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salt stress response

68186 relationships annotated with this phrase. Showing first 500 of 68186.
Source entity Relationship Target entity Species
(ATAZG1, AZG1, AT3G10960) expression in lateral root (LR) primordia is sensitive to NaCl Arabidopsis thaliana
CIPKs show pronounced salt-responsive transcriptional changes transcriptional expression Marchantia polymorpha
salt responses may be some of the early functions of CBL-CIPK networks
50 mM NaCl treatment from 16 DPG onward causes changes in Photosystem II efficiency (ΦPSII) over 67 days Oryza sativa
Maize (Zea mays L.) is highly susceptible to elevated NaCl concentrations Zea mays
(ATAZG1, AZG1, AT3G10960) confers sensitivity to salinity Arabidopsis thaliana
effects of impairing xylem K+ load under salt stress were assessed by studying slskor plants Solanum lycopersicum
Regarding shoot Na+ content it was 30–38% higher in slskor plants than in the WT after the salt treatment Solanum lycopersicum
Schrenkiella parvula roots do not avoid salt Schrenkiella parvula
salt treatment (20 mM NaCl) greatly reduces IR-64 stomatal conductance (gsw) Oryza sativa
MpPUB9 modulates angle of thallus growth relative to the ground Marchantia polymorpha
amount of the MpPUB9 protein was dramatically increased via both posttranscriptional and posttranslational regulation Marchantia polymorpha
(ATNHX7, ATSOS1, SOS1, AT2G01980) was not up-regulated in (ANN1, ANNAT1, AtANN1, ATOXY5, OXY5, AT1G35720) Arabidopsis thaliana
primary root growth of Arabidopsis is strongly reduced under 125 mM NaCl Arabidopsis thaliana
In 2015 is characterized by dramatic drop in (GPP, VTC4, AT3G02870) ET, and gs for shoreline trees at GWI and MS
pH-stabilizing effect during salt stress was demonstrated K+/H+ antiport at tonoplast
NaCl causes greater net Na+ influx at root epidermal cells of (ANN1, ANNAT1, AtANN1, ATOXY5, OXY5, AT1G35720) than wild type Arabidopsis thaliana
(VQ9, AT1G78310) leads to the inactivation of (ATWRKY8, WRKY8, AT5G46350) Arabidopsis thaliana
salt stress induces abscisic acid (ABA) levels Schrenkiella parvula; Arabidopsis thaliana
SKT1506 cultivar is more salt-sensitive than PN28 cultivar with respect to shoot growth Zea mays
MpPUB9 protein functions as positive regulator of stress response under high-salt conditions Marchantia polymorpha
salt stress suppresses root growth by interfering with cell cycle progression in the root apical meristem (RAM)
ABA levels in roots of S. parvula are further elevated under 175 mM NaCl after 3 h Schrenkiella parvula
reduction in gs and Ψleaf from R.M. alone at GWI and MS becomes more significant after 2015
Sixteen-day-old seedlings were treated with 150 mM NaCl for 6 h Oryza sativa L. ssp. Japonica
net H+ efflux in roots persists at mild and intermediate stress (60 and 120 mM NaCl) Zea mays
MpPUB9 level is affected by high-salt treatments Marchantia polymorpha
genes in cluster 1 have similar expression profiles at 3 h but diverge at 2-d/48 h timepoint Schrenkiella parvula; Arabidopsis thaliana
OsEPF1oe plants are less susceptible to salinity toxicity Oryza sativa
relative insensitivity of S. parvula root growth under salt stress is consistent with more stable carbon partitioning toward roots Schrenkiella parvula
MpCBL-C was downregulated in Tak-1 under 50 and 100 mM NaCl treatments Marchantia polymorpha
OsEPF1oe plant leaves continue to show slower decline in health than majority of other varieties after 41 DPG Oryza sativa
MpEXO70.1-overexpressing transgenic plants were generated to reinforce the functional and physiological relation between MpPUB9 and MpEXO70.1 under high-salt conditions Marchantia polymorpha
regulation of autoubiquitination level may not serve as primary mechanism for the extended half-life of MpPUB9 under high salinity Marchantia polymorpha
(ATNHX7, ATSOS1, SOS1, AT2G01980) was up-regulated in wild-type roots to levels comparable with a previous study on chronic salinity stress Arabidopsis thaliana
(ATAZG1, AZG1, AT3G10960) expression pattern in the root system is highly dependent on NaCl Arabidopsis thaliana
xylem K+ transport is crucial for salt tolerance in different plant species
ABA levels in roots of Arabidopsis are increased under salt but much lower than in S. parvula roots Arabidopsis thaliana; Schrenkiella parvula
salt treatment (20 mM NaCl) results in increase in stomatal density (SD) Oryza sativa
OsEPF1oe plants maintained higher leaf photosystem II quantum yield (ΦPSII) values when grown in salt water Oryza sativa
decreased level of MpEXO70.1 resulting in hyponastic growth of thallus Marchantia polymorpha
primary root growth of S. parvula is enhanced by 125 mM NaCl Schrenkiella parvula
MAP KINASE17 (ATMPK17, MPK17, AT2G01450) is involved in peroxisome proliferation in response to NaCl stress Arabidopsis thaliana
(PMD1, AT3G58840) mutant shows no substantial impact on survival or growth under high-NaCl conditions Arabidopsis thaliana
CHXs contribute to tolerance to salt stress Glycine max
salt-treated epidermal bladder cells (EBC) can reach diameters of 1.6 mm Mesembryanthemum crystallinum
(WDL5, AT4G32330) participates in microtubule reassembly
microtubule reorganization is associated with increased [Ca2+]cyt levels under salt stress
transgenic plants overexpressing only (AT-NHX1, ATNHX, ATNHX1, NHX1, AT5G27150) failed to detect any increased salt tolerance in more than 100 independent transgenic lines Arabidopsis thaliana
(PFD3, AT5G49510) mutant shows dramatic inhibition of leaf development Arabidopsis thaliana
experiments under salinity conditions showed that SlSKOR could be an important factor for tomato salt tolerance Solanum lycopersicum
higher NaCl bypass in suberin-deficient mutants fits well with higher salt tolerance of increased suberin mutants Arabidopsis thaliana
MpPUB9-Citrine from thalli treated with CHX and 300 mM NaCl had significantly extended half-life of 60 min Marchantia polymorpha
changes in MpCBL-A/B expression were not consistent between two accessions Marchantia polymorpha
both cipk-b mutants showed increased chlorosis and death from as low as 50 mM NaCl compared with WT plants Marchantia polymorpha
protein stabilities of MpPUB9-Citrine and MpEXO70.1-3xFlag were increased and decreased, respectively, in response to high-salt conditions Marchantia polymorpha
sodium chloride induced (ATAZG1, AZG1, AT3G10960) transcription at a higher rate than Arabidopsis thaliana
PpCIPK1 has been characterised to function in salt tolerance Physcomitrium patens
upland trees at BC show much slower decline in leaf (GPP, VTC4, AT3G02870) ET, and gs
salinity impacts maize cultivars differing in salt tolerance Zea mays
GABA shunt is activated by acidification of the cytosol and salinity Zea mays
common underlying stress responses exist between S. parvula and Arabidopsis Schrenkiella parvula; Arabidopsis thaliana
calcineurin B-like (CBL) and CBL-interacting protein kinase (CIPK) expression analysed during salt stress Marchantia polymorpha
stomatal size (SS) and stomatal density (SD) do not appear to be associated with degree of salinity tolerance Oryza sativa
seawater exposure affects likelihood of mortality
(ANN1, ANNAT1, AtANN1, ATOXY5, OXY5, AT1G35720) loss-of-function mutant has maximum mean net Na+ influx significantly higher than wild type Arabidopsis thaliana
