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drought response

12664 relationships annotated with this phrase. Showing first 500 of 12664.
Source entity Relationship Target entity Species
stomatal closure is employed during soil water limitation or atmospheric drying
drought-induced reduction in normalized rhizosheath mass is universal trend for all maize varieties Zea mays
ABA (abscisic acid) is known to initiate responses to drought stress
high ABA concentration acts as signal for plants to close their stomata and prevent water loss
Conyza canadensis populations examined for among-population variation in performance and functional traits in response to drought Conyza canadensis
drought impacts on natural forests include tree mortality
(CPD45, FHY3, AT3G22170) mutant shows more severe drought stress phenotype than wild-type plants Arabidopsis thaliana
tree species richness should have a negative relationship with δ 13 C during droughts
H1 proposes a negative relationship between tree species richness and δ 13 C during droughts
species-specific responses are expected to be driven by desiccation tolerance
drought stress reduces rhizosheath mass normalized by root biomass Zea mays
drought stress causes reductions in stability and SUMOylation of CaAITP1 protein Capsicum annuum
macroclimate drought conditions will affect each species in a forest differently each species in a forest
more negative midday leaf water potential in Fagus sylvatica is an indication of increased soil moisture impacts experienced by the beech species compared with the oak
ospp18 mutant is sensitive to drought stress Oryza sativa
amiR-OsPP18 plants are sensitive to drought stress Oryza sativa
OsPP18 expression level is higher in SNAC1-overexpressing plant than in wild type under drought stress condition Oryza sativa
MdMYB88/124 RNAi plants have lower root-to-shoot ratio than GL-3 plants under drought stress Malus domestica
native range populations from xeric habitats show less reduction in plant performance by drought compared to native range populations from mesic habitats Conyza canadensis
Capsicum annuum DeSUMOylating Isopeptidase 2 (CaDeSI2) positively regulates drought tolerance Capsicum annuum
tree diversity has mitigating effects on functional responses to droughts
range-specific patterns in drought responses are consistent across recruitment, juvenile, and adult life stages Conyza canadensis
seedling dry matter content was the only trait with significant two-way interaction between drought and climatic water deficit (CWD) Conyza canadensis
Quercus pubescens may have reduced stomatal sensitivity to soil moisture or atmospheric drought
drought deciduousness can occur, primarily in stressed individuals Populus tremuloides
impaired expression of stress-inducible marker genes in (AtMAX2, MAX2, ORE9, PPS, AT2G42620) mutant might contribute, at least partly, to drought-sensitive phenotypes of (AtMAX2, MAX2, ORE9, PPS, AT2G42620) Arabidopsis thaliana
PtSUT4 down-regulation under drought stress confirms involvement of PtSUT4 in the drought response Populus trichocarpa
25 reproductive-specific lincRNAs were detected as down-regulated in response to drought Oryza sativa
(ATFP6, AtHMP40, FP6, HIPP26, AT4G38580) accumulation in nucleus and nucleolus leads to up-regulation of dehydration-responsive gene expression in the vasculature Nicotiana benthamiana
MdMYB88 or MdMYB124 overexpression plants have higher shoot hydraulic conductivity than GL-3 plants in response to drought stress Malus domestica
H1 proposes that tree diversity reduces drought-related increases in leaf δ 13 C
some LSMs do not accurately consider effects of drought on phenology
(H2B, HTB2, AT5G22880) proposes that droughts are expected to increase leaf δ 15 N
trees in particularly dry years or in seasonally dry forests shed leaves to avoid high water demand and associated stress
desiccation tolerance and mycorrhizal association type are expected to mediate interspecific leaf δ 13 C and δ 15 N patterns
drought impacts on natural forests include early leaf senescence
φ PSII is better indicator of early drought stress Arabidopsis thaliana
response of leaf δ 15 N to droughts is not well understood current knowledge
(CPD45, FHY3, AT3G22170) and (FAR1, AT5G22500) promote drought tolerance Arabidopsis thaliana
species with greater degrees of shrinkage before turgor loss point (TLP) are hypothesized to experience greater loss of leaf hydraulic conductance (K leaf)
DROUGHT-HYPERSENSITIVE MUTANT1 (DHM1) loss of function caused increased sensitivity to drought stress
(AtMAX2, MAX2, ORE9, PPS, AT2G42620) mutant is strongly hypersensitive to drought stress Arabidopsis thaliana
potential role for CA in drought responses was defined in Zea mays ca1ca2 double mutant plants grown under watering regimes Zea mays
virus exploits systemic signaling response to drought
MdMYB88 or MdMYB124 overexpression plants have clearly higher root hydraulic conductivity than GL-3 plants Malus domestica
simplifications in LSM representation of S0 ignore water stress effects on vegetation
tree species diversity theoretically suggests positive effects on forest drought responses
H1 proposes that tree diversity lowers need to close the stomata
ospp18 mutant is sensitive to drought stress at seedling stage Oryza sativa
expression levels of stress-inducible marker genes were reduced in (AtMAX2, MAX2, ORE9, PPS, AT2G42620) compared with wild-type plants during dehydration treatment Arabidopsis thaliana
drought treatment significantly affects dry weight of shoots Malus domestica
(FAR1, AT5G22500) mutant shows more severe drought stress phenotype than wild-type plants Arabidopsis thaliana
RNAi lines maintained green leaves throughout drought treatment Kalanchoe fedtschenkoi
32 reproductive-specific lincRNAs were detected as up-regulated in response to drought Oryza sativa
ospp18 mutant is sensitive to drought stress at young panicle differentiation stage Oryza sativa
compromise between carbon assimilation and water transpiration is required for optimal growth under drought
higher susceptibility to drought stress correlated with low content of GABA Arabidopsis thaliana
drought-sensitive species experience strong leaf thickness shrinkage
tissue shrinkage would lead to declines in extraxylem hydraulic conductance
larger root systems may be caused partially by role of CK in regulating the response to drought
concentrations of ABA and its catabolites PA and (DPA, AT5G02470) increased under experimental drought conditions Hordeum vulgare
hypersensitivity to drought conditions in (AtMAX2, MAX2, ORE9, PPS, AT2G42620) is not due to difference in stomatal architecture Arabidopsis thaliana
(AtMAX2, MAX2, ORE9, PPS, AT2G42620) mutant shows very high sensitivity to drought conditions Arabidopsis thaliana
