| SUMOylation |
is important mechanism for |
rapid redirection of molecular pathways during stress signaling |
|
| chloroplast-derived hydrogen peroxide signals |
in response to high light, wounding, or infection with incompatible hypersensitive response-inducing pathogen are localized specifically to |
vascular bundle |
Arabidopsis thaliana |
| NaCl |
caused oscillatory intracellular Ca2+ signals specifically in |
spongy mesophyll and vascular cells |
Arabidopsis thaliana |
| MAPKs |
are involved in |
numerous stress responses, including high-temperature stress, cold stress, salt stress, and biotic stresses |
|
| Calcium (Ca 2+) signaling |
has been described in |
stress responses to environmental stimuli |
Chlamydomonas reinhardtii |
| MYC |
supports |
stress response |
|
| consistency in dynamics of response to cold across cell types |
suggests that there are not |
cell-specific responses to cold in terms of Ca2+ signaling |
Arabidopsis thaliana |
| progesterone (pregn-4-ene-3,20-dione; PO) |
influences |
stress responses |
|
| epidermal pavement cells |
have |
large mechanical stimulation-induced intracellular Ca2+ transient |
Arabidopsis thaliana |
| FERONIA (FER, AT3G51550) |
functions as regulator of |
response to abiotic stress |
|
| overexpression of (STZ, ZAT10, AT1G27730) (AtZAT12, RHL41, ZAT12, AT5G59820) (ATCBF1, CBF1, DREB1B, AT4G25490) and (ATCBF2, CBF2, DREB1C, FTQ4, AT4G25470) in why1why3polIb-1 |
supports |
hypothesis that ROS-mediated genetic reprogramming occurs |
Arabidopsis thaliana |
| protein kinases |
especially function as integrators in pathways involved in |
plant stress responses |
|
| strigolactone (SL) |
play a pivotal role in |
biotic stress responses |
|
| abscisic acid (ABA) |
plays critical role in |
plant biotic and abiotic stress response |
|
| low-molecular weight carboxylic acids |
is |
by-product from anaerobic bacterial activity acting as environmental signal for barrier formation |
|
| ROS in several environmental signaling pathways |
plays role in |
environmental signaling pathways |
|
| (ATCDPK3, ATCPK6, CPK6, AT2G17290) |
is a convergent point of |
signaling pathways for stomatal closure in response to abiotic and biotic stress |
Arabidopsis thaliana |
| NaCl-induced oscillatory intracellular Ca2+ signals in endodermis and pericycle of roots |
is consistent with |
previous studies that found that NaCl caused oscillatory intracellular Ca2+ signals specifically in endodermis and pericycle of roots |
Arabidopsis thaliana |
| serine/threonine-protein kinase (AtCTR1, CTR1, SIS1, AT5G03730) |
is involved in |
stress signaling |
Ipomoea purpurea |
| OPEN STOMATA1/SUCROSE-NON-FERMENTING-1-RELATED 2.6 ( (ATOST1, OST1, P44, SNRK2-6, SNRK2.6, SRK2E, AT4G33950) ) |
is |
member of the SnRK2 protein kinase family |
Arabidopsis thaliana |
| hydrogen peroxide |
induces |
intracellular Ca2+ elevation |
Arabidopsis thaliana |
| intracellular Ca2+ signals induced by mechanical stimulation and NaCl |
identify cell-specific dynamics to |
|
Arabidopsis thaliana |
| cytokinin (CK) |
affects |
response to abiotic stresses in roots |
Arabidopsis thaliana |
| high similitude of genetic expression remodeling in why1why3polIb-1 with ROS-inducing conditions |
suggests that |
ROS, and not ptDNA rearrangements, mediate this response |
Arabidopsis thaliana |
| mechanical stimulation |
induces |
intracellular Ca2+ elevation |
Arabidopsis thaliana |
| miR394 |
fine-tunes tissue response to ABA under |
drought stress |
Arabidopsis thaliana |
| VmRDRs |
influence |
abiotic stress response |
Valsa mali |
| contribution to intracellular Ca2+ dynamics made by mechanical stimulation |
when taken into account |
all cells, including epidermal pavement cells, had essentially monophasic response to hydrogen peroxide |
Arabidopsis thaliana |
| calcium and ethylene signaling pathways |
have important roles in |
regulation and signalization of abiotic stresses |
|
| dynamics of response to cold stimulation |
is similar to |
dynamics described previously for whole plants, root-specific cell types, and guard cell populations |
Arabidopsis thaliana |
| miR394 |
fine-tunes tissue response to ABA under |
salt stress |
Arabidopsis thaliana |
| endodermis and pericycle of roots |
exhibit complex cell-specific behaviors in response to |
NaCl |
Arabidopsis thaliana |
| abscisic acid (ABA) |
is involved in |
abiotic stress responses |
|
| SA (salicylic acid) accumulation |
is reported to be responsible for |
dwarf phenotype of some phenylpropanoid mutants |
Arabidopsis thaliana |
| Arabidopsis (ATMAPK6, ATMPK6, MAPK6, MPK6, AT2G43790) |
is activated by |
abiotic stresses |
Arabidopsis thaliana |
| suberization in the endodermis |
is induced by |
abscisic acid (ABA) and salt stress |
|
| endogenous miR394 |
regulates |
stress response |
Arabidopsis thaliana |
| Calcium (Ca 2+) signaling |
has been described in |
stress responses to bacterial toxins |
Chlamydomonas reinhardtii |
| (ATCDPK3, ATCPK6, CPK6, AT2G17290) |
is involved in activation of |
inward-rectifying potassium (IKin) channels induced by abiotic and biotic stimuli |
Arabidopsis thaliana |
| salt tolerance receptor-like cytoplasmic kinase1 |
is |
plasma membrane protein |
|
| GmCaM4 |
plays crucial role in |
abiotic and biotic signaling pathways |
Glycine max |
| intracellular signaling cascades |
have been studied to |
control stress responses |
|
| SlMPK1 |
is |
p47-MBPK |
Solanum lycopersicum |
| OsFBK1 |
is induced by |
abscisic acid (ABA) |
Oryza sativa |
| brassinosteroids (BRs) |
play key roles in regulating |
responses to abiotic stresses |
|
| stress signaling pathways |
reduce |
photosynthetic efficiency |
|
| abscisic acid (ABA) |
responds to |
abiotic stress |
|
| drought-responsive element (DRE) binding factors (DREB) |
is also called |
cold-responsive element (CRT) binding factors (CBF) |
|
| plant stress responses |
involve changes in |
protein interactions |
|
| polyamines |
act as signals in |
plant stress tolerance |
|
| Calcium Protein Kinase8 |
is |
plasma membrane protein |
|
| MAPK cascades |
are known to regulate |
biotic stress response pathways |
|
| CALCINEURIN B-LIKE10 (ATCBL10, CBL10, SCABP8, AT4G33000) |
homolog shows |
increased copy number or basal-level expression in S. parvula |
Schrenkiella parvula; Arabidopsis thaliana |
| OsFBK1 |
transcript levels are higher in seedlings treated with |
abscisic acid (ABA) |
Oryza sativa |
| extracellular ATP (eATP) |
could serve as |
early signal of biotic stress |
|
| salt stress |
