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F-actin forms mobile and unwinding ring-shaped structures in germinating Arabidopsis pollen expressing Lifeact

The flowering plant pollen tube is the fastest elongating plant cell and transports the sperm cells for double fertilization. The highly dynamic formation and reorganization of the actin cytoskeleton is essential for pollen germination and pollen tube growth. To drive pollen-specific expression of f...

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Autores principales: Vogler, Frank, Sprunck, Stefanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4883927/
https://www.ncbi.nlm.nih.gov/pubmed/26337326
http://dx.doi.org/10.1080/15592324.2015.1075684
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author Vogler, Frank
Sprunck, Stefanie
author_facet Vogler, Frank
Sprunck, Stefanie
author_sort Vogler, Frank
collection PubMed
description The flowering plant pollen tube is the fastest elongating plant cell and transports the sperm cells for double fertilization. The highly dynamic formation and reorganization of the actin cytoskeleton is essential for pollen germination and pollen tube growth. To drive pollen-specific expression of fluorescent marker proteins, commonly the strong Lat52 promoter is used. Here we show by quantitative fluorescent analysis that the gametophyte-specific ARO1 promoter from Arabidopsis drives an about 3.5 times weaker transgene expression than the Lat52 promoter. In one third of the pollen of F-actin-labeled ARO1p:tagRFP-T-Lifeact transgenic lines we observed mobile ring-shaped actin structures in pollen grains and pollen tubes. Pollen tube growth, transgene transmission and seed production were not affected by tagRFP-T-Lifeact expression. F-actin rings were able to integrate into emerging actin filaments and they may reflect a particular physiological state of the pollen or a readily available storage form provided for rapid actin network remodeling.
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spelling pubmed-48839272016-06-13 F-actin forms mobile and unwinding ring-shaped structures in germinating Arabidopsis pollen expressing Lifeact Vogler, Frank Sprunck, Stefanie Plant Signal Behav Article Addendum The flowering plant pollen tube is the fastest elongating plant cell and transports the sperm cells for double fertilization. The highly dynamic formation and reorganization of the actin cytoskeleton is essential for pollen germination and pollen tube growth. To drive pollen-specific expression of fluorescent marker proteins, commonly the strong Lat52 promoter is used. Here we show by quantitative fluorescent analysis that the gametophyte-specific ARO1 promoter from Arabidopsis drives an about 3.5 times weaker transgene expression than the Lat52 promoter. In one third of the pollen of F-actin-labeled ARO1p:tagRFP-T-Lifeact transgenic lines we observed mobile ring-shaped actin structures in pollen grains and pollen tubes. Pollen tube growth, transgene transmission and seed production were not affected by tagRFP-T-Lifeact expression. F-actin rings were able to integrate into emerging actin filaments and they may reflect a particular physiological state of the pollen or a readily available storage form provided for rapid actin network remodeling. Taylor & Francis 2015-09-04 /pmc/articles/PMC4883927/ /pubmed/26337326 http://dx.doi.org/10.1080/15592324.2015.1075684 Text en © 2015 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Article Addendum
Vogler, Frank
Sprunck, Stefanie
F-actin forms mobile and unwinding ring-shaped structures in germinating Arabidopsis pollen expressing Lifeact
title F-actin forms mobile and unwinding ring-shaped structures in germinating Arabidopsis pollen expressing Lifeact
title_full F-actin forms mobile and unwinding ring-shaped structures in germinating Arabidopsis pollen expressing Lifeact
title_fullStr F-actin forms mobile and unwinding ring-shaped structures in germinating Arabidopsis pollen expressing Lifeact
title_full_unstemmed F-actin forms mobile and unwinding ring-shaped structures in germinating Arabidopsis pollen expressing Lifeact
title_short F-actin forms mobile and unwinding ring-shaped structures in germinating Arabidopsis pollen expressing Lifeact
title_sort f-actin forms mobile and unwinding ring-shaped structures in germinating arabidopsis pollen expressing lifeact
topic Article Addendum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4883927/
https://www.ncbi.nlm.nih.gov/pubmed/26337326
http://dx.doi.org/10.1080/15592324.2015.1075684
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