Notice: Database construction is still in progress. Certain features may be incomplete, slower than usual, or temporarily unavailable while we re-ingest the knowledge graph with citation data. Thank you for your patience.
← All pathways

jasmonic acid signaling

17634 relationships annotated with this phrase. Showing first 500 of 17634.
Source entity Relationship Target entity Species
GhMYC3 downstream genes are significantly enriched in pathways associated with oxidative stress responses, flowering time, signal transduction, metabolic process, JA, root development, and embryo development Gossypium hirsutum
point mutation D94N in the JAZ-interacting domain of (MYC3, AT5G46760) abolishes interaction with most JAZ proteins Arabidopsis thaliana
MdNAC72-MdABI5 interface combines with MdJAZ2 Malus domestica
NbBBLd expression does not increase following exposure to methyl jasmonate (MeJA) Nicotiana benthamiana
P. syringae suppresses SA responses by inducing coronatine-mediated JA signaling Arabidopsis thaliana
(AIB, ATAIB, bHLH017, bHLH17, JAM1, AT2G46510) (bHLH013, bHLH13, JAM2, AT1G01260) and (bHLH003, bHLH03, bHLH3, JAM3, AT4G16430) expression decreased in coi1-1 mutant Arabidopsis thaliana
(ATVSP2, VSP2, AT5G24770) expression significantly increased in MJ-treated jam x3 plants Arabidopsis thaliana
inhibitors of JA signaling block induction of Momilactone B by (−)-loliolide
JA receptor was definitively elucidated a few years later
WT apple plants treated with exogenous ABA upregulates JA signaling and synthesis genes Malus domestica
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) mutant exhibited longer roots than wild-type Arabidopsis thaliana
(IAA26, PAP1, AT3G16500) (DFR, M318, TT3, AT5G42800) and (ATVSP2, VSP2, AT5G24770) expression phenotypes in 0.5% Suc attenuated by (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) mutation Arabidopsis thaliana
FERONIA (FER, AT3G51550) phosphorylates and destabilizes (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) (myelocytomatosis proteins 2)
(AtERF#092, ERF1, ERF1B, AT3G23240) expression induced by MJ treatments Arabidopsis thaliana
2-wk-old cotton seedlings are treated with MeJA treatment Gossypium hirsutum
(AIB, ATAIB, bHLH017, bHLH17, JAM1, AT2G46510) (bHLH013, bHLH13, JAM2, AT1G01260) and (bHLH003, bHLH03, bHLH3, JAM3, AT4G16430) have redundant functions antagonistic to (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) in JA responses Arabidopsis thaliana
97 genes corresponding to 90 probes regarded as candidate downstream targets of JAMs Arabidopsis thaliana
14 genes encoding transcription factors found among 98 genes regulated by JAMs Arabidopsis thaliana
wild-type plants support slower growth of aphids Arabidopsis thaliana
JA-responsive genes expressed at higher levels in Bla-2 included CORONATINE-INDUCED PROTEIN1, JASMONATE RESPONSIVE1, and JASMONATE RESPONSIVE2 Arabidopsis thaliana
GST-ZTL pulls down most MBP-His-JAZs Nicotiana attenuata
jasmonic acid acts through the regulation of MdERF genes and ethylene biosynthetic genes by MdMYC2 Malus domestica
TCP transcription factors are involved in JA signaling pathway Arabidopsis thaliana; Oryza sativa
gene encoding a basic helix-loop-helix (bHLH) transcription factor in nearest neighbor clade with JAZ genes Arabidopsis thaliana
jam1jam2 double mutant exhibited intermediate root lengths between wild-type and jam x3 Arabidopsis thaliana
MdPYL4 enhanced disease resistance by promoting accumulation of JA Malus domestica
Arabidopsis (MED25, PFT1, AT1G25540) interacted with transcription factor (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) Arabidopsis thaliana
(LCR77, PDF1.2, PDF1.2A, AT5G44420) expression almost comparable to wild-type in MJ-treated jam x3 plants Arabidopsis thaliana
JAMs negatively regulate (ANAC019, ANAC19, NAC019, AT1G52890) expression Arabidopsis thaliana
(ERF59, ORA59, AT1G06160) levels in myc2jam x3 higher than (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) mutant and closely correlated to (LCR77, PDF1.2, PDF1.2A, AT5G44420) Arabidopsis thaliana
JA accumulation leads to proteasome-dependent degradation of (JAZ9, TIFY7, AT1G70700)
(ANAC019, ANAC19, NAC019, AT1G52890) and (AtERF#092, ERF1, ERF1B, AT3G23240) can be target points of JAMs to negatively regulate downstream metabolic genes Arabidopsis thaliana
caterpillar (Pieris rapae) and early thrips (Frankliniella occidentalis) herbivory are known to activate JA signaling Arabidopsis thaliana
LOV domain of (ADO1, FKL2, LKP1, ZTL, AT5G57360) is sufficient to bind JAZb Nicotiana attenuata
increased JA concentration (4 µg g−1 fresh weight) is considered high enough to promote JA signaling pathway Oryza sativa
enhanced resistance was accompanied by suppression of jasmonic acid-dependent pathway Oryza sativa
MeJA treatment improves MdNAC72 promoter activity Malus domestica
MdPYL4-RNAi transgenic line exhibits reduced expression of MdMYC2 Malus domestica
cluster 7 includes 128 early and strong JA- and wound-responsive genes Arabidopsis thaliana
8 probes showed enhanced MJ-responsive reduction in jam x3 compared with wild-type Arabidopsis thaliana
(IAA26, PAP1, AT3G16500) (AtMYB47, MYB47, AT1G18710) (ERF113, RAP2.6, AT1G43160) and (AT1G10585) can be target points by JAMs to regulate JA-responsive metabolic genes Arabidopsis thaliana
blocking of PIF action by DELLA proteins inhibits growth
WT plants show expression of VSP2 marker not induced Arabidopsis thaliana
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) overexpression ( OE) plants shows phenotype of MYC2-dependent JA pathway activity Populus trichocarpa
plants exposed to control and fresh damage volatiles did not show significant differences in jasmonic acid (JA) and jasmonic acid-isoleucine (JA-Ile) levels Gossypium hirsutum
jam2jam3 double mutant exhibited intermediate root lengths between wild-type and jam x3 Arabidopsis thaliana
(AtERF#092, ERF1, ERF1B, AT3G23240) and (LCR77, PDF1.2, PDF1.2A, AT5G44420) expression profiles not consistent with jam x3 phenotype Arabidopsis thaliana
knocking down NlVg reduced levels of JA and JA-Ile induced by the ovary extract
MeJA is produced in plants in response to wounding by herbivore pathogens Arabidopsis thaliana
(AtJAZ1, JAZ1, TIFY10A, AT1G19180) expression increased by 50 μm methyl jasmonate (MJ) treatment Arabidopsis thaliana
WT-GmBIR1 samples had significantly higher level of JA-Ile Glycine max
epistatic relationship between myc mutations and jazD is consistent with the hypothesis that one or more JAZ proteins repress the ability of (MYC3, AT5G46760) to boost (TRP, AT3G56390) metabolism Arabidopsis thaliana
