| constitutive expresser of PR genes22 (cpr22) mutant |
displays |
autoimmune phenotypes with increased SA accumulation |
Arabidopsis thaliana |
| itpa plants |
accumulate |
SA |
Arabidopsis thaliana |
| E3-mediated ubiquitination of NON-EXPRESSOR OF PR GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
is critical for |
SA perception and establishment of systemic acquired resistance (SAR) |
|
| salicylic acid (SA) production |
increases |
(AtRDR1, ATRDRP1, RDR1, AT1G14790) expression |
|
| several pathogenic viruses |
induce |
salicylic acid (SA) production |
|
| salicylic acid (SA) |
showed no significant effect on |
plants exposed to different volatile treatments |
Gossypium hirsutum |
| (ARAPPT, CUE1, NOX1, PPT, AT5G33320) mutants |
have decreased level of |
salicylic acid (SA) in leaves |
Arabidopsis thaliana |
| free SA levels in 3FLAG-TLP6 OE lines |
were |
intermediate between that in WT and pi4kβ1,2 |
Arabidopsis thaliana |
| DELLA loss-of-function mutants |
have primed |
salicylic acid with earlier, more robust expression of pathogenesis-related (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) and (AtBG2, AtPR2, BG2, BGL2, GNS2, PR-2, PR2, AT3G57260) genes |
Arabidopsis thaliana |
| ENHANCED DISEASE SUSCEPTIBILITY 1a (GmEDS1a) and ENHANCED DISEASE SUSCEPTIBILITY 1b (GmEDS1b) silenced plants |
were defective in |
pathogen-inducible salicylic acid accumulation |
Glycine max |
| enhanced salicylic acid (SA) accumulation and increased expression of SA-responsive marker genes in 35S::BiP4 line |
may serve as |
priming state for further induction of salicylic acid (SA) signaling upon biological activation |
Glycine max |
| spatial and temporal controlled experiments on salicylic acid (SA) accumulation and plant growth in (CYP98A3, REF8, AT2G40890) mutant |
may be useful to |
better understand the underlying mechanism for dwarfism |
Arabidopsis thaliana |
| SA |
has a role in |
nematode resistance |
Glycine max |
| GO terms 'salicylic acid biosynthetic process' and 'salicylic acid-mediated signaling pathway' |
were enriched among |
uniquely downregulated genes in WT-GmBIR1 |
Glycine max |
| plants with more unrepaired DNA double-strand breaks |
have increased |
concentration of SA |
Arabidopsis thaliana |
| high basal salicylic acid (SA) level |
is required for sustained expression of |
OsWRKY45 |
Oryza sativa |
| PRR2-like proteins in vascular plants |
are implicated in |
SA-mediated defense responses |
|
| defense, no death1 (ATCNGC2, CNGC2, DND1, AT5G15410) mutant |
displays |
elevated levels of salicylic acid (SA) |
Arabidopsis thaliana |
| rdd1-1D cngc2-3 mutant |
has lower levels of |
total salicylic acid compared to (ATCNGC2, CNGC2, DND1, AT5G15410) and -3 |
Arabidopsis thaliana |
| SCF E3-mediated ubiquitination |
is linked to |
SA inactivation |
|
| cngc2-3 mutant |
displays elevated levels of |
salicylic acid (SA) |
Arabidopsis thaliana |
| STEAROYL-ACYL CARRIER PROTEIN Δ9-DESATURASE6 (AAD6, FTM1, HUP7, SAD6, AT1G43800) |
was ectopically expressed in the background of |
ssi2-2 mutant |
Arabidopsis thaliana |
| (AAD6, FTM1, HUP7, SAD6, AT1G43800) ectopic expression in ssi2-2 mutant background |
rescued |
all known ssi2-2 phenotypes |
Arabidopsis thaliana |
| phb3-3 mutant plants |
show lower accumulation of |
(AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) (PATHOGENESIS-RELATED 1) protein after infection |
Arabidopsis thaliana |
| salicylic acid (SA) |
primes plant for |
better adaptation under both biotic and abiotic stress conditions |
|
| MdPR1 |
is |
SA-regulated gene |
Malus domestica |
| (BIP, BIP2, AT5G42020) overexpression in response to salicylic acid (SA) signaling |
induced further |
N-rich protein (NRP, NRP1, AT5G42050) -mediated cell death signaling |
Glycine max |
| SA homeostasis |
is linked to |
plant growth |
Arabidopsis thaliana |
| (ATPAD4, PAD4, AT3G52430) 35S::PROTEIN PHOSPHATASE 2C-LIKE (GmPAD4) plants |
contained significantly reduced |
basal and pathogen-induced levels of salicylic acid |
Arabidopsis thaliana |
| BiP-mediated amplification of hypersensitive response (HR) programmed cell death (PCD) |
may be linked to |
activation of salicylic acid (SA) signaling |
Glycine max |
| (BIK1, AT2G39660) |
suppresses |
salicylic acid (SA) accumulation |
Arabidopsis thaliana |
| salicylic acid (SA)-mediated induction of N-rich protein (NRP, NRP1, AT5G42050) cell death signaling |
likely occurs via |
pathway distinct from unfolded protein response (UPR) |
Glycine max |
| reduced epidermal fluorescence8 (CYP98A3, REF8, AT2G40890) mutant |
accumulates higher levels of |
salicylic acid (SA) |
Arabidopsis thaliana |
| Mutations in (EDS5, SCORD3, SID1, AT4G39030) |
impair |
SA responsiveness |
|
| (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) |
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 |
| accession-specific Rhizoctonia solani resistance in Bd3-1 |
is |
salicylic acid (SA) dependent |
Brachipodium distachyon |
| enhanced induction of N-rich protein (NRP, NRP1, AT5G42050) -mediated cell death signaling in BiP-overexpressing leaves |
