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Selective egg cell polyspermy bypasses the triploid block

Polyploidization, the increase in genome copies, is considered a major driving force for speciation. We have recently provided the first direct in planta evidence for polyspermy induced polyploidization. Capitalizing on a novel sco1-based polyspermy assay, we here show that polyspermy can selectivel...

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Autores principales: Mao, Yanbo, Gabel, Alexander, Nakel, Thomas, Viehöver, Prisca, Baum, Thomas, Tekleyohans, Dawit Girma, Vo, Dieu, Grosse, Ivo, Groß-Hardt, Rita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004562/
https://www.ncbi.nlm.nih.gov/pubmed/32027307
http://dx.doi.org/10.7554/eLife.52976
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author Mao, Yanbo
Gabel, Alexander
Nakel, Thomas
Viehöver, Prisca
Baum, Thomas
Tekleyohans, Dawit Girma
Vo, Dieu
Grosse, Ivo
Groß-Hardt, Rita
author_facet Mao, Yanbo
Gabel, Alexander
Nakel, Thomas
Viehöver, Prisca
Baum, Thomas
Tekleyohans, Dawit Girma
Vo, Dieu
Grosse, Ivo
Groß-Hardt, Rita
author_sort Mao, Yanbo
collection PubMed
description Polyploidization, the increase in genome copies, is considered a major driving force for speciation. We have recently provided the first direct in planta evidence for polyspermy induced polyploidization. Capitalizing on a novel sco1-based polyspermy assay, we here show that polyspermy can selectively polyploidize the egg cell, while rendering the genome size of the ploidy-sensitive central cell unaffected. This unprecedented result indicates that polyspermy can bypass the triploid block, which is an established postzygotic polyploidization barrier. In fact, we here show that most polyspermy-derived seeds are insensitive to the triploid block suppressor admetos. The robustness of polyspermy-derived plants is evidenced by the first transcript profiling of triparental plants and our observation that these idiosyncratic organisms segregate tetraploid offspring within a single generation. Polyspermy-derived triparental plants are thus comparable to triploids recovered from interploidy crosses. Our results expand current polyploidization concepts and have important implications for plant breeding.
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spelling pubmed-70045622020-02-10 Selective egg cell polyspermy bypasses the triploid block Mao, Yanbo Gabel, Alexander Nakel, Thomas Viehöver, Prisca Baum, Thomas Tekleyohans, Dawit Girma Vo, Dieu Grosse, Ivo Groß-Hardt, Rita eLife Developmental Biology Polyploidization, the increase in genome copies, is considered a major driving force for speciation. We have recently provided the first direct in planta evidence for polyspermy induced polyploidization. Capitalizing on a novel sco1-based polyspermy assay, we here show that polyspermy can selectively polyploidize the egg cell, while rendering the genome size of the ploidy-sensitive central cell unaffected. This unprecedented result indicates that polyspermy can bypass the triploid block, which is an established postzygotic polyploidization barrier. In fact, we here show that most polyspermy-derived seeds are insensitive to the triploid block suppressor admetos. The robustness of polyspermy-derived plants is evidenced by the first transcript profiling of triparental plants and our observation that these idiosyncratic organisms segregate tetraploid offspring within a single generation. Polyspermy-derived triparental plants are thus comparable to triploids recovered from interploidy crosses. Our results expand current polyploidization concepts and have important implications for plant breeding. eLife Sciences Publications, Ltd 2020-02-06 /pmc/articles/PMC7004562/ /pubmed/32027307 http://dx.doi.org/10.7554/eLife.52976 Text en © 2020, Mao et al http://creativecommons.org/licenses/by/4.0/ 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 Developmental Biology
Mao, Yanbo
Gabel, Alexander
Nakel, Thomas
Viehöver, Prisca
Baum, Thomas
Tekleyohans, Dawit Girma
Vo, Dieu
Grosse, Ivo
Groß-Hardt, Rita
Selective egg cell polyspermy bypasses the triploid block
title Selective egg cell polyspermy bypasses the triploid block
title_full Selective egg cell polyspermy bypasses the triploid block
title_fullStr Selective egg cell polyspermy bypasses the triploid block
title_full_unstemmed Selective egg cell polyspermy bypasses the triploid block
title_short Selective egg cell polyspermy bypasses the triploid block
title_sort selective egg cell polyspermy bypasses the triploid block
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004562/
https://www.ncbi.nlm.nih.gov/pubmed/32027307
http://dx.doi.org/10.7554/eLife.52976
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