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Persistent directional growth capability in Arabidopsis thaliana pollen tubes after nuclear elimination from the apex

During the double fertilization process, pollen tubes deliver two sperm cells to an ovule containing the female gametes. In the pollen tube, the vegetative nucleus and sperm cells move together to the apical region where the vegetative nucleus is thought to play a crucial role in controlling the dir...

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Autores principales: Motomura, Kazuki, Takeuchi, Hidenori, Notaguchi, Michitaka, Tsuchi, Haruna, Takeda, Atsushi, Kinoshita, Tetsu, Higashiyama, Tetsuya, Maruyama, Daisuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8062503/
https://www.ncbi.nlm.nih.gov/pubmed/33888710
http://dx.doi.org/10.1038/s41467-021-22661-8
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author Motomura, Kazuki
Takeuchi, Hidenori
Notaguchi, Michitaka
Tsuchi, Haruna
Takeda, Atsushi
Kinoshita, Tetsu
Higashiyama, Tetsuya
Maruyama, Daisuke
author_facet Motomura, Kazuki
Takeuchi, Hidenori
Notaguchi, Michitaka
Tsuchi, Haruna
Takeda, Atsushi
Kinoshita, Tetsu
Higashiyama, Tetsuya
Maruyama, Daisuke
author_sort Motomura, Kazuki
collection PubMed
description During the double fertilization process, pollen tubes deliver two sperm cells to an ovule containing the female gametes. In the pollen tube, the vegetative nucleus and sperm cells move together to the apical region where the vegetative nucleus is thought to play a crucial role in controlling the direction and growth of the pollen tube. Here, we report the generation of pollen tubes in Arabidopsis thaliana whose vegetative nucleus and sperm cells are isolated and sealed by callose plugs in the basal region due to apical transport defects induced by mutations in the WPP domain-interacting tail-anchored proteins (WITs) and sperm cell-specific expression of a dominant mutant of the CALLOSE SYNTHASE 3 protein. Through pollen-tube guidance assays, we show that the physiologically anuclear mutant pollen tubes maintain the ability to grow and enter ovules. Our findings provide insight into the sperm cell delivery mechanism and illustrate the independence of the tip-localized vegetative nucleus from directional growth control of the pollen tube.
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spelling pubmed-80625032021-05-11 Persistent directional growth capability in Arabidopsis thaliana pollen tubes after nuclear elimination from the apex Motomura, Kazuki Takeuchi, Hidenori Notaguchi, Michitaka Tsuchi, Haruna Takeda, Atsushi Kinoshita, Tetsu Higashiyama, Tetsuya Maruyama, Daisuke Nat Commun Article During the double fertilization process, pollen tubes deliver two sperm cells to an ovule containing the female gametes. In the pollen tube, the vegetative nucleus and sperm cells move together to the apical region where the vegetative nucleus is thought to play a crucial role in controlling the direction and growth of the pollen tube. Here, we report the generation of pollen tubes in Arabidopsis thaliana whose vegetative nucleus and sperm cells are isolated and sealed by callose plugs in the basal region due to apical transport defects induced by mutations in the WPP domain-interacting tail-anchored proteins (WITs) and sperm cell-specific expression of a dominant mutant of the CALLOSE SYNTHASE 3 protein. Through pollen-tube guidance assays, we show that the physiologically anuclear mutant pollen tubes maintain the ability to grow and enter ovules. Our findings provide insight into the sperm cell delivery mechanism and illustrate the independence of the tip-localized vegetative nucleus from directional growth control of the pollen tube. Nature Publishing Group UK 2021-04-22 /pmc/articles/PMC8062503/ /pubmed/33888710 http://dx.doi.org/10.1038/s41467-021-22661-8 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
Motomura, Kazuki
Takeuchi, Hidenori
Notaguchi, Michitaka
Tsuchi, Haruna
Takeda, Atsushi
Kinoshita, Tetsu
Higashiyama, Tetsuya
Maruyama, Daisuke
Persistent directional growth capability in Arabidopsis thaliana pollen tubes after nuclear elimination from the apex
title Persistent directional growth capability in Arabidopsis thaliana pollen tubes after nuclear elimination from the apex
title_full Persistent directional growth capability in Arabidopsis thaliana pollen tubes after nuclear elimination from the apex
title_fullStr Persistent directional growth capability in Arabidopsis thaliana pollen tubes after nuclear elimination from the apex
title_full_unstemmed Persistent directional growth capability in Arabidopsis thaliana pollen tubes after nuclear elimination from the apex
title_short Persistent directional growth capability in Arabidopsis thaliana pollen tubes after nuclear elimination from the apex
title_sort persistent directional growth capability in arabidopsis thaliana pollen tubes after nuclear elimination from the apex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8062503/
https://www.ncbi.nlm.nih.gov/pubmed/33888710
http://dx.doi.org/10.1038/s41467-021-22661-8
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