leads to decrease of |
gibberellic acid (GA) levels |
Arabidopsis thaliana |
| mitochondria |
can act as sensors and initiate |
stress responses in plants |
|
| Arabidopsis (ATMAPK6, ATMPK6, MAPK6, MPK6, AT2G43790) |
is involved in integrating and transducing |
signal transduction for stress responses |
Arabidopsis thaliana |
| differential responsiveness of Thellungiella and Arabidopsis to stresses |
may be evident at the level of |
hormones and secondary messengers upstream of the transcriptional response |
Thellungiella; Arabidopsis thaliana |
| unsaturated fatty acids (FA) |
are assumed to be involved in |
hypoxia/reactive oxygen species (ROS) signaling |
Arabidopsis thaliana |
| (ATMPK17, MPK17, AT2G01450) |
is essentially uncharacterized compared to |
(ATMAPK3, ATMPK3, MPK3, AT3G45640) and (ATMAPK6, ATMPK6, MAPK6, MPK6, AT2G43790) |
Arabidopsis thaliana |
| rising MEcDP (2-C-methylerythritol-2,4-cyclodiphosphate) levels |
may signal |
any broader changes in the physiology of the plant |
Arabidopsis thaliana |
| ethylene |
is important for |
plant responses to biotic and abiotic stresses |
|
| mitochondrial stress response |
overlaps with |
ABA (abscisic acid) signaling responses |
Arabidopsis thaliana |
| early signaling events |
are probably triggered by |
small perturbations in the environment |
|
| reactive oxygen species (ROS) |
serve as |
important signaling molecules in stress response |
|
| aldehyde dehydrogenase (ALDH) |
are NAD(P)+-dependent oxidoreductases that contribute to |
abiotic stress response |
|
| PA |
is a secondary messenger involved in |
stress signal transduction |
|
| responses to pathogen infection |
overlap with |
responses to mitochondrial dysfunction |
|
| plant stress responses |
involve changes in |
phytohormones |
|
| (TOR, AT1G50030) (target of rapamycin) |
is regulated in response to |
osmotic stress |
Arabidopsis thaliana |
| activities of regulatory components |
are controlled by |
post-translational modification or intracellular translocation |
|
| (ATMYB30, MYB30, AT3G28910) |
can link together |
reactive oxygen species (ROS) signaling, root cell elongation and plant immune response |
Arabidopsis thaliana |
| (ATR4, CYP83B1, RED1, RNT1, SUR2, AT4G31500) mutant |
shows pronounced effects on |
stress responses |
|
| sugars |
modulate |
stress responses |
|
| (AKIN10, KIN10, SnRK1, SnRK1α1, SNRK1.1, AT3G01090) kinases |
are central integrators of |
stress, carbon, and energy signaling |
|
| phosphatidic acid (PA) |
is involved in |
biotic/abiotic stress responses |
|
| siRNA translocation through the phloem |
is suggested as mechanism for |
long-distance communication |
Arabidopsis thaliana |
| exocyst |
is involved in regulation of |
stress responses |
|
| phenylpropanoids |
are indicators of |
plant stress responses upon variation of light or mineral treatment |
|
| Ca2+ |
functions as |
messenger system in response to external stresses |
|
| lipid signaling |
provides suggestive link between |
chromatin-modifying activity |
Arabidopsis thaliana |
| direct manipulation of the active form of a regulator |
could bypass |
control from upstream modifier |
|
| (MED25, PFT1, AT1G25540) |
is involved in |
abiotic stress responses |
|
| RALFs and CrRLK1Ls |
link |
abiotic and biotic stress responses |
|
| plant hormones |
implicated in |
responses to biotic and abiotic environmental stresses |
|
| S-group bZIPs |
are involved in |
stress responses |
Arabidopsis thaliana |
| (ATRBOHD, DELT1, RBOHD, AT5G47910) |
plays important role in |
systemic signaling upon challenge by biotic and abiotic stresses |
|
| regulatory genes |
are |
important stress regulators |
|
| ABA-activated kinase (AAPK) |
belongs to |
SnRK2 family of kinases |
Vicia faba |
| transcriptional programs |
are essential for |
stress responses in plants |
|
| Arabidopsis (ARAKIN, ATMEKK1, MAPKKK8, MEKK1, AT4G08500) |
is transcriptionally up-regulated by |
drought stress |
Arabidopsis thaliana |
| BABA |
induces |
stress response |
Arabidopsis thaliana |
| ABA-independent signal transduction cascade |
is |
one of at least two independent signal transduction pathways in plants under abiotic stresses |
|
| heavy metal stress |
is influenced by |
ROS signaling |
|
| 35S-TaABC1 plants |
had high transcript levels of |
(DREB2, DREB2A, AT5G05410) |
Arabidopsis thaliana |
| (ATHDA6, AXE1, HDA6, HDAC6, RPD3B, RTS1, SIL1, AT5G63110) |
plays important role in |
plant response to abiotic stresses |
Arabidopsis thaliana |
| soldat mutants |
promote |
constitutive stress response in the nucleus |
Arabidopsis thaliana |
| Pleiotropic Regulatory Locus 1 |
coordinates |
stress responses |
Arabidopsis thaliana |
| MAPK pathway |
is easily activated by |
environmental stresses (such as wounding, touch, etc.) |
|
| ABA-activated kinase (AAPK) |
is homologous to |
(SNRK2-2, SNRK2.2, SPK-2-2, SRK2D, AT3G50500) (SNRK2-3, SNRK2.3, SRK2I, AT5G66880) and (ATOST1, OST1, P44, SNRK2-6, SNRK2.6, SRK2E, AT4G33950) |
Arabidopsis thaliana |
| hydrogen peroxide (H2O2) at low concentrations |
acts as |
signal molecule involved in adaptation to abiotic and biotic stresses |
|
| tethering complexes |
have roles in |
abiotic stress responses |
|
| nitrogen starvation |
signals |
terrein involvement in seed germination inhibition and lesion production |
|
| redox state of cells |
regulates |
responses to the environment |
|
| mitogen-activated protein kinases (MAPKs) signaling |
activates |
oxidative stress signaling |
|
| β-ionone |
contributes to |
abiotic stress response |
|
| CcCIPK14 |
might be involved in tolerance to |
various stresses |
Cajanus cajan |
| primary cell wall |
is involved in |
biotic/abiotic stress response |
|
| RsbQ and RsbP binding |
initiates |
downstream signaling cascade |
Bacillus subtilis |
| RALFs |
play key roles in |
plant stress responses |
|
| abiotic stress signals |
include |
ABA |
|
| target of rapamycin (TOR, AT1G50030) protein kinase |
plays central role in regulating |
stress responses |
|
| salt-stress-triggered cleavage and activation of RALF22/23 by SITE-1 PROTEASE (ATS1P, ATSBT6.1, S1P, AT5G19660) |
causes |
(FER, AT3G51550) internalization |
|
| plant elicitor peptides (Peps) |
are |
DAMPs |
|
| ROS |
act as signalling molecules during |
abiotic stress |
|
| reactive oxygen species (ROS) |
play key roles in regulating |
drought and salt stresses signaling |
|
| allene oxide synthase (AOS, CYP74A, DDE2, AT5G42650) mutant root growth |
is as sensitive to phytoprostane PPA1 as |
