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osmotic stress response

14095 relationships annotated with this phrase. Showing first 500 of 14095.
Source entity Relationship Target entity Species
osmotin proteins have been shown to protect against osmotic shock during abiotic stress
osmotin proteins protect against osmotic shock through compartmentalizing solutes
MpCIPK-A showed no significant changes in gene expression Marchantia polymorpha
fluorescent Förster Resonance Energy Transfer (FRET)-based calcium (Ca 2+) reporter proteins revealed specific chloroplast calcium (Ca 2+) signals in response to osmotic stress
GO:0006972 (hyperosmotic response) was enriched in SOM7 Setaria viridis
osmotic stress accelerates release of (CBNAC, NTL9, AT4G35580) from the membrane
(ATSAHH1, EMB1395, HOG1, MEE58, SAH1, SAHH1, AT4G13940) and Msn2/4 are considered as core components of the Hog1-MAPK signaling pathway Saccharomyces cerevisiae
PH02Gene46833 (ATCIPK23, CIPK23, LKS1, PKS17, SnRK3.23, AT1G30270) from Salt sample is involved in osmotic stress Phyllostachys edulis
azg1-1 × azg2-1 double mutant roots respond in the same way as wild-type (WT) roots when exposed to mannitol concentrations of up to 100 mM in the absence of sodium chloride (NaCl) Arabidopsis thaliana
wild-type and both cipk-b mutant lines showed decreased growth in response to increasing concentrations of sorbitol Marchantia polymorpha
raised concentrations in soil solution or irrigation water perturb osmotic relations
pseudogene (AT3G29725) seems unlikely to influence Pro accumulation Arabidopsis thaliana
(ATELP, ATELP1, ATVSR1, BP-80, BP80, BP80-1;1, BP80B, GFS1, MTV18, VSR1, VSR1;1, AT3G52850) mutants show lower induction of (ATNCED3, NCED3, SIS7, STO1, AT3G14440) expression Arabidopsis thaliana
21 mannitol-responsive phosphopeptides showed reproducible mannitol-induced phosphorylation Arabidopsis thaliana
osmotic stress response is associated with rapid accumulation of the phospholipid species PI(3,5)P2 Arabidopsis thaliana
increased expression of osmotic stress-responsive genes can lead to increased drought tolerance Arabidopsis thaliana
raffinose acts as osmoprotectant Arabidopsis thaliana
CIPK-B does not have role in osmotic stress Marchantia polymorpha
rapidly changing solute concentration results in potential osmotic shock Hordeum vulgare
high salinities induce production of hemolytic toxins in Phaeocystis globosa Phaeocystis globosa
transgenic lines with 35S-driven expression of (AT5G35380) had Pro increased by 28 to 50 μmol g fresh weight −1 (144%–178% of Col wild type) Arabidopsis thaliana
mitogen-activated protein kinase (MAPK) family members are specifically phosphorylated in response to osmotic stress Arabidopsis thaliana
(VAC1, VAC14, AT2G01690) phosphoregulation mechanism is unique to plants Arabidopsis thaliana
(VAC1, VAC14, AT2G01690) (ASK1, SNRK2-4, SNRK2.4, SRK2A, AT1G10940) and (MyoB1, AT1G08800) displayed maximal phosphorylation at 2 min Arabidopsis thaliana
phosphorylation may mediate complex assembly with PI3P-5-kinase (ATKAS2, FAB1, KAS2, AT1G74960) during the stress response Arabidopsis thaliana
NaCl treatment (300 mM) increases transcript abundance of (COR78, LTI140, LTI78, RD29A, AT5G52310) gene in (ELO4, HOS3-1, AT4G36830) and hos3-2 Arabidopsis thaliana
flavonoids, quercetin and coumaroyl derivatives identified as defensive compounds to osmotic stress
preliminary analysis on wheat root exudates indicates that BNI trait is reduced upon an osmotic stress in certain genotypes
MpCIPK-B showed significant upregulation with sorbitol Marchantia polymorpha
cipk-b mutants did not respond to sorbitol of isoosmolar concentrations Marchantia polymorpha
osmotin proteins protect against osmotic shock through altering metabolism or structure in cells
abiotic stress marker gene LEA-like4 was again strongly induced by growth on treatment plates Marchantia polymorpha
MpPUB9 involvement in plant-specific regulation implies involvement of MpPUB9 in plant-specific regulation to deal with changes in water potential Marchantia polymorpha
MpCIPK-B does not respond to osmotic stress Marchantia polymorpha
PEG treatment induces similar pattern of expression as dehydration-induced CaDeSI2 expression Capsicum annuum
(ATELP, ATELP1, ATVSR1, BP-80, BP80, BP80-1;1, BP80B, GFS1, MTV18, VSR1, VSR1;1, AT3G52850) mutant shows increased sensitivity to osmotic stress Arabidopsis thaliana
ced2 mutant is defective in osmotic stress-induced ABA accumulation Arabidopsis thaliana
ced2 mutant is impaired in osmotic stress regulation of a large number of genes Arabidopsis thaliana
(VAC1, VAC14, AT2G01690) is required for stress-induced PI(3,5)P2 production Saccharomyces cerevisiae
pht4;6-1 seedlings is not hypersensitive to osmotic stress caused by mannitol Arabidopsis thaliana
RiMsn2 regulates osmotic homeostasis Saccharomyces cerevisiae
AM fungal inoculation reduces free proline content in Medicago truncatula leaves Medicago truncatula
glutamyl-ACC (GACC) may be involved in regulation of early osmotic stresses
firefly luciferase reporter gene driven by the stress-responsive (ATNCED3, NCED3, SIS7, STO1, AT3G14440) promoter is used to enable genetic dissection of plant responses to osmotic stress Arabidopsis thaliana
vacuolar protein Vac14p regulates levels of phosphatidylinositol 3,5-bisphosphate Saccharomyces cerevisiae
Vacuolar ATPase D subunit shows phosphorylation increase of 2.91-fold in response to mannitol Arabidopsis thaliana
(VAC1, VAC14, AT2G01690) is required for stress-induced PI(3,5)P2 production Saccharomyces cerevisiae
genes with lower expression in response to elevated red light:far-red light ratio in bud n-2 enriched for osmotic stress response Gene Ontology terms Arabidopsis thaliana
(GOSAMT2, AT4G27720) and (ATOPT6, OPT6, AT4G27730) are contiguous and likely only one affects Pro accumulation Arabidopsis thaliana
(ATELP, ATELP1, ATVSR1, BP-80, BP80, BP80-1;1, BP80B, GFS1, MTV18, VSR1, VSR1;1, AT3G52850) (ATVSR3, BP80-2;2, UXS2, VSR2;2, VSR3, AT2G14740) double mutant shows obvious inhibition during germination and postgermination growth Arabidopsis thaliana
molecular mechanisms involved in initial perception and response to dehydration are not well understood current understanding
shifts in active protein translation suggests heightened levels of posttranscriptional regulation
(AHA2, AtHA2, HA2, PMA2, AT4G30190) null mutants are not hypersensitive to sorbitol or NaCl treatment Arabidopsis thaliana
untargeted and targeted proteomic results indicate new pathways that may be important for osmotic adaptation Arabidopsis thaliana
