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On the origin of the widespread self-compatible allotetraploid Capsella bursa-pastoris (Brassicaceae)

Polyploidy, or whole-genome duplication, is a common speciation mechanism in plants. An important barrier to polyploid establishment is a lack of compatible mates. Because self-compatibility alleviates this problem, it has long been hypothesized that there should be an association between polyploidy...

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Autores principales: Bachmann, Jörg A., Tedder, Andrew, Fracassetti, Marco, Steige, Kim A., Lafon-Placette, Clément, Köhler, Claudia, Slotte, Tanja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8249383/
https://www.ncbi.nlm.nih.gov/pubmed/33875831
http://dx.doi.org/10.1038/s41437-021-00434-9
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author Bachmann, Jörg A.
Tedder, Andrew
Fracassetti, Marco
Steige, Kim A.
Lafon-Placette, Clément
Köhler, Claudia
Slotte, Tanja
author_facet Bachmann, Jörg A.
Tedder, Andrew
Fracassetti, Marco
Steige, Kim A.
Lafon-Placette, Clément
Köhler, Claudia
Slotte, Tanja
author_sort Bachmann, Jörg A.
collection PubMed
description Polyploidy, or whole-genome duplication, is a common speciation mechanism in plants. An important barrier to polyploid establishment is a lack of compatible mates. Because self-compatibility alleviates this problem, it has long been hypothesized that there should be an association between polyploidy and self-compatibility (SC), but empirical support for this prediction is mixed. Here, we investigate whether the molecular makeup of the Brassicaceae self-incompatibility (SI) system, and specifically dominance relationships among S-haplotypes mediated by small RNAs, could facilitate loss of SI in allopolyploid crucifers. We focus on the allotetraploid species Capsella bursa-pastoris, which formed ~300 kya by hybridization and whole-genome duplication involving progenitors from the lineages of Capsella orientalis and Capsella grandiflora. We conduct targeted long-read sequencing to assemble and analyze eight full-length S-locus haplotypes, representing both homeologous subgenomes of C. bursa-pastoris. We further analyze small RNA (sRNA) sequencing data from flower buds to identify candidate dominance modifiers. We find that C. orientalis-derived S-haplotypes of C. bursa-pastoris harbor truncated versions of the male SI specificity gene SCR and express a conserved sRNA-based candidate dominance modifier with a target in the C. grandiflora-derived S-haplotype. These results suggest that pollen-level dominance may have facilitated loss of SI in C. bursa-pastoris. Finally, we demonstrate that spontaneous somatic tetraploidization after a wide cross between C. orientalis and C. grandiflora can result in production of self-compatible tetraploid offspring. We discuss the implications of this finding on the mode of formation of this widespread weed.
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spelling pubmed-82493832021-07-20 On the origin of the widespread self-compatible allotetraploid Capsella bursa-pastoris (Brassicaceae) Bachmann, Jörg A. Tedder, Andrew Fracassetti, Marco Steige, Kim A. Lafon-Placette, Clément Köhler, Claudia Slotte, Tanja Heredity (Edinb) Article Polyploidy, or whole-genome duplication, is a common speciation mechanism in plants. An important barrier to polyploid establishment is a lack of compatible mates. Because self-compatibility alleviates this problem, it has long been hypothesized that there should be an association between polyploidy and self-compatibility (SC), but empirical support for this prediction is mixed. Here, we investigate whether the molecular makeup of the Brassicaceae self-incompatibility (SI) system, and specifically dominance relationships among S-haplotypes mediated by small RNAs, could facilitate loss of SI in allopolyploid crucifers. We focus on the allotetraploid species Capsella bursa-pastoris, which formed ~300 kya by hybridization and whole-genome duplication involving progenitors from the lineages of Capsella orientalis and Capsella grandiflora. We conduct targeted long-read sequencing to assemble and analyze eight full-length S-locus haplotypes, representing both homeologous subgenomes of C. bursa-pastoris. We further analyze small RNA (sRNA) sequencing data from flower buds to identify candidate dominance modifiers. We find that C. orientalis-derived S-haplotypes of C. bursa-pastoris harbor truncated versions of the male SI specificity gene SCR and express a conserved sRNA-based candidate dominance modifier with a target in the C. grandiflora-derived S-haplotype. These results suggest that pollen-level dominance may have facilitated loss of SI in C. bursa-pastoris. Finally, we demonstrate that spontaneous somatic tetraploidization after a wide cross between C. orientalis and C. grandiflora can result in production of self-compatible tetraploid offspring. We discuss the implications of this finding on the mode of formation of this widespread weed. Springer International Publishing 2021-04-19 2021-07 /pmc/articles/PMC8249383/ /pubmed/33875831 http://dx.doi.org/10.1038/s41437-021-00434-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Bachmann, Jörg A.
Tedder, Andrew
Fracassetti, Marco
Steige, Kim A.
Lafon-Placette, Clément
Köhler, Claudia
Slotte, Tanja
On the origin of the widespread self-compatible allotetraploid Capsella bursa-pastoris (Brassicaceae)
title On the origin of the widespread self-compatible allotetraploid Capsella bursa-pastoris (Brassicaceae)
title_full On the origin of the widespread self-compatible allotetraploid Capsella bursa-pastoris (Brassicaceae)
title_fullStr On the origin of the widespread self-compatible allotetraploid Capsella bursa-pastoris (Brassicaceae)
title_full_unstemmed On the origin of the widespread self-compatible allotetraploid Capsella bursa-pastoris (Brassicaceae)
title_short On the origin of the widespread self-compatible allotetraploid Capsella bursa-pastoris (Brassicaceae)
title_sort on the origin of the widespread self-compatible allotetraploid capsella bursa-pastoris (brassicaceae)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8249383/
https://www.ncbi.nlm.nih.gov/pubmed/33875831
http://dx.doi.org/10.1038/s41437-021-00434-9
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