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drought stress response

69202 relationships annotated with this phrase. Showing first 500 of 69202.
Source entity Relationship Target entity Species
RiMsn2 enhances plant tolerance to drought stress
RiMsn2 regulates STRE-controlled genes from R. irregularis Rhizophagus irregularis
dryland ecosystems are composed of diverse biological strategies for dealing with water stress
differences between plant and air temperature can be used to infer plant water stress
These comparisons were true across seasonal or drought-induced soil moisture variation
stomatal closure minimizes water loss
CaDeSI2 modulates CaAITP1 protein in plant cells during drought stress Capsicum annuum
leaf δ13C can be immediately affected by droughts
this study aimed to identify cause of sensitivity of C4 assimilation to dehydration
dephosphorylated BpMADS11 plays a key role in drought tolerance conferred by BpMADS11 Betula pendula
dephosphorylation of BpMADS11 plays a role in drought tolerance Betula pendula
BpPP2C22 knockout resulted in BpMADS11 maintaining its phosphorylated state Betula pendula
silencing of RiMsn2 can influence expression levels of drought stress-responsive genes in Rhizophagus irregularis Rhizophagus irregularis; Medicago truncatula
difference in resistance to dehydration between poplar and lavender may explain difference in (PLD, PLDALPHA1, AT3G15730) lethal values between species
seedlings are less drought resistant than adults
drought stress induces CaOSR1 expression Capsicum annuum
treating sapwood capacitance (CS) as constant in models may overestimate buffering capacity under drought conditions
BpERF61 overexpression lines (BpERF61-OE5, BpERF61-OE6, BpERF61-OE7) suffer lowest degree of damage from dehydration Betula pendula
plant–plant interactions can exacerbate hot drought impacts
ANNEXIN 1 (ANN1, ANNAT1, AtANN1, ATOXY5, OXY5, AT1G35720) was found to be important for drought tolerance Arabidopsis thaliana
fET GLDAS displays several tails that decrease linearly with progressing CWD at medium fET sites
(PAC, AT2G48120) treatment plants show recovery rate of 100%
Arabidopsis thaliana plants divided into Water, Semi-drought, and Drought groups Arabidopsis thaliana
apoplastic water potential drops more than xylem water potential and leaf water potential as xylem potential decreases to turgor loss point
dehydration causes subsequent increase in CaDeSI2 expression Capsicum annuum
BpERF61 mainly binds to three other kinds of motifs Betula pendula
35S:PYL4 A194T transgenic plants showed enhanced drought resistance compared with nontransformed or 35S:PYL4 plants
(PAC, AT2G48120) concentration has concentration-dependent effect on PAC-enhancing drought tolerance
IbBBX24 enhances plant tolerance to drought stress Ipomoea batatas
greater proportion of bark in WL trees compared with WW and LL trees may contribute to difference in (PLD, PLDALPHA1, AT3G15730) lethal
flash-drought event causes only slight change in respiration rate (R) Betula pendula Roth
tree populations may be at risk of population declines with increased aridity
BpMADS11 regulates expression of BpERF61 Betula platyphylla
BpERF61 binds to DNA motif (GGGCCCC) to regulate drought stress-related genes Betula platyphylla
(FAR1, AT5G22500) (FAR-RED IMPAIRED RESPONSE 1) confers increased resistance to drought
(ATAZG1, AZG1, AT3G10960) does not confer sensitivity to drought Arabidopsis thaliana
(LGO, SMR1, AT3G10525) and (SMR5, AT1G07500) induction occurs under mild drought stress Arabidopsis thaliana
GintAQPF1 and GintAQPF2 respond to drought stress Rhizophagus irregularis
stomatal conductance were measured drought stress response Populus
CaSnRK2.6 is substrate of (AtUBP12, UBP12, AT5G06600) /13 Arabidopsis thaliana
semi-dwarf varieties typically do not outperform taller counterparts under drought
drought-stressed sunflowers show increased macroporosity in the rhizosheath Helianthus annuus
preserved rhizodeposition mitigates drought effects on the microbial community
RcOST1L overexpression line (RcOST1L-OE) shows better performance in drought tolerance Arabidopsis thaliana
AM and ECM trees may differ in their sensitivities to water stress
delayed mortality is hard to attribute to climate due to its delayed onset which depends on carbon storage filling prior drought and uncertain carbon use strategies which differ among tree species
Ri14-3-3 is significantly enhanced under severe drought conditions Medicago truncatula; Rhizophagus irregularis
abscisic acid (ABA) levels in leaves were shown to be relatively constant and only to substantially increase during repeated drought stress cycles
root barrier to radial O2 loss (ROL) is possibly of importance as drought tolerance trait
RiMsn2 and drought-responsive genes positively respond to drought stress during AM symbiosis Medicago truncatula; Rhizophagus irregularis
RiMsn2 knockdown through VIGS and HIGS resulted in significant decreases in relative water content (RWC) in mycorrhizal plants Medicago truncatula; Rhizophagus irregularis
RiMsn2 knock-down results in decreased plant tolerance to drought stress Rhizophagus irregularis
reducing stomatal conductance (gs) is one of the first responses of plants to high vapor pressure deficit (VPD) and drying soil Pinus sylvestris
drought causes biochemical responses
WL and LL trees showed the greatest difference in (PLD, PLDALPHA1, AT3G15730) lethal values
soil desiccation affects nutrient and water uptake
labile C inputs into the soil via rhizodeposition can increase in response to drought
drought did not affect transition traits Conyza canadensis
BpERF61 binds to DNA motif (TTGGAT) to regulate drought stress-related genes Betula platyphylla
SLR1-TAD1-PYLs module coordinates growth and survival during drought response Oryza sativa
inhibited GA accumulation contributes to rice survival under drought stress
all plots showed reduced gas exchange through most of 2021 Pinus edulis
electrolyte leakage were measured drought stress response Populus
C4 plants are superb drought avoiders
sensitivity or elasticity quantifies reciprocal of tolerance
growth repression and yield reduction deliver more energy to stress response
(PYL9, RCAR1, AT1G01360) (PYL10, RCAR4, AT4G27920) slr1-d1 mutant restored survival rate to wild-type background levels
WL trees had higher PLD lethal value compared with WW and LL trees
Scots pine is known to suffer from drought Pinus sylvestris
