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cold acclimation

13623 relationships annotated with this phrase. Showing first 500 of 13623.
Source entity Relationship Target entity Species
cold hardiness enables trees to tolerate adverse growing conditions for photosynthesis
means of site level parameters different from PFT-level parameters
plants in climates with low spring temperatures and high spring temperature variability deploy higher leaf freezing resistance
sucrose (Suc) accumulation correlates with cold stress tolerance Arabidopsis thaliana
cold-acclimation effects on light use efficiency (LUE) considers delayed effects of minimum temperatures
many trees, especially evergreens maintain cold hardiness
successful cold acclimation of Col-0 to 10°C leads to flowering Arabidopsis thaliana
REIL proteins are required for rapid accumulation of cytosolic ribosome subunits after cold shift Arabidopsis thaliana
(ATMSRB3, MSRB3, AT4G04800) reveals a critical role of MSRs in process of cold acclimation in plants Arabidopsis thaliana
cold acclimation results in global reprogramming of metabolism Arabidopsis thaliana
reil1-1 reil2-1 remains physiologically capable of wild-type cold acclimation responses at transcriptomic level Arabidopsis thaliana
cold stress induced cell wall biogenesis Triticum aestivum
relationships between fitted parameters and other environmental variables found no consistent patterns
noncoding polymorphism in the FLOWERING LOCUS C (AGL25, FLC, FLF, RSB6, AT5G10140) promoter enables adaptation to cold winter temperatures Arabidopsis thaliana
relationship between parameters and T min in different PFTs not significant
largest (GPP, VTC4, AT3G02870) reductions (lowest mean f T) simulated for sites with lowest winter-mean T min
remodeling of translational apparatus is confirmed with expected delay between gene expression maximum and subsequent protein accumulation Arabidopsis thaliana
REIL either directly or indirectly modifies temperature perception by suppressing premature low-temperature acclimation responses Arabidopsis thaliana
delayed shoot apex development is linked to induction of cold tolerance Triticum aestivum
Wcor410 is responsive to ABA
smaller fitted parameter values for τ, X 0, and S max in ENF indicates faster acclimation rate, lower temperature threshold for initiation of acclimation, and lower temperature upper limit for inhibiting photosynthesis
Col-0 shows mostly nonresponsive chloroplast ribosomal protein genes Arabidopsis thaliana
INDUCER OF CBF EXPRESSION (ICE)-C-REPEAT-BINDING FACTORS (CBF)-COLD REGULATED (COR) transcriptional cascade is only well-characterized cold acclimation pathway
47 CORs (DHNS, ECHID, AT1G60550) emphasized important role in cold tolerance during autumn cold acclimation Triticum aestivum
active translation after cold shift is required for cold acclimation Arabidopsis thaliana
reduced polysome abundance agrees with growth arrest Arabidopsis thaliana
activation of DREB/CBF regulon was highly similar to wild type Arabidopsis thaliana
cold-responsive genes containing the C-repeat/dehydration-responsive motif and ABA response cis-elements are responsive to ABA
reil1-1 reil2-1 mutant acquired freezing tolerance Arabidopsis thaliana
cold acclimation pathways is conserved among different plant species
spring Norstar (SN) is almost as cold tolerant as winter Norstar (NO) under short days that delay plant development Triticum aestivum
nonacclimated reil1-1 reil2-1 shows preference for cold acclimation factors (ATCBF1, CBF1, DREB1B, AT4G25490) , (ATCBF2, CBF2, DREB1C, FTQ4, AT4G25470) , and (ATCBF3, CBF3, DREB1A, AT4G25480) over heat and osmotic components (DREB2, DREB2A, AT5G05410) and (DREB2, DREB2B, AT3G11020) Arabidopsis thaliana
(CHY1, AT5G65940) mutant plants compared to wild-type Arabidopsis thaliana
REILs clearly play role in cold-acclimating mature leaves Arabidopsis thaliana
cold acclimation occurs in response to period of exposure to low temperatures prior to onset of −0°C
soil temperature increase after September 22 resulted in greater cold tolerance (LT 50)
cold stress induced various signaling pathways from temperature, hormones, and oxygen-containing molecules Triticum aestivum
cold responses showed genes in signaling receptor kinases and RNA regulation of transcription were up-regulated (C3–C7) Triticum aestivum
HvCBF2 in barley and TaCBF14, TaCBF15, and TaCBF16 in wheat are expressed at higher levels in winter genotype than in spring genotype Hordeum vulgare; Triticum aestivum
investigations of reil1-1 reil2-1 show surprisingly limited effects largely not confounded by cell death during cold acclimation Arabidopsis thaliana
molecular basis of cold acclimation and acquired freezing tolerance has been studied extensively in Arabidopsis thaliana Arabidopsis thaliana
(REM39, VRN1, AT3G18990) directly regulates CBF genes
delaying the VRT confers greater cold tolerance in wheat Triticum aestivum
cold acclimation helps plants adapt to low temperature
evergreen species leaves lack growth and interference of endodormancy transition during cold acclimation (CA)
results from this study provide comprehensive recognition of differences between field and artificial cold acclimation (CA)
Artificial cold acclimation (A-CA) treatment increases leaf freezing tolerance (LFT)
high light stress in overwintering leaves could positively increase freezing tolerance (FT)
(VIN3, AT5G57380) is induced within 1 day of experiencing cold temperatures
Arabidopsis (FZF, REIL2, STCH4, AT2G24500) gene expression is activated after shift to low temperatures Arabidopsis thaliana
cold-activated (ATICE1, ICE1, SCREAM, SCRM, AT3G26744) genes rapidly up-regulate expression of CBF genes Triticum aestivum
47 CORs (DHNS, ECHID, AT1G60550) but only one (ATICE1, ICE1, SCREAM, SCRM, AT3G26744) gene were up-regulated Triticum aestivum
cold-induced expression of VRN2L in leaves is reminiscent to that of C-REPEAT BINDING FACTOR genes Brachypodium spp.