JA corepressor (JAZ6, TIFY11B, AT1G72450) inhibits activity of Populus (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) transcription factors Populus
Response to JA stimulus (GO:0009753) is common to both FS and 3- to 24-h data sets Arabidopsis thaliana
jasmonic acid and JA-Ile levels peak at around 45 min after treatment Nicotiana attenuata
(COI1, AT2G39940) regulates nicotine biosynthesis Nicotiana attenuata
Activation of the JA pathway via de-repression of MYC transcription factors leads to induced expression of VEGETATIVE STORAGE PROTEIN 2 (ATVSP2, VSP2, AT5G24770) Arabidopsis thaliana
MeJA treatment continuously induces transcription of MdNAC72 Malus domestica
coexpression gene networks constructed with 2,220 JA-responsive genes Arabidopsis thaliana
JAM genes expression positively regulated by (COI1, AT2G39940) and (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) Arabidopsis thaliana
(ANAC019, ANAC19, NAC019, AT1G52890) expression in myc2jam1jam2 and myc2jam x3 almost comparable to (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) mutant Arabidopsis thaliana
vegetative storage protein1 (ATVSP1, VSP1, AT5G24780) constitutive expression mutant shows reduced population expansion of green peach aphids (Myzus persicae) Arabidopsis thaliana; Myzus persicae
similarity of gene expression profiles between spider mite- and methyl jasmonate/OPDA-triggered responses suggested that JA-mediated signaling is important in Arabidopsis defense responses to spider mite herbivory Arabidopsis thaliana
CORONATINE INSENSITIVE1B (OsCOI1b) is JA signaling component gene Oryza sativa
JASMONATE ZIM-DOMAIN PROTEIN8 (OsJAZ8) is JA signaling component gene Oryza sativa
(AGB1, ATAGB1, ELK4, AT4G34460) mutant is impaired in induction of (LCR77, PDF1.2, PDF1.2A, AT5G44420) by methyl jasmonate (MeJA) Arabidopsis thaliana
(AtERF#092, ERF1, ERF1B, AT3G23240) expression in MJ-treated myc2jam1jam2 and myc2jam x3 higher in (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) mutant Arabidopsis thaliana
(ANAC019, ANAC19, NAC019, AT1G52890) expression enhanced MJ-inducible expression in jam1jam2 and jam x3 Arabidopsis thaliana
JA-Ile peak concentration is significantly lower in ir-ztl lines compared with EV plants 45 min after treatment Nicotiana attenuata
12-hydroxy-JA and dicarboxy-JA-Ile levels accumulate equally in ir-ztl and EV under all treatments Nicotiana attenuata
OsTCP21 is involved in synthesis and signaling of JA in response to cold stress Oryza sativa
methyl jasmonate (MeJA) would demonstrate disease-rescue effect on wild-type and transgenic rice Oryza sativa
jasmonic acid induces expression of (LCR77, PDF1.2, PDF1.2A, AT5G44420) Arabidopsis thaliana
(ADO1, FKL2, LKP1, ZTL, AT5G57360) and (COI1, AT2G39940) contribute to and perhaps function independently in regulation of JAZ-MYC2 module Nicotiana attenuata
coi1-1 mutant plants are hypersensitive to thrips Arabidopsis thaliana
fad3-2 fad7-2 (AtFAD8, FAD8, AT5G05580) triple mutant is susceptible to infection by Pythium spp. Arabidopsis thaliana
jasmonic acid (JA)-inducible serine protease inhibitors have been used as reliable markers of jasmonic acid (JA)-induced tomato defenses to spider mite herbivory Solanum lycopersicum
wild-type rice showed JA signaling reporter gene and JA synthesis/signaling components induced by Guy11 infection at early stage Oryza sativa; Magnaporthe oryzae
defense responses induced by Nilaparvata lugens mucin-like protein (NlMLP) in plant cells are related to JA signaling pathway Oryza sativa
JA synthesis and signaling are affected by (MIR319, MIR319B, AT5G41663) /OsTCP21 regulatory module Oryza sativa
(PDF1.2b, AT2G26020) is induced by jasmonic acid application Arabidopsis thaliana
B. cinerea and A. brassicicola trigger JA-responsive pathway Arabidopsis thaliana
coi1-16 mutant plants in low-K medium experienced lethal thrips damage thrips damage Arabidopsis thaliana
jasmonic acid (JA)-Ile is major biologically active jasmonate
Jas domain of JAZb is not sufficient for full-length (ADO1, FKL2, LKP1, ZTL, AT5G57360) binding Nicotiana attenuata
oleic acid (FA18:1) reduction indicates that fatty acid signaling affects jasmonic acid (JA) signaling Arabidopsis thaliana
jasmonic acid (JA) biosynthesis and signaling are central to Arabidopsis's defense Arabidopsis thaliana
miR319-mediated regulation of OsTCP21 might affect rice resistance against blast disease by manipulating JA signaling Oryza sativa
(COI1, AT2G39940) mutant shows extremely severe fatty acid changes due to severe defect in jasmonic acid (JA) signaling Arabidopsis thaliana
2-aminoadipate may induce jasmonic acid (JA) accumulation in HFL rice Oryza sativa
TIFY domain-containing N-terminal sequence of JAZb is sufficient for full-length (ADO1, FKL2, LKP1, ZTL, AT5G57360) binding Nicotiana attenuata
JA-responsive genes in the FS sample (149) included regulators of hormonal responses Arabidopsis thaliana
transient in planta expression of Mp10 activates jasmonic acid (JA) signaling pathway
hevein-like chitinase is associated primarily with JA responses Nicotiana benthamiana
majority of JAZs in N. attenuata bind to MYC2a and MYC2b Nicotiana attenuata
JAM genes are negative regulators of (ATVSP2, VSP2, AT5G24770) expression but not of (LCR77, PDF1.2, PDF1.2A, AT5G44420) Arabidopsis thaliana
(ERF59, ORA59, AT1G06160) expression independent from jam x3 Arabidopsis thaliana
mite feeding induces the expression of JASMONATE-ZIM-DOMAIN PROTEIN repressors Arabidopsis thaliana
NbPR3 is chitinase gene associated with JA-dependent defenses Nicotiana benthamiana
defense responses triggered by Nilaparvata lugens mucin-like protein (NlMLP) are associated with JA signaling pathway Nicotiana benthamiana
jasmonic acid levels show increased or decreased level in only one ir-ztl line compared with EV plants under some treatments ir-ztl lines Nicotiana attenuata
JA stress responses may play major role in connection between different metabolic pathways and endosperm appearance in HFL rice Oryza sativa
(LCR77, PDF1.2, PDF1.2A, AT5G44420) mRNA induced levels in hsf mutant plants exceed (LCR77, PDF1.2, PDF1.2A, AT5G44420) mRNA induced levels in WT plants Arabidopsis thaliana
(MYC3, AT5G46760) interacts with (JAZ8, TIFY5A, AT1G30135)
JA-Ile basal levels and levels 90 min after treatment are not different between ir-ztl and EV plants Nicotiana attenuata
Magnaporthe oryzae strain Guy11 suppresses jasmonic acid (JA) signaling Oryza sativa
MiSSP7 not only prevents the degradation of PtaJAZ6 Populus trichocarpa; Laccaria bicolor
MeJA treatment rapidly activates transcription of MdABI5 Malus domestica
plant defensin 1.3 (PDF1.3, AT2G26010) is one of the JA biosynthesis and signaling genes Arabidopsis thaliana