(TOL2, AT1G06210) /3/5/6 quadruple mutant plant line is significantly more drought-tolerant
growing trees on oceanic island in Japan frequently receive tree drought-induced mortality
rapid dehydration caused nonstomatal limitation to rise three times more steeply in C4 maize and sorghum
BpERF61 regulates expression of drought tolerance-related genes Betula pendula
bpmads11 knockout lines (bpmads11#-3, bpmads11#-5, bpmads11#-10) show significantly increased H2O2 content Betula pendula
stomatal closure before embolism formation has been theoretically advanced as another fundamental component of plant drought tolerance
MdMYB88 slightly induced by simulated drought in roots of M. sieversii Malus sieversii
(ATVAMP711, VAMP711, AT4G32150) deletion mutant shows slower stomatal closure in response to drought stress Arabidopsis thaliana
ost2-2D-OE-VAMP711-1#/2# transgenic lines display phenotype similar to ost2-2D-OE-VAMP711 plants Arabidopsis thaliana
HVA22P:CBF3 transgenic families shows significantly higher relative yield (RY) Oryza sativa
HVA22P:CBF3 transgenic families shows significantly higher RY than wild-type (WT) Oryza sativa
Actin1:LOS5 transgenic families shows significantly higher relative yield (RY) Oryza sativa
constitutive and/or inducible overexpression of (ATCBF3, CBF3, DREB1A, AT4G25480) conferred drought resistance
constitutive and/or inducible overexpression of (ABA3, ACI2, ATABA3, AtLOS5, GIN5, LOS5, SIR3, AT1G16540) conferred drought resistance
(ATTSPO, TSPO, AT2G47770) expression and activity increase in response to water stress or ABA treatment Physcomitrella patens
DRE-like elements have been found in 5' sequences upstream of dehydration-induced genes Physcomitrella patens
aridity index exerted negative effects on root N concentrations implying plant root growth and N uptake are inhibited by drought conditions woody plant species
reductions in water availability affects rice yields Oryza sativa
reduced crop water loss leads to better drought avoidance
medium to high stomatal density (SD) varieties (IR-64, HATRI-61, Bharathy, C-7306) perform better than low stomatal density varieties under drought stress Oryza sativa
reduced stomatal density (SD) and stomatal conductance (g sw) improved drought tolerance Oryza sativa
RiMsn2 may regulate downstream drought stress-responsive genes in Rhizophagus irregularis Rhizophagus irregularis
mechanism of nutrient stress enhancing tree mortality has been rarely addressed in tropical systems
mycorrhizal associations can facilitate land plants to mitigate drought stress
RiMsn2 binds to STRE elements of drought-responsive genes Rhizophagus irregularis
seedlings after dehydration 2 h (D2h) identified 1320 upregulated genes
seedlings after dehydration 4 h (D4h) compared with D2h identified 3941 upregulated genes
slr1-d1 mutants have slower water loss rate than wild-type (WT)
extreme short-term drought manipulation applied to mature piñon Pinus edulis
CmBBX19 physically interacts with CmABF3 Chrysanthemum morifolium
complete disconnection of the vascular bundle from the photosynthetic tissue of lycopods during drought is analogous behavior to transfusion tracheid collapse
comparative field studies by Taylor et al. (2014) found C4 species experienced water limitation in correspondence to midday depressions of leaf water potential (ΨL)
BpERF61 regulates drought stress genes Betula pendula
drought tolerance-related genes enhance drought tolerance Betula pendula
nutrient stress was found to enhance tree mortality after droughts
high levels of biodiversity, interactions among species, trait plasticity, and variation in species' relative abundance make difficult characterisation of community-level hydraulic vulnerability of tropical rainforests
savannah and grassland sites exhibit rapid declines of fET to 10% of water-unlimited rate
differences between plant and air temperature have been used to assess plant moisture stress
leaves with declining xylem water potential and declining leaf water potential show no signs of macroscopic loss of turgor
saplings of a hybrid poplar grown under well-watered (WW), water-limited (WL), or light-limited (LL) conditions were exposed to a severe drought Populus species (hybrid poplar)
drought affected functional traits Conyza canadensis
(TOL2, AT1G06210) /3/5/6 mutant shows clear drought tolerance Arabidopsis thaliana
leaf δ 13 C decrease indicates less drought stress
tree diversity experiments experienced extreme natural drought event in 2018
leaf hydraulic conductance under high irradiance may be more vulnerable to dehydration (lower safety) dehydration vulnerability
vapor pressure deficit (VPD) is a significant independent predictor of Kmax (leaf hydraulic efficiency)
modest dips in leaf water potential (ΨL) did not trigger stress indicators in C3 plants
(AtPYL4, PYL4, RCAR10, AT2G38310) OE lines showed survival of around 30% after drought stress Arabidopsis thaliana
growth in semi-dwarf genotypes under drought may not prioritize reproductive parts
aridity gradient affects Δ performance Conyza canadensis
drought had weaker effects in recruitment life stage Conyza canadensis
Capsicum annuum DeSUMOylating Isopeptidase 2 (CaDeSI2) influences drought responses of pepper Capsicum annuum
pan-European 2018 summer drought impacted forest ecosystems
tree species richness increases leaf δ15N under high drought intensity
BpERF61 knockout exhibits decreased drought tolerance Betula platyphylla
drought resistance experiments under greenhouse conditions performed to test plant survival under drought stress Arabidopsis thaliana
(AtATL78, ATL78, PRU2, AT1G49230) is a positive regulator of drought stress response Arabidopsis thaliana
percentage loss of branch diameter (PLD) is a result of decrease in branch diameter during the drought relative to the maximum diameter of the branch before dehydration
drought stress decouples enzyme activity
water potential decreases during drought
TRV2:CaDeSI2/TRV2:CaAITP1 plants show survival almost as high as TRV2:CaAITP1 plants Capsicum annuum
decrease of CaDeSI2 gene expression during early dehydration/PEG exposure may be mediated via ABA-independent pathway Capsicum annuum
MpPUB9 gene expression levels increased precipitously under drought treatment Marchantia polymorpha
natural field conditions across a transect in Western China showed five C4 Amaranthaceae species had greater depression of photosynthesis due to water limitation compared to C3 neighbours
