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OsHKT1;4-mediated Na(+) transport in stems contributes to Na(+) exclusion from leaf blades of rice at the reproductive growth stage upon salt stress

BACKGROUND: Na(+) exclusion from leaf blades is one of the key mechanisms for glycophytes to cope with salinity stress. Certain class I transporters of the high-affinity K(+) transporter (HKT) family have been demonstrated to mediate leaf blade-Na(+) exclusion upon salinity stress via Na(+)-selectiv...

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Autores principales: Suzuki, Kei, Yamaji, Naoki, Costa, Alex, Okuma, Eiji, Kobayashi, Natsuko I., Kashiwagi, Tatsuhiko, Katsuhara, Maki, Wang, Cun, Tanoi, Keitaro, Murata, Yoshiyuki, Schroeder, Julian I., Ma, Jian Feng, Horie, Tomoaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4719677/
https://www.ncbi.nlm.nih.gov/pubmed/26786707
http://dx.doi.org/10.1186/s12870-016-0709-4
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author Suzuki, Kei
Yamaji, Naoki
Costa, Alex
Okuma, Eiji
Kobayashi, Natsuko I.
Kashiwagi, Tatsuhiko
Katsuhara, Maki
Wang, Cun
Tanoi, Keitaro
Murata, Yoshiyuki
Schroeder, Julian I.
Ma, Jian Feng
Horie, Tomoaki
author_facet Suzuki, Kei
Yamaji, Naoki
Costa, Alex
Okuma, Eiji
Kobayashi, Natsuko I.
Kashiwagi, Tatsuhiko
Katsuhara, Maki
Wang, Cun
Tanoi, Keitaro
Murata, Yoshiyuki
Schroeder, Julian I.
Ma, Jian Feng
Horie, Tomoaki
author_sort Suzuki, Kei
collection PubMed
description BACKGROUND: Na(+) exclusion from leaf blades is one of the key mechanisms for glycophytes to cope with salinity stress. Certain class I transporters of the high-affinity K(+) transporter (HKT) family have been demonstrated to mediate leaf blade-Na(+) exclusion upon salinity stress via Na(+)-selective transport. Multiple HKT1 transporters are known to function in rice (Oryza sativa). However, the ion transport function of OsHKT1;4 and its contribution to the Na(+) exclusion mechanism in rice remain to be elucidated. RESULTS: Here, we report results of the functional characterization of the OsHKT1;4 transporter in rice. OsHKT1;4 mediated robust Na(+) transport in Saccharomyces cerevisiae and Xenopus laevis oocytes. Electrophysiological experiments demonstrated that OsHKT1;4 shows strong Na(+) selectivity among cations tested, including Li(+), Na(+), K(+), Rb(+), Cs(+), and NH(4)(+), in oocytes. A chimeric protein, EGFP-OsHKT1;4, was found to be functional in oocytes and targeted to the plasma membrane of rice protoplasts. The level of OsHKT1;4 transcripts was prominent in leaf sheaths throughout the growth stages. Unexpectedly however, we demonstrate here accumulation of OsHKT1;4 transcripts in the stem including internode II and peduncle in the reproductive growth stage. Moreover, phenotypic analysis of OsHKT1;4 RNAi plants in the vegetative growth stage revealed no profound influence on the growth and ion accumulation in comparison with WT plants upon salinity stress. However, imposition of salinity stress on the RNAi plants in the reproductive growth stage caused significant Na(+) overaccumulation in aerial organs, in particular, leaf blades and sheaths. In addition, (22)Na(+) tracer experiments using peduncles of RNAi and WT plants suggested xylem Na(+) unloading by OsHKT1;4. CONCLUSIONS: Taken together, our results indicate a newly recognized function of OsHKT1;4 in Na(+) exclusion in stems together with leaf sheaths, thus excluding Na(+) from leaf blades of a japonica rice cultivar in the reproductive growth stage, but the contribution is low when the plants are in the vegetative growth stage. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-016-0709-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-47196772016-01-21 OsHKT1;4-mediated Na(+) transport in stems contributes to Na(+) exclusion from leaf blades of rice at the reproductive growth stage upon salt stress Suzuki, Kei Yamaji, Naoki Costa, Alex Okuma, Eiji Kobayashi, Natsuko I. Kashiwagi, Tatsuhiko Katsuhara, Maki Wang, Cun Tanoi, Keitaro Murata, Yoshiyuki Schroeder, Julian I. Ma, Jian Feng Horie, Tomoaki BMC Plant Biol Research Article BACKGROUND: Na(+) exclusion from leaf blades is one of the key mechanisms for glycophytes to cope with salinity stress. Certain class I transporters of the high-affinity K(+) transporter (HKT) family have been demonstrated to mediate leaf blade-Na(+) exclusion upon salinity stress via Na(+)-selective transport. Multiple HKT1 transporters are known to function in rice (Oryza sativa). However, the ion transport function of OsHKT1;4 and its contribution to the Na(+) exclusion mechanism in rice remain to be elucidated. RESULTS: Here, we report results of the functional characterization of the OsHKT1;4 transporter in rice. OsHKT1;4 mediated robust Na(+) transport in Saccharomyces cerevisiae and Xenopus laevis oocytes. Electrophysiological experiments demonstrated that OsHKT1;4 shows strong Na(+) selectivity among cations tested, including Li(+), Na(+), K(+), Rb(+), Cs(+), and NH(4)(+), in oocytes. A chimeric protein, EGFP-OsHKT1;4, was found to be functional in oocytes and targeted to the plasma membrane of rice protoplasts. The level of OsHKT1;4 transcripts was prominent in leaf sheaths throughout the growth stages. Unexpectedly however, we demonstrate here accumulation of OsHKT1;4 transcripts in the stem including internode II and peduncle in the reproductive growth stage. Moreover, phenotypic analysis of OsHKT1;4 RNAi plants in the vegetative growth stage revealed no profound influence on the growth and ion accumulation in comparison with WT plants upon salinity stress. However, imposition of salinity stress on the RNAi plants in the reproductive growth stage caused significant Na(+) overaccumulation in aerial organs, in particular, leaf blades and sheaths. In addition, (22)Na(+) tracer experiments using peduncles of RNAi and WT plants suggested xylem Na(+) unloading by OsHKT1;4. CONCLUSIONS: Taken together, our results indicate a newly recognized function of OsHKT1;4 in Na(+) exclusion in stems together with leaf sheaths, thus excluding Na(+) from leaf blades of a japonica rice cultivar in the reproductive growth stage, but the contribution is low when the plants are in the vegetative growth stage. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-016-0709-4) contains supplementary material, which is available to authorized users. BioMed Central 2016-01-19 /pmc/articles/PMC4719677/ /pubmed/26786707 http://dx.doi.org/10.1186/s12870-016-0709-4 Text en © Suzuki et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Suzuki, Kei
Yamaji, Naoki
Costa, Alex
Okuma, Eiji
Kobayashi, Natsuko I.
Kashiwagi, Tatsuhiko
Katsuhara, Maki
Wang, Cun
Tanoi, Keitaro
Murata, Yoshiyuki
Schroeder, Julian I.
Ma, Jian Feng
Horie, Tomoaki
OsHKT1;4-mediated Na(+) transport in stems contributes to Na(+) exclusion from leaf blades of rice at the reproductive growth stage upon salt stress
title OsHKT1;4-mediated Na(+) transport in stems contributes to Na(+) exclusion from leaf blades of rice at the reproductive growth stage upon salt stress
title_full OsHKT1;4-mediated Na(+) transport in stems contributes to Na(+) exclusion from leaf blades of rice at the reproductive growth stage upon salt stress
title_fullStr OsHKT1;4-mediated Na(+) transport in stems contributes to Na(+) exclusion from leaf blades of rice at the reproductive growth stage upon salt stress
title_full_unstemmed OsHKT1;4-mediated Na(+) transport in stems contributes to Na(+) exclusion from leaf blades of rice at the reproductive growth stage upon salt stress
title_short OsHKT1;4-mediated Na(+) transport in stems contributes to Na(+) exclusion from leaf blades of rice at the reproductive growth stage upon salt stress
title_sort oshkt1;4-mediated na(+) transport in stems contributes to na(+) exclusion from leaf blades of rice at the reproductive growth stage upon salt stress
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4719677/
https://www.ncbi.nlm.nih.gov/pubmed/26786707
http://dx.doi.org/10.1186/s12870-016-0709-4
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