transgenic barley lines were less sensitive to drought stress Hordeum vulgare
continued growth of roots of CKX-modulated lines may facilitate water sensing and root branching process Hordeum vulgare
altered ABA content besides this, several other metabolic changes in leaves of transgenic lines could support improved tolerance to drought Hordeum vulgare
MdMYB88/124 RNAi plants have lower dry weight of shoots than GL-3 plants Malus domestica
higher root hydraulic conductivity in MdMYB88 or MdMYB124 overexpression plants is suggestive of stronger water transportation ability under long-term drought stress Malus domestica
drought stress causes productivity loss
MdMYB88/124 RNAi plants have much thinner stems than GL-3 plants under drought Malus domestica
(ATCCD8, CCD8, MAX4, AT4G32810) mutant did not display any phenotypic difference compared with wild type under drought conditions Arabidopsis thaliana
species from moist habitats are hypothesized to have greater degrees of leaf shrinkage
(CYP711A1, MAX1, AT2G26170) mutant did not display any phenotypic difference compared with wild type under drought conditions Arabidopsis thaliana
208 lincRNAs up-regulated in response to drought conditions in reproductive tissues Oryza sativa
(AHG3, ATPP2CA, PP2CA, AT3G11410) is important PP2C for plant tolerance to drought stress
ZmPTPN overexpression in maize results in increased drought tolerance Zea mays
OsPP18 is unique drought-responsive PP2C gene in rice Oryza sativa
mock-inoculated plants survived drought treatment at rate of 27% Nicotiana benthamiana
MdMYB88 and MdMYB124 positively regulate drought tolerance of apple roots Malus domestica
SNAC1 is induced by drought Oryza sativa
dor1 mutant displayed drought-resistant phenotypes Arabidopsis thaliana
shrinkage occurring simultaneously with vein xylem embolism would arise if association of leaf shrinkage with decline of leaf hydraulic conductance (K leaf)
oaks (Quercus spp.) experience less thickness shrinkage Quercus spp.
Arabidopsis thaliana exhibits varying levels of proline accumulation under low water potential Arabidopsis thaliana
lower ABA concentrations in CKX-overexpressing lines indicates that the former experienced weaker stress level Hordeum vulgare
MdMYB88/124 RNAi plants have lower dry weight of roots than GL-3 plants Malus domestica
increasing CK breakdown in the root decreases the sensitivity to drought stress Hordeum vulgare
noninfected N. benthamiana plants showed signs of wilting after 13 d of water withholding Nicotiana benthamiana
increased basal levels of certain amino acids might contribute to reduced sensitivity to drought conditions
MdMYB88/124 RNAi plants have much lower root hydraulic conductivity than GL-3 plants Malus domestica
drought treatment significantly affects stem diameter Malus domestica
G protein-coupled receptor 1 (ATGCR1, GCR1, AT1G48270) is involved in drought response
OsZFP252-mediated drought tolerance was correlated with induced expression of OsDREB1A Oryza sativa
OsiSAP8 overexpression plants survived water withdrawal for 23 d Oryza sativa
higher plants have evolved sophisticated mechanisms to respond to drought
detached Atptpn-1 leaves lose water much faster than wild-type leaves Arabidopsis thaliana
HSFA6a-OE/p transgenic plants are more sensitive to drought and have lower survival rates than Arabidopsis thaliana
lincRNA loci to detect any that may be involved in responding to drought Oryza sativa
Zea mays ca1ca2 double mutant plants were grown under several watering regimes Zea mays
effective drought-avoidance mechanism may be at least partially attributed to enhanced root system Hordeum vulgare
concentrations of ABA and its catabolites PA and (DPA, AT5G02470) in CKX-overexpressing lines were only about half of those in wild type Hordeum vulgare
increased ABA sensitivity is accompanied by reduced transpiration water loss Arabidopsis thaliana
increased drought sensitivity of (AtMAX2, MAX2, ORE9, PPS, AT2G42620) mutant is not due to difference in ABA contents of wild-type and (AtMAX2, MAX2, ORE9, PPS, AT2G42620) plants Arabidopsis thaliana
(AtMAX2, MAX2, ORE9, PPS, AT2G42620) overexpression showed similar phenotypes to wild-type plants in water loss and drought treatment assays Arabidopsis thaliana
concentrations of amino acids (Pro, Asn, Ser, Thr, and GABA) under drought conditions increased less strongly in CKX-transgenic barley, indicating, similar to the behavior of ABA, reduced drought sensitivity Hordeum vulgare
MdMYB88 and MdMYB124 are induced slightly in roots under simulated drought conditions Malus sieversii
drought treatment significantly affects dry weight of roots Malus domestica
hydraulic conductivity decreases in both roots and shoots under drought stress
(NF-YA7, AT1G30500) is of interest because its close homolog (NF-YA5, NFYA5, AT1G54160) has been reported to affect drought response Arabidopsis thaliana
stomatal closure induced by abscisic acid (ABA) contributes to tolerance to drought conditions Arabidopsis thaliana
112 lincRNAs down-regulated by drought in inflorescence six were up-regulated at vegetative stage Oryza sativa
detached Atptpn-2 leaves lose water much faster than wild-type leaves Arabidopsis thaliana
PsRD29 expression was highly upregulated 46.85-fold increase Pisum sativum
(ATR4, CYP83B1, RED1, RNT1, SUR2, AT4G31500) mutant displays altered transcriptome Arabidopsis thaliana
AtPTPN mutation by T-DNA insertion increased sensitivity to drought and osmotic stresses Arabidopsis thaliana
cpk11-2 mutant is less able to withhold water under drought conditions Arabidopsis thaliana
cpk4-1 and cpk11-2 mutants show lower survival rate following re-watering after 15-day drought period Arabidopsis thaliana
AtPTPN plays positive roles in plant drought tolerance Arabidopsis thaliana
drought-induced gene products are up-regulated in (ATR4, CYP83B1, RED1, RNT1, SUR2, AT4G31500) mutant Arabidopsis thaliana
OsZFP252 might be upstream regulator of OsDREB1A Oryza sativa
OsZFP252-mediated drought tolerance was correlated with higher accumulation of soluble sugars Oryza sativa
long-distance coordination and phloem-mediated change in allocation or recycling of components contribute to drought-avoidance strategy based on decreased above-ground growth
OsZFP252-mediated drought tolerance was correlated with higher accumulation of free proline Oryza sativa
FTB down-regulation via antisense technology improves drought tolerance Brassica napus
cpk21-1 mutant does not show higher survival rates with statistical significance under drought conditions Arabidopsis thaliana
down-regulation of ARABIDOPSIS THALIANA (AtPUB19, PUB19, AT1G60190) leads to enhanced drought tolerance Arabidopsis thaliana
PTPN have positive and conserved roles in drought responses Arabidopsis thaliana; Zea mays
