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A miR172 target-deficient AP2-like gene correlates with the double flower phenotype in roses

One of the well-known floral abnormalities in flowering plants is the double-flower phenotype, which corresponds to flowers that develop extra petals, sometimes even containing entire flowers within flowers. Because of their highly priced ornamental value, spontaneous double-flower variants have bee...

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Autores principales: François, Léa, Verdenaud, Marion, Fu, Xiaopeng, Ruleman, Darcy, Dubois, Annick, Vandenbussche, Michiel, Bendahmane, Abdelhafid, Raymond, Olivier, Just, Jérémy, Bendahmane, Mohammed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6110776/
https://www.ncbi.nlm.nih.gov/pubmed/30150746
http://dx.doi.org/10.1038/s41598-018-30918-4
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author François, Léa
Verdenaud, Marion
Fu, Xiaopeng
Ruleman, Darcy
Dubois, Annick
Vandenbussche, Michiel
Bendahmane, Abdelhafid
Raymond, Olivier
Just, Jérémy
Bendahmane, Mohammed
author_facet François, Léa
Verdenaud, Marion
Fu, Xiaopeng
Ruleman, Darcy
Dubois, Annick
Vandenbussche, Michiel
Bendahmane, Abdelhafid
Raymond, Olivier
Just, Jérémy
Bendahmane, Mohammed
author_sort François, Léa
collection PubMed
description One of the well-known floral abnormalities in flowering plants is the double-flower phenotype, which corresponds to flowers that develop extra petals, sometimes even containing entire flowers within flowers. Because of their highly priced ornamental value, spontaneous double-flower variants have been found and selected for in a wide range of ornamental species. Previously, double flower formation in roses was associated with a restriction of AGAMOUS expression domain toward the centre of the meristem, leading to extra petals. Here, we characterized the genomic region containing the mutation associated with the switch from simple to double flowers in the rose. An APETALA2-like gene (RcAP2L), a member of the Target Of EAT-type (TOE-type) subfamily, lies within this interval. In the double flower rose, two alleles of RcAP2L are present, one of which harbours a transposable element inserted into intron 8. This insertion leads to the creation of a miR172 resistant RcAP2L variant. Analyses of the presence of this variant in a set of simple and double flower roses demonstrate a correlation between the presence of this allele and the double flower phenotype. These data suggest a role of this miR172 resistant RcAP2L variant in regulating RcAGAMOUS expression and double flower formation in Rosa sp.
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spelling pubmed-61107762018-08-30 A miR172 target-deficient AP2-like gene correlates with the double flower phenotype in roses François, Léa Verdenaud, Marion Fu, Xiaopeng Ruleman, Darcy Dubois, Annick Vandenbussche, Michiel Bendahmane, Abdelhafid Raymond, Olivier Just, Jérémy Bendahmane, Mohammed Sci Rep Article One of the well-known floral abnormalities in flowering plants is the double-flower phenotype, which corresponds to flowers that develop extra petals, sometimes even containing entire flowers within flowers. Because of their highly priced ornamental value, spontaneous double-flower variants have been found and selected for in a wide range of ornamental species. Previously, double flower formation in roses was associated with a restriction of AGAMOUS expression domain toward the centre of the meristem, leading to extra petals. Here, we characterized the genomic region containing the mutation associated with the switch from simple to double flowers in the rose. An APETALA2-like gene (RcAP2L), a member of the Target Of EAT-type (TOE-type) subfamily, lies within this interval. In the double flower rose, two alleles of RcAP2L are present, one of which harbours a transposable element inserted into intron 8. This insertion leads to the creation of a miR172 resistant RcAP2L variant. Analyses of the presence of this variant in a set of simple and double flower roses demonstrate a correlation between the presence of this allele and the double flower phenotype. These data suggest a role of this miR172 resistant RcAP2L variant in regulating RcAGAMOUS expression and double flower formation in Rosa sp. Nature Publishing Group UK 2018-08-27 /pmc/articles/PMC6110776/ /pubmed/30150746 http://dx.doi.org/10.1038/s41598-018-30918-4 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
François, Léa
Verdenaud, Marion
Fu, Xiaopeng
Ruleman, Darcy
Dubois, Annick
Vandenbussche, Michiel
Bendahmane, Abdelhafid
Raymond, Olivier
Just, Jérémy
Bendahmane, Mohammed
A miR172 target-deficient AP2-like gene correlates with the double flower phenotype in roses
title A miR172 target-deficient AP2-like gene correlates with the double flower phenotype in roses
title_full A miR172 target-deficient AP2-like gene correlates with the double flower phenotype in roses
title_fullStr A miR172 target-deficient AP2-like gene correlates with the double flower phenotype in roses
title_full_unstemmed A miR172 target-deficient AP2-like gene correlates with the double flower phenotype in roses
title_short A miR172 target-deficient AP2-like gene correlates with the double flower phenotype in roses
title_sort mir172 target-deficient ap2-like gene correlates with the double flower phenotype in roses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6110776/
https://www.ncbi.nlm.nih.gov/pubmed/30150746
http://dx.doi.org/10.1038/s41598-018-30918-4
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