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Bypassing reproductive barriers in hybrid seeds using chemically induced epimutagenesis

The triploid block, which prevents interploidy hybridizations in flowering plants, is characterized by a failure in endosperm development, arrest in embryogenesis, and seed collapse. Many genetic components of triploid seed lethality have been successfully identified in the model plant Arabidopsis t...

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Autores principales: Huc, Jonathan, Dziasek, Katarzyna, Pachamuthu, Kannan, Woh, Tristan, Köhler, Claudia, Borges, Filipe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894923/
https://www.ncbi.nlm.nih.gov/pubmed/34792584
http://dx.doi.org/10.1093/plcell/koab284
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author Huc, Jonathan
Dziasek, Katarzyna
Pachamuthu, Kannan
Woh, Tristan
Köhler, Claudia
Borges, Filipe
author_facet Huc, Jonathan
Dziasek, Katarzyna
Pachamuthu, Kannan
Woh, Tristan
Köhler, Claudia
Borges, Filipe
author_sort Huc, Jonathan
collection PubMed
description The triploid block, which prevents interploidy hybridizations in flowering plants, is characterized by a failure in endosperm development, arrest in embryogenesis, and seed collapse. Many genetic components of triploid seed lethality have been successfully identified in the model plant Arabidopsis thaliana, most notably the paternally expressed genes (PEGs), which are upregulated in tetraploid endosperm with paternal excess. Previous studies have shown that the paternal epigenome is a key determinant of the triploid block response, as the loss of DNA methylation in diploid pollen suppresses the triploid block almost completely. Here, we demonstrate that triploid seed collapse is bypassed in Arabidopsis plants treated with the DNA methyltransferase inhibitor 5-Azacytidine during seed germination and early growth. We identified strong suppressor lines showing stable transgenerational inheritance of hypomethylation in the CG context, as well as normalized expression of PEGs in triploid seeds. Importantly, differentially methylated loci segregate in the progeny of “epimutagenized” plants, which may allow epialleles involved in the triploid block response to be identified in future studies. Finally, we demonstrate that chemically induced epimutagenesis facilitates hybridization between different Capsella species, thus potentially emerging as a strategy for producing triploids and interspecific hybrids with high agronomic interest.
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spelling pubmed-88949232022-03-07 Bypassing reproductive barriers in hybrid seeds using chemically induced epimutagenesis Huc, Jonathan Dziasek, Katarzyna Pachamuthu, Kannan Woh, Tristan Köhler, Claudia Borges, Filipe Plant Cell Research Articles The triploid block, which prevents interploidy hybridizations in flowering plants, is characterized by a failure in endosperm development, arrest in embryogenesis, and seed collapse. Many genetic components of triploid seed lethality have been successfully identified in the model plant Arabidopsis thaliana, most notably the paternally expressed genes (PEGs), which are upregulated in tetraploid endosperm with paternal excess. Previous studies have shown that the paternal epigenome is a key determinant of the triploid block response, as the loss of DNA methylation in diploid pollen suppresses the triploid block almost completely. Here, we demonstrate that triploid seed collapse is bypassed in Arabidopsis plants treated with the DNA methyltransferase inhibitor 5-Azacytidine during seed germination and early growth. We identified strong suppressor lines showing stable transgenerational inheritance of hypomethylation in the CG context, as well as normalized expression of PEGs in triploid seeds. Importantly, differentially methylated loci segregate in the progeny of “epimutagenized” plants, which may allow epialleles involved in the triploid block response to be identified in future studies. Finally, we demonstrate that chemically induced epimutagenesis facilitates hybridization between different Capsella species, thus potentially emerging as a strategy for producing triploids and interspecific hybrids with high agronomic interest. Oxford University Press 2021-11-18 /pmc/articles/PMC8894923/ /pubmed/34792584 http://dx.doi.org/10.1093/plcell/koab284 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of American Society of Plant Biologists. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Huc, Jonathan
Dziasek, Katarzyna
Pachamuthu, Kannan
Woh, Tristan
Köhler, Claudia
Borges, Filipe
Bypassing reproductive barriers in hybrid seeds using chemically induced epimutagenesis
title Bypassing reproductive barriers in hybrid seeds using chemically induced epimutagenesis
title_full Bypassing reproductive barriers in hybrid seeds using chemically induced epimutagenesis
title_fullStr Bypassing reproductive barriers in hybrid seeds using chemically induced epimutagenesis
title_full_unstemmed Bypassing reproductive barriers in hybrid seeds using chemically induced epimutagenesis
title_short Bypassing reproductive barriers in hybrid seeds using chemically induced epimutagenesis
title_sort bypassing reproductive barriers in hybrid seeds using chemically induced epimutagenesis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894923/
https://www.ncbi.nlm.nih.gov/pubmed/34792584
http://dx.doi.org/10.1093/plcell/koab284
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