(XBAT35, AT3G23280) functions positively in plant drought response Arabidopsis thaliana
terminal drought tolerance QTL explains differences in FTSW thresholds pearl millet
partial stomatal closure is common in dry season in Banksia habitats Banksia
experimental drought decreases via photosynthetic capacity (Pmax, Jmax, and Vcmax) down-regulation under severe water shortage
Atptpn-1 and Atptpn-2 mutants are more sensitive to drought stress Arabidopsis thaliana
ZmNF-YB2 transgenic maize has less leaf rolling Zea mays
ZmPTPN overexpression enhanced plant drought tolerance Zea mays
cpk21-1 mutant shows enhanced accumulation of proline Arabidopsis thaliana
histone H1 variant is induced through ABA-dependent pathway Solanum lycopersicum
SNF1-related protein kinase subfamily 2 (SnRK2s)-encoding genes are important for plant drought tolerance Arabidopsis thaliana
(STZ, ZAT10, AT1G27730) overexpression conferred drought tolerance Oryza sativa
changes in metabolite profile coincide with activation of drought response Arabidopsis thaliana
xbat35-1 mutant is more sensitive to drought stress Arabidopsis thaliana
protein farnesylation has potential role in drought response Arabidopsis thaliana
(AT-HSFA6A, HSFA6A, AT5G43840) has positive role in drought response Arabidopsis thaliana
GmNTF2B-1 transgenic lines show upregulation of (ATWRKY46, WRKY46, AT2G46400) Glycine max
increased metabolite levels triggers physiological responses aimed at conserving energy
root traits are proposed to contribute to plant performance under drought conditions
limited water availability results in decrease of growth
abscisic acid (ABA) promotes stomatal guard cell closure
TcLOX did not show delayed expression in roots
soybean orthologs of conserved DRGs were analyzed drought-regulated gene expression Glycine max
AtPTPN overexpression were more tolerant to drought Arabidopsis thaliana
Sobic.003g244100 expression increased after drought stress Sorghum
photosynthesis and diffusional conductances are correlated with yield Oryza sativa
endogenous TaNAC69 transcript level is markedly up-regulated in wheat leaves and roots during drought stress Triticum aestivum
TaZFP transcript level is markedly up-regulated in wheat leaves and roots during drought stress Triticum aestivum
tonoplast-specific v-SNAREs (AtVAMP71/AtVAMP7C) function in plant's response to water deficit Arabidopsis thaliana
very low July soil water availability causes gs at seasonal low
linking physiology, 'omics and quantitative genetics has been proposed for understanding drought response
genetic studies have not permitted effective dissection of the drought response Triticum aestivum
experimental drought pushes response of Deschampsia beyond threshold where dry conditions could be handled solely by acclimation Deschampsia
conserved DRGs were obtained based on cross-species meta-analysis of drought-regulated genes Arabidopsis thaliana; Oryza sativa; Triticum aestivum; Hordeum vulgare
OE-5 and OE-6 plants have higher survival rates than wild-type plants after drought stress Arabidopsis thaliana
lower rate of water loss per unit leaf area (Tr) in well-watered plants of tolerant genotypes might simply be a consequence of lower FTSW threshold for beginning of transpiration drop pearl millet
rapid and cheap procedures to characterize components of the drought response will be critical in improving genetic resolution Triticum aestivum
ectopic expression of (ATHB-7, ATHB7, HB-7, AT2G46680) mimics phenotype of wild-type plants grown under water-limiting conditions Arabidopsis thaliana
TcSTK was down-regulated in response to drought starting at 7 d PW in cacao roots
suppression of MdbZIP39 alone did not increase drought tolerance Malus domestica
PLDα1-OE plants have significantly higher relative conductivity
myriad of genes involved in plant response to water deficits is reason for limited success in water limitation breeding
lower FTSW threshold where transpiration declines makes drought-stressed plant behave like well-watered plants until soil has become dryer than for sensitive lines pearl millet
soluble sugars are components of osmotic readjustments in Nicotiana sylvestris CMSII mutants and wild-type plants Nicotiana sylvestris
Ccrboh transcript was expressed in tissue-specific pattern following drought stress Citrullus colocynthis
water deficit (WD) causes stomatal closure
vulnerability to cavitation during peak midday transpiration demand could contribute to observed depression in midday stomatal conductance (g s) in chamber-grown, water-stressed soybean leaves Glycine max
RLD (root length density) at depth was not significantly greater in +QTL BILs when grown in soil with higher clay content soil with higher clay content (about 50%) Oryza sativa
PLDα1-OE plants have significantly higher MDA
drought causes biomass reductions
ectopic expression of (ATHB-12, ATHB12, HB-12, HB12, AT3G61890) mimics phenotype of wild-type plants grown under water-limiting conditions Arabidopsis thaliana
patchy stomatal closure has been observed under water stress
gs of co-occurring C. vulgaris decreases in response to dry conditions Calluna vulgaris
different QTL combinations result in different levels of improvement over IR64 Oryza sativa
qDTY 2.2 has been reported to show effect on grain yield under upland reproductive-stage drought stress Oryza sativa
Helianthus deserticola in 2002 with meagre 9 mm precipitation in July and August had significantly lower P75 than Helianthus anomalus Helianthus anomalus; Helianthus deserticola
transpiration rate (TR) of drought-exposed plants upwards would consequently drive upwards normalized transpiration rate (NTR) pearl millet
Trichoderma hamatum isolate DIS 219b colonization delayed drought-induced changes in green fluorescence emissions Theobroma cacao
drought causes impaired photosynthesis
TcNR did not show delayed expression in roots
resisting severe stress through survival mechanisms is typically not relevant to agriculture
ABA signaling has been suggested to be important during drought conditions Picea abies
superior NILs-QTL (near-isogenic lines with QTL) had FTSW threshold similar to QTL donor parent pearl millet
Wdhn13 is responsive to drought Triticum aestivum
ESTs putatively involved in the production of osmoprotectants and/or regulatory metabolites were responsive to drought
osmolytes accumulate under drought stress
reduced membrane water permeability encourages water conservation during periods of drought
RLD (root length density) at depth was greater in NILs and +QTL BIL in some field experiments Oryza sativa
lower FTSW threshold in tolerant lines means that transpiration dropped upon progressive soil drying in relatively dryer soil in tolerant lines than in sensitive lines pearl millet