wild-type root growth |
Arabidopsis thaliana |
| caleosin |
may have key signaling roles in |
development and abiotic stress tolerance |
|
| plasma membrane (PM) integrity surveillance |
might be essential for |
plant stress responses |
|
| plasma membrane (PM) |
plays central role in perception and relay of |
information about external stimuli |
|
| abscisic acid (ABA) |
affects |
shared components of stress signaling |
|
| ABA |
is activated under |
drought stress |
Glycine max |
| VOC analysis |
should be extended to |
abiotic stress responses |
|
| ABA |
promotes |
growth inhibition |
|
| MAPK cascades |
are involved in |
plant stress responses |
|
| Polycomb group (PcG) |
coordinate |
stress responses |
|
| ROS |
is suggested to play a role in |
stress responses |
|
| (MED25, PFT1, AT1G25540) |
is involved in |
biotic stress responses |
|
| calcium gradients |
can be imaged with corresponding |
cytoskeleton dynamics near nucleus |
|
| nitric oxide (NO) |
regulates |
adaptive responses to abiotic stresses |
|
| subtle changes in reactive oxygen species (ROS) production |
can act as |
initial signal of stress |
|
| blumenols |
contribute to |
abiotic stress response |
|
| environmental stress cues |
trigger |
rapid intracellular changes of Ca2+ ion concentration |
|
| abscisic acid |
is vital in regulating |
stress response |
|
| microRNAs (miRNAs) |
control |
stress responses |
|
| flavonols acting as reactive oxygen species (ROS) scavengers and inhibitors of auxin transport |
modulate |
responses to abiotic stresses |
|
| bls1 low expression |
showed increase in |
abscisic acid |
|
| CIPKs and CBLs |
commonly play a regulatory role in |
plants |
|
| nuclear bodies |
reversibly form in reaction to |
osmotic stress |
|
| triacylglycerols (TAGs) |
is involved in |
stress responses in plant vegetative tissues |
|
| ethylene |
plays pivotal role in |
abiotic stress responses |
|
| inhibition of oxidative phosphorylation |
results in de-repression of |
(ATPK10, CIPK15, PKS3, SIP2, SNRK3.1, AT5G01810) expression |
Oryza sativa |
| anthocyanin |
accumulates upon |
BABA treatment |
Arabidopsis thaliana |
| ABA |
was detected in |
G. elata |
Gastrodia elata |
| abscisic acid (ABA) |
modulates |
plant response to biotic stress |
|
| Rapid alkalinization factor (RALFs) |
are |
DAMPs |
|
| stress responses |
is context for |
cellular events |
Arabidopsis thaliana |
| ethylene |
regulates |
responses to stress |
|
| mitochondrial alternative oxidase (AOX) |
is involved in |
H2O2 signalling |
Oryza sativa |
| glutamate receptor-like calcium-permeable channels |
have conserved roles in |
general stress responses |
Arabidopsis thaliana |
| AP2-family genes |
respond to |
cold, salt, and drought stress |
Arabidopsis thaliana |
| ethylene |
is involved in |
responses to abiotic stresses |
|
| inositol 1,4,5-trisphosphate (IP3) and 1,2-diacylglycerol (DAG) |
are |
second messengers in stress signalling |
|
| ROS at non-lethal levels |
influence |
stress responses |
|
| high light stress |
is influenced by |
ROS signaling |
|
| (DREB2, DREB2A, AT5G05410) expression |
underwent increased expression under normal conditions in |
35S-TaABC1 plants |
Arabidopsis thaliana |
| hexenal |
is |
stress response distributor |
|
| mitogen-activated protein kinase (MAPK) |
is activated by |
osmotic stress |
|
| CaSnRK2.6 (Capsicum annuum sucrose non-fermenting 1-related protein kinase 2.6) |
is homolog of |
Arabidopsis (ATOST1, OST1, P44, SNRK2-6, SNRK2.6, SRK2E, AT4G33950) (OPEN STOMATA 1) |
Capsicum annuum; Arabidopsis thaliana |
| Arabidopsis (CIPK3, SnRK3.17, AT2G26980) |
was previously shown to physically interact with |
(ATCBL9, CBL9, AT5G47100) |
Arabidopsis thaliana |
| CcCIPK14 |
might play important roles together with |
CcCBL1 or AtCBL9-like proteins |
Cajanus cajan; Arabidopsis thaliana |
| glutathione |
has crucial functions in |
stress responses |
|
| trehalose |
is implicated in |
stress response |
|
| in vivo substrates of stress-responsive protein kinases |
remain |
unknown |
|
| identification of the in vivo substrates of stress-responsive protein kinases or other post-translational modifiers |
is |
one of the great challenges ahead |
|
| F-box proteins |
play important roles in regulating |
stress responses |
|
| plant proteostasis |
is important for |
stress responses |
|
| high-light stress signaling |
converges with |
abscisic acid (ABA) signaling |
Arabidopsis thaliana |
| (PLD, PLDALPHA1, AT3G15730) in plasma membrane |
generates PA when activated by |
multiple stress-related signals |
|
| high temperature stress |
is influenced by |
ROS signaling |
|
| post-translational modifications such as phosphorylation |
is possible mechanism for |
activation by AZC |
Oryza sativa |
| SsLTP1 gene expression |
is regulated through |
distinct pathways under non-freezing low temperature and osmotic treatments |
Solanum sogarandinum; Solanum tuberosum |
| abscisic acid (ABA) |
regulates |
abiotic environmental stresses |
|
| heat stress (HS) |
cross-talk exists between |
oxidative stress signalling |
|
| plants |
evolved |
complex signaling networks |
|
| selective modifications of lipid and/or recognition of specific lipid features |
seems to be crucial for controlling |
biotic and abiotic stress signaling |
|
| ROS |
may mainly regulate |
stromule formation |
|
| complex receptor formation |
analysis is essential for understanding |
sophisticated role of plasma membrane in stress response |
Arabidopsis thaliana |
| promoter region in a phytochrome-regulated gene |
is required for |
down-regulation in response to oxidative stress or high light |
|
| OsMAPK2 |
was not induced by |
HS (heat shock) |
Oryza sativa |
| abscisic acid (ABA) |
is synthesized in response to |
many abiotic stresses |
|
| N-myristoylation |
is considered crucial in |
plant signal transduction in response to environmental stress |
|
| Ccrboh gene |
accumulates in tissue-specific pattern during |
jasmonic acid (JA) treatment |
Citrullus colocynthis |
| transcription factors (TFs) |
mediate |
stress signal transduction pathways |
|
| abscisic acid (ABA) |
crosstalk in |
stress responses |
|
| MAPK signalling |
interacts with |
ABA signalling pathways |
|
| protein kinases |
have important roles in |
stress signalling |
|
| mycorradicins |
contribute to |
abiotic stress response |
|
| phosphatidic acid and polyphosphoinositides |
accumulate in response to |
biotic and abiotic stresses |
|
| reactive oxygen species (ROS) |
regulates |
responses to the environment |
