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heat stress response

35982 relationships annotated with this phrase. Showing first 500 of 35982.
Source entity Relationship Target entity Species
thousands of genes associated with multiple biological pathways are involved in plant responses to heat stress
AtHsfA binding to heat shock elements (HSEs) regulates plant heat resistance
Arabidopsis homologue GAST1 PROTEIN HOMOLOG 4 constitutive expression improves thermotolerance by influencing (BIP, BIP2, AT5G42020) transcript abundance Arabidopsis thaliana
expression of (ATHSFA2, HSFA2, AT2G26150) in seedlings is strictly controlled by HSFA1s upon stress Arabidopsis thaliana
young leaves were less prone to heating Vitis vinifera L.
heterooligomeric complexes can synergistically activate the expression of a small HSP Solanum lycopersicum
genes involved in thermotolerance dissecting underlying molecular mechanisms will help breeders develop strategies to improve thermotolerance of wheat germplasm Triticum aestivum
HsfA2-II protein cooperates with (ATHSF1, ATHSFA1A, HSF1, HSFA1A, AT4G17750) Solanum lycopersicum
ectopic expression of (ATHSFA2, HSFA2, AT2G26150) regulates metabolism and redox homeostasis-related genes Arabidopsis thaliana
HSFA1s induce the expression of diverse transcription regulators, including HSFs of other classes (class A2, A3, A7, B1, and B2) Arabidopsis thaliana
marginal gain theory often fails in hot environments
HSFA2-I isoform enhances acquired thermotolerance following repeated heat stress episodes Solanum lycopersicum
TaHSFC2 played a role in response to heat stress Triticum aestivum
(ATHSF1, ATHSFA1A, HSF1, HSFA1A, AT4G17750) (ATHSF3, ATHSFA1B, HSF3, HSFA1B, AT5G16820) (ATHSFA1D, HSFA1D, AT1G32330) (ATHSFA1E, HSFA1E, AT3G02990) activates transcription of (ATHSFA2, HSFA2, AT2G26150) Arabidopsis thaliana
HSFA1s induce the expression of (BZIP28, AT3G10800) Arabidopsis thaliana
(DREB2, DREB2A, AT5G05410) expression ratio of heat-treated hsfa2 versus A2QK plants 3.34 Arabidopsis thaliana
heat stress induces alternative splicing Triticum aestivum
genes with no preference for HSFA1s or (ATHSFA2, HSFA2, AT2G26150) contains 14 small HSPs Arabidopsis thaliana
first mild and later applied severe heat stress does not change HSC70.1 transcription
Tahsp70s-KO-31 and Tahsp70s-KO-55 were more sensitive than WT to heat stress Triticum aestivum
(ATHSP101, HOT1, HSP101, AT1G74310) is identical to ScHsp104 ortholog in yeast Arabidopsis thaliana; Saccharomyces cerevisiae
(ATHSP101, HOT1, HSP101, AT1G74310) expression in yeast rescues thermotolerance defect of Δ Hsp104 mutant Saccharomyces cerevisiae
(ATHSP101, HOT1, HSP101, AT1G74310) is induced by heat stress Arabidopsis thaliana; Saccharomyces cerevisiae
quadruple KO (QK) mutants show dramatic defects in tolerance to different heat stress regimes Arabidopsis thaliana
(ATHSFA2, HSFA2, AT2G26150) at high levels regulates ROTAMASE FKBP2 (ATFKBP65, FKBP65, ROF2, AT5G48570) Arabidopsis thaliana
total (ATHSFA2, HSFA2, AT2G26150) transcripts significantly higher in accordance with (ATHSP101, HOT1, HSP101, AT1G74310) transcript levels Arabidopsis thaliana
endogenous (ATHSFA2, HSFA2, AT2G26150) transcripts slightly increased in A2QK-10 after heat treatment Arabidopsis thaliana
endogenous (ATHSFA2, HSFA2, AT2G26150) transcripts much less abundant than in wild type and A2Wt after heat treatment Arabidopsis thaliana
TaHSFA6e directly binds to and upregulates TaHSP70s Triticum aestivum
240 probe sets strongly heat induced in wild type, (ATHSFA2, HSFA2, AT2G26150) or A2QK Arabidopsis thaliana
two pathways control heat induction of (AT-HSFA3, FGT3, HSFA3, AT5G03720) Arabidopsis thaliana
severe heat stress induces HSC70.1 transcription
heat shock transcription factor (HSF)-mediated transcriptional upregulation of heat shock protein genes (HSPs) plays an essential role in regulating heat stress responses
HSF-mediated reprograming of HSP gene expression is the most well-known pathway involved in heat stress responses
(ATHSFA2, HSFA2, AT2G26150) forms heterooligomeric complexes with (ATHSF1, ATHSFA1A, HSF1, HSFA1A, AT4G17750) (ATHSF3, ATHSFA1B, HSF3, HSFA1B, AT5G16820) (ATHSFA1D, HSFA1D, AT1G32330) (ATHSFA1E, HSFA1E, AT3G02990) Arabidopsis thaliana
(ATHSFA2, HSFA2, AT2G26150) without substantial positive autoregulation by (ATHSFA2, HSFA2, AT2G26150) Arabidopsis thaliana
TaHSFA6e loss-of-function led to enhanced heat stress sensitivity of mutants Triticum aestivum
leaf conductance increase with temperature did not find any evidence in the literature that it could occur at least up to 45°C in grapevine Vitis vinifera L.
AtHsfA regulates expression of heat shock proteins and stress-related genes
A2QK transgenic line promotes callus formation Arabidopsis thaliana
heat stress conditions can induce stabilization of (RCA, AT2G39730) transcript levels Gossypium hirsutum; Arabidopsis thaliana
high growing season temperature threatens rice productivity Oryza sativa
(HSA32, AT4G21320) is required for maintaining high level of (ATHSP101, HOT1, HSP101, AT1G74310) Oryza sativa
japonica rice cultivar Nipponbare has higher LAT level than indica rice cultivar N22 Oryza sativa
HSF-HSP module was simultaneously determined in response to heat stress Triticum aestivum
total and endogenous (ATHSFA2, HSFA2, AT2G26150) transcripts no substantial difference in A2Wt line after heat treatment Arabidopsis thaliana
(ATHSFA2, HSFA2, AT2G26150) is a relatively weak activator of heat-induced transcription regulators such as (AT-HSFA7A, HSFA7A, AT3G51910) (AT-HSFA7B, HSFA7B, AT3G63350) (ATHAP5B, HAP5B, NF-YC2, AT1G56170) (DREB2, DREB2A, AT5G05410) (AT-HSFB2B, HSF7, HSFB2B, AT4G11660) and (ATHSFA2, HSFA2, AT2G26150) itself Arabidopsis thaliana
heat damage to leaf tissues leads to reduced photosynthetic efficiency
cuticle permeability could increase at high temperature Vitis vinifera L.