paralleled |
increased expression of pathogenesis-related (PR) proteins |
Glycine max |
| aphid feeding |
activates |
salicylic acid (SA) signaling pathway |
|
| wild type |
accumulates lower levels of |
salicylic acid (SA) |
Arabidopsis thaliana |
| mutations in enhanced disease susceptibility1 (ATEDS1, EDS1, AT3G48090) |
impair |
SA responsiveness |
|
| basal and pathogen-induced levels of salicylic acid glucoside in (ATPAD4, PAD4, AT3G52430) and 35S::PROTEIN PHOSPHATASE 2C-LIKE (GmPAD4) plants |
were comparable to |
wild-type levels |
Arabidopsis thaliana |
| WRKY42-OE lines |
have dramatically increased |
free salicylic acid (SA) levels |
Arabidopsis thaliana |
| (BIP, BIP2, AT5G42020) |
modulates N-rich protein (NRP)-mediated cell death signaling pathway by stimulating |
salicylic acid (SA) signaling |
Glycine max |
| pathogen-induced PME activity |
did not require |
salicylic acid signaling |
Arabidopsis thaliana |
| dwarfism of Arabidopsis (CYP98A3, REF8, AT2G40890) mutants |
does not depend on |
salicylic acid (SA) accumulation |
Arabidopsis thaliana |
| 35S-driven NahG overexpression in (CYP98A3, REF8, AT2G40890) |
may not be effective in reducing |
salicylic acid (SA) accumulation in certain cell types or tissues |
Arabidopsis thaliana |
| silencing of GmEDS1a and GmEDS1b |
reduced |
pathogen-inducible salicylic acid accumulation |
Glycine max |
| salicylic acid (SA)-responsive marker genes |
include |
PR10 |
Glycine max |
| endoplasmic reticulum (ER)-resident gene (BIP, BIP2, AT5G42020) |
is induced before |
(AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) accumulation |
|
| hyperaccumulation of salicylic acid (SA) |
is unlikely to be responsible for |
dwarfism in the (CYP98A3, REF8, AT2G40890) mutant |
Arabidopsis thaliana |
| MEcDP (2-C-methylerythritol-2,4-cyclodiphosphate) diversion resulting from pathogen attack |
is part of |
a stress response mediated by salicylic acid (SA) |
Arabidopsis thaliana |
| decreasing PAL activity by suppressing PAL expression or applying PAL inhibitors |
resulted in |
reduced levels of salicylic acid (SA) |
Nicotiana tabacum; Arabidopsis thaliana |
| silencing of GmPAD4 |
reduced |
pathogen-inducible salicylic acid accumulation |
Glycine max |
| Phytophthora sojae infection |
did not result in increase in |
salicylic acid levels in ENHANCED DISEASE SUSCEPTIBILITY 1a (GmEDS1a) and ENHANCED DISEASE SUSCEPTIBILITY 1b (GmEDS1b) and PROTEIN PHOSPHATASE 2C-LIKE (GmPAD4) silenced plants |
Glycine max |
| PROTEIN PHOSPHATASE 2C-LIKE (GmPAD4) gene |
was unable to complement |
defect in salicylic acid accumulation |
Arabidopsis thaliana |
| Altered GIPC headgroup glycosylation |
results in |
constitutive defense response mediated by increased salicylic acid biosynthesis |
|
| salicylic acid (SA)-induced PR gene expression |
is repressed in |
(FHY2, FRE1, HY8, PHYA, AT1G09570) mutant |
Arabidopsis thaliana |
| PATHOGENESIS-RELATED 1 (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) |
is |
one of the SA biosynthesis and signaling genes |
Arabidopsis thaliana |
| pipecolate |
positively regulates |
salicylic acid (SA) biosynthesis |
dicots |
| (ATCNGC2, CNGC2, DND1, AT5G15410) mutant |
has significantly higher |
total salicylic acid levels compared to Columbia wild-type |
Arabidopsis thaliana |
| 35S::BiP4 line |
compared with wild type displayed |
enhanced salicylic acid (SA) accumulation and increased expression of SA-responsive marker genes |
Glycine max |
| (ATPAD4, PAD4, AT3G52430) protein |
functions independently of |
SA-mediated pathway |
|
| silencing of GmPAD4 gene |
affects |
pathogen-induced salicylic acid (SA) accumulation |
Glycine max |
| phb3-3 mutant |
may fail to sense adequately |
SA |
Arabidopsis thaliana |
| SA signaling |
is not altered in |
phb3-3 plants |
Arabidopsis thaliana |
| cpr22 double mutants with (NDR1, AT4G14350) |
did not affect |
SA levels |
|
| Chlorella fusca application |
highly upregulates |
PATHOGENESIS-RELATED 1 (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) |
Arabidopsis thaliana |
| free and total salicylic acid (SA) |
are significantly induced in all three genotypes upon induction |
pathogen-induced defense response |
Arabidopsis thaliana |
| cpr22 double mutants with (ATPAD4, PAD4, AT3G52430) |
did not affect |
SA levels |
|
| overlap between NahG plants and shRBOHD plants |
expected, as |
expression of (ATRBOHD, DELT1, RBOHD, AT5G47910) is repressed in NahG plants |
Solanum tuberosum |
| (AtWRKY42, WRKY42, AT4G04450) expression |
was significantly reduced under |
500 μM SA treatment |
Arabidopsis thaliana |
| (ANAC059, ATNAC3, NAC3, ORS1, AT3G29035) and (ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) genes |
expression is controlled by |
stress, wound, or salicylic acid factors |
Arabidopsis thaliana |
| TGA transcription factors |
interact with |
NPRs |
Arabidopsis thaliana |
| salicylic acid (SA)-induced PR gene expression |
is repressed in |
(FHY2, FRE1, HY8, PHYA, AT1G09570) (HY3, OOP1, PHYB, AT2G18790) mutant |
Arabidopsis thaliana |