BpERF61 binding to different DNA motifs improves birch drought tolerance Betula pendula
15-d-old seedlings submitted to dehydration for 12 h in a laminar flow hood, followed by rehydration used to measure survival rate 3 d afterward Arabidopsis thaliana
other barley lines senesced and gave lower yields Hordeum vulgare
reduced metabolic demand for root growth is particularly important under water stress Zea mays
water deficit reduced stomatal conductance in transgenic plants to 25% to 29% of control conditions Hordeum vulgare
MdVND6 and MdMYB46 target genes expression is influenced under drought conditions Malus × domestica
T2 transgenic families were selected for drought resistance re-testing
(AtHPR1, AtTHO1, HPR1, RAE3, THO1, AT5G09860) expression was not inducible under all types of drought-imposed conditions such as desiccation of plants on filter paper Arabidopsis thaliana
drought causes need for cellular architecture reconstruction
hydrophilic, disordered regions spanning the length of LEAs are thought to fold upon water loss into amphipathic alpha-helices that stabilize cellular membranes
plants have evolved sophisticated mechanisms to cope with drought stress
extreme drought may cause drought-induced embolism in tropical French Guiana
GLDAS overestimates water stress
Pinus edulis trees experiencing extreme short-term drought (−90% ambient precipitation plot, 2020–2021) contrasted with Pinus edulis trees experiencing a decade of severe drought (−45% plot, 2010–2021) Pinus edulis
functional traits have weak or complex effects on how Conyza canadensis copes with drought stress Conyza canadensis
TRV2:CaDeSI2/TRV2:CaAITP1 plants show higher survival than TRV2:00 control plants Capsicum annuum
C4 grasses and Cyperaceae species showed 50% reduction in assimilation at −1.5 MPa leaf water potential
phosphorylation of BpMADS11 is critical for enhancing drought tolerance Betula pendula
leaf hydraulic conductance (Kleaf) and stomatal conductance (gs) are co-regulated by drought
(FAR1, AT5G22500) mutant are more sensitive to drought Arabidopsis thaliana
hot droughts are especially hard on trees
water potential measured as physiological metric to investigate mechanisms underlying drought-induced changes in NSC pool age Pinus edulis
irrigated trees were also more sensitive to changes in temperature when soil was drying Pinus sylvestris
14-day drought treatment causes changes in photosynthetic apparatus Arabidopsis thaliana
observation of apoplastic water potential becoming more negative than turgor loss point is consistent with recent assessments of undersaturation using indirect techniques
relative water content (RWC) is a parameter related to tree water status
LL trees had the weakest PLD lethal value and resistance to cell damage
C3 grass and Cyperaceae species showed 50% reduction in assimilation at −3.8 MPa leaf water potential
increasing drought in dry areas may threaten survival of EcM gymnosperms more than AM gymnosperms
bpmads11 knockout lines (bpmads11#-3, bpmads11#-5, bpmads11#-10) show significantly increased MDA content Betula pendula
dephosphorylation of BpMADS11 induced the expression of BpERF61 Betula pendula
greater plasticity in vegetative phase change (VPC) timing would occur in a more severe drought treatment Arabidopsis thaliana
GO:0009414 (response to water deprivation) was enriched in SOM9 Setaria viridis
stressful outdoor conditions in middle of day can create temporary mild drought stress Nicotiana tabacum
drought is associated with tree mortality and forest dieback
trees were dehydrated to varying drought levels Populus species (hybrid poplar)
genome size (GS) plays unclear role in influencing species' response to reduced water availability
detailed studies of other NRLs can reveal how plants sense and respond to water limitation
(CPD45, FHY3, AT3G22170) and (FAR1, AT5G22500) proteins confer drought tolerance
Col-0 wild-type plants did not survive after drought stress Arabidopsis thaliana
mannitol induced (ATAZG1, AZG1, AT3G10960) transcription at a lower rate than sodium chloride Arabidopsis thaliana
most forests exhibit mild fET reductions
plants have evolved sophisticated molecular regulatory networks
stability of plasma membrane and its rupture were found to be linked to plant water status
WL (water-limited) trees had higher PLD lethal value of 11.47%
LL (light-limited) trees had PLD lethal value of 7.58%
tree populations may be sensitive to fluctuations in soil moisture
transfusion tracheids have been observed collapsing under drought
drought-impacted forests show significantly more loss in vegetation index
(CPD45, FHY3, AT3G22170) and/or (FAR1, AT5G22500) knockout mutants are less tolerant to drought stress
delayed mortality after drought events due to carbon starvation cannot be ruled out
control plants show survival rate of approximately 26%
strong decline in OXZ conductance preceding stomatal closure provided nonstomatal limitation of transpiration rate Solanum lycopersicum
difference in (PLD, PLDALPHA1, AT3G15730) lethal could also be attributed to physiological parameters, such as age or cell anatomy
alix-1 and (FREE1, FYVE1, PDE330, AT1G20110) mutant plant lines are difficult targets for engineering drought tolerance Arabidopsis thaliana
leaf water potential (ψL) should be measured in terms of stress intensity
modest dips in leaf water potential (ΨL) did not affect assimilation in C3 plants
BpERF61 does not mainly bind to DRE/CRT elements and GCC-boxes Betula pendula
plant heat shock transcription factors act on downstream drought-responsive element-binding factors (DREB2, DREB2A, AT5G05410) and (AtERF48, DREB2C, AT2G40340)
abscisic acid (ABA) accumulation is required to maintain root growth of maize (Zea mays L.), Arabidopsis, and rice (Oryza sativa L.) in response to water deficit Zea mays; Arabidopsis thaliana; Oryza sativa
small plant size together with very low stomatal density (SD) is ideal combination of traits for growth of rice under drought conditions Oryza sativa
epiphytic material (EM) segments moved from upper montane cloud forest to lower elevations in Costa Rica showed plants at lower, drier sites had significantly higher leaf mortality, lower leaf production, and reduced longevity
RiMsn2 regulates STRE-controlled genes Rhizophagus irregularis
tropical rainforests are susceptible to increases in mortality
RiPbs2 is required for drought resistance of the host plant Rhizophagus irregularis
