ArticleEvolution; international journal of organic evolution2019
Physical linkage and mate preference generate linkage disequilibrium for behavioral isolation in two parapatric crickets.
Article in Evolution; international journal of organic evolution, 2019. 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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Who cites it
5 citing papers in PubMed, 12 citations in OpenAlex.
- The evolution of preferred male traits, female preference and the G matrix: "Toto, I've a feeling we're not in Kansas anymore".Heredity · 2025Article
- Negative Coupling: The Coincidence of Premating Isolating Barriers Can Reduce Reproductive Isolation.Cold Spring Harbor perspectives in biology · 2024Review
- The neurodevelopmental genes alan shepard and Neuroglian contribute to female mate preference in African Drosophila melanogaster.Journal of evolutionary biology · 2024Article
- Dissecting cricket genomes for the advancement of entomology and entomophagy.Biophysical reviews · 2022Review
- A high-density genetic map and molecular sex-typing assay for gerbils.Mammalian genome : official journal of the International Mammalian Genome Society · 2019Article
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Authors and funding
4 authors at 3 institutions in 3 countries.
Funding
Abstract
Behavioral isolation is a potent barrier to gene flow and a source of striking diversity in the animal kingdom. However, it remains unclear if the linkage disequilibrium (LD) between sex-specific traits required for behavioral isolation results mostly from physical linkage between signal and preference loci or from directional mate preferences. Here, we test this in the field crickets Gryllus rubens and G. texensis. These closely related species diverged with gene flow and have strongly differentiated songs and preference functions for the mate calling song rhythm. We map quantitative trait loci for signal and preference traits (pQTL) as well as for gene expression associated with these traits (eQTL). We find strong, positive genetic covariance between song traits and between song and preference. Our results show that this is in part explained by incomplete physical linkage: although both linked pQTL and eQTL couple male and female traits, major effect loci for different traits were never on the same chromosome. We suggest that the finely tuned, highly divergent preference functions are likely an additional source of LD between male and female traits in this system. Furthermore, pleiotropy of gene expression presents an underappreciated mechanism to link sexually dimorphic phenotypes.
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