jasmonic acid (JA)-insensitive mutant coronatine-insensitive1 (COI1, AT2G39940) supports more rapid growth of aphids Arabidopsis thaliana
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) expression was not altered by aphid infestation Arabidopsis thaliana
JASMONATE RESPONSIVE2 is JA-responsive gene Arabidopsis thaliana
S. littoralis treatment causes JAs to peak at around 45 min Nicotiana attenuata
salicylic acid (SA) regulates JA-responsive genes Arabidopsis thaliana
PR1b responds to jasmonic acid Nicotiana tabacum
(MYC3, AT5G46760) responds more slowly and mildly to JA
fresh weights of MYC3–OE1 are significantly reduced compared with fresh weights of wild-type seedlings Arabidopsis thaliana
fresh weights of MYC3–OE2 are significantly reduced compared with fresh weights of wild-type seedlings Arabidopsis thaliana
Chlorella fusca application highly upregulates PLANT DEFENSIN 1.2 (LCR77, PDF1.2, PDF1.2A, AT5G44420) Arabidopsis thaliana
JA signalling pathway was activated in GhnsLTPsA10-silenced plants Gossypium hirsutum
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) binds to promoter of (ERF115, AT5G07310) Arabidopsis thaliana
cross-talk between JA and other hormone signaling pathways prioritizes JA responses Arabidopsis thaliana
genes up-regulated during K-starvation and down-regulated upon K re-supply is transcriptional profile most clearly related to JA signaling Arabidopsis thaliana
(MYC3, AT5G46760) interacts with (JAZ9, TIFY7, AT1G70700)
MYC3–OE2 seedlings shows relative root length of 30% of root length without JA treatment Arabidopsis thaliana
transgenic plants with overexpression of (MYC3, AT5G46760) are hypersensitive to JA treatment Arabidopsis thaliana
(ATWRKY11, WRKY11, AT4G31550) and (ATWRKY17, WRKY17, AT2G24570) are positive regulators of (AOS, CYP74A, DDE2, AT5G42650) Arabidopsis thaliana
MYC3–OE1 seedlings shows relative root length of 27.6% of root length without JA treatment Arabidopsis thaliana
(LCR77, PDF1.2, PDF1.2A, AT5G44420) expression is significantly upregulated by >2-fold in Chlorella fusca-treated Arabidopsis leaves compared with control leaves at 12 hpi with Pseudomonas syringae pv. tomato DC3000 Arabidopsis thaliana
JA pre-treatment reduces Frankliniella occidentalis numbers on Brassica rapa Brassica rapa; Frankliniella occidentalis
MYC3–OE1 is severely inhibited by MeJA compared with wild-type (Col-0) seedlings Arabidopsis thaliana
gain-of-function experiments of several genes of group IX suggested that they might play roles in regulation of JA-responsive genes Arabidopsis thaliana
genes participating in jasmonic acid (JA) signaling includes 13-LOX, 9-LOX, (ACX3, ATACX3, AT1G06290) Solanum tuberosum
MYC3–OE1 shows increased expression level of (MYC3, AT5G46760) Arabidopsis thaliana
MYC3–OE2 is more sensitive to JA-inhibitory root growth Arabidopsis thaliana
allantoin activates MYC2-regulated jasmonic acid (JA) signaling pathway Arabidopsis thaliana
change of (REM11, VAL, AT5G60140) /Ile to Ala in (COI1, AT2G39940) leads to switch in JAs ligand specificity from dn-iso-OPDA to (+)-7-iso-JA-Ile
(MYC3, AT5G46760) interacts with (JAS1, JAZ10, PW220, TIFY9, AT5G13220)
seedling sizes of MYC3–OE1 are much smaller than wild-type seedling sizes Arabidopsis thaliana
increase in JA-mediated defense during K-deficiency has evolved to counteract increased susceptibility to biological enemies
CORONATINE INSENSITIVE 1-jasmonate zinc-finger inflorescence meristem domain (JAZ) protein complex is receptor for jasmonates
eight probes whose expression was down-regulated by both stress treatments but not from stages S0 to S2 included gibberellin (GA)-regulated protein and defence response protein and S-adenosyl-L-methionine:jasmonic acid (SAM:JA) carboxyl methyltransferase
jasmonic acid (JA) employs COI1-independent signaling pathways Arabidopsis thaliana
thrips attack is dependent on (COI1, AT2G39940) Arabidopsis thaliana
DEGs revealed enrichment in JA signaling Arabidopsis thaliana
MeJA level is decreased in GmPLDα1OE roots compared to GUS roots Glycine max
jasmonic acid (JA) has been implicated in regulation of plant resistance responses
ALLENE OXIDE SYNTHASE 2 (AOS2) overexpression increases resistance to Magnaporthe grisea Oryza sativa
DELLA proteins binding to JAZ proteins activates expression of JA-responsive genes
prophylactic defense response is mediated by jasmonic acid (JA) and CORONATINE INSENSITIVE 1 (COI1, AT2G39940)
(MYC3, AT5G46760) interacts with (AtJAZ1, JAZ1, TIFY10A, AT1G19180)
(MYC3, AT5G46760) interacts with (JAZ6, TIFY11B, AT1G72450)
MYC3–RNAi1 contains about 70% of wild-type (MYC3, AT5G46760) Arabidopsis thaliana
T-DNA insertion mutant of (MYC3, AT5G46760) did not show clear defects in JA response Arabidopsis thaliana
(ATWRKY11, WRKY11, AT4G31550) and (ATWRKY17, WRKY17, AT2G24570) are positive regulators of (ATLOX2, LOX2, AT3G45140) Arabidopsis thaliana
JA-dependent signal pathway induces resistance to necrotrophs
MdJAZ2 interferes with interaction between MdbHLH3 and promoter of MdMYB9 Malus domestica
JAZ proteins interact with (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640)
jar1-1 mutant shows no significant difference in pathogen population density between Chlorella fusca-treated and BG11 medium-treated leaves Arabidopsis thaliana
jasmonate (JA), methyl JA (MeJA) and jasmonoyl-l-isoleucine (JA-Ile) levels are decreased in GmPLDα1OE hairy roots compared to GUS hairy roots Glycine max
MeJA level is increased in GmPLDα1KD roots compared to GUS roots Glycine max
plants can respond to jasmonic acid (JA) signaling
ureide allantoin has been shown to induce expression of JA-responsive genes Oryza sativa
ALLENE OXIDE SYNTHASE 2 (AOS2) overexpression increases PATHOGENESIS-RELATED 1 (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) gene expression Oryza sativa
coi1-2 seedlings shows growth not affected by MeJA treatment Arabidopsis thaliana
dinor-oxo-phytodienoic acid (dnOPDA) level is increased in GmPLDα1OE compared to GUS hairy roots Glycine max
C-terminal Jas motif of JAZ proteins bind (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640)
Mediator subunit integrates effects of general splicing factors into specific signaling pathway
induction of PME activity by Pseudomonas syringae pv maculicola ES4326 was contributed to by (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) branch of jasmonic acid signaling Arabidopsis thaliana; Pseudomonas syringae pv maculicola ES4326
responses to methyl jasmonate/OPDA clustered together with mite-triggered responses Arabidopsis thaliana
differential metabolites (DMs) and differentially expressed genes (DEGs) involved in stress response most were involved in JA pathway Oryza sativa