heat stress can generate two distinct signals correlating with different gene sets Arabidopsis thaliana
OsEPF1oeS leaf 5 with very low stomatal density (SD) and small stomatal size (SS) had slower rates of photosynthetic rate (A) decline at higher temperature as leaf vapor pressure deficit (VPD) increased Oryza sativa
heat stress induces global repression of protein synthesis
morning-phased DMGs are enriched in response to heat Petunia hybrida
total (ATHSFA2, HSFA2, AT2G26150) transcripts significantly higher in accordance with (HSA32, AT4G21320) transcript levels Arabidopsis thaliana
genotypes classified as traditionally heat tolerant were sensitive to small increases in night-time temperature
knockout mutants of TahsfA6e exhibit reduced thermotolerance Triticum aestivum
disruption of eukaryotic translation initiation factor 5B (eIF5B) resulted in heat sensitivity Arabidopsis thaliana
(ATHSFA2, HSFA2, AT2G26150) is involved in the late phase of heat stress response Arabidopsis thaliana
ectopic expression of (ATHSFA2, HSFA2, AT2G26150) in Arabidopsis mutant lacking all four HSFA1s allows assessment of independent function of (ATHSFA2, HSFA2, AT2G26150) Arabidopsis thaliana
(ATHSFA2, HSFA2, AT2G26150) performs triggering heat stress response Arabidopsis thaliana
(AT-HSFA3, FGT3, HSFA3, AT5G03720) is preferentially regulated by (ATHSFA2, HSFA2, AT2G26150) Arabidopsis thaliana
(AT-HSFA3, FGT3, HSFA3, AT5G03720) late induction profile under heat stress is in good agreement with preferential regulation by (ATHSFA2, HSFA2, AT2G26150) Arabidopsis thaliana
class A1 and A2 heat shock factors have overlapping and distinct functions in heat stress response and development Arabidopsis thaliana
heat-induced callus formation mediated by overexpression of (ATHSFA2, HSFA2, AT2G26150) in the absence of HSFA1s Arabidopsis thaliana
pathway through HSFA1s-HSFA2 controls heat induction of (AT-HSFA3, FGT3, HSFA3, AT5G03720) Arabidopsis thaliana
(ATHSP17.4, HSP17.4, AT3G46230) and (AT-HSP17.6A, HSP17.6, HSP17.6A, AT5G12030) are targets of HSFA1s in heat stress response Arabidopsis thaliana
current high-temperature-tolerant genotypes may not be adapted to rising Tmin
TaHSFA6e and TaHSP70s interaction occurs in response to heat stress Triticum aestivum
TaHSFA6e-II, TaHSFA6e-III and TaHSFA6e-III variants compared for transcriptional activity under heat stressed conditions (40°C, 1 h) Triticum aestivum
WT (CB037) has survival rate of 66.6% Triticum aestivum
stomatal closure is likely to dominate over potential increase in cuticular permeance Vitis vinifera L.
heat stress increases CaDeSI2 expression Capsicum annuum
(ATHSFA2, HSFA2, AT2G26150) knockout mutant compared with A2QK-10 overexpression line Arabidopsis thaliana
TaHSP70 knockout increases heat sensitivity Triticum aestivum
constitutive expression of SlHSP21 enhanced thermotolerance Solanum lycopersicum
GID-2465 and GID-7129721 were classified as having high heat tolerance
heat treatment at 37°C for 1 h did not further increase (ATHSFA2, HSFA2, AT2G26150) protein levels Arabidopsis thaliana
240 probe sets not strongly heat induced in QK mutant Arabidopsis thaliana
fluorescent Förster Resonance Energy Transfer (FRET)-based calcium (Ca 2+) reporter proteins revealed specific chloroplast calcium (Ca 2+) signals in response to heat stress
(ATHSF1, ATHSFA1A, HSF1, HSFA1A, AT4G17750) (ATHSF3, ATHSFA1B, HSF3, HSFA1B, AT5G16820) (ATHSFA1D, HSFA1D, AT1G32330) are master regulators of heat stress response in Arabidopsis Arabidopsis thaliana
(ATHS83, AtHsp90-1, ATHSP90.1, HSP81-1, HSP81.1, HSP83, HSP90.1, AT5G52640) expression ratio of heat-treated hsfa2 versus A2QK plants 0.5 Arabidopsis thaliana
(HSA32, AT4G21320) and (ATHSP101, HOT1, HSP101, AT1G74310) are not obviously induced by heat in mature leaf Oryza sativa
heat tolerance involves multiple mechanisms and various genetic components Oryza sativa
high temperature-induced sHSP22 transcription was also observed in hypocotyls Arabidopsis thaliana
15 genes showed significantly higher expression levels in WT compared to (AT-HSFB1, ATHSF4, HSF4, HSFB1, TBF1, AT4G36990) /B2b plants
heat stress can cause high stem hydraulic damage
heat reduces growth Populus tremuloides
silencing of (ATHSP101, HOT1, HSP101, AT1G74310) severely impaired thermotolerance Arabidopsis thaliana
(ATHSFA1E, HSFA1E, AT3G02990) does not confer thermotolerance in absence of (ATHSF1, ATHSFA1A, HSF1, HSFA1A, AT4G17750) (ATHSF3, ATHSFA1B, HSF3, HSFA1B, AT5G16820) and (ATHSFA1D, HSFA1D, AT1G32330) Arabidopsis thaliana
(ATCPN21, CHCPN10, CPN10, CPN20, CPN21, AT5G20720) expression increases in SlMPK1 RNAi lines Solanum lycopersicum
(cpHsc70-2, HSC70-7, HSP70-7, AT5G49910) expression increases in SlMPK1 RNAi lines Solanum lycopersicum
sHSP22 expression is dramatically induced under heat shock conditions Arabidopsis thaliana
WT plants show maximum signal at 2 h heat stress Arabidopsis thaliana
TaHSFA6e knockout increases heat sensitivity Triticum aestivum
Tahsp70s-KO-31 has survival rate of 7.7% Triticum aestivum
(AT-HSFA3, FGT3, HSFA3, AT5G03720) is partially regulated by (DREB2, DREB2A, AT5G05410) Arabidopsis thaliana
heterooligomers formed by HSFA1s and (ATHSFA2, HSFA2, AT2G26150) have not been investigated for synergetic effect Arabidopsis thaliana
japonica Nipponbare rice cultivar shows opposite performance in basal thermotolerance and long-term acquired thermotolerance (LAT) Oryza sativa
Arabidopsis plants overexpressing SlSPRH1 were more sensitive to HT Arabidopsis thaliana
SlMPK1 responds to heat stress Solanum lycopersicum
(HSA32, AT4G21320) knockout (KO) mutants characterized by biochemical and physiological responses to heat stress conditions Oryza sativa
deficiency of (AT-HSFB1, ATHSF4, HSF4, HSFB1, TBF1, AT4G36990) and (AT-HSFB2B, HSF7, HSFB2B, AT4G11660) has little if any effect on expression profiles of typical Hsf-A1a/1b target genes Arabidopsis thaliana
synthetic HSEs were used as probe in EMSA Arabidopsis thaliana
HEAT STRESS-ASSOCIATED 32-KD PROTEIN (HSA32, AT4G21320) protein level is substantially higher in cv Nipponbare than in cv N22 after long recovery following heat acclimation treatment cultivar difference in long-term acquired thermotolerance (LAT) phenotype Oryza sativa
(ATHSP101, HOT1, HSP101, AT1G74310) transcripts are reduced to prestress level after recovery for 60 min in wild type Oryza sativa
lesions in chloroplast membranes at high temperature would cause mimosinase to leak out of chloroplast Leucaena leucocephala
(AT-HSFB1, ATHSF4, HSF4, HSFB1, TBF1, AT4G36990) and (AT-HSFB2B, HSF7, HSFB2B, AT4G11660) are heat-induced heat stress
(AT-HSFB1, ATHSF4, HSF4, HSFB1, TBF1, AT4G36990) /B2b plants show earlier onset at 60 min heat stress Arabidopsis thaliana