cytokinin influences plants' ability to tolerate sodium chloride in the soil Arabidopsis thaliana
transcriptomic changes in WT liverwort under high-salt conditions were analyzed to investigate the biological processes involved in the regulation of MpPUB9-mediated salt stress responses Marchantia polymorpha
(VQ9, AT1G78310) and (ATWRKY8, WRKY8, AT5G46350) act antagonistically to mediate salt stress response Arabidopsis thaliana
modules of coexpressed genes with different expression strengths in salt-adapted species Eutrema salsugineum were identified compared with Arabidopsis thaliana Eutrema salsugineum; Arabidopsis thaliana
atnig1-1 knockout mutant shows enhanced sensitivity to salt stress Arabidopsis thaliana
increased salt tolerance is usually assumed to result from greater antiporter activity of (ATNHX7, ATSOS1, SOS1, AT2G01980) Saccharomyces cerevisiae
root cells of Thellungiella and Arabidopsis under identical salt treatment experience the same Na+ concentration identical salt treatment Thellungiella; Arabidopsis thaliana
knock-down of (ATNHX7, ATSOS1, SOS1, AT2G01980) by RNAi transforms Thellungiella into a salt-sensitive species Thellungiella
lower Na+ permeability of VICs is not sufficient for salt tolerance
overexpression of (ATNHX7, ATSOS1, SOS1, AT2G01980) increases salt tolerance in transgenic plants Arabidopsis thaliana
(ATGH9A1, DEC, GH9A1, IRX2, KOR, KOR1, RSW2, TSD1, AT5G49720) mutant is salt-sensitive Arabidopsis thaliana
(ATAZG1, AZG1, AT3G10960) gene expression is rapidly induced in roots after treatment with 150 mM sodium chloride Arabidopsis thaliana
WT plants showed tolerance up to 150 mM NaCl Marchantia polymorpha
salt-treated IR-64 plants have A and gsw rates no longer significantly higher than OsEPF1oe lines Oryza sativa
R.M. (root mortality) alone at BC, MS, and GWI affects physiological traits, growth and mortality of shoreline trees in similar ways shoreline trees
phosphorylation of Ser108 of AtUNE12 activated its binding to G-box and LTRE15 motifs Arabidopsis thaliana
(ATAZG1, AZG1, AT3G10960) localization makes it unlikely to be involved in cytokinin (CK)-based root-shoot communication in response to increased soil sodicity Arabidopsis thaliana
(CC1, AT2G16940) and (CC2, AT5G42860) aid plant growth and biomass production during salt stress Arabidopsis thaliana
prolonged exposure to elevated salt concentrations will cause root damage
15-d-old seedlings were treated with 150 mM NaCl solution for 3–5 d Oryza sativa L. ssp. Japonica
long-term H+ influx was previously reported in NaCl-exposed Populus roots Populus trichocarpa
impairment in [Ca2+]cyt signaling is reflected in poor ability of (ANN1, ANNAT1, AtANN1, ATOXY5, OXY5, AT1G35720) roots to up-regulate NaCl-responsive transcripts Arabidopsis thaliana
(ANN1, ANNAT1, AtANN1, ATOXY5, OXY5, AT1G35720) could contribute to plasma membrane Ca2+ influx pathway acting downstream of NADPH oxidase activity in salt stress Arabidopsis thaliana
salt stress also imposes osmotic stress to plants
OsEPF1oe plants have stomatal conductance (gsw) remain low between freshwater controls and salt-treated equivalents Oryza sativa
fluorescent Förster Resonance Energy Transfer (FRET)-based calcium (Ca 2+) reporter proteins revealed specific chloroplast calcium (Ca 2+) signals in response to salt stress
leaf (GPP, VTC4, AT3G02870) rapidly drops to near zero in the first year after seawater exposure
upregulation of MpPUB9 in response to salt stress is via translational regulation Marchantia polymorpha
effect of azg1-1 × azg2-1 mutations on lateral root density depended on salt concentration Arabidopsis thaliana
140 mM NaCl treatment causes decrease in Arabidopsis root growth rate Arabidopsis thaliana
salt treatment does not affect stomatal size (SS) Oryza sativa
plants with lowest stomatal density (SD) accumulate significantly less salt in their leaves Oryza sativa
higher NaCl bypass in suberin-deficient mutants fits well with salt hypersensitivity of further decreased suberin mutants Arabidopsis thaliana
osmads56 mutants, OsMADS56 overexpressing lines, and corresponding WT were assessed for seed germination under salt treatment Oryza sativa L. ssp. Japonica
MpPUB9 plays crucial roles as a positive regulator under conditions of high salinity Marchantia polymorpha
Schrenkiella parvula seedlings experienced much less inhibition of primary root growth under salt concentrations up to 200 mM NaCl Schrenkiella parvula
MpPUB9 gene expression levels increased precipitously under high-salt treatment Marchantia polymorpha
sustained increases in [Ca 2+ ] i following NaCl stimulation detected in all cell types except the epidermal pavement cells
salinisation of arable land reduces plant yield
Tak-1, Tak-2, Cam-1 and Cam-2 plants demonstrate similar salt tolerance responses from 0 to 150 mM salt Marchantia polymorpha
salt toxicity often leads to deficiencies in potassium ions (K+)
net H+ efflux in roots of PN28 is particularly pronounced in more tolerant PN28 cultivar Zea mays
NaCl treatment provoked upregulation of 1400 genes and the down-regulation of 309 genes Marchantia polymorpha
root transcriptomic analysis of Schrenkiella parvula revealed induction of sugar transporters Schrenkiella parvula
effects of R.M. + C.V. on gs and Ψleaf at GWI and MS start to slightly decrease around 2012 and become more significant after 2015
seeds were placed in ½-strength Murashige & Skoog medium (½ MS medium) supplemented with 150 mM NaCl Oryza sativa L. ssp. Japonica
partial recovery of Arabidopsis root growth from 5 to 9 h after salt treatment results in slower growth rates overall compared with control conditions Arabidopsis thaliana
suberin deposition between the endodermal plasma membrane and the cell wall is induced by salt stress Arabidopsis thaliana
MpCIPK-B responds specifically to ionic stress Marchantia polymorpha
both cipk-b mutant lines showed decreased growth and biomass under mild salt stress (50 mM NaCl) compared with WT plants Marchantia polymorpha
potassium (K) levels show no differences across genotypes or treatments Oryza sativa
From 2000 to 2013 is characterized by slight drop in % live crown and k/kmax of shoreline trees at GWI and MS
MpPUB9 is upregulated in response to salt stress conditions Marchantia polymorpha
dynamics of the NaCl-induced [Ca 2+ ] i signals from mesophyll and vasculature cells more complex mesophyll cells reporting a sustained [Ca 2+ ] i peaking 120 s after stimulation
dynamics of the NaCl-induced [Ca 2+ ] i signals from mesophyll and vasculature cells in the vasculature, prolonged relaxation kinetics following initial transient
reducing active cytokinin amount increases resistance to salt stress
75 and 125 mM NaCl treatment reduces lateral root elongation more than primary root elongation Arabidopsis thaliana
halotropism is common strategy used by glycophytic species such as Arabidopsis and Solanum lycopersicum Arabidopsis thaliana; Solanum lycopersicum
halotropism enables primary root active growth away from high salt concentrations Arabidopsis thaliana; Solanum lycopersicum
relative insensitivity of S. parvula root growth under salt stress is consistent with suberization Schrenkiella parvula