relative content of N δ-acetyl-Orn was increased by 20-fold in HFL mature seeds Oryza sativa
OsTCP21 is involved in synthesis and signaling of JA in response to virus infection Oryza sativa
single-cell ablation of the root elongation zone does not trigger robust JA response Arabidopsis thaliana
potassium (K) deficiency induces jasmonic acid (JA) signal
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) interacts with all 12 JAZ proteins
JA-Ile content is increased in GmPLDα1KD roots compared to GUS hairy roots Glycine max
(ERF115, AT5G07310) is also activated by JA/MYC2-dependent homologue (ERF109, RRTF1, AT4G34410) Arabidopsis thaliana
(ATPEPR1, PEPR1, AT1G73080) is transcriptionally induced by methyl jasmonate (MeJA) Arabidopsis thaliana
jasmonate is perceived by (COI1, AT2G39940) Arabidopsis thaliana
HopZ1a acetylation of JAZ proteins leads to activation of JA signaling
VEGETATIVE STORAGE PROTEIN 2 (ATVSP2, VSP2, AT5G24770) had increased transcript levels in MYC overexpression seedlings Arabidopsis thaliana
JA content accumulation were determined in potato plants after insect attack Solanum tuberosum
JAZ4.2 has reduced affinity for (COI1, AT2G39940) Arabidopsis thaliana
JAZ4.1 interacts with (COI1, AT2G39940) Arabidopsis thaliana
JA-Ile content is decreased in GmPLDα1OE roots compared to GUS hairy roots Glycine max
JAZ4.2 interacts with (MYC3, AT5G46760) Arabidopsis thaliana
plant 'odorant-binding proteins' include CORONATINE INSENSITIVE 1-jasmonate zinc-finger inflorescence meristem domain (JAZ) protein complex
vegetative storage protein (VSP) expression level is significantly increased in AevPAL1-silenced plants Aegilops variabilis
JAZ4.2 retains functionality of JA signaling repression Arabidopsis thaliana
jasmonic acid-mediated phytohormone signaling pathways mediate long term resistance to herbivores
(MED25, PFT1, AT1G25540) (PRP39, PRP39a, AT1G04080) and (ATPRP40A, PRP40A, AT1G44910) module keeps balance between JAZ splice variant-mediated repression of MMC and JAZ degradation-mediated activation of MMC
DAP-seq, RNA-seq, Histone ChIP, Proteomics, Phosphoproteomics enable identification of novel TFs of JA responses downstream of master TF (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) Arabidopsis thaliana
self-DNA induced jasmonic acid-dependent defense responses
(ATNIG1, bhlh28, MYC5, NIG1, AT5G46830) did not show interaction with (AtJAZ1, JAZ1, TIFY10A, AT1G19180) Arabidopsis thaliana
JAZ genes are among earliest genes induced by JA signalling Arabidopsis thaliana
TaWRKY78 is weakly affected by MeJA treatment Triticum aestivum
COR/MeJA role in JA-signalling pathway
JA-deficient plants are usually more susceptible towards herbivore attacks
GFP::JAZ4.1 protein is degraded within 20 min of exposure to 2 µM COR Arabidopsis thaliana
apple MdTRB1 plays role in jasmonic acid (JA)-mediated plant developmental processes Malus domestica
critical amino acid residues of the Jas domain are retained for interaction with NINJA and MYC transcription factors Arabidopsis thaliana
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) is repressed by C-terminal Jas motif of JAZ proteins
hormone-dependent degradation of JAZ repressors leads to derepression (activation) of MMC
JA-induced de novo production of JAZ splice variants strictly depends on (MED25, PFT1, AT1G25540)
12-oxo-phytodienoic acid (OPDA) level is increased in GmPLDα1OE compared to GUS hairy roots Glycine max
JAZ splicing variants retain ability to repress (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640)
(MED25, PFT1, AT1G25540) plays critical role in preventing excessive desensitization of JA signaling mediated by JAZ splice variants
(MYC3, AT5G46760) interacts with (JAZ2, TIFY10B, AT1G74950)
(MYC3, AT5G46760) interacts with (JAZ5, TIFY11A, AT1G17380)
methyl-JA may cause increased production of inositol 1,4,5-trisphosphate (InsP3) Arabidopsis thaliana
altering JA accumulation can affect herbivore host selection
MeJA treatment of coi1-16 seedlings reduces root length to 79.1% of control Arabidopsis thaliana
endogenous jasmonic acid (JA) release occurs without concurrent wound stimulation Arabidopsis thaliana
coi1-1 mutant is JA-insensitive mutant Arabidopsis thaliana
MJ application in EV plants increased NaTPI activity levels 9.5-fold in EV plants Nicotiana attenuata
jasmonic acid (JA) may bind to JAZ1–SCF–COI1 receptor complex
TIBA-treated WT plants shows lower expression of (LCR77, PDF1.2, PDF1.2A, AT5G44420) Arabidopsis thaliana
(TAT, TAT3, AT2G24850) is induced upon Pectobacterium cucumerina infection in TIBA-treated WT plants Arabidopsis thaliana
jasmonic acid is known to mediate plant defences
ability of hl plants to produce PI-II in response to wounding indicates that mutant is probably not defective in JA-induced changes in leaf chemistry Solanum lycopersicum
JA-amido synthetase catalyzes formation of biologically active JA–Ile conjugate Arabidopsis thaliana
GFP::JAZ4.1 protein displays reduction in protein levels of approximately 93% in response to COR Arabidopsis thaliana
germin-like protein is related to jasmonic acid signaling pathway Pyrus pyrifolia Nakai
dominant JAZ splice variants repress MMC
restricted cell damage in root meristematic zones triggers JA signaling Arabidopsis thaliana
coronatine binds to AtCOI1/AtJAZ
expression patterns of (TAT, TAT3, AT2G24850) and (ATLOX3, LOX3, AT1G17420) were not impaired in axr1-12 and axr2-1 mutants upon Pectobacterium cucumerina infection Arabidopsis thaliana
(ABCD1, ACN2, AtABCD1, CTS, PED3, PXA1, AT4G39850) mutants have reduced JA levels
100 μM JA is component of JA treatment spray solution Oryza sativa
jasmonic acid (JA) signaling pathway is activated in (AT-SYR1, ATSYP121, ATSYR1, PEN1, SYP121, SYR1, AT3G11820) (ATSYP122, SYP122, AT3G52400) double mutant
endogenous production and perception of jasmonates is required for induction of NaHD20 mRNA levels Nicotiana attenuata
overexpression of (MYC3, AT5G46760) and (MYC4, AT4G17880) produced JA-related phenotype, anthocyanin accumulation Arabidopsis thaliana
dnOPDA level is decreased in GmPLDα1KD relative to GUS hairy roots Glycine max
JAZ4.1 participates in repression of canonical JA signaling Arabidopsis thaliana
binding of jasmonic acid (JA) to JAZ1–SCF–COI1 receptor complex may involve inositolpolyphosphates
JASMONATE INSENSITIVE1 (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) encodes (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) transcriptional activator Arabidopsis thaliana
JA pathway response mutants such as coi1-1 and jar1-1 showed that JA plays a key role in Arabidopsis resistance to Pythium sp., Pectobacterium cucumerina and Botrytis cinerea Arabidopsis thaliana