ectopic expression of (ATHB6, HB6, AT2G22430) mimics phenotype of wild-type plants grown under water-limiting conditions Arabidopsis thaliana
endophytic colonization of cacao by Trichoderma hamatum isolate DIS 219b resulted in delay in many aspects of the drought response Theobroma cacao
TcNI was induced by drought in leaves only
drought-altered expression of TcMAPK3 was delayed in colonized seedlings
drought stress increases MDA
experimental drought decreases Pn via gs reduction
interactions among multiple drought-yield QTLs have effects on drought responses in field conditions Oryza sativa
higher root hydraulic conductivity and higher root length density at depth result in better leaf water status Oryza sativa
glucose content of cacao leaves increased during drought stress
increased root growth during period of drought provided most reasonable explanation for change in kr
defect in stomatal closure and enhanced water loss in (AtNMNAT, NMNAT, AT5G55810) were complemented by (AtNMNAT, NMNAT, AT5G55810) over-expression Arabidopsis thaliana
colonized seedlings show delayed drop in stomatal conductance
NR enzyme activity and transcript abundance are known to be sensitive to repression by drought
drought-altered expression of TcrbcS was delayed in colonized seedlings
rboh transcript level in watermelon showed no change under drought stress Citrullus lanatus
drought-responsive genes include transcription factors Solanum lycopersicum
protein regulation, metabolic adjustment, and physiological status of plants under drought is not well understood in relation to role of nitrogen fixation in nodules Medicago sativa
TcHK did not show delayed expression in roots
drought-altered expression of TcTPP was delayed in colonized seedlings
accumulation of Arg in response to water deprivation was also observed in wheat
GABA concentrations in cacao leaves increased in response to drought
signal transduction results in activation of components of the drought response
drought-induced changes in gene expression patterns were delayed in leaves of colonized seedlings
drought-induced stomatal closure of pea results in higher Ψ leaf Pisum sativum
genotypes with qDTY 2.2 and qDTY 4.1 showed improvement in canopy temperature Oryza sativa
lack of difference in HI in well-watered conditions points to T (transpiration) as main factor behind yield under drought Oryza sativa
rice typically shows reduced ability to draw down soil moisture levels compared to other crops Oryza sativa
drought altered expression of 19 expressed sequence tags (ESTs) Theobroma cacao
TcTIP (P31) was repressed in the roots by drought at 7 d PW roots
TcTPP did not show delayed expression in roots
NILs with different QTL combinations show different levels of drought response Oryza sativa
NILs in this study did not exhibit conservative water uptake Oryza sativa
experiments with additional aquaporin inhibitors may reveal more-detailed mechanisms behind higher Lpr of 2-QTL NILs Oryza sativa
drought stress affects water use efficiency (WUE) and yield Oryza sativa
single QTL NILs and 2-QTL NILs show higher NDVI Oryza sativa
tolerant parental genotypes had lower FTSW (fraction of transpirable soil water) threshold pearl millet
Sullu cultivar exhibits different drought responses at leaf level
drought stress intensity affects effects of drought on leaf osmotic potential (Lo)
SALK_011529 and SALK_004690 lines have been used to unravel the role of (ABO1, AtELP1, ELO2, AT5G13680) in modulating ABA and drought response
drought causes cessation of shoot growth
TcPR5 was induced by drought 10 d PW in leaves and roots
TcPP2C was induced in cacao roots 7 d PW cacao roots
Wrab19 is responsive to drought Triticum aestivum
drought-responsive ESTs have characterized involvement in drought
soluble carbohydrates (glucose, fructose, sucrose, stachyose, mannitol, and pinitol) can accumulate in leaves in a response that varies among plant species
genotypes with higher photosynthesis and conductances were more productive Oryza sativa
stomata closure occurs once continuous increase in (PLD, PLDALPHA1, AT3G15730)
low-rainfall ecotypes show no evidence for drought tolerance Lupinus luteus
NF-YA transcription factor is important in drought stress regulation
qDTY 2.2 and qDTY 4.1 showed greatest degree of improvement under drought compared with IR64 Oryza sativa
+QTL BILs showed large differences in transpiration under severe stress compared to –QTL BILs and IR64 Oryza sativa
genotypes with small xylem vessel diameters (+QTL BILs) yielded more under drought than genotypes with larger xylem vessel diameters (–QTL BILs) Oryza sativa
whole root system water conductance (kr) of drought-tolerant root system increased during period of drought
Trichoderma hamatum isolate DIS 219b colonization delayed drought-induced changes in net photosynthesis Theobroma cacao
DIS 219b-colonized seedlings show delayed drought-induced changes in net photosynthesis
TcODC is responsive to drought
TcTPP induction was a late response to drought in leaves
plant drought tolerance, as indicated by maintenance of vegetative biomass growth under drought is not associated with distinct belowground drought reactions Zea mays
Arabidopsis proteins (ANAC019, ANAC19, NAC019, AT1G52890) (ANAC055, ANAC55, ATNAC3, NAC055, NAC3, AT3G15500) and (ANAC072, ANAC72, AtRD26, RD26, AT4G27410) bind to downstream gene promoters Arabidopsis thaliana
(CaS, AT5G23060) correlates with stomatal movements
reduced 18O exchange between CO2 and H2O at the shoot level under drought is in accordance with reduction in carbonic anhydrase (CA) activity after long drought period in wheat
causal mechanisms affecting amount of useable water include higher root hydraulic conductivity and higher root length density at depth Oryza sativa
introgressing AdaySel-derived drought-yield QTLs into IR64 affects multiple root traits Oryza sativa
lines with three or four QTLs introgressed together showed smaller differences from IR64 in terms of yield, canopy temperature, and NDVI Oryza sativa
drought impacts on natural forests include canopy dieback
smaller xylem vessels may be beneficial in rice under drought since rice is susceptible to xylem vessel cavitation caused by drought stress Oryza sativa
differences in Lpr point to improved root function in 2-QTL NILs Oryza sativa
this report investigates relationships between (CaS, AT5G23060) WUE, and drought tolerance
2-QTL NILs do not confer traits related to TE (transpiration efficiency) or HI (harvest index) Oryza sativa
generation advancement to NILs revealed 2-QTL NILs to show generally higher Lpr (root hydraulic conductivity) Oryza sativa
drought stress does not induce responsive gene expression in drought-sensitive cultivar S. lycopersicum cv. M82 Solanum lycopersicum