treatments with 100 and 150 mM NaCl caused significant decreases in fresh weight relative to control plants Marchantia polymorpha
mppub9 knock-out mutant lines were more susceptible to high-salinity conditions Marchantia polymorpha
Up-regulation of AtRD29A was significantly lower in (ANN1, ANNAT1, AtANN1, ATOXY5, OXY5, AT1G35720) compared with wild type Arabidopsis thaliana
Arabidopsis mutant in the SYP41-interacting protein Tonneau1 is sensitive to salt stress Arabidopsis thaliana
improved salt tolerance through maintaining ΔpH and reducing vacuolar calcium release Arabidopsis thaliana
increase in ploidy may contribute to salt tolerance Mesembryanthemum crystallinum
EBC transcriptome had 8,285 out of 37,341 transcripts significantly differentially expressed in response to salt stress Mesembryanthemum crystallinum
ectopic expression of GhMPK6a reduced salt tolerance Nicotiana benthamiana
wdl5-1 mutant seedlings show approximately 50% death at 125 mM NaCl treatment Arabidopsis thaliana
ethylene signaling positively regulates cortical microtubule reassembly
IDS1 bound to promoter region of (ATNHX7, ATSOS1, SOS1, AT2G01980) Oryza sativa
(ATNHX7, ATSOS1, SOS1, AT2G01980) + (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) + (ATSOS3, CBL4, SOS3, AT5G24270) genes improved salt tolerance in yeast Saccharomyces cerevisiae
loss-of-function mutations in (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) cause hypersensitivity to NaCl Arabidopsis thaliana
(ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) is involved in the regulation of H+/Ca2+ antiporter Arabidopsis thaliana
triple mutant m123-2 shows decreased tolerance to salt stress Arabidopsis thaliana
cytoskeleton plays an essential role in plant tolerance to salt stress Arabidopsis thaliana
suberin deposition extends coverage of endodermal cells Arabidopsis thaliana
increased amount of MpPUB9 protein in response to high-salt treatment subsequently level of MpEXO70.1 decreased in a proteasome-dependent manner Marchantia polymorpha
(ATMPK17, MPK17, AT2G01450) and (PMD1, AT3G58840) act in salt-responsive peroxisome division pathway Arabidopsis thaliana
salt-induced alterations in ploidy levels were not observed in shoot tissue Sorghum bicolor
SOS2-like proteins (PKS/CIPKs) there are 23 additional SOS2-like proteins Arabidopsis thaliana
transgenic plants overexpressing (AT-NHX1, ATNHX, ATNHX1, NHX1, AT5G27150) + (ATSOS3, CBL4, SOS3, AT5G24270) found similar salt-tolerant phenotypes compared to transgenic plants overexpressing only (ATSOS3, CBL4, SOS3, AT5G24270) Arabidopsis thaliana
control plants exhibit decreased total chlorophyll content
plasma membrane Na+/H+ antiporter (ATNHX7, ATSOS1, SOS1, AT2G01980) transcript level was higher in Thellungiella than in Arabidopsis in control conditions Thellungiella; Arabidopsis thaliana
(ATNHX7, ATSOS1, SOS1, AT2G01980) is required to avoid Na+ influx from the root tip into the root elongation zone during early stages of salt stress Thellungiella
autophosphorylation plays a role in regulation of (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) Arabidopsis thaliana
autophosphorylation on Ser228 is involved in function of (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) under salt stress
(PFD5, AT5G23290) mutants are hypersensitive to elevated concentrations of NaCl Arabidopsis thaliana
salt stress suppresses root growth by reducing elongation of mature cells
downregulation of CIPK-B was observed in greater number of salt stress treatments than CIPK-A Marchantia polymorpha
rising salinity affects rice yields Oryza sativa
salt-treated OsEPF1oeW seedlings have significantly more stomata per mm² than fresh-water grown plants Oryza sativa
H+ influx was not observed in salt-sensitive SKT1506 when roots were challenged with 180 mM NaCl Zea mays
degradation pattern of HA-MpEXO70.1 was also slightly promoted in the presence of 300 mM NaCl-treated WT crude extract Marchantia polymorpha
SOS3-SOS2 complex directly phosphorylates (ATNHX7, ATSOS1, SOS1, AT2G01980) C terminus Arabidopsis thaliana
(ABI1, AtABI1, AT4G26080) and (AHG3, ATPP2CA, PP2CA, AT3G11410) are essential for plant tolerance to salt stress Arabidopsis thaliana
(AtbZIP59, bZIP59, PosF21, AT2G31370) functions downstream of salt overly sensitive signaling pathway Arabidopsis thaliana
wild-type (ATMPK17, MPK17, AT2G01450) expressed under its native promoter in -1 background restores peroxisome proliferation on NaCl Arabidopsis thaliana
high salinity conditions induces hyperosmotic stress
ethylene signaling is critical for microtubule reassembly in response to salt stress Arabidopsis thaliana
transgenic plants overexpressing (ATNHX7, ATSOS1, SOS1, AT2G01980) + (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) + (ATSOS3, CBL4, SOS3, AT5G24270) salt tolerance appeared similar to transgenic plants overexpressing (ATNHX7, ATSOS1, SOS1, AT2G01980) alone Arabidopsis thaliana
(ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) and (ATSOS3, CBL4, SOS3, AT5G24270) overexpression line alleviates salt inhibition of lateral root development
(ATNHX7, ATSOS1, SOS1, AT2G01980) (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) and (ATSOS3, CBL4, SOS3, AT5G24270) overexpression line alleviates salt inhibition of lateral root development
transgenic plants and control plants show inhibited lateral root development
Thellungiella accumulates less Na+ in shoot than Arabidopsis Thellungiella; Arabidopsis thaliana
Thellungiella effectively restricts Na+ accumulation in the shoots Thellungiella
seedlings on MS plates were transferred to filter paper saturated with 300 mM NaCl in deionized water
m23-2 mutant shows decreased tolerance to high salinity
actin levels in (PFD5, AT5G23290) mutants decrease in (PFD5, AT5G23290) mutants when growing in conditions of NaCl stress Arabidopsis thaliana
wdl5-1 mutant seedlings show approximately 10% survival at 200 mM NaCl treatment Arabidopsis thaliana
ethylene signaling mediates salt tolerance
transgenic plants overexpressing (AT-NHX1, ATNHX, ATNHX1, NHX1, AT5G27150) show no difference in K+ content compared to control plants with or without salt treatment
transgenic plants expressing the T168D form of (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) in wild-type background had improved salt tolerance Arabidopsis thaliana
cell files in primary root elongation zone appeared undisturbed by NaCl stress Arabidopsis thaliana
pht4;6-1 allele is linked tightly to NaCl-sensitive phenotype Arabidopsis thaliana
SOS3-like CALCIUM-BINDING PROTEIN1 (ATCBL2, CBL2, SCaBP1, AT5G55990) -regulated SOS2-like protein kinase24 (ATCIPK14, ATSR1, CIPK14, PKS24, SnRK3.15, SR1, AT5G01820) kinase activity is important for inactivating Arabidopsis plasma membrane proton-translocating adenosine triphosphatase (H+-ATPase) Arabidopsis thaliana
pmd1-1 mutant does not proliferate peroxisomes in response to NaCl stress Arabidopsis thaliana
peeled bract leaf from salt-treated plant much larger proportion of 32C and 64C nuclei Mesembryanthemum crystallinum
transgenic lines overexpressing (ATSOS3, CBL4, SOS3, AT5G24270) exhibit lesser decline in total chlorophyll content
(AT-NHX1, ATNHX, ATNHX1, NHX1, AT5G27150) and (ATSOS3, CBL4, SOS3, AT5G24270) overexpression line alleviates salt inhibition of lateral root development