higher expression level of (ATCTIMC, CYTOTPI, TPI, AT3G55440) in Rivera compared to Christmas Drumhead probably result of higher expression level of (ATLOX2, LOX2, AT3G45140) in Rivera Brassica oleracea
myc2-1 mutant is less sensitive to JA for root meristem size
JA-signalling pathway coordinates primary and secondary metabolism
jasmonates have key regulatory role Solanum lycopersicum
NaBAK1 silencing impaired accumulation of JA-Ile after wounding Nicotiana attenuata
(ARF1-BP, ARF2, AtARF2, HSS, ORE14, AT5G62000) seedlings have responses to MJ similar to wild-type seedlings Arabidopsis thaliana
NaGSNOR-VIGS plants challenged with W+W showed reduced JA accumulation Nicotiana attenuata
MJ treatment resulted in same transcript levels of NaJAZ3 and NaTD in NaGSNOR-VIGS and EV plants Nicotiana attenuata
JA-Ile is responsible for eliciting most of the JA-induced responses
JA (methyl jasmonate) treatment increased PhERF1–PhERF8 mRNA levels Petunia hybrida
methyl jasmonic acid (JA) induced little expression of (ATWRKY48, WRKY48, AT5G49520) Arabidopsis thaliana
Arabidopsis thaliana Col gl wild-type seedlings displays response to root growth inhibition induced by MeJA Arabidopsis thaliana
degradation of JAZ repressors releases (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) transcription factors
24 differentially expressed genes are involved in jasmonic acid signaling pathway Gossypium hirsutum
methyl jasmonate (MeJA) is applied as chemical treatment
methyl jasmonate treatment reduced specific guaiacol peroxidase activity of PM vesicles Zea mays
(AtTEM1, EDF1, TEM1, AT1G25560) and RAV3 transcripts after MJ treatment decrease 20 h after MJ treatment Arabidopsis thaliana
ectopic expression of HAHB4 stimulates increased accumulation of JA Arabidopsis thaliana
dde2-2 plants support enhanced growth of Plutella xylostella caterpillars Arabidopsis thaliana; Plutella xylostella
enhanced susceptibility of (AXR1, AT1G05180) to different isolates of the soil-borne pathogen Pythium spp correlated with a defect in JA signaling Arabidopsis thaliana
5-d-old maize seedlings were treated with methyl jasmonate Zea mays
EV plants accumulate JA after wounding treatment Nicotiana attenuata
MdJAZ2 protein degradation releases MdbHLH3 Malus domestica
whole rosettes of 6 week old plants were treated with external application of methyl-JA Arabidopsis thaliana
NaGSNOR is required for wounding- and herbivory-induced accumulation of JA Nicotiana attenuata
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) transcription factors are responsible for activating JA response Arabidopsis
overexpression of (bHLH, AT5G51780) transcription factors caused increased transcript levels of JA-mediated wound-response genes Arabidopsis thaliana
subtle damage caused by needles does not seem to trigger JA pathway
JA transporter (ABCG16, AtABCG16, ATJAT1, JAT1, AT3G55090) transports jasmonyl-isoleucine (JA-Ile)
NaBAK1 negatively modulates JA-induced (ATCTIMC, CYTOTPI, TPI, AT3G55440) levels Nicotiana attenuata
G-proteins have possible roles in JA signalling Arabidopsis thaliana
JA content is decreased in GmPLDα1OE roots compared to GUS hairy roots Glycine max
alterations in plant cell wall structural polysaccharides can simulate signalling molecules and induce antistress response of jasmonic acid (JA) signalling
(ERF59, ORA59, AT1G06160) is major target for modulation by other hormones Arabidopsis thaliana
GSNOR-silenced plants decreased herbivory-induced accumulation of jasmonic acid (JA) Nicotiana attenuata
W+OS treatment in EV plants elicited 2-fold higher levels of JA by 1 h compared with W+W Nicotiana attenuata
NaHD20-silenced plants show similar accumulation of JA Nicotiana attenuata
methyl jasmonate induces expression of RACK1 Oryza sativa
loliolides induces jasmonic acid-related responses
pepper ERF gene CaPF1 was induced by JA
methyl jasmonate (MJ) is jasmonic acid derivative
MeJA treatment of wild-type seedlings reduces mature cell length to 46.7% of control Arabidopsis thaliana
coi1-16; F-box transgenic line shows statistical difference compared with wild-type in response to MeJA Arabidopsis thaliana
NaSIPK and NaWIPK are important regulators of wounding- and M. sexta herbivory-induced JA and JA–Ile accumulation Nicotiana attenuata
coi1-16 mutant was examined after various COI1 constructs had been introduced (COI1, AT2G39940) constructs Arabidopsis thaliana
MJ application in NaGSNOR-VIGS plants increased NaTPI activity levels only 1.7-fold in NaGSNOR-VIGS plants Nicotiana attenuata
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) interacts with (AtJAZ1, JAZ1, TIFY10A, AT1G19180) Arabidopsis thaliana
(MYC3, AT5G46760) associates with (JAI3, JAZ3, TIFY6B, AT3G17860) Arabidopsis thaliana
(MYC4, AT4G17880) associates with (AtJAZ1, JAZ1, TIFY10A, AT1G19180) Arabidopsis thaliana
(MYC4, AT4G17880) associates with (JAZ9, TIFY7, AT1G70700) Arabidopsis thaliana
jasmonic acid (JA) is key factor in resistance to biotic stress
JA mediates direct defence by inducing secondary metabolites
NaGSNOR is required for certain, but not all, JA-induced responses Nicotiana attenuata
Arabidopsis GH3-11 (JAR1) specifically adenylates jasmonic acid Arabidopsis thaliana
0.1mM JA treatment applied 7 days before four T. urticae infestation results in JA levels similar to control treatment Phaseolus lunatus; Tetranychus urticae
JA-repressed genes are downregulated in (FER, AT3G51550) mutants Arabidopsis thaliana
JA biosynthesis and responsive gene expressions are unaffected by red light treatment Ranunculus aquatica
GmERF081 expression rapidly accumulated until 5 h after JA treatment, and subsequently declined JA treatment Glycine max
gene expression was examined in response to methyl jasmonate (MeJA) Arabidopsis thaliana
coronatine (COR) utilizes (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) Arabidopsis thaliana
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) interacts with (JAI3, JAZ3, TIFY6B, AT3G17860) Arabidopsis thaliana
jasmonic acid (JA) plays key role in signal transduction pathway resulting in activation of induced defence response against insects and pathogens
AtHEL promoter contains JA-responsive elements Arabidopsis thaliana
JA-deficient plants are usually more susceptible towards pathogens
silencing NaBAK1 decreases wounding-induced jasmonic acid (JA) Nicotiana attenuata
brassinosteroid negatively acts on trichome formation by controlling some point of jasmonic acid pathway upstream of (COI1, AT2G39940) Solanum lycopersicum
sesquiterpene synthase expression seems to be jasmonic acid controlled Solanum lycopersicum
