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Presence versus absence of CYP734A50 underlies the style-length dimorphism in primroses

Heterostyly is a wide-spread floral adaptation to promote outbreeding, yet its genetic basis and evolutionary origin remain poorly understood. In Primula (primroses), heterostyly is controlled by the S-locus supergene that determines the reciprocal arrangement of reproductive organs and incompatibil...

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Autores principales: Huu, Cuong Nguyen, Kappel, Christian, Keller, Barbara, Sicard, Adrien, Takebayashi, Yumiko, Breuninger, Holger, Nowak, Michael D, Bäurle, Isabel, Himmelbach, Axel, Burkart, Michael, Ebbing-Lohaus, Thomas, Sakakibara, Hitoshi, Altschmied, Lothar, Conti, Elena, Lenhard, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5012859/
https://www.ncbi.nlm.nih.gov/pubmed/27596932
http://dx.doi.org/10.7554/eLife.17956
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author Huu, Cuong Nguyen
Kappel, Christian
Keller, Barbara
Sicard, Adrien
Takebayashi, Yumiko
Breuninger, Holger
Nowak, Michael D
Bäurle, Isabel
Himmelbach, Axel
Burkart, Michael
Ebbing-Lohaus, Thomas
Sakakibara, Hitoshi
Altschmied, Lothar
Conti, Elena
Lenhard, Michael
author_facet Huu, Cuong Nguyen
Kappel, Christian
Keller, Barbara
Sicard, Adrien
Takebayashi, Yumiko
Breuninger, Holger
Nowak, Michael D
Bäurle, Isabel
Himmelbach, Axel
Burkart, Michael
Ebbing-Lohaus, Thomas
Sakakibara, Hitoshi
Altschmied, Lothar
Conti, Elena
Lenhard, Michael
author_sort Huu, Cuong Nguyen
collection PubMed
description Heterostyly is a wide-spread floral adaptation to promote outbreeding, yet its genetic basis and evolutionary origin remain poorly understood. In Primula (primroses), heterostyly is controlled by the S-locus supergene that determines the reciprocal arrangement of reproductive organs and incompatibility between the two morphs. However, the identities of the component genes remain unknown. Here, we identify the Primula CYP734A50 gene, encoding a putative brassinosteroid-degrading enzyme, as the G locus that determines the style-length dimorphism. CYP734A50 is only present on the short-styled S-morph haplotype, it is specifically expressed in S-morph styles, and its loss or inactivation leads to long styles. The gene arose by a duplication specific to the Primulaceae lineage and shows an accelerated rate of molecular evolution. Thus, our results provide a mechanistic explanation for the Primula style-length dimorphism and begin to shed light on the evolution of the S-locus as a prime model for a complex plant supergene. DOI: http://dx.doi.org/10.7554/eLife.17956.001
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spelling pubmed-50128592016-09-07 Presence versus absence of CYP734A50 underlies the style-length dimorphism in primroses Huu, Cuong Nguyen Kappel, Christian Keller, Barbara Sicard, Adrien Takebayashi, Yumiko Breuninger, Holger Nowak, Michael D Bäurle, Isabel Himmelbach, Axel Burkart, Michael Ebbing-Lohaus, Thomas Sakakibara, Hitoshi Altschmied, Lothar Conti, Elena Lenhard, Michael eLife Genes and Chromosomes Heterostyly is a wide-spread floral adaptation to promote outbreeding, yet its genetic basis and evolutionary origin remain poorly understood. In Primula (primroses), heterostyly is controlled by the S-locus supergene that determines the reciprocal arrangement of reproductive organs and incompatibility between the two morphs. However, the identities of the component genes remain unknown. Here, we identify the Primula CYP734A50 gene, encoding a putative brassinosteroid-degrading enzyme, as the G locus that determines the style-length dimorphism. CYP734A50 is only present on the short-styled S-morph haplotype, it is specifically expressed in S-morph styles, and its loss or inactivation leads to long styles. The gene arose by a duplication specific to the Primulaceae lineage and shows an accelerated rate of molecular evolution. Thus, our results provide a mechanistic explanation for the Primula style-length dimorphism and begin to shed light on the evolution of the S-locus as a prime model for a complex plant supergene. DOI: http://dx.doi.org/10.7554/eLife.17956.001 eLife Sciences Publications, Ltd 2016-09-06 /pmc/articles/PMC5012859/ /pubmed/27596932 http://dx.doi.org/10.7554/eLife.17956 Text en © 2016, Huu et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Genes and Chromosomes
Huu, Cuong Nguyen
Kappel, Christian
Keller, Barbara
Sicard, Adrien
Takebayashi, Yumiko
Breuninger, Holger
Nowak, Michael D
Bäurle, Isabel
Himmelbach, Axel
Burkart, Michael
Ebbing-Lohaus, Thomas
Sakakibara, Hitoshi
Altschmied, Lothar
Conti, Elena
Lenhard, Michael
Presence versus absence of CYP734A50 underlies the style-length dimorphism in primroses
title Presence versus absence of CYP734A50 underlies the style-length dimorphism in primroses
title_full Presence versus absence of CYP734A50 underlies the style-length dimorphism in primroses
title_fullStr Presence versus absence of CYP734A50 underlies the style-length dimorphism in primroses
title_full_unstemmed Presence versus absence of CYP734A50 underlies the style-length dimorphism in primroses
title_short Presence versus absence of CYP734A50 underlies the style-length dimorphism in primroses
title_sort presence versus absence of cyp734a50 underlies the style-length dimorphism in primroses
topic Genes and Chromosomes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5012859/
https://www.ncbi.nlm.nih.gov/pubmed/27596932
http://dx.doi.org/10.7554/eLife.17956
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