drought causes morphological responses
strong decline in conductance of OXZ preceded stomatal closure during dry down Solanum lycopersicum
growth conditions influence relationship between stem diameter variations and drought damage mechanisms Populus
severe stress response can be accompanied by changes in leaf wax composition
drought reduced root : shoot ratio (RSR) Conyza canadensis
vein width is related to drought stress negatively drought stress
greater hydraulic safety leads to large decline in Kleaf and stomatal closure during drought
increased likelihood of drought-tolerant species may contribute to mitigated effect of drought on the middle growing-season plant community
BpMADS11 is M-Type MADS-box transcription factor
physical/anatomical mechanisms, such as the xylem and apoplastic (cell walls) structure are the main contributors to control of water movement out of the xylem, especially under drought
ABA biosynthetic pathway can be considered as potential target to improve plant performance under drought
drought stress coping mechanisms prevent water loss
increased frequency and intensity of droughts is expected to exacerbate tree mortality and forest dieback events
WW (well-watered) trees had PLD lethal value of 6.62%
turgor loss and embolism spread increase risk of hydraulic failure
tree diversity can regulate drought impacts in natural forests
bpmads11 knockout lines (bpmads11#-3, bpmads11#-5, bpmads11#-10) show increased plant height Betula pendula
BpMADS11 can regulate the expression of BpERF61 Betula pendula
BpERF61 directly regulates drought tolerance-related genes Betula pendula
202 target genes of BpERF61 are mainly involved in response to water deprivation Betula pendula
drought stress coping mechanisms maintain cell water content
drought-induced tree mortality globally is reported to increase research priority for characterising hydraulic traits
drought-activated (ATSAHH1, EMB1395, HOG1, MEE58, SAH1, SAHH1, AT4G13940) MAP kinase signalling cascade culminates at RiMsn2 Rhizophagus irregularis
high fET sites show almost no effect of water stress on plants
little plasticity in the timing of vegetative phase change (VPC) in response to drought was found Arabidopsis thaliana
(PLD, PLDALPHA1, AT3G15730) lethal value in lavender species was 21.3%
plasticity of responses to drought was comparable between native and non-native ranges Conyza canadensis
CaDeSI2 plays a positive role in drought resistance Capsicum annuum
CaDeSI2-OX plants show less severe wilting than wild-type plants Arabidopsis thaliana
leaf shedding occurs during drought conditions
warming and drying environment increased mortality rate of large trees in subtropical forest
PEG-induced drought stress highly induces expression of BpMADS11 in roots and leaves Betula pendula
abscisic acid (ABA) is recognized as critical hormonal regulator of plant response to water stress
(AtPYL4, PYL4, RCAR10, AT2G38310) A194T OE lines showed survival of 60% to 70% after drought stress Arabidopsis thaliana
enhanced abscisic acid (ABA) biosynthesis and signaling regulates gene expression under water stress conditions
low stomatal density (SD) varieties (Nang Thom BIS, Sathi, UCP-188, OM-479) do not perform well under drought stress Oryza sativa
RiHog1-RiMsn2-STREs module controls drought stress-responsive genes Rhizophagus irregularis
water deficits influence crop productivity
difference in proportion of bark between poplar and lavender could also explain difference between the two species in (PLD, PLDALPHA1, AT3G15730) lethal
scenario (c) presents opposite response (increasing Δ performance) Conyza canadensis
intact plants grown in hydroponics showed assimilation decline at more negative ΨL in C3 wheat and sunflower
BpMADS11 overexpression lines (BpMADS11-OE1, BpMADS11-OE2, BpMADS11-OE3) recover quickly and grow well after rehydration, whereas drought tolerance Betula pendula
BpERF61 binds to DNA motifs such as G-boxes to regulate drought tolerance-related genes Betula pendula
ABSCISIC ACID INSENSITIVE 5 (ABI5, AtABI5, DPBF1, GIA1, AT2G36270) expression is induced by drought stress
plant growth during the subsequent 5-d period was reduced in nontransformed Col-0 and (AtPYL4, PYL4, RCAR10, AT2G38310) OE plants compared with A194T OE plants Arabidopsis thaliana
transgenic plants performed better than parental line (wild type; WT) under stress Hordeum vulgare
LN plants showed effective coordination of assimilation with balanced transpiration under drought stress Hordeum vulgare
modulated abscisic acid (ABA) homeostasis benefits plants under long-term stress Hordeum vulgare
greater water acquisition enables improved growth and yield under water stress Zea mays
(AtMAX2, MAX2, ORE9, PPS, AT2G42620) mutant at seedling stage displays strong hypersensitivity to drought stress Arabidopsis thaliana
(AtMAX2, MAX2, ORE9, PPS, AT2G42620) mutant at adult stage displays strong hypersensitivity to drought stress Arabidopsis thaliana
capacity of plants to resist embolism formation in the xylem is hypothesized to be a major component of plant drought tolerance and survival
Actin1:NHX1 is one of eight constructs showing significantly higher relative yield under both drought stress conditions
relative yield is used as criterion to evaluate drought resistance performance
CACG-like motifs is bound by (ANAC072, ANAC72, AtRD26, RD26, AT4G27410)
msi1-cs plants have increased drought tolerance Arabidopsis thaliana
aquaporin gene expression in Physcomitrella patens is stimulated by water stress and ABA Physcomitrella patens
RRS1-KO mutant significantly increased grain yield per plant under drought stress
declining xylem water potential and declining leaf water potential causes to become significantly more negative apoplastic water potential
severe drought events results in increased mortality Pinus sylvestris
functional traits mediate effects of drought on plant performance
comparison of among-population variation (APV) in drought responses across life stages may be important because impact of drought can significantly differ between seedlings and adults
ESCRT machinery components including (TOL2, AT1G06210) and (TOL5, AT5G63640) are highly upregulated in early drought stress responses plant cell suspension cultures
CaDeSI2-silenced pepper plants show enhanced susceptibility to drought stress Capsicum annuum
TRV2:00 plants show higher survival than TRV2:CaDeSI2 plants Capsicum annuum