| salicylic acid (SA)-induced PR gene expression |
is repressed in |
(ATCRY1, BLU1, CRY1, HY4, OOP2, AT4G08920) mutant |
Arabidopsis thaliana |
| endogenous salicylic acid (SA) |
positively regulates |
accession-specific R. solani resistance |
Brachypodium distachyon |
| (AtWRKY42, WRKY42, AT4G04450) mutant plants |
have decreased |
free salicylic acid (SA) levels |
Arabidopsis thaliana |
| salicylic acid (SA)-induced PR gene expression |
is repressed in |
(HY3, OOP1, PHYB, AT2G18790) mutant |
Arabidopsis thaliana |
| (ATRBOHA, RBOHA, AT5G07390) activation |
attenuated in |
NahG plants |
Solanum tuberosum |
| PR gene expression induction |
rules out |
inhibition of the SA pathway by acarbose |
Arabidopsis thaliana |
| (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
directs expansion of |
protein import and folding capacities in the ER |
Arabidopsis thaliana |
| phytochrome signaling |
specifically controls |
SA accumulation |
Arabidopsis thaliana |
| aberrant defense activation |
includes |
increased SA accumulation |
Arabidopsis thaliana |
| (ATRBOHD, DELT1, RBOHD, AT5G47910) |
under the regulation of |
salicylic acid (SA) |
Solanum tuberosum |
| EAR motif |
might not be diagnostic domain to predict |
positive or negative role of NPR homologs in SA signaling |
|
| NRR |
interacts with |
paralogs of NH1 (rice (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) homolog 1) |
|
| salt stress and salicylic acid (SA)-induced degradation of (OTS1, ULP1D, AT1G60220) /2 |
is important for |
SA biosynthesis |
|
| BdWRKY44 |
is |
SA-responsive |
Brachipodium distachyon |
| (EDS5, SCORD3, SID1, AT4G39030) |
is |
one of the SA biosynthesis and signaling genes |
Arabidopsis thaliana |
| (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
interacts with |
TGAs |
Arabidopsis thaliana |
| (LecRK-IX.2, AT5G65600) |
is also involved in |
SA signaling |
|
| coronatine, (COI1, AT2G39940) and (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) |
is required for |
reduction of pathogen-induced SA levels |
Arabidopsis thaliana |
| atypical DP-E2F-LIKE1 ( (DEL1, E2FE, E2L3, AT3G48160) ) |
negatively regulates |
ENHANCED DISEASE SUSCEPTIBILITY5 (EDS5, SCORD3, SID1, AT4G39030) |
Arabidopsis thaliana |
| microarray experiment |
detected |
up-regulation of protein secretory pathway genes |
Arabidopsis thaliana |
| NON-EXPRESSOR OF PR GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
induces |
transcriptional changes |
Arabidopsis thaliana |
| PHOSPHATE TRANSPORTER 4;1 (PHT4;1) |
acts upstream of |
salicylic acid (SA) pathway |
Arabidopsis thaliana |
| BdWRKY36 |
is |
SA-responsive |
Brachipodium distachyon |
| genes participating in salicylic acid (SA) signaling |
includes |
(AHBP-1B, AtTGA2, TGA2, AT5G06950) |
Solanum tuberosum |
| ENHANCED DISEASE SUSCEPTIBILITY 1 (ATEDS1, EDS1, AT3G48090) |
is |
one of the SA biosynthesis and signaling genes |
Arabidopsis thaliana |
| AevPAL1 expression |
is induced by |
100 µm salicylic acid (SA) |
Aegilops variabilis |
| (AtGH3.12, GDG1, GH3.12, PBS3, WIN3, AT5G13320) |
interacts with EDS1 in |
nucleus |
Arabidopsis thaliana |
| chloroplasts and mitochondria |
activate |
salicylic acid |
|
| complementation of (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) by Mp NPR |
suggests that |
MpNPR can still bind SA |
Marchantia polymorpha |
| suspension of low concentration (1 × 10^6 cfu mL^−1, OD 600 = 0.002) of virulent pathogen Pst. DC3000 |
was injected into leaves |
2 d after SA treatment |
|
| (ATICS1, EDS16, ICS1, SID2, AT1G74710) double mutants |
did not rescue |
HR attenuation phenotype in (ATCNGC2, CNGC2, DND1, AT5G15410) and (ATCNGC4, CNGC4, DND2, HLM1, AT5G54250) |
|
| (UGT76D1, AT2G26480) expression pattern similarity |
in line with the evidence that |
(ATRBOHD, DELT1, RBOHD, AT5G47910) is repressed in NahG plants |
Solanum tuberosum |
| (ATNPR3, NPR3, AT5G45110) and (ATNPR4, NPR4, AT4G19660) |
missing in |
Gastrodia elata genome |
Gastrodia elata |
| NON-EXPRESSOR OF PR GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) and (TGA3, AT1G22070) interaction |
promotes |
PR gene expression |
|
| (ATNPR3, NPR3, AT5G45110) (ATNPR4, NPR4, AT4G19660) |
constitutively localize to |
nucleus |
Arabidopsis thaliana |
| MpNPR |
has been proposed to be |
negative regulator of SA responses |
Marchantia polymorpha |
| 35S::BiP4 line |
displayed under normal conditions |
increased expression of salicylic acid (SA)-responsive marker genes |
Glycine max |
| N-rich protein (NRP, NRP1, AT5G42050) -mediated cell death signaling |
is induced by |
salicylic acid (SA) signaling |
Glycine max |
| silencing of GmEDS1a and GmEDS1b |
reduced |
basal salicylic acid accumulation |
Glycine max |
| AevPAL1 |
may not be induced instantaneously by |
salicylic acid (SA) |
Aegilops variabilis |
| FB1-induced cell death |
is blocked in |
transgenic plants expressing bacterial salicylate hydroxylase |
Arabidopsis thaliana |
| salicylic acid (SA) binding to (ATNPR3, NPR3, AT5G45110) |
facilitates |
NPR3–NPR1 interaction |
|