results indicate that REIL function also may be important for young leaf or root tissue that grows and develops in cold Arabidopsis thaliana
rapid increase in histone H3 acetylation at region VIN3.1 may be required for (VIN3, AT5G57380) expression in response to short-term cold treatment
endogenous phytohormone abscisic acid (ABA) levels increase in Arabidopsis thaliana during low-temperature exposure Arabidopsis thaliana
clusters C8 to C10 was down-regulated as autumn progressed to winter Triticum aestivum
differential histone modifications mediate cold sensing
(MEX1, RCP1, AT5G17520) is a modulator of cold acclimation Arabidopsis thaliana
cold acclimation of Col-0 to 10°C increases (FZF, REIL2, STCH4, AT2G24500) mRNA Arabidopsis thaliana
cold acclimation enables plants to acquire freezing tolerance
thousands of genes in wheat were affected during cold treatment in controlled environments Triticum aestivum
most biological processes were affected but numbers of genes in each pathway varied according to types of gene expression Triticum aestivum
cold responses showed protein synthesis, protein degradation, and amino acid metabolism were down-regulated (C8–C10) Triticum aestivum
MA genetic background is more sensitive to cold stress relative to that of NO Triticum aestivum
wheat has evolved cold tolerance strategies Triticum aestivum
C-REPEAT/DRE BINDING FACTOR1/DEHYDRATION-RESPONSIVE ELEMENT BINDING PROTEIN1B ( (ATCBF1, CBF1, DREB1B, AT4G25490) , .1), (ATCBF2, CBF2, DREB1C, FTQ4, AT4G25470) ( .1), and (ATCBF3, CBF3, DREB1A, AT4G25480) ( .1) were part of set of DEGs that belonged to cold acclimation and response to cold GO terms Arabidopsis thaliana
plants lacking (ATMSRB3, MSRB3, AT4G04800) lose their ability to tolerate freezing temperatures following a pre-treatment to cold conditions Arabidopsis thaliana
subunit composition changes dynamically relative abundance of 60S (AtGGPPS11, AtGGPS11, AtLSU, GGPPS11, GGPS1, IDS11, LSU, AT4G36810) Arabidopsis thaliana
strong and specific activation of cytosolic ribosomal protein gene expression supports conclusion that 10°C acclimation of Col-0 involves activation of cytosolic ribosome biogenesis Arabidopsis thaliana
cold stress induced membrane lipid remolding Triticum aestivum
ABA-dependent pathway contains 14 DEGs Triticum aestivum
CBF genes subsequently initiate transcription of various COR genes Triticum aestivum
plant acclimation to cold conditions involves alterations in lipid composition
(CHY1, AT5G65940) mutant plants are less tolerant to freezing stress Arabidopsis thaliana
PRPL33, (EMB3113, PRPS5, RPS5, SCA1, uS5c, AT2G33800) and RDB1 mutants are associated with impaired acclimation to cold Arabidopsis thaliana
NO genetic background gave SN a cold tolerance advantage over WM Triticum aestivum
expression of CBFs displayed diurnal pattern Triticum aestivum
cold treatments in Arabidopsis seedlings down-regulate GA20ox transcript levels Arabidopsis thaliana
(ATICE1, ICE1, SCREAM, SCRM, AT3G26744) mutation significantly reduces chilling tolerance
(VIN3, AT5G57380) induction occurs via distinct transcriptional pathways Arabidopsis thaliana
previous microarray studies identified 16 CBFs and three ICE1-encoding genes as cold-regulated genes Triticum aestivum
ectopic overexpression of (ATCBF3, CBF3, DREB1A, AT4G25480) results in increased freezing tolerance Arabidopsis thaliana
CBF regulon has critical role in cold acclimation
80 genes that were up-regulated and 41 down-regulated genes in cold-responsive pathways were identified in cold-responsive pathways Triticum aestivum
cold treatments in Arabidopsis seedlings up-regulate GA2ox transcript levels Arabidopsis thaliana
nonacclimated reil1-1 reil2-1 mimics metabolic phenotype of 10°C cold-acclimating Col-0 Arabidopsis thaliana
cold tolerance strategies optimize autumn seedling growth and development Triticum aestivum
CBF pathway contains 47 genes up-regulated and 6 down-regulated Triticum aestivum
Col-0 wild-type plants resumed growth and development after lag phase of approximately 1 or 2 weeks upon temperature shift from 20°C to 10°C or 4°C regime Arabidopsis thaliana
cytosolic translational apparatus is remodeled at level of translation initiation factors Arabidopsis thaliana
accumulation of compatible osmolytes includes proline
plants transferred to 4°C growth cabinet at 16-h day length with 90 μE m−2 s−1 for 14 d Arabidopsis thaliana
cold-acclimation responses includes activation of DREB/CBF regulon Arabidopsis thaliana
translation elongation factor2-like protein mutants demonstrate requirement of active translation after cold shift Arabidopsis thaliana
wheat winter survival involves cold acclimation Triticum aestivum
Gene Ontology (GO) enrichment analysis revealed that various biological processes were affected during cold acclimation Triticum aestivum
up-regulated genes (clusters C3–C7) were highly enriched in cell wall organization or biogenesis, lipid metabolism, response to stimulus and hormones, and response to oxygen-containing compound Triticum aestivum
total magnitude of metabolic changes was not related to increase in freezing tolerance of different Arabidopsis accessions during acclimation Arabidopsis thaliana
acidic PEPC2 forms increased in abundance upon cold treatment
Ca2+, ABA and JA signaling transduction promotes plant growth cessation and cold acclimation (CA)
nine genes encoding (ATCBF3, CBF3, DREB1A, AT4G25480) COLD REGULATED314 THYLAKOID MEMBRANE 2 (COR314-TM2, COR413IM2, AT1G29390) COLD-REGULATED413 PLASMA MEMBRANE PROTEIN1, COLD SHOCK120 (CS120), three CS66s, cold acclimation protein WCOR410b, and LOW EXPRESSION OF OSMOTICALLY RESPONSIVE GENES2 (ENO2, LOS2, AT2G36530) were highly expressed in NO and SN Triticum aestivum
ICE-CBF-COR pathway has been suggested to be functionally conserved in different plant species
SAGA-like transcriptional co-activator complex regulates expression of cold-regulated (COR) genes Arabidopsis thaliana
ABA increase could induce tissues to cease growing and enter cold acclimation (CA) status
Dehydroascorbic acid dimer contributes to the prediction of freezing tolerance Arabidopsis thaliana
plants grown under short-day conditions were acclimated at 4°C for 1 week Arabidopsis thaliana
transcriptional and metabolic reprogramming increases freezing tolerance
leaves with higher freezing tolerance (FT) had DEG encoding (HY5, TED 5, AT5G11260) and its expression increased ~3.4-fold (HY5, TED 5, AT5G11260) expression
fructose contributes to the prediction of freezing tolerance Arabidopsis thaliana
C-repeat/DRE binding factors (CBFs) are induced in (ADA2B, PRZ1, AT4G16420) mutants
