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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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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. |
format | Online Article Text |
id | pubmed-7004562 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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