|
| Os09g35010 |
encodes |
(ATCBF1, CBF1, DREB1B, AT4G25490) transcription factor |
Oryza sativa |
| glutathione (GSH) |
is essential component of |
plant stress response |
|
| ascorbate |
has crucial functions in |
stress responses |
|
| BABA |
acts as |
stress agent |
Arabidopsis thaliana |
| extracellular ATP |
was shown to act as |
signal potentially in wound and stress response |
|
| host–pathogen interactions |
stimulate |
biphasic PA response |
|
| phospholipase C (PLC) |
catalyzes hydrolysis of |
phosphatidylinositol 4,5-bisphosphate (PIP2) |
|
| Arabidopsis AP2-family genes |
function as |
important mediators of responses to environmental stress signals |
Arabidopsis thaliana |
| low temperature stress |
is influenced by |
ROS signaling |
|
| chitinase activity |
can be induced by |
ethylene, jasmonic and salicylic acid, auxin, cytokinin, and abscisic acid (ABA) |
|
| hydrogen peroxide (H2O2) |
is considered as |
central signalling molecule in plant responses to biotic and abiotic stresses |
|
| reactive oxygen species (ROS) |
are involved in |
regulation of multiple plant responses to a variety of stresses |
|
| nitric oxide |
is probably involved in transmitting |
stress signal to EIN2-associated (ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) pathway |
Arabidopsis thaliana |
| interconnected regulatory pathways |
steer |
stress responses |
|
| HvNAC013 |
was shown to be elevated in response to |
abscisic acid (ABA) |
Hordeum vulgare |
| Executer proteins |
form part of |
signalling network for the perception of environmental perturbation in plants |
Arabidopsis thaliana |
| cytokinin metabolism |
is highly regulated during |
response to abiotic stress |
|
| H2O2 |
can act as |
signal |
|
| 35S-TaABC1 plants |
had high transcript levels of |
(KIN1, AT5G15960) |
Arabidopsis thaliana |
| abscisic acid (ABA) treatment |
induces proteins which are or may be linked to |
stress response |
Vitis vinifera |
| OsMAPK2 transcripts and kinase activity |
similar activation effects were found on |
AZC treatment |
Oryza sativa |
| abscisic acid (ABA) |
is |
important signal against various stresses |
|
| slight drop in RWC |
triggers |
long-distance signal transduction |
|
| EXECUTER1 (EX1, EXE1, AT4G33630) |
plays a crucial role in |
regulating the singlet-oxygen-triggered retrograde signaling pathway |
|
| reactive oxygen species |
may act as |
signalling intermediates |
|
| Arabidopsis (ARAKIN, ATMEKK1, MAPKKK8, MEKK1, AT4G08500) |
is transcriptionally up-regulated by |
cold stress |
Arabidopsis thaliana |
| (ATCBF3, CBF3, DREB1A, AT4G25480) expression |
showed no clear changes in |
35S-TaABC1 plants |
Arabidopsis thaliana |
| AA oxidation to DHA |
constitutes |
vital signal transduction module governing plant reaction to stressful environmental conditions |
|
| signalling cross-talk |
occurs in |
biotic stress signalling |
|
| phytochrome signaling |
converges with |
abscisic acid (ABA) signaling |
Arabidopsis thaliana |
| Arabidopsis (AtWIND1, ERF59, RAP2.4, WIND1, AT1G78080) and its homologous genes |
may share conserved function in mediating responses to |
light and other environmental stresses |
Arabidopsis thaliana |
| (GAI, RGA2, AT1G14920) |
is responsive to |
salt stress, ABA and ethylene |
Solanum tuberosum subsp. tuberosum |
| jasmonic acid (JA) |
regulates |
abiotic defense responses |
|
| (ABF3, AtABF3, DPBF5, AT4G34000) (KIN1, AT5G15960) and (ATCBF1, CBF1, DREB1B, AT4G25490) |
are thought to be involved in |
different stress regulation pathways |
|
| phospholipids |
modulate |
stress processes |
|
| phosphatidylinositol transfer proteins (PITPs) |
have proposed roles in |
physiological stress responses |
|
| extrachromosomal circular DNA (eccDNA) |
contribute to |
stress response |
|
| mitogen-activated protein (MAP) kinase gene |
is more strongly expressed in |
SL15 genotype |
Oryza sativa |
| ABA-dependent signal transduction cascade |
is |
one of at least two independent signal transduction pathways in plants under abiotic stresses |
|
| plants |
trigger |
orchestrated complex network of signal events |
|
| (ATPGLP2, ATPK5, PGLP2, AT5G47760) (AtRPK1, RPK1, AT1G69270) |
is induced by |
abscisic acid and abiotic stress conditions |
Arabidopsis thaliana |
| eATP |
plays signal role in |
plant stress response |
|
| zaxinone |
contributes to |
abiotic stress response |
|
| ethylene |
is activated under |
drought stress |
Glycine max |
| apple MdTRB1 |
responded to |
multiple hormones and stresses |
Malus domestica |
| target of rapamycin (TOR, AT1G50030) protein kinase |
is modulated by |
stress inputs |
|
| plasma membrane (PM) structure |
analysis is essential for understanding |
sophisticated role of plasma membrane in stress response |
Arabidopsis thaliana |
| BR-induced ROS production |
is important for |
BR-induced stress tolerance in cucumber and tomato |
Solanum lycopersicum; Cucumis sativus |
| nitric oxide |
is suggested to be |
signalling component that mediates stress responses |
|
| calcium signalling |
leads to |
retrograde regulation |
Arabidopsis thaliana |
| H2O2 |
is generated by plants during response to |
pathogen attack |
|
| condensate-PM interactions |
are involved in |
signal transduction during biotic and abiotic stress |
|
| hormone signalling (e.g. ethylene or abscisic acid) |
may be playing an additional role in |
response to organ removal stress |
|
| TaABC1 |
may act upstream of |
(DREB2, DREB2A, AT5G05410) (COR78, LTI140, LTI78, RD29A, AT5G52310) (ABF3, AtABF3, DPBF5, AT4G34000) (KIN1, AT5G15960) and (ATCBF1, CBF1, DREB1B, AT4G25490) |
Arabidopsis thaliana |
| cross-talk of signalling pathways in plants |
is speculated to be |
common phenomenon |
|
| transient Ca 2+ content in cells |
presumably results in |
acquired tolerance/resistance to environmental stresses |
|
| C20+ VLCPUFAs |
play roles in |
abiotic stress responses in plants |
|
| ROS |
crosstalk in |
stress responses |
|
| high soil salinity |
may be triggered by |
multiple signals |
Mesembryanthemum crystallinum |
| plant chitinases |
play important roles in |
stress response |
|
| (ABCG36, ATABCG36, ATPDR8, PDR8, PEN3, AT1G59870) / (PLEIOTROPIC DRUG RESISTANCE8/PENETRATION RESISTANCE3) |
was shown to be phosphorylated by |
range of biotic and abiotic stimuli |
Arabidopsis thaliana |
| abscisic acid and salicylic acid |
mediate |
plant responses to abiotic stress |
|
| SV channel mediated increase of free cytosolic Ca2+ of ≤70 nM min−1 |
is by several orders of magnitude slower than |
