Dual‐species origin of an adaptive chemical defense polymorphism

Summary Allopolyploid speciation and chemical defense diversification are two of the most characteristic features of plant evolution; although the former has likely shaped the latter, this has rarely been documented. Here we document allopolyploidy‐mediated chemical defense evolution in the origin o...

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Veröffentlicht in:The New phytologist 2021-11, Vol.232 (3), p.1477-1487
Hauptverfasser: Olsen, Kenneth M., Goad, David M., Wright, Sara J., Dutta, Maya L., Myers, Samantha R., Small, Linda L., Li, Lin‐Feng
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container_end_page 1487
container_issue 3
container_start_page 1477
container_title The New phytologist
container_volume 232
creator Olsen, Kenneth M.
Goad, David M.
Wright, Sara J.
Dutta, Maya L.
Myers, Samantha R.
Small, Linda L.
Li, Lin‐Feng
description Summary Allopolyploid speciation and chemical defense diversification are two of the most characteristic features of plant evolution; although the former has likely shaped the latter, this has rarely been documented. Here we document allopolyploidy‐mediated chemical defense evolution in the origin of cyanogenesis (HCN release upon tissue damage) in white clover (Trifolium repens). We combined linkage mapping of the loci that control cyanogenesis (Ac, controlling production of cyanogenic glucosides; and Li, controlling production of their hydrolyzing enzyme linamarase) with genome sequence comparisons between white clover, a recently evolved allotetraploid, and its diploid progenitors (Trifolium pallescens, Trifolium occidentale). The Ac locus (a three‐gene cluster comprising the cyanogenic glucoside pathway) is derived from T. occidentale; it maps to linkage group 2O (occidentale subgenome) and is orthologous to a highly similar cluster in the T. occidentale reference genome. By contrast, Li maps to linkage group 4P (pallescens subgenome), indicating an origin in the other progenitor species. These results indicate that cyanogenesis evolved in white clover as a product of the interspecific hybridization that created the species. This allopolyploidization‐derived chemical defense, together with subsequent selection on intraspecific cyanogenesis variation, appears to have contributed to white clover’s ecological success as a globally distributed weed species.
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Here we document allopolyploidy‐mediated chemical defense evolution in the origin of cyanogenesis (HCN release upon tissue damage) in white clover (Trifolium repens). We combined linkage mapping of the loci that control cyanogenesis (Ac, controlling production of cyanogenic glucosides; and Li, controlling production of their hydrolyzing enzyme linamarase) with genome sequence comparisons between white clover, a recently evolved allotetraploid, and its diploid progenitors (Trifolium pallescens, Trifolium occidentale). The Ac locus (a three‐gene cluster comprising the cyanogenic glucoside pathway) is derived from T. occidentale; it maps to linkage group 2O (occidentale subgenome) and is orthologous to a highly similar cluster in the T. occidentale reference genome. By contrast, Li maps to linkage group 4P (pallescens subgenome), indicating an origin in the other progenitor species. These results indicate that cyanogenesis evolved in white clover as a product of the interspecific hybridization that created the species. 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Here we document allopolyploidy‐mediated chemical defense evolution in the origin of cyanogenesis (HCN release upon tissue damage) in white clover (Trifolium repens). We combined linkage mapping of the loci that control cyanogenesis (Ac, controlling production of cyanogenic glucosides; and Li, controlling production of their hydrolyzing enzyme linamarase) with genome sequence comparisons between white clover, a recently evolved allotetraploid, and its diploid progenitors (Trifolium pallescens, Trifolium occidentale). The Ac locus (a three‐gene cluster comprising the cyanogenic glucoside pathway) is derived from T. occidentale; it maps to linkage group 2O (occidentale subgenome) and is orthologous to a highly similar cluster in the T. occidentale reference genome. By contrast, Li maps to linkage group 4P (pallescens subgenome), indicating an origin in the other progenitor species. These results indicate that cyanogenesis evolved in white clover as a product of the interspecific hybridization that created the species. This allopolyploidization‐derived chemical defense, together with subsequent selection on intraspecific cyanogenesis variation, appears to have contributed to white clover’s ecological success as a globally distributed weed species.</description><subject>allopolyploid speciation</subject><subject>Allopolyploidy</subject><subject>Chemical defense</subject><subject>Cyanogenesis</subject><subject>cyanogenic glucoside</subject><subject>Diploids</subject><subject>Evolution</subject><subject>Gene mapping</subject><subject>Genomes</subject><subject>Glucosides</subject><subject>Glycosides</subject><subject>Hybridization</subject><subject>Interspecific hybridization</subject><subject>intraspecific polymorphism</subject><subject>Linamarase</subject><subject>Loci</subject><subject>Nucleotide sequence</subject><subject>Plant growth</subject><subject>Polymorphism</subject><subject>Speciation</subject><subject>Species</subject><subject>Trifolium</subject><subject>Trifolium repens</subject><subject>Trifolium repens (Fabaceae)</subject><subject>Weeds</subject><issn>0028-646X</issn><issn>1469-8137</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp10M1KxDAQB_AgCq6rB9-g4EUPXZPmo81R148VFvWg4C0kaeJmaZuabJW9-Qg-o09idD0JzmVg-M0w_AE4RHCCUp12_WKCSkbJFhghwnheIVxugxGERZUzwp52wV6MSwghp6wYgfOLQTaf7x-xN9qZmPngnl2XeZvJLpO17Ffu1WR6YVqnZZPVxpoumqz3zbr1oV-42O6DHSubaA5--xg8Xl0-TGf5_O76Zno2zzVO_-QWKqaoUSUmCluucSFrQqWBFdKEU6K4LrQlnNWmlqXSitVUWalJGpXSYjwGx5u7ffAvg4kr0bqoTdPIzvghioJShitGeJXo0R-69EPo0ndJlRyiilUkqZON0sHHGIwVfXCtDGuBoPhOU6Q0xU-ayZ5u7JtrzPp_KG7vZ5uNLyC8d8Y</recordid><startdate>202111</startdate><enddate>202111</enddate><creator>Olsen, Kenneth M.</creator><creator>Goad, David M.</creator><creator>Wright, Sara J.</creator><creator>Dutta, Maya L.</creator><creator>Myers, Samantha R.</creator><creator>Small, Linda L.</creator><creator>Li, Lin‐Feng</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7SN</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H95</scope><scope>L.G</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8658-6660</orcidid><orcidid>https://orcid.org/0000-0002-8338-3638</orcidid></search><sort><creationdate>202111</creationdate><title>Dual‐species origin of an adaptive chemical defense polymorphism</title><author>Olsen, Kenneth M. ; 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subjects allopolyploid speciation
Allopolyploidy
Chemical defense
Cyanogenesis
cyanogenic glucoside
Diploids
Evolution
Gene mapping
Genomes
Glucosides
Glycosides
Hybridization
Interspecific hybridization
intraspecific polymorphism
Linamarase
Loci
Nucleotide sequence
Plant growth
Polymorphism
Speciation
Species
Trifolium
Trifolium repens
Trifolium repens (Fabaceae)
Weeds
title Dual‐species origin of an adaptive chemical defense polymorphism
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