SlMPK1 suppression improves heat tolerance in RNAi-SlMPK1 tomato plants Solanum lycopersicum
16 genes showed lower expression levels in WT compared to (AT-HSFB1, ATHSF4, HSF4, HSFB1, TBF1, AT4G36990) /B2b plants
33 genes from cluster 1 respond rapidly and strongly but transiently to heat stress
SlSPRH1 has a negative effect on heat tolerance is suggested by SlSPRH1-expressing plant phenotypes Arabidopsis thaliana
unspecific constitutive binding complexes are marked by asterisks in EMSA gel Arabidopsis thaliana
(AtTN10, TIR, TN10, AT1G72930) class disease resistance gene is down-regulated after heat stress in wild-type plants Arabidopsis thaliana
(AtHsp90-7, AtHsp90.7, HSP90, HSP90.7, SHD, AT4G24190) accumulation is induced by warm temperatures Arabidopsis thaliana
Jmax of DJ 123 showed opposing response to heat stress and decreased Oryza sativa
negative association between Tcrit and (ATNYE1, NYE1, SGR, SGR1, AT4G22920) demonstrates that lines that enter the rapid temperature response phase at higher temperatures also have improved vegetative heat tolerance as adult plants Oryza sativa
(ATHSFA2, HSFA2, AT2G26150) mutation leads to heat-sensitive phenotype Arabidopsis thaliana
(AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) and (ATHSFA2, HSFA2, AT2G26150) participate in regulation of heat shock response Arabidopsis thaliana
(ATHSP101, HOT1, HSP101, AT1G74310) is induced to similarly high levels in wild type and hsa32-1 after heat treatment at 42°C for 2 h Oryza sativa
heat-induced expression of (HSA32, AT4G21320) and sHSP-CI exhibited shorter duration in cv N22 than in cv Nipponbare Oryza sativa
rice cultivar tolerant to one type of heat stress is not necessarily tolerant to other types of heat stress Oryza sativa
SlMPK1 is activated in tomato leaves under high-temperature stress Solanum lycopersicum
heterologous expression of SlSPRH1 in Arabidopsis led to a decrease in thermotolerance Arabidopsis thaliana
double knockout mutations in (ATHSF1, ATHSFA1A, HSF1, HSFA1A, AT4G17750) (ATHSF3, ATHSFA1B, HSF3, HSFA1B, AT5G16820) caused attenuation of induction of (HSP70, AT4G16660) Arabidopsis thaliana
(ATHSP101, HOT1, HSP101, AT1G74310) transcripts are slightly higher in (HSA32, AT4G21320) KO lines than in wild type Oryza sativa
(ATSUC4, ATSUT4, SUC4, SUT4, AT1G09960) expression showed the same response under heat stress in the tested monocots
(CPN60B, Cpn60beta1, CPNB1, LEN1, AT1G55490) possibly protects Rubisco activase from thermal denaturation
(LCR77, PDF1.2, PDF1.2A, AT5G44420) is differentially regulated upon heat stress in (AT-HSFB1, ATHSF4, HSF4, HSFB1, TBF1, AT4G36990) /B2b mutant plants compared to wild-type Arabidopsis thaliana
rice (HSA32, AT4G21320) expression is highly induced by heat treatment Oryza sativa
high temperature (HT) induces activities of 46-kD HAMK Nicotiana tabacum
CPN60B2 expression increases in SlMPK1 RNAi lines Solanum lycopersicum
OsPP18 is not significantly changed under heat stress Oryza sativa
(ATCPN21, CHCPN10, CPN10, CPN20, CPN21, AT5G20720) is heat-regulated protein Solanum lycopersicum
SlMPK1 functions as negative regulator in heat stress Solanum lycopersicum
(LCR77, PDF1.2, PDF1.2A, AT5G44420) is up-regulated in (AT-HSFB1, ATHSF4, HSF4, HSFB1, TBF1, AT4G36990) /B2b plants Arabidopsis thaliana
plants grown under long-day conditions were exposed to heat stress at 42°C for 48 h Arabidopsis thaliana
HSP100 encoded by (ATHSP101, HOT1, HSP101, AT1G74310) is essential for thermo-tolerance in Arabidopsis Arabidopsis thaliana
losses in the main panicle yield from shoot heating were caused by reduction in the number of seeds produced Chenopodium quinoa
Vcmax showed significant variation between pre- and post-heat-stress initiation Oryza sativa
mutants lacking mitochondrial-localized mTERF4 have increased tolerance to heat Arabidopsis thaliana
Arabidopsis (HSP70, AT4G16660) family has five cytoplasmic members Arabidopsis thaliana
(ATHSP101, HOT1, HSP101, AT1G74310) transcript and protein are significantly upregulated in response to HS Arabidopsis thaliana
(AtHsp70-2, Hsp70-2, AT5G02490) single-mutant shows heat-sensitive phenotype Arabidopsis thaliana
constitutive presence of (AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) may have repercussions in proposed role of (AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) as negative regulator noted in basal thermotolerance seedling assay Arabidopsis thaliana
progression of (ATHSP70, HSC70-4, HSP70, HSP70-4, AT3G12580) transcript expression takes place in parallel to increasing heat stress Arabidopsis thaliana
RNA-seq on three tolerant and three susceptible genotypes was conducted in order to identify differentially expressed genes (DEGs) under heat stress Solanum lycopersicum
ZmRCAα may contribute to synthesis of larger heat-induced (RCA, AT2G39730) polypeptide Zea mays
(ATHSP101, HOT1, HSP101, AT1G74310) is major heat-inducible HSP gene Solanum lycopersicum
STP3 is down-regulated after heat stress in wild-type plants Arabidopsis thaliana
Arabidopsis (ATHSP101, HOT1, HSP101, AT1G74310) mutants show enhanced expression of other chaperones Arabidopsis thaliana
(ATHSP101, HOT1, HSP101, AT1G74310) positively affects level of (HSA32, AT4G21320) Oryza sativa
AtMPK6-phosphorylated (ATHSFA2, HSFA2, AT2G26150) might participate in HT response Arabidopsis thaliana
SlMPK1 negatively regulates HT response Solanum lycopersicum
(HSP70-5, Hsp70b, AT1G16030) is highly induced in HT-treated plants Solanum lycopersicum
SlMPK1-mediated CPN60 accumulation may protect chloroplast proteins from heat-induced denaturation Solanum lycopersicum
molecular chaperone activity of (TRP3, TSA1, AT3G54640) promotes resistance to heat shock yeast
down-regulation of (SUT1, AT5G63020) and (ATSUC4, ATSUT4, SUC4, SUT4, AT1G09960) under heat stress matches observed strong reduction of growth in all tissues in heat-stressed grasses
heat stress at 37°C for 1 h increases (AT-HSFB1, ATHSF4, HSF4, HSFB1, TBF1, AT4G36990) mRNA transcript levels in wild-type plants Arabidopsis thaliana
heat stress up-regulates (AT-HSFB2B, HSF7, HSFB2B, AT4G11660) mRNA levels in wild-type plants Arabidopsis thaliana
rice (HSA32, AT4G21320) accumulation does not exhibit obvious delay in accumulation after heat treatment Oryza sativa
(ATHSFA2, HSFA2, AT2G26150) is major heat-inducible HSF gene Solanum lycopersicum
SlSPRH1 S44A mutation blocked SlMPK1-mediated inhibition in protoplasts under heat stress Solanum lycopersicum
(ATHSFA2, HSFA2, AT2G26150) is a downstream gene of HSFA1 Arabidopsis thaliana
HSFA1s-preferring genes most enriched categories transcription Arabidopsis thaliana