(ATCDSP32, CDSP32, TRXL1, AT1G76080) thioredoxin abundance is higher under salt treatment Thellungiella; Arabidopsis thaliana
ThSOS1 induction in Thellungiella leaves during salt stress was confirmed at the protein level using antibody against (ATNHX7, ATSOS1, SOS1, AT2G01980) Thellungiella
transgenic plants expressing mutated (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) at Ser228 phenotype is consistent with enhancement of activity Arabidopsis thaliana
(PFD3, AT5G49510) mutants are hypersensitive to elevated concentrations of NaCl Arabidopsis thaliana
cytoskeleton might involve in proper localization of specific Na+ transporters such as (ATNHX7, ATSOS1, SOS1, AT2G01980) Arabidopsis thaliana
Col-0 parental line used as parental line in salt-stress experiments
wild-type seedlings carrying GFP-PTS1 reporter treated with NaCl and oryzalin increased peroxisome numbers were not reduced in seedlings treated with NaCl and oryzalin Arabidopsis thaliana
epidermal bladder cells (EBC) show spatially related differences in cell size Mesembryanthemum crystallinum
165 genes in RECT gene set 43 genes (39%) show significantly differential expression between salt-treated and control EBC Mesembryanthemum crystallinum
histones down-regulated in EBC from salt-treated plants Mesembryanthemum crystallinum
root transcriptome compared with only 53 differentially expressed transcripts out of 53,516 in roots Mesembryanthemum crystallinum
(GL2, AT1G79840) in roots showed no change in expression upon salt stress Mesembryanthemum crystallinum
ethylene signaling is involved in plant salt tolerance
ethylene signaling enhances salt tolerance
ethylene-mediated salt tolerance occurs via EIN3-dependent manner
plasma membrane (PM) H+-ATPase plays regulatory roles in response to saline stress Arabidopsis thaliana
NAMATAF1/2 and CUC TFs (NACs) regulate salinity tolerance in rice Oryza sativa
rice QTLs control salt tolerance Oryza sativa
transgenic plants overexpressing (ATSOS3, CBL4, SOS3, AT5G24270) accumulate same level of K+ as control plants under normal conditions but more K+ than control plants under salt treatment
transgenic plants overexpressing (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) and (ATSOS3, CBL4, SOS3, AT5G24270) accumulate same level of K+ as control plants under normal conditions but more K+ than control plants under salt treatment
(PHT4;6, AT5G44370) is a determinant of salt tolerance Arabidopsis thaliana
N-glycosylation of proteins and cell wall synthesis are essential for salt tolerance Arabidopsis thaliana
(ATSOS3, CBL4, SOS3, AT5G24270) and -like CALCIUM-BINDING PROTEIN8 (ATCBL10, CBL10, SCABP8, AT4G33000) interact with and activate (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) protein kinase Arabidopsis thaliana
43 genes showing differential expression compared with only 22% of total transcripts in EBC transcriptome (8,285 out of 37,341) Mesembryanthemum crystallinum
IDS1 regulates plant salt tolerance Oryza sativa
(ATCBL10, CBL10, SCABP8, AT4G33000) appears to be the main mediator for salt tolerance in shoots Arabidopsis thaliana
additive effect of (AT-NHX1, ATNHX, ATNHX1, NHX1, AT5G27150) overexpression when combined with (ATSOS3, CBL4, SOS3, AT5G24270) was not detected under assay conditions tested Arabidopsis thaliana
Thellungiella treated with 250 mM NaCl showed similar transcript response as Arabidopsis treated with 150 mM NaCl Thellungiella; Arabidopsis thaliana
(ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) is involved in the regulation of (ATNHX7, ATSOS1, SOS1, AT2G01980) Arabidopsis thaliana
reduction of actin levels in the (PFD5, AT5G23290) mutant does not appear to increase sensitivity to NaCl Arabidopsis thaliana
NPK1-like genes (OsNPKLs) are strongly induced by salt stress Oryza sativa
OsCIPK15 overexpression line results in increased salinity tolerance Oryza sativa
hasty mutant is heightened in sensitivity to salt Arabidopsis thaliana
transcriptomic analysis identified alternative oxidase 1a (AOX1A, ATAOX1A, AtHSR3, HSR3, AT3G22370) Arabidopsis thaliana
(AOX1A, ATAOX1A, AtHSR3, HSR3, AT3G22370) overexpression in myb30-2 background exhibit elevated salt tolerance Arabidopsis thaliana
sumoylation of (ATMYB30, MYB30, AT3G28910) contributes to transcriptional upregulation of (ATMYB30, MYB30, AT3G28910) Arabidopsis thaliana
salt stress causes inhibition of specific protein expression
largest leaf nuclei detected in epidermal peels from lower surface of leaves from salt-treated plants Mesembryanthemum crystallinum
epidermal bladder cells (EBC) of flower buds diameters of up to 136 μm detected Mesembryanthemum crystallinum
single round of endoreduplication induced by salinity from 256C to 512C detected initially solely from flow cytometry data Mesembryanthemum crystallinum
M. crystallinum SMR gene was down-regulated upon salt treatment Mesembryanthemum crystallinum
high salinity conditions induces ionic stress
ethylene signaling participates in regulation of cortical microtubule reorganization in response to salt stress Arabidopsis thaliana
ids1-1 mutant had expression levels of ZFP179 significantly increased in ZFP179 Oryza sativa
GmCaM4 mediates salt-induced Ca2+ signaling Glycine max
(ATNHX7, ATSOS1, SOS1, AT2G01980) overexpression line alleviates salt inhibition of lateral root development
(ATNHX7, ATSOS1, SOS1, AT2G01980) is required to recover Na+ from the xylem during prolonged salt stress Thellungiella
yeast gim3Δ mutant exhibits almost wild-type phenotype to NaCl Saccharomyces cerevisiae
(PFD5, AT5G23290) mutant has fresh weight approximately 32% of wild-type plants under 100 mM NaCl Arabidopsis thaliana
constitutive expression of PHT4;6:GFP in pht4;6-1 and pht4;6-2 genetic backgrounds restored salt tolerance to level comparable to isogenic wild-type lines Arabidopsis thaliana
Arabidopsis is sensitive to soil concentrations of Na+, K+, Mg2+, Li+, and borate Arabidopsis thaliana
(ATGSTU24, GST, GSTU24, AT1G17170) gene from Escherichia coli overexpression in tobacco enhanced salt tolerance Nicotiana tabacum
mpk17-1 mutant does not proliferate peroxisomes in response to NaCl stress Arabidopsis thaliana
stems and flower buds from salt-treated plants possessed largest nuclei found in plant Mesembryanthemum crystallinum
genes associated with replicative helicase and GINS complex significantly up-regulated in EBC from salt-treated plants Mesembryanthemum crystallinum
root transcripts associated with positive regulators of endoreplication were not significantly up-regulated under salt stress Mesembryanthemum crystallinum
(WDL5, AT4G32330) participates in ethylene-mediated microtubule reassembly
(ATNHX7, ATSOS1, SOS1, AT2G01980) plays important roles in regulating Arabidopsis salt tolerance Arabidopsis thaliana
m123-2 mutant shows increased inhibition of seedling growth by salt compared to wild-type
lower epidermis of salt-treated branch leaves ploidy up to 512C was detected Mesembryanthemum crystallinum
transgenic plants overexpressing (ATNHX7, ATSOS1, SOS1, AT2G01980) shows reduced salt-induced decrease in lateral root number
HOS3 ORF under control of 35SCaMV promoter restores wild-type NaCl-root growth sensitivity Arabidopsis thaliana
all mutants containing the m3-2 mutant allele showed decreased tolerance to high salinity Arabidopsis thaliana