(ATCBF1, CBF1, DREB1B, AT4G25490) might stimulate transcription through recruitment of SAGA-like complexes
non-freezing cold temperature exposure activates metabolic reprogramming
ABA-deficient mutant of Arabidopsis lost ability to increase freezing tolerance (FT) during cold acclimation (CA) Arabidopsis thaliana
seasonal adaptation of cellular functions reflects acclimation that could account for the survival of Norway spruce needles in harsh boreal environmental conditions Picea abies
plants need to adapt their metabolism to increase freezing tolerance
DEG encoding (LHY, LHY1, AT1G01060) exhibited strong upregulation during cold acclimation (CA) in Experiment I cold acclimation (CA)
plants from temperate climates increase in freezing tolerance during exposure to low, non-freezing temperatures
galactose contributes to the prediction of freezing tolerance Arabidopsis thaliana
cold induces association with insoluble cell structures Arabidopsis thaliana
light signals before low temperatures are essential for further increasing freezing tolerance (FT)
cold-induced changes of gene expression and metabolism are critical for plant survival of freezing Arabidopsis thaliana
light quality could induce ABA increase
(BGT, GCN5, HAC3, HAG01, HAG1, HAT1, AT3G54610) mutants show reduced transcription of cold-regulated (COR) genes
ABA and JA concentrations in Experiment II showed opposite changes under long photoperiod
Col-0 accession shows intermediate changes in metabolite pool sizes during cold acclimation Arabidopsis thaliana
TCA cycle intermediates are associated with heterosis in freezing tolerance Arabidopsis thaliana
chlorophyll (a + b) in Experiment III were higher than in Experiment II Experiment II
non-acclimated gcn5-1 mutant plants are not more freezing tolerant than non-acclimated wild-type plants
different processes of field cold acclimation (F-CA) and artificial cold acclimation (A-CA) result in different freezing tolerance (FT) after complete or incomplete cold acclimation (CA)
all differences between field cold acclimation (F-CA) and artificial cold acclimation (A-CA) result in weak freezing tolerance (FT) in artificial cold acclimation (A-CA)
metabolite profiling has indicated major reprogramming of plant metabolism in the cold
AtGCN5 and AtADA2b-containing SAGA-like complex may function together with C-repeat/DRE binding factors (CBFs)
PUFAs are reported to accumulate during cold stress
constitutive expression of (ATCBF1, CBF1, DREB1B, AT4G25490) led to frost tolerance Arabidopsis thaliana
plants stressed following 24 h acclimation period show suppression of downstream PLDα transcription Gossypium hirsutum
light intensity could induce ABA increase
high light intensity stress during cold acclimation (CA) would result in great freezing tolerance (FT)
upregulation of (HY5, TED 5, AT5G11260) ensured complete development of cold acclimation (CA) in Arabidopsis via integrating low temperature and light signaling Arabidopsis thaliana
processes of field cold acclimation (F-CA) and artificial cold acclimation (A-CA) are quite different, including hormone signaling transduction, degree of photoinhibition/photoprotection, fatty acid metabolism and respiration
anthocyanin increases freezing tolerance (FT)
non-freezing cold temperature exposure activates transcriptional reprogramming
starch-degrading genes were up-regulated in 1 or 4 d under cold conditions Arabidopsis thaliana
glucan-water dikinase ( (GWD, GWD1, SEX1, SOP, SOP1, AT1G10760) and (ATGWD2, GWD3, PWD, AT4G24450, At4g24450) ) were up-regulated in 1 or 4 d under cold conditions Arabidopsis thaliana
plants exposed to reduced light intensity during cold acclimation (CA) and/or unchanged day-length were studied with short-term cold acclimation (CA) period Arabidopsis thaliana
(HP59, pSUT, AT5G59250) is a modulator of cold acclimation Arabidopsis thaliana
C24 accession shows largest changes in metabolite pool sizes during cold acclimation Arabidopsis thaliana
TCA cycle intermediates increased rapidly in early stage within 4 h of cold treatment Arabidopsis thaliana
tomato leaves with relatively high expression of SlHY5 exhibited enhanced freezing tolerance (FT) Solanum lycopersicum
exposure of plants to low temperature causes metabolism was largely reprogrammed Arabidopsis thaliana
fumaric acid contributes to the prediction of freezing tolerance Arabidopsis thaliana
ABA increase could increase low freezing tolerance (LFT)
proline contributes to the prediction of freezing tolerance Arabidopsis thaliana
ABA level gradually decreased with increase of freezing tolerance (FT)
photoperiod could induce ABA increase
cellular cold signalling networks prepares the cell for onset of winter
successful cold acclimation of Col-0 to 10°C starts with growth arrest of approximately 1 week Arabidopsis thaliana
much less effort has been devoted to elucidating the underlying molecular mechanisms to gradual temperature decline during the autumn-winter progression in natural conditions Triticum aestivum
cytosolic MSRA protein abundance increases during acclimation to low temperature Secale cereale
transcript levels of biosynthetic genes responded more slowly increased during 12–24 h and sustained Arabidopsis thaliana
MtCBF4 activation of downstream genes regulates cold tolerance Medicago truncatula
3 °C is used as acclimation temperature Gossypium hirsutum
RNA secondary structure unwinding has important roles in regulating freezing tolerance
MtCBF4 regulation by MtMYB3 and MtMYB61 occurs during cold acclimation Medicago truncatula
CBF regulons of Solanum commersonii and Solanum tuberosum differ in sets of genes Solanum commersonii; Solanum tuberosum
Cor (LEA, AT2G21490) genes transcript accumulation is higher in freezing-tolerant M808 Triticum aestivum
90 mM sucrose in lower epidermis had much less effect than 40 mM sucrose on (COR78, LTI140, LTI78, RD29A, AT5G52310) transcript abundance
PpCBF1 T166 transgenic apple trees showed increased cold tolerance Malus domestica
(CP29A, AT3G53460) is a modulator of cold acclimation Arabidopsis thaliana
M. falcata accumulates more soluble sugars than alfalfa Medicago sativa subsp. falcata; Medicago sativa subsp. sativa
C3 leaves are protected from freezing injury through cold acclimation process Amaranthus semialata
three C3 and two C4 species displayed cold acclimation response
Wsc120 from Triticum aestivum expression profiles at proteomic level Triticum aestivum
MtCBF4 activates expression of MtCAS15 Medicago truncatula
low nonfreezing temperatures triggers development of freezing tolerance
