The genetic architecture of local adaptation and reproductive isolation in sympatry within the Mimulus guttatus species complex
The genetic architecture of local adaptation has been of central interest to evolutionary biologists since the modern synthesis. In addition to classic theory on the effect size of adaptive mutations by Fisher, Kimura and Orr, recent theory addresses the genetic architecture of local adaptation in t...
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Veröffentlicht in: | Molecular ecology 2017-01, Vol.26 (1), p.208-224 |
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description | The genetic architecture of local adaptation has been of central interest to evolutionary biologists since the modern synthesis. In addition to classic theory on the effect size of adaptive mutations by Fisher, Kimura and Orr, recent theory addresses the genetic architecture of local adaptation in the face of ongoing gene flow. This theory predicts that with substantial gene flow between populations local adaptation should proceed primarily through mutations of large effect or tightly linked clusters of smaller effect loci. In this study, we investigate the genetic architecture of divergence in flowering time, mating system‐related traits, and leaf shape between Mimulus laciniatus and a sympatric population of its close relative M. guttatus. These three traits are probably involved in M. laciniatus’ adaptation to a dry, exposed granite outcrop environment. Flowering time and mating system differences are also reproductive isolating barriers making them ‘magic traits’. Phenotypic hybrids in this population provide evidence of recent gene flow. Using next‐generation sequencing, we generate dense SNP markers across the genome and map quantitative trait loci (QTLs) involved in flowering time, flower size and leaf shape. We find that interspecific divergence in all three traits is due to few QTL of large effect including a highly pleiotropic QTL on chromosome 8. This QTL region contains the pleiotropic candidate gene TCP4 and is involved in ecologically important phenotypes in other Mimulus species. Our results are consistent with theory, indicating that local adaptation and reproductive isolation with gene flow should be due to few loci with large and pleiotropic effects. |
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In addition to classic theory on the effect size of adaptive mutations by Fisher, Kimura and Orr, recent theory addresses the genetic architecture of local adaptation in the face of ongoing gene flow. This theory predicts that with substantial gene flow between populations local adaptation should proceed primarily through mutations of large effect or tightly linked clusters of smaller effect loci. In this study, we investigate the genetic architecture of divergence in flowering time, mating system‐related traits, and leaf shape between Mimulus laciniatus and a sympatric population of its close relative M. guttatus. These three traits are probably involved in M. laciniatus’ adaptation to a dry, exposed granite outcrop environment. Flowering time and mating system differences are also reproductive isolating barriers making them ‘magic traits’. Phenotypic hybrids in this population provide evidence of recent gene flow. Using next‐generation sequencing, we generate dense SNP markers across the genome and map quantitative trait loci (QTLs) involved in flowering time, flower size and leaf shape. We find that interspecific divergence in all three traits is due to few QTL of large effect including a highly pleiotropic QTL on chromosome 8. This QTL region contains the pleiotropic candidate gene TCP4 and is involved in ecologically important phenotypes in other Mimulus species. Our results are consistent with theory, indicating that local adaptation and reproductive isolation with gene flow should be due to few loci with large and pleiotropic effects.</description><identifier>ISSN: 0962-1083</identifier><identifier>EISSN: 1365-294X</identifier><identifier>DOI: 10.1111/mec.13763</identifier><identifier>PMID: 27439150</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Adaptation ; Adaptation, Biological - genetics ; Biological Evolution ; Evolutionary biology ; flowering time ; Flowers & plants ; Flowers - physiology ; Gene Flow ; genetic architecture ; Genetic Pleiotropy ; local adaptation ; mating system ; Mimulus ; Mimulus - genetics ; Mimulus - physiology ; Mimulus guttatus ; Mimulus guttatus species complex ; Mimulus laciniatus ; Plant reproduction ; Polymorphism, Single Nucleotide ; Quantitative Trait Loci ; Reproductive Isolation ; Sympatry</subject><ispartof>Molecular ecology, 2017-01, Vol.26 (1), p.208-224</ispartof><rights>2016 John Wiley & Sons Ltd</rights><rights>2016 John Wiley & Sons Ltd.