MITOCHONDRIAL HEAT SHOCK COGNATE 70-kD PROTEIN-2 (HSC70-5, HSP70-10, MTHSC70-2, AT5G09590) expression ratio of heat-treated hsfa2 versus A2QK plants 3.65 Arabidopsis thaliana
(ATHSP101, HOT1, HSP101, AT1G74310) level is induced to similar level after 2 h of recovery in cv N22 and Nipponbare Oryza sativa
Arabidopsis thaliana contains heat shock factor (HSF) homologs Arabidopsis thaliana
(ATHSFA2, HSFA2, AT2G26150) mediates the amplification of a subset of heat stress response genes Arabidopsis thaliana
indica N22 rice cultivar shows opposite performance in basal thermotolerance and long-term acquired thermotolerance (LAT) Oryza sativa
SlMPK1 may be negative regulator of heat stress signaling Solanum lycopersicum
class A-Hsfs have functions in heat stress response Arabidopsis thaliana
(PDF1.2b, AT2G26020) promoter contains variant HSE (nGAAn/nTTCn) Arabidopsis thaliana
plants respond differently to heat in roots versus shoots heat stress response
short heat exposure during anthesis may be sufficient to cause significant yield losses Chenopodium quinoa
Jmax rates increasing substantially for majority of genotypes except IR 64 and BRRI 28 Oryza sativa
parameters determined from juvenile leaf segments demonstrating the effectiveness of these for forecasting vegetative heat tolerance in adult plants Oryza sativa
(ATHSFA1D, HSFA1D, AT1G32330) and (ATHSFA1E, HSFA1E, AT3G02990) are involved in transcriptional regulation of (ATHSFA2, HSFA2, AT2G26150) function Arabidopsis thaliana
knl2-2 single-mutant shows heat-sensitive phenotype Arabidopsis thaliana
XTH gene expression is regulated by heat shock
HSPs/molecular chaperones are heat-regulated protein-coding gene transcripts Solanum lycopersicum
(AT-HSFB2B, HSF7, HSFB2B, AT4G11660) single mutant shows no obvious phenotypic effect on thermotolerance Arabidopsis thaliana
nitric oxide (NO) is involved in responses to heat stress
heating quinoa shoots results in yield loss Chenopodium quinoa
changes in maturity in shoot-heated samples, especially HRS, in combination with increases in tertiary panicle yield and number suggest this accession of quinoa uses a heat-avoidance strategy rather than an escape strategy Chenopodium quinoa
BRRI 28 yielded negative percentage decrease in ɸPSII Oryza sativa
plasticity for Amax ranged from 0.02 to 0.23 Oryza sativa
phenotypic plasticity for Vcmax ranged between 0.01 and 0.41 Oryza sativa
(APD9, FGT2, AT5G66080) does not affect acquisition of thermotolerance
expression of (ATHSFA2, HSFA2, AT2G26150) was not affected in (ATHSF1, ATHSFA1A, HSF1, HSFA1A, AT4G17750) /b double knockout (KO) lines Arabidopsis thaliana
CaMV35S:Hsc70-1 transgenic line shows phenotype comparable to Col-0 Arabidopsis thaliana
deletion of Hsc70-1-like negative regulators may lead to more heat-tolerant crops without negative effects on plant growth and development under non-heat stress conditions Arabidopsis thaliana
(ATHSFA2, HSFA2, AT2G26150) complementary DNA introduced into (ATHSF1, ATHSFA1A, HSF1, HSFA1A, AT4G17750) (ATHSF3, ATHSFA1B, HSF3, HSFA1B, AT5G16820) (ATHSFA1D, HSFA1D, AT1G32330) (ATHSFA1E, HSFA1E, AT3G02990) QK mutant background Arabidopsis thaliana
(ATHSFA2, HSFA2, AT2G26150) at high levels regulates (AtHsp70-15, HSP70-15, AT1G79920) Arabidopsis thaliana
SlMPK1 is activated during high-temperature stress Solanum lycopersicum
(ARC2, CH-CPN60A, CPN60A, Cpn60alpha1, CPNA1, SLP, AT2G28000) expression increases in SlMPK1 RNAi lines Solanum lycopersicum
AtHSFB2b is heat shock transcription factor
HSFA1s-preferring genes classified as chaperones and cochaperones Arabidopsis thaliana
heat-induced expression of (ATHSP101, HOT1, HSP101, AT1G74310) is drastically reduced at the transcript level in RNAi lines compared with control line Oryza sativa
Arabidopsis (HSA32, AT4G21320) transcript level remained unchanged after 16 h recovery from heat Arabidopsis thaliana
SlMPK1 has negative role in heat tolerance Solanum lycopersicum
SlMPK1-mediated phosphorylation of SlSPRH1 at Ser-44 regulates antioxidant defense Arabidopsis thaliana
double knockout mutations in (ATHSF1, ATHSFA1A, HSF1, HSFA1A, AT4G17750) (ATHSF3, ATHSFA1B, HSF3, HSFA1B, AT5G16820) caused attenuation of induction of (ATHSP101, HOT1, HSP101, AT1G74310) Arabidopsis thaliana
class B-Hsf mutations (AT-HSFB1, ATHSF4, HSF4, HSFB1, TBF1, AT4G36990) /B2B had no effect on the expression of known heat shock genes Arabidopsis thaliana
(LCR77, PDF1.2, PDF1.2A, AT5G44420) is up-regulated in (AT-HSFB1, ATHSF4, HSF4, HSFB1, TBF1, AT4G36990) plants Arabidopsis thaliana
heat treatment of seedlings clusters together with heat treatment of cell cultures Arabidopsis thaliana
heat shock protein (HSC70-5, HSP70-10, MTHSC70-2, AT5G09590) is protein with altered abundance under heat stress Arabidopsis thaliana
HS plants had 14% smaller seed area than control plants Chenopodium quinoa
HRS treatment resulted in approximately 78% lower estimated seed number than control Chenopodium quinoa
main panicle from HS plants produced 85% fewer seeds than control plants Chenopodium quinoa
homozygous salk_087844 mutant seedlings lack (AtHsp70-2, Hsp70-2, AT5G02490) transcript Arabidopsis thaliana
(HSP70-3, AT3G09440) and (HSP70-5, Hsp70b, AT1G16030) transcript levels are ~1.5- to fourfold higher in hx and (AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) seedlings Arabidopsis thaliana
(AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) may be negatively regulating downstream target genes Arabidopsis thaliana
GUS transcript and enzymatic activity are upregulated by (ATHSFA1D, HSFA1D, AT1G32330) (ATHSFA1E, HSFA1E, AT3G02990) and (ATHSFA2, HSFA2, AT2G26150) Arabidopsis thaliana
G lines ( (AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) overexpression lines) show drastically reduced (ATHSP101, HOT1, HSP101, AT1G74310) protein levels under heat stress conditions Arabidopsis thaliana
(AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) mutant shows increased (AT-HSFA7A, HSFA7A, AT3G51910) transcript levels Arabidopsis thaliana
hx mutant shows increased (AT-HSFA7A, HSFA7A, AT3G51910) transcript levels Arabidopsis thaliana
root and shoot responses to heat may involve different mechanisms
(AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) over-expression resulted in increased heat sensitivity Arabidopsis thaliana
native pro-Hsc70-1 lines (G lines) show differences in Hsp101 expression and phenotype compared to CaMV35S:Hsc70-1 lines and FMV34S:Hsc70-1 lines Arabidopsis thaliana
(AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) protein may be holding HsfA1s in cytoplasmic compartment Arabidopsis thaliana
(AT-HSFB1, ATHSF4, HSF4, HSFB1, TBF1, AT4G36990) (AT-HSFB2B, HSF7, HSFB2B, AT4G11660) double-mutant plants exhibit higher heat tolerance than wild-type Arabidopsis thaliana