(ATELP, ATELP1, ATVSR1, BP-80, BP80, BP80-1;1, BP80B, GFS1, MTV18, VSR1, VSR1;1, AT3G52850) transcript level returns to control level after prolonged stress Arabidopsis thaliana
ced2 mutant accumulates more ROS Arabidopsis thaliana
pH cyt regulates osmotic stress responses
MAPK phosphorylation likely plays important role in osmotic stress response
mannitol-responsive phosphorylation events provide insight to cellular processes involved in early signaling and adaptation Arabidopsis thaliana
six-day-old seedlings were transferred onto basal media containing mannitol (0, 200, 300, or 400 mM)
down-regulated genes in ced2 mutant include larger number of osmotic stress- or ABA-inducible genes
changes in the electrophysiological properties of the plasma membrane and vacuole membrane occurred prior to changes in gene expression
SnRK2 proteins play role in non-ABA-mediated dehydration responses
novel type of nuclear CaM-binding protein (ATCAMBP25, CAMBP25, AT2G41010) functions as negative regulator of osmotic stress responses Arabidopsis thaliana
ThCBL9 overexpression enhanced tolerance to osmotic stress Arabidopsis thaliana
overexpression (OE) of OsPP18 in transgenic rice enhanced osmotic tolerance Oryza sativa
(ATHM4, ATM4, TRX-M4, AT3G15360) mutants had enhanced root elongation at low water potential Arabidopsis thaliana
effect of MADS box and UspA gene mutants on Pro metabolism may not have been strong enough or of correct type to significantly affect low water potential tolerance Arabidopsis thaliana
osmotic stress inhibits root growth Arabidopsis thaliana
higher [Ca2+]cyt in ced2 (ATELP, ATELP1, ATVSR1, BP-80, BP80, BP80-1;1, BP80B, GFS1, MTV18, VSR1, VSR1;1, AT3G52850) mutants is consistent with more depolarized membrane potentials in the mutant
(ATCCD7, CCD7, MAX3, AT2G44990) mutant does not display defects in osmotic stress response Arabidopsis thaliana
this study investigates proteins involved in early response to hyperosmotic stress Arabidopsis thaliana
(bZIP30, DKM, AT2G21230) shows phosphorylation increase of 2.70-fold in response to mannitol Arabidopsis thaliana
(ELO4, HOS3-1, AT4G36830) mutant shows enhanced primary root growth on mannitol osmotic-stress media
OsPP18-overexpressing plants showed improved tolerance to osmotic stress Oryza sativa
greater root elongation in (ATHM4, ATM4, TRX-M4, AT3G15360) cannot conclusively be attributed to increased Pro Arabidopsis thaliana
turgor recovery is accompanied by arrest of cell growth and expansion
transgenic wheat that accumulated mannitol was found to have mannitol concentration too low to function as osmolyte Triticum aestivum
abscisic acid (ABA) reprograms gene expression
T-DNA mutants of (ATTRX H1, ATTRX1, TRX1, AT3G51030) (THIOREDOXIN1 [ ]) had more than 30% reduction in Pro accumulation at −1.2 MPa Arabidopsis thaliana
transgenic lines overexpressing (AT5G35380) had Pro levels indistinguishable from wild type under unstressed conditions (−0.25 MPa) Arabidopsis thaliana
MAP3K Raf18 shows phosphorylation increase of 2.50-fold in response to mannitol Arabidopsis thaliana
proline acts as osmoprotectant
expression of ABA- and osmotic-stress-responsive genes is increased in msi1-cs plants Arabidopsis thaliana
accumulated metabolites under heat or osmotic stress act as osmolites, protecting cells from dehydration
ospp18 mutant is sensitive to osmotic stress Oryza sativa
untargeted and targeted isotope-assisted mass spectrometric methods used to characterize proteins whose degree of phosphorylation is rapidly altered by hyperosmotic treatment Arabidopsis thaliana
data from this study implicate new proteins and points of regulation in osmotic stress response Arabidopsis thaliana
MAP4Kα1 shows phosphorylation increase of 4.87-fold in response to mannitol Arabidopsis thaliana
11 phosphopeptides cluster together in phosphorylation heat map Arabidopsis thaliana
proline acts as compatible solute
other differences in mutants may mitigate effect of having higher or lower Pro Arabidopsis thaliana
turgor recovery is accompanied by shifts in active protein translation
UspA domain proteins (AT5G20310) and (GRUSP, USP, AT3G58450) had effect on Pro accumulation opposite to UspA kinase (AT3G35380) Arabidopsis thaliana
osmotic stress increased expression of 1,849 genes Arabidopsis thaliana
(AtMAX2, MAX2, ORE9, PPS, AT2G42620) mutant seedlings showed lower percentage with green cotyledons than wild type at various days of growth and in presence of different concentrations of mannitol Arabidopsis thaliana
hyper-osmotic stress causes growth attenuation or cessation
trehalose is sugar osmolyte
mass spectrometric methods for quantifying changes in phosphoproteome provide opportunity to identify key phosphorylation events involved in osmotic stress response Arabidopsis thaliana
microtubule subunit TUA clusters in osmotic-responsive phosphorylation group Arabidopsis thaliana
KCl and mannitol concentrations tested failed to stimulate peroxisome proliferation in wild type Arabidopsis thaliana
(ELO4, HOS3-1, AT4G36830) mutant seedlings shows reduced luminescence compared to wild-type C24 RD29A:LUC seedlings after NaCl treatment Arabidopsis thaliana
wild-type plants show reduced root growth in response to NaCl stress Arabidopsis thaliana
OsPP18-OE plants show significantly less suppression of shoot growth than wild-type plants Oryza sativa
mutants of several other genes in Region 9 including (AT1G30470) had no significant effect on Pro accumulation Arabidopsis thaliana
(ATELP, ATELP1, ATVSR1, BP-80, BP80, BP80-1;1, BP80B, GFS1, MTV18, VSR1, VSR1;1, AT3G52850) mutant differs from wild type in calcium flux under osmotic stress Arabidopsis thaliana
VACUOLAR SORTING RECEPTOR 1 (ATELP, ATELP1, ATVSR1, BP-80, BP80, BP80-1;1, BP80B, GFS1, MTV18, VSR1, VSR1;1, AT3G52850) is critical for osmotic stress tolerance Arabidopsis thaliana
ced2 mutant shows reduced ABA accumulation Arabidopsis thaliana
MAP4K Ste20 functions downstream of osmosensor Sho1 Saccharomyces cerevisiae
MAP4K Ste20 activates (ATSAHH1, EMB1395, HOG1, MEE58, SAH1, SAHH1, AT4G13940) MAPK cascade Saccharomyces cerevisiae
(VAC1, VAC14, AT2G01690) function is indicated to be highly responsive to osmotic perturbations Arabidopsis thaliana
osmotic stress (200 mM mannitol) is one of 12 specific treatments Arabidopsis thaliana
(ELO4, HOS3-1, AT4G36830) mutant exhibits tolerance to NaCl stress Arabidopsis thaliana
cells re-establish turgor by osmotic adjustment
mutant of (AT5G35380) reduced Pro content by nearly 20% Arabidopsis thaliana
