ArticleMolecular ecology2014
The genomic signature of parallel adaptation from shared genetic variation.
Article in Molecular ecology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.
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75 citing papers in PubMed.
- Natural selection and recombination interact to structure genome-wide variation in pines.The Plant journal : for cell and molecular biology · 2026Article
- High Gene Flow With Patterns of Asymmetric Connectivity and Adaptive Divergence in the New Zealand Southern Rock Lobster,Evolutionary applications · 2026Article
- Complex Patterns of Hitchhiking Mutation Load Among Stickleback Populations.Genome biology and evolution · 2026Article
- Article
- Rapid genome modifications including chromosomal fusions and large-scale inversions are key features in Arctic codfish species.Genome biology · 2026Article
- A species interaction kick-starts ecological speciation in allopatry.Proceedings of the National Academy of Sciences of the United States of America · 2025Article
- Strong but diffuse genetic divergence underlies differentiation in an incipient species of marine stickleback.bioRxiv : the preprint server for biology · 2025Article
- Inversions contribute disproportionately to parallel genomic divergence in dune sunflowers.Nature ecology & evolution · 2025Article
- Genomic variation in weedy and cultivated broomcorn millet accessions uncovers the genetic architecture of agronomic traits.Nature genetics · 2024Article
- Ancient dolphin genomes reveal rapid repeated adaptation to coastal waters.Nature communications · 2023Article
- The role of recombination landscape in species hybridisation and speciation.Frontiers in plant science · 2023Review
- Climatic similarity and genomic background shape the extent of parallel adaptation in Timema stick insects.Nature ecology & evolution · 2022Article
- The ectodysplasin-A receptor is a candidate gene for lateral plate number variation in stickleback fish.G3 (Bethesda, Md.) · 2022Article
- Chromosomal Fusions Facilitate Adaptation to Divergent Environments in Threespine Stickleback.Molecular biology and evolution · 2022Article
- The maintenance of standing genetic variation: Gene flow vs. selective neutrality in Atlantic stickleback fish.Molecular ecology · 2022Article
- Genome-Environment Associations, an Innovative Tool for Studying Heritable Evolutionary Adaptation in Orphan Crops and Wild Relatives.Frontiers in genetics · 2022Review
- Comparing genome scans among species of the stickleback order reveals three different patterns of genetic diversity.Ecology and evolution · 2022Article
- Highly Replicated Evolution of Parapatric Ecotypes.Molecular biology and evolution · 2021Article
- Parallel introgression, not recurrent emergence, explains apparent elevational ecotypes of polyploid Himalayan snowtrout.Royal Society open science · 2021Article
- Clinal genomic analysis reveals strong reproductive isolation across a steep habitat transition in stickleback fish.Nature communications · 2021Article
15 more citing papers are in PubMed but not listed here.
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5 authors.
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Abstract
Parallel adaptation is common and may often occur from shared genetic variation, but the genomic consequences of this process remain poorly understood. We first use individual-based simulations to demonstrate that comparisons between populations adapted in parallel to similar environments from shared variation reveal a characteristic genomic signature around a selected locus: a low-divergence valley centred at the locus and flanked by twin peaks of high divergence. This signature is initiated by the hitchhiking of haplotype tracts differing between derived populations in the broader neighbourhood of the selected locus (driving the high-divergence twin peaks) and shared haplotype tracts in the tight neighbourhood of the locus (driving the low-divergence valley). This initial hitchhiking signature is reinforced over time because the selected locus acts as a barrier to gene flow from the source to the derived populations, thus promoting divergence by drift in its close neighbourhood. We next empirically confirm the peak-valley-peak signature by combining targeted and RAD sequence data at three candidate adaptation genes in multiple marine (source) and freshwater (derived) populations of threespine stickleback. Finally, we use a genome-wide screen for the peak-valley-peak signature to discover additional genome regions involved in parallel marine-freshwater divergence. Our findings offer a new explanation for heterogeneous genomic divergence and thus challenge the standard view that peaks in population divergence harbour divergently selected loci and that low-divergence regions result from balancing selection or localized introgression. We anticipate that genome scans for peak-valley-peak divergence signatures will promote the discovery of adaptation genes in other organisms.
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