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High V‐PPase activity is beneficial under high salt loads, but detrimental without salinity

The membrane‐bound proton‐pumping pyrophosphatase (V‐PPase), together with the V‐type H(+)‐ATPase, generates the proton motive force that drives vacuolar membrane solute transport. Transgenic plants constitutively overexpressing V‐PPases were shown to have improved salinity tolerance, but the relati...

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Autores principales: Graus, Dorothea, Konrad, Kai R., Bemm, Felix, Patir Nebioglu, Meliha Görkem, Lorey, Christian, Duscha, Kerstin, Güthoff, Tilman, Herrmann, Johannes, Ferjani, Ali, Cuin, Tracey Ann, Roelfsema, M. Rob G., Schumacher, Karin, Neuhaus, H. Ekkehard, Marten, Irene, Hedrich, Rainer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099232/
https://www.ncbi.nlm.nih.gov/pubmed/29938800
http://dx.doi.org/10.1111/nph.15280
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author Graus, Dorothea
Konrad, Kai R.
Bemm, Felix
Patir Nebioglu, Meliha Görkem
Lorey, Christian
Duscha, Kerstin
Güthoff, Tilman
Herrmann, Johannes
Ferjani, Ali
Cuin, Tracey Ann
Roelfsema, M. Rob G.
Schumacher, Karin
Neuhaus, H. Ekkehard
Marten, Irene
Hedrich, Rainer
author_facet Graus, Dorothea
Konrad, Kai R.
Bemm, Felix
Patir Nebioglu, Meliha Görkem
Lorey, Christian
Duscha, Kerstin
Güthoff, Tilman
Herrmann, Johannes
Ferjani, Ali
Cuin, Tracey Ann
Roelfsema, M. Rob G.
Schumacher, Karin
Neuhaus, H. Ekkehard
Marten, Irene
Hedrich, Rainer
author_sort Graus, Dorothea
collection PubMed
description The membrane‐bound proton‐pumping pyrophosphatase (V‐PPase), together with the V‐type H(+)‐ATPase, generates the proton motive force that drives vacuolar membrane solute transport. Transgenic plants constitutively overexpressing V‐PPases were shown to have improved salinity tolerance, but the relative impact of increasing PP(i) hydrolysis and proton‐pumping functions has yet to be dissected. For a better understanding of the molecular processes underlying V‐PPase‐dependent salt tolerance, we transiently overexpressed the pyrophosphate‐driven proton pump (NbVHP) in Nicotiana benthamiana leaves and studied its functional properties in relation to salt treatment by primarily using patch‐clamp, impalement electrodes and pH imaging. NbVHP overexpression led to higher vacuolar proton currents and vacuolar acidification. After 3 d in salt‐untreated conditions, V‐PPase‐overexpressing leaves showed a drop in photosynthetic capacity, plasma membrane depolarization and eventual leaf necrosis. Salt, however, rescued NbVHP‐hyperactive cells from cell death. Furthermore, a salt‐induced rise in V‐PPase but not of V‐ATPase pump currents was detected in nontransformed plants. The results indicate that under normal growth conditions, plants need to regulate the V‐PPase pump activity to avoid hyperactivity and its negative feedback on cell viability. Nonetheless, V‐PPase proton pump function becomes increasingly important under salt stress for generating the pH gradient necessary for vacuolar proton‐coupled Na(+) sequestration.
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spelling pubmed-60992322018-08-23 High V‐PPase activity is beneficial under high salt loads, but detrimental without salinity Graus, Dorothea Konrad, Kai R. Bemm, Felix Patir Nebioglu, Meliha Görkem Lorey, Christian Duscha, Kerstin Güthoff, Tilman Herrmann, Johannes Ferjani, Ali Cuin, Tracey Ann Roelfsema, M. Rob G. Schumacher, Karin Neuhaus, H. Ekkehard Marten, Irene Hedrich, Rainer New Phytol Research The membrane‐bound proton‐pumping pyrophosphatase (V‐PPase), together with the V‐type H(+)‐ATPase, generates the proton motive force that drives vacuolar membrane solute transport. Transgenic plants constitutively overexpressing V‐PPases were shown to have improved salinity tolerance, but the relative impact of increasing PP(i) hydrolysis and proton‐pumping functions has yet to be dissected. For a better understanding of the molecular processes underlying V‐PPase‐dependent salt tolerance, we transiently overexpressed the pyrophosphate‐driven proton pump (NbVHP) in Nicotiana benthamiana leaves and studied its functional properties in relation to salt treatment by primarily using patch‐clamp, impalement electrodes and pH imaging. NbVHP overexpression led to higher vacuolar proton currents and vacuolar acidification. After 3 d in salt‐untreated conditions, V‐PPase‐overexpressing leaves showed a drop in photosynthetic capacity, plasma membrane depolarization and eventual leaf necrosis. Salt, however, rescued NbVHP‐hyperactive cells from cell death. Furthermore, a salt‐induced rise in V‐PPase but not of V‐ATPase pump currents was detected in nontransformed plants. The results indicate that under normal growth conditions, plants need to regulate the V‐PPase pump activity to avoid hyperactivity and its negative feedback on cell viability. Nonetheless, V‐PPase proton pump function becomes increasingly important under salt stress for generating the pH gradient necessary for vacuolar proton‐coupled Na(+) sequestration. John Wiley and Sons Inc. 2018-06-25 2018-09 /pmc/articles/PMC6099232/ /pubmed/29938800 http://dx.doi.org/10.1111/nph.15280 Text en © 2018 The Authors. New Phytologist © 2018 New Phytologist Trust This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Graus, Dorothea
Konrad, Kai R.
Bemm, Felix
Patir Nebioglu, Meliha Görkem
Lorey, Christian
Duscha, Kerstin
Güthoff, Tilman
Herrmann, Johannes
Ferjani, Ali
Cuin, Tracey Ann
Roelfsema, M. Rob G.
Schumacher, Karin
Neuhaus, H. Ekkehard
Marten, Irene
Hedrich, Rainer
High V‐PPase activity is beneficial under high salt loads, but detrimental without salinity
title High V‐PPase activity is beneficial under high salt loads, but detrimental without salinity
title_full High V‐PPase activity is beneficial under high salt loads, but detrimental without salinity
title_fullStr High V‐PPase activity is beneficial under high salt loads, but detrimental without salinity
title_full_unstemmed High V‐PPase activity is beneficial under high salt loads, but detrimental without salinity
title_short High V‐PPase activity is beneficial under high salt loads, but detrimental without salinity
title_sort high v‐ppase activity is beneficial under high salt loads, but detrimental without salinity
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099232/
https://www.ncbi.nlm.nih.gov/pubmed/29938800
http://dx.doi.org/10.1111/nph.15280
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