cold acclimation obtains cold tolerance
compatible osmolytes include proline
plants from temperate and cold climates increase in freezing tolerance during exposure to low, but non-freezing, temperatures
four structurally unknown metabolites are highly predictive for a complex trait such as freezing tolerance Arabidopsis thaliana
AtGCN5 and AtADA2b-containing SAGA-like complex regulates cold-regulated (COR) gene expression
different changes in respiration during field cold acclimation (F-CA) and artificial cold acclimation (A-CA) were presented during field cold acclimation (F-CA) and artificial cold acclimation (A-CA)
cold acclimation activates multiple regulatory pathways Arabidopsis thaliana
ectopic expression of (ATCBF1, CBF1, DREB1B, AT4G25490) driven by the CaMV-35S constitutive promoter significantly enhanced freezing tolerance Arabidopsis thaliana
cold-regulated (COR) genes function is to protect cell membranes
Miscanthus show greater degree of cold acclimation capacity Miscanthus
MtCBF4 is regulated by MtMYB3 Medicago truncatula
temperate plants are capable of developing freezing tolerance
RNA splicing has important roles in regulating chilling tolerance
transient nature of gene expression induced by cold treatment may reflect activation of transcriptional cascades Alstroemeria
PLDα1 deficient plants showed stronger expression in response to cold acclimation Arabidopsis thaliana
cold acclimation leads to freezing tolerance
CRT (C-repeat)/DRE (dehydration response element) is present in the promoter of COR (cold-regulated) genes Arabidopsis thaliana
(ATCBF1, CBF1, DREB1B, AT4G25490) (ATCBF2, CBF2, DREB1C, FTQ4, AT4G25470) and (ATCBF3, CBF3, DREB1A, AT4G25480) is followed by expression of CBF-targeted genes (the CBF regulon) Arabidopsis thaliana
reduced ABA levels impair freezing tolerance Arabidopsis thaliana
Field non-acclimation (F-NA) sample has leaf LT 50 of −4.3°C
circadian rhythm pathway is common pathway enriched in each two-pair comparison
lack of correlation between (HY5, TED 5, AT5G11260) expression and ABA accumulation may be one of differences identified between herbaceous plants and woody perennials
DREB1/CBF and (HOS9, PFS2, WOX6, AT2G01500) /HOS10 pathways play a pivotal role in development of freezing tolerance upon low-temperature treatment
chilling, non-freezing temperatures leads to development of resistance under freezing temperatures
sorbitol did not induce high (COR78, LTI140, LTI78, RD29A, AT5G52310) expression Arabidopsis thaliana
depression of osmotic potential was associated with acquisition of cold acclimation in some C3 and C4 species
cold acclimation occurs after exposure to low temperatures >0°C
cellular metabolic signals have important roles in regulating chilling tolerance
plants develop tolerance to freezing after exposure to low, non-freezing temperatures Arabidopsis thaliana
cold-regulated (COR) genes function is to prevent cellular dehydration
ectopic expression of (ATCBF1, CBF1, DREB1B, AT4G25490) driven by the CaMV-35S constitutive promoter induced expression of COR genes Arabidopsis thaliana
10 °C is not acclimation temperature Gossypium hirsutum
(AtFAD2, FAD2, AT3G12120) expression patterns correlates with lipid profiles Gossypium hirsutum
CBF cold-response pathway includes activity of three transcription factors, namely (ATCBF1, CBF1, DREB1B, AT4G25490) (ATCBF2, CBF2, DREB1C, FTQ4, AT4G25470) and (ATCBF3, CBF3, DREB1A, AT4G25480) Arabidopsis thaliana
HOS10 is speculated to regulate ABA-mediated cold acclimation Arabidopsis thaliana
CBF regulon collectively known as stress-responsive genes Arabidopsis thaliana
cold acclimation is process of acquiring freezing tolerance
Arabidopsis increase frost tolerance in response to low, non-freezing temperatures Arabidopsis thaliana
Solanum commersonii and Solanum tuberosum have CBF regulons composed of hundreds of genes Solanum commersonii; Solanum tuberosum
spring habit and winter habit are tightly linked to frost tolerance genes Triticum aestivum L.
winter Manitou reaches lowest LT 50 of –13.3 °C at 42 d cold hardiness
sugars are implicated in regulation of cold-acclimation
C4 species from this ecosystem have no inherent barrier to the development of cold acclimation
Egu CBF 1a/b genes exhibit very fast and strong cold regulation Eucalyptus gunnii
cold acclimation at 17 °C resulted in induction of one of the four PLDα variants Gossypium hirsutum
differences in composition of CBF regulons may involve differences in freezing tolerance response to CBF overexpression Arabidopsis thaliana; poplar; tomato; rice
dehydrins are among COR genes that have been extensively studied
reciprocal near-isogenic lines (NILs) for the Vrn-A1 locus were developed to determine genetic and biochemical effect of Vrn-A1 locus on wheat LT tolerance Triticum aestivum L.
(COR78, LTI140, LTI78, RD29A, AT5G52310) transcript abundance increase is detectable earlier than 6–24 h time point
40 mM sorbitol in lower epidermis in cold and dark did not increase (COR78, LTI140, LTI78, RD29A, AT5G52310) transcript abundance
oxygen-evolving enhancer protein, Rubisco activase, phosphoglycerate kinase, NAD-dependent isocitrate dehydrogenase, Rieske protein, chlorophyll a / b binding protein, glyceraldehyde 3-phosphate dehydrogenase, thioredoxin M-type, triosephosphate isomerase, glutamate-1-semialdehyde 2,1-aminomutase, GDP-mannose 3,5-epimerase, thiamine biosynthetic enzyme, and translation elongation factor Tu have already been found after cold treatment in Arabidopsis thaliana or Oryza sativa Arabidopsis thaliana; Oryza sativa
cold-regulated genes constitute 4–20% of the genome Arabidopsis thaliana
sucrose supply in cold and dark had similar effects on freezing tolerance as on GUS activity and (COR78, LTI140, LTI78, RD29A, AT5G52310) transcript abundance Arabidopsis thaliana
cryoprotection probably requires high concentrations of sucrose Arabidopsis thaliana
overwintering plants that contain carbohydrate reserve do not require light for acclimation Triticum aestivum
modulation of activities of various enzymes plays a role in preventing freezing-induced cellular damage
proteomic analysis has not been previously conducted on frost tolerance in grasses Lolium–Festuca complex
more accumulation of soluble sugars in M. falcata is associated with greater freezing tolerance Medicago sativa subsp. falcata
spring habit and winter habit have been shown to influence level of LT tolerance Triticum aestivum L.
gene expression patterns during LT acclimation have been conducted on RNA extracted from leaves Triticum aestivum L.