150 mM NaCl treatment inhibits seedling growth
pht4;6-1 mutant is moderately sensitive to K2SO4 stress Arabidopsis thaliana
antisense plants of Arabidopsis Vesicle-Associated Membrane Protein 7C showed improved salt tolerance Arabidopsis thaliana
actin cytoskeleton is required for NaCl-induced peroxisome division Arabidopsis thaliana
root tissue from salt-treated plants mean ploidy level showed significant increase between salt-treated and untreated root tissue Mesembryanthemum crystallinum
bract leaf lower epidermis EBC from salt-treated plants ploidy levels of up to 2,048C estimated Mesembryanthemum crystallinum
plants have evolved transcriptional cascade
soil salinity is a common factor affecting rice grain yield Oryza sativa
TsVP overexpression improves salt tolerance Zea mays; Gossypium hirsutum
Ser228 is autophosphorylation site on (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410)
(ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) phosphorylates Ser or Thr residues in RXX(S/T) and KXX(S/T) motifs Arabidopsis thaliana
late embryogenesis abundant (LEA, AT2G21490) proteins are induced in by salt vegetative tissues
DICER-LIKE (DCL) 1 mutant alleles engenders hypersensitivity to high salt stress Arabidopsis thaliana
(HOS15, OLI1, AT5G67320) protein is induced by high-salinity stress Arabidopsis thaliana
nitric oxide (NO) is involved in responses to salt stress
two-week-old seedlings treated with NaCl (300 mM)
(ATSIZ1, SIZ1, AT5G60410) SUMOylates (ATMYB30, MYB30, AT3G28910) Arabidopsis thaliana
SIZ1-mediated SUMOylation is involved in plant salt tolerance Arabidopsis thaliana
Fe, P and S were not significantly different between genotypes Hordeum vulgare
salt-treatment caused significant increase in K concentration in maturation zone of Sahara Hordeum vulgare
Sahara has increased mature cortical cell size in response to salt stress barley
salt stress decreases branch angle
(XTH23, XTR6, AT4G25810) mutant LRs sensitive to salt Arabidopsis thaliana
posttranslational regulation is one way in which MAPs can facilitate microtubule reorganization
(ERF109, RRTF1, AT4G34410) is involved in regulation of salt tolerance in plants
salt stress is characterized by excess of toxic ions such as Na+ and Cl-
different PFD subunits do not have exactly the same function in response of yeast to salt stress Saccharomyces cerevisiae
yeast mutants sensitivity to salt stress was assessed by growth on YEPD plus 1.2 M NaCl Saccharomyces cerevisiae
High extracellular salinity increases net K+ efflux from roots
ZmPP2C overexpression in Arabidopsis decreased tolerance to salt stress Arabidopsis thaliana
mpk17-1 mutant does not display detectable tolerance to NaCl Arabidopsis thaliana
IDS1 plays negative role in rice salt tolerance Oryza sativa
transgenic lines overexpressing (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) and (ATSOS3, CBL4, SOS3, AT5G24270) exhibit lesser decline in total chlorophyll content
two large gene clusters represented expression profile of up-regulated and down-regulated genes Thellungiella
autophosphorylation on Ser228 might be involved in (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) function under salt stress
ERF#011 is involved in salt stress response Arabidopsis thaliana
MT defects in (PFD3, AT5G49510) and (PFD5, AT5G23290) mutants only affect Arabidopsis response to elevated concentrations of NaCl Arabidopsis thaliana
sucrose exacerbates mutant phenotypes Arabidopsis thaliana
Transcripts of Dehydration-Responsive Element Binding2A (AtDREB2A) were significantly up-regulated in wild type and (ANN1, ANNAT1, AtANN1, ATOXY5, OXY5, AT1G35720) roots at 24 h of NaCl exposure Arabidopsis thaliana
(FLA4, SOS5, AT3G46550) SALT-OVERLY SENSITIVE5 was identified in screen for salt sensitivity in roots Arabidopsis thaliana
(AtLEA14, LEA1, LEA14, LSR3, AT1G01470) positively regulates rice salt tolerance Oryza sativa
transgenic Arabidopsis plants overexpressing (ATNHX7, ATSOS1, SOS1, AT2G01980) + (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) + (ATSOS3, CBL4, SOS3, AT5G24270) did not observe greatly increased salt tolerance in compared to transgenic plants overexpressing either (ATNHX7, ATSOS1, SOS1, AT2G01980) or (ATSOS3, CBL4, SOS3, AT5G24270) alone Arabidopsis thaliana
(ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) is involved in the regulation of NUCLEOSIDE DIPHOSPHATE KINASE2 (ATNDPK2, NDPK IA, NDPK IA IA, NDPK1A, NDPK2, AT5G63310) Arabidopsis thaliana
SOS3-like CALCIUM-BINDING PROTEIN (SCaBP) and SOS2-like protein kinase (PKS) regulatory mechanism is novel regulatory mechanism in plants Arabidopsis thaliana
Wm and TyrA23 have been previously reported to negatively affect ROS production in RbohD-dependent manner in response to salt stimulus Arabidopsis thaliana
negative regulators of endoreplication (E−) show significant increases in transcript levels in EBC when treated with salt Mesembryanthemum crystallinum
(GL2, AT1G79840) in EBC shows almost 6-fold increase in expression upon salt stress Mesembryanthemum crystallinum
cortical microtubules participate in adaptation of plants to salt stress
wild-type seedlings treated with NaCl and Ag+ show dramatically decreased survival rates Arabidopsis thaliana
phosphatidic acid (PA) directly binds (ATMAP65-1, MAP65-1, AT5G55230)
protein degradation and PA-mediated posttranslational regulation appear to contribute to microtubule-mediated salt stress responses
plants have evolved salt overly sensitive (SOS) pathway
APETALA2/ethylene response factors ( (AP2, AtAP2, FL1, FLO2, AT4G36920) /ERFs) regulate salinity tolerance in rice Oryza sativa
salt stress requires ion transport and compartmentation Oryza sativa
IDS1-OE plants had survival rate significantly lower than wild-type plants Oryza sativa
transgenic lines overexpressing (AT-NHX1, ATNHX, ATNHX1, NHX1, AT5G27150) and (ATSOS3, CBL4, SOS3, AT5G24270) exhibit lesser decline in total chlorophyll content
(ATNHX7, ATSOS1, SOS1, AT2G01980) was more strongly induced by salt in Thellungiella than in Arabidopsis in shoots Thellungiella; Arabidopsis thaliana
150 mM NaCl treatment causes chlorosis of cotyledons and leaves
epidermal bladder cells (EBC) swell significantly when plants are treated with salt Mesembryanthemum crystallinum
peeled branch leaf from salt-treated plants salt treatment resulted in significant increase in 32C and 64C nuclei Mesembryanthemum crystallinum
ethylene signaling facilitates salt stress-induced reassembly of cortical microtubules Arabidopsis thaliana
alteration of biphasic dynamics of cortical microtubules significantly decreases survival rate of seedlings under salt stress Arabidopsis thaliana
IDS1 RNAi lines (RI-1, RI-2, RI-3) showed greatly enhanced salt tolerance Oryza sativa
IDS1-OE plants had expression levels of LEA1 downregulated in (AtLEA14, LEA1, LEA14, LSR3, AT1G01470) Oryza sativa
ionic stress and osmotic stress lead to nutritional disorders
transgenic Arabidopsis plants overexpressing (ATNHX7, ATSOS1, SOS1, AT2G01980) + (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) + (ATSOS3, CBL4, SOS3, AT5G24270) did not show greatly improved salt tolerance Arabidopsis thaliana
