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Selection and gene flow shape niche-associated variation in pheromone response
Daehan Lee1, Stefan Zdraljevic1,2, Daniel E Cook1,2,3
1Department of Molecular Biosciences, Northwestern University, Evanston, IL, USA.
Nature Ecology & Evolution
|September 25, 2019
Summary
Genetic variation in C. elegans pheromone receptor genes influences how individuals respond to chemical signals. A recent deletion in the srg-37 gene reduces pheromone sensitivity globally, with balancing selection maintaining this diversity.
Area of Science:
- Evolutionary Biology
- Genetics
- Animal Behavior
Background:
- Chemical communication is vital for social interactions in many species.
- In *C. elegans*, ascaroside pheromones regulate population density, inhibiting reproduction at high levels.
- Natural genetic diversity's impact on pheromone response is poorly understood.
Purpose of the Study:
- To investigate how natural genetic variation affects *C. elegans* pheromone responses.
- To identify genetic mechanisms underlying differences in pheromone sensitivity across diverse habitats.
Main Methods:
- Analysis of pheromone receptor genes (*srg-36*, *srg-37*) for loss-of-function deletions.
- Investigating the evolutionary history and global distribution of identified genetic variations.
- Assessing the relationship between genetic genotypes and population dynamics/niche diversity.
Main Results:
- Identified deletions in *srg-36* and *srg-37* impair pheromone receptor function.
- A recent, globally distributed deletion in *srg-37* reduces pheromone sensitivity in *C. elegans*.
- Balancing selection maintains both wild-type and deletion alleles of *srg-37* in natural populations, linked to niche diversity.
Conclusions:
- Niche-associated variation in pheromone receptor genes drives natural differences in pheromone response.
- The *srg-37* deletion's maintenance suggests a role in adapting to fluctuating population dynamics.
- Human activities may have influenced the spread and selection of *srg-37* variation through species migration and habitat modification.
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