the Ca2+ responses to most abiotic stresses |
|
| MAP kinases in yeast |
are activated by |
multiple stresses including acid stress |
Saccharomyces cerevisiae |
| SnRK2 family members in Arabidopsis thaliana |
9 out of 10 members activated upon |
osmotic stress |
Arabidopsis thaliana |
| sugar-signalling |
is connected with |
ABA signalling |
|
| (AOS, CYP74A, DDE2, AT5G42650) signalling |
may be associated with |
nitric oxide (NO) |
|
| DHA (dihydroascorbate) |
acts supposedly upstream of |
H2O2 production by NADH oxidase and ABA synthesis |
|
| reactive oxygen species (ROS) |
form |
important group of signal mediators |
|
| DHA (dihydroascorbate) |
is potential factor in |
signalling pathway |
|
| DHA (dihydroascorbate) |
can modulate |
plant responses to stress in different ways, regulating ABA synthesis and increasing hydrogen peroxide production |
|
| cytoplasmic calcium concentration ([Ca2+]cyt) |
changes occur during |
drought |
|
| phosphoinositide levels |
show transient changes during |
plant responses to environmental stresses |
|
| abscisic acid (ABA) |
is stress signal in |
castor bean plants |
Ricinus |
| abscisic acid (ABA) biosynthesis, signalling, and molecular effects |
are activated under |
water-, salt-, and cold-stress |
|
| (ABF3, AtABF3, DPBF5, AT4G34000) expression |
underwent increased expression under normal conditions in |
35S-TaABC1 plants |
Arabidopsis thaliana |
| Eukaryotic cold shock domain proteins |
are involved in |
stress responses |
|
| microRNA (miRNA) pathway |
is involved in |
response to abiotic stresses |
|
| stress perception and signalling pathways |
are |
multiple and some specific whereas others cross-talk at various steps |
|
| plant hormones, such as ethylene |
are proposed to play an important role in |
plant thermotolerance |
|
| elevated levels of NO |
appear to act downstream of |
ROS in BR-induced stress tolerance |
|
| (ATMAPK3, ATMPK3, MPK3, AT3G45640) |
plays important roles in |
stress response |
Arabidopsis thaliana |
| 14-3-3 isoform specificity or different heterodimers |
may be involved in |
different stress perceptions/signalling |
Arabidopsis thaliana |
| class IV chitinases |
are implicated in |
response to abiotic stress |
|
| abscisic acid (ABA) |
serves as |
long-distance stress signal |
|
| LIN6 promoter |
is induced by |
ABA (abscisic acid) |
|
| root-yield-1.06 QTL |
does not show appreciable effects on |
leaf abscisic acid (L-ABA) concentration |
|
| stress responses in plants |
are mediated by |
temporal–spatial coordination between ROS and other signals |
|
| cross-talk between high light stress and responses to pathogens |
involves |
control of growth and development under optimal and stress conditions |
Arabidopsis thaliana |
| oxylipins |
participate in |
biotic or abiotic stress responses |
|
| (ATOST1, OST1, P44, SNRK2-6, SNRK2.6, SRK2E, AT4G33950) protein kinase |
is activated by |
low-humidity stress |
Arabidopsis thaliana |
| β-carotene oxidation products |
have been proposed to be |
stress signals that mediate gene responses to singlet oxygen (1O2) |
|
| calmodulin (CaM)-like (CML) |
have been implicated in |
abiotic stress responses |
|
| nitric oxide |
is involved in |
stress responses |
|
| mutants partially defective in BR biosynthesis |
compared with |
mutants defective in ABA biosynthesis and RBOH1-silenced plants |
Solanum lycopersicum |
| ERFs |
mediate |
biotic stress responses |
|
| MAPKs |
regulate |
biotic stress response |
|
| OXIDATIVE SIGNAL INDUCIBLE 1 (AGC2, AGC2-1, AtOXI1, OXI1, AT3G25250) |
is required for |
(ATMAPK6, ATMPK6, MAPK6, MPK6, AT2G43790) activation by reactive oxygen species |
Arabidopsis thaliana |
| 14-3-3 proteins |
are involved in |
stress responses |
|
| relatively high frequency of AAGTCAA cis-regulatory element (CRE) |
suggests that it plays a role in mediating |
more general stress signals |
Arabidopsis thaliana |
| (ATGPX7, GPX7, GPXL7, AT4G31870) and (ATGPX1, GPX1, GPXL1, AT2G25080) |
contribute to |
cross-talk between high light stress and responses to pathogens |
Arabidopsis thaliana |
| reciprocal grafting experiments with abscisic acid (ABA)-deficient wilty pea mutants |
have generally established that |
an abscisic acid (ABA)-deficient root system has little impact on xylem ABA concentration or stomatal closure in response to soil drying |
Pisum sativum |
| VTE compounds |
participate in |
plant responses to abiotic stress |
|
| (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) and (AtERF#092, ERF1, ERF1B, AT3G23240) |
differential regulation of pathogen attack and wound response by |
pathogen attack and wound response |
|
| reactive oxygen species (ROS) |
down-regulate |
photosynthesis-related genes |
|
| secondary oxidative stress |
leads to |
signaling responses |
|
| 35S-TaABC1 plants |
had high transcript levels of |
(ATCBF1, CBF1, DREB1B, AT4G25490) |
Arabidopsis thaliana |
| (ATCBF1, CBF1, DREB1B, AT4G25490) expression |
underwent increased expression under normal conditions in |
35S-TaABC1 plants |
Arabidopsis thaliana |
| stress |
can cause influx of |
Ca2+ and H+ |
|
| sugar and starch metabolism |
is interconnected with |
hormone and ROS pathways |
|
| Lsp5cs and Lslea genes |
are regulated by |
ABA-dependent and ABA-independent pathways |
|
| cytoplasmic calcium concentration ([Ca2+]cyt) |
changes occur during |
osmotic stress |
|
| reduced iron |
is |
by-product from anaerobic bacterial activity acting as environmental signal for barrier formation |
|
| phosphorylation of (ACS2, AT-ACC2, AT1G01480) and (ACS6, ATACS6, AT4G11280) by stress-responsive MAPKs ( (ATMAPK3, ATMPK3, MPK3, AT3G45640) and (ATMAPK6, ATMPK6, MAPK6, MPK6, AT2G43790) ) |
causes |
(ACS2, AT-ACC2, AT1G01480) and (ACS6, ATACS6, AT4G11280) accumulation |
Arabidopsis thaliana |
| NO and NADPH oxidase-dependent oxidative bursts |
are regulated by |
MAPK signals |
Nicotiana benthamiana; Solanum lycopersicum |
| paraquat acclimation (PA) |
induced |
H2O2 accumulation at the apoplast |
Solanum lycopersicum |
| Executer proteins |
might participate in |
basal repression of defence responses in chloroplasts under normal irradiance |
Arabidopsis thaliana |
| dominant allele of receptor-like wall associated kinase (WAK2, AT1G21270) ( -cTAP fusion) |
triggers |
constitutive stress responses |
Arabidopsis |
| ABA |
activates |
(APX1B, APX2, AtAPX2, AT3G09640) promoter |
Arabidopsis thaliana |
| SNAREs (soluble N-ethyl-maleimide sensitive factor attachment receptor proteins) |
are engaged in |
