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Cellular dynamics during early barley pollen embryogenesis revealed by time-lapse imaging

Plants display a remarkable capacity for cellular totipotency. An intriguing and useful example is that immature pollen cultured in vitro can pass through embryogenic development to form haploid or doubled haploid plants. However, a lack of understanding the initial mechanisms of pollen embryogenesi...

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Autores principales: Daghma, Diaa Eldin S., Hensel, Goetz, Rutten, Twan, Melzer, Michael, Kumlehn, Jochen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4259004/
https://www.ncbi.nlm.nih.gov/pubmed/25538715
http://dx.doi.org/10.3389/fpls.2014.00675
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author Daghma, Diaa Eldin S.
Hensel, Goetz
Rutten, Twan
Melzer, Michael
Kumlehn, Jochen
author_facet Daghma, Diaa Eldin S.
Hensel, Goetz
Rutten, Twan
Melzer, Michael
Kumlehn, Jochen
author_sort Daghma, Diaa Eldin S.
collection PubMed
description Plants display a remarkable capacity for cellular totipotency. An intriguing and useful example is that immature pollen cultured in vitro can pass through embryogenic development to form haploid or doubled haploid plants. However, a lack of understanding the initial mechanisms of pollen embryogenesis hampers the improvement and more effective and widespread employment of haploid technology in plant research and breeding. To investigate the cellular dynamics during the onset of pollen embryogenesis, we used time-lapse imaging along with transgenic barley expressing nuclear localized Green Fluorescent Protein. The results enabled us to identify nine distinct embryogenic and non-embryogenic types of pollen response to the culture conditions. Cell proliferation in embryogenic pollen normally started via a first symmetric mitosis (54.3% of pollen observed) and only rarely did so via asymmetric pollen mitosis I (4.3% of pollen observed). In the latter case, proliferation generally originated from the vegetative-like cell, albeit the division of the generative-like cell was observed in few types of pollen. Under the culture conditions used, fusion of cell nuclei was the only mechanism of genome duplication observed.
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spelling pubmed-42590042014-12-23 Cellular dynamics during early barley pollen embryogenesis revealed by time-lapse imaging Daghma, Diaa Eldin S. Hensel, Goetz Rutten, Twan Melzer, Michael Kumlehn, Jochen Front Plant Sci Plant Science Plants display a remarkable capacity for cellular totipotency. An intriguing and useful example is that immature pollen cultured in vitro can pass through embryogenic development to form haploid or doubled haploid plants. However, a lack of understanding the initial mechanisms of pollen embryogenesis hampers the improvement and more effective and widespread employment of haploid technology in plant research and breeding. To investigate the cellular dynamics during the onset of pollen embryogenesis, we used time-lapse imaging along with transgenic barley expressing nuclear localized Green Fluorescent Protein. The results enabled us to identify nine distinct embryogenic and non-embryogenic types of pollen response to the culture conditions. Cell proliferation in embryogenic pollen normally started via a first symmetric mitosis (54.3% of pollen observed) and only rarely did so via asymmetric pollen mitosis I (4.3% of pollen observed). In the latter case, proliferation generally originated from the vegetative-like cell, albeit the division of the generative-like cell was observed in few types of pollen. Under the culture conditions used, fusion of cell nuclei was the only mechanism of genome duplication observed. Frontiers Media S.A. 2014-12-08 /pmc/articles/PMC4259004/ /pubmed/25538715 http://dx.doi.org/10.3389/fpls.2014.00675 Text en Copyright © 2014 Daghma, Hensel, Rutten, Melzer and Kumlehn. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Daghma, Diaa Eldin S.
Hensel, Goetz
Rutten, Twan
Melzer, Michael
Kumlehn, Jochen
Cellular dynamics during early barley pollen embryogenesis revealed by time-lapse imaging
title Cellular dynamics during early barley pollen embryogenesis revealed by time-lapse imaging
title_full Cellular dynamics during early barley pollen embryogenesis revealed by time-lapse imaging
title_fullStr Cellular dynamics during early barley pollen embryogenesis revealed by time-lapse imaging
title_full_unstemmed Cellular dynamics during early barley pollen embryogenesis revealed by time-lapse imaging
title_short Cellular dynamics during early barley pollen embryogenesis revealed by time-lapse imaging
title_sort cellular dynamics during early barley pollen embryogenesis revealed by time-lapse imaging
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4259004/
https://www.ncbi.nlm.nih.gov/pubmed/25538715
http://dx.doi.org/10.3389/fpls.2014.00675
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