genotype × acclimation period interaction affects LT 50
cold acclimation induces genes with various functions
Wdreb2 transcript accumulation is higher in freezing-tolerant M808 Triticum aestivum
significant differences in protein accumulation profiles appeared most often after 26 h (2nd day) of cold acclimation Festuca pratensis
(ATFP6, AtHMP40, FP6, HIPP26, AT4G38580) Fp17, Fp23, Fp30, Fp34, Fp38, and Fp39 plants show high values of regrowth after freezing at –8 °C Festuca pratensis
evg mutant trees remain capable of some cold hardiness induction in response to cold temperatures Prunus persica
(ATRBP31, ATRBP33, CP31, CP31A, RBP31, AT4G24770) is a modulator of cold acclimation Arabidopsis thaliana
compatible osmolytes include glycine betaine
cellular metabolic signals have important roles in regulating freezing tolerance
ability to germinate at low temperature probably involves induction of cold-acclimation mechanisms
53 groups of putative orthologous genes are cold-regulated in Solanum commersonii, Solanum tuberosum, and Arabidopsis thaliana Solanum commersonii; Solanum tuberosum; Arabidopsis thaliana
rapid evolution of CBF pathways may contribute to differences in freezing tolerance Solanum commersonii; Solanum tuberosum
cold shock proteins (CSPs) are induced at high levels during cold acclimation phase
acclimation period affects LT 50
LT acclimation patterns were consistent with previously reported patterns
ectopic expression of Wcbf2 and Wdreb2 improved freezing tolerance Nicotiana tabacum
ICE-DREB1/CBF system drives cold-acclimation processes
(COR78, LTI140, LTI78, RD29A, AT5G52310) typically reaches peak of expression at 6–24 h in the cold
0 mM sucrose in leaves without lower epidermis in other environments gave higher COR78 transcript abundance than controls on soil
0 mM sucrose in leaves without lower epidermis in warm and dark gave higher transcript abundance than 40 mM and 90 mM sucrose
underlying mechanisms of cold acclimation response have not been reported scientific literature
timing of floral transition is one of the determining factors for low temperature (LT) tolerance winter wheat
time point at which differences were most often observed was at 26 h of cold acclimation Festuca pratensis
Norstar reaches lowest LT 50 of –23 °C at 49 d cold hardiness
chilling pretreatment indicates development of frost protection in C3 subspecies Amaranthus semialata
(HOS9, PFS2, WOX6, AT2G01500) /HOS10 pathway contributes to only a part of plant's acclimation capacity
sucrose promoted expression in warm environment Arabidopsis thaliana
six C3 and three C4 Mongolian steppe grasses were exposed to 20 d chilling or control pre-treatments
timing of floral transition is an important factor that affects LT tolerance levels in winter wheat Triticum aestivum
more frost-tolerant plants, including species from Lolium–Festuca complex tend to be more tolerant to cold-induced photoinhibition of photosynthesis Lolium–Festuca complex
downstream genes play important roles in development of freezing tolerance
cold acclimation is generally associated with changes in gene-expression levels
CBF/DREB1 regulon is important pathway involved in cold acclimation Arabidopsis thaliana
PA/PC+PE ratio does not increase during cold acclimation in light Gossypium hirsutum
LT tolerance shows most rapid changes during initial stages of LT acclimation Triticum aestivum L.
light strongly affects acclimation to cold
cold acclimation is associated with many structural, physiological, and biochemical changes within plant cells
MS analyses of differentially accumulated proteins could be an efficient way for the identification of crucial proteins involved in tolerance to low temperature stress
proteins directly involved in photosynthesis were major group selected as differentially accumulated proteins before and during cold acclimation between plants of different frost tolerance levels Festuca pratensis
cold acclimation is associated with accumulation of compatible osmolytes
sucrose concentrations used in experiments reflected concentrations found in plants during normal acclimation to cold Arabidopsis thaliana
Festuca pratensis is used as model for research on cold acclimation of forage grasses Festuca pratensis
freezing at –11 °C is used to discriminate Festuca genotypes according to their frost tolerance Festuca pratensis
chloroplast proteins constituted main group of differentially accumulated proteins identified in current work Festuca pratensis
cold-acclimated (CA) plants were grown under light and dark conditions (12/12 h light/dark, 120 μmol m⁻² s⁻¹) Arabidopsis thaliana
increase in freezing tolerance helps plants to survive freezing Arabidopsis thaliana
Solanum commersonii can cold acclimate Solanum commersonii
40 mM sucrose in lower epidermis in cold dark and warm light gave COR78 transcript abundance 25 times higher than 0 mM solution
proteomic research is first comprehensive study of cold acclimation in monocotyledonous species Festuca pratensis
Oryza sativa cannot cold acclimate and develop frost tolerance Oryza sativa
chlorophyll a / b -binding protein accumulation shows recovery only in HFT plants Festuca pratensis
low winter temperatures induce cold acclimation
reproductive stage limits plants' ability to cold acclimate Triticum aestivum L.
chilling pretreatment modifies patterns of leaf freezing injury substantially, with differential response between C3 and C4 subspecies Amaranthus semialata
cold acclimation in C4 subspecies does not develop in C4 leaves Amaranthus semialata
osmotic adjustment may accompany acclimation to chilling in C3 but not C4 grasses
Festuca pratensis cv. Skra population shows high variation in frost tolerance Festuca pratensis
sucrose effect on (COR78, LTI140, LTI78, RD29A, AT5G52310) transcript abundance in leaves without lower epidermis was much less than effect in lower epidermis
plants respond by activating mechanism of cold acclimation (CA)
maximal differences in frost tolerance between HFT and LFT genotypes were finally observed at 21 days of cold acclimation Festuca pratensis
Solanum commersonii increases in freezing tolerance in response to low temperature Solanum commersonii
differences in cold regulatory programmes may contribute to differences in freezing tolerance Solanum commersonii; Solanum tuberosum
Wlip19 transcript accumulation is higher in freezing-tolerant M808 Triticum aestivum
Solanum tuberosum cv. Irga displays low capacity for cold acclimation Solanum tuberosum
noticeable Ss (ATLTP1, AtLtpI-4, LP1, LTP1, AT2G38540) accumulation upon cold treatment was observed only in plants able to acclimate to low temperature Solanum
sugars may regulate cold-acclimation
optimal sucrose concentration was not constant, changing from 40 mM to 3 mM between second and fourth days of treatment Arabidopsis thaliana
10 proteins (spot nos 4, 7, 8, 9, 21, 24, 25, 26, 28, and 30) showed differences in abundance after 21 days of cold acclimation Festuca pratensis
Egu CBF 1a/b genes exhibit robust induction of 118-fold and 190-fold Eucalyptus gunnii
cold acclimation is characterized by growth cessation, bud dormancy, leaf senescence, and abscission
(ATCBF1, CBF1, DREB1B, AT4G25490) overexpression causes phenotypes associated with freezing tolerance Arabidopsis thaliana
plants adapted to temperate environments have considerable freezing tolerance
CBF regulon has fundamental role in cold acclimation Arabidopsis thaliana
Cereal lip19 genes are assumed to play regulatory role in gene expression during cold acclimation
ns-LTP1 participates in is supported by the fact that two S. sogarandinum lines displaying the same genetic background and only differing in their capacity to acclimatize to cold were used Solanum sogarandinum
(COR78, LTI140, LTI78, RD29A, AT5G52310) transcript levels at 24 h in warm and light in peeled lower epidermis were lower than transcript levels at 2 h
epidermis is well positioned to receive cold-induced signal Arabidopsis thaliana
Fp13 plant is low-frost-tolerant plant Festuca pratensis
photosynthetic apparatus plays role in cold acclimation Lolium–Festuca complex
other proteins differentially accumulated during cold acclimation in HFT and LFT Fp plants have not yet been detected in model plants Festuca pratensis
upregulated genes in mvp mutant encode CBF transcription factors
WCS120 family of proteins are thought to have significant role in frost tolerance Triticum aestivum L.