shoot heating results in much greater yield losses than heating roots Chenopodium quinoa
increased tertiary panicle yield was only statistically significant in HRS plants Chenopodium quinoa
genetic variation in gas-exchange traits is quantified in response to heat stress Oryza sativa
Rd after heat-stress initiation positively associated with Tcrit Oryza sativa
IR 64 has been demonstrated to be fairly susceptible to moderate temperature increases Oryza sativa
heat resistance is distinct from heat tolerance
heat stress (HS) results in rapid accumulation of reactive oxygen species (ROS) Arabidopsis thaliana
many DEGs according to the temperature difference were identified in ovaries
heat shock impairs nutrient uptake
abscisic acid (ABA) imparts thermotolerance
glutamate dehydrogenase (GDH1, AT5G18170) is protein with altered abundance under heat stress Arabidopsis thaliana
HRS plants had 61% less seed yield than control plants Chenopodium quinoa
Jmax : Vcmax ratio was upregulated significantly under heat stress in all genotypes Oryza sativa
PPI values close to 1 denote strong response Oryza sativa
m1 and Tcrit parameters but not prior to heat stress Oryza sativa
high basal thermotolerance (BT) phenotype of salk_087844 mutant is due to deletion of (AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) gene Arabidopsis thaliana
(AtHsp70-2, Hsp70-2, AT5G02490) transcript levels are ~sixfold higher in (AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) seedlings in 2-day recovery conditions Arabidopsis thaliana
(KNL2, AT5G02520) genomic fragment is complemented in hx line Arabidopsis thaliana
(ATHSFA2, HSFA2, AT2G26150) transcript is strongly induced by HS Arabidopsis thaliana
hx mutant shows higher levels of (ATHSP101, HOT1, HSP101, AT1G74310) protein Arabidopsis thaliana
Rd before initiation of heat stress did not correlate with aforementioned parameters Oryza sativa
(ATHSP101, HOT1, HSP101, AT1G74310) plays critical role in heat tolerance
(ATHSFA2, HSFA2, AT2G26150) mutant showed overly sensitive phenotype and reduced expression of many heat stress-inducible genes Arabidopsis thaliana
(HSP17.6II, AT5G12020) Hsp17.7 and Hsp90-1 transcript levels are mostly higher in hx and (AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) mutants compared with Col-0 Arabidopsis thaliana
(ATHSP101, HOT1, HSP101, AT1G74310) transcript and protein are below detection levels in heat-stressed G lines Arabidopsis thaliana
hx mutant shows increased transcript levels of (ATHS83, AtHsp90-1, ATHSP90.1, HSP81-1, HSP81.1, HSP83, HSP90.1, AT5G52640) Arabidopsis thaliana
hx seedlings show comparable heat stress response to Col-0 seedlings in AT-seedling assay Arabidopsis thaliana
(ATHSFA1D, HSFA1D, AT1G32330) and (ATHSFA2, HSFA2, AT2G26150) together in tobacco system shows lower extent of GUS activity than (ATHSFA1D, HSFA1D, AT1G32330) and (ATHSFA1E, HSFA1E, AT3G02990) alone Nicotiana tabacum
hx mutant shows upregulated (ATHSFA2, HSFA2, AT2G26150) transcript levels Arabidopsis thaliana
temperatures above 32°C causes physiological and phenotypic changes Chenopodium quinoa
salk_087844 mutant possessed basal seedling thermotolerance (BT-seedling) phenotype Arabidopsis thaliana
(ATHSFA2, HSFA2, AT2G26150) does not show physical interaction with (AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) Arabidopsis thaliana
(ATHSFA1D, HSFA1D, AT1G32330) and (ATHSFA1E, HSFA1E, AT3G02990) are good candidates in activating (ATHSP101, HOT1, HSP101, AT1G74310) promoter Nicotiana tabacum
heat stress observed to increase rate of Rd significantly in all genotypes Oryza sativa
iWUE response to heat stress primarily associated with >50% reduction experienced by IR 64 Oryza sativa
rapid methodology for assaying heat tolerance is correlated with independent estimates of heat tolerance in genetically diverse adult rice plants Oryza sativa
PLDα2 and PLDα3 are not required for basal thermotolerance
(ATHSP101, HOT1, HSP101, AT1G74310) transcript and protein levels are comparable in C and Col-0 seedlings Arabidopsis thaliana
(ATHSFA2, HSFA2, AT2G26150) seedlings show stress response-like Col-0 seedlings Arabidopsis thaliana
after heat stress HsfA1d/HsfA1e are set free of Hsc70-1 binding during (ATHSFA1D, HSFA1D, AT1G32330) and (ATHSFA1E, HSFA1E, AT3G02990) Arabidopsis thaliana
brassinosteroids (BRs) promote resistance to high temperature by protein synthesis
PLDα2 is required for heat shock memory
(ATHSFA2, HSFA2, AT2G26150) over-expressing plants show higher heat tolerance Arabidopsis thaliana
(AtHsp70-2, Hsp70-2, AT5G02490) single-mutant shows heat-sensitive phenotype Arabidopsis thaliana
knl2-1 single-mutant shows heat-sensitive phenotype Arabidopsis thaliana
(AtHsp70-2, Hsp70-2, AT5G02490) is close paralog of (AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) Arabidopsis thaliana
(AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) complemented lines show thermosensitive phenotype Arabidopsis thaliana
fruit weight (fw) did not decrease in stress conditions occurred in those lines with positive fw plasticity index Solanum lycopersicum
29 genotypes from the CC panel were not negatively impacted by heat stress for fruit weight Solanum lycopersicum
466 and 130 DEGs in susceptible and tolerant accessions corresponded to a total of 837 unique DEGs Solanum lycopersicum
261 (AtCGS1, AtCYS1, CGS, CGS1, MTO1, AT3G01120) with their polymorphisms could be reliably associated to tomato heat response
(XTH29, AT4G18990) is upregulated in roots in response to heat stress Arabidopsis thaliana
mutants with altered thermotolerance extended understanding of complexity of the heat stress response in plants
heat has effects on hormone signaling
GmWRKY54 transgenic Arabidopsis does not show enhanced tolerance to heat stress Arabidopsis thaliana
localization of OsFKBP20-1b to nuclear speckles was higher under heat stress than under normal conditions Nicotiana benthamiana
root heating had a more pronounced effect than shoot heating on grain yield Triticum aestivum
coefficients extracted from segmented models (Tcrit and m1) compared to variation in heat tolerance parameters from heat-stress experiment on adult plants Oryza sativa
model where HSFs are activated by releasing bound chaperones towards denatured proteins is insufficient to explain HS sensing Arabidopsis thaliana
remaining four cytosolic (HSP70, AT4G16660) genes are heat-induced Arabidopsis thaliana
hx mutant seedlings show higher transcript levels of (AtHsp70-2, Hsp70-2, AT5G02490) − (HSP70-5, Hsp70b, AT1G16030) genes under heat stress and 2-day recovery conditions Arabidopsis thaliana
endoplasmic reticulum localized (FKBP15-1, AT3G25220) and (FKBP15-2, AT5G48580) respond differentially to heat stress Oryza sativa L.