drought-responsive genes include genes controlling plant height Solanum lycopersicum
greenhouse seedling experiments showed no differences in water uptake or root growth Oryza sativa
aquaporins have been implicated in differential transpiration and conservative water uptake function in wheat Triticum aestivum
field experiments showed no differences in water uptake or root growth Oryza sativa
Trichoderma hamatum isolate DIS 219b colonization of 9-day-old seedlings altered expression of drought-responsive ESTs Theobroma cacao
drought-responsive genes include signalling proteins Solanum lycopersicum
responsive genes are involved in signalling and metabolic pathways
improved leaf water status under drought appears to be consequence of causal mechanisms affecting amount of useable water Oryza sativa
transient water deficit treatment is applied to seedlings Hordeum vulgare; Zea mays
relationship between drought resistance and sap bleeding rate requires more research to understand Oryza sativa
qDTY 2.2 shows effect specific to most severe stress conditions Oryza sativa
abscisic acid (ABA) has well-known roles in drought signaling
aquaporins have been implicated in differential transpiration and conservative water uptake function in peanut Arachis hypogaea
decrease in stomatal conductance (g s) without maximum K leaf acclimation suggests that stomatal sensitivity to dry soil protects against hydraulic failure Glycine max
qDTY 2.2 and qDTY 4.1 combination could be complementary to achieve yield advantages under wider range of stress severities Oryza sativa
2-QTL NILs show slightly higher biomass Oryza sativa
small root xylem vessel diameter has been reported to result in conservative water uptake in wheat Triticum aestivum
small xylem vessel diameter trait was not associated with yield under drought in best-performing lines (2-QTL NILs) Oryza sativa
2-QTL NILs show generally higher Lpr than IR64 across experiments and treatments Oryza sativa
sap bleeding rate from root zones of +QTL BILs and 2-QTL NILs did not correlate with trends seen for Lpr Oryza sativa
difficulties in detecting significant differences among genotypes for many traits measured in field experiments could be addressed by more-detailed measurements in controlled conditions Oryza sativa
drought-responsive genes enriched among putative (APRR7, PRR7, AT5G02810) targets Arabidopsis thaliana
(ATHB9, PHV, AT1G30490) A and HVA22 upregulation highlights genotype-specific responses Aegilops tauschii
drought causes accumulation of solutes
cool-season grass endophytes result in reduced water loss
complex interactions among major-effect drought-yield QTLs highlight Oryza sativa
optimal combination of QTLs that act to complement each other is needed when present in common genetic background Oryza sativa
NMNAT-ox1 and NMNAT-ox2 plants tended to be tolerant to drought stress Arabidopsis thaliana
drought stress effects on C18OO fluxes occur at different temporal and spatial scales
qDTY 2.2 and qDTY 4.1 are major-effect drought-yield QTLs Oryza sativa
smaller xylem vessels may be less likely to cavitate under high evapo-transpiration demand Oryza sativa
better leaf water status is evidenced by canopy temperature, LWP, LRWC, leaf osmotic potential, and Δ 13 C Oryza sativa
reduced cuticle thickness correlates with drought-sensitive phenotype Arabidopsis thaliana
drought treatment significantly affects plant height Malus domestica
RWC (relative water content) indicates higher levels of leaf hydration and transpiration Oryza sativa
increase in ABA can be regarded as an indicator of drought stress
ABA-responsive genes are drought-related genes Aegilops tauschii
ectopic expression of Arabidopsis thaliana RING Zinc Finger 1 (AtRZF1, BTL02, RZF1, AT3G56580) gene is very significantly influential in proline content Arabidopsis thaliana
large xylem vessel diameter may be beneficial for improving drought response Oryza sativa
lines showing highest yield under drought in this study show trends of higher Lpr and no evidence of conservative water uptake Oryza sativa
investment in costly roots, as indicated by higher root tissue density under drought is consistently negatively associated with drought response of assessed rhizosheath properties Zea mays
study investigated effects of tree species richness on responses to an extreme drought event
plant resource allocation to root growth typically increases under drought
(CYP711A1, MAX1, AT2G26170) mutant does not display defects in drought-sensitive phenotype Arabidopsis thaliana
transgenic barley plants compared with wild-type plants under long-term drought conditions Hordeum vulgare
genes satisfy selection criteria Hordeum vulgare
field and chamber experiments suggest that K leaf in soybean does not acclimate to drought Glycine max
+QTL BILs and NILs would have achieved improved leaf hydration via increased water uptake through greater root length at depth Oryza sativa
larger root diameters have been associated with drought resistance in OsNAC10 and OsNAC5 transgenics Oryza sativa
(ANAC019, ANAC19, NAC019, AT1G52890) (ANAC055, ANAC55, ATNAC3, NAC055, NAC3, AT3G15500) and (ANAC072, ANAC72, AtRD26, RD26, AT4G27410) proteins could bind promoter of the drought-inducible (CLPD, ERD1, SAG15, AT5G51070) gene Arabidopsis thaliana
LCB phosphate is implicated in ABA-dependent stomatal closure
ABA is responsible for drought stress response
drought induced an increase in the concentration of many amino acids in cacao leaves Theobroma cacao
DIS 219b colonization caused a significant lag in initiation of the drought response in the leaf
highest-yielding QTL combination (qDTY 2.2 + qDTY 4.1) confers multiple drought response mechanisms related to improved transpiration Oryza sativa
transgenic canola under drought stress shows reduced stomatal conductance Brassica napus
AtPTPN expression is upregulated by drought Arabidopsis thaliana
TaNF-Y transcript level is markedly up-regulated in wheat leaves and roots during drought stress Triticum aestivum
drought stress stimulates stomatal closure
SNAC1-overexpressing rice exhibits significantly enhanced drought resistance under field conditions Oryza sativa
dehydration treatment led to increased expression of Kinase1 (KIN1, AT5G15960) gene Arabidopsis thaliana
112 lincRNAs down-regulated in response to drought conditions in reproductive tissues Oryza sativa
208 lincRNAs up-regulated by drought in inflorescence tissue five were down-regulated in vegetative stage Oryza sativa
PTPN has positive and conserved role in regulation of plant drought tolerance
non-native range populations do not show relationship between habitat aridity and drought-reduced plant performance Conyza canadensis
drought impacts on natural forests include growth reduction