CaDeSI2 positively modulates drought tolerance Capsicum annuum
CaDeSI2 transcript levels decrease during early dehydration/PEG exposure Capsicum annuum
comparative field studies by Taylor et al. (2014) found C3 species did not experience water limitation in correspondence to midday depressions of leaf water potential (ΨL)
NRL5 is involved in drought resistance Arabidopsis thaliana
OsPP18 confers drought stress tolerance Oryza sativa
ospp18 mutant shows significantly reduced tiller number compared with wild-type plants Oryza sativa
water stress in field reduces grain yield Zea mays
abscisic acid (ABA) is involved in drought stress tolerance
dehydration proteins accumulate to protect plants from damage of stress conditions
(ATVAMP711, VAMP711, AT4G32150) overexpression partially rescues drought-sensitive phenotype of ost2-2D mutant Arabidopsis thaliana
stomatal pores play an important role in the control of water loss in response to drought stress
(ATCBF3, CBF3, DREB1A, AT4G25480) is one of five genes showing significantly higher relative yield under both drought stress conditions
aquaporin gene knockouts wilt faster than wild-type gametophores during moderate water stress Physcomitrella patens
varieties with higher stomatal density (SD) and smaller stomatal size (SS) respond better to drought stress Oryza sativa
RiMsn2 may positively regulate expression of STRE-controlled genes Rhizophagus irregularis
forests growing under higher vapour pressure deficit (VPD) are expected to be more hydraulically resistant
chlorophyll fluorescence measured as physiological metric to investigate mechanisms underlying drought-induced changes in NSC pool age Pinus edulis
90% plot had significantly more negative water potentials than control in September 2020 and June 2021 Pinus edulis
loss of hydraulic conductance assessed as AquaDust or SPC conductance proceeds through steeper drop based on best-fit exponents of sigmoidal dependence Solanum lycopersicum
modulated root aquaporin expression occurs under drought
Ectomycorrhiza-associated oaks (Quercus) were reported to have better growth performance than other trees during drought Quercus
BpMADS11 interacts with protein phosphatase 2C22 (BpPP2C22) Betula platyphylla
BpERF61 can confer drought tolerance Betula pendula
(ABCC2, AtABCC2, ATMRP2, EST4, MRP2, AT2G34660) transcript levels were considerably increased after exposure to drought for at least 4 d Arabidopsis thaliana
2-week-old seedlings subjected to drought (polyethylene glycol [PEG]-infused plates) or osmotic (mannitol) stress for 1 week showed no evident differences in wilting appearance and root and shoot growth between mutant and wild-type seedlings Arabidopsis thaliana
mutations that enhance abscisic acid (ABA)-dependent inhibition of PP2Cs can be used for ameliorating drought stress
leaf death occurs as gs approaches zero and Kleaf declines by more than 88% Metasequoia glyptostroboides
LOHi lines suffered to lesser extent stress-induced reduction in assimilation Hordeum vulgare
OsPP18 mediates drought stress responses Oryza sativa
root system size correlates with tolerance to drought stress
wilting rate of leaves in ost2-2D mutant is much higher than other plants Arabidopsis thaliana
(ATVAMP711, VAMP711, AT4G32150) and (AHA1, HA1, OST2, PMA, AT2G18960) (AHA2, AtHA2, HA2, PMA2, AT4G30190) work together to regulate stomatal closure in response to drought stress Arabidopsis thaliana
(ABA3, ACI2, ATABA3, AtLOS5, GIN5, LOS5, SIR3, AT1G16540) overexpression leads to reduced leaf transpiration under drought conditions Arabidopsis thaliana
transgenic families of two gene constructs showed significantly higher relative spikelet fertility than wild-type
reduction in irrigation in Kipp resulted in only 1–11% reduction in yield of BnFTA transgenic lines Brassica napus
Tortula ruralis has two distinct cDNAs with high homology to PpDBF1 Tortula ruralis
incipient point of leaf death corresponds to 88% loss of leaf hydraulic conductivity (Kleaf) Metasequoia glyptostroboides
drought stress markedly inhibited stomatal conductance, transpiration, and assimilation Hordeum vulgare
genes in response to stimulus category have altered drought-responsive expression patterns in ospp18 mutant Oryza sativa
Leucaena leucocephala is highly tolerant to drought Leucaena leucocephala
low water potential-induced Pro accumulation has been widely observed in plants
Piriformospora indica confers drought stress tolerance to Arabidopsis seedlings Arabidopsis thaliana; Piriformospora indica
(ATCBF3, CBF3, DREB1A, AT4G25480) transgenic plants with HVA22P promoter showed high drought resistance (LDS < 1)
ThZF1 is upregulated by drought
LP103 plants remained green for longer duration before senescence under postanthesis drought Hordeum vulgare
(ATCBF3, CBF3, DREB1A, AT4G25480) transgenic plants with Actin1 promoter showed high drought resistance (LDS < 1)
Actin1:ZAT10 showed significantly higher relative spikelet fertility than wild-type
Physcomitrella patens contains at least one DREB, PpDBF1 Physcomitrella patens
water-use efficiency under drought conditions is the focus of most studies
drought tolerance involves guard cell regulation
(ATCBF3, CBF3, DREB1A, AT4G25480) transgenic plants had better drought resistance performance than other genes in pre-screening
reduction in irrigation in Kipp resulted in 21% decrease in yield of control Brassica napus
Tr288, a Tortula ruralis protein with 78% similarity to Physcomitrella patens DHNA is thought to be involved in cellular protection, perhaps repair, during rehydration Tortula ruralis
severe levels of water stress sufficient to cause damage to the hydraulic system and incipient leaf damage Metasequoia glyptostroboides
sugar accumulation is important for osmotic adjustment under drought stress
MdMYB transcription factors cannot be expressed at higher levels in response to simulated drought treatment Malus domestica
Actin1:NHX1 transgenic families (T2) shows higher spikelet fertility Oryza sativa
exogenous candidate genes showed certain effects in improving drought resistance of rice Oryza sativa
HVA22P:CBF3 is one of eight constructs showing significantly higher relative yield under both drought stress conditions
constitutive and/or inducible overexpression of (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) conferred drought resistance