stress responses |
|
| (ATNOA1, ATNOS1, NOA1, NOS1, RIF1, SVR10, AT3G47450) null mutants |
lack |
some NO-dependent stress responses |
Arabidopsis thaliana |
| ROS |
are |
important signaling molecules that ensure response to biotic and abiotic stresses |
|
| calcium and ethylene signaling molecules |
might be important for |
proper adaptation to plastid genome instability |
Arabidopsis thaliana |
| (ATGSTU24, GST, GSTU24, AT1G17170) expression |
is stimulated by |
H2O2 |
|
| PLDα1 and its cleavage product phosphatidic acid (PA) |
are important players in |
plant stress responses |
Arabidopsis thaliana |
| paraquat acclimation (PA) |
induced |
RBOH1 transcription |
Solanum lycopersicum |
| polyamines (PAs) |
regulate |
stress responses |
|
| (AP2, AtAP2, FL1, FLO2, AT4G36920) transcription factor family |
have been linked to |
stress responses |
|
| nitric oxide (NO) |
participates in |
stress responses |
|
| ethylene |
is involved in |
response to abiotic stresses |
|
| reactive oxygen species (ROS) |
are key messengers in |
plant responses to biotic and abiotic stresses |
|
| (ATCDPK3, ATCPK6, CPK6, AT2G17290) |
is a key component in activation of |
S-type anion channels induced by abiotic and biotic stimuli |
Arabidopsis thaliana |
| cold stimulation |
showed consistency in dynamics of response across |
cell types |
Arabidopsis thaliana |
| summation of behavior of many individual cells |
probably obscures |
underlying oscillatory nature of NaCl-induced intracellular Ca2+ increases in root cells |
Arabidopsis thaliana |
| chloroplast ROS |
provide warning that |
photosynthetic electron transport chain (PET) has been affected and plant must adapt to stress |
Arabidopsis thaliana |
| ABA |
could trigger |
apoplastic H2O2 generation |
|
| glutathione homeostasis |
could influence |
stress response |
|
| control mechanism involving oxidative stress and hormones |
may take place in |
fruits |
Solanum lycopersicum |
| Tobacco VCaB42 |
shows high homology to |
(ANNAT4, AtANN4, AT2G38750) |
Nicotiana tabacum; Arabidopsis thaliana |
| brassinosteroids (BRs) |
induce |
nitric oxide (NO) |
|
| MAPK signalling |
interacts with |
NO signalling pathways |
|
| BRs |
could trigger |
apoplastic H2O2 generation |
|
| soil water deficit |
also triggers an increase in |
leaf ABA concentration ([ABA]) at high RH |
|
| virus-induced gene silencing of (ATMPK1, MPK1, AT1G10210) |
compromises |
associated stress responses |
Solanum lycopersicum |
| a significant increase in endogenous H2O2 level at the apoplast |
is associated with |
upregulation of RBOH1 transcription |
Solanum lycopersicum |
| mitogen-activated protein kinase (MAPK) cascades |
regulate |
stress responses |
|
| NAC transcription factor family |
is key regulatory family for |
abiotic stress responses |
Hordeum vulgare |
| transient spike of cytokinin |
occurs in |
initial response to stress |
|
| elongator complex in Arabidopsis thaliana |
mediates part of |
response to abiotic stress |
Arabidopsis thaliana |
| cytosolic Ca2+ signaling in response to abiotic or biotic stresses |
has been documented extensively |
in literature |
|
| plants |
were treated for |
up to 2h with 50 μM ABA or 1000 ppm CO2 |
Arabidopsis thaliana |
| (ATMPK4, MAPK4, MPK4, AT4G01370) mutant |
shows upregulation of genes related to |
stress responses |
Arabidopsis thaliana |
| MAPKs |
are activated in response to |
drought and other environmental stresses |
|
| (ASK2, SNRK2-1, SNRK2.1, SRK2G, AT5G08590) ; (CIPK9, PKS6, SnRK3.12, AT1G01140) / (CIPK3, SnRK3.17, AT2G26980) |
are significantly down-regulated in |
(ATTOP6B, BIN3, HLQ, HYP6, RHL3, TOP6B, AT3G20780) |
Arabidopsis thaliana |
| paraquat acclimation (PA) |
induced |
NADPH oxidase activity |
Solanum lycopersicum |
| (AT-PHH1, ATCRY2, CRY2, FHA, PHH1, AT1G04400) domains |
are involved in |
stress responses |
|
| Ca2+ |
plays vital roles in |
response to environmental stimuli |
|
| softened green berries cultured on medium with exogenous ABA |
was used to evaluate |
effect of exogenous ABA application |
Vitis vinifera |
| HvNAC013 protein |
interacts with |
RADICAL-INDUCED CELL DEATH 1 protein (ATP8, AtRCD1, CEO, CEO1, RCD1, RIMB1, AT1G32230) |
Hordeum vulgare |
| ABA signalling |
is mediated by |
ROS and NO |
|
| liming |
increased |
root-derived xylem sap abscisic acid (ABA) |
Pisum sativum |
| elongator complex subunit 2 (AtELP2, ELP2, AT1G49540) |
participates in |
abiotic stress responses |
Arabidopsis thaliana |
| link between stress and the cytoskeleton |
could be |
largely indirect |
|
| AHLs (AT-hook containing proteins) |
activate |
stress responses |
Arabidopsis thaliana |
| sucrose non-fermenting-related kinase 2 family (SnRK2) |
activated upon |
salt and osmotic stress |
Zea mays; Triticum aestivum L.; Glycine max; Nicotiana tabacum |
| phosphatidic acid |
rapidly accumulates in response to |
several stress conditions |
|
| increases in [Ca 2+] cyt observed in response to H 2 O 2 |
differ markedly to that of ozone in both magnitude and temporal dynamics |
increases in [Ca 2+] cyt observed in response to ozone |
|
| accumulation of ABA |
result in |
increased tolerance |
|
| (ATMAPK3, ATMPK3, MPK3, AT3G45640) (ATMPK4, MAPK4, MPK4, AT4G01370) and (ATMAPK6, ATMPK6, MAPK6, MPK6, AT2G43790) |
act redundantly in |
osmotic stress response |
Arabidopsis thaliana |
| abscisic acid (ABA) |
is |
abscisic acid |
|
| H2O2 |
plays important functions in |
plant stress responses |
|
| MAPK cascade |
participates in |
several stress responses |
Arabidopsis thaliana |
| RBOHs |
regulate signalling in response to |
wounding stress |
Arabidopsis thaliana |
| liming |
increased both root and leaf xylem sap abscisic acid (ABA) concentrations equally over |
unlimed controls |
Pisum sativum |
| ABA-mediated abiotic stress signaling |
interact antagonistically with |
SA and JA/ET biotic stress signaling |
Arabidopsis thaliana |
| VOZs |
might integrate |
abiotic and biotic stress signals |
Arabidopsis thaliana |
| hydrogen sulfide (H2S) |
acts as |
gasotransmitter |
|
| sensory hub |
decodes |
stress-related signal signatures |
|
| cytokinins (CKs) |
regulate |
environmental stress responses |
Arabidopsis thaliana |
| ethylene gas |
is essential for |
stress responses |
|
| cross-talk among different stress signalling pathways |
occurs in |
TaABC1-induced stress responses |
Arabidopsis thaliana |
| (AtCLO3, AtRD20, CLO-3, CLO3, PXG3, RD20, AT2G33380) |
is involved in |
generation of oxidized fatty acids in stress-related signalling pathways |
