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      Clines on the seashore: The genomic architecture underlying rapid divergence in the face of gene flow

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          Abstract

          Adaptive divergence and speciation may happen despite opposition by gene flow. Identifying the genomic basis underlying divergence with gene flow is a major task in evolutionary genomics. Most approaches (e.g., outlier scans) focus on genomic regions of high differentiation. However, not all genomic architectures potentially underlying divergence are expected to show extreme differentiation. Here, we develop an approach that combines hybrid zone analysis (i.e., focuses on spatial patterns of allele frequency change) with system‐specific simulations to identify loci inconsistent with neutral evolution. We apply this to a genome‐wide SNP set from an ideally suited study organism, the intertidal snail Littorina saxatilis, which shows primary divergence between ecotypes associated with different shore habitats. We detect many SNPs with clinal patterns, most of which are consistent with neutrality. Among non‐neutral SNPs, most are located within three large putative inversions differentiating ecotypes. Many non‐neutral SNPs show relatively low levels of differentiation. We discuss potential reasons for this pattern, including loose linkage to selected variants, polygenic adaptation and a component of balancing selection within populations (which may be expected for inversions). Our work is in line with theory predicting a role for inversions in divergence, and emphasizes that genomic regions contributing to divergence may not always be accessible with methods purely based on allele frequency differences. These conclusions call for approaches that take spatial patterns of allele frequency change into account in other systems.

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          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.
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            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.
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              Gene flow and the limits to natural selection

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                Author and article information

                Contributors
                anja.westram@ist.ac.at
                Journal
                Evol Lett
                Evol Lett
                10.1002/(ISSN)2056-3744
                EVL3
                Evolution Letters
                John Wiley and Sons Inc. (Hoboken )
                2056-3744
                07 August 2018
                August 2018
                : 2
                : 4 ( doiID: 10.1002/evl3.2018.2.issue-4 )
                : 297-309
                Affiliations
                [ 1 ] Department of Animal and Plant Sciences University of Sheffield UK
                [ 2 ] Current address: IST Austria Am Campus 1 3400 Klosterneuburg Austria
                [ 3 ] Department of Marine Sciences University of Gothenburg 40530 Gothenburg Sweden
                [ 4 ] Department of Physics University of Gothenburg 41296 Gothenburg Sweden
                [ 5 ] Department of Marine Sciences ‐ Tjärnö University of Gothenburg 45296 Strömstad Sweden
                [ 6 ] CEES (Centre for Ecological and Evolutionary Synthesis) University of Oslo Oslo 0316 Norway
                [ 7 ] Department of Chemistry and Molecular Biology University of Gothenburg 40530 Gothenburg Sweden
                Article
                EVL374
                10.1002/evl3.74
                6121805
                30283683
                123cf25f-ad30-4a92-acbb-d6af867adb38
                © 2018 The Author(s). Evolution Letters published by Wiley Periodicals, Inc. on behalf of Society for the Study of Evolution (SSE) and European Society for Evolutionary Biology (ESEB).

                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
                : 08 March 2018
                : 14 June 2018
                : 29 June 2018
                Page count
                Figures: 4, Tables: 0, Pages: 13, Words: 9260
                Funding
                Funded by: Vetenskapsrådet
                Funded by: Svenska Forskningsrådet Formas
                Funded by: Natural Environment Research Council
                Funded by: H2020 European Research Council
                Funded by: Adlerbert Research Foundation
                Categories
                Letter
                Letters
                Custom metadata
                2.0
                evl374
                August 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.4.7.1 mode:remove_FC converted:04.09.2018

                clines,hybrid zones,inversions,local adaptation,molluscs,speciation

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