Ss (ATLTP1, AtLtpI-4, LP1, LTP1, AT2G38540) abundance was higher in cold-hardened plants Solanum sogarandinum
cold signalling in dark period increases freezing tolerance even when plants are exposed to light period in cold
global changes in gene expression during CA in plants from winter and spring Triticum aestivum (wheat) cultivars have been demonstrated at transcriptome level Triticum aestivum
CBF (CRT/DRE-binding factor) pathway controls a significant part of changes in gene expression
clones showed different responses to low temperatures
cold acclimation induces production of compatible solutes
CBF overexpression increases freezing tolerance Brassica napus
CBF overexpression increases freezing tolerance potato
Cor (LEA, AT2G21490) gene expression profiles show good correlation with development of freezing tolerance Triticum aestivum
Wcbf2 transcript accumulation is lower in freezing-sensitive CS Triticum aestivum
cold acclimation is associated with changes in cell wall properties
CBF (C-repeat binding factor)/DREB (dehydration responsive element binding protein) transcriptional factor family play a key role in expression of Cor (cold-regulated) genes Arabidopsis thaliana
94.9% of detected proteins did not show significant differences in abundance during cold acclimation between HFT and LFT plants Festuca pratensis
acclimation to cold-induced photoinhibition and to frost have partially overlapping mechanisms Lolium–Festuca complex
duration of the cold induction is specific feature of Eucalyptus genes Eucalyptus
CBF genes show differences in cold expression profiles grape
quantitative analysis of cold induction is performed on each Egu CBF 1 gene Eucalyptus gunnii
export generally recovers as plant acclimates to the cold
Solanum phureja (ATCHS, CHS, TT4, AT5G13930) (diploid potato) is cold-acclimating potato Solanum phureja
cold-acclimation processes may exist in cold-sensitive species
protein accumulation profiles show wide range of different patterns in Fp genotypes with distinct levels of frost tolerance Festuca pratensis
increased accumulation of phosphoglycerate kinase protein was observed during whole period of cold acclimation in HFT genotypes Festuca pratensis
amplitude of shrinkage in 'Dvina' increased with succession of negative thermal events Populus deltoides
(GALS1, AT2G33570) (GALS2, AT5G44670) (GALS3, AT4G20170) triple mutant does not exhibit changes in cell wall extensibility and rigidity Arabidopsis thaliana
increase in pectic galactan during CA was found in several freezing-tolerant plants
CBF regulon brings about increase in freezing tolerance Arabidopsis thaliana
amounts of (PPDK, AT4G15530) in Miscanthus×giganteus (M.×giganteus) are elevated greatly when grown at 14 °C Miscanthus×giganteus
subspecies and treatment show significant interactions for leaf mortality and damage Amaranthus semialata
cold acclimation in the C3 subspecies is associated with changes in the pattern of moisture release at low water potentials Alloteropsis semialata
changes in the pattern of moisture release at low water potentials indicates possible involvement of water relations in the acclimation response Alloteropsis semialata
cold acclimation rate controls level of accumulated LT tolerance Triticum aestivum
thioredoxin was accumulated at higher amounts in HFT plants Festuca pratensis
CBF genes show differences in cold expression profiles Chinese cabbage
C3 leaves developed protection via cold acclimation mechanism Alloteropsis semialata
Solanum tuberosum cv. Irga displays very low capacity to acclimatize to low temperature Solanum tuberosum
sucrose causes increase in GUS activity Arabidopsis thaliana
young barley plants exposed to 10 h photoperiod followed by 14 h dark period in 6/2 °C day/night achieved several degrees K more freezing tolerance compared to constant 6 °C Hordeum vulgare
transcript profiling analyses indicate cold acclimation is a very complex response resulting from global changes in gene expression Arabidopsis thaliana
C4 subspecies shows leaf damage that is low across pretreatments Amaranthus semialata
leaf protein accumulation analyzed before and after cold acclimation time points Festuca pratensis
mechanism of cold acclimation (CA) increases level of frost tolerance
comprehensive analysis of the protein complement of plant tissues in response to low temperature has been largely restricted to Arabidopsis thaliana and Oryza sativa Arabidopsis thaliana; Oryza sativa
decreased accumulation of Rubisco activase protein after prolonged cold-acclimation was observed in LFT genotypes Festuca pratensis
total transcript copy number ng-1 of cDNA is still four times higher than basal level Eucalyptus gunnii
mean f T values in different vegetation types at coldest sites approximately 0.3–0.5, indicating 50–70% reduction of (GPP, VTC4, AT3G02870)
disagreement between minimum air temperature and peak stem shrinkage could explain need for poplar clones to perceive recurrent negative temperatures below threshold Populus × canadensis; Populus deltoides
cold acclimation induces accumulation of osmolytes
(GALS1, AT2G33570) (GALS2, AT5G44670) (GALS3, AT4G20170) triple mutant exhibits impaired freezing tolerance during initial stages of cold acclimation Arabidopsis thaliana
compositional modification of the cell wall during CA is important for improving freezing tolerance through changes in cell wall properties Arabidopsis thaliana
40 mM sucrose enhanced freezing tolerance in cold and dark conditions
approximately 800 protein profiles revealed 41 proteins with minimum 1.5-fold difference in abundance Festuca pratensis
photosynthesis was highly depressed by cold acclimation Festuca pratensis
plant cells started to establish new homeostasis under low temperature stress Festuca pratensis
northern and southern ecotypes of Betula pendula show differences in rates and degrees of cold acclimation Betula pendula
accumulation of specific carbohydrates (sucrose, galactinol, myoinositol, and raffinose) may be important to improve tolerance to freezing stress Arabidopsis thaliana
minimum temperature (T min) during winter related to mean spring cold-acclimated temperature modifier (f T) and relative mean (GPP, VTC4, AT3G02870) bias
cold-acclimatized plants show significantly reduced effects of cold on (ANAC062, NAC062, NTL6, AT3G49530) processing and protein stability Arabidopsis thaliana
COLD REGULATED (COR) genes are expressed during cold acclimation
(GWD, GWD1, SEX1, SOP, SOP1, AT1G10760) locus is genetically linked to plant freezing tolerance Arabidopsis thaliana
greening of pale-yellow (PGP1, PGPS1, PGS1, AT2G39290) resulted in simultaneous decrease in 29 kD polypeptide Arabidopsis thaliana
putrescine pathway is involved in potato cold acclimation Solanum tuberosum
calibrated parameters from site-level calibration compared with variation of T min during period between 60 d before start of photosynthesis resumption period and peak of (GPP, VTC4, AT3G02870)
cold acclimation induces accumulation of abscisic acid (ABA)
(EMB2107, MSA, RPN5A, AT5G09900) (4x) 'PF30153' is the only clone showing similar pattern of response to Mxg (3x) 'Illinois' with nearly full acclimatization Miscanthus sacchariflorus
Solanum tuberosum does not increase in freezing tolerance in response to low temperature Solanum tuberosum
rate component decides degree of expression of LT-induced genes Triticum aestivum L.