</rights><rights>Copyright © 2017 John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3863-58ec73fd40817dca93551421d0037eaca5bd07dec53885ddb3933c897069899a3</citedby><cites>FETCH-LOGICAL-c3863-58ec73fd40817dca93551421d0037eaca5bd07dec53885ddb3933c897069899a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fmec.13763$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fmec.13763$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27439150$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ferris, Kathleen G.</creatorcontrib><creatorcontrib>Barnett, Laryssa L.</creatorcontrib><creatorcontrib>Blackman, Benjamin K.</creatorcontrib><creatorcontrib>Willis, John H.</creatorcontrib><title>The genetic architecture of local adaptation and reproductive isolation in sympatry within the Mimulus guttatus species complex</title><title>Molecular ecology</title><addtitle>Mol Ecol</addtitle><description>The genetic architecture of local adaptation has been of central interest to evolutionary biologists since the modern synthesis. In addition to classic theory on the effect size of adaptive mutations by Fisher, Kimura and Orr, recent theory addresses the genetic architecture of local adaptation in the face of ongoing gene flow. This theory predicts that with substantial gene flow between populations local adaptation should proceed primarily through mutations of large effect or tightly linked clusters of smaller effect loci. In this study, we investigate the genetic architecture of divergence in flowering time, mating system‐related traits, and leaf shape between Mimulus laciniatus and a sympatric population of its close relative M. guttatus. These three traits are probably involved in M. laciniatus’ adaptation to a dry, exposed granite outcrop environment. Flowering time and mating system differences are also reproductive isolating barriers making them ‘magic traits’. Phenotypic hybrids in this population provide evidence of recent gene flow. Using next‐generation sequencing, we generate dense SNP markers across the genome and map quantitative trait loci (QTLs) involved in flowering time, flower size and leaf shape. We find that interspecific divergence in all three traits is due to few QTL of large effect including a highly pleiotropic QTL on chromosome 8. This QTL region contains the pleiotropic candidate gene TCP4 and is involved in ecologically important phenotypes in other Mimulus species. Our results are consistent with theory, indicating that local adaptation and reproductive isolation with gene flow should be due to few loci with large and pleiotropic effects.</description><subject>Adaptation</subject><subject>Adaptation, Biological - genetics</subject><subject>Biological Evolution</subject><subject>Evolutionary biology</subject><subject>flowering time</subject><subject>Flowers & plants</subject><subject>Flowers - physiology</subject><subject>Gene Flow</subject><subject>genetic architecture</subject><subject>Genetic Pleiotropy</subject><subject>local adaptation</subject><subject>mating system</subject><subject>Mimulus</subject><subject>Mimulus - genetics</subject><subject>Mimulus - physiology</subject><subject>Mimulus guttatus</subject><subject>Mimulus guttatus species complex</subject><subject>Mimulus laciniatus</subject><subject>Plant reproduction</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Quantitative Trait Loci</subject><subject>Reproductive Isolation</subject><subject>Sympatry</subject><issn>0962-1083</issn><issn>1365-294X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU2LFDEQhoMo7rh68A9IwIseejfp6nSSowzrB-ziZQVvTSap2cmS_jAfrnPyrxvt1YMgBopUkYeHCi8hzzk74_Wcj2jPOMgeHpANh140re4-PyQbpvu24UzBCXmS0i1jHFohHpOTVnaguWAb8v36gPQGJ8zeUhPtwWe0uUSk856G2ZpAjTNLNtnPEzWToxGXOLtis_-K1Kc5rE9-ouk4LibHI73z-VDnXNVXfiyhJHpTcnXUJi1oPSZq53EJ-O0pebQ3IeGz-_uUfHp7cb1931x-fPdh--aysaB6aIRCK2HvOqa4dNZoEIJ3LXeMgURjjdg5Jh1aAUoJ53agAazSkvVaaW3glLxavXX5LwVTHkafLIZgJpxLGrjqFTDgtf6Ptr1spe54RV_-hd7OJU71I5USumvrFl2lXq-UjXNKEffDEv1o4nHgbPgZ4FADHH4FWNkX98ayG9H9IX8nVoHzFbjzAY__Ng1XF9tV-QNV4qXd</recordid><startdate>201701</startdate><enddate>201701</enddate><creator>Ferris, Kathleen G.</creator><creator>Barnett, Laryssa L.</creator><creator>Blackman, Benjamin K.</creator><creator>Willis, John H.