overexpression of OsMFT1 results in drought tolerance Oryza sativa
how plant diversity mediates drought impacts on leaf δ 15 N is unclear current knowledge
C 3 plants under drought conditions may close their stomata to prevent desiccation
tree species in interspecific and intraspecific mixtures show how community interactions modulate individual plant responses to hotter droughts
H1b proposes that the higher the drought intensity, the stronger effects of tree species richness on leaf δ 13 C become
Contig_10961 expression is downregulated rapidly upon water deficit treatment Hordeum vulgare
species originating from moist habitats showed substantial shrinkage during dehydration before reaching turgor loss point (TLP)
plant drought response is regulated by multiple molecular and cellular pathways Arabidopsis thaliana
lower level of ABA accumulation could be due to the avoidance of detrimental effects of increased ABA levels on photosynthesis and growth
(ADR1-L1, AT4G33300) is involved in drought tolerance Abies alba
7-d drought treatment causes leaves to exhibit phenotypic alterations Arabidopsis thaliana
H1a proposes negative relationship between tree species richness and δ 13 C during droughts
(H2B, HTB2, AT5G22880) has no a priori expectations on differences in this increase between diversity levels
metabolite analysis by GC-MS reveals changes in metabolite profile Arabidopsis thaliana
KAR pathway controls drought stress tolerance Arabidopsis thaliana; Oryza sativa; Lotus japonicus; Brachypodium distachyon
increasing CWD generally reduces fET across sites
woody plants have traits associated with drought responses at the species' rear edge
prolonged hot drought leads to decreased stomatal conductance
OsMFT1 enhances drought tolerance in a dose-dependent manner drought tolerance Oryza sativa
OsMYB26 is responsible for drought-sensitive phenotype of Osmyb26 Oryza sativa
accumulation of sugars (e.g. carbohydrates) help plants to resist dehydration and desiccation
drought-induced reduction in total rhizosheath mass is universal trend for all maize varieties Zea mays
variety effects on drought response of bulk element concentrations in rhizosheath are of little importance Zea mays
simultaneous impacts of species diversity and drought on leaf δ 15 N have not been investigated current knowledge
arbuscular mycorrhizal (AM) or ectomycorrhizal (ECM) associations conferring superior drought resistance may result in lower δ 13 C
prolonged hot drought leads to thinner leaf production
water stress reduces CO2 availability due to stomata closure Arabidopsis thaliana
carbohydrate metabolism is described in the literature as important component of drought response in conifers
naturally regenerated forests and planted forests have documented differences in drought vulnerability
C4 Eragrostis curvula showed high sensitivity of nonstomatal limitation to dehydration when dehydration was imposed over days Eragrostis curvula
GhWRKY207 expression is induced by drought stress Gossypium hirsutum
cpk4-1 mutant is less able to withhold water under drought conditions Arabidopsis thaliana
HSFA6a-OE/C plants have higher survival rates than wild-type plants after drought stress Arabidopsis thaliana
(AT-HSFA6A, HSFA6A, AT5G43840) has downstream targets that remain elusive in plant drought response Arabidopsis thaliana
most plants close their stomata in response to drying soil conditions
drought stress treatments varied methodically in corresponding experiments Arabidopsis thaliana
One association affects (AtERF#092, ERF1, ERF1B, AT3G23240) drought response regulator Arabidopsis thaliana
rice MOTHER OF FT AND (TFL-1, TFL1, AT5G03840) (OsMFT1) plays crucial role in response to drought treatment Oryza sativa
OsMFT1 regulates transcriptional ability of OsbZIP66 and OsMYB26 Oryza sativa
OsFTIP1 impeding OsMFT1 translocation affects drought response in rice Oryza sativa
OsMFT1 in nucleus interacts with OsMYB26 Oryza sativa
ABA- or drought-responsive genes were not modified in expression in microarray experiment of ERF#111-OE lines Arabidopsis thaliana
strong effects on yield under drought of qDTY 2.2 and qDTY 4.1 may be due to additive effects of QTLs on root traits or complementarity of distinct traits Oryza sativa
hydraulic properties have been implicated in drought response of other crops
root pressure has been hypothesized as important for rice drought response as mechanism for refilling of xylem embolism Oryza sativa
improved lowland rice genotypes more than 95% genetically similar to IR64 aimed to characterize physiological mechanisms behind drought response conferred by AdaySel-derived QTLs Oryza sativa
OsMFT1 in the nucleus under drought stress enhances activation of OsbZIP66 and impairs the repression of OsMYB26 on drought-responsive genes Oryza sativa
genes in this study (OsFTIP1, OsMFT1, OsMYB26, OsbZIP66) may serve as useful candidates for crop biotechnology to improve drought tolerance Oryza sativa
OsMFT1 interacts directly with OsMYB26 Oryza sativa
ectopic expression of Arabidopsis thaliana RING Zinc Finger 1 (AtRZF1, BTL02, RZF1, AT3G56580) gene is very significantly influential in water loss Arabidopsis thaliana
C3H2C3-type RING domain is likely important for biological function of Arabidopsis thaliana RING Zinc Finger 1 (AtRZF1, BTL02, RZF1, AT3G56580) in drought response Arabidopsis thaliana
MYB and (AtbZIP, bZIP, AT1G68880) transcription factors positively or negatively regulate drought response in plants
(ABI3, AtABI3, SIS10, AT3G24650) is ABA-associated drought response factor
accumulation of sugars and sugar alcohols in phloem sap reflects responses of pea plants to drought Pisum sativum
approximately 70% (39 of 56 genes) of conserved DRGs were upregulated (log2 fold-change >1) by drought in either leaves or roots Glycine max
wild-type leaves were closed up (in-rolled shape) around stem Kalanchoe fedtschenkoi
dehydration treatment led to increased expression of Responsive to Dehydration29B (LTI65, RD29B, AT5G52300) gene Arabidopsis thaliana
SNAC1-overexpressing plants exhibits drought-resistant phenotype Oryza sativa
knock-down of Grain Number, Plant Height, and Heading Date7 (Ghd7) enhanced drought tolerance Oryza sativa
Arabidopsis thaliana exhibits natural genetic variation in drought response Arabidopsis thaliana
analysis of drought-induced changes in the metabolome of two different barley cultivars revealed that the level of Pro was already high in drought-tolerant cultivar in the absence of drought stress Hordeum vulgare
cpk4-1 and cpk11-2 mutants show lower survival rate compared to Col-0 ecotype Arabidopsis thaliana
MdbZIP2 and MdbZIP39 are negative regulators of drought tolerance Malus domestica
OsHB22 positively regulates drought response Oryza sativa L.
