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Plasma membrane H(+)-ATPases sustain pollen tube growth and fertilization
Pollen tubes are highly polarized tip-growing cells that depend on cytosolic pH gradients for signaling and growth. Autoinhibited plasma membrane proton (H(+)) ATPases (AHAs) have been proposed to energize pollen tube growth and underlie cell polarity, however, mechanistic evidence for this is lacki...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7224221/ https://www.ncbi.nlm.nih.gov/pubmed/32409656 http://dx.doi.org/10.1038/s41467-020-16253-1 |
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author | Hoffmann, Robert D. Portes, Maria Teresa Olsen, Lene Irene Damineli, Daniel Santa Cruz Hayashi, Maki Nunes, Custódio O. Pedersen, Jesper T. Lima, Pedro T. Campos, Cláudia Feijó, José A. Palmgren, Michael |
author_facet | Hoffmann, Robert D. Portes, Maria Teresa Olsen, Lene Irene Damineli, Daniel Santa Cruz Hayashi, Maki Nunes, Custódio O. Pedersen, Jesper T. Lima, Pedro T. Campos, Cláudia Feijó, José A. Palmgren, Michael |
author_sort | Hoffmann, Robert D. |
collection | PubMed |
description | Pollen tubes are highly polarized tip-growing cells that depend on cytosolic pH gradients for signaling and growth. Autoinhibited plasma membrane proton (H(+)) ATPases (AHAs) have been proposed to energize pollen tube growth and underlie cell polarity, however, mechanistic evidence for this is lacking. Here we report that the combined loss of AHA6, AHA8, and AHA9 in Arabidopsis thaliana delays pollen germination and causes pollen tube growth defects, leading to drastically reduced fertility. Pollen tubes of aha mutants had reduced extracellular proton (H(+)) and anion fluxes, reduced cytosolic pH, reduced tip-to-shank proton gradients, and defects in actin organization. Furthermore, mutant pollen tubes had less negative membrane potentials, substantiating a mechanistic role for AHAs in pollen tube growth through plasma membrane hyperpolarization. Our findings define AHAs as energy transducers that sustain the ionic circuit defining the spatial and temporal profiles of cytosolic pH, thereby controlling downstream pH-dependent mechanisms essential for pollen tube elongation, and thus plant fertility. |
format | Online Article Text |
id | pubmed-7224221 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72242212020-05-15 Plasma membrane H(+)-ATPases sustain pollen tube growth and fertilization Hoffmann, Robert D. Portes, Maria Teresa Olsen, Lene Irene Damineli, Daniel Santa Cruz Hayashi, Maki Nunes, Custódio O. Pedersen, Jesper T. Lima, Pedro T. Campos, Cláudia Feijó, José A. Palmgren, Michael Nat Commun Article Pollen tubes are highly polarized tip-growing cells that depend on cytosolic pH gradients for signaling and growth. Autoinhibited plasma membrane proton (H(+)) ATPases (AHAs) have been proposed to energize pollen tube growth and underlie cell polarity, however, mechanistic evidence for this is lacking. Here we report that the combined loss of AHA6, AHA8, and AHA9 in Arabidopsis thaliana delays pollen germination and causes pollen tube growth defects, leading to drastically reduced fertility. Pollen tubes of aha mutants had reduced extracellular proton (H(+)) and anion fluxes, reduced cytosolic pH, reduced tip-to-shank proton gradients, and defects in actin organization. Furthermore, mutant pollen tubes had less negative membrane potentials, substantiating a mechanistic role for AHAs in pollen tube growth through plasma membrane hyperpolarization. Our findings define AHAs as energy transducers that sustain the ionic circuit defining the spatial and temporal profiles of cytosolic pH, thereby controlling downstream pH-dependent mechanisms essential for pollen tube elongation, and thus plant fertility. Nature Publishing Group UK 2020-05-14 /pmc/articles/PMC7224221/ /pubmed/32409656 http://dx.doi.org/10.1038/s41467-020-16253-1 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Hoffmann, Robert D. Portes, Maria Teresa Olsen, Lene Irene Damineli, Daniel Santa Cruz Hayashi, Maki Nunes, Custódio O. Pedersen, Jesper T. Lima, Pedro T. Campos, Cláudia Feijó, José A. Palmgren, Michael Plasma membrane H(+)-ATPases sustain pollen tube growth and fertilization |
title | Plasma membrane H(+)-ATPases sustain pollen tube growth and fertilization |
title_full | Plasma membrane H(+)-ATPases sustain pollen tube growth and fertilization |
title_fullStr | Plasma membrane H(+)-ATPases sustain pollen tube growth and fertilization |
title_full_unstemmed | Plasma membrane H(+)-ATPases sustain pollen tube growth and fertilization |
title_short | Plasma membrane H(+)-ATPases sustain pollen tube growth and fertilization |
title_sort | plasma membrane h(+)-atpases sustain pollen tube growth and fertilization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7224221/ https://www.ncbi.nlm.nih.gov/pubmed/32409656 http://dx.doi.org/10.1038/s41467-020-16253-1 |
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