Intercontinental genomic parallelism in multiple three-spined stickleback adaptive radiations
Parallelism, the evolution of similar traits in populations diversifying in similar conditions, provides strong evidence of adaptation by natural selection. Many studies of parallelism focus on comparisons of different ecotypes or contrasting environments, defined a priori, which could upwardly bias...
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Veröffentlicht in: | Nature ecology & evolution 2021-02, Vol.5 (2), p.251-261 |
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creator | Magalhaes, Isabel S. Whiting, James R. D’Agostino, Daniele Hohenlohe, Paul A. Mahmud, Muayad Bell, Michael A. Skúlason, Skúli MacColl, Andrew D. C. |
description | Parallelism, the evolution of similar traits in populations diversifying in similar conditions, provides strong evidence of adaptation by natural selection. Many studies of parallelism focus on comparisons of different ecotypes or contrasting environments, defined a priori, which could upwardly bias the apparent prevalence of parallelism. Here, we estimated genomic parallelism associated with components of environmental and phenotypic variation at an intercontinental scale across four freshwater adaptive radiations (Alaska, British Columbia, Iceland and Scotland) of the three-spined stickleback (
Gasterosteus aculeatus
). We combined large-scale biological sampling and phenotyping with restriction site associated DNA sequencing (RAD-Seq) data from 73 freshwater lake populations and four marine ones (1,380 fish) to associate genome-wide allele frequencies with continuous distributions of environmental and phenotypic variation. Our three main findings demonstrate that (1) quantitative variation in phenotypes and environments can predict genomic parallelism; (2) genomic parallelism at the early stages of adaptive radiations, even at large geographic scales, is founded on standing variation; and (3) similar environments are a better predictor of genome-wide parallelism than similar phenotypes. Overall, this study validates the importance and predictive power of major phenotypic and environmental factors likely to influence the emergence of common patterns of genomic divergence, providing a clearer picture than analyses of dichotomous phenotypes and environments.
Using data from four adaptive radiations of the three-spined stickleback, the authors examine levels of genomic parallelism and the phenotypic and environmental factors that predict parallelism. |
doi_str_mv | 10.1038/s41559-020-01341-8 |
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Gasterosteus aculeatus
). We combined large-scale biological sampling and phenotyping with restriction site associated DNA sequencing (RAD-Seq) data from 73 freshwater lake populations and four marine ones (1,380 fish) to associate genome-wide allele frequencies with continuous distributions of environmental and phenotypic variation. Our three main findings demonstrate that (1) quantitative variation in phenotypes and environments can predict genomic parallelism; (2) genomic parallelism at the early stages of adaptive radiations, even at large geographic scales, is founded on standing variation; and (3) similar environments are a better predictor of genome-wide parallelism than similar phenotypes. Overall, this study validates the importance and predictive power of major phenotypic and environmental factors likely to influence the emergence of common patterns of genomic divergence, providing a clearer picture than analyses of dichotomous phenotypes and environments.
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Gasterosteus aculeatus
). We combined large-scale biological sampling and phenotyping with restriction site associated DNA sequencing (RAD-Seq) data from 73 freshwater lake populations and four marine ones (1,380 fish) to associate genome-wide allele frequencies with continuous distributions of environmental and phenotypic variation. Our three main findings demonstrate that (1) quantitative variation in phenotypes and environments can predict genomic parallelism; (2) genomic parallelism at the early stages of adaptive radiations, even at large geographic scales, is founded on standing variation; and (3) similar environments are a better predictor of genome-wide parallelism than similar phenotypes. Overall, this study validates the importance and predictive power of major phenotypic and environmental factors likely to influence the emergence of common patterns of genomic divergence, providing a clearer picture than analyses of dichotomous phenotypes and environments.
