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Selection and gene flow shape niche-associated variation in pheromone response
From quorum sensing in bacteria to pheromone signaling in social insects, chemical communication mediates interactions among individuals in a local population. In Caenorhabditis elegans, ascaroside pheromones can dictate local population density, in which high levels of pheromones inhibit the reprod...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764921/ https://www.ncbi.nlm.nih.gov/pubmed/31548647 http://dx.doi.org/10.1038/s41559-019-0982-3 |
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author | Lee, Daehan Zdraljevic, Stefan Cook, Daniel E. Frézal, Lise Hsu, Jung-Chen Sterken, Mark G. Riksen, Joost A.G. Wang, John Kammenga, Jan E. Braendle, Christian Félix, Marie-Anne Schroeder, Frank C. Andersen, Erik C. |
author_facet | Lee, Daehan Zdraljevic, Stefan Cook, Daniel E. Frézal, Lise Hsu, Jung-Chen Sterken, Mark G. Riksen, Joost A.G. Wang, John Kammenga, Jan E. Braendle, Christian Félix, Marie-Anne Schroeder, Frank C. Andersen, Erik C. |
author_sort | Lee, Daehan |
collection | PubMed |
description | From quorum sensing in bacteria to pheromone signaling in social insects, chemical communication mediates interactions among individuals in a local population. In Caenorhabditis elegans, ascaroside pheromones can dictate local population density, in which high levels of pheromones inhibit the reproductive maturation of individuals. Little is known about how natural genetic diversity affects the pheromone responses of individuals from diverse habitats. Here, we show that a niche-associated variation in pheromone receptor genes contributes to natural differences in pheromone responses. We identified putative loss-of-function deletions that impair duplicated pheromone receptor genes (srg-36 and srg-37), which were shown previously to be lost in population-dense laboratory cultures. A common natural deletion in srg-37 arose recently from a single ancestral population that spread throughout the world and underlies reduced pheromone sensitivity across the global C. elegans population. We found that many local populations harbor individuals with wild-type or a deletion allele of srg-37, suggesting that balancing selection has maintained the recent variation in this pheromone receptor gene. The two srg-37 genotypes are associated with niche diversity underlying boom-and-bust population dynamics. We hypothesize that human activities likely contributed to the gene flow and balancing selection of srg-37 variation through facilitating migration of species and providing favorable niche for recently arose srg-37 deletion. |
format | Online Article Text |
id | pubmed-6764921 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-67649212020-03-23 Selection and gene flow shape niche-associated variation in pheromone response Lee, Daehan Zdraljevic, Stefan Cook, Daniel E. Frézal, Lise Hsu, Jung-Chen Sterken, Mark G. Riksen, Joost A.G. Wang, John Kammenga, Jan E. Braendle, Christian Félix, Marie-Anne Schroeder, Frank C. Andersen, Erik C. Nat Ecol Evol Article From quorum sensing in bacteria to pheromone signaling in social insects, chemical communication mediates interactions among individuals in a local population. In Caenorhabditis elegans, ascaroside pheromones can dictate local population density, in which high levels of pheromones inhibit the reproductive maturation of individuals. Little is known about how natural genetic diversity affects the pheromone responses of individuals from diverse habitats. Here, we show that a niche-associated variation in pheromone receptor genes contributes to natural differences in pheromone responses. We identified putative loss-of-function deletions that impair duplicated pheromone receptor genes (srg-36 and srg-37), which were shown previously to be lost in population-dense laboratory cultures. A common natural deletion in srg-37 arose recently from a single ancestral population that spread throughout the world and underlies reduced pheromone sensitivity across the global C. elegans population. We found that many local populations harbor individuals with wild-type or a deletion allele of srg-37, suggesting that balancing selection has maintained the recent variation in this pheromone receptor gene. The two srg-37 genotypes are associated with niche diversity underlying boom-and-bust population dynamics. We hypothesize that human activities likely contributed to the gene flow and balancing selection of srg-37 variation through facilitating migration of species and providing favorable niche for recently arose srg-37 deletion. 2019-09-23 2019-10 /pmc/articles/PMC6764921/ /pubmed/31548647 http://dx.doi.org/10.1038/s41559-019-0982-3 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Lee, Daehan Zdraljevic, Stefan Cook, Daniel E. Frézal, Lise Hsu, Jung-Chen Sterken, Mark G. Riksen, Joost A.G. Wang, John Kammenga, Jan E. Braendle, Christian Félix, Marie-Anne Schroeder, Frank C. Andersen, Erik C. Selection and gene flow shape niche-associated variation in pheromone response |
title | Selection and gene flow shape niche-associated variation in pheromone response |
title_full | Selection and gene flow shape niche-associated variation in pheromone response |
title_fullStr | Selection and gene flow shape niche-associated variation in pheromone response |
title_full_unstemmed | Selection and gene flow shape niche-associated variation in pheromone response |
title_short | Selection and gene flow shape niche-associated variation in pheromone response |
title_sort | selection and gene flow shape niche-associated variation in pheromone response |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764921/ https://www.ncbi.nlm.nih.gov/pubmed/31548647 http://dx.doi.org/10.1038/s41559-019-0982-3 |
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