drought stress affects geographical distribution and productivity of crops
OsLEA3 and Rab21 expression occurs in response to drought stress Oryza sativa
canopy temperature showed significant positive correlations with flowering (FLW)
Haplotype I accessions displayed mean canopy temperature under drought of 34.24 °C Oryza sativa
OsPP18 positively affects drought tolerance Oryza sativa
(FPA, AT2G43410) has been shown to play role in post-transcriptional modification of mRNAs from other expressed genes in response to dehydration stress
HB7 and (ATHB-12, ATHB12, HB-12, HB12, AT3G61890) are up-regulated in (ATR4, CYP83B1, RED1, RNT1, SUR2, AT4G31500) mutant Arabidopsis thaliana
leaf shrinkage relates to decline of leaf hydraulic conductance (K leaf)
oaks (Quercus spp.) experience increase in intercellular airspace Quercus spp.
leaf shrinkage is hypothesized to relate to decline of leaf hydraulic conductance (K leaf) during dehydration
drought stress increases ABA content Arabidopsis thaliana
(ABO3, ATWRKY63, WRKY63, AT1G66600) mutant shows increased transpiration water loss Arabidopsis thaliana
model species with larger root systems are more tolerant to drought
increased basal levels of these amino acids represent a biochemical predisposition acting as efficient drought tolerance mechanism
OsPP18 is positive regulator of drought tolerance in rice Oryza sativa
available RNA-seq data from drought experiment at two stages of development (inflorescence and vegetative stages) were assessed for potential modulation by drought within reproductive tissue Oryza sativa
abscisic acid (ABA) is important for plant drought responses
(AT-HSFA6A, HSFA6A, AT5G43840) is a direct target of AtPTPN Arabidopsis thaliana
intronless sub-family genes enriched in 'transcriptional regulation' function in drought responsive pathways
OsPP18 is first member of PP2C family identified as positive regulator of drought stress tolerance in ABA-independent pathway Oryza sativa
(AtMAX2, MAX2, ORE9, PPS, AT2G42620) is involved in drought responses Arabidopsis thaliana
shoot hydraulic conductivity of MdMYB88/124 RNAi plants is much lower than GL-3 plants under drought stress Malus domestica
(ABI1, AtABI1, AT4G26080) is important PP2C for plant tolerance to drought stress
ced2 mutant does not show increase in ABA content Arabidopsis thaliana
potato and tomato varieties used here are drought-sensitive Solanum tuberosum; Solanum lycopersicum
OsFTIP6 may positively modulate drought response Oryza sativa L.
trp2-8 mutants exhibited reduced water-loss rates under water deficit
proteins that significantly changed their accumulation pattern in drought conditions identified Hordeum vulgare
moderate drought alone can stimulate isoprene emission
ZmPP2C overexpression in Arabidopsis decreased tolerance to drought stress Arabidopsis thaliana
rNAD-ME1 held its leaves in open position Kalanchoe fedtschenkoi
dehydration treatment led to increased expression of Responsive to ABA (RAB, RBE, AT5G06070) gene Arabidopsis thaliana
447 lincRNAs were affected by drought in at least one comparison Oryza sativa
ospp18 mutant is sensitive to drought stress at flowering stage Oryza sativa
TGB1 interaction with NbHIPP26 leading to drought tolerance activates expression of dehydration-inducible genes Nicotiana benthamiana
MdMYB88 or MdMYB124 overexpression plants are taller than GL-3 plants after 2 months of drought stress Malus domestica
increasing CK production in leaves during periods of severe drought stress caused drought tolerance
increasing the endogenous GABA level rescued drought susceptibility defect Arabidopsis thaliana
root hydraulic conductivity is reduced remarkably after 2-month exposure to drought conditions Malus domestica
loss of extraxylem hydraulic conductance is hypothesized to have greater impact on leaf hydraulic conductance at less negative water potentials when xylem tensions are too weak to trigger embolism
abscisic acid (chemical signal from vein xylem) is converted by bundle sheath cells into decrease in K leaf (leaf hydraulic conductance) by deactivating aquaporins Arabidopsis
greater oxidative damage in ospp18 mutant is associated with increased sensitivity of ospp18 mutant to drought stress Oryza sativa
increased ABA sensitivity is accompanied by increased drought tolerance Arabidopsis thaliana
(AtLSM5, AtSAD1, LSM5, SAD1, AT5G48870) mutant shows increased transpiration water loss Arabidopsis thaliana
dehydration treatment led to increased expression of Responsive to Dehydration29A (COR78, LTI140, LTI78, RD29A, AT5G52310) gene Arabidopsis thaliana
lower level of ABA accumulation correlates with drought tolerance
MdMYB88 or MdMYB124 overexpression plants have higher root-to-shoot ratio than GL-3 plants in response to long-term drought stress Malus domestica
G protein-coupled receptor 1 (ATGCR1, GCR1, AT1G48270) binds to GUANINE NUCLEOTIDE-BINDING PROTEIN ALPHA-1 SUBUNIT (ATGPA1, GP ALPHA 1, GPA1, AT2G26300)
MdMYB88/124 RNAi plants are much shorter than GL-3 plants after 2 months of drought stress Malus domestica
membrane cuticle thickness is associated with drought response Arabidopsis thaliana
(ATCCD7, CCD7, MAX3, AT2G44990) mutant did not display any phenotypic difference compared with wild type under drought conditions Arabidopsis thaliana
