journal article Jul 18, 2017

The Role of Na+ and K+ Transporters in Salt Stress Adaptation in Glycophytes

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References
171
[1]
Ahmad "Cellular and tissue distribution of potassium: physiological relevance, mechanisms and regulation" J. Plant Physiol. (2014) 10.1016/j.jplph.2013.10.016
[2]
Alemán "The F130S point mutation in the Arabidopsis high-affinity K+ transporter AtHAK5 increases K+ over Nacontinuously decreasing and Cs+ selectivity and confers Na+ and Cs+ tolerance to yeast under heterologous expression" Front. Plant Sci. (2014) 10.3389/fpls.2014.00430
[3]
Alemán "Differential regulation of the HAK5 genes encoding the high-affinity K+ transporters of Thellungiella halophila and Arabidopsis thaliana" Environ. Exper. Bot. (2009) 10.1016/j.envexpbot.2008.09.011
[4]
Ali "TsHKT1; 2, a HKT1 homolog from the extremophile Arabidopsis relative Thellungiella salsuginea, shows K+ specificity in the presence of NaCl" Plant Physiol. (2012) 10.1104/pp.111.193110
[5]
Almeida "Differences in shoot Na+ accumulation between two tomato species are due to differences in ion affinity of HKT1; 2" J. Plant Physiol. (2014) 10.1016/j.jplph.2013.12.001
[6]
Amin "Enhanced salt tolerance conferred by the complete 2.3 kb cDNA of the rice vacuolar Na+/H+ antiporter gene compared to 1.9 kb coding region with 5′ UTR in transgenic lines of rice" Front. Plant Sci. (2016) 10.3389/fpls.2016.00014
[7]
Andrés "Control of vacuolar dynamics and regulation of stomatal aperture by tonoplast potassium uptake" Proc. Natl. Acad Sci. U.S.A. (2014) 10.1073/pnas.1320421111
[8]
Anschütz "Going beyond nutrition: regulation of potassium homoeostasis as a common denominator of plant adaptive responses to environment" J. Plant Physiol. (2014) 10.1016/j.jplph.2014.01.009
[9]
Apse "Salt tolerance conferred by overexpression of a vacuolar Na+/H+ antiport in Arabidopsis" Science (1999) 10.1126/science.285.5431.1256
[10]
Álvarez-Aragón "Salt intolerance in Arabidopsis: shoot and root sodium toxicity, and inhibition by sodium-plus-potassium overaccumulation" Planta (2016) 10.1007/s00425-015-2400-7
[11]
Ashnest "Arabidopsis intracellular NHX-type sodium-proton antiporters are required for seed storage protein processing" Plant Cell Physiol. (2015) 10.1093/pcp/pcv138
[12]
Assaha "Salinity-induced expression of HKT may be crucial for Na+ exclusion in the leaf blade of huckleberry (Solanum scabrum Mill.), but not of eggplant (Solanum melongena L.)" Biochem. Biophys. Res. Commun. (2015) 10.1016/j.bbrc.2015.03.048
[13]
Bacha "High Ca 2+ reverts the repression of high-affinity K+ uptake produced by Na+ in Solanum lycopersycum L.(var. microtom) plants" J. Plant Physiol. (2015) 10.1016/j.jplph.2015.03.014
[14]
Barragán "Ion exchangers NHX1 and NHX2 mediate active potassium uptake into vacuoles to regulate cell turgor and stomatal function in Arabidopsis" Plant Cell (2012) 10.1105/tpc.111.095273
[15]
Bassil "The ins and outs of intracellular ion homeostasis: NHX-type cation/H+ transporters" Curr. Opin. Plant Biol. (2014) 10.1016/j.pbi.2014.08.002
[16]
Bassil "Cellular ion homeostasis: emerging roles of intracellular NHX Na+/H+ antiporters in plant growth and development" J. Exp. Bot. (2012) 10.1093/jxb/ers250
[17]
Bassil "The Arabidopsis Na+/H+ antiporters NHX1 and NHX2 control vacuolar pH and K+ homeostasis to regulate growth, flower development, and reproduction" Plant Cell (2011) 10.1105/tpc.111.089581
[18]
Benito "The twins K+ and Na+ in plants" J. Plant Physiol. (2014) 10.1016/j.jplph.2013.10.014
[19]
Berthomieu "Functional analysis of AtHKT1 in Arabidopsis shows that Na+ recirculation by the phloem is crucial for salt tolerance" EMBO J. (2003) 10.1093/emboj/cdg207
[20]
Böhm "Venus flytrap HKT1-type channel provides for prey sodium uptake into carnivorous plant without conflicting with electrical excitability" Mol. Plant (2016) 10.1016/j.molp.2015.09.017
[21]
Differential Activity of Plasma and Vacuolar Membrane Transporters Contributes to Genotypic Differences in Salinity Tolerance in a Halophyte Species, Chenopodium quinoa

Edgar Bonales-Alatorre, Igor Pottosin, Lana Shabala et al.

International Journal of Molecular Sciences 10.3390/ijms14059267
[22]
Bonales-Alatorre "Reduced tonoplast fast-activating and slow-activating channel activity is essential for conferring salinity tolerance in a facultative halophyte, quinoa" Plant Physiol. 10.1104/pp.113.216572
[23]
Bose "Kinetics of xylem loading, membrane potential maintenance, and sensitivity of K+-permeable channels to reactive oxygen species: physiological traits that differentiate salinity tolerance between pea and barley" Plant Cell Environ. (2014) 10.1111/pce.12180
[24]
Bose "Haem oxygenase modifies salinity tolerance in Arabidopsis by controlling K+ retention via regulation of the plasma membrane H+-ATPase and by altering SOS1 transcript levels in roots" J. Exp. Bot. (2013) 10.1093/jxb/ers343
[25]
Sodium efflux in plant roots: What do we really know?