sandbox system allows for independent temperature control of roots and shoots
rapid accumulation of reactive oxygen species (ROS) in the chloroplast may trigger parallel pathway of HSFA1 activation Arabidopsis thaliana
(ATHSF1, ATHSFA1A, HSF1, HSFA1A, AT4G17750) expression is increased in (AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) and hx mutant plants Arabidopsis thaliana
(ATHSF1, ATHSFA1A, HSF1, HSFA1A, AT4G17750) (ATHSFA1D, HSFA1D, AT1G32330) (ATHSF3, ATHSFA1B, HSF3, HSFA1B, AT5G16820) (AT-HSFA3, FGT3, HSFA3, AT5G03720) HsfA4a, (AT-HSFA5, HSFA5, AT4G13980) and (AT-HSFA7A, HSFA7A, AT3G51910) expression is higher in hx and (AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) mutants compared with WT plants in recovery phase Arabidopsis thaliana
(AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) physically interacts with (ATHSFA1E, HSFA1E, AT3G02990) Arabidopsis thaliana
flowering date (flw) and leaf length (leaf) had the strongest heat stress impact at the population level (−40% and −45% respectively) Solanum lycopersicum
processes and pathways involved in heat stress response were already known to be important in heat stress response Solanum lycopersicum
Solyc03g117590 gene showed a strong increase in expression in most of the genotypes during heat stress Solanum lycopersicum
female organs are also impacted by heat independently of pollen quality heat stress
misfolding and aggregation of proteins causes heat-induced proteotoxic stress
genotypic differences in germinating pollen on stigma are associated with spikelet fertility under high temperatures Oryza sativa
thirteen proteins were differentially expressed in response to temperature Oryza sativa
RCAII showed complex expression profile in Oryza meridionalis Oryza meridionalis
concentration of thiamine in leaves of Oryza meridionalis fell significantly during heat stress Oryza meridionalis
EGTA treatment abolishes protection against cellular leakage Glycine max
stress-inducible or constitutive ectopic expression of maize ZmDREB2A resulted in improved tolerance to heat stress Arabidopsis thaliana
Sobic.004g228900 encodes (HSP23.5, AT5G51440) Sorghum
flowering stage is most susceptible developmental stage to heat stress
average yield of all the secondary panicles from each HS plant was 85% lower than in control plants Chenopodium quinoa
lipid composition changes rapidly after heat shock (HS)
hx seedlings lack (AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) transcript Arabidopsis thaliana
(AtHsp70-2, Hsp70-2, AT5G02490) transcript levels are at undetectable levels in hx mutant Arabidopsis thaliana
(ATHSP101, HOT1, HSP101, AT1G74310) expression is extremely crucial for survival of Arabidopsis plants against heat stress conditions Arabidopsis thaliana
free state of (ATHSFA1D, HSFA1D, AT1G32330) (ATHSFA1E, HSFA1E, AT3G02990) activates downstream (ATHSFA2, HSFA2, AT2G26150) Arabidopsis thaliana
increased (ATHSP101, HOT1, HSP101, AT1G74310) transcripts lead to enhanced defence to heat stress conditions Arabidopsis thaliana
main panicles from HS plants yielded 87% less than control plants Chenopodium quinoa
percentage reduction in ɸPSII negatively correlated with Tcrit Oryza sativa
m1 and Tcrit parameters were also significantly associated in the expected direction with Rd during heat stress Oryza sativa
HEAT SHOCK FACTOR A1 (HSFA1) isoforms A1A, A1B, A1D, and A1E are master regulators of the immediate HS responses Arabidopsis thaliana
(AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) over-expressing Col-0 transgenic plants did not accumulate (ATHSP101, HOT1, HSP101, AT1G74310) transcript/protein under heat stress (HS) and recovery time points Arabidopsis thaliana
(AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) is suggested to play a role as negative regulator upstream to (ATHSFA1D, HSFA1D, AT1G32330) (ATHSFA2, HSFA2, AT2G26150) cascading Arabidopsis thaliana
(AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) is present in detectable levels under non-HS conditions Arabidopsis thaliana
(AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) mutant shows increased transcript levels of (ATHS83, AtHsp90-1, ATHSP90.1, HSP81-1, HSP81.1, HSP83, HSP90.1, AT5G52640) Arabidopsis thaliana
use of natural promoter in driving chaperone genes in trans-hosts reflects effectiveness in driving chaperone gene expression Arabidopsis thaliana
(AtHsp70-2, Hsp70-2, AT5G02490) and (ATHSP70, HSC70-4, HSP70, HSP70-4, AT3G12580) transcripts show most predominant increase in 2-day recovery condition Arabidopsis thaliana
heat is a major limitation to quinoa cultivation expansion Chenopodium quinoa
M2 did not observe any association between (ATNYE1, NYE1, SGR, SGR1, AT4G22920) or the percentage reduction in ɸPSII Oryza sativa
(ATHSP101, HOT1, HSP101, AT1G74310) was repressed in (AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) over-expressing plants after post-HS conditions Arabidopsis thaliana
hx mutant shows higher levels of (ATHSP101, HOT1, HSP101, AT1G74310) transcript Arabidopsis thaliana
heat treatment triggers avoidance strategy of prioritizing growth over development Chenopodium quinoa
HRS plants produced more than double the number of tertiary panicles than control plants Chenopodium quinoa
lines with improved heat tolerance have reduced heat resistance
plant Hsp100 genes complement thermotolerance defects in yeast hsp104 mutant strain
(AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) shows binding with (ATHSFA1E, HSFA1E, AT3G02990) Arabidopsis thaliana
under non-heat stress conditions Hsc70-1 keeps HsfA1d and HsfA1e in bound/quiescent state during (ATHSFA1D, HSFA1D, AT1G32330) and (ATHSFA1E, HSFA1E, AT3G02990) Arabidopsis thaliana
Ca2+-dependent phosphorylation cascade results in HEAT SHOCK FACTOR A1 (HsfA1) activation Arabidopsis thaliana
PLDα3 is required for heat shock memory
lipid composition changes counteract increased membrane fluidity upon temperature increase
(ATHSF1, ATHSFA1A, HSF1, HSFA1A, AT4G17750) and (ATHSF3, ATHSFA1B, HSF3, HSFA1B, AT5G16820) binding with (ATHSFA2, HSFA2, AT2G26150) regulates downstream heat stress cascade Arabidopsis thaliana
(AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) shows clear physical binding with (ATHSFA1D, HSFA1D, AT1G32330) and (ATHSFA1E, HSFA1E, AT3G02990) Arabidopsis thaliana
HS tolerance is a complex mechanism that must be interpreted in a trait- and genotype-dependent manner
Solyc06g007970 expression strongly increased in HS conditions and was much more expressed in tolerant genotypes
RdDM pathway is involved in plant response to heat stress
pollen viability is compromised by high temperatures Triticum aestivum; Oryza sativa; Sorghum bicolor
chromatin structural changes are more pronounced in heat-resilient indica variety Oryza sativa
Low H2K27me3 marks (ATHSP22.0, HSP22, AT4G10250)
meiocyte perceives heat stress Arabidopsis thaliana
root heating did not show substantial effects on secondary panicle yield Chenopodium quinoa
average tertiary panicle yield from HS plants was fourfold higher than that of the control Chenopodium quinoa
intrinsic water-use efficiency (iWUE) demonstrated significant response to heat stress Oryza sativa
non-modelled metrics of photosynthetic assimilation of CO2 demonstrated lowest phenotypic plasticity for all genotypes Oryza sativa
overexpression of (ATCBF3, CBF3, DREB1A, AT4G25480) enhanced plant heat tolerance Arabidopsis thaliana
mechanisms underlying initial sensing of HS and activation of HS response remain poorly understood Arabidopsis thaliana
(ATHSFA2, HSFA2, AT2G26150) expression is increased in (AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) and hx mutant plants Arabidopsis thaliana
(ATHSFA1D, HSFA1D, AT1G32330) (ATHSFA1E, HSFA1E, AT3G02990) (ATHSFA2, HSFA2, AT2G26150) proteins positively regulate (ATHSP101, HOT1, HSP101, AT1G74310) promoter Arabidopsis thaliana
HSP70s show co-immunoprecipitation with (ATHSFA1D, HSFA1D, AT1G32330) Arabidopsis thaliana
69 plasticity QTLs (pQTLs) were involved in tomato heat response for 11 traits Solanum lycopersicum