(ATSOS3, CBL4, SOS3, AT5G24270) functions mainly in roots may not show more salt tolerance because (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) and (ATSOS3, CBL4, SOS3, AT5G24270) may not function optimally with (ATNHX7, ATSOS1, SOS1, AT2G01980) in shoots Arabidopsis thaliana
Arabidopsis exposed to a very short salt shock (2 h in 250 mM NaCl) identified by RIKEN array as having 40 transcripts as up-regulated Arabidopsis thaliana
seedlings on filter paper saturated with 300 mM NaCl were incubated for 4 hours
disruption of MTs prevented seedling lethality Arabidopsis thaliana
pht4;6-1 mutant is hypersensitive to KCl stress Arabidopsis thaliana
pht4;6.2 mutant line used in salt-stress experiments
(APR, APR1, ATAPR1, PRH19, AT4G04610) (adenosine-5′-phosphosulfate reductase) is regulated by salinity levels
ced2 mutant shows no significant difference in seed germination Arabidopsis thaliana
relocalization and dissociation of (RIC1, AT2G33460) from microtubules favors microtubule reassembly
IDS1 repressed expression of (ATNHX7, ATSOS1, SOS1, AT2G01980) Oryza sativa
regulatory pathway that coordinately controls the transport of Na+ across cellular membranes has been established ion homeostasis
constitutive overexpression of (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) and (ATSOS3, CBL4, SOS3, AT5G24270) in other cells could disturb coordinative functions of other proteins Arabidopsis thaliana
transgenic plants overexpressing (ATSOS3, CBL4, SOS3, AT5G24270) accumulate less Na+ than control plants under normal and salt treatment conditions
triple mutant m123-2 showed decreased tolerance to salt stress Arabidopsis thaliana
ABA signaling is critical in plant response to salt stress
gim1Δ mutants are sensitive to salt stress Saccharomyces cerevisiae
(ATSOS3, CBL4, SOS3, AT5G24270) and -like CALCIUM-BINDING PROTEIN8 (ATCBL10, CBL10, SCABP8, AT4G33000) perceive calcium signal Arabidopsis thaliana
SOS3-SOS2 complex further activates (ATNHX7, ATSOS1, SOS1, AT2G01980) Arabidopsis thaliana
GhMPK17 overexpression in Arabidopsis leads to increased tolerance of salinity stress Arabidopsis thaliana
512C ploidy level in salt-treated leaves indicating at least one, and in some cases two, additional rounds of endoreduplication Mesembryanthemum crystallinum
(WDL5, AT4G32330) expression up-regulation occurs in response to salt stress Arabidopsis thaliana
microtubule reassembly in ein2-5 mutants is abnormal
transgenic plants overexpressing only (AT-NHX1, ATNHX, ATNHX1, NHX1, AT5G27150) did not show difference in salt tolerance compared to wild-type plants Arabidopsis thaliana
(ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) kinase activity level may need to be tightly regulated (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) function Arabidopsis thaliana
salt-treated whole leaves highest ploidy levels increased from 128C in untreated whole leaves up to 512C Mesembryanthemum crystallinum
MYB domain protein (ATMYB3R-1, ATMYB3R1, MYB3R-1, MYB3R1, PC-MYB1, AT4G32730) shows significant increase in transcript levels in EBC when treated with salt Mesembryanthemum crystallinum
(AtTCP15, TCP15, AT1G69690) and (AT-TCP20, ATTCP20, PCF1, TCP20, AT3G27010) are significantly down-regulated upon salt stress Mesembryanthemum crystallinum
ASR (Q2QJT5) is related to salt tolerance
ein3eil1 mutant is hypersensitive to NaCl treatment Arabidopsis thaliana
salt tolerance receptor-like cytoplasmic kinase1 interacts with, phosphorylates, and activates Catalase C (in rice) Oryza sativa
disturbance of normal function in salt tolerance results from constitutive overexpression of (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) and (ATSOS3, CBL4, SOS3, AT5G24270) in other cells Arabidopsis thaliana
transgenic plants overexpressing (AT-NHX1, ATNHX, ATNHX1, NHX1, AT5G27150) show no difference in Na+ content compared to control plants with or without salt treatment
transgenic plants overexpressing (ATNHX7, ATSOS1, SOS1, AT2G01980) (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) and (ATSOS3, CBL4, SOS3, AT5G24270) accumulate less Na+ than control plants under normal and salt treatment conditions
loss-of-function mutations in (ATNHX7, ATSOS1, SOS1, AT2G01980) cause hypersensitivity to NaCl Arabidopsis thaliana
(ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) with combined mutation of S228D and T168A cannot rescue the survival defect of sos2-2 under salt stress Arabidopsis thaliana
roots of transgenic (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) -2 plants expressing S228A were shorter than roots of transgenic (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) -2 plants expressing wild-type
high (AtAVP1, ATAVP3, AtVHP1;1, AVP-3, AVP1, FUGU5, VHP1, AT1G15690) and SALT OVERLY SENSITIVE1 (ATNHX7, ATSOS1, SOS1, AT2G01980) expression levels have been associated with increased salt tolerance
43 significantly differentially expressed RECT genes in EBC compared with only one differentially expressed gene detected in root transcriptome in response to salt stress Mesembryanthemum crystallinum
M. crystallinum showed salinity-induced polyploidy Mesembryanthemum crystallinum
certain MAPs promote plant cell adaptation to high salinity
proteasome-mediated protein degradation pathway mediates degradation of (SKU6, SPR1, AT2G03680)
(ATNHX7, ATSOS1, SOS1, AT2G01980) was constitutively higher in Thellungiella than in Arabidopsis in roots in control conditions Thellungiella; Arabidopsis thaliana
detailed profiling of transcripts and proteins is necessary before species-specific regulation of genes that are potentially important for salt tolerance can be assessed Thellungiella; Arabidopsis thaliana
complex regulation of (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) activation makes it possible for SOS2 to coordinate the function of various salt tolerance effector proteins under salt stress Arabidopsis thaliana
Ser228 of (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) is involved in function of (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) under salt stress
response to high salinity is specifically associated with (ABC1, ABCI8, ATABC1, ATNAP1, LAF6, AT4G04770) ;3-2 mutant allele
salt stress treatment applied to four to 5-week-old Arabidopsis thaliana plants Arabidopsis thaliana
(PFD3, AT5G49510) mutant has fresh weight approximately 32% of wild-type plants under 100 mM NaCl Arabidopsis thaliana
(ABA3, ACI2, ATABA3, AtLOS5, GIN5, LOS5, SIR3, AT1G16540) mutant had reduced tolerance to salt stress Arabidopsis thaliana
polyamines (PAs) are implicated in salt stress response
Binding sites for ORESARA1 ( (ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) also called and ) were found to be present in 26 of the salt-regulated SAGs Arabidopsis thaliana
sodium (Na+) toxicity is not directly reducing cell division in salt-sensitive genotype Sahara Hordeum vulgare
increased chlorophyll contents with salinity is in accordance with findings in Medicago sativa Medicago sativa
CAPE1 is salt-responsive Arabidopsis thaliana
(ATXTH19, XTH19, AT4G30290) and (XTH23, XTR6, AT4G25810) respond to salt Arabidopsis thaliana
BRs take part in Arabidopsis salt stress response Arabidopsis thaliana
ced2 mutant shows no significant difference in postgermination growth Arabidopsis thaliana