GmERF069 expression rapidly increased at 1 h after JA treatment, and remained at this high level of expression for at least 24 h JA treatment Glycine max
further transcriptome analyses showed that 29% of the JA-regulated genes are misregulated by the loss of the Gα subunit Arabidopsis thaliana
NaGSNOR modulates wounding- and simulated herbivory-induced levels of JA/JA-Ile Nicotiana attenuata
NaHD20-silenced plants show similar accumulation of JA–Ile Nicotiana attenuata
JA levels in transgenic Arabidopsis plants ectopically expressing HAHB10 differentially decrease after wounding Arabidopsis thaliana
JASMONATE-ZIM DOMAIN (JAZ) proteins repress JA signalling
(MYC3, AT5G46760) and (MYC4, AT4G17880) physically associate with JAZ repressors Arabidopsis thaliana
(AtCPB, CPB, AT1G71790) seems unable to activate JA pathway
TIC is involved in jasmonic acid-mediated root development
degradation of JASMONATE-ZIM-DOMAIN (JAZ) proteins frees transcriptional regulation activity of (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) Arabidopsis thaliana
myc2-1 mutant is less sensitive to JA compared with wild-type plants
0.1mM JA treatment increases PlOS transcript levels Phaseolus lunatus
TMV and Pseudomonas syringae infection has little or no effects on JA-dependent PI I and PI II transcript expression Solanum lycopersicum
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) (MYC3, AT5G46760) and (MYC4, AT4G17880) act as transcriptional activators during early JA signalling Arabidopsis thaliana
pTRV:PI-silenced plants exhibit significantly reduced PI I and PI II transcript expression Solanum lycopersicum
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) is involved in JA signaling Arabidopsis thaliana
N. attenuata accumulated high contents of JA Nicotiana attenuata
(ATWRKY70, WRKY70, AT3G56400) negatively regulates JA-dependent gene expression Arabidopsis thaliana
transcriptional responses in field-grown plants have been studied after exposure to methyl jasmonate
infiltrated leaves treated with coronatine Arabidopsis thaliana
JA (methyl jasmonate) treatment did not affect PhERF9, PhERF10, PhERF12, and PhERF13 mRNA levels Petunia hybrida
F-box protein is involved in de-repression of JA-signalling pathway through ubiquitination
DELLA proteins block action of PIFs
VmPR1c-mediated attenuation of jasmonic acid (JA) levels impairs JA-dependent immune responses Malus domestica
two-time treatment with NlVgN effect on hatch rate and number of eggs laid disappeared in rice lines with impaired JA pathway Oryza sativa
Laccaria bicolor effector MiSSP7 stabilizes JA corepressor (JAZ6, TIFY11B, AT1G72450) Laccaria bicolor; Populus
wild-type plants show higher sensitivity to exogenous JA in morning than in evening
accumulation of OPDA is associated with inhibition of germination Arabidopsis thaliana
observed changes in N allocation after simulated herbivory only indirectly depend on JA signaling Nicotiana attenuata
(COI1, AT2G39940) is required for jasmonic acid-regulated fertility Arabidopsis thaliana
strong increase in LOX activity suggests JA signalling seems to be a very promising one
one of the 12 differentially regulated genes has shown to be directly linked with JA responses Arabidopsis thaliana
j1256 mutant does not show induced expression of (ATVSP2, VSP2, AT5G24770) Arabidopsis thaliana
MeJA treatment inhibits expression of MdSINA2 Malus domestica
constitutive expresser of PR genes22 (cpr22) mutant constitutively expresses JA-inducible antifungal defensin gene (LCR77, PDF1.2, PDF1.2A, AT5G44420) Arabidopsis thaliana
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) RNAi plants shows phenotype of MYC2-dependent JA pathway activity Populus trichocarpa
Serotonin (5-hydroxytryptamine) activated expression of JASMONATE ZIM-domain (JAZ) proteins (AtJAZ1, JAZ1, TIFY10A, AT1G19180) Arabidopsis thaliana
NtCOI1 silencing in floral nectary provides critical molecular evidence for JA in mediating primary metabolism and carotenoid synthesis Nicotiana tabacum
PI silencing significantly reduces PI I and PI II expression Solanum lycopersicum
(MIR319, MIR319B, AT5G41663) (MEE35, PCF4, TCP4, AT3G15030) module affected endogenous JA level Solanum lycopersicum
Arabidopsis quadruple DELLA mutant is partially insensitive to gene induction by methyl jasmonate Arabidopsis thaliana
reduction in JA defence marker gene expression by low R:FR-induced phytochrome inactivation has been shown in Arabidopsis Arabidopsis thaliana
HvRAF expression is induced by methyl jasmonate Hordeum vulgare
activated JA signaling pathway decreases number of eggs laid by BPH female adults Oryza sativa
WT-GmBIR1 samples had significantly higher level of OPDA Glycine max
(AtERF#092, ERF1, ERF1B, AT3G23240) expression in MJ-treated jam1jam2 and jam x3 clearly higher than wild-type Arabidopsis thaliana
jam3-2 mutant exhibited slightly shorter roots on MJ-containing medium Arabidopsis thaliana
(IAA26, PAP1, AT3G16500) (DFR, M318, TT3, AT5G42800) and (ATVSP2, VSP2, AT5G24770) expression in MJ-treated seedlings grown on 0.5% Suc higher in jam x3 compared with wild-type Arabidopsis thaliana
Botrytis cinerea-induced increases in JA contents are much lower in plants grown under elevated CO2 compared with ambient CO2 plants Solanum lycopersicum
infected (GAI, RGA2, AT1G14920) plants display earlier and stronger (LCR77, PDF1.2, PDF1.2A, AT5G44420) mRNA induction Arabidopsis thaliana
TIC represses (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) protein accumulation
expression of OsRAN1 is induced by jasmonic acid Oryza sativa
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) suppresses expression of PLETHORA genes Arabidopsis thaliana
jasmonic acid (JA) is signaling molecule
caterpillar salivary effectors suppress JA-induced plant responses
Transcript abundances of JA-inducible genes were reduced in leaves of barley RNAi lines Hordeum vulgare
JA-Ile promotes binding of (COI1, AT2G39940) to jasmonate-ZIM domain (JAZ) proteins
Jasmonate-induced protein homologue exhibits increased steady-state transcript abundance in CAM-performing leaves Mesembryanthemum crystallinum
most of these genes respond to jasmonic acid stimuli Gossypium hirsutum
CORONATINE INSENSITIVE 1 (COI1, AT2G39940) receptor promotes degradation of JASMONATE-ZIM-DOMAIN (JAZ) proteins Arabidopsis thaliana
elevated [CO2] does not significantly affect JA content in mock plants Solanum lycopersicum
many foliar pathogens activate JA signaling
0.5 μM MeJA and 1 mM DIECA were sprayed every 12 h for 12 days Prunus persica
(COI1, AT2G39940) regulates male fertility
(ATNPR1, NIM1, NPR1, SAI1, AT1G64280) induction suppresses expression of JA-dependent genes PI I and PI II Solanum lycopersicum
