12
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Targeted re‐sequencing confirms the importance of chemosensory genes in aphid host race differentiation

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Host‐associated races of phytophagous insects provide a model for understanding how adaptation to a new environment can lead to reproductive isolation and speciation, ultimately enabling us to connect barriers to gene flow to adaptive causes of divergence. The pea aphid ( Acyrthosiphon pisum) comprises host races specializing on legume species and provides a unique system for examining the early stages of diversification along a gradient of genetic and associated adaptive divergence. As host choice produces assortative mating, understanding the underlying mechanisms of choice will contribute directly to understanding of speciation. As host choice in the pea aphid is likely mediated by smell and taste, we use capture sequencing and SNP genotyping to test for the role of chemosensory genes in the divergence between eight host plant species across the continuum of differentiation and sampled at multiple locations across western Europe. We show high differentiation of chemosensory loci relative to control loci in a broad set of pea aphid races and localities, using a model‐free approach based on principal component analysis. Olfactory and gustatory receptors form the majority of highly differentiated genes and include loci that were already identified as outliers in a previous study focusing on the three most closely related host races. Consistent indications that chemosensory genes may be good candidates for local adaptation and barriers to gene flow in the pea aphid open the way to further investigations aiming to understand their impact on gene flow and to determine their precise functions in response to host plant metabolites.

          Related collections

          Most cited references82

          • Record: found
          • Abstract: found
          • Article: not found

          Hybridization and speciation.

          Hybridization has many and varied impacts on the process of speciation. Hybridization may slow or reverse differentiation by allowing gene flow and recombination. It may accelerate speciation via adaptive introgression or cause near-instantaneous speciation by allopolyploidization. It may have multiple effects at different stages and in different spatial contexts within a single speciation event. We offer a perspective on the context and evolutionary significance of hybridization during speciation, highlighting issues of current interest and debate. In secondary contact zones, it is uncertain if barriers to gene flow will be strengthened or broken down due to recombination and gene flow. Theory and empirical evidence suggest the latter is more likely, except within and around strongly selected genomic regions. Hybridization may contribute to speciation through the formation of new hybrid taxa, whereas introgression of a few loci may promote adaptive divergence and so facilitate speciation. Gene regulatory networks, epigenetic effects and the evolution of selfish genetic material in the genome suggest that the Dobzhansky-Muller model of hybrid incompatibilities requires a broader interpretation. Finally, although the incidence of reinforcement remains uncertain, this and other interactions in areas of sympatry may have knock-on effects on speciation both within and outside regions of hybridization. © 2013 The Authors. Journal of Evolutionary Biology © 2013 European Society For Evolutionary Biology.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            The genomic basis of adaptive evolution in threespine sticklebacks

            Summary Marine stickleback fish have colonized and adapted to innumerable streams and lakes formed since the last ice age, providing an exceptional opportunity to characterize genomic mechanisms underlying repeated ecological adaptation in nature. Here we develop a high quality reference genome assembly for threespine sticklebacks. By sequencing the genomes of 20 additional individuals from a global set of marine and freshwater populations, we identify a genome-wide set of loci that are consistently associated with marine-freshwater divergence. Our results suggest that reuse of globally-shared standing genetic variation, including chromosomal inversions, plays an important role in repeated evolution of distinct marine and freshwater sticklebacks, and in the maintenance of divergent ecotypes during early stages of reproductive isolation. Both coding and regulatory changes occur in the set of loci underlying marine-freshwater evolution, with regulatory changes likely predominating in this classic example of repeated adaptive evolution in nature.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Widespread parallel evolution in sticklebacks by repeated fixation of Ectodysplasin alleles.

              Major phenotypic changes evolve in parallel in nature by molecular mechanisms that are largely unknown. Here, we use positional cloning methods to identify the major chromosome locus controlling armor plate patterning in wild threespine sticklebacks. Mapping, sequencing, and transgenic studies show that the Ectodysplasin (EDA) signaling pathway plays a key role in evolutionary change in natural populations and that parallel evolution of stickleback low-plated phenotypes at most freshwater locations around the world has occurred by repeated selection of Eda alleles derived from an ancestral low-plated haplotype that first appeared more than two million years ago. Members of this clade of low-plated alleles are present at low frequencies in marine fish, which suggests that standing genetic variation can provide a molecular basis for rapid, parallel evolution of dramatic phenotypic change in nature.
                Bookmark

                Author and article information

                Contributors
                i.eyres@sheffield.ac.uk
                Journal
                Mol Ecol
                Mol. Ecol
                10.1111/(ISSN)1365-294X
                MEC
                Molecular Ecology
                John Wiley and Sons Inc. (Hoboken )
                0962-1083
                1365-294X
                15 September 2016
                January 2017
                : 26
                : 1 , MOLECULAR MECHANISMS OF ADAPTATION AND SPECIATION: INTEGRATING GENOMIC AND MOLECULAR APPROACHES ( doiID: 10.1111/mec.2017.26.issue-1 )
                : 43-58
                Affiliations
                [ 1 ] Department of Animal and Plant Sciences University of Sheffield Western Bank, Alfred Denny Building Sheffield S10 2TN UK
                [ 2 ] Edinburgh Genomics Ashworth Laboratories University of Edinburgh EH9 3JT Edinburgh UK
                [ 3 ] Institut de Génétique, Environnement et Protection des Plantes, UMR 1349 IGEPP, Domaine de la Motte INRA 35653 Le Rheu Cedex France
                [ 4 ] Department of Biology University of York York YO10 5DD UK
                [ 5 ] Institut des Sciences de l'Evolution (UMR 5554 CNRS‐IRD‐CIRAD‐Université de Montpellier) Université de Montpellier cc065, Place Bataillon, Campus Triolet 34095 Montpellier Cedex 05 France
                Author notes
                [*] [* ]Correspondence: Isobel Eyres, Fax: 0114 2220002; E‐mail: i.eyres@ 123456sheffield.ac.uk
                [†]

                Joint last authors.

                Author information
                http://orcid.org/0000-0003-0960-0312
                Article
                MEC13818
                10.1111/mec.13818
                6849616
                27552184
                af355178-48af-4353-8747-db88d8859f3c
                © 2016 The Authors. Molecular Ecology published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 02 February 2016
                : 18 August 2016
                : 22 August 2016
                Page count
                Figures: 4, Tables: 1, Pages: 16, Words: 11495
                Funding
                Funded by: NERC , open-funder-registry 10.13039/501100000270;
                Award ID: NE/H004521/1
                Award ID: NE/J021660/1
                Funded by: Leverhulme Trust , open-funder-registry 10.13039/501100000275;
                Award ID: RPG‐2013‐198
                Categories
                Special Issue: The Molecular Mechanisms of Adaptation and Speciation: Integrating Genomic and Molecular Approaches
                Genomic Adaptation
                Custom metadata
                2.0
                January 2017
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.1 mode:remove_FC converted:12.11.2019

                Ecology
                acyrthosiphon pisum,adaptation,chemosensory genes,genome scan,speciation,targeted resequencing
                Ecology
                acyrthosiphon pisum, adaptation, chemosensory genes, genome scan, speciation, targeted resequencing

                Comments

                Comment on this article