combined transcriptome results were used to propose candidate genes for HS response QTLs Solanum lycopersicum
seven other HSPs or chaperone proteins previously identified as DEGs in pollen or anthers were also located in the pQTLs
overexpression of (BZR1, AT1G75080) improves thermotolerance Solanum lycopersicum
(AT-HSFA7A, HSFA7A, AT3G51910) is induced by priming and triggering treatments at the SAM Arabidopsis thaliana
quinoa accession QQ74 undergoes physiological changes during and after heat treatment Chenopodium quinoa
temperatures above 32°C impairs yield Chenopodium quinoa
Rd after heat-stress initiation negatively associated with M1 Oryza sativa
(AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) genomic fragment is complemented in hx line Arabidopsis thaliana
(ATHSFA1D, HSFA1D, AT1G32330) and (ATHSFA1E, HSFA1E, AT3G02990) and (ATHSFA2, HSFA2, AT2G26150) together in tobacco system shows lower extent of GUS activity than (ATHSFA1D, HSFA1D, AT1G32330) and (ATHSFA1E, HSFA1E, AT3G02990) alone Nicotiana tabacum
(AT-HSFA7B, HSFA7B, AT3G63350) is induced by priming and triggering treatments at the SAM Arabidopsis thaliana
heat stress causes changes in large-scale chromatin interactions Arabidopsis thaliana
(ATHSFA2, HSFA2, AT2G26150) overexpression triggers stress response Arabidopsis thaliana
independent role of (ATHSFA2, HSFA2, AT2G26150) can only be fulfilled after prolonged or reexposure to stress conditions or ectopic overexpression Arabidopsis thaliana
new type of thermotolerance constitutes thermotolerance diversity orchestrated by master regulators of heat stress response Arabidopsis thaliana
long-term acquired thermotolerance (LAT) assay is valuable for exploring thermotolerance diversity in rice Oryza sativa
SlMPK1 overexpression results in decreased heat tolerance Solanum lycopersicum
AtCSP41B overexpression exhibited heat stress tolerance Arabidopsis thaliana
(LCR77, PDF1.2, PDF1.2A, AT5G44420) promoter contains imperfect HSE (nGAAn/nATCn) Arabidopsis thaliana
plants treated with combined heat stress and methyl jasmonate (MeJ) were kept in growth chamber at 37°C
(ATMYB30, MYB30, AT3G28910) is involved in heat stress response Arabidopsis thaliana
2 months delay in the sowing date led to plant growth exposed to the hottest months in heat stress (HS) condition Solanum lycopersicum
fruit color (col_a) and pH were positively impacted by heat stress in both populations Solanum lycopersicum
yield plasticity was correlated to the plasticity of its components fruit number (nfr), fruit set (fset) and fruit weight (fw) Solanum lycopersicum
almost 9,500 significantly differentially expressed genes had more than 75% identified in both control and heat stress conditions Solanum lycopersicum
837 DEGs comprised 33% specific to the contrast using all six genotypes together Solanum lycopersicum
tomato reproduction is hampered when temperature exceeds critical value of 30°C
ovaries may play an important role in HS response and fruit development
RESTRICTED TO NUCLEOLUS 1 (REN1) is member of heat shock transcription factor family Arabidopsis thaliana
INTACT-ATAC-seq, Histone-, RNAPII- and TF-ChIP-seq, Nuclear RNA-seq, RNA-seq, TRAP-seq identify temporal discordance between transcription and mRNA accumulation of heat-responsive and other genes Arabidopsis thaliana
responsiveness of miR156 to heat stress is conserved in plants including Arabidopsis, Brassica rapa and wheat Arabidopsis thaliana; Brassica rapa; Triticum aestivum
(AT-HSFA3, FGT3, HSFA3, AT5G03720) is induced by priming and triggering treatments at the SAM Arabidopsis thaliana
(AT-HSFB2A, HSFB2A, AT5G62020) is induced by priming and triggering treatments at the SAM Arabidopsis thaliana
Low H3K27me3, inhibition of siRNA marks hTTP
aconitate hydratase (ACO2, AT4G26970) is protein with altered abundance under heat stress Arabidopsis thaliana
temporal dynamics of HS responses are highly relevant
plants have evolved complex molecular mechanisms in fight against heat stress
(AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) and (ATHSFA1D, HSFA1D, AT1G32330) double-mutant shows heat stress-sensitive phenotype like Col-0 in basal thermotolerance seedling assay Arabidopsis thaliana
(ATSIZ1, SIZ1, AT5G60410) is the main driver of sumoylation during heat shock Arabidopsis thaliana
heat stress activates downstream transcriptional responses
Low H2K27me3 marks (HSP17.6C, AT1G53540)
Four unknown proteins were constitutively expressed at a high level in N22 compared to Moroberekan Oryza sativa
heat stress at 45 °C does not affect leaf growth of Oryza meridionalis Oryza meridionalis
transketolase became more abundant over 24 h period in heat stress Oryza sativa
Hsp17.4-CII is responsible for recruitment of (ATHSFA2, HSFA2, AT2G26150) into heat stress granules Solanum lycopersicum
(ATHSFA2, HSFA2, AT2G26150) is markedly activated in young anthers in response to heat stress (hs) regimes Solanum lycopersicum
transgenic plants with (AtSAG12, SAG12, AT5G45890) promoter were exposed to 35 °C heat stress Agrostis stolonifera
HRS plants produced an average of 79% less yield from secondary panicles than in control plants Chenopodium quinoa
IR 64 and BRRI 28 showed only minor increases in Jmax Oryza sativa
Tcrit demonstrated negative correlation with (ATNYE1, NYE1, SGR, SGR1, AT4G22920) Oryza sativa
HEAT SHOCK FACTOR A1 (HSFA1) isoforms A1A, A1B, A1D, and A1E induce the expression of HEAT SHOCK FACTOR A2 (ATHSFA2, HSFA2, AT2G26150) Arabidopsis thaliana
(ATHSFA1D, HSFA1D, AT1G32330) transcript were at higher levels in (AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) mutant compared with wild-type Arabidopsis thaliana
flowering date (flw) of the 5th truss occurred 9 and 16 days earlier on average under heat stress in the MAGIC and CC populations, respectively Solanum lycopersicum
susceptibility of male reproductive traits is mostly due to
adaptive behavior of these genotypes seems to be related to their capacity to reallocate resources from growth to fruit development by increasing their yield capacity
HEAT INTOLERANT 4 (HIT4, AT5G10010) is involved in decondensation of chromocenters during extended periods of heat stress Arabidopsis thaliana
stabilized (ESD6, HOS1, AT2G39810) increases thermotolerance Arabidopsis thaliana
sudden increase in ambient temperature increases plasma membrane (PM) permeability
heat treatment sometimes confers lethal damage
chromatin remodeling complex that includes (EMB1135, FGT1, AT1G79350) (ATBRM, BRM, CHA2, CHR2, FFO3, AT2G46020) (CHR11, AT3G06400) and (CHR17, AT5G18620) targets transcription start site (TSS) of memory genes
heat stress raises nadir of heat-responsive genes but not their peak
ethylene imparts thermotolerance
69 genotypes (13 and 19% of the CC and MAGIC populations, respectively) were considered as heat-tolerant Solanum lycopersicum
heat stress appears to involve calcium signaling
sensitization to increases in heat triggers priming to protect plants from subsequent stresses
(FWA, HDG6, AT4G25530) gene activation is also observed in wild-type plants under heat stress Arabidopsis thaliana
High H3K4me2/3 marks (APX1B, APX2, AtAPX2, AT3G09640)
distinct band of Rubisco activase was not evident in lanes corresponding to control plants Arabidopsis thaliana
function of cpn60β in chloroplasts during heat shock would be analogous to function in other organisms
(ATHSFA2, HSFA2, AT2G26150) seemed to be activated at later time period after heat shock later time period after heat shock Solanum lycopersicum
25 protein spots (spots 1–5, 7, 8, 15, 18, 21, 22, 25–27, 29, 32, 33, 36–42, and 44) were decreased in both A. scabra and A. stolonifera under heat stress Agrostis scabra; Agrostis stolonifera
13 protein spots (spots 9, 10, 19, 20, 23, 28, 30, 31, 34, 35, 43, 46, and 47) were decreased only in A. scabra under heat stress Agrostis scabra
cessation of mitochondrial movement is one of alterations in mitochondrial dynamics in (ATHSFA2, HSFA2, AT2G26150) mutant protoplasts Arabidopsis thaliana
(ATHSFA2, HSFA2, AT2G26150) knockout mutant displays reduced basal thermotolerance Arabidopsis thaliana
