter biotic responses to global change, including range expansion dynamics and biological invasions. Models predicting range dynamics often make highly simplifying assumptions about the genetic architecture underlying relevant traits. However, genetic architecture defines evolvability and higher-order evolutionary processes, which determine whether evolution will be able to keep up with environmental change or not. Therefore, we here study the impact of the genetic architecture of dispersal and local adaptation, two central traits of high relevance for range expansions, on the dynamics and predictability of invasion into an environmental gradient, such as temperature. In our theoretical model we assume that dispersal and local adaptation traits result from the products of two noninteracting gene-regulatory networks (GRNs). We compare our model to simpler quantitative genetics models and show that in the GRN model, range expansions are accelerating and less predictable. We further find that accelerating dynamics in the GRN model are primarily driven by an increase in the rate of local adaptation to novel habitats which results from greater sensitivity to mutation (decreased robustness) and increased gene expression. Our results highlight how processes at microscopic scales, here within genomes, can impact the predictions of large-scale, macroscopic phenomena, such as range expansions, by modulating the rate of evolution.
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