</creator><general>Blackwell Publishing Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SN</scope><scope>7SS</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201701</creationdate><title>The genetic architecture of local adaptation and reproductive isolation in sympatry within the Mimulus guttatus species complex</title><author>Ferris, Kathleen G. ; Barnett, Laryssa L. ; Blackman, Benjamin K. ; Willis, John H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3863-58ec73fd40817dca93551421d0037eaca5bd07dec53885ddb3933c897069899a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adaptation</topic><topic>Adaptation, Biological - genetics</topic><topic>Biological Evolution</topic><topic>Evolutionary biology</topic><topic>flowering time</topic><topic>Flowers & plants</topic><topic>Flowers - physiology</topic><topic>Gene Flow</topic><topic>genetic architecture</topic><topic>Genetic Pleiotropy</topic><topic>local adaptation</topic><topic>mating system</topic><topic>Mimulus</topic><topic>Mimulus - genetics</topic><topic>Mimulus - physiology</topic><topic>Mimulus guttatus</topic><topic>Mimulus guttatus species complex</topic><topic>Mimulus laciniatus</topic><topic>Plant reproduction</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Quantitative Trait Loci</topic><topic>Reproductive Isolation</topic><topic>Sympatry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ferris, Kathleen G.</creatorcontrib><creatorcontrib>Barnett, Laryssa L.</creatorcontrib><creatorcontrib>Blackman, Benjamin K.</creatorcontrib><creatorcontrib>Willis, John H.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular ecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ferris, Kathleen G.</au><au>Barnett, Laryssa L.</au><au>Blackman, Benjamin K.</au><au>Willis, John H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The genetic architecture of local adaptation and reproductive isolation in sympatry within the Mimulus guttatus species complex</atitle><jtitle>Molecular ecology</jtitle><addtitle>Mol Ecol</addtitle><date>2017-01</date><risdate>2017</risdate><volume>26</volume><issue>1</issue><spage>208</spage><epage>224</epage><pages>208-224</pages><issn>0962-1083</issn><eissn>1365-294X</eissn><abstract>The genetic architecture of local adaptation has been of central interest to evolutionary biologists since the modern synthesis. In addition to classic theory on the effect size of adaptive mutations by Fisher, Kimura and Orr, recent theory addresses the genetic architecture of local adaptation in the face of ongoing gene flow. This theory predicts that with substantial gene flow between populations local adaptation should proceed primarily through mutations of large effect or tightly linked clusters of smaller effect loci. In this study, we investigate the genetic architecture of divergence in flowering time, mating system‐related traits, and leaf shape between Mimulus laciniatus and a sympatric population of its close relative M. guttatus. These three traits are probably involved in M. laciniatus’ adaptation to a dry, exposed granite outcrop environment. Flowering time and mating system differences are also reproductive isolating barriers making them ‘magic traits’. Phenotypic hybrids in this population provide evidence of recent gene flow. Using next‐generation sequencing, we generate dense SNP markers across the genome and map quantitative trait loci (QTLs) involved in flowering time, flower size and leaf shape. We find that interspecific divergence in all three traits is due to few QTL of large effect including a highly pleiotropic QTL on chromosome 8. This QTL region contains the pleiotropic candidate gene TCP4 and is involved in ecologically important phenotypes in other Mimulus species. Our results are consistent with theory, indicating that local adaptation and reproductive isolation with gene flow should be due to few loci with large and pleiotropic effects.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>27439150</pmid><doi>10.1111/mec.13763</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adaptation Adaptation, Biological - genetics Biological Evolution Evolutionary biology flowering time Flowers & plants Flowers - physiology Gene Flow genetic architecture Genetic Pleiotropy local adaptation mating system Mimulus Mimulus - genetics Mimulus - physiology Mimulus guttatus Mimulus guttatus species complex Mimulus laciniatus Plant reproduction Polymorphism, Single Nucleotide Quantitative Trait Loci Reproductive Isolation Sympatry |
title | The genetic architecture of local adaptation and reproductive isolation in sympatry within the Mimulus guttatus species complex |
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