| regulatory elements in (ANAC059, ATNAC3, NAC3, ORS1, AT3G29035) and (ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) promoters |
have function in |
stress, wound, or salicylic acid responses |
Arabidopsis thaliana |
| (ATRBOHD, DELT1, RBOHD, AT5G47910) gene activity |
under the regulation of |
salicylic acid (SA) |
Solanum tuberosum |
| (ATEDS1, EDS1, AT3G48090) (ATPAD4, PAD4, AT3G52430) (ALD1, AtALD1, EDTS5, AT2G13810) and (FMO1, AT1G19250) |
important downstream genes of SA signaling, all missing in |
Gastrodia elata and Cuscuta australis |
Gastrodia elata; Cuscuta australis |
| salicylic acid (SA) |
binds to |
NONEXPRESSOR OF PATHOGENESIS-RELATED GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
|
| salicylic acid (SA) |
is also a key player in redox signalling by modulating the activity of |
NON-EXPRESSOR OF PR GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
|
| (BGLU2, AT5G16580) and PR1B response |
differs markedly in |
SA-depleted system |
Solanum tuberosum |
| (ATPAL1, PAL1, AT2G37040) in Capsicum annuum |
is dependent on |
salicylic acid (SA) signaling |
Capsicum annuum |
| NON-EXPRESSOR OF PR GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) nuclear activity |
is tightly regulated by |
post-translational modifications (PTMs) |
|
| NPRs from non-seed plants |
constitutively localize in |
nucleus |
|
| SUMOylation |
affects |
(ATNPR1, NIM1, NPR1, SAI1, AT1G64280) differential associations with TGA and WRKY transcription factors |
|
| Physcomitrella patens (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) (PpNPR1) |
partially complemented |
(ATNPR1, NIM1, NPR1, SAI1, AT1G64280) mutant |
Physcomitrella patens; Arabidopsis thaliana |
| (COI1, AT2G39940) mutant roots |
show de-repression of |
salicylic acid (SA)-related genes |
Arabidopsis thaliana |
| (AtGH3.12, GDG1, GH3.12, PBS3, WIN3, AT5G13320) |
interacts with EDS1 in |
cytoplasm |
Arabidopsis thaliana |
| (ATEDS1, EDS1, AT3G48090) |
is receptor of |
(AtTN10, TIR, TN10, AT1G72930) enzymatic products |
flowering plants |
| presence of SA and JAs (OPDA/dn-cis-OPDA) in algae |
supports |
presence of receptor-independent pathways |
|
| salicylic acid |
regulates |
different PhERF transcripts |
Petunia |
| HAFT |
expression is up-regulated by |
salicylic acid (SA) treatment |
Helianthus annuus |
| AevPAL1 expression |
is probably in a concentration-dependent manner |
salicylic acid (SA) concentration |
Aegilops variabilis |
| salicylic acid (SA)-induced changes in cellular redox |
triggers release of |
NON-EXPRESSOR OF PR GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) monomers |
|
| similar transcriptional response to SA after 6 h in wild-type and Mp npr |
led to conclusion that |
MpNPR is not a master regulator of SA responses |
Marchantia polymorpha |
| BdWRKY38 and BdWRKY44 |
positively regulate |
accession-specific R. solani resistance |
Brachypodium distachyon |
| (GBSS1, AT1G32900) expression downregulation |
not true in |
NahG plants |
Solanum tuberosum |
| PEROXIDASE 52 expression |
was altered in |
fumonisin B1-resistant salicylic acid induction-deficient (ATICS1, EDS16, ICS1, SID2, AT1G74710) mutants |
Arabidopsis thaliana |
| complex posttranslational regulation of NPR1-dependent transcription |
occurs during |
immune responses |
|
| phenomenon of signal transmission from egg-stimulated plants to bacteria-infected plants |
did not require |
functional production of SA in the sender plant |
|
| salicylic acid (SA) |
is perceived by |
Nonexpresser of PR 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
Arabidopsis thaliana |
| Arabidopsis (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) mutant |
has SA hypersensitivity attributed to |
SA hyperaccumulation |
Arabidopsis thaliana |
| rising temperatures |
suppress |
SA synthesis |
|
| salicylic acid (SA) |
can block |
UV irradiation-induced RACK1 expression |
Nicotiana tabacum |
| CORONATINE INSENSITIVE 1 (COI1, AT2G39940) |
constitutively represses |
SA-related genes in roots |
Arabidopsis thaliana |
| FB1-induced cell death |
is blocked in |
phytoalexin-deficient 4-1 mutant plants |
Arabidopsis thaliana |
| (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) mutant |
was complemented by |
EAR-containing (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) homologs from Physcomitrella patens |
Arabidopsis thaliana; Physcomitrella patens |
| (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) binding efficiency to SA |
is low in vitro when compared with |
(ATNPR3, NPR3, AT5G45110) and (ATNPR4, NPR4, AT4G19660) binding efficiency to SA |
Arabidopsis thaliana |
| (EDS5, SCORD3, SID1, AT4G39030) (ATNPR3, NPR3, AT5G45110) and (ATNPR4, NPR4, AT4G19660) |
also absent in |
Cuscuta australis genome |
Cuscuta australis |
| (SIM, AT5G04470) |
is required for |
elevated SA |
Arabidopsis thaliana |
| (AtGH3.12, GDG1, GH3.12, PBS3, WIN3, AT5G13320) |
interacts with |
immune regulator (ATEDS1, EDS1, AT3G48090) |
Arabidopsis thaliana |
| activation of the SA pathway by Pseudomonas syringae pv. maculicola ES4326 (Psm ES4326) |