Arabidopsis thaliana |
| ROS (specifically H2O2) |
can act as a signal for |
turning on stress-related genes |
|
| further increase of H 2 O 2 production |
and |
BR-induced stress responses |
|
| (AKIN10, KIN10, SnRK1, SnRK1α1, SNRK1.1, AT3G01090) protein kinase |
is |
regulator of starvation stress responses in plants |
|
| RBOHs |
regulate signalling in response to |
cold stress |
Arabidopsis thaliana |
| (ATMPK2, MPK2, AT1G59580) (ATMAPK3, ATMPK3, MPK3, AT3G45640) (ATMPK4, MAPK4, MPK4, AT4G01370) and (ATMAPK6, ATMPK6, MAPK6, MPK6, AT2G43790) |
are all activated under |
heavy metal stress |
|
| chloroplasts |
can act as sensors and initiate |
stress responses in plants |
|
| (AOX1A, ATAOX1A, AtHSR3, HSR3, AT3G22370) rpoTmp response to the simultaneous restriction of the cytochrome and alternative respiratory pathways |
likely overlaps with |
ABA signaling |
Arabidopsis thaliana |
| limitation of the capacity of the cytochrome oxidase |
results in |
unique and overlapping responses in Arabidopsis depending on the growth conditions |
Arabidopsis thaliana |
| stress responses |
are regulated at |
chromatin level |
|
| MAPK1 |
is involved in |
stress responses |
|
| virus-induced gene silencing of (ATMPK2, MPK2, AT1G59580) |
compromises |
associated stress responses |
Solanum lycopersicum |
| activity of INVs and SUSs |
were suggested to be involved in |
plant stress responses and signalling cascades |
|
| WRKY transcription factor family |
have been linked to |
stress responses |
|
| diverse functional interactions between NO and ABA |
range to |
different responses to stress |
|
| cytokinins (CKs) |
play major roles in |
stress responses |
|
| biotic stresses |
activate |
signal transduction pathways |
|
| (AP2, AtAP2, FL1, FLO2, AT4G36920) transcription factors |
play essential roles in |
stress response |
Arabidopsis thaliana |
| increased wall peroxidase expression |
could serve as |
key convergence point in the signaling pathways that cross over in stress signaling networks |
|
| wounding and mechanical pressure |
trigger |
release of ATP |
|
| stress |
alters |
Ca 2+ level |
|
| ROS production |
is associated with |
activation of anion channels |
|
| brassinosteroids (BRs) |
involved in |
stress response |
|
| (ATCIPK6, CIPK6, SIP3, SNRK3.14, AT4G30960) null mutation |
abolished |
CBP-mediated induction of (COR78, LTI140, LTI78, RD29A, AT5G52310) |
Arabidopsis thaliana |
| protons |
can serve as |
second messengers in plant cells |
|
| virus-induced gene silencing of RBOH1 |
compromises |
associated stress responses |
Solanum lycopersicum |
| Ca2+ |
could also be involved in |
acclimation and cross-tolerance |
|
| abiotic and biotic stress responses |
have similarities in |
recognition and signalling pathways |
|
| lack of (AtMYB60, MYB60, AT1G08810) transcripts in the mutant |
is perceived by guard cell as |
signal that triggers a stress response |
Arabidopsis thaliana |
| osmotic stress |
can activate |
signaling pathways |
|
| ethylene |
mediates |
plant stress responses |
|
| LjMYB36 |
affects |
stress responses |
Lotus japonicus |
| SSB1 |
regulates |
stress responses |
Fusarium oxysporum |
| abscisic acid (ABA) |
is |
key stress signaling hormone |
Arabidopsis thaliana |
| both Ser171 and Ser175 in Arabidopsis OPEN STOMATA 1 (ATOST1, OST1, P44, SNRK2-6, SNRK2.6, SRK2E, AT4G33950) |
were phosphorylated after |
hyperosmotic or abscisic acid treatment |
Arabidopsis thaliana |
| Type one protein phosphatases (TOPPs) |
modulate |
stress responses |
|
| Cryptochromes (CRYs) |
are involved in mediating |
enhancement of stress responses |
Arabidopsis thaliana |
| (AtbZIP, bZIP, AT1G68880) transcription factors |
is translocated to nucleus upon |
hypo-osmotic shock |
Arabidopsis thaliana |
| Ca2+ |
is implicated in regulating |
stress responses |
|
| cold stress |
is mediated by |
EF-hand proteins |
|
| transcriptional response of ozone-responsive vesicle transport genes |
is not induced by |
[Ca 2+ ] cyt changes stimulated by other oxidative stresses and ROS |
Arabidopsis thaliana |
| Ghd7 |
might be involved in |
stress pathways |
Oryza sativa |
| ROS and reactive nitrogen species |
may add |
specific feedback inputs under diverse environmental stresses |
Arabidopsis thaliana |
| Hsf-dependent negative regulation |
provides evidence for interconnection of Hsf in regulation of |
biotic and abiotic responses |
|
| limitation of the capacity of the alternative oxidase |
results in |
unique and overlapping responses in Arabidopsis depending on the growth conditions |
Arabidopsis thaliana |
| large area exposure to white light |
likely triggers |
uniform systemic stress response involving broader signaling and defense mechanisms |
Arabidopsis thaliana |
| other abiotic stress cues |
may establish |
specificity in the pathway |
|
| ABA |
is used in |
transient ABA treatment |
Hordeum vulgare; Zea mays |
| mild cold, PQ, or drought pretreatment |
triggers |
a significant increase in endogenous H2O2 level at the apoplast |
Solanum lycopersicum |
| circadian clock |
enables the plant to trigger |
stress responses |
|
| chromatin remodelling and modifying enzymes |
may be direct targets of |
stress signalling pathways |
|
| reactive oxygen species (ROS) |
can serve as |
signaling molecules that help plants adapt to stress conditions |
Arabidopsis thaliana |
| diamine oxidases (DAO) |
plays important roles in |
defence responses against abiotic stress |
|
| cell flattening and smaller cell size phenotype |
might be related to |
alterations in regulatory pathways after sensing lack in cell wall/cuticle integrity |
|
| (ATMAPK6, ATMPK6, MAPK6, MPK6, AT2G43790) mutant |
suppresses |
exacerbated stress responses |
Arabidopsis |
| SnRK2 family members in Oryza sativa |
all 10 members activated upon |
osmotic stress |
Oryza sativa |
| TbSRPPs |
may mediate |
abiotic stress responses |
Taraxacum brevicorniculatum |
| BBX proteins |
play critical roles in |
stress responses |
|
| polyamine oxidases (PAO) |
plays important roles in |
defence responses against biotic stress |
|
| abscisic acid (ABA) |
is involved in |
stress responses |
|
| (PPR40, AT3G16890) mutants |
are hypersensitive to |
abscisic acid (ABA) |
Arabidopsis thaliana |
| osmotic stress |
leads to |
phosphorylation of mitochondrial pyruvate dehydrogenase complex (mtPDC) |
|
| calcium-dependent protein kinase (CDPK) |
is activated by |
abscisic acid (ABA) |
|
| natural variation in biochemical and metabolic pathways |
affects |
stress responses |