Using data from four adaptive radiations of the three-spined stickleback, the authors examine levels of genomic parallelism and the phenotypic and environmental factors that predict parallelism.</description><subject>45</subject><subject>45/23</subject><subject>631/158</subject><subject>631/158/2452</subject><subject>631/158/2459</subject><subject>631/158/670</subject><subject>631/158/857</subject><subject>Animal behavior</subject><subject>Animals</subject><subject>Biological and Physical Anthropology</subject><subject>Biological sampling</subject><subject>Biomedical and Life Sciences</subject><subject>British Columbia</subject><subject>Deoxyribonucleic acid</subject><subject>Divergence</subject><subject>DNA</subject><subject>DNA sequencing</subject><subject>Ecology</subject><subject>Ecotypes</subject><subject>Environmental factors</subject><subject>Evolutionary Biology</subject><subject>Freshwater lakes</subject><subject>Gene frequency</subject><subject>Genetics, Population</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Life Sciences</subject><subject>Natural selection</subject><subject>Paleontology</subject><subject>Phenotypes</subject><subject>Phenotypic variations</subject><subject>Phenotyping</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Population genetics</subject><subject>Populations</subject><subject>Radiation</subject><subject>Scotland</subject><subject>Smegmamorpha - genetics</subject><subject>Zoology</subject><issn>2397-334X</issn><issn>2397-334X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kUFrFjEQhhdRbKn9Ax5kwYuX1WSTTXYvgpRqCwUvCl4kzCaTr2mzyZpkC_570361Vg-eJjDPvDNv3qZ5SclbStj4LnM6DFNHetIRyjjtxifNYc8m2THGvz199D5ojnO-IoRQKYdJiOfNAWP9IEcqD5vv56Fg0jEUFzAU8O0OQ1ycbldI4D16l5fWhXbZfHGrx7ZcJsQur5U3bS5OX3ucQV-3YGAt7gbbBMZBcTHkF80zCz7j8X09ar5-PP1yctZdfP50fvLhotNc8tJxtNzMhmptBuSgpeGjZVKwmbDeWgOzAZjFTLiBaeQWBm3FPKEVxghglh017_e66zYvaHR1Uo9Xa3ILpJ8qglN_d4K7VLt4o-Q4jD1jVeDNvUCKPzbMRS0ua_QeAsYtq54LQZigPa_o63_Qq7ilUO1VahzqzzJyK9jvKZ1izgntwzGUqNsA1T5AVQNUdwGqsQ69emzjYeR3XBVgeyDXVthh-rP7P7K_AH0rqxM</recordid><startdate>20210201</startdate><enddate>20210201</enddate><creator>Magalhaes, Isabel S.</creator><creator>Whiting, James R.</creator><creator>D’Agostino, Daniele</creator><creator>Hohenlohe, Paul A.</creator><creator>Mahmud, Muayad</creator><creator>Bell, Michael A.</creator><creator>Skúlason, Skúli</creator><creator>MacColl, Andrew D. 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C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intercontinental genomic parallelism in multiple three-spined stickleback adaptive radiations</atitle><jtitle>Nature ecology & evolution</jtitle><stitle>Nat Ecol Evol</stitle><addtitle>Nat Ecol Evol</addtitle><date>2021-02-01</date><risdate>2021</risdate><volume>5</volume><issue>2</issue><spage>251</spage><epage>261</epage><pages>251-261</pages><issn>2397-334X</issn><eissn>2397-334X</eissn><abstract>Parallelism, the evolution of similar traits in populations diversifying in similar conditions, provides strong evidence of adaptation by natural selection. Many studies of parallelism focus on comparisons of different ecotypes or contrasting environments, defined a priori, which could upwardly bias the apparent prevalence of parallelism. Here, we estimated genomic parallelism associated with components of environmental and phenotypic variation at an intercontinental scale across four freshwater adaptive radiations (Alaska, British Columbia, Iceland and Scotland) of the three-spined stickleback (
Gasterosteus aculeatus
). We combined large-scale biological sampling and phenotyping with restriction site associated DNA sequencing (RAD-Seq) data from 73 freshwater lake populations and four marine ones (1,380 fish) to associate genome-wide allele frequencies with continuous distributions of environmental and phenotypic variation. Our three main findings demonstrate that (1) quantitative variation in phenotypes and environments can predict genomic parallelism; (2) genomic parallelism at the early stages of adaptive radiations, even at large geographic scales, is founded on standing variation; and (3) similar environments are a better predictor of genome-wide parallelism than similar phenotypes. Overall, this study validates the importance and predictive power of major phenotypic and environmental factors likely to influence the emergence of common patterns of genomic divergence, providing a clearer picture than analyses of dichotomous phenotypes and environments.
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subjects | 45 45/23 631/158 631/158/2452 631/158/2459 631/158/670 631/158/857 Animal behavior Animals Biological and Physical Anthropology Biological sampling Biomedical and Life Sciences British Columbia Deoxyribonucleic acid Divergence DNA DNA sequencing Ecology Ecotypes Environmental factors Evolutionary Biology Freshwater lakes Gene frequency Genetics, Population Genomes Genomics Life Sciences Natural selection Paleontology Phenotypes Phenotypic variations Phenotyping Polymorphism, Single Nucleotide Population genetics Populations Radiation Scotland Smegmamorpha - genetics Zoology |
title | Intercontinental genomic parallelism in multiple three-spined stickleback adaptive radiations |
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