is reverted to wild-type levels in |
(COI1, AT2G39940) expressing the SA-degrading enzyme NahG |
Arabidopsis thaliana |
| MpNPR |
cannot substitute for |
(ATNPR4, NPR4, AT4G19660) |
Marchantia polymorpha; Arabidopsis thaliana |
| Mp npr mutant |
shows hypersensitivity to |
SA exogenous treatment |
Marchantia polymorpha |
| palmitate in (TGA3, AT1G22070) dimer |
regulates |
SA-mediated gene expression |
|
| NON-EXPRESSOR OF PR GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
is stabilized in |
systemic tissue |
|
| AevPAL1 gene expression |
was obviously induced by |
100 µm salicylic acid (SA) at 48 h |
Aegilops variabilis |
| (ATNPR3, NPR3, AT5G45110) and (ATNPR4, NPR4, AT4G19660) |
act as |
negative regulators of SA-responsive genes |
Arabidopsis thaliana |
| NRR F40G (FG) transgenic Arabidopsis |
does not suppress |
PR gene induction |
Arabidopsis thaliana |
| inactivation of SA signaling genes in (AT-SYR1, ATSYP121, ATSYR1, PEN1, SYP121, SYR1, AT3G11820) (ATSYP122, SYP122, AT3G52400) |
only partially rescues |
lesion-mimic phenotype |
Arabidopsis thaliana |
| (ATNPR4, NPR4, AT4G19660) |
directly binds |
salicylic acid (SA) |
|
| Eui overexpressor |
decreased |
SA level |
Oryza sativa |
| ELONGATED HYPOCOTYL 5 (HY5, TED 5, AT5G11260) |
may be involved in regulating |
salicylic acid (SA)-induced PR gene expression |
Arabidopsis thaliana |
| (FBI1, HFR1, REP1, RSF1, AT1G02340) |
may be involved in regulating |
salicylic acid (SA)-induced PR gene expression |
Arabidopsis thaliana |
| HR attenuation in (ATCNGC2, CNGC2, DND1, AT5G15410) and (ATCNGC4, CNGC4, DND2, HLM1, AT5G54250) |
was not due to |
high levels of salicylic acid (SA) |
|
| differential regulation of (ATWRKY70, WRKY70, AT3G56400) by the two elicitors |
suggests that either |
some SA-mediated responses are induced by Flg22 but not OGs |
Arabidopsis thaliana |
| biotrophic pathogens |
activate preferentially |
SA-mediated transduction pathway |
|
| increased SA synthesis through activation of the isochorismate pathway |
is hypothesized to be instrumental for |
increased expression of the whole group of SA-related genes |
Arabidopsis thaliana |
| SA pathway |
is not constitutively activated in |
(COI1, AT2G39940) shoots |
Arabidopsis thaliana |
| conservation in MpNPR of a key arginine involved in SA binding |
suggests that |
MpNPR can still bind SA |
Marchantia polymorpha |
| plant immune system incompatibilities |
downregulate jasmonic acid-dependent responses through their effect on expression of |
salicylic acid (SA)-dependent pathway |
|
| orthologous protein from beet curly top virus |
triggers expression of |
SA-responsive genes |
|
| cytosolic effectors |
undermine |
salicylic acid (SA)-dependent immunity |
|
| differences in SA binding affinities for (ATNPR3, NPR3, AT5G45110) and (ATNPR4, NPR4, AT4G19660) and opposing effects of SA binding |
allows |
(ATNPR1, NIM1, NPR1, SAI1, AT1G64280) degradation in high SA concentration cells |
|
| cytosolic (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
translocates to nucleus upon |
SA treatment |
Arabidopsis thaliana |
| bacterial flagellin peptide flg22 |
substantially induces |
SA-dependent secretory pathway genes |
Arabidopsis thaliana |
| SA signaling |
was shown to contribute to |
Flg22-induced repression of the chlorophyll a/b-binding protein gene |
Arabidopsis thaliana |
| salicylic acid |
plays important roles in |
induced defences |
|
| NO activation of SIPK |
is through |
salicylic acid (SA)-dependent pathway |
Nicotiana tabacum |
| oligogalacturonides (OGs) |
do not substantially induce |
PATHOGENESIS-RELATED 1 (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) |
Arabidopsis thaliana |
| (ATMPK4, MAPK4, MPK4, AT4G01370) mutant |
does not exhibit |
SA-hypersensitivity |
|
| CaPAL1 and CaPR1 |
involved in |
SA-dependent defence signalling during Xcv infection |
Capsicum annuum |
| free SA and total SA levels |
measured in |
leaves of WT and CaPAL1-OX transgenic lines during Pst infection |
Arabidopsis thaliana |
| NON-EXPRESSOR OF PR GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) monomers |
localize to |
nucleus |
|
| phosphorylation at Ser55/Ser59 and phosphorylation at Ser11/Ser15 |
interplay with |
SUMOylation |
|
| introgression of (AtGH3.12, GDG1, GH3.12, PBS3, WIN3, AT5G13320) mutant background |
reverses |
autoimmune phenotype |
Arabidopsis thaliana |
| (EDS5, SCORD3, SID1, AT4G39030) |
were down-regulated in |
35S:HAHB10 plants |
Arabidopsis thaliana |
| (AHG2, ATPARN, PARN, AT1G55870) mutant |
displays |
hypersensitivity to salicylic acid |
Arabidopsis thaliana |
| NRR |
binds directly to |
NON-EXPRESSOR OF PR GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
Arabidopsis thaliana |
| EV and NaGSNOR-VIGS when untreated |
showed statistically no significantly different levels of |
SA |
Nicotiana attenuata |
| tomato H52 silencing |
induces |
overaccumulation of conjugated salicylic acid (SA) |
Solanum lycopersicum |
| elevated [CO2] |
causes significant increase of |
SA accumulation in mock plants |
Solanum lycopersicum |