D.T. Britto, H.J. Kronzucker

Journal of Plant Physiology 2015 10.1016/j.jplph.2015.08.002
[26]
Byrt "Non-selective cation channel activity of aquaporin AtPIP2; 1 regulated by Ca2+ and pH" Plant Cell Environ (2017) 10.1111/pce.12832
[27]
Cabot "Lessons from crop plants struggling with salinity" Plant Sci. (2014) 10.1016/j.plantsci.2014.04.013
[28]
Carraretto "Ion channels in plant bioenergetic organelles, chloroplasts and mitochondria: from molecular identification to function" Mol. Plant (2016) 10.1016/j.molp.2015.12.004
[29]
Chakraborty "Difference in root K+ retention ability and reduced sensitivity of K+-permeable channels to reactive oxygen species confer differential salt tolerance in three Brassica species" J. Exp. Bot. (2016) 10.1093/jxb/erw236
[30]
Chaumont "Aquaporins: highly regulated channels controlling plant water relations" Plant Physiol. (2014) 10.1104/pp.113.233791
[31]
Cheong "Two calcineurin B-like calcium sensors, interacting with protein kinase CIPK23, regulate leaf transpiration and root potassium uptake in Arabidopsis" Plant J. (2007) 10.1111/j.1365-313x.2007.03236.x
[32]
Chevalier "Trafficking of plant plasma membrane aquaporins: multiple regulation levels and complex sorting signals" Plant Cell Physiol. (2014) 10.1093/pcp/pcu203
[33]
Coskun "How high do ion fluxes go? A re-evaluation of the two-mechanism model of K+ transport in plant roots" Plant Sci. (2016) 10.1016/j.plantsci.2015.12.003
[34]
Cotsaftis "A two-staged model of Na+ exclusion in rice explained by 3D modeling of HKT transporters and alternative splicing" PLoS ONE (2012) 10.1371/journal.pone.0039865
[35]
Na+ transport in glycophytic plants: what we know and would like to know

DARREN CRAIG PLETT, INGE SKRUMSAGER MØLLER

Plant, Cell & Environment 2010 10.1111/j.1365-3040.2009.02086.x
[36]
Cuin "A root's ability to retain K+ correlates with salt tolerance in wheat" J. Exp. Bot. (2008) 10.1093/jxb/ern128
[37]
Deinlein "Plant salt-tolerance mechanisms" Trends Plant Sci. (2014) 10.1016/j.tplants.2014.02.001
[38]
Demidchik "Mechanisms and physiological roles of K+ efflux from root cells" J. Plant Physiol. (2014) 10.1016/j.jplph.2014.01.015
[39]
Demidchik "Arabidopsis root K+-efflux conductance activated by hydroxyl radicals: single-channel properties, genetic basis and involvement in stress-induced cell death" J. Cell Sci. (2010) 10.1242/jcs.064352
[40]
Demidchik "Physiological roles of nonselective cation channels in plants: from salt stress to signalling and development" New Phytol. (2007) 10.1111/j.1469-8137.2007.02128.x
[41]
Demidchik "Stress-induced electrolyte leakage: the role of K+-permeable channels and involvement in programmed cell death and metabolic adjustment" J. Exp. Bot. (2014) 10.1093/jxb/eru004
[42]
Plasma Membrane H + -ATPase Regulation in the Center of Plant Physiology

Janus Falhof, Jesper Torbøl Pedersen, Anja Thoe Fuglsang et al.

Molecular Plant 2016 10.1016/j.molp.2015.11.002
[43]
Feki "A constitutively active form of a durum wheat Na+/H+ antiporter SOS1 confers high salt tolerance to transgenic Arabidopsis" Plant Cell Rep. (2014) 10.1007/s00299-013-1528-9
[44]
Feki "Regulation of durum wheat Na+/H+ exchanger TdSOS1 by phosphorylation" Plant Mol. Biol. (2011) 10.1007/s11103-011-9787-8
[45]
Flowers "Salinity tolerance in halophytes" New Phytol. (2008) 10.1111/j.1469-8137.2008.02531.x
[46]
Fraile-Escanciano "The SOS1 transporter of Physcomitrella patens mediates sodium efflux in planta" New Phytol. (2010) 10.1111/j.1469-8137.2010.03405.x
[47]
Fujimaki "Base to tip and long-distance transport of sodium in the root of common reed (Phragmites australis Cav.) Trin. ex Steud.] at steady state under constant high-salt conditions" Plant Cell Physiol. (2015) 10.1093/pcp/pcv021
[48]
Furumoto "A plastidial sodium-dependent pyruvate transporter" Nature (2011) 10.1038/nature10250
[49]
Garciadeblás "Cloning of two SOS1 transporters from the seagrass Cymodocea nodosa. SOS1 transporters from Cymodocea and Arabidopsis mediate potassium uptake in bacteria" Plant Mol. Biol. (2007) 10.1007/s11103-006-9102-2
[50]
Garciadeblás "Sodium transport and HKT transporters: the rice model" Plant J. (2003) 10.1046/j.1365-313x.2003.01764.x

Showing 50 of 171 references

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References
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Published
Jul 18, 2017
Vol/Issue
8
Funding
The Research Council Award: 151
Cite This Article
Dekoum V. M. Assaha, Akihiro Ueda, Hirofumi Saneoka, et al. (2017). The Role of Na+ and K+ Transporters in Salt Stress Adaptation in Glycophytes. Frontiers in Physiology, 8. https://doi.org/10.3389/fphys.2017.00509
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