SNAC1 is transcription factor involved in drought response
drought treatment significantly affects root-to-shoot ratio Malus domestica
Haplotype I and Haplotype II accessions showed highly significant canopy temperature difference under drought canopy temperature Oryza sativa
most families showed decrease in δ 15 N under drought treatment Juglans regia
tppi1 mutant shows survival rate after drought stress and rehydration Arabidopsis thaliana
drought treatment has stronger effect on M82 growth Solanum lycopersicum
PsRD29 expression was highly upregulated at 7 days after drought stress Pisum sativum
drought leads to stomatal closure
interaction of droughts with nutrient availability and uptake is important for understanding drought impacts on trees
Fagus sylvatica did not experience the same change in stomatal conductance
inactivation of (AtKPNB1, IMB1, KPNB1, AT5G53480) reduced rate of water loss Arabidopsis thaliana
plant resource allocation to root growth enhances water acquisition
increased water loss correlates with drought-sensitive phenotype Arabidopsis thaliana
transgenic barley plants displayed a 1.5- to 2-fold higher stomatal conductance Hordeum vulgare
drought induces the accumulation of ABA
microarray experiment by Nishiyama et al. did not show effect of drought stress on AtERF#111 expression Arabidopsis thaliana
stomatal closure prevents excessive water loss
drought stress reduces total rhizosheath mass Zea mays
drought stress reduces rhizosheath mass normalized by root length Zea mays
gOsbZIP66-9myc rescued drought-sensitive phenotype of Osbzip66 Oryza sativa
Osftip6-1 mutant was rescued by supplying OsHB22 activity in the nucleus Oryza sativa
minor alleles at qCT1 had negative effect on grain yield (GY) under stress Oryza sativa
enhanced activation of OsbZIP66 and impaired repression of OsMYB26 on drought-responsive genes enhances drought tolerance in rice Oryza sativa
OsMYB26 expression may contribute to drought regulation of OsFTIP1-OsMFT1-OsMYB26/OsbZIP66 module Oryza sativa
OsbZIP66 expression may contribute to drought regulation of OsFTIP1-OsMFT1-OsMYB26/OsbZIP66 module Oryza sativa
four loci in the study colocalized within previously reported drought-related QTLs Oryza sativa
OsHB22 mutant displayed drought-sensitive phenotype Oryza sativa
AtERF#111 transcript level was observed to increase upon drought stress Arabidopsis thaliana
drought escape triggers acceleration of floral transition and reproductive success
canopy temperature under drought stress showed highest correlation coefficients with grain yield (GY)
OsSRO1c is induced in guard cells by drought stress Oryza sativa
(ATCCD7, CCD7, MAX3, AT2G44990) mutant does not display defects in drought-sensitive phenotype Arabidopsis thaliana
reduced cuticle thickness of (AtMAX2, MAX2, ORE9, PPS, AT2G42620) could contribute to drought-sensitive phenotype of (AtMAX2, MAX2, ORE9, PPS, AT2G42620) mutant Arabidopsis thaliana
11 lincRNAs appear to be responding to abiotic stress, drought, in a manner dependent on developmental stage Oryza sativa
Atptpn-2 mutants have lower survival rates than wild-type plants after drought stress Arabidopsis thaliana
Overexpression of Grain Number, Plant Height, and Heading Date7 (Ghd7) increased drought sensitivity Oryza sativa
first response to drought is a reduction in stomatal conductance
plants have naturally developed over-riding survival mechanism that will trigger stomatal closure even in presence of light when drought signal is perceived
(ATCPK23, CPK23, GCA2, AT4G04740) mutant allele (SALK_007958) is more tolerant towards non-watering for 6-day period Arabidopsis thaliana
OsMFT1 interacts directly with OsbZIP66 Oryza sativa
overexpression of OsbZIP66 in Osmyb26 protoplasts led to higher expression of OsLEA3 Oryza sativa
suppression of MdbZIP80 alone increases drought tolerance Malus domestica
apple C/S1 (AtbZIP, bZIP, AT1G68880) network negatively modulates drought tolerance Malus domestica
expression of lincRNA loci analyzed within duplicate RNA-seq data sets derived from drought-treated and control plants Oryza sativa
(ATFTA, FTA, PFT/PGGT-IALPHA, PLP, AT3G59380) down-regulation via RNAi techniques improves drought tolerance Brassica napus
HSFA6a-OE/C plants are more tolerant to drought and have higher survival rates than Arabidopsis thaliana
OsFTIP1 RNA interference (RNAi) transgenic lines displayed enhanced drought tolerance similar to Osftip1-1 and Osftip1-2 mutants Oryza sativa
overexpression of OsbZIP66 in Osmyb26 protoplasts led to higher expression of RAB21 Oryza sativa
transgenic Curinga lines grown under confined field drought conditions revealed distinctive capability of regulating drought avoidance and drought tolerance mechanisms Oryza sativa
drought stress induces expression of AtPTPN Arabidopsis thaliana
complemented lines expressing CALCIUM-DEPENDENT PROTEIN KINASE 21 (AtCPK21, CPK21, AT4G04720) under P35S control show no altered drought response drought conditions Arabidopsis thaliana
TaNAC69 genes is up-regulated >10-fold during drought stress in roots Triticum aestivum
drought up-regulated transcription factors transcript level is markedly up-regulated in wheat leaves and roots during drought stress Triticum aestivum