| salicylic acid treatment of uninfected (CHS4, LSD1, AT4G20380) mutants |
caused |
necrosis |
Arabidopsis thaliana |
| wild-type plants |
respond to exogenous SA by induction of |
PR-1 gene |
|
| (ATWRKY48, WRKY48, AT5G49520) T-DNA insertion mutants |
show enhanced resistance associated with increased induction of |
salicylic acid-regulated (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) |
Arabidopsis thaliana |
| syntaxin double mutant ( (AT-SYR1, ATSYP121, ATSYR1, PEN1, SYP121, SYR1, AT3G11820) (ATSYP122, SYP122, AT3G52400) ) |
is |
hypersensitive to salicylic acid (SA) |
|
| pathways that did not contribute to lesion phenotype in (AT-SYR1, ATSYP121, ATSYR1, PEN1, SYP121, SYR1, AT3G11820) (ATSYP122, SYP122, AT3G52400) |
were not involved in |
SA-hypersensitivity |
|
| NONEXPRESSOR OF PATHOGENESIS-RELATED PROTEINS1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) and TGA and WRKY transcription factors |
activates expression of |
thousands of genes |
Arabidopsis thaliana |
| NB-LRR-mediated resistance |
is associated with |
salicylic acid (SA)-dependent signalling pathway |
|
| salicylic acid treatment |
did not exhibit any effect on |
total peroxidase activity of membrane proteins |
Zea mays |
| MpNPR |
can substitute for |
(ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
Marchantia polymorpha; Arabidopsis thaliana |
| salicylic acid (SA) |
is |
plant hormone signaling pathway |
|
| HAHB10 |
expression is up-regulated by |
salicylic acid (SA) treatment |
Helianthus annuus |
| HASEP3 transcripts |
remained almost constant |
72 h after SA treatment |
Helianthus annuus |
| wild-type plants infested by caterpillars with normal salivary secretions |
have similar |
SA levels |
Arabidopsis thaliana |
| Arabidopsis ssi mutation |
causes |
accumulation of SA |
Arabidopsis thaliana |
| NRR |
may interfere with |
NPR2 function |
Arabidopsis thaliana |
| SA-dependent, NON-EXPRESSOR OF PR GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) -independent processes |
exist in |
Arabidopsis thaliana |
Arabidopsis thaliana |
| salicylic acid (SA) |
is applied as |
chemical treatment |
|
| SA treatment |
causes continued increase in stability of |
AXR3NT–GUS protein |
Arabidopsis thaliana |
| (ATICS1, EDS16, ICS1, SID2, AT1G74710) mutant |
did not significantly affect MgCl2- and pathogen-induced WRKY48 expression in |
(ATWRKY48, WRKY48, AT5G49520) expression |
Arabidopsis thaliana |
| AtHEL |
is inducible after |
SA treatment |
Arabidopsis thaliana |
| SA-dependent signal pathway |
activates |
resistance to biotrophs |
|
| salicylic acid (SA) |
has been shown to have a role in |
regulation of expression of some senescence-associated genes during developmentally regulated senescence |
Arabidopsis thaliana |
| NaHD20-silenced plants |
show similar accumulation of |
SA |
Nicotiana attenuata |
| GmERF057 |
expression peaked at 2 h with |
SA treatment |
Glycine max |
| phenomenon of signal transmission from egg-stimulated plants to bacteria-infected plants |
enhanced |
SA production in the receiver plant |
|
| (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) expression |
is higher in |
CaPAL1-OX plants |
Arabidopsis thaliana |
| enhancement of SA effectiveness |
is responsible for activating |
SA-dependent signal transduction pathway |
Solanum tuberosum L. |
| glutathione accumulation per se |
does not necessarily induce |
SA accumulation |
Nicotiana tabacum |
| salicylic acid (SA) |
induces translocation of |
NONEXPRESSOR OF PATHOGENESIS-RELATED PROTEINS1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
Arabidopsis thaliana |
| (AT-SYR1, ATSYP121, ATSYR1, PEN1, SYP121, SYR1, AT3G11820) (ATSYP122, SYP122, AT3G52400) mutants |
undergo programmed cell death (PCD) in response to exogenous |
salicylic acid (SA) |
|
| SA levels in the SAR – plants |
were consistently low |
caterpillar herbivory |
Arabidopsis thaliana |
| HAFT expression in sunflower leaves |
is induced after |
12 hours of salicylic acid treatment |
Helianthus annuus |
| HAHB10 |
expression was induced by |
exogenous SA |
Helianthus annuus |
| NRR |
may interact with |
(ATNPR4, NPR4, AT4G19660) |
Arabidopsis thaliana |
| constitutive expresser of PR genes 22 (cpr22) mutant |
shows heightened |
salicylic acid (SA) accumulation |
Arabidopsis thaliana |
| SA-responsive elements (TCA-elements) |
found in promoters of |
65 PtrWRKY genes |
Populus trichocarpa |
| constitutive MPKK-mediated activation of MAPK3/6 in Arabidopsis |
was sufficient to activate |
most of the SA-responsive genes in a SA-independent manner |
Arabidopsis thaliana |
| (ATWRKY33, WRKY33, AT2G38470) mutants |
show increased expression of |
salicylic acid (SA)-regulated PR genes |
Arabidopsis thaliana |
| DELLAs |
repress |
SA signaling and biosynthesis during Pto DC3000 infection |
Arabidopsis thaliana |
| (ATWRKY1, WRKY1, ZAP1, AT2G04880) |
mediates |
salicylic acid (SA) signalling response |
Solanum tuberosum subsp. andigena |
| interaction between plants and Pseudomonas syringae |
triggers resistance via |
SA-signalling pathway |