(AtHPR1, AtTHO1, HPR1, RAE3, THO1, AT5G09860) expression kinetics is different from other drought-inducible genes such as (COR78, LTI140, LTI78, RD29A, AT5G52310) and (ATNCED3, NCED3, SIS7, STO1, AT3G14440) Arabidopsis thaliana
protection of photosynthetic electron transport chain (ETC) from excess light by alternative pathway (AP) was demonstrated in drought-stressed wheat Triticum aestivum
ABA-independent transcription occurs through activation of dehydration-responsive elements (DREs) in dehydration-induced gene promoters
60 protein spots are irreversible in IR64 genotype Oryza sativa
HvDhn4s: TaNAC69-1 lines show 13-fold increase of TaNAC69-1 expression in roots under drought stress Triticum aestivum
drought stress sufficient to impact photosynthesis has relatively little effect on translocation
PIP expression induced by water deficit is complicated response Oryza sativa
(ASL11, LBD15, AT2G40470) mutant has increased sensitivity to water-deficit stress
LBD15-overexpressing lines show slower water loss
senescence is response to terminal drought Hordeum vulgare
lines with large cortical cell size (CCS) under water stress have greater stomatal conductance Zea mays
fad7-1/fad8-1 double mutant shows no significant difference in tumor size compared to wild-type at high relative humidity (75%–100%) Arabidopsis thaliana
(AT-POX, ATPDH, ATPOX, ERD5, PDH1, PRO1, PRODH, AT3G30775) mutants had the same low water potential-sensitive phenotype as (ATP5CS, P5CS1, AT2G39800) mutants Arabidopsis thaliana
(AtMAX2, MAX2, ORE9, PPS, AT2G42620) mutants are drought sensitive Arabidopsis thaliana
plants always lost turgor before experiencing stem embolism Quercus
plasma membrane (PM) H+-ATPase plays regulatory roles in response to drought stress Arabidopsis thaliana
(AHA1, HA1, OST2, PMA, AT2G18960) open stomata2-2D ( -2D) mutant plants with constitutive higher PM H+-ATPase activity are hypersensitive to drought stress Arabidopsis thaliana
rice MAPK overexpression significantly increases tolerance of rice to drought Oryza sativa
(ATNCED2, NCED2, AT4G18350) transgenic plants with HVA22P promoter showed high drought resistance (LDS < 1)
drought resistance of transgenic plants tested in field conditions
drought tolerance occurs in naturally fluctuating evaporative demand and soil moisture Zea mays
abscisic acid (ABA) accumulation occurs in response to drought
xylem resistance to embolism appears to be important property of drought tolerance in land plants
1130 T1 families for 14 constructs were evaluated by leaf drying score (LDS)
drought stress applied by withholding water until relative water content was 70% caused (ATHPR1, HPR, AT1G68010) expression increased 1.6-fold compared to non-stressed plants Arabidopsis thaliana
Tortula ruralis aquaporins may be involved in recovery of desiccation-tolerant moss Tortula ruralis
stay-green Lochow-Petkus (LP103) line displayed reasonable level of drought tolerance Hordeum vulgare
overexpression of STRESS-RESPONSIVE (anac021, ANAC022, NAC1, AT1G56010) (SNAC1) resulted in improved drought tolerance Oryza sativa
lines with large cortical cell size (CCS) under water stress in mesocosms have greater shoot biomass Zea mays
several groups constructing transgenic plants with increased Pro accumulation have collectively led to ambiguous results on whether increasing Pro accumulation can by itself increase drought tolerance
Pro does contribute to drought resistance Arabidopsis thaliana
overexpression of a stress-responsive transcription factor in rice resulted in significantly improved drought resistance under field conditions Oryza sativa
laboratory or greenhouse conditions may be partially consistent with results from drought-stressed field environments
steady increase in transcripts of (COR78, LTI140, LTI78, RD29A, AT5G52310) and (ATNCED3, NCED3, SIS7, STO1, AT3G14440) suggests that plants started to experience water deficiency after 2 days Arabidopsis thaliana
abscisic acid (ABA) remains elevated long after initial dehydration drying moss Physcomitrella patens
overexpression of certain individual stress protein or transcription factor regulating multiple stress proteins was shown to confer increased tolerance to drought
msi1-cs plants were deprived of water
purified (LEA, AT2G21490) protein promoted formation of a sucrose-LEA glass
(CBNAC, NTL9, AT4G35580) or Ca2+/CaM binding to may positively regulate RD29
(IRX14, AT4G36890) mutants exhibit drought-tolerant phenotype Arabidopsis thaliana
water deficit affects crop yield Oryza sativa
(AtPUB19, PUB19, AT1G60190) expression level is inversely correlated with degree of tolerance to water stress Arabidopsis thaliana
various root hydraulic conductances directly resulting in differing resistance to water deficiency Oryza sativa
number of dehydration-regulated genes was almost 10 times greater than number of genes under hydration conditions Arabidopsis thaliana
drought stress compromises grain yield
cortical cell size (CCS) in well-watered conditions is positively correlated with cortical cell size (CCS) in water-stressed conditions Zea mays
water stress in field reduces shoot biomass Zea mays
HVA22P:ZAT10 transgenic families shows significantly higher relative yield (RY) Oryza sativa
(ABA3, ACI2, ATABA3, AtLOS5, GIN5, LOS5, SIR3, AT1G16540) transgenic plants with Actin1 promoter showed high drought resistance (LDS < 1)
barley late embryogenesis abundant (LEA, AT2G21490) B19.3 promoter is induced in vegetative tissues during postanthesis drought stress Hordeum vulgare
ospp18 mutant shows slower growth than wild-type plants Oryza sativa
stomatal closure maintains water status in plant cells
decreased chlorophyll and relative water contents in ost2-2D mutant are partially rescued in Col-0:OE-VAMP711 plants Arabidopsis thaliana
constitutive and/or inducible overexpression of (ABA3, ACI2, ATABA3, AtLOS5, GIN5, LOS5, SIR3, AT1G16540) can contribute to improvement of drought resistance at level of yield per plant and/or spikelet fertility
limited number of transgenic families for (ATNCED2, NCED2, AT4G18350) might be reason why promising transgenic families with significant drought resistance have not been identified from (ATNCED2, NCED2, AT4G18350)
each plant was stressed to same degree at which leaves of main tillers were completely rolled Oryza sativa
down-regulation of (ATFTA, FTA, PFT/PGGT-IALPHA, PLP, AT3G59380) in canola using (AtHPR1, AtTHO1, HPR1, RAE3, THO1, AT5G09860) promoter driving RNAi construct resulted in yield protection against drought stress Brassica napus L.
