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Functional Characterization of the Arabidopsis Abscisic Acid Transporters NPF4.5 and NPF4.6 in Xenopus Oocytes
Few proteins have been characterized as abscisic acid transporters. Several of them are NRT1/PRT Family (NPF) transporters which have been characterized in yeast using reporter systems. Because several members of the NPF4 subfamily members were identified in yeast as ABA transporters, here, we scree...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054286/ https://www.ncbi.nlm.nih.gov/pubmed/32174938 http://dx.doi.org/10.3389/fpls.2020.00144 |
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author | Léran, Sophie Noguero, Mélanie Corratgé-Faillie, Claire Boursiac, Yann Brachet, Chantal Lacombe, Benoit |
author_facet | Léran, Sophie Noguero, Mélanie Corratgé-Faillie, Claire Boursiac, Yann Brachet, Chantal Lacombe, Benoit |
author_sort | Léran, Sophie |
collection | PubMed |
description | Few proteins have been characterized as abscisic acid transporters. Several of them are NRT1/PRT Family (NPF) transporters which have been characterized in yeast using reporter systems. Because several members of the NPF4 subfamily members were identified in yeast as ABA transporters, here, we screened for ABA transport activity the seven members of the NPF4 subfamily in Xenopus oocytes using cRNA injection and (3)H-ABA accumulation. The ABA transport capacities of NPF4.2, NPF4.5, NPF4.6, and NPF4.7 were confirmed. The transport properties of NPF4.5 and NPF4.6 were studied in more detail. Both ABA transporter activities are pH-dependent and slightly pH-dependent apparent Km around 500 μM. There is no competitive inhibition of the ABA-analogs pyrabactin and quinabactin on ABA accumulation demonstrating a different selectivity compared to the ABA receptors. Functional expression of these ABA transporters in Xenopus oocyte is an opportunity to start structure–function studies and also to identify partner proteins of these hormone transporters. |
format | Online Article Text |
id | pubmed-7054286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70542862020-03-13 Functional Characterization of the Arabidopsis Abscisic Acid Transporters NPF4.5 and NPF4.6 in Xenopus Oocytes Léran, Sophie Noguero, Mélanie Corratgé-Faillie, Claire Boursiac, Yann Brachet, Chantal Lacombe, Benoit Front Plant Sci Plant Science Few proteins have been characterized as abscisic acid transporters. Several of them are NRT1/PRT Family (NPF) transporters which have been characterized in yeast using reporter systems. Because several members of the NPF4 subfamily members were identified in yeast as ABA transporters, here, we screened for ABA transport activity the seven members of the NPF4 subfamily in Xenopus oocytes using cRNA injection and (3)H-ABA accumulation. The ABA transport capacities of NPF4.2, NPF4.5, NPF4.6, and NPF4.7 were confirmed. The transport properties of NPF4.5 and NPF4.6 were studied in more detail. Both ABA transporter activities are pH-dependent and slightly pH-dependent apparent Km around 500 μM. There is no competitive inhibition of the ABA-analogs pyrabactin and quinabactin on ABA accumulation demonstrating a different selectivity compared to the ABA receptors. Functional expression of these ABA transporters in Xenopus oocyte is an opportunity to start structure–function studies and also to identify partner proteins of these hormone transporters. Frontiers Media S.A. 2020-02-26 /pmc/articles/PMC7054286/ /pubmed/32174938 http://dx.doi.org/10.3389/fpls.2020.00144 Text en Copyright © 2020 Léran, Noguero, Corratgé-Faillie, Boursiac, Brachet and Lacombe http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Léran, Sophie Noguero, Mélanie Corratgé-Faillie, Claire Boursiac, Yann Brachet, Chantal Lacombe, Benoit Functional Characterization of the Arabidopsis Abscisic Acid Transporters NPF4.5 and NPF4.6 in Xenopus Oocytes |
title | Functional Characterization of the Arabidopsis Abscisic Acid Transporters NPF4.5 and NPF4.6 in Xenopus Oocytes |
title_full | Functional Characterization of the Arabidopsis Abscisic Acid Transporters NPF4.5 and NPF4.6 in Xenopus Oocytes |
title_fullStr | Functional Characterization of the Arabidopsis Abscisic Acid Transporters NPF4.5 and NPF4.6 in Xenopus Oocytes |
title_full_unstemmed | Functional Characterization of the Arabidopsis Abscisic Acid Transporters NPF4.5 and NPF4.6 in Xenopus Oocytes |
title_short | Functional Characterization of the Arabidopsis Abscisic Acid Transporters NPF4.5 and NPF4.6 in Xenopus Oocytes |
title_sort | functional characterization of the arabidopsis abscisic acid transporters npf4.5 and npf4.6 in xenopus oocytes |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054286/ https://www.ncbi.nlm.nih.gov/pubmed/32174938 http://dx.doi.org/10.3389/fpls.2020.00144 |
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