sucrose regulatory role in cold acclimation may be important during diurnal dark periods Arabidopsis thaliana
40 mM sucrose in lower epidermis gave COR78 transcript abundance well above transcript abundance in controls on soil
sucrose effect was transient in warm environment Arabidopsis thaliana
Eragrostis curvula markedly increased leaf freezing resistance Eragrostis curvula
CBF transcription factors bind specifically to C-repeat (CRT)/dehydration responsive element (DRE)/low temperature responsive (LTR) motif
cold acclimation (CA) activates cellular protection mechanism
enhanced levels of soluble sugars, nitrogenous metabolites, and citric acid in L er plants grown in low R:FR at 16°C is consistent with expression of the CBF regulon in these conditions Arabidopsis thaliana
decreased PG generates reversible, yellow phenotype during cold acclimation Arabidopsis thaliana
greening of pale-yellow (PGP1, PGPS1, PGS1, AT2G39290) concomitantly resulted in accumulation of Lhcas Arabidopsis thaliana
effect of sucrose on (COR78, LTI140, LTI78, RD29A, AT5G52310) promoter activity or transcript abundance would not necessarily require cold Arabidopsis thaliana
sucrose increases plant survival of freezing tolerance
sufficient soluble carbohydrates might help trigger first steps in acclimation
transfer of cabbage plants from constant 5 °C to 5/0 °C day/night caused increase in freezing tolerance Brassica oleracea
C4 grass species have the capability for developing cold acclimation during exposure to chilling
RH7 promotes plant development at low temperatures Arabidopsis thaliana
cytosolic translational apparatus is remodeled at level of ribosome biogenesis factors Arabidopsis thaliana
fully acclimated wheat plants may survive as low as −22°C or colder Triticum aestivum
behaviour of 'Dvina' shrinkage amplitude increase could be related to cold acclimation processes mediated by recurring low thermal cycles Populus deltoides
cold acclimation pathways are highly interactive and modulated by multiple signaling pathways
successful cold acclimation of Col-0 to 10°C leads to vegetative-to-regenerative phase transition Arabidopsis thaliana
cytosolic translational apparatus is remodeled at level of structural ribosomal proteins Arabidopsis thaliana
down-regulated genes (clusters C8–C10) were enriched mainly in biosynthetic processes, carbohydrate metabolic process, ribosome assembly, and DNA packaging Triticum aestivum
Cvi accession of Arabidopsis displays lower freezing tolerance than temperate accessions such as Wassilewskija and L er Arabidopsis thaliana
(AtRH3, emb1138, RH3, AT5G26742) (EMB3108, HS3, RH22, AT1G59990) and (RH39, AT4G09730) are involved in acclimation to cold stress Arabidopsis thaliana
rh50-1 plants polysome loading is perturbed in cold-acclimated plants Arabidopsis thaliana
field experiments were designed to systematically identify differentially expressed genes (DEGs) that low temperature activated in wheat NILs Triticum aestivum
cold stress often modulates lipid compositions in cellular membranes Triticum aestivum
NO genetic background indicates superiority of for cold tolerance Triticum aestivum
(ATICE1, ICE1, SCREAM, SCRM, AT3G26744) and CBFs are induced rapidly by cold Triticum aestivum
cold acclimation genes induction occurs via distinct transcriptional pathways Arabidopsis thaliana
chloroplast is targeted by action of COR genes
Arabidopsis thaliana plants (35S::MdS6PDH and WT) grown at cold temperatures only transgenic lines survived while WT plants underwent severe dehydration damage and died Arabidopsis thaliana
altered gene expression of (AGL25, FLC, FLF, RSB6, AT5G10140) and (AGL19, GL19, AT4G22950) is apparently part of premature triggering of limited cold responses in nonacclimated reil1-1 reil2-1 Arabidopsis thaliana
only ∼12% of cold-responsive genes are controlled by CBFs
VRN-A1 down-regulates expression of CORs (cold-responsive genes) or (DHNS, ECHID, AT1G60550) (dehydrins) Triticum aestivum
transcriptional changes during cold acclimation in wheat have been conducted under controlled environments Triticum aestivum
β-1,4-galactan accumulates in cell walls during cold acclimation Arabidopsis thaliana
COLD REGULATED (COR) genes are downstream components of the C-repeat Binding Factor (CBF) regulon
expanded leaves of L er plants grown in low R:FR at 16°C displayed elevated levels of soluble sugars and cold acclimation products Arabidopsis thaliana
cold acclimation in wild type results in decrease in extensibility and increase in rigidity of cell wall Arabidopsis thaliana
galactan accumulation was accompanied by changes in the mechanical properties of the cell wall Arabidopsis thaliana
CBF overexpression does not result in increased freezing tolerance tomato
loss of ability to cold acclimate in S. tuberosum cv. Irga may indicate inactivation of a signalling element upstream of DREB1/CBF in this cultivar Solanum tuberosum
low temperature results in increase in Ss LTP1 level in Solanum species or cultivar able to acclimatize to cold Solanum species
iron–sulphur Rieske protein (spot no. 30) shows increased accumulation at early stages of cold acclimation in HFT plant Festuca pratensis
SaADC1 overexpression in Solanum tuberosum cv. E3 exhibits enhanced cold-acclimated freezing tolerance Solanum tuberosum
cluster of DEGs induced by ethylene characterized by genes putatively involved in protection mechanisms against cold stress
increased structural stabilization of membranes through production of unsaturated and long chain fatty acids and sorbitol is hypothesized to be responsible for improved tolerance to low temperatures in 1-MCP-treated fruit
arginine decarboxylase gene ADC1-associated putrescine pathway probably enhances expression of C-repeat binding factor genes (CBFs) Solanum tuberosum; Solanum acaule
cell wall changes are necessary for enhancement of freezing tolerance during CA
itaconic acid contributes to the prediction of freezing tolerance in C24-crosses Arabidopsis thaliana
beta-amylase was up-regulated in 1 or 4 d under cold conditions Arabidopsis thaliana
evergreen cultivar in the genus Rhododendron 'Elsie Lee' was used as system to study cold acclimation (CA) in woody perennials Rhododendron
Physiological statuses of artificial non-acclimation (A-NA) and field non-acclimation (F-NA) are different each other
cold acclimation in the model plant Arabidopsis thaliana involves changes in the expression levels of several hundred genes Arabidopsis thaliana
Ler accession shows intermediate changes in metabolite pool sizes during cold acclimation Arabidopsis thaliana
cold exposure induces cold acclimation Arabidopsis thaliana