Solanum lycopersicum |
| soybean GH2/4 gene |
is inducible by |
inactive SA analogues (3-hydroxybenzoic acid, 4-hydroxybenzoic acid) |
|
| induction of SA-related defence markers PR-1, (AtBG2, AtPR2, BG2, BGL2, GNS2, PR-2, PR2, AT3G57260) and (PR-5, PR5, AT1G75040) in wrky75At22 mutant |
is considerably delayed and greatly reduced in |
wrky75At22 mutant compared to wild type |
Arabidopsis thaliana |
| H2O2 |
was neither necessary nor sufficient for |
SA accumulation |
Nicotiana tabacum |
| SA signalling |
crucial in |
defence responses induced by pathogen attacks |
|
| SA treatment |
was performed on |
Arabidopsis thaliana plants |
Arabidopsis thaliana |
| GmERF069 |
expression peaked at 5 h with |
SA treatment |
Glycine max |
| SA-dependent (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) and ROS-producing NADPH oxidase (ATRBOHD, DELT1, RBOHD, AT5G47910) expression |
higher in |
leaves of CaPAL1-OX plants than in leaves of WT plants |
Arabidopsis thaliana |
| Deficiency in SA signalling |
leads to susceptibility to |
pathogen attack |
|
| activation of (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) target genes |
is known to require |
phosphorylation at the N-terminal phosphodegron |
Nicotiana tabacum |
| elevated [CO2]-induced TMV resistance |
is completely abolished in |
pTRV:NPR1-silenced plants |
Solanum lycopersicum |
| GmERF079 |
expression peaked at 1 h with |
SA treatment |
Glycine max |
| induction of PR-1, (AtBG2, AtPR2, BG2, BGL2, GNS2, PR-2, PR2, AT3G57260) and (PR-5, PR5, AT1G75040) in Lc10 transgenics |
is not recovered to wild-type level but considerably delayed and reduced |
wild-type plants |
Arabidopsis thaliana |
| 24 differentially expressed genes |
are involved in |
salicylic acid signaling pathway |
Gossypium hirsutum |
| age-related changes (ARCs) at the level of salicylic acid |
may contribute to establish |
senescence-competent status of the leaf |
|
| cellular redox state |
is of crucial importance for |
salicylic acid (SA)–NON-EXPRESSOR OF PR GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) signalling pathway |
|
| elevated CO2 and pathogen infection |
increases SA and SA-related transcripts in |
plants |
Solanum lycopersicum |
| HASEP3 expression in sunflower leaves |
does not change after |
salicylic acid treatment |
Helianthus annuus |
| (ATWRKY25, WRKY25, AT2G30250) overexpression |
suppresses |
SA-regulated (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) gene expression |
Arabidopsis thaliana |
| (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) induction by Flg22 when administered at a sub-saturating dose |
is lost |
|
Arabidopsis thaliana |
| salicylic acid (SA) |
is required for |
induction of systemic acquired resistance (SAR) |
|
| salicylic acid |
typically mediates |
defence |
|
| high endogenous salicylic acid (SA) level in syntaxin double mutant |
may contribute to |
SA-hypersensitivity of syntaxin double mutant |
|
| salicylic acid treatment |
showed strong up-regulation of |
pmPOX2b |
Zea mays |
| EV, NaMKK1-VIGS, and NaMEK2-VIGS plants |
show no difference in |
basal and W+W-induced SA levels |
Nicotiana attenuata |
| HAFT |
expression was induced by |
exogenous SA |
Helianthus annuus |
| (AGP17, ATAGP17, AT2G23130) |
might reduce |
free salicylic acid levels |
Arabidopsis thaliana |
| arbuscular mycorrhizal fungi (AMF) inoculation |
partially suppress |
SA-dependent responses |
|
| salicylic acid (SA) |
is |
signaling molecule |
|
| SA induction by avirulent Pst DC3000 (avrRpm1) infection |
much higher than |
SA induction by virulent Pst DC3000 infection |
Arabidopsis thaliana |
| defence-related genes |
induce |
defence-like response |
Solanum tuberosum L. |
| SA or SAG levels |
show no significant changes in |
upper noninoculated leaves |
Solanum tuberosum |
| npr1-5 mutant |
has |
NPR1-dependent salicylic acid signaling |
Arabidopsis thaliana |
| (AtBG2, AtPR2, BG2, BGL2, GNS2, PR-2, PR2, AT3G57260) |
is known to be activated by |
SA in NPR1-dependent and -independent modes |
|
| transcripts related to salicylic acid (SA) response |
were upregulated in |
plants lacking ITPA |
Arabidopsis thaliana |
| ROS and NO |
known to increase |
SA-mediated responses |
|
| SA-mediated defense |
linking to |
resistance to biotrophic pathogens |
Arabidopsis thaliana |
| (BAH1, NLA, SYG1, AT1G02860) mutant plants |
show |
increased levels of salicylic acid (SA) |
Arabidopsis thaliana |
| SA-mediated resistance mechanisms in (AP-3 beta, PAT2, WAT1, AT3G55480) and (CPR5, HYS1, OLD1, AT5G64930) |
may not be conserved between |
(AP-3 beta, PAT2, WAT1, AT3G55480) and (CPR5, HYS1, OLD1, AT5G64930) mutants |
Arabidopsis thaliana |
| low red:far-red light ratio (R:FR)-mediated phytochrome inactivation |
suppresses |
SA-mediated defences |
Arabidopsis thaliana |
| (HY3, OOP1, PHYB, AT2G18790) mutant |
has reduced |
SA-dependent resistance against Pst |
|
| (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) |
is |
SA-dependent defense gene |
Arabidopsis thaliana |
| (ATGLR3.3, GLR3.3, AT1G42540) feedback mechanism |