|
| WNKs |
may play role in |
abiotic stress |
Arabidopsis thaliana |
| (ATGCN2, GCN2, AT3G59410) N-terminal kinase domain |
turns on |
downstream signaling |
yeasts; mammals |
| calcium |
can serve as |
second messengers in plant cells |
|
| (SNRK2-3, SNRK2.3, SRK2I, AT5G66880) (ATCIPK6, CIPK6, SIP3, SNRK3.14, AT4G30960) /SOS3-INTERACTING3; (ATSR2, ATSRPK1, CIPK7, PKS7, SnRK3.10, AT3G23000) ; (ATCIPK14, ATSR1, CIPK14, PKS24, SnRK3.15, SR1, AT5G01820) /PSK24 |
are significantly up-regulated in |
(ATTOP6B, BIN3, HLQ, HYP6, RHL3, TOP6B, AT3G20780) |
Arabidopsis thaliana |
| MAPKs |
regulate |
abiotic stress response |
|
| SlAREB1 OE lines |
could have |
abiotic stress signal activated |
Solanum lycopersicum |
| 14-3-3 proteins |
are found to stabilize |
AREB/ABF transcription factor family |
Arabidopsis thaliana |
| regulatory genes |
are originally isolated and characterized based on |
transcriptional induction by various stresses |
|
| brassinosteroids (BRs) |
play key roles in regulating |
responses to biotic stresses |
|
| abscisic acid (ABA) |
is involved in |
adaptive response to abiotic stresses |
|
| heat |
triggers |
phosphatidylinositol 4,5-bisphosphate (PIP2) response |
|
| Attpc1-2 seedlings and plants |
show behavior consistent with |
response to cold, hyperosmotic, salt, and oxidative stress |
Arabidopsis thaliana |
| ABA |
is |
stress hormone |
|
| HKMTs |
are known to be involved in |
stress responses |
|
| OsPP18 |
regulates ROS homeostasis through |
ABA-independent pathways |
Oryza sativa |
| nitric oxide (NO) |
modulates |
stress responses |
Arabidopsis thaliana |
| loss of complex I |
induces changes in genes involved in |
stress responses |
|
| UV-B exposure |
triggers |
stress responses |
|
| signalling effect of hydrogen sulphide |
is fast and similar to |
signalling effect of stagnant conditions |
|
| reduced mechanical strength due to reduced cross-linking |
could induce |
cell wall integrity response mechanism |
Brachypodium distachyon |
| mitochondrial proteins and transcripts |
showed upregulation of genes involved in |
mitochondrial stress signaling |
Arabidopsis thaliana |
| NAC transcription factors |
are involved in |
various plant stress responses |
Arabidopsis thaliana |
| abscisic acid (ABA) |
is involved in |
biotic stress responses |
|
| ABA (abscisic acid) |
is |
common stress response (CSR) hormone |
|
| H2S |
is a global regulator of |
plant stress responses |
Arabidopsis thaliana |
| jasmonic acid (JA) |
participates in |
stress responses |
Arabidopsis thaliana |
| RNAi |
participates in |
stress response |
fungi |
| intracellular Ca2+ in response to stress signals |
was first identified based on |
intracellular Ca2+ elevations detected in seedlings constitutively expressing aequorin |
Arabidopsis thaliana |
| N-glycosylation |
is required for |
salt stress responses |
|
| (AtbZIP, bZIP, AT1G68880) transcription factor |
is involved in |
regulation of stress signaling |
Arabidopsis thaliana |
| cold and hydrogen peroxide stimulus-induced intracellular free Ca2+ concentration ([Ca2+]i) dynamics |
are common to |
all cell types tested |
Arabidopsis thaliana |
| deubiquitinating enzymes |
are involved in |
stress response |
Fusarium graminearum |
| elevated chloroplast ROS levels in why1why3polIb-1 |
are perceived by cells and lead to |
genetic reprogramming |
Arabidopsis thaliana |
| apparent absence of genetic reprogramming in low-light-grown why1why3polIb-1 plants |
further supports |
ROS-mediated genetic reprogramming hypothesis |
Arabidopsis thaliana |
| increased cytosolic Ca2+ levels |
leads to activation of |
nuclear factor (NF)-κB |
|
| strigolactone (SL) |
play a pivotal role in |
abiotic stress responses |
|
| NaCl-induced oscillatory intracellular Ca2+ signals in vasculature and spongy mesophyll cells |
are indicative of |
role in signal transduction and regulation of NaCl-regulated downstream responses |
Arabidopsis thaliana |
| conserved WD-protein |
functions as |
global regulator of sugar, stress, and hormone responses |
Arabidopsis thaliana |
| SnRK2 family |
is |
family of 10 kinases |
Arabidopsis thaliana |
| FERONIA (FER, AT3G51550) |
alters |
ROS bursts in leaf cells |
|
| phosphatidic acid (PA) |
act in |
stress signaling and acclimation |
Arabidopsis thaliana |
| (−)-loliolide |
is |
general signal of plant stress |
|
| epidermis |
is the location of |
major mechanical stimulation-induced intracellular Ca2+ signals |
Arabidopsis thaliana |
| receptor-like kinases |
are often involved in pathways that detect |
biotic and abiotic stresses |
|
| genes upregulated in Mp cry ge plants |
were associated with |
response to water deprivation |
Marchantia polymorpha |
| (CPK28, AT5G66210) |
has roles in |
stress responses |
Arabidopsis thaliana |
| canonical intracellular Ca2+ response to stress stimuli |
exhibits considerable variation dependent on |
signal applied |
Arabidopsis thaliana |
| GOLDEN2-LIKE (GLK) |
have diverse roles in |
stress responses |
|
| mechanical stimulation-induced intracellular Ca2+ signals |
are largely restricted to |
epidermal pavement cells in the leaf |
Arabidopsis thaliana |
| 35S:PYL4 A194T plants |
are primed for |
accelerated response to stress conditions |
Arabidopsis thaliana |
| NaCl |
induces |
intracellular Ca2+ elevation |
Arabidopsis thaliana |
| NaCl |
appears to alter only |
steady-state intracellular Ca2+ in guard cell |
Arabidopsis thaliana |
| jasmonic acid (JA) |
is involved in |
stress responses |
|
| protein kinases |
are often involved in pathways that detect |
biotic and abiotic stresses |
|
| (APX1, ATAPX01, ATAPX1, CS1, MEE6, AT1G07890) |
is S-nitrosylated |
S-nitrosylation |
|
| reactive oxygen species (ROS) |
participate in |
responses to biotic and abiotic environmental cues |
|
| OsbZIP47 homologs |
influence |
stress responses |
|
| hydrogen sulfide (H2S) secreted by Cronobacter muytjensii strain JZ38 |
induces |
plant resistance to abiotic and biotic stress |
|
| TIC |
affects gene expression for |
abiotic stress response |
Arabidopsis thaliana |
| polyamine oxidases (PAO) |
plays important roles in |
defence responses against abiotic stress |
|
| nitric oxide (NO) |
may be |
link between polyamine (PA)-mediated stress responses |
|
| comprehensive network of signaling pathways |
includes |
transduction of stress signals |
|
| abscisic acid (ABA) |
mediates |
environmental stress responses |
|
| hyperosmotic stress |
triggers |
phosphatidylinositol 4,5-bisphosphate (PIP2) response |
|