succinate is associated with heterosis in freezing tolerance Arabidopsis thaliana
upstream and downstream of C-repeat binding factor (CBF) transcription factors were gradually uncovered through research Arabidopsis thaliana
clusters C3 to C7 was up-regulated as autumn progressed to winter Triticum aestivum
cold responses included Ca 2+ signaling and kinase cascades, CBFs, CORs, and ABA-dependent pathways Triticum aestivum
day-length is essential component for poplar bud set and dormancy Populus
(VEN4, AT5G40270) is a modulator of cold acclimation Arabidopsis thaliana
parameters for MF had large variation and did not have clear linkage with ones in DBF and ENF
calcium/calmodulin-regulated receptor-like kinase 1 (CRLK1, AT5G54590) interaction with (ARAKIN, ATMEKK1, MAPKKK8, MEKK1, AT4G08500) leads to MAPK activation and freezing tolerance
(CaS, AT5G23060) (SVK, AT4G07395) positively controls expression of C-repeat-binding factor 1 (ATCBF1, CBF1, DREB1B, AT4G25490) Arabidopsis thaliana
cold-responsive protein kinase 1 (CRPK1, AT1G16670) is activated by cold stress Arabidopsis thaliana
PFT-level parameters in DBF and ENF generally have consistent pattern compared with site-level parameters
positive, albeit nonsignificant relationship between τ and T min for DBF and ENF sites in boreal climates (Dfc-ENF) emerged
(CAMTA1, EICBP.B, AT5G09410) /3 double mutant plants were impaired in ability to acclimate to cold Arabidopsis thaliana
fructose (Fru) accumulation correlates with cold stress tolerance Arabidopsis thaliana
reil1-1 reil2-1 mutant showed premature triggering of cold-acclimation responses Arabidopsis thaliana
(ATCBF3, CBF3, DREB1A, AT4G25480) activation explains cold-induced carbohydrate metabolism and starch degradation Arabidopsis thaliana
previous microarray studies were limited to examining relative differences of gene expression under cold treatments in controlled environment Triticum aestivum
metabolite profiling studies indicated major restructuring of plant metabolism during cold acclimation
Co-2 accession shows largest changes in metabolite pool sizes during cold acclimation Arabidopsis thaliana
glycine contributes to the prediction of freezing tolerance in C24-crosses Arabidopsis thaliana
TCA cycle intermediates increase during cold shock
low temperatures resulted in zeaxanthin being mainly allocated for photoprotection
JA induces relative protein accumulation (dehydrin)
posttranslational regulation of Inducer of CBF expression 1 (ATICE1, ICE1, SCREAM, SCRM, AT3G26744) is essential for Inducer of CBF expression 1 (ATICE1, ICE1, SCREAM, SCRM, AT3G26744) function
(ATMKK2, MK1, MKK2, AT4G29810) activates (ATMPK4, MAPK4, MPK4, AT4G01370) and (ATMAPK6, ATMPK6, MAPK6, MPK6, AT2G43790)
fitted parameter values for τ, X 0, and S max tended to be smaller for ENF than for DBF
cold-acclimated (CAMTA1, EICBP.B, AT5G09410) /3 double mutant plants had EL 50 values of −8°C Arabidopsis thaliana
C-repeat/DRE binding factors (CBFs) are induced in wild-type plants
rapid accumulation of maltose protects plant cells against freezing damage Arabidopsis thaliana
overwintering woody species experience combination of short day-length and low temperatures through fall and winter
seasonal leaf color change in Rhododendron 'Elsie Lee' provides opportunity to study significant function of anthocyanin during cold acclimation (CA) Rhododendron
Leaf freezing tolerance (LFT) is temperature causing 50% injury (LT 50)
stems of 13 out of 15 woody species significantly increased respiration in response to near freezing temperature
circadian rhythm pathway was shown to be important for cold acclimation (CA)
cold acclimation is mediated by transcriptional network
freezing sensitive accessions show low CBF expression levels 2h after transfer to 5°C Arabidopsis thaliana
changes in gene expression at low temperature affect multiple aspects of plant growth and development Arabidopsis thaliana
CBF/DREB1-dependent pathway is involved in cold-stress response Arabidopsis thaliana
cold acclimation of (PGP1, PGPS1, PGS1, AT2G39290) at 5 °C limits accumulation of Lhcbs Arabidopsis thaliana
plants treated with low R:FR at 16°C but not 22°C display increased expression of COLD REGULATED (COR) genes
CBF/DREB1-independent pathway is involved in cold-stress response Arabidopsis thaliana
CSCD ablation enables better recovery of root growth from freezing stress without prior chilling treatment Arabidopsis thaliana
multi-photon laser ablation was used to mimic chilling stress-induced death of CSCDs Arabidopsis thaliana
phytochrome-interacting factor 4/7 ( (AtPIF4, PIF4, SRL2, AT2G43010) /7) regulates CBF expression
(ATMYB15, ATY19, MYB15, AT3G23250) regulates CBF expression
(ATMYB15, ATY19, MYB15, AT3G23250) binds to promoters of CBF genes
Arabidopsis thaliana develops greater ability to withstand freezing after exposure to chilling stress induced by low but above-freezing temperatures Arabidopsis thaliana
(ATMYB15, ATY19, MYB15, AT3G23250) physically interacts with INDUCER OF CBF EXPRESSION 1 (ATICE1, ICE1, SCREAM, SCRM, AT3G26744)
(PUB25, AT3G19380) and (PUB26, AT1G49780) positively regulate freezing tolerance Arabidopsis thaliana
cultivated potato (Solanum tuberosum) generally lacks capacity to acquire partial tolerance following cold acclimation Solanum tuberosum
freezing tolerance reaches maximum in approximately 1–2 weeks Arabidopsis thaliana
cold or freezing temperature acclimation requires reprogramming of gene expression
OST1-mediated phosphorylation of (ATBTF3, BTF3, AT1G17880) proteins facilitates interaction of (ATBTF3, BTF3, AT1G17880) proteins and CBF proteins Arabidopsis thaliana
OsICE1 stabilization enhances plant chilling tolerance Oryza sativa
HIGH EXPRESSION OF OSMOTICALLY RESPONSIVE GENE 1 (ESD6, HOS1, AT2G39810) degrades INDUCER OF CBF EXPRESSION 1 (ATICE1, ICE1, SCREAM, SCRM, AT3G26744) Arabidopsis thaliana
cold acclimation results in increase in cell wall rigidity Arabidopsis thaliana
plants that acclimate to cold interpret chilling temperatures as forerunner of potential freezing temperatures Arabidopsis thaliana
L er plants grown in low R:FR at 16°C display enhanced levels of nitrogenous metabolites, including glycine, 5-oxo-proline and glutamic acid Arabidopsis thaliana
(ATCBF2, CBF2, DREB1C, FTQ4, AT4G25470) expression levels relationship with CBF1 or CBF3 expression strongly depends on genetic background of RNAi lines Arabidopsis thaliana
Fourier transform ion cyclotron mass spectrometry (MS) and nontargeted metabolic fingerprinting approach was used to study effects of cold acclimation on the metabolome Arabidopsis thaliana