{"title":"Bumblebee Pollination and Herbivory Alter Genomic Adaptation of Plants to Soil.","authors":"Tyler Figueira, Léa Frachon, Florian P Schiestl","doi":"10.1111/mec.17811","DOIUrl":null,"url":null,"abstract":"<p><p>Adaptation to environmental heterogeneity is a key driver of between-population genomic differentiation, yet we know very little about how genomic divergence is affected by adaptation to multiple ecological factors. Using an experimental evolution approach, we whole-genome re-sequenced 'fast-cycling' Brassica rapa plants which had evolved during eight generations of selection from different combinations of soil type, aphid herbivore presence or absence, and either bee- or hand pollination. Our results show that bumblebee pollination was the strongest driver of genomic divergence and that the degree of genomic divergence was strongly associated with the number of SNP markers identified in genomic selection scans. Furthermore, we found that the number of SNPs under selection was affected by herbivory in a soil-dependent way. More specifically, aphid herbivory was associated with an increased number of selected SNPs for bee-pollinated plants that evolved in tuff soil but was associated with a decreased number of selected SNPs for bee-pollinated plants that evolved in the more resource-limiting limestone soil. We also found that a higher number of selected SNPs was associated with higher rates of phenotypic evolution for 27 phenotypic traits including morphology and scent. Finally, we found that variation in pleiotropy between treatments was related to both the degree of genomic divergence and the number of SNPs under selection. Our results demonstrate that different soil types promote unique adaptive genomic architectures in response to biotic interactions, thus increasing genomic divergence between plant populations.</p>","PeriodicalId":210,"journal":{"name":"Molecular Ecology","volume":" ","pages":"e17811"},"PeriodicalIF":4.5000,"publicationDate":"2025-06-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Ecology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/mec.17811","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Adaptation to environmental heterogeneity is a key driver of between-population genomic differentiation, yet we know very little about how genomic divergence is affected by adaptation to multiple ecological factors. Using an experimental evolution approach, we whole-genome re-sequenced 'fast-cycling' Brassica rapa plants which had evolved during eight generations of selection from different combinations of soil type, aphid herbivore presence or absence, and either bee- or hand pollination. Our results show that bumblebee pollination was the strongest driver of genomic divergence and that the degree of genomic divergence was strongly associated with the number of SNP markers identified in genomic selection scans. Furthermore, we found that the number of SNPs under selection was affected by herbivory in a soil-dependent way. More specifically, aphid herbivory was associated with an increased number of selected SNPs for bee-pollinated plants that evolved in tuff soil but was associated with a decreased number of selected SNPs for bee-pollinated plants that evolved in the more resource-limiting limestone soil. We also found that a higher number of selected SNPs was associated with higher rates of phenotypic evolution for 27 phenotypic traits including morphology and scent. Finally, we found that variation in pleiotropy between treatments was related to both the degree of genomic divergence and the number of SNPs under selection. Our results demonstrate that different soil types promote unique adaptive genomic architectures in response to biotic interactions, thus increasing genomic divergence between plant populations.
期刊介绍:
Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include:
* population structure and phylogeography
* reproductive strategies
* relatedness and kin selection
* sex allocation
* population genetic theory
* analytical methods development
* conservation genetics
* speciation genetics
* microbial biodiversity
* evolutionary dynamics of QTLs
* ecological interactions
* molecular adaptation and environmental genomics
* impact of genetically modified organisms