(ATMPK17, MPK17, AT2G01450) and (PMD1, AT3G58840) are necessary for salt-induced peroxisome proliferation Arabidopsis thaliana
root tissue from salt-treated plants no increase in maximum ploidy level detected with salt treatment Mesembryanthemum crystallinum
(WDL5, AT4G32330) is positive regulator of salt tolerance
(ATEIN2, CKR1, EIN2, ERA3, ORE2, ORE3, PIR2, AT5G03280) mutants suppress cortical microtubule reassembly
(AtLEA14, LEA1, LEA14, LSR3, AT1G01470) plays important roles in regulating rice salt tolerance Oryza sativa
structural differences between ThSOS1 and (ATNHX7, ATSOS1, SOS1, AT2G01980) may enhance stress-induced induction of ThSOS1 Thellungiella
soil salinity limits plant productivity
autophosphorylation on Ser228 of (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) is important for (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) function under salt stress
transgenic (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) -2 plants expressing S228A remained alive on MS plates with 100 mM NaCl
(PFD3, AT5G49510) mutant tolerance to 100 mM NaCl quantified based on percentage of fresh weight relative to wild-type seedlings Arabidopsis thaliana
T-DNA insertion lines screened for NaCl sensitivity Arabidopsis thaliana
glyceraldehyde-3-phosphate dehydrogenase (GAPC, GAPC-1, GAPC1, AT3G04120) is protein with altered abundance under salt stress Arabidopsis thaliana
K+ : Na+ ratio is parameter that gives clues about plant salt tolerance
Schrenkiella parvula roots deploy multiple physiological and developmental adjustments under salt stress Schrenkiella parvula
Arabidopsis root growth under 140 mM NaCl shows partial recovery from 5 to 9 hours after salt treatment Arabidopsis thaliana
salt stress conditions result in CSCs depletion from plasma membrane
functional gene expression altered stomatal aperture Arabidopsis thaliana
characteristics of transport systems and mechanisms regulating them may be of importance for salt tolerance
IR29 genotype shows significantly higher shoot Na+ concentration than IR63731 genotype Oryza sativa
salt stress treatment includes sodium chloride (NaCl) Oryza sativa
drought up-regulated NAC gene overexpression shows improved salt tolerance Arabidopsis thaliana; Oryza sativa
SIZ1-mediated SUMOylation of (ATMYB30, MYB30, AT3G28910) modulates plant salt tolerance Arabidopsis thaliana
chloride (Cl−) ions reduce root growth Hordeum vulgare
2D elemental images of Na show difference in spatial distribution of Na developmentally along root with approximately 10-fold difference in signal intensity between control and salt-treated root tips Hordeum vulgare
fold-change in Na in Clipper in maturation zone was 9.5-fold Hordeum vulgare
soil salinity limits plant growth and productivity
35S::HSFA2 transgenic line in QK background does not complement defects in tolerance to salt stress Arabidopsis thaliana
epidermal bladder cells (EBC) show spatially related differences in ploidy Mesembryanthemum crystallinum
Supplemental Tables S2 and S3 give transcripts showing significantly different expression in response to salt stress Mesembryanthemum crystallinum
(ATDPB, DPB, AT5G03415) is significantly up-regulated with salt Mesembryanthemum crystallinum
OsMAPK5 overexpression increased tolerance to salt stress Oryza sativa
det2-1 mutant have increased sensitivity to salt stress
microtubule depolymerization in ein2-5 mutants is similar to microtubule depolymerization in wild-type cells
alteration of (WDL5, AT4G32330) expression through ethylene signaling resulted in abnormal microtubule reassembly
high concentrations of salt cause ionic stress
(AT-NHX1, ATNHX, ATNHX1, NHX1, AT5G27150) overexpression line does not alleviate salt inhibition of lateral root development
Ser228 is not essential for salt tolerance Arabidopsis thaliana
root growth in the presence under salt stress requires greater SOS2 activity than survival under salt stress Arabidopsis thaliana
(PFD5, AT5G23290) mutant shows dramatic inhibition of leaf development Arabidopsis thaliana
insertion mutations disrupting PHT4;6 function cause NaCl hypersensitivity of seedlings Arabidopsis thaliana
mannitol at equiosmolar concentrations does not exacerbate mutant phenotypes Arabidopsis thaliana
OsPP18 is induced by high salinity Oryza sativa
salt stress induces at least one extra round of endoreduplication Mesembryanthemum crystallinum
EBC cell type-specific RNA-sequencing (RNA-seq) replicated data set generated from control and salt-treated plants (200 mM NaCl for 2 weeks) of same developmental age (8 weeks) Mesembryanthemum crystallinum
salt-treated M. crystallinum plants showed at least two to possibly six additional rounds of endoreduplication Mesembryanthemum crystallinum
multiple coordinated pathways modulate activity and expression levels of MAPs
SERF1 (SALT-RESPONSIVE (AtERF#092, ERF1, ERF1B, AT3G23240) ) responds to salt stress Oryza sativa
(ATCBL10, CBL10, SCABP8, AT4G33000) mutants exhibit moderate salt sensitivity in roots Arabidopsis thaliana
salt tolerance in the whole plant may need other unidentified components that cooperate with SOS genes Arabidopsis thaliana
Na+ accumulation reduction in transgenic plants overexpressing SOS genes indicates that (ATNHX7, ATSOS1, SOS1, AT2G01980) antiporter activity can be increased by overexpression of SOS genes Arabidopsis thaliana
WD40-repeat protein (HOS15, OLI1, AT5G67320) is involved in tolerance to inhibition of seed germination by salt Arabidopsis thaliana
F1 progeny of pht4;6-1 x pht4;6-2 cross exhibit NaCl sensitivity similar to pht4;6-1 or pht4;6-2 Arabidopsis thaliana
mitochondrial processing peptidase (MPPBETA, AT3G02090) is protein with altered abundance under salt stress Arabidopsis thaliana
(DREB2, DREB2A, AT5G05410) expression is more responsive to salt stress Arabidopsis thaliana
FL478 has 682 salt-responsive probe sets specific to FL478 Oryza sativa
salt treatment resulted in differential regulation of 481 salt-responsive probe sets in IR63731 Oryza sativa
salt stress increases polyamine levels in rice shoot Oryza sativa
sodium (Na+) ions reduce root growth Hordeum vulgare
(XTH23, XTR6, AT4G25810) single mutant is more sensitive to salt stress Arabidopsis thaliana
(BES1, BZR2, AT1G19350) and (ATXTH19, XTH19, AT4G30290) (XTH23, XTR6, AT4G25810) overexpression verify that (BES1, BZR2, AT1G19350) mediates salt stress tolerance upstream of (ATXTH19, XTH19, AT4G30290) and (XTH23, XTR6, AT4G25810) in Arabidopsis Arabidopsis thaliana
reduced endocytosis and ROS production in transgenic plants with reduced (ATVPS34, PI3K, VPS34, AT1G60490) levels results in salt-oversensitive phenotype Arabidopsis thaliana
mutants in jasmonate signaling show uncoupling of response of mRNA and activity
mutants in gibbereline signaling show uncoupling of response of mRNA and activity
OsTIP2;1 (Os02g44080) possibly has function in salinity tolerance Oryza sativa
FL478 shows lower Na+ and slightly higher K+ concentrations in shoot shoot ion composition
myo-inositol oxygenase gene is significantly down-regulated in Pokkali upon salt treatment Oryza sativa
Ca concentration was higher in Sahara roots independent of treatment Hordeum vulgare
salt-treatment caused decrease in Mg concentration in Clipper Hordeum vulgare
salt treatment with 50 mM NaCl induces smaller, thicker leaves Gossypium spp.
