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Vacuolar Na(+)/H(+) NHX-Type Antiporters Are Required for Cellular K(+) Homeostasis, Microtubule Organization and Directional Root Growth

Na(+)/H(+) antiporters (NHXs) are integral membrane transporters that catalyze the electroneutral exchange of K(+) or Na(+) for H(+) and are implicated in cell expansion, development, pH and ion homeostasis and salt tolerance. Arabidopsis contains four vacuolar NHX isoforms (NHX1–NHX4), but only the...

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Autores principales: McCubbin, Tyler, Bassil, Elias, Zhang, Shiqi, Blumwald, Eduardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4844347/
https://www.ncbi.nlm.nih.gov/pubmed/27135511
http://dx.doi.org/10.3390/plants3030409
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author McCubbin, Tyler
Bassil, Elias
Zhang, Shiqi
Blumwald, Eduardo
author_facet McCubbin, Tyler
Bassil, Elias
Zhang, Shiqi
Blumwald, Eduardo
author_sort McCubbin, Tyler
collection PubMed
description Na(+)/H(+) antiporters (NHXs) are integral membrane transporters that catalyze the electroneutral exchange of K(+) or Na(+) for H(+) and are implicated in cell expansion, development, pH and ion homeostasis and salt tolerance. Arabidopsis contains four vacuolar NHX isoforms (NHX1–NHX4), but only the functional roles for NHX1 and NHX2 have been assessed thus far. Colocalization studies indicated that NHX3 and NHX4 colocalize to the tonoplast. To investigate the role of all vacuolar NHX isoforms, a quadruple knockout nhx1nhx2nhx3nhx4, lacking all vacuolar NHXs, was generated. Seedlings of nhx1nhx2nhx3nhx4 displayed significantly reduced growth, with markedly shorter hypocotyls. Under high K(+), but not Na(+), pronounced root skewing occurred in nhx1nhx2nhx3nhx4, suggesting that the organization of the cytoskeleton might be perturbed. Whole mount immunolabeling of cortical microtubules indicated that high K(+) caused significant microtubule reorganization in nhx1nhx2nhx3nhx4 root cells of the elongation zone. Using microtubule stabilizing (Taxol) and destabilizing (propyzamide) drugs, we found that the effect of K(+) on nhx1nhx2nhx3nhx4 root growth was antagonistic to that of Taxol, whereas elevated K(+) exacerbated the endogenous effect of propyzamide on root skewing. Collectively, our results suggest that altered K(+) homeostasis leads to an increase in the dynamics of cortical microtubule reorganization in nhx1nhx2nhx3nhx4 root epidermal cells of the elongation zone.
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spelling pubmed-48443472016-04-29 Vacuolar Na(+)/H(+) NHX-Type Antiporters Are Required for Cellular K(+) Homeostasis, Microtubule Organization and Directional Root Growth McCubbin, Tyler Bassil, Elias Zhang, Shiqi Blumwald, Eduardo Plants (Basel) Article Na(+)/H(+) antiporters (NHXs) are integral membrane transporters that catalyze the electroneutral exchange of K(+) or Na(+) for H(+) and are implicated in cell expansion, development, pH and ion homeostasis and salt tolerance. Arabidopsis contains four vacuolar NHX isoforms (NHX1–NHX4), but only the functional roles for NHX1 and NHX2 have been assessed thus far. Colocalization studies indicated that NHX3 and NHX4 colocalize to the tonoplast. To investigate the role of all vacuolar NHX isoforms, a quadruple knockout nhx1nhx2nhx3nhx4, lacking all vacuolar NHXs, was generated. Seedlings of nhx1nhx2nhx3nhx4 displayed significantly reduced growth, with markedly shorter hypocotyls. Under high K(+), but not Na(+), pronounced root skewing occurred in nhx1nhx2nhx3nhx4, suggesting that the organization of the cytoskeleton might be perturbed. Whole mount immunolabeling of cortical microtubules indicated that high K(+) caused significant microtubule reorganization in nhx1nhx2nhx3nhx4 root cells of the elongation zone. Using microtubule stabilizing (Taxol) and destabilizing (propyzamide) drugs, we found that the effect of K(+) on nhx1nhx2nhx3nhx4 root growth was antagonistic to that of Taxol, whereas elevated K(+) exacerbated the endogenous effect of propyzamide on root skewing. Collectively, our results suggest that altered K(+) homeostasis leads to an increase in the dynamics of cortical microtubule reorganization in nhx1nhx2nhx3nhx4 root epidermal cells of the elongation zone. MDPI 2014-08-29 /pmc/articles/PMC4844347/ /pubmed/27135511 http://dx.doi.org/10.3390/plants3030409 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
McCubbin, Tyler
Bassil, Elias
Zhang, Shiqi
Blumwald, Eduardo
Vacuolar Na(+)/H(+) NHX-Type Antiporters Are Required for Cellular K(+) Homeostasis, Microtubule Organization and Directional Root Growth
title Vacuolar Na(+)/H(+) NHX-Type Antiporters Are Required for Cellular K(+) Homeostasis, Microtubule Organization and Directional Root Growth
title_full Vacuolar Na(+)/H(+) NHX-Type Antiporters Are Required for Cellular K(+) Homeostasis, Microtubule Organization and Directional Root Growth
title_fullStr Vacuolar Na(+)/H(+) NHX-Type Antiporters Are Required for Cellular K(+) Homeostasis, Microtubule Organization and Directional Root Growth
title_full_unstemmed Vacuolar Na(+)/H(+) NHX-Type Antiporters Are Required for Cellular K(+) Homeostasis, Microtubule Organization and Directional Root Growth
title_short Vacuolar Na(+)/H(+) NHX-Type Antiporters Are Required for Cellular K(+) Homeostasis, Microtubule Organization and Directional Root Growth
title_sort vacuolar na(+)/h(+) nhx-type antiporters are required for cellular k(+) homeostasis, microtubule organization and directional root growth
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4844347/
https://www.ncbi.nlm.nih.gov/pubmed/27135511
http://dx.doi.org/10.3390/plants3030409
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