NtCOI1-silenced tobacco mimicked hallmarks of the Arabidopsis (COI1, AT2G39940) mutant Nicotiana tabacum; Arabidopsis thaliana
(COI1, AT2G39940) is co-receptor for jasmonoyl-L-isoleucine (JA-Ile)
NtCOI1-silenced tobacco exhibits jasmonic acid insensitivity Nicotiana tabacum
coronatine (COR) is mimic of the bioactive phytohormone jasmonic acid-isoleucine (JA-Ile)
activated (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) directly regulates expression of transcription factors (ANAC019, ANAC19, NAC019, AT1G52890)
JA-responsive gene induction is sensitized in (GAI, RGA2, AT1G14920) mutant Arabidopsis thaliana
coronatine (COR) structurally and functionally mimics jasmonic acid-isoleucine (JA-Ile)
MeJA-responsive elements (CGTCA-motif) found in promoters of 64 PtrWRKY genes Populus trichocarpa
external application of jasmonic acid (JA) rescues anther indehiscence in AIF-C+SRDX flowers Arabidopsis thaliana
jasmonic acid (JA) is perceived by CORONATINE INSENSITIVE 1 (COI1, AT2G39940) receptor Arabidopsis thaliana
NPR1-silenced plants show significantly induced PI I and PI II transcripts Solanum lycopersicum
elevated CO2 does not increase jasmonic acid (JA) concentrations Solanum lycopersicum
(HY3, OOP1, PHYB, AT2G18790) mutant has reduced JA-dependent defence against Bc
JAZ degradation upon JA perception allows JA-induced gene expression
extra-floral nectaries of lima bean respond to jasmonic acid Phaseolus lunatus
Jasmonate ZIM-domain protein 5 ( (JAZ5, TIFY11A, AT1G17380) ) is JA-responsive gene Arabidopsis thaliana
(BAH1, NLA, SYG1, AT1G02860) mutant plants show further increase in jasmonic acid (JA) levels upon pathogen infection Arabidopsis thaliana
NaBAK1 silencing impaired accumulation of JA-Ile after herbivory Nicotiana attenuata
untreated plants with similar levels of jasmonic acid (JA) have similar levels of jasmonic acid (JA) Nicotiana attenuata
(MYC3, AT5G46760) associates with (AtJAZ1, JAZ1, TIFY10A, AT1G19180) Arabidopsis thaliana
lipoxygenase 3 (ATLOX3, LOX3, AT1G17420) had increased transcript levels in MYC overexpression seedlings Arabidopsis thaliana
four T. urticae infestation does not increase JA levels Phaseolus lunatus; Tetranychus urticae
(ATWRKY33, WRKY33, AT2G38470) mutants show reduced expression of jasmonic acid (JA)-regulated genes such as (LCR77, PDF1.2, PDF1.2A, AT5G44420) Arabidopsis thaliana
four T. urticae infestation applied 7 days after water treatment does not affect JA levels Phaseolus lunatus; Tetranychus urticae
effects of jasmonates on seed germination appear to be species and even ecotype specific
OsPP18 is transiently induced by jasmonic acid (JA) treatment Oryza sativa
LOX encodes lipoxygenase Nicotiana benthamiana
elevated Lys and/or its metabolites somehow induced JA biosynthesis as well as associated stress responses Oryza sativa
Five-week-old plants were sprayed with methyl jasmonate (MeJ) solution
tyrosine aminotransferase-1 (AtTAT1, TAT1, TAT7, AT5G53970) is JA-dependent marker Arabidopsis thaliana
quadruple-DELLA mutant treated with MeJA shows delayed upregulation of (LCR77, PDF1.2, PDF1.2A, AT5G44420) (ATLOX2, LOX2, AT3G45140) and (AtTAT1, TAT1, TAT7, AT5G53970) mRNA Arabidopsis thaliana
coronatine (COR) hijacks host JA-signaling pathway Arabidopsis thaliana
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) activates NAC transcription factors Arabidopsis thaliana
methyl jasmonate treatment inhibited root growth to same extent in clasp-1 mutants as in wild-type Arabidopsis thaliana
Arabidopsis homologue ( (ATWRKY50, WRKY50, AT5G26170) ) is induced by jasmonic acid (JA) Arabidopsis thaliana
roots of cts-1 lines expressing HvABCD2 but not HvABCD1 exhibited sensitivity to exogenously applied OPDA similar to wild-type controls Arabidopsis thaliana
elevated [CO2] has no effect on PI I and PI II transcript expression Solanum lycopersicum
(ATNPR1, NIM1, NPR1, SAI1, AT1G64280) gene silencing results in large and significant increases in PI I and PI II transcript expression Solanum lycopersicum
(ADO1, FKL2, LKP1, ZTL, AT5G57360) interacts strongly with JAZb Nicotiana attenuata
JAZe transcriptional abundance has mild diurnal pattern in EV but shows no difference between EV and ir-ztl plants Nicotiana attenuata
MeJA treatment induces expression of MdABI5 promoter Malus domestica
arbuscular mycorrhizal fungi (AMF) inoculation enhance JA-regulated responses
Pseudomonas syringae YopJ-like HopZ1a acetylates JASMONATE ZIM-domain (JAZ) transcriptional repressors Arabidopsis thaliana
JA-induced genes are upregulated in (FER, AT3G51550) mutants Arabidopsis thaliana
JASMONATE-ZIM-DOMAIN PROTEIN repressors act as negative regulators of jasmonic acid (JA) perception and signaling Arabidopsis thaliana
GFP alone does not immunoprecipitate Myc-JAZb Nicotiana benthamiana
enhanced serotonin accumulation and dark-brown pigmentation is led to by low-temperature treatment-induced JA biosynthesis and signaling Oryza sativa
hsf mutant plants show higher induction of (LCR77, PDF1.2, PDF1.2A, AT5G44420) mRNA Arabidopsis thaliana
JAs are maintained at very low levels without treatment and show no difference between ir-ztl and EV plants Nicotiana attenuata
12-hydroxy-JA-Ile levels show increased or decreased level in only one ir-ztl line compared with EV plants under some treatments ir-ztl lines Nicotiana attenuata
JA signaling pathway is induced in HFL rice endosperm Oryza sativa
0.5 μM MeJA and 1 mM DIECA were sprayed on peach shoots Prunus persica
differentially expressed genes in barley showed significant enrichment of genes involved in jasmonic acid hormone pathway Hordeum vulgare
extrafloral nectar quantities show insensitivity to external application of jasmonic acid Acacia cornigera
RESPONSIVE TO DESICCATION 26 (ANAC072, ANAC72, AtRD26, RD26, AT4G27410) is upregulated in (FER, AT3G51550) mutants Arabidopsis thaliana
PLANT DEFENSIN 1.2 (LCR77, PDF1.2, PDF1.2A, AT5G44420) expression in RALF23ox shows increased JA induction jasmonic acid (JA) treatment Arabidopsis thaliana
COR activates JA signaling
35S:DAF-H137Y plants show phenotype rescued by external application of JA Arabidopsis thaliana
TYROSINE AMINO TRANSFERASE (TAT, TAT3, AT2G24850) is upregulated in (FER, AT3G51550) mutants Arabidopsis thaliana
VEGETATIVE STORAGE PROTEIN 1 (ATVSP1, VSP1, AT5G24780) is upregulated in (FER, AT3G51550) mutants Arabidopsis thaliana
Jasmonoyl-S-isoleucine is jasmonic acid derivative
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) /3/4 mutant showed increased bacterial colonization Xcc8004 ΔxopAC Tn5:lux Arabidopsis thaliana
CaDEF1 is JA-responsive marker gene Capsicum annuum
