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GABA operates upstream of H(+)-ATPase and improves salinity tolerance in Arabidopsis by enabling cytosolic K(+) retention and Na(+) exclusion

The non-protein amino acid γ-aminobutyric acid (GABA) rapidly accumulates in plant tissues in response to salinity. However, the physiological rationale for this elevation remains elusive. This study compared electrophysiological and whole-plant responses of salt-treated Arabidopsis mutants pop2-5 a...

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Autores principales: Su, Nana, Wu, Qi, Chen, Jiahui, Shabala, Lana, Mithöfer, Axel, Wang, Haiyang, Qu, Mei, Yu, Min, Cui, Jin, Shabala, Sergey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859739/
https://www.ncbi.nlm.nih.gov/pubmed/31420662
http://dx.doi.org/10.1093/jxb/erz367
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author Su, Nana
Wu, Qi
Chen, Jiahui
Shabala, Lana
Mithöfer, Axel
Wang, Haiyang
Qu, Mei
Yu, Min
Cui, Jin
Shabala, Sergey
author_facet Su, Nana
Wu, Qi
Chen, Jiahui
Shabala, Lana
Mithöfer, Axel
Wang, Haiyang
Qu, Mei
Yu, Min
Cui, Jin
Shabala, Sergey
author_sort Su, Nana
collection PubMed
description The non-protein amino acid γ-aminobutyric acid (GABA) rapidly accumulates in plant tissues in response to salinity. However, the physiological rationale for this elevation remains elusive. This study compared electrophysiological and whole-plant responses of salt-treated Arabidopsis mutants pop2-5 and gad1,2, which have different abilities to accumulate GABA. The pop2-5 mutant, which was able to overaccumulate GABA in its roots, showed a salt-tolerant phenotype. On the contrary, the gad1,2 mutant, lacking the ability to convert glutamate to GABA, showed oversensitivity to salinity. The greater salinity tolerance of the pop2-5 line was explained by: (i) the role of GABA in stress-induced activation of H(+)-ATPase, thus leading to better membrane potential maintenance and reduced stress-induced K(+) leak from roots; (ii) reduced rates of net Na(+) uptake; (iii) higher expression of SOS1 and NHX1 genes in the leaves, which contributed to reducing Na(+) concentration in the cytoplasm by excluding Na(+) to apoplast and sequestering Na(+) in the vacuoles; (iv) a lower rate of H(2)O(2) production and reduced reactive oxygen species-inducible K(+) efflux from root epidermis; and (v) better K(+) retention in the shoot associated with the lower expression level of GORK channels in plant leaves.
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spelling pubmed-68597392019-11-21 GABA operates upstream of H(+)-ATPase and improves salinity tolerance in Arabidopsis by enabling cytosolic K(+) retention and Na(+) exclusion Su, Nana Wu, Qi Chen, Jiahui Shabala, Lana Mithöfer, Axel Wang, Haiyang Qu, Mei Yu, Min Cui, Jin Shabala, Sergey J Exp Bot Research Papers The non-protein amino acid γ-aminobutyric acid (GABA) rapidly accumulates in plant tissues in response to salinity. However, the physiological rationale for this elevation remains elusive. This study compared electrophysiological and whole-plant responses of salt-treated Arabidopsis mutants pop2-5 and gad1,2, which have different abilities to accumulate GABA. The pop2-5 mutant, which was able to overaccumulate GABA in its roots, showed a salt-tolerant phenotype. On the contrary, the gad1,2 mutant, lacking the ability to convert glutamate to GABA, showed oversensitivity to salinity. The greater salinity tolerance of the pop2-5 line was explained by: (i) the role of GABA in stress-induced activation of H(+)-ATPase, thus leading to better membrane potential maintenance and reduced stress-induced K(+) leak from roots; (ii) reduced rates of net Na(+) uptake; (iii) higher expression of SOS1 and NHX1 genes in the leaves, which contributed to reducing Na(+) concentration in the cytoplasm by excluding Na(+) to apoplast and sequestering Na(+) in the vacuoles; (iv) a lower rate of H(2)O(2) production and reduced reactive oxygen species-inducible K(+) efflux from root epidermis; and (v) better K(+) retention in the shoot associated with the lower expression level of GORK channels in plant leaves. Oxford University Press 2019-11-01 2019-08-17 /pmc/articles/PMC6859739/ /pubmed/31420662 http://dx.doi.org/10.1093/jxb/erz367 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Experimental Biology. 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 Research Papers
Su, Nana
Wu, Qi
Chen, Jiahui
Shabala, Lana
Mithöfer, Axel
Wang, Haiyang
Qu, Mei
Yu, Min
Cui, Jin
Shabala, Sergey
GABA operates upstream of H(+)-ATPase and improves salinity tolerance in Arabidopsis by enabling cytosolic K(+) retention and Na(+) exclusion
title GABA operates upstream of H(+)-ATPase and improves salinity tolerance in Arabidopsis by enabling cytosolic K(+) retention and Na(+) exclusion
title_full GABA operates upstream of H(+)-ATPase and improves salinity tolerance in Arabidopsis by enabling cytosolic K(+) retention and Na(+) exclusion
title_fullStr GABA operates upstream of H(+)-ATPase and improves salinity tolerance in Arabidopsis by enabling cytosolic K(+) retention and Na(+) exclusion
title_full_unstemmed GABA operates upstream of H(+)-ATPase and improves salinity tolerance in Arabidopsis by enabling cytosolic K(+) retention and Na(+) exclusion
title_short GABA operates upstream of H(+)-ATPase and improves salinity tolerance in Arabidopsis by enabling cytosolic K(+) retention and Na(+) exclusion
title_sort gaba operates upstream of h(+)-atpase and improves salinity tolerance in arabidopsis by enabling cytosolic k(+) retention and na(+) exclusion
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859739/
https://www.ncbi.nlm.nih.gov/pubmed/31420662
http://dx.doi.org/10.1093/jxb/erz367
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