25% of the MAGIC genotypes had a positive fruit weight (fw) plasticity index Solanum lycopersicum
heat-tolerant genotypes showed negative plasticity index for leaf (−33%) and diameter (−16%) Solanum lycopersicum
HS condition reduced fw by 25% in the CC population
direction of the effect of HS was consistent between populations
peptide with Met-to-AHA modification was detected in heat shock samples only Arabidopsis thaliana
chromatin around memory genes is poor in histone H3K4 methylation before heat stress
free HSFA1 activates heat stress-responsive genes
(ATBZIP60, BZIP60, AT1G42990) promotes expression of key HSF in maize heat stress response Zea mays
(NDL1, AT5G56750) mutants carry transcriptional signatures of enhanced stress response when grown in warm temperature Zea mays
heat-stress responsive ONSEN displayed an insertion site preference for exonic regions enriched for H3K27me3, (H2A.Z, HTA11, AT3G54560) and (H3.1, HTR1, AT5G65360) Arabidopsis thaliana
HR plants produced approximately 43% more tertiary panicles than control plants Chenopodium quinoa
higher yield of tertiary panicles observed in HRS plants resulted from median 12% higher individual seed weight than in control plants Chenopodium quinoa
pollen viability has been reported to be affected by heat in quinoa Chenopodium quinoa
low phenotypic plasticity for A400 and Amax suggests relatively reduced response to temperature of instantaneous rates of photosynthesis Oryza sativa
(APD9, FGT2, AT5G66080) does not affect basal thermotolerance
(ATHSF1, ATHSFA1A, HSF1, HSFA1A, AT4G17750) and (ATHSF3, ATHSFA1B, HSF3, HSFA1B, AT5G16820) physically bind with (ATHSFA2, HSFA2, AT2G26150) Arabidopsis thaliana
dissociation of (HSP70, AT4G16660) from HSFs has been shown in response to heat stress (HS)
(AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) single-mutant shows lower phenotype intensity than hx line Arabidopsis thaliana
increased intensity of transcript expression of selected Hsps leads to development of basal thermotolerance (BT) Arabidopsis thaliana
(AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) represses downstream heat stress-responsive genes expression via (ATHSFA1D, HSFA1D, AT1G32330) (ATHSFA1E, HSFA1E, AT3G02990) and (ATHSFA2, HSFA2, AT2G26150) Arabidopsis thaliana
heat shock represses hair-cell–specific genes in hair cells Arabidopsis thaliana
circadian control of the heat stress response translatome observed that only 70% of cycling heat-responsive transcripts were also responsive at translatome level
acquired thermotolerance is plant thermotolerance
ABA enables plants to enhance thermal acclimation under various stresses
promoter–enhancer interactions enable expression of genes involved in the HS response Solanum lycopersicum
transcriptome changes in the ovary of six genotypes with contrasted responses to HS were studied heat stress response in reproductive tissue Solanum lycopersicum
spring maize season in South Asia is particularly prone to severe heat stress during flowering/early grain filling stages
HSFA1 proteins are retained in cytosol
HEAT SHOCK TRANSCRIPTION FACTOR A2 (ATHSFA2, HSFA2, AT2G26150) protects plants against organelle dysfunction Arabidopsis thaliana
heated peach shows induction of small heat shock proteins (smHSPs) of 17–18 kDa
heated peach shows induction of (HSP70, AT4G16660) (heat shock protein 70)
effect of salicylic acid in alleviating chilling injury (CI) of peach has been attributed, at least in part, to induction of heat shock proteins (HSPs) Prunus persica
heat stress affects Rubisco activase (RCA, AT2G39730) expression Triticum aestivum; Zea mays; Arabidopsis thaliana
root hair-less plants exhibited reduced capacity for heat adaptation Arabidopsis thaliana
decrease in translation efficiency may explain differences in magnitude of response to heat stress between transcriptome and translatome Arabidopsis thaliana
four candidate genes among the most DEGs in control versus heat stress conditions were selected for illustration Solanum lycopersicum
six (AtCGS1, AtCYS1, CGS, CGS1, MTO1, AT3G01120) (Solyc02g088610, Solyc03g007890, Solyc03g113930, Solyc03g115230, Solyc11g071830, Solyc11g066100) have been previously identified as DEGs under heat conditions in ovaries
acquired thermotolerance depends on OsHSA32 (HEAT STRESS-ASSOCIATED 32-KD PROTEIN) Oryza sativa
heat stress promotes the production of eccDNA derived from the heat-stress responsive ONSEN retrotransposon Arabidopsis thaliana
two large experimental populations revealed large diversity in response to HS
induction of most heat-up-regulated genes occurred when heat stress occurred outside of gene's peak expression
rapid transcriptional changes include induction of cochaperones
PHLOEM INTERCALATED WITH XYLEM-LIKE 1 (ATPXL1, PXL1, AT1G08590) overexpression results in enhanced heat tolerance
(FLORE, AT1G69572) transcripts show increased accumulation at transcriptome and translatome levels in response to heat stress Arabidopsis thaliana
heat-responsive transcriptome shows time-of-day-dependent significance under extreme heat stress specific time point Arabidopsis thaliana
heat shock proteins are preferentially translated during heat stress response Arabidopsis thaliana
heat stress causes changes in local chromatin interactions Arabidopsis thaliana
nucleus-localized (ATFKBP62, FKBP62, ROF1, AT3G25230) and (ATFKBP65, FKBP65, ROF2, AT5G48570) proteins function antagonistically during adaptation to high temperature Oryza sativa L.
quinoa does poorly in high temperature climates Chenopodium quinoa
root heating did not have substantial effect on seed yield Chenopodium quinoa
greatest plasticity of Rd to heat stress indicating role for respiration in heat tolerance Oryza sativa
heat tolerance is constrained by space for growing plants and facilities and equipment for experimentally increasing temperature
(AT-HSFA7A, HSFA7A, AT3G51910) transcript is strongly induced by HS Arabidopsis thaliana
(AT-HSC70-1, AtHsp70-1, HSC70, HSC70-1, HSP70-1, AT5G02500) mutant shows increased transcript levels of Hsp17.7 Arabidopsis thaliana
(ATHSFA2, HSFA2, AT2G26150) and Hsp17-CII are further induced under prolonged heat stress conditions Solanum lycopersicum
(ATHSFA2, HSFA2, AT2G26150) mRNA levels transiently decline quickly after 2 h heat stress Solanum lycopersicum
GAPDH (Spots #264 and 267) expression levels were not changed in NT or S41 under heat stress
HS-increased intracellular Ca2+ level serves as cellular second messenger through Ca2+-CaM heat stress signal transduction pathway
L-glutamine did not affect level of heat resistance Arabidopsis thaliana
heat response was studied in both populations (MAGIC and CC) Solanum lycopersicum
nfr-nflw correlation was lower in heat stress (HS) condition compared with the control condition Solanum lycopersicum
fruit weight (fw) decreased on average in the MAGIC population under heat stress Solanum lycopersicum
837 DEGs in control versus HS conditions found only eight HSPs or chaperone proteins and two HSFs
multiple NPCs are involved in responses to high temperature
heat shock treatment at 37°C for 30 or 60 min increases expression of (SEC31A, AT1G18830) Arabidopsis thaliana
heat shock impairs protein function
copia-like retrotransposon ONSEN can confer heat-responsiveness to genes near new insertion sites Arabidopsis thaliana
heat-responsive transcriptome shows time-of-day-dependent significance under moderate heat stress specific time point Arabidopsis thaliana
heat shock impairs hormone metabolism
Ca 2+ treatment could improve cell survival Arabidopsis thaliana
Ba2+ supplementation with EGTA significantly rescues seedling survival Glycine max
Ca2+ treatment counteracts EGTA effect on fluorescence signals Glycine max
apoplastic Ca2+ homeostasis participates in development of thermotolerance Glycine max
elevated temperatures can lead to misfolding and aggregation of proteins
serine protease, ribosomal, and dirigent proteins do not change significantly in Moroberekan Oryza sativa
(HSP70, AT4G16660) family is directly correlated with thermotolerance in plants