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Auxin Influx Carrier AUX1 Confers Acid Resistance for Arabidopsis Root Elongation Through the Regulation of Plasma Membrane H(+)-ATPase

The plant plasma membrane (PM) H(+)-ATPase regulates pH homeostasis and cell elongation in roots through the formation of an electrochemical H(+) gradient across the PM and a decrease in apoplastic pH; however, the detailed signaling for the regulation of PM H(+)-ATPases remains unclear. Here, we sh...

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Autores principales: Inoue, Shin-ichiro, Takahashi, Koji, Okumura-Noda, Hiromi, Kinoshita, Toshinori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434668/
https://www.ncbi.nlm.nih.gov/pubmed/27503216
http://dx.doi.org/10.1093/pcp/pcw136
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author Inoue, Shin-ichiro
Takahashi, Koji
Okumura-Noda, Hiromi
Kinoshita, Toshinori
author_facet Inoue, Shin-ichiro
Takahashi, Koji
Okumura-Noda, Hiromi
Kinoshita, Toshinori
author_sort Inoue, Shin-ichiro
collection PubMed
description The plant plasma membrane (PM) H(+)-ATPase regulates pH homeostasis and cell elongation in roots through the formation of an electrochemical H(+) gradient across the PM and a decrease in apoplastic pH; however, the detailed signaling for the regulation of PM H(+)-ATPases remains unclear. Here, we show that an auxin influx carrier, AUXIN RESISTANT1 (AUX1), is required for the maintenance of PM H(+)-ATPase activity and proper root elongation. We isolated a low pH-hypersensitive 1 (loph1) mutant by a genetic screen of Arabidopsis thaliana on low pH agar plates. The loph1 mutant is a loss-of-function mutant of the AUX1 gene and exhibits a root growth retardation restricted to the low pH condition. The ATP hydrolysis and H(+) extrusion activities of the PM H(+)-ATPase were reduced in loph1 roots. Furthermore, the phosphorylation of the penultimate threonine of the PM H(+)-ATPase was reduced in loph1 roots under both normal and low pH conditions without reduction of the amount of PM H(+)-ATPase. Expression of the DR5:GUS reporter gene and auxin-responsive genes suggested that endogenous auxin levels were lower in loph1 roots than in the wild type. The aux1-7 mutant roots also exhibited root growth retardation in the low pH condition like the loph1 roots. These results indicate that AUX1 positively regulates the PM H(+)-ATPase activity through maintenance of the auxin accumulation in root tips, and this process may serve to maintain root elongation especially under low pH conditions.
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spelling pubmed-54346682017-05-22 Auxin Influx Carrier AUX1 Confers Acid Resistance for Arabidopsis Root Elongation Through the Regulation of Plasma Membrane H(+)-ATPase Inoue, Shin-ichiro Takahashi, Koji Okumura-Noda, Hiromi Kinoshita, Toshinori Plant Cell Physiol Regular Papers The plant plasma membrane (PM) H(+)-ATPase regulates pH homeostasis and cell elongation in roots through the formation of an electrochemical H(+) gradient across the PM and a decrease in apoplastic pH; however, the detailed signaling for the regulation of PM H(+)-ATPases remains unclear. Here, we show that an auxin influx carrier, AUXIN RESISTANT1 (AUX1), is required for the maintenance of PM H(+)-ATPase activity and proper root elongation. We isolated a low pH-hypersensitive 1 (loph1) mutant by a genetic screen of Arabidopsis thaliana on low pH agar plates. The loph1 mutant is a loss-of-function mutant of the AUX1 gene and exhibits a root growth retardation restricted to the low pH condition. The ATP hydrolysis and H(+) extrusion activities of the PM H(+)-ATPase were reduced in loph1 roots. Furthermore, the phosphorylation of the penultimate threonine of the PM H(+)-ATPase was reduced in loph1 roots under both normal and low pH conditions without reduction of the amount of PM H(+)-ATPase. Expression of the DR5:GUS reporter gene and auxin-responsive genes suggested that endogenous auxin levels were lower in loph1 roots than in the wild type. The aux1-7 mutant roots also exhibited root growth retardation in the low pH condition like the loph1 roots. These results indicate that AUX1 positively regulates the PM H(+)-ATPase activity through maintenance of the auxin accumulation in root tips, and this process may serve to maintain root elongation especially under low pH conditions. Oxford University Press 2016-10 2016-08-08 /pmc/articles/PMC5434668/ /pubmed/27503216 http://dx.doi.org/10.1093/pcp/pcw136 Text en © The Author 2016. Published by Oxford University Press on behalf of Japanese Society of Plant Physiologists. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Regular Papers
Inoue, Shin-ichiro
Takahashi, Koji
Okumura-Noda, Hiromi
Kinoshita, Toshinori
Auxin Influx Carrier AUX1 Confers Acid Resistance for Arabidopsis Root Elongation Through the Regulation of Plasma Membrane H(+)-ATPase
title Auxin Influx Carrier AUX1 Confers Acid Resistance for Arabidopsis Root Elongation Through the Regulation of Plasma Membrane H(+)-ATPase
title_full Auxin Influx Carrier AUX1 Confers Acid Resistance for Arabidopsis Root Elongation Through the Regulation of Plasma Membrane H(+)-ATPase
title_fullStr Auxin Influx Carrier AUX1 Confers Acid Resistance for Arabidopsis Root Elongation Through the Regulation of Plasma Membrane H(+)-ATPase
title_full_unstemmed Auxin Influx Carrier AUX1 Confers Acid Resistance for Arabidopsis Root Elongation Through the Regulation of Plasma Membrane H(+)-ATPase
title_short Auxin Influx Carrier AUX1 Confers Acid Resistance for Arabidopsis Root Elongation Through the Regulation of Plasma Membrane H(+)-ATPase
title_sort auxin influx carrier aux1 confers acid resistance for arabidopsis root elongation through the regulation of plasma membrane h(+)-atpase
topic Regular Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434668/
https://www.ncbi.nlm.nih.gov/pubmed/27503216
http://dx.doi.org/10.1093/pcp/pcw136
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