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Arabidopsis class I formins control membrane-originated actin polymerization at pollen tube tips

A population of dynamic apical actin filaments is required for rapid polarized pollen tube growth. However, the cellular mechanisms driving their assembly remain incompletely understood. It was postulated that formin is a major player in nucleating apical actin assembly, but direct genetic and cytol...

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Detalles Bibliográficos
Autores principales: Lan, Yaxian, Liu, Xiaonan, Fu, Ying, Huang, Shanjin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6258422/
https://www.ncbi.nlm.nih.gov/pubmed/30418966
http://dx.doi.org/10.1371/journal.pgen.1007789
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author Lan, Yaxian
Liu, Xiaonan
Fu, Ying
Huang, Shanjin
author_facet Lan, Yaxian
Liu, Xiaonan
Fu, Ying
Huang, Shanjin
author_sort Lan, Yaxian
collection PubMed
description A population of dynamic apical actin filaments is required for rapid polarized pollen tube growth. However, the cellular mechanisms driving their assembly remain incompletely understood. It was postulated that formin is a major player in nucleating apical actin assembly, but direct genetic and cytological evidence remains to be firmly established. Here we found that both Arabidopsis formin 3 (AtFH3) and formin 5 (AtFH5) are involved in the regulation of apical actin polymerization and actin array construction in pollen tubes, with AtFH3 playing a more dominant role. We found that both formins have plasma membrane (PM) localization signals but exhibit distinct PM localization patterns in the pollen tube, and loss of their function reduces the amount of apical actin filaments. Live-cell imaging revealed that the reduction in filamentous actin is very likely due to the decrease in filament elongation. Furthermore, we found that the rate of tip-directed vesicle transport is reduced and the pattern of apical vesicle accumulation is altered in formin loss-of-function mutant pollen tubes, which explains to some extent the reduction in pollen tube elongation. Thus, we provide direct genetic and cytological evidence showing that formin is an important player in nucleating actin assembly from the PM at pollen tube tips.
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spelling pubmed-62584222018-12-06 Arabidopsis class I formins control membrane-originated actin polymerization at pollen tube tips Lan, Yaxian Liu, Xiaonan Fu, Ying Huang, Shanjin PLoS Genet Research Article A population of dynamic apical actin filaments is required for rapid polarized pollen tube growth. However, the cellular mechanisms driving their assembly remain incompletely understood. It was postulated that formin is a major player in nucleating apical actin assembly, but direct genetic and cytological evidence remains to be firmly established. Here we found that both Arabidopsis formin 3 (AtFH3) and formin 5 (AtFH5) are involved in the regulation of apical actin polymerization and actin array construction in pollen tubes, with AtFH3 playing a more dominant role. We found that both formins have plasma membrane (PM) localization signals but exhibit distinct PM localization patterns in the pollen tube, and loss of their function reduces the amount of apical actin filaments. Live-cell imaging revealed that the reduction in filamentous actin is very likely due to the decrease in filament elongation. Furthermore, we found that the rate of tip-directed vesicle transport is reduced and the pattern of apical vesicle accumulation is altered in formin loss-of-function mutant pollen tubes, which explains to some extent the reduction in pollen tube elongation. Thus, we provide direct genetic and cytological evidence showing that formin is an important player in nucleating actin assembly from the PM at pollen tube tips. Public Library of Science 2018-11-12 /pmc/articles/PMC6258422/ /pubmed/30418966 http://dx.doi.org/10.1371/journal.pgen.1007789 Text en © 2018 Lan et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Lan, Yaxian
Liu, Xiaonan
Fu, Ying
Huang, Shanjin
Arabidopsis class I formins control membrane-originated actin polymerization at pollen tube tips
title Arabidopsis class I formins control membrane-originated actin polymerization at pollen tube tips
title_full Arabidopsis class I formins control membrane-originated actin polymerization at pollen tube tips
title_fullStr Arabidopsis class I formins control membrane-originated actin polymerization at pollen tube tips
title_full_unstemmed Arabidopsis class I formins control membrane-originated actin polymerization at pollen tube tips
title_short Arabidopsis class I formins control membrane-originated actin polymerization at pollen tube tips
title_sort arabidopsis class i formins control membrane-originated actin polymerization at pollen tube tips
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6258422/
https://www.ncbi.nlm.nih.gov/pubmed/30418966
http://dx.doi.org/10.1371/journal.pgen.1007789
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