seedlings subjected to drought stress
Physcomitrella patens DREB is expressed following water stress Physcomitrella patens
BiP-mediated negative regulation of N-rich protein (NRP, NRP1, AT5G42050) -mediated cell death signaling attenuates dehydration-induced cell death
mesophytic plants such as Arabidopsis face drought stress Arabidopsis thaliana
dor1 mutant displays drought-tolerant phenotype Arabidopsis thaliana
msi1-cs plants were monitored for wilting of rosette leaves
formation of a glassy matrix in dehydrated Physcomitrella patens tissue likely through (LEA, AT2G21490) accumulation Physcomitrella patens
senescing line showed markedly inhibited stomatal conductance, transpiration, and assimilation Hordeum vulgare
LN and LOHi lines possessed higher relative leaf water content at 4 DAS Hordeum vulgare
down-regulation of HvABA8′OH genes resulted in improved assimilation and water use efficiency (WUE) under terminal drought Hordeum vulgare
SNAC1 may have as downstream gene OsPP18 Oryza sativa
root traits correlate positively with crop performance under drought
VESICLE-ASSOCIATED MEMBRANE PROTEIN 711 (ATVAMP711, VAMP711, AT4G32150) is involved in regulating stomatal closure in response to drought stress Arabidopsis thaliana
(ATVAMP711, VAMP711, AT4G32150) repressing PM H+-ATPase activity is achieved by regulating (AHA1, HA1, OST2, PMA, AT2G18960) (AHA2, AtHA2, HA2, PMA2, AT4G30190) trafficking Arabidopsis thaliana
HVA22P:NPK1 transgenic families (T2) shows significantly higher yield per plant Oryza sativa
HVA22P:LOS5 transgenic families (T2) shows significantly higher yield per plant Oryza sativa
inducible promoter (HVA22P) had relatively better effect for (AT-NHX1, ATNHX, ATNHX1, NHX1, AT5G27150) drought resistance
transgenic families from nine constructs showed significantly higher relative yield than wild-type
(STZ, ZAT10, AT1G27730) is one of three genes showing significantly higher relative yield under both stress-inducible and constitutive promoter control
(ATFTA, FTA, PFT/PGGT-IALPHA, PLP, AT3G59380) could also be effective if expression of transgene is controlled by conditional promoter
abscisic acid (ABA) is central player in plant responses to drought stress
ospp18 mutant is more sensitive than wild-type to drought stress Oryza sativa
abscisic acid (ABA) induces stomatal closure
rao3/big and rao6/ (AS1, ATMYB91, ATPHAN, LL2, MYB91, AT2G37630) mutants conferred enhanced drought tolerance Arabidopsis thaliana
water deficit reduced transpiration rate in wild-type plants to 18% of control conditions Hordeum vulgare
drought tolerance involves alterations in photosynthesis
lines with large cortical cell size (CCS) in field under water stress have greater rooting depth (D95) Zea mays
fad7-1/fad8-1 double mutant shows no significant difference in tumor size compared to wild-type at normal relative humidity (45%–50%) Arabidopsis thaliana
reductions in water potential that mimic the effects of soil drying during drought elicit up to a 100-fold increase of Pro content in the Col reference accession Arabidopsis thaliana
447 drought-responsive lincRNAs of which 208 were specific to the agronomically important and drought-sensitive reproductive stage of O. sativa Oryza sativa
OsFBK1 expression is enhanced in seedlings exposed to drought stress Oryza sativa
developing secondary phloem will increase in wooden plants under drought stress
transgenic plants of four genes showed significantly higher relative spikelet fertility than wild-type
different stress responsive genes may be clustered by means of crossing transgenic families with promising drought resistance
drought resistance testing in PVC pipes measures spikelet fertility
(AtERG1, Era-1, ERA1, AT5G66470) is one target that has previously been validated in transgenic canola in field Brassica napus
protection that ABA provides Physcomitrella patens, Funaria hygrometrica, and Atrichum androgynum is most likely partially attributable to protein synthesis Physcomitrella patens; Funaria hygrometrica; Atrichum androgynum
cortical cell size (CCS) may improve drought tolerance of maize and possibly other cereal crops Zea mays
drop in water content of air causes increase in abscisic acid (ABA) content Arabidopsis thaliana
(ABA3, ACI2, ATABA3, AtLOS5, GIN5, LOS5, SIR3, AT1G16540) is one of four genes showing significantly higher relative spikelet fertility under both promoter control in PVC pipes
reduced expression of (ATGSTU24, GST, GSTU24, AT1G17170) genes contributes to hypersensitivity of ospp18 mutants to drought stress Oryza sativa
water stress in mesocosms reduces shoot biomass Zea mays
MdMYB124 slightly induced by simulated drought in roots of M. sieversii Malus sieversii
PVCs with a small portion of (ATVAMP711, VAMP711, AT4G32150) could move close to or fuse with plasma membrane Arabidopsis thaliana
HVA22P:CBF3 transgenic families (T2) shows significantly higher yield per plant Oryza sativa
(LEA, AT2G21490) (late embryogenesis abundant) proteins are involved in formation of a glassy matrix
leaf water potential (Ψl) close to the turgor loss point of the leaf is still before incipient point of leaf death Metasequoia glyptostroboides
stay-green type plants survived longer under terminal drought Hordeum vulgare
ospp18 mutant shows earlier and more severe wilting symptoms compared with wild-type siblings Oryza sativa
lines with large cortical cell size (CCS) under water stress correlate with deeper rooting depth (D95) Zea mays
shoot growth is inhibited under water-limited conditions
number of transgenic families used in drought resistance experiments perhaps limited for (ATNCED2, NCED2, AT4G18350)
BnFTA2 and BnFTA4 under limited irrigation in Taber showed no reduction and 5% increase in yield respectively compared to optimal conditions yield under limited irrigation Brassica napus
ABA accumulation triggers production of hardening protein(s) that limit damage Atrichum androgynum
(AtERG1, Era-1, ERA1, AT5G66470) mutants exhibit drought resistance Arabidopsis thaliana
OsDREB1A overexpression in rice improves drought stress tolerance Oryza sativa
HvDhn4s-driven TaNAC69-1 lines produce very high levels of TaNAC69-1 transcript under drought-stress conditions Triticum aestivum
WT plants exhibit low survival rate under drought stress
PUB19-OX2 plants are hypersensitive to dehydration Arabidopsis thaliana