(AtTAT1, TAT1, TAT7, AT5G53970) transcripts in MeJA-treated (GAI, RGA2, AT1G14920) plants display approximately 1000-fold induction versus approximately 5-fold induction in La-er controls Arabidopsis thaliana
PLANT DEFENSIN 1.2 (LCR77, PDF1.2, PDF1.2A, AT5G44420) is upregulated in (FER, AT3G51550) mutants Arabidopsis thaliana
(AtGBF1, GBF1, AT4G36730) plants may be regarded as more sensitive towards MeJA application Arabidopsis thaliana
jasmonic acid regulatory model is heavily loaded with amplification and feedback loops
(ATLOX3, LOX3, AT1G17420) is upregulated by MJ treatment
low red:far-red light ratio (R:FR) inhibits jasmonic acid (JA)-dependent disease resistance Arabidopsis thaliana
expression of the JAZ genes is rapidly upregulated by herbivory
(ATRBOH F, ATRBOHF, RBOH F, RBOHAP108, RBOHF, AT1G64060) is involved in jasmonic acid-induced ROS production Arabidopsis thaliana
Medtr1g086530 transcript levels increased within 30 min of methyl jasmonate (MeJA) treatment Medicago truncatula
singlet oxygen (1O2) can activate JA signaling pathway Arabidopsis thaliana
(FER, AT3G51550) mutants is hypersensitive to jasmonic acid (JA) Arabidopsis thaliana
activated (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) directly regulates expression of transcription factors (ANAC072, ANAC72, AtRD26, RD26, AT4G27410)
jasmonic acid (JA) regulates root stem cell niche maintenance and meristem activity Arabidopsis thaliana
(COI1, AT2G39940) regulates secondary metabolism
JA-signalling pathway is important in coordinating overall primary metabolism in plants
(ATRALF23, RALF23, AT3G16570) stabilizes (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) Arabidopsis thaliana
ABA receptor (PYL6, RCAR9, AT2G40330) inhibit MYC2-mediated trans-activation of (JAZ6, TIFY11B, AT1G72450) promoter
(LCR78, PDF1.4, AT1G19610) is one of the JA biosynthesis and signaling genes Arabidopsis thaliana
jasmonic acid (JA) biosynthesis induces defense gene expression Solanum lycopersicum
MYC3–OE2 seedlings shows severely inhibited aerial part growth Arabidopsis thaliana
MeJA treatments applied at 10 μM final concentration Rorippa aquatica
(ML3, AT5G23820) mutants are compromised in wound-induced JA signaling Arabidopsis thaliana
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) regulates expression of downstream metabolic genes through transcription factor-encoding genes such as (ANAC019, ANAC19, NAC019, AT1G52890) (AtERF#092, ERF1, ERF1B, AT3G23240) and (ERF59, ORA59, AT1G06160) Arabidopsis thaliana
plant resistance to fungal pathogens is known to be related to jasmonic acid signaling
physiological processes regulated by jasmonates were first described almost 30 years before JA mechanism was established
VmSpm1 overexpression in apple leaves suppresses JA-related gene expression Malus domestica
jasmonic acid (JA) signaling pathway shows alterations in (ATCNGC2, CNGC2, DND1, AT5G15410) (ATCNGC4, CNGC4, DND2, HLM1, AT5G54250) , and cpr22 mutants Arabidopsis thaliana
ER body formation is promoted by jasmonic acid (JA) Arabidopsis thaliana
(AOC4, AT1G13280) is upregulated by MJ treatment
(AtOPR3, DDE1, OPR3, AT2G06050) is upregulated by MJ treatment
jam1jam2jam3 triple mutants (jam x3) exhibited shorter roots on 50 μm MJ-containing medium Arabidopsis thaliana
acetate treatment did not enhance disease tolerance in tomato mutant deficient in JA biosynthesis Solanum lycopersicum
jasmonic acid induces nectar secretion Brassica sp.
MYC2-dependent JA pathway is important in defence against herbivores and pathogens Populus trichocarpa
(LCR77, PDF1.2, PDF1.2A, AT5G44420) is not expressed in defense, no death1 (ATCNGC2, CNGC2, DND1, AT5G15410) mutant Arabidopsis thaliana
jasmonates have phytohormone role that is firmly accepted phytohormone
jazD mutant shows induced expression of (ATVSP2, VSP2, AT5G24770) Arabidopsis thaliana
(ML3, AT5G23820) and (NAI1, AT2G22770) abundance is induced by MeJA treatments Arabidopsis thaliana
(ATVSP2, VSP2, AT5G24770) expression in jam x3 attenuated by (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) mutation Arabidopsis thaliana
DELLA proteins interact with PIFs
MdNAC72-MdABI5 module combines with MdJAZ2 Malus domestica
control of bHLH18 by (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) suggests redundant and/or additive role within the jasmonic acid (JA) pathway Populus trichocarpa
MdNAC72 interacts with MdJAZ2 Malus domestica
activated JA signaling pathway decreases hatching rate of BPH eggs Oryza sativa
VmPR1c attenuates levels of jasmonic acid (JA) Malus domestica
82 probes showed enhanced MJ-inducible expression in jam x3 compared with wild-type Arabidopsis thaliana
FERONIA (FER, AT3G51550) functions to inhibit jasmonic acid (JA) signaling
jasmonic acid (JA) content reduction impairs JA signal transduction Malus domestica
jasmonic acid-isoleucine (JA-Ile) were higher in plants exposed to emitters with old damage Gossypium hirsutum
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) and (ERF59, ORA59, AT1G06160) negatively regulate each other each other Arabidopsis thaliana
activated (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) directly regulates expression of transcription factors (ANAC055, ANAC55, ATNAC3, NAC055, NAC3, AT3G15500)
jasmonic acid (JA) promotes (ML3, AT5G23820) gene expression Arabidopsis thaliana
(AIB, ATAIB, bHLH017, bHLH17, JAM1, AT2G46510) expression clearly induced by 50 μm methyl jasmonate (MJ) treatment Arabidopsis thaliana
(bHLH013, bHLH13, JAM2, AT1G01260) expression clearly induced by 50 μm methyl jasmonate (MJ) treatment Arabidopsis thaliana
plant response to aphids involves genes regulated by jasmonic acid (JA)
OsCOI2 is JA signaling component gene Oryza sativa
JA signaling inhibits growth through JAZ-DELLA-PIF signaling module
MeJA treatment affects pigment gland development Gossypium hirsutum
(COI1, AT2G39940) functions as jasmonic acid receptor Arabidopsis thaliana
altered cell wall polysaccharide levels stimulate JA-regulatory pathways
MiSSP7 also strengthens interaction between PtaJAZ6 and the two poplar paralogs PtaMYC2.1 and PtaMYC2.2 Populus trichocarpa; Laccaria bicolor
(NAI1, AT2G22770) transcription is induced by MeJA Arabidopsis thaliana
myc2jam1jam2 triple mutant showed no obvious effects on (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) phenotype Arabidopsis thaliana
(AIB, ATAIB, bHLH017, bHLH17, JAM1, AT2G46510) originally selected as JA-responsive gene Arabidopsis thaliana
JAZ repressors recruit TPL-related (TPR) Arabidopsis thaliana
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) probably resides on DNA directly interacting with JAZ repressors Arabidopsis thaliana
knockdown of NlVg in the insect did not affect JA and JA-Ile levels