Na+ -induced depolarization of the membrane potential could play a role in regulation of high-affinity HAK transporter gene expression Solanum lycopersicum
reductions in the expression of high-affinity HAK transporter genes by NaCl are not so severe in halophytes such as Thellungiella halophila Thellungiella halophila
(ATP5CS, P5CS1, AT2G39800) overexpression lines are more salt-tolerant
tpc1-2 mutant plants exposed to 200 mM salt for 3 days did not exhibit pronounced differences in stomatal activity and leaf turgor Arabidopsis thaliana
unannotated PACs increased dramatically after 6 h of salt treatment Sorghum
Gossypium trilobum is least tolerant to high salinity Gossypium trilobum
domestication does not cause significant changes in salt tolerance Gossypium spp.
G. barbadense and G. darwinii displayed good growth performance under 100 mM NaCl during the first week of treatment salt tolerance phenotype Gossypium barbadense; Gossypium darwinii
G. davidsonii and G. klotzschianum species pair differ dramatically in salt-stress physiology Gossypium davidsonii; Gossypium klotzschianum
reactive oxygen species (ROS) accumulation plays important role in oxidative damage caused by salt stress Arabidopsis thaliana
(ATMYB30, MYB30, AT3G28910) is involved in salt tolerance Arabidopsis thaliana
RdDM gene targets provide potential source for the search of targets for improving future farming on salt-affected soils Arabidopsis thaliana
BET1s physically interact with calmodulin-binding receptor-like cytoplasmic kinase 1s (CRCK1s)
DELLAs mediate salt-induced delay of the floral transition Arabidopsis thaliana
mutants characterized by transfer DNA insertions in (AtRAV2, EDF2, RAP2.8, RAV2, TEM2, AT1G68840) are more tolerant to salt stress during the vegetative phase Arabidopsis thaliana
(AtTEM1, EDF1, TEM1, AT1G25560) overexpression plants exhibit hypersensitivity in response to salinity Arabidopsis thaliana
second interval of salt stress corresponding to ionic phase of salt stress Arabidopsis thaliana
WT plants recover cortical MT array after salt stress
lyk4lyk5 double mutant displays wild-type-like response to salt Arabidopsis thaliana
BRASSINOSTEROID INSENSITIVE 1-ASSOCIATED RECEPTOR KINASE 1 (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) contributes to salt tolerance Arabidopsis thaliana
chromatin landscape rapidly activating proximal (ATNACK2, NACK2, TES, AT3G43210) Oryza sativa
(ATMYB30, MYB30, AT3G28910) K283R does not significantly increase (AOX1A, ATAOX1A, AtHSR3, HSR3, AT3G22370) expression Arabidopsis thaliana
loss of function of (ATSIZ1, SIZ1, AT5G60410) leads to salt-sensitive phenotype in Arabidopsis Arabidopsis thaliana
RWC in allopolyploids after 50 mM NaCl treatment becomes more A2-like Gossypium spp.
hot pepper CaXTH3 participates in protection of Arabidopsis mesophyll cells from salt stress Arabidopsis thaliana; Capsicum annuum
salt stress restricts growth and development of plants
Na+ competes for K+ binding sites that are essential for cellular function
cpk4-1 and cpk11-2 mutants display increased salt-insensitive seed germination rate Arabidopsis thaliana
IR29 genotype shows significantly higher root Na+ concentration than FL478 genotype Oryza sativa
differences in duration and severity of salinity treatment do not allow safe comparisons between two datasets from different studies Oryza sativa
OsCIPK07, OsCIPK08, OsCIPK09, OsCIPK10, OsCIPK11, OsCIPK15, OsCIPK16, OsCIPK17, OsCIPK21, OsCIPK22, OsCIPK29, OsCIPK30 are induced by salt treatment Oryza sativa
expression of OsFKBP20-1b was increased by 40-fold under salt treatment Oryza sativa
SIZ1-mediated SUMOylation of (ATMYB30, MYB30, AT3G28910) regulates alternative respiration (Alt) and cellular redox homeostasis via (AOX1A, ATAOX1A, AtHSR3, HSR3, AT3G22370) Arabidopsis thaliana
salt-treatment caused decrease in potassium concentration in Clipper roots Hordeum vulgare
S showed no significant difference between genotypes or treatments Hordeum vulgare
S in both genotypes is slightly higher in salt-treated samples in maturation zone Hordeum vulgare
salt treatment upregulated both XTH19 and XTH23 more than ten-fold for 6 hours expression of (ATXTH19, XTH19, AT4G30290) and (XTH23, XTR6, AT4G25810) Arabidopsis thaliana
35S:: (BES1, BZR2, AT1G19350) -HA transgenic plants salt tolerance enhanced compared with wild type Arabidopsis thaliana
Pokkali rice plants cultured in sand tanks for 22 d after germination, then subjected to ramped salinity treatment for 7 d salt stress treatment Oryza sativa
quantitative real-time polymerase chain reaction (Q-PCR) was performed on 12 genes selected on the basis of their transcript levels across accessions, salt responsiveness, and/or functional annotation Oryza sativa
Pokkali shows lower Na+ and slightly higher K+ concentrations in shoot shoot ion composition
unannotated PACs increased dramatically after 1 h of salt treatment Sorghum
curves fitted for salt-treatment relative to control show significant difference for both genotypes Hordeum vulgare
overexpressed transgenic plants significantly improved LR initiation events compared with wild-type plants Arabidopsis thaliana
growth of 35S:: (BES1, BZR2, AT1G19350) -HA transgenic plants less inhibited by salt stress Arabidopsis thaliana
cpk21-1 mutant shows no obvious growth advantage under salt conditions
OsRHC19 expression was induced by salt stress (200 mM) Oryza sativa
ORS1-dependent genes are induced by long-term salinity stress long-term salinity stress (4 d, 150 mM NaCl) Arabidopsis thaliana
ORS1-dependent genes are not induced by short-term salinity stress short-term salinity stress (6 h, 150 mM NaCl) Arabidopsis thaliana
osmotic effect of NaCl outside of the roots may inhibit cell elongation
Mg concentration in root tip was genotype and treatment dependent Hordeum vulgare
allopolyploid cottons do not necessarily show higher salinity tolerance than diploid species Gossypium spp.
TaNAC69-4 expression level varies considerably among samples root samples of control and salt-stressed plants Triticum aestivum
(AtTIFY1, GATA25, TIFY1, ZIM, AT4G24470) family protein is highly correlated in expression with TaNAC69 genes Triticum aestivum
salt stress elevates transcriptional activity of (ATMYB30, MYB30, AT3G28910) towards (AOX1A, ATAOX1A, AtHSR3, HSR3, AT3G22370) Arabidopsis thaliana
Gossypium trilobum is least tolerant species to salt stress Gossypium trilobum
salt stress has more serious effect on activation of (ATXTH19, XTH19, AT4G30290) mutant LRs than in (XTH23, XTR6, AT4G25810) mutants Arabidopsis thaliana
Wheat SRO PARP activity improve growth of seedlings exposed to salinity stress Triticum aestivum
H2O2 homeostasis maintenance occurs under salt stress condition Oryza sativa