(AtMAX2, MAX2, ORE9, PPS, AT2G42620) mutants displayed hypersensitivity to mannitol Arabidopsis thaliana
protein phosphorylation is rapidly altered by hyperosmotic treatment Arabidopsis thaliana
rapid protein phosphorylation response to dehydration is distinct from slower molecular phenotypes associated with mRNA changes Arabidopsis thaliana
osmotic stress induces accumulation of osmolytes
(AT5G20310) mutants of had increased Pro accumulation Arabidopsis thaliana
Cellulose synthase-like (ATCSLD3, CSLD3, KJK, RHD7, AT3G03050) shows phosphorylation increase of 2.10-fold in response to mannitol Arabidopsis thaliana
AHA activity appears to be down-regulated through decreased penultimate Thr phosphorylation in (AHA1, HA1, OST2, PMA, AT2G18960) and (AHA2, AtHA2, HA2, PMA2, AT4G30190) Arabidopsis thaliana
(MyoB1, AT1G08800) shows highest degree of phosphorylation at 2 min Arabidopsis thaliana
light induces sucrose accumulation
ced2 mutant is defective in osmotic stress tolerance Arabidopsis thaliana
CED2/ (ATELP, ATELP1, ATVSR1, BP-80, BP80, BP80-1;1, BP80B, GFS1, MTV18, VSR1, VSR1;1, AT3G52850) is essential for osmotic stress resistance
phosphatidylinositol 3,5-bisphosphate is osmotic stress-induced phospholipid Saccharomyces cerevisiae
ZmMPK17 transcript increases upon osmotic stress Zea mays
(ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) mutant phenotype is not a result of osmotic stress Arabidopsis thaliana
(AT5G54920) (MNM1, AT5G54930) and (AT5G54940) are contiguous and likely only one affects Pro accumulation Arabidopsis thaliana
mutants of (RTH, AT3G51040) and (NERD1, AT3G51050) had no effect on Pro accumulation Arabidopsis thaliana
membrane potentials of the vacuole and plasma membrane rapidly respond to osmotic stress Arabidopsis thaliana
(VAC1, VAC14, AT2G01690) clusters in osmotic-responsive phosphorylation group Arabidopsis thaliana
(AHA2, AtHA2, HA2, PMA2, AT4G30190) null mutants are hypersensitive to KCl treatment Arabidopsis thaliana
osmotic stress response network includes MAP4K family proteins Arabidopsis thaliana
(MyoB1, AT1G08800) is phosphorylated specifically in response to osmotic stress Arabidopsis thaliana
(ATELP, ATELP1, ATVSR1, BP-80, BP80, BP80-1;1, BP80B, GFS1, MTV18, VSR1, VSR1;1, AT3G52850) mutants phenocopy osmotic stress-sensitive phenotype of ced2 Arabidopsis thaliana
(ATELP, ATELP1, ATVSR1, BP-80, BP80, BP80-1;1, BP80B, GFS1, MTV18, VSR1, VSR1;1, AT3G52850) is required for full induction of (ATNCED3, NCED3, SIS7, STO1, AT3G14440) gene Arabidopsis thaliana
phosphorylation changes involved in cross talk with other signaling pathways Arabidopsis thaliana
protein phosphorylation and mRNA measurements reveal minimal overlap between protein phosphorylation and mRNA measurements Arabidopsis thaliana
osmotic stress response network includes (AtbZIP, bZIP, AT1G68880) transcription factors Arabidopsis thaliana
(ATELP, ATELP1, ATVSR1, BP-80, BP80, BP80-1;1, BP80B, GFS1, MTV18, VSR1, VSR1;1, AT3G52850) mutant differs from wild type in membrane potential under osmotic stress Arabidopsis thaliana
rapid phosphorylation analysis is important for observing phosphorylation responses before the onset of significant changes in protein synthesis/breakdown Arabidopsis thaliana
some phosphopeptides show highest response to mannitol after only 2 min of treatment Arabidopsis thaliana
(ELO4, HOS3-1, AT4G36830) mutant shows enhanced transcript abundance of (COR78, LTI140, LTI78, RD29A, AT5G52310) gene Arabidopsis thaliana
(PFD3, AT5G49510) mutants are not sensitive to mannitol Arabidopsis thaliana
5-day-old seedlings transferred to GM medium supplemented with 300 mM mannitol Arabidopsis thaliana
(ATELP, ATELP1, ATVSR1, BP-80, BP80, BP80-1;1, BP80B, GFS1, MTV18, VSR1, VSR1;1, AT3G52850) does so, at least in part, by regulating many osmotic stress-induced genes
turgor recovery is accompanied by restructuring of the cytoskeleton
(bZIP30, DKM, AT2G21230) phosphorylation is responsive to 30 min of mannitol treatment Arabidopsis thaliana
myosin-binding proteins (MyoB) family members were shown to undergo increased phosphorylation in response to mannitol Arabidopsis thaliana
osmolytes function for osmotic adjustment
elongation factor EF-Tu (AT4G02930) is protein with altered abundance under osmotic stress Arabidopsis thaliana
vacuolar sugars can serve as production of osmoprotectants
osmotic stress- or ABA-inducible genes include those encoding protein kinases
similar pathway may be present in plants
TPR domain containing protein shows phosphorylation increase of 2.61-fold in response to mannitol Arabidopsis thaliana
AHA proton pumps are speculated to be hyperactivated during osmotic stress response Arabidopsis thaliana
cells respond to hyper-osmotic stress
malate dehydrogenase (MDH, pNAD-MDH, AT3G47520) is protein with altered abundance under osmotic stress Arabidopsis thaliana
common compounds responding to variation in osmotic pressure across elevation gradient
increased levels of sugars and amino acids is indicative for production of compatible solutes Hordeum vulgare
(ATTRX H1, ATTRX1, TRX1, AT3G51030) and (ATHM4, ATM4, TRX-M4, AT3G15360) mutants had different effects on growth at low water potential Arabidopsis thaliana
mutants of two genes in Region 81 clearly did not affect Pro accumulation Arabidopsis thaliana
two T-DNA mutants of (eL24z, RPL24A, AT2G36620) had more than 20% increase in Pro accumulation Arabidopsis thaliana
Two T-DNA lines of (AT5G46320) had significantly higher Pro accumulation than Col wild type Arabidopsis thaliana
vsr1-3 allele is sensitive to osmotic stress Arabidopsis thaliana
1,299 phosphorylated peptides represent 833 unique proteins Arabidopsis thaliana
12 proteins possess greater than 3-fold phosphorylation change Arabidopsis thaliana
enhanced root growth upon osmotic stress is consistent with HOS3 functioning as negative regulator of stress-induced root growth inhibition Arabidopsis thaliana
high osmotic stress induced by 300 mM mannitol causes highly reduced leaf development Arabidopsis thaliana
sequestering of inorganic ions (Na+, K+ and Cl−) into the vacuole is one mechanism to cope with osmotic stress
proline is compatible solute
(CIPK11, PKS5, SIP4, SNRK3.22, AT2G30360) is normally enhanced by osmotic stress Arabidopsis thaliana
CaUBP12 expression is significantly induced by mannitol treatment Capsicum annuum
serrate (se) mutant is heightened in sensitivity to high osmoticum Arabidopsis thaliana
high accumulation of mannitol causes severe abnormalities Triticum aestivum