(AtPUB19, PUB19, AT1G60190) overexpression increases sensitivity to dehydration Arabidopsis thaliana
MsGME overexpression enhances drought tolerance Arabidopsis thaliana
OsPIP1;3 gene in upland rice cultivar (subspecies indica cv. Zhonghan 3) was responsive to drought stress Oryza sativa
drought resistance genes were identified in Acer truncatum Acer truncatum
(LEA, AT2G21490) gene family in Acer truncatum expanded to 82 genes Acer truncatum
H2O2 production was progressively enhanced in both wild type and (AtATL78, ATL78, PRU2, AT1G49230) mutant under dehydration Arabidopsis thaliana
MYB, MYC, and WRKY transcription factor families regulate genes in response to drought stress Arabidopsis thaliana
10 up-regulated MdMYB genes were not highly induced by simulated drought stress Malus sieversii
(STZ, ZAT10, AT1G27730) transgenic families (both promoters) shows significantly higher relative spikelet fertility Oryza sativa
drought resistance testing in PVC pipes measures yield
(ATMSI1, MEE70, MSI1, AT5G58230) has a proposed new role in negative regulation of the drought stress response Arabidopsis thaliana
low proline accumulation alleviates plant drought stress
mitogen-activated protein kinase (MAPK) cascade participates in AM fungal and host plant symbionts in responses to drought stress
higher expression of three Hog1-MAPK genes increased resistance of mycorrhizal plants to drought stress
GiTPS2 responds to drought stress Rhizophagus irregularis
RiAQP-2, RiNTH1/2, RiTPS-1/-2, and Ri14-3-3 are significantly decreased under drought stress (DS) conditions Medicago truncatula; Nicotiana benthamiana; Rhizophagus irregularis
long, dry periods is when high NSC in Mediterranean roots aids recovery hydraulic conductivity recovery
GA metabolic genes are associated with drought-resistant coefficient
obscuring of the full magnitude of the drop in potential across tissues and between symplast and apoplast limits our understanding of coupling of outside-xylem zone (OXZ) water status to stomatal closure, embolism avoidance, and collapse of leaf xylem conduits
dehydration threshold is suggested by observation from Lamacque et al. on Lavender
difference in resistance of poplar and lavender to dehydration probably explains difference in mortality timing between species
reduced photosynthetic activity reinforces trade-off for the plant to partition recent photoassimilates efficiently
RcOST1L has conserved functions in regulating drought response Arabidopsis thaliana; Rosa chinensis
plants may grow less in dry treatments than wet treatments
leaf carbon isotopic ratio (δ 13 C) is used as proxy for drought response
tree species richness decreases leaf δ15N under low drought intensity
(ABF3, AtABF3, DPBF5, AT4G34000) and (ABF4, AREB2, AtAREB2, AT3G19290) overexpression results in improved drought tolerance Arabidopsis thaliana
AtDREB1C overexpression in rice improves drought stress tolerance Oryza sativa
AtNF-YA5 is induced by drought Arabidopsis thaliana
variation in gene expression for the CWIN IVR1 occurs in pollen during water deficits wheat
irx14L mutant does not share drought-tolerant phenotype
bulliform cells lose turgor under water stress Oryza sativa
xanthine dehydrogenase suppression transgenic lines shows enhanced growth retardation during drought stress Arabidopsis thaliana
(ATRD22, RD22, AT5G25610) is significantly up-regulated in pub19-1 mutant plants under drought stress
(COR78, LTI140, LTI78, RD29A, AT5G52310) is significantly up-regulated in pub19-1 mutant plants under drought stress
PUB19-OX1 plants are hypersensitive to dehydration Arabidopsis thaliana
Atptpn-1 T-DNA insertion mutant is hypersensitive to drought Arabidopsis thaliana
ectopic expression of OsPIP1;3 gene resulted in higher resistance to water deficit Nicotiana benthamiana
(ATPIP1, PIP1, PIP1;1, PIP1A, AT3G61430) ;3 expression increased in response to drought stress Arabidopsis thaliana
(ASL11, LBD15, AT2G40470) protein possibly integrates vascular differentiation and stomatal aperture to enhance tolerance of water-deficit stress
Arabidopsis (AtGolS1, GolS1, AT2G47180) is induced by drought stress Arabidopsis thaliana
abscisic acid (ABA) is largely attributed to survival over continued growth in vegetative tissues during drought stress
avoidance strategies when fail, repair strategies may prevent excessive shoot dieback
water stress significantly reduces rooting depth (D95) Zea mays
abscisic acid (ABA) levels are elevated in crown galls Arabidopsis thaliana
(AtMAX2, MAX2, ORE9, PPS, AT2G42620) mutant shows impaired expression of stress-responsive genes Arabidopsis thaliana
increased temperature and larger variability of water stress results in higher mortality rate during terminal drought
(ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) plants responded to drought stress by producing higher ABA concentrations Arabidopsis thaliana
(ATNCED2, NCED2, AT4G18350) transgenic plants with Actin1 promoter showed high drought resistance (LDS < 1)
(AtHPR1, AtTHO1, HPR1, RAE3, THO1, AT5G09860) expression is up-regulated by drought Arabidopsis thaliana
ABA pretreatment promoted formation of a glassy matrix in dehydrated Physcomitrella patens tissue Physcomitrella patens
drought stress exposure for 1 week reduced WUE in senescing plants Hordeum vulgare
ethylene triggers expression of drought stress-responsive genes
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) binding site in (ATRD22, RD22, AT5G25610) motif is associated with dehydration-responsive gene; abscisic acid induction, water stress Arabidopsis thaliana
inducible MdMYBs showed lower expression levels by simulated drought Malus domestica
Actin1:LOS5 transgenic families (T2) shows significantly higher yield per plant Oryza sativa
HVA22P:LOS5 transgenic families (T2) shows higher spikelet fertility Oryza sativa
(ATMSI1, MEE70, MSI1, AT5G58230) protein binding partners together with MSI1 control expression of drought stress-inducible genes Arabidopsis thaliana
ectopic expression of plant AQP genes like apple MdPIP1;3 enhanced plant resistance to water deficit under osmotic stress or extreme temperatures Malus domestica
(AtLtpI-5, cdf3, LP2, LTP2, AT2G38530) interaction with OsPIP proteins negatively affected drought resistance Oryza sativa
decline in photosynthesis is central consequence of drought