increasing |
SA biosynthesis |
Arabidopsis thaliana |
| increased salicylic acid (SA) content |
leads to increased |
resistance to adapted powdery mildew |
Arabidopsis thaliana |
| menthol |
increases transcript accumulation levels of |
(AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) |
Glycine max |
| arbuscular mycorrhizal fungi (AMF) |
regulates |
salicylic acid signaling pathway |
|
| transcript accumulation of PtrWRKY89 |
decreased significantly after |
24h of SA treatment |
Populus trichocarpa |
| NON-EXPRESSOR OF PR GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
plays a role in mediating |
SA-induced cell death |
Arabidopsis thaliana |
| (PR-5, PR5, AT1G75040) |
is known to be activated by |
SA in NPR1-dependent and -independent modes |
|
| SA |
induced remarkable increase in mRNA levels of |
PtrWRKY60 and PtrWRKY89 |
Populus trichocarpa |
| stress-induced formation of glutathione |
appears to be required for |
SA accumulation |
Arabidopsis thaliana |
| elevated CO2 |
induces |
SA accumulation |
|
| elevated CO2 |
increased expression of |
(ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
Solanum lycopersicum |
| CaPAL1 silencing |
significantly compromised |
SA-dependent CaPR1 expression |
Capsicum annuum |
| (AtNUDT7, GFG1, NUDT7, AT4G12720) mutant |
has constitutively expressed |
NPR1-independent salicylic acid signaling pathway |
Arabidopsis thaliana |
| augmented transcript increases for SA-dependent genes, expeditious SA accumulation, and more callose depositions in HGLs |
suggest |
strong SA-dependent defence response upon infection |
Nicotiana tabacum |
| elevated CO2 |
increased |
SA level upon uninfected treatments in tomato plants |
Solanum lycopersicum |
| elevated CO2 |
increases SA and SA-related transcripts in |
uninfected plants |
Solanum lycopersicum |
| TdERF1 transcript levels |
highly upregulated after |
SA treatment |
Triticum turgidum subsp. durum |
| nitric oxide |
promotes |
(ATNPR1, NIM1, NPR1, SAI1, AT1G64280) translocation to the nucleus |
Arabidopsis thaliana |
| wild-type plants eaten by cauterized caterpillars |
have similar |
SA levels |
Arabidopsis thaliana |
| SA levels |
did not change in response to |
caterpillar herbivory |
Arabidopsis thaliana |
| strongly triggered production of (AOS, CYP74A, DDE2, AT5G42650) |
is supposed to indicate |
enhanced SA synthesis |
|
| (ATWRKY38, WRKY38, AT5G22570) (ATWRKY46, WRKY46, AT2G46400) (ATWRKY53, WRKY53, AT4G23810) (ATWRKY54, WRKY54, AT2G40750) (ATWRKY62, WRKY62, AT5G01900) and (ATWRKY70, WRKY70, AT3G56400) |
were early SA-induced with highest expression levels |
2h after SA treatment |
Arabidopsis thaliana |
| representative genes of the SA pathway |
include |
PATHOGENESIS-RELATED 1 (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) |
Arabidopsis thaliana |
| CaPAL1 overexpression |
significantly induced |
free SA accumulation in healthy leaves |
Arabidopsis thaliana |
| constitutive SA accumulation in the cpr and (ATCNGC2, CNGC2, DND1, AT5G15410) mutants |
affected |
the glutathione pool size |
Arabidopsis thaliana |
| signaling double mutant (SARD1, AT1G73805) (CBP60G, AT5G26920) |
did not show increased bacterial colonization |
Xcc8004 ΔxopAC Tn5:lux |
Arabidopsis thaliana |
| SIE141 |
affects |
salicylic acid (SA) signaling |
Arabidopsis thaliana |
| glutathione accumulation in the presence of pronounced oxidative stress |
does induce |
SA accumulation |
Nicotiana tabacum |
| elevated CO2 |
generally increases |
SA-related transcripts |
Solanum lycopersicum |
| elevated CO2 |
favours |
SA signalling |
Solanum lycopersicum |
| transient treatment with salicylic acid (SA) |
triggers |
significant clock phase delay |
Arabidopsis |
| transient SA treatment |
is mediated by |
NONEXPRESSER OF PR GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
Arabidopsis thaliana |
| SA responses |
are partly mediated by |
rapid increase of reactive oxygen species (ROS) |
Arabidopsis thaliana |
| SIE141-transformants |
show SA accumulation in |
roots |
Arabidopsis thaliana |
| SIE141 |
is |
secreted effector protein |
|
| CaPR1 induction levels |
distinctly lower in |
silenced plants than in empty-vector control plants during Xcv infection |
Capsicum annuum |
| salicylic acid (SA) |
mediates expression of |
defence-related genes |
Solanum tuberosum L. |
| elevated [CO2] |
increases transcript level of |
(AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) |
Solanum lycopersicum |
| BTH |
is |
benzothiadiazole S-methylester |
|
| (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) mutant |
does not develop |
salicylic-acid-inducible programmed cell death (PCD) |
|
| MPK6-modulated signalling pathway |
is responsible for |
gene expression of NON-EXPRESSOR OF PR GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
Arabidopsis thaliana |
| Suppression of CaPAL1 induction in silenced leaves |
reduced |
expression of the SA-dependent gene CaPR1 |
Capsicum annuum |
| (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) and (TGA1, AT5G65210) |
are subject to |