kinase-inactive (AtCPK21, CPK21, AT4G04720) variants remained tolerant to osmotic stress treatment Arabidopsis thaliana
Qiān Shŏu kinase (QSK1), inflorescence meristem kinase 2, and CYSTEINE-RICH RECEPTOR-LIKE KINASE2 (ASG6, CRK2, AT1G70520) rapidly relocate and cluster to plasmodesmata pores
CARAV1 triggers tolerance to osmotic stresses Capsicum annuum
maltose has been shown to act as compatible solute
(ABI5, AtABI5, DPBF1, GIA1, AT2G36270) in Arabidopsis thaliana under osmotic stress restrains seed germination and embryo development Arabidopsis thaliana
suppression of (AT-P5C1, AT-P5R, EMB2772, P5CR, AT5G14800) in soybean results in increased sensitivity to osmotic stress Glycine max
Maize overexpressing ZmPLC1 exhibited higher cellular solute content Zea mays
tomato P5CS expression in yeast cells showed that yeast growth is inversely correlated with proline accumulation under osmotic stress conditions
glycine betaine (GB) can be exogenously applied to plant cells
cpk21-1 mutant shows no enhanced tolerance on PEG-containing plates Arabidopsis thaliana
(SNRK2-8, SNRK2.8, SRK2C, AT1G78290) /C is strongly stimulated by hyperosmotic stress Arabidopsis thaliana
osmotic stress triggers rapid relocation and clustering of Qiān Shŏu kinase (QSK1), inflorescence meristem kinase 2, and CYSTEINE-RICH RECEPTOR-LIKE KINASE2 (ASG6, CRK2, AT1G70520)
PDX mutants react hypersensitively when exposed to mannitol Arabidopsis thaliana
7-day-old seedlings were transferred to plates 1 MS, 3% sucrose 1.5% agar overlayed with PEG to osmotic potential of –0.45 and –0.95 MPa Arabidopsis thaliana
(AtCPK21, CPK21, AT4G04720) mutant shows tolerance to osmotic stress treatment Arabidopsis thaliana
SnRK2 kinases are essential for ABA accumulation in osmotic stress conditions Arabidopsis thaliana
(AtMAX2, MAX2, ORE9, PPS, AT2G42620) mutant seedlings is hypersensitive to osmotic stress Arabidopsis thaliana
(PFD5, AT5G23290) mutant shows lower root growth than wild-type plants Arabidopsis thaliana
proline level shows no significant difference among WT, mtctlk1 mutants, and MtCTLK1-OE plants before cold treatment Medicago truncatula
salt (Na+) stress exerts osmotic stress on living plant cells
succinyl-CoA ligase (AT2G20420) is protein with altered abundance under osmotic stress Arabidopsis thaliana
high level of osmolyte accumulation in plants is biologically expensive metabolic cost
heat stress increases levels of amino acids Hordeum vulgare
TEM modulates regulators of osmotic component of abiotic stress response Arabidopsis thaliana
ZFP179 is induced by PEG 6000 Oryza sativa
(AtCPK21, CPK21, AT4G04720) may contribute to mannitol uptake or metabolism Arabidopsis thaliana
UWO has optimal growth temperature that is salt dependent Chlamydomonas raudensis
(ABI4, ATABI4, GIN6, ISI3, SAN5, SIS5, SUN6, AT2G40220) transcripts are high in, to a lesser extent, in seedlings exposed to osmotic agents
(AtCOR47, COR47, RD17, AT1G20440) is induced by osmotic stress Arabidopsis thaliana
proline, sorbitol, and trehalose were higher after 5 weeks of salt stress in Clipper roots Hordeum vulgare
(SNRK2-8, SNRK2.8, SRK2C, AT1G78290) exhibited similar relative expression levels in (AAO3, AOdelta, At-AO3, AtAAO3, AT2G27150) KO roots Arabidopsis thaliana
tall fescue had higher proline contents proline content Festuca arundinacea
osmolyte-mediated osmotic adjustment (OA) is responsible for cell turgor maintenance
OsClo5 overexpression increased contents of proline Oryza sativa
AtCIPK3 transcription was induced by hyperosmosis treatment Arabidopsis thaliana
plants have adaptive robustness to osmotic stresses
(AtG3BP-1, AtG3BP8, NTF2, AT5G60980) is targeted by hyperosmotic stress signals
CaOSR1 expression is lower in CaSnRK2.6-silenced plants than control after dehydration stress Capsicum annuum
low amount of low molecular weight (LMW) PEG in PEG 6000 product suggests osmotic potential decrease did not affect root growth Phaseolus vulgaris
Bu-5, Bur-0, Ll-1, Wl-0, and Zu-0 accessions showed osmotic stress tolerance after SA Arabidopsis thaliana
OsGMST1 transcript level is unaffected by PEG4000 Oryza sativa
(AtbZIP, bZIP, AT1G68880) transcription factor heterodimer requires phosphorylation of Sucrose–non-Fermenting1-Related kinase1 (AKIN10, KIN10, SnRK1, SnRK1α1, SNRK1.1, AT3G01090)
zmsro1e mutant showed no obvious difference from (B73, CHL6, CNX, CNX1, SIR4, AT5G20990) under osmotic stress Zea mays
GmDREB2 overexpression confers enhanced tolerance to osmotic stress (salt and drought) Arabidopsis thaliana
cinnamic acid (CA) decreases leaf osmotic potential Dactylis glomerata; Lolium perenne; Rumex acetosa
osmolytes (maltose) serve as active response against osmotic stress
H2O2 accumulation at 24 h in salinized broccoli roots is mainly due to osmotic stress induced by external NaCl concentration Brassica oleracea
osmotolerance of Bu-5 plants after SA is semi-dominant Arabidopsis thaliana
ZmDBF1 overexpression confers enhanced tolerance to osmotic stress (salt and drought) Arabidopsis thaliana
Annexin 1 gene (ANN1, ANNAT1, AtANN1, ATOXY5, OXY5, AT1G35720) plays a role in osmotic stress response Arabidopsis thaliana
ZFP179-ox plants accumulated more free proline Oryza sativa
Bu-5, Bur-0, Ll-1, Wl-0, and Zu-0 accessions except Wl-0 showed marked osmotic stress tolerance compared with Col-0 plants Arabidopsis thaliana
TaSnRK2.4 is involved in the regulation of enhanced osmotic potential Arabidopsis thaliana
SNAC2-overexpressing plants showed improved tolerance to osmotic stress Oryza sativa
transgene-induced increase in compatible solutes represented only a small portion of total osmotic adjustment (OA) of plant cells under osmotic stress
salt-acclimated Bu-5 plants exhibited marked tolerance of 750 mM sorbitol stress Arabidopsis thaliana
PKABA1 was induced by hyperosmotic stress Triticum aestivum
GSH is required during initial phase of osmotic stress induced by salt stress Brassica oleracea
SnRK2 family is involved in hyperosmotic stress responses
δ1-pyrroline-5-carboxylate synthetase (P5CS) functions in protection of cells during osmotic stress
(AtTudor1, TSN1, Tudor1, AT5G07350) (AtTudor2, TSN2, Tudor2, AT5G61780) RNAi transgenic lines (R#4–R#7) show more severely affected growth under 200mM mannitol stress Arabidopsis thaliana
no clear accumulation of compatible solutes was observed under tebuconazole and GT treatments Lolium perenne
OsClo5 overexpression increased contents of soluble sugar Oryza sativa
osmotic stress promotes accumulation of proline (Pro)
PEG supply of 250 g l −1 is lethal to plants Phaseolus vulgaris
mannitol had similar effect to NaCl Arabidopsis
freezing-induced cellular dehydration is cold-induced osmotic stress
(HHP1, AT5G20270) may contribute to osmotic stress sensitivity Arabidopsis thaliana
salt-acclimated osmotolerance mechanism of tolerant accessions is not dependent on expression level of responsible gene between tolerant and sensitive accessions Arabidopsis thaliana
microtubule bundling is relied on for control of protoplast volume during hyperosmotic stress response
Arabidopsis knock-out (KO) mutants reveal specific phenotypes in response to osmotic stress Arabidopsis thaliana
proline has proposed role in control of osmotic homeostasis
proteins absent before the stress-treatment and appearing at 10min and/or 3h time point are stress-induced 14-3-3 targets
peroxidase, EARLY-RESPONSIVE TO DEHYDRATION 2, and CATALASE2 are stress-responsive 14-3-3 targets
proline helps maintain cell turgor and growth Triticum aestivum
genetic, physiological, and media manipulations show that under normal growth conditions epidermal plastids of leaf experience hypoosmotic stress Arabidopsis thaliana
dehydrated leaves mounted in water caused leaf epidermal plastids became large and round Arabidopsis thaliana
AtSRK2C and NtOSAK show extremely early activation in cultured plant cells Arabidopsis thaliana; Nicotiana tabacum
saline treatments decreases leaf osmotic potential Vicia faba
ABA-responsive CaRAV1 overexpression line enhances osmotic stress resistance Arabidopsis thaliana
OPEN STOMATA 1 (ATOST1, OST1, P44, SNRK2-6, SNRK2.6, SRK2E, AT4G33950) is activated by hyperosmotic stress independently of abscisic acid (ABA) Arabidopsis thaliana
eight to ten week old plants were treated by adding 0.8 M sorbitol to hydroponic media Arabidopsis thaliana
osmotic stress induces ZFP179 transcripts Oryza sativa
Col-0 plants showed complete chlorosis under 750 mM sorbitol stress Arabidopsis thaliana
decrease in water availability induced by osmotic stress might lead to turgor reduction
polyols and trehalose in Sahara roots rose 2-3-fold after short-term exposure to salt Hordeum vulgare
osmotolerance of Bu-5 plants after SA is thought to be semi-dominant phenotype Arabidopsis thaliana
Ss (ATLTP1, AtLtpI-4, LP1, LTP1, AT2G38540) accumulation is observed in cold-acclimating and non-acclimating Solanum species Solanum sogarandinum; Solanum tuberosum
(LTI65, RD29B, AT5G52300) is induced by osmotic stress Arabidopsis thaliana
SnRK2s might be activated almost from the beginning of osmotic stress
salinity imposes osmotic component resulting from reduced water availability caused by increased osmotic pressure in soil
Late embryogenesis abundant (LEA) proteins function in protection of cells during osmotic stress
35S::Wlip19 transgenic tobacco became tolerant to high mannitol stress Nicotiana tabacum
various plants adopt RAM premature differentiation
water stress induces osmotic adjustment of swollen root tips Triticum aestivum
osmotic stress treatment reduces transcription of OsRAN2 Oryza sativa
PEG 6000 dehydrates root apoplast more than PEG 1000 Phaseolus vulgaris
free proline increases osmotic potential
TaSnRK2.4 was identified in common wheat Triticum aestivum
TaSnRK2.7 responds to polyethylene glycol Triticum aestivum
free proline plays important role in buffering cellular redox
salts perturb water content of the cell
Sahara genotype has significantly higher Ψs compared with other three genotypes
high salt concentration in the root medium causes water stress
compatible solutes act as osmoprotectants to stabilize enzymes
roots exposed to higher salinity were reduced in growth mainly because of osmotic effect of salt Triticum turgidum
VvSIP1 expression in suspension-cultured cells (CSB, Cabernet Sauvignon Berry) did not change after treatment with osmotic stress (2% w/v PEG) Vitis vinifera
proline accumulates during water stress Triticum aestivum
Arabidopsis mutant lacking two plastid-localized MS channels was used as sensitized background for analysis of plastidic osmotic stress Arabidopsis thaliana
MS channels offer likely molecular mechanism by which endosymbiotic organelles respond to hypoosmotic stress Arabidopsis thaliana
hyperosmotic conditions increases nuclear stiffness
hyperosmotic stress relationship with gene expression remains to be fully characterized in plants
chromatin can become more compact upon hyperosmotic treatment
leaf osmotic potential in salt treatments also decreased in salt treatments compared with control
dimethylsulphoniopropionate (DMSP) acts as compatible solute to counter osmotic stress
percentage of plants with healthy green cotyledons decreased more rapidly in wild-type plants than in 35S::Wlip19-#9 and 35S::Wlip19-#15 plants during 4 d of mannitol treatment Nicotiana tabacum
salt stress induces expression of (HHP1, AT5G20270) (hepta helical protein 1) Arabidopsis thaliana
7B-1 mutant shows resistance to osmotic stress Solanum lycopersicum
0.15 M mannitol treatment does not induce significant gene expression in selected genes Arabidopsis thaliana
nuclear shape contributes to plant response to osmotic stress
plasmolysis treatment is osmotic stress condition
alternative oxidase (AOX1A, ATAOX1A, AtHSR3, HSR3, AT3G22370) is important for osmotic stress tolerance
TaSnRK2.7 plants grew slowly under severe osmotic stress Arabidopsis thaliana
water deficit treatment induces Ss (ATLTP1, AtLtpI-4, LP1, LTP1, AT2G38540) accumulation Solanum sogarandinum; Solanum tuberosum
(ADH, ADH1, ATADH, ATADH1, AT1G77120) is induced by osmotic stress Arabidopsis thaliana
(HHP1, AT5G20270) expression is induced by osmotic stress Arabidopsis thaliana
osmotic stress (339 mM sorbitol) results in cell viability of approximately 40% after 48 h Micrasterias
(AtCOR15A, COR15, COR15A, AT2G42540) is induced by osmotic stress Arabidopsis thaliana
sorbitol was at 7-fold level in Clipper roots after 5 weeks of salt stress Hordeum vulgare
(ATCBF3, CBF3, DREB1A, AT4G25480) expression is up-regulated in wild-type and transgenic plants Arabidopsis thaliana
sulphotransferase 12 (AtSOT1, AtSOT12, ATST1, AtSULT202A1, RAR047, SOT12, ST, ST1, SULT202A1, AT2G03760) is highly expressed under osmotic stress Arabidopsis thaliana
salt treatment induces Ss (ATLTP1, AtLtpI-4, LP1, LTP1, AT2G38540) accumulation Solanum sogarandinum; Solanum tuberosum
drought and salt-stress conditions result in noticeable accumulation of Ss LTP1 protein in two groups of Solanum species and lines Solanum species
anthocyanins have correlative evidence for a relationship with osmotic stress
aluminium-treated cells were extensively plasmolysed in 0.3 M mannitol Nicotiana tabacum
14-3-3 mutants show different responses to mannitol treatment Arabidopsis thaliana
large, spherical appearance of nongreen plastids is suggestive of increased osmotic pressure within the plastids Arabidopsis thaliana
(ATGA20OX3, GA20OX3, YAP169, AT5G07200) mutants ( -1 and -2) show more severely inhibited growth under 200mM mannitol stress Arabidopsis thaliana
transgenic plants subjected to mannitol (200mM) stress accumulated higher levels of reducing sugars compared with WT and VT plants Arabidopsis thaliana
osmotic stress induces expression of (HHP1, AT5G20270) (hepta helical protein 1) Arabidopsis thaliana
salinity stress causes reduction of water uptake
osmolytes are thought to counteract dehydration effect of low water activity
anthocyanin synthesis is inducible under sugar treatments
aluminium-treated cells were not plasmolysed in 0.25 M mannitol (370 mOsm kg−1) Nicotiana tabacum
14-3-3 interactome is markedly affected by mannitol treatment
addition of 30 mM Mtl suggests that this non-metabolizable sugar might generate additional stress Arabidopsis thaliana
prolonged exposure to osmotic stress induced widening of ageing roots
overexpression of IAA in S. meliloti 1021 played positive role in adaptation to osmotic stress in free-living bacteria Sinorhizobium meliloti
osmotolerance locus of Bur-0, Cal-0, Ll-1, and Zu-0 showed strong linkage to same position as Bu-5 osmotolerance locus Arabidopsis thaliana
OsRAN2 expression was determined under osmotic stress Oryza sativa
Hydrogen sulphide (H2S) alleviates oxidative damage from osmotic stress Ipomoea batatas
immersion of excised leaves in a hypertonic solution reliably and reversibly ameliorates large, round leaf epidermal plastid phenotype of msl2-1 msl3-1 plants Arabidopsis thaliana
seedlings were subjected to iso- or hypo-osmotic treatments Arabidopsis thaliana
gip1gip2 nuclei fully mimic WT nuclei under hyperosmotic stress Arabidopsis thaliana
gip1gip2 nuclear shapes remain unchanged in harsher osmotic conditions (0.4 M and 0.6 M mannitol) Arabidopsis thaliana
increased expression of AOX genes and ND genes in (SLG1, AT5G08490) may still be insufficient to reduce ROS level when responding to osmotic stress Arabidopsis thaliana
overexpression of IAA in S. meliloti 1021 played positive role in adaptation to osmotic stress Sinorhizobium meliloti
glycerol-3-P and inositol were at higher concentration in Sahara roots after short-term salt exposure Hordeum vulgare
proline is best known compatible solute in plants
(HHP1, AT5G20270) might play role in osmotic stress signaling Arabidopsis thaliana
osmotic stress (339 mM sorbitol) results in cell viability of approximately 60% after 12 h Micrasterias
osmoregulation mechanism is conserved in yeast Saccharomyces cerevisiae
(ATHSFA2, HSFA2, AT2G26150) overexpression in Arabidopsis wild-type background was shown to enhance tolerance of seedlings germinating on medium with high salt or mannitol concentrations Arabidopsis thaliana
experiments analysed effects of osmotic stress induced by polyethylene glycol (PEG) Vitis vinifera
un is not the only background showing reduced sensitivity to mannitol
existing media was replaced by CM containing 600 nM ISX but without mannitol or PEG Arabidopsis thaliana
hyperosmotic stress shrinks nucleus
hyperosmotic conditions reduces nuclear area
nucleoplasm crowding may reduce nucleus size
nucleoplasm crowding may increase nuclear internal density
(SLG1, AT5G08490) is more sensitive than WT to osmotic stress Arabidopsis thaliana
ns-LTP1 transcripts are up-regulated in response to various environmental stimuli leading to cell dehydration
high-level overexpression of the Arabidopsis (ATHSFA2, HSFA2, AT2G26150) gene confers salt/osmotic stress tolerance Arabidopsis thaliana
sugars help maintain osmotic balance
genes with higher expression in response to elevated red light:far-red light ratio in bud n-2 enriched for osmotic stress Gene Ontology terms Arabidopsis thaliana
high levels of sucrose and fructose may be acting as osmoprotectants Arabidopsis thaliana
defective EGM genotypes behave like plants that do not perceive and respond to mannitol Arabidopsis thaliana
(RLK, AT5G67280) kinases are involved in transduction of osmotic stress signals
FvWRKY42 may play an important role in salt stress response regulation
transgenic T(2) plants showed increased levels of soluble sugars Avena sativa
OsACA6 transgenic plants exhibited enhanced tolerance to PEG stress Oryza sativa
(EGM1, AT1G11300) and EGM2 control plant growth responses to mannitol Arabidopsis thaliana
(EGM1, AT1G11300) and EGM2 act together to induce EGM response Arabidopsis thaliana
(LEA, AT2G21490) proteins are associated with osmotic stress
salt supplementation increases proline content Arabidopsis thaliana
yeast protein kinase (ATSAHH1, EMB1395, HOG1, MEE58, SAH1, SAHH1, AT4G13940) (high osmolarity glycerol 1) regulates many target genes through transcriptional activators Msn2/4, (ATHSP101, HOT1, HSP101, AT1G74310) and Sko1
RiMsn2 can complement growth defect induced by hyperosmosis in ScMsn2/4 knock-out strains Saccharomyces cerevisiae
osmotic stress shows no significant induction of TG markers Arabidopsis thaliana
14-3-3 root interactome markedly responds to mannitol application Arabidopsis thaliana
control cells were distinctly plasmolysed in 0.35 M mannitol (490 mOsm kg−1) Nicotiana tabacum
IgASE1 transgenic seedlings exhibit greater osmotic tolerance than WT seedlings Arabidopsis thaliana
nNOS transgenic plants accumulated higher levels of osmolytes (proline, sucrose, and total soluble sugars) Arabidopsis thaliana
sag mutants show much lower germination and green cotyledon rates than wild-type seeds Arabidopsis thaliana
polyethylene glycol treatment does not greatly increase OsRAN1 mRNA levels Oryza sativa
osmolytes are induced in response to water deficit
upsilon and nu show unequal redundancy in mannitol insensitivity
(BAM3, AT4G20270) is symmetrically repressed under osmotic stress
hhp1-1 mutant shows higher sensitivity to osmotic stress Arabidopsis thaliana
hhp1-1 mutant shows more sensitive induction of stress-responsive genes to osmotic stress Arabidopsis thaliana
mannitol does not show significant induction of LIN6 promoter Nicotiana tabacum
osmotic stress treatment (mannitol) causes 14-3-3 interactome changes Arabidopsis thaliana
nu added to kl background shows larger leaf elongation under hyperosmotic stress (LEH) compared to wild-type on mannitol Arabidopsis thaliana
leaf epidermal plastid phenotype of the msl2-1 msl3-1 mutant can be attributed to abnormally high stromal osmolarity Arabidopsis thaliana
(DAL1, SP1, AT1G63900) mutant plants showed similar results under osmotic stress conditions Arabidopsis thaliana
chlorophyll accumulation used as measure of stress tolerance Arabidopsis thaliana
cell wall softening and hypo-osmotic treatment induces cell swelling Arabidopsis thaliana
increased nuclear stiffness provides mechanical shielding through resistance to hyperosmotic stress
remaining ABA and/or osmostress-upregulated genes were either SnRK2 regulated (14.0%) or HK regulated (10.4%) Physcomitrella patens
(ATP5CS, P5CS1, AT2G39800) is differentially regulated according to osmotic stress responses Medicago truncatula
exogenous application of NO induces proline accumulation in plants under osmotic stress
tebuconazole was hypothesized to induce compatible solute accumulation
bacterial MS ion channel MscS protects against cellular lysis during osmotic downshock
hyperosmotic stress (0.3 M mannitol) on gip1gip2 seedlings does not induce further nuclear deformation in gip1gip2 nuclei Arabidopsis thaliana
PpARK/ (AtCTR1, CTR1, SIS1, AT5G03730) was essential for SnRK2 activation Physcomitrella patens
plants defective in GIP proteins exhibit this response constitutively nuclear stiffness and touch gene expression scaling with osmotic environment Arabidopsis thaliana
nuclear envelope factors contribute to plant response to osmotic stress
AR7 mutant protonemata were killed by osmotic stress and desiccation treatments Physcomitrella patens
knock-out mutant of TAIR: (ATLAC2, LAC2, AT2G29130) shows slightly reduced root elongation under osmotic stress Arabidopsis thaliana
efflux of osmolytes prevents cellular lysis Escherichia coli
regain in cellular turgor triggers in systemic tissues At GLR3.3-dependent cytosolic Ca2+ increase Arabidopsis thaliana
73 proteins were identified at different time points
nine proteins exclusively found in the control plants indicate negative regulation by mannitol stress
complemented lines restore sensitivity to mannitol to wild-type levels Arabidopsis thaliana
pEGM1:EGM1 construct fully complemented (EGM1, AT1G11300) mutant Arabidopsis thaliana
mannose, mannitol and sorbitol alter osmotic status Arabidopsis thaliana
IP3 rapidly accumulates after treatment with NaCl, KCl and sorbitol
proline putatively acts as osmolyte Picochlorum celeri
(KIN1, AT5G15960) expression is up-regulated in wild-type and transgenic plants Arabidopsis thaliana
nitrate reductase (NR) is involved in NO production during osmotic stress response in roots Arabidopsis thaliana
NaCl (200 mM) and sorbitol (400 mM) induce osmolality shifts Nicotiana tabacum
(P5CS2, AT3G55610) is differentially regulated according to osmotic stress responses Medicago truncatula
(MSL2, AT5G10490) are required to release ions from the plastid in response to changes in envelope-membrane tension Arabidopsis thaliana
level of Pro accumulation is not always strong indicator of stress tolerance Arabidopsis thaliana
PEG-induced osmotic stress causes transient increase in membrane depolarization Arabidopsis thaliana
ced2, (ATELP, ATELP1, ATVSR1, BP-80, BP80, BP80-1;1, BP80B, GFS1, MTV18, VSR1, VSR1;1, AT3G52850) (ATVSR3, BP80-2;2, UXS2, VSR2;2, VSR3, AT2G14740) and (BP80-2;1, MTV2, MTV4, VSR2;1, VSR4, AT2G14720) mutants show significantly higher membrane depolarization Arabidopsis thaliana
triple mutants in the un background show larger LEH on mannitol
silicon treatment reduces decrease in total dry weight under osmotic stress Sorghum bicolor
(GRUSP, USP, AT3G58450) mutants of had increased Pro accumulation Arabidopsis thaliana
T-DNA mutants of (NF-YA5, NFYA5, AT1G54160) did have increased Pro accumulation Arabidopsis thaliana
(ATELP, ATELP1, ATVSR1, BP-80, BP80, BP80-1;1, BP80B, GFS1, MTV18, VSR1, VSR1;1, AT3G52850) (ATVSR3, BP80-2;2, UXS2, VSR2;2, VSR3, AT2G14740) mutants were more depolarized relative to wild-type plants
ced2 (ATELP, ATELP1, ATVSR1, BP-80, BP80, BP80-1;1, BP80B, GFS1, MTV18, VSR1, VSR1;1, AT3G52850) mutants had higher [Ca2+]cyt upon osmotic stress treatment osmotic stress treatment
water loss is important for identifying genetic and chemical interventions
11 proteins displaying relatively osmotic-specific phosphorylation responses highlight new processes that may play important roles Arabidopsis thaliana
seedlings grown in presence of mannitol shows no significant difference in growth compared with control samples Arabidopsis thaliana
multiple members of Arabidopsis UspA domain proteins are effectors of Pro accumulation Arabidopsis thaliana
mutants of other three adjacent genes including (AT2G36630) did not significantly differ from wild type Arabidopsis thaliana
arHIF[Col] shows induction of (EGM1, AT1G11300) and EGM2 Arabidopsis thaliana
truncated version of (MSL3, AT1G58200) is capable of rescuing osmotic-shock sensitivity of MJF465
IPTG-inducible expression of MscS is sufficient to restore hypo-osmotic-shock survival to MJF465 Escherichia coli
(ATELP, ATELP1, ATVSR1, BP-80, BP80, BP80-1;1, BP80B, GFS1, MTV18, VSR1, VSR1;1, AT3G52850) mutant differs from wild type in vacuolar pH changes under osmotic stress Arabidopsis thaliana
ced2 mutant shows markedly inhibited early seedling growth Arabidopsis thaliana
vacuolar trafficking mediated by (ATELP, ATELP1, ATVSR1, BP-80, BP80, BP80-1;1, BP80B, GFS1, MTV18, VSR1, VSR1;1, AT3G52850) is important for osmotic stress tolerance Arabidopsis thaliana
proteins implicated in the osmotic response did not show stress-induced changes in gene expression Arabidopsis thaliana
several proteins experiencing osmotic stress-induced phosphoregulation provide insight into cellular mechanisms occurring during the initial stress response Arabidopsis thaliana
osmotic stress treatment applied to four to 5-week-old Arabidopsis thaliana plants Arabidopsis thaliana
osmotic stress results in decrease in transcript abundance for several genes Arabidopsis thaliana
adenosine kinase (ADK1, ATADK1, AT3G09820) is protein with altered abundance under osmotic stress Arabidopsis thaliana
msl2-1 msl3-1 plants exhibit large, round leaf epidermal plastid phenotype Arabidopsis thaliana
gip1gip2 mutant is resistant to lethal hyperosmotic conditions Arabidopsis thaliana
nuclei in gip1gip2 mutant are almost insensitive to osmotic changes Arabidopsis thaliana
hyperosmotic stress for 16 h followed by recovery on normal medium for 7 h results in no significant induction of selected genes Arabidopsis thaliana
T-DNA mutation of (LON1, LON_ARA_ARA, AT5G26860) led to reduced Pro accumulation Arabidopsis thaliana
observation that (ATHM4, ATM4, TRX-M4, AT3G15360) had higher Pro may be consistent with greater root elongation in (ATHM4, ATM4, TRX-M4, AT3G15360) Arabidopsis thaliana
osmotic stress perturbation induces protein phosphorylation changes Arabidopsis thaliana
(RPN13, AT2G26590) shows phosphorylation increase of 3.84-fold in response to mannitol Arabidopsis thaliana
MAP4Kα1 gene expression shows no response in array data Arabidopsis thaliana
N-rich protein (NRP, NRP1, AT5G42050) -mediated cell death signaling is induced by osmotic stress Glycine max
mutants of (ATHM4, ATM4, TRX-M4, AT3G15360) had higher Pro accumulation than Col wild type Arabidopsis thaliana
phosphorylation changes represent phosphorylation increases rather than changes in protein abundance Arabidopsis thaliana
Unknown protein (AT5G58510) shows phosphorylation increase of 2.10-fold in response to mannitol Arabidopsis thaliana
AtALDH7B4 is encoded by osmotic stress-inducible ALDH gene Arabidopsis thaliana
growth attenuation or cessation is attributable to turgor reduction
reversibility of gene expression upon recovery is consistent with idea that induction of genes relates to hyperosmotic stress Arabidopsis thaliana
monitoring of osmotic shocks by MSL family members maintains cell viability
ABA- or osmostress-activated SnRK2 activities were not observed in (AHK5, CKI2, HK5, AT5G10720) /13/20/24 QKO plants Physcomitrella patens
PEG-infused agar produced similar results to mannitol
nuclear response to hyperosmotic stress is rescued upon return to iso-osmotic conditions Arabidopsis thaliana
hyperosmotic stress (0.3 M mannitol) causes mild cytoplasmic detachment from cell wall Arabidopsis thaliana
extracted WT nuclei upon mannitol treatment maintain shape defects Arabidopsis thaliana
nu, phi, and (A11, AtCHI, CFI, CHI, TT5, AT3G55120) mutations in the kl background result in LEH phenotypes similar to un phenotype
(FER, AT3G51550) mutants do not show hypersensitivity to hyper-osmotic stress from mannitol or sorbitol Arabidopsis thaliana
gip1gip2 mutant resists hyperosmotic stress better than wild-type
confocal images were captured after salt treatment Arabidopsis thaliana
organelles may respond similarly to abrupt changes in cytoplasmic osmolarity
WT leaves subjected to dehydration and rehydration regime showed no lysis Arabidopsis thaliana
(MSL2, AT5G10490) and (MSL3, AT1G58200) are required to relieve hypoosmotic stress in the stroma of leaf epidermal plastids Arabidopsis thaliana
hyperosmotic stress decreases nuclear circularity Arabidopsis thaliana
WT nuclei in surviving cells upon 0.4 M and 0.6 M mannitol treatment are strongly deformed compared to iso-osmotic control nuclei Arabidopsis thaliana
hyperosmotic stress (0.3 M mannitol) induces response comparable to gip1gip2 mutant Arabidopsis thaliana
ETR-HKs of Physcomitrella patens are integral part of core module for ABA and osmostress responses Physcomitrella patens
quadruple mutant of ABA-independent class I SnRK2 members ( (ASK2, SNRK2-1, SNRK2.1, SRK2G, AT5G08590) /2.4/2.5/2.10) revealed elevated proline levels in response to osmotic stress Arabidopsis thaliana
increased level of expression of (EGM1, AT1G11300) and EGM2 resulted in stronger growth reduction on Man60 Arabidopsis thaliana
T-DNA mutants in several SD1 members showed no obvious phenotypic indication for involvement in mannitol response Arabidopsis thaliana
150 μL of either water or 140 mM mannitol was injected to produce hypo-osmotic or iso-osmotic treatments Arabidopsis thaliana
root meristematic nuclei after 0.3 M mannitol treatment exhibit deformed shape compared to non-treated plants Arabidopsis thaliana
withholding water rescues msl2-1 msl3-1 leaf epidermal plastid phenotype Arabidopsis thaliana
WT roots treated with 280 mM mannitol showed far fewer [Ca2+] transients Arabidopsis thaliana
sorbitol treatment affects root growth Arabidopsis thaliana
cell swelling is a fundamental property of cellular response to osmotic challenges
WT nuclei at 0.6 M mannitol have lower nuclear area than WT nuclei at 0.3 M mannitol Arabidopsis thaliana
GIP would indirectly control gel-like properties of chromatin
ABA and/or osmostress-upregulated genes in Physcomitrella patens were regulated by HK and/or SnRK2 Physcomitrella patens
regain in cellular turgor triggers in systemic tissues increase of apoplastic L-Glu Arabidopsis thaliana
osmotic stress denatures cytosolic proteins
putative receptor-like kinases (RLKs) are not involved in osmotic effect of mannitol osmotic effect of mannitol Arabidopsis thaliana
EGM2 containing putative mannose-binding and putative carbohydrate-binding domains suggests that variation in shoot growth results from osmotic stress imposed by mannitol or action specific to mannitol Arabidopsis thaliana
WT and GFP plants stopped growing under severe osmotic stress Arabidopsis thaliana
NOJ accumulates higher levels of proline Solanum tuberosum subsp. andigena
Sinorhizobium meliloti RD64 strain accumulates higher level of trehalose Sinorhizobium meliloti
trehalose increased in roots of both cultivars Hordeum vulgare
(DAL1, SP1, AT1G63900) transcript levels are elevated under osmotic stress Arabidopsis thaliana
(AHK5, CKI2, HK5, AT5G10720) /13/20/24 QKO mutant shows defects in establishing osmostress tolerance Physcomitrella patens
WT (SLG1, AT5G08490) transformation rescues mutant phenotypes in terms of response to osmotic stress Arabidopsis thaliana
Treatment of Arabidopsis seedlings with NaCl, sucrose, or mannitol has been demonstrated to decrease leaf osmotic potential Arabidopsis thaliana
Lettuce and radish roots are grown with or without sorbitol at 20°C or 28°C Lactuca sativa; Raphanus sativus
transcriptomes at different stages were analyzed to determine response mechanisms of P. patens to diluted seawater Physcomitrella patens
significant numbers of (ANAC008, SOG1, AT1G25580) target genes were upregulated in response to osmotic stress Arabidopsis thaliana
mannitol treatment affects root growth Arabidopsis thaliana
seedlings were vertically grown on CM plates supplemented with 140 mM mannitol or PEG Arabidopsis thaliana
overexpression of ABA receptor (AtPYL4, PYL4, RCAR10, AT2G38310) enhances osmolyte levels Arabidopsis thaliana
hyperosmotic stress responses are reversible upon return to iso-osmotic conditions
(ATCBF3, CBF3, DREB1A, AT4G25480) was expressed under the control of osmotic stress-inducible (COR78, LTI140, LTI78, RD29A, AT5G52310) promoter
(ATCESA8, CESA8, IRX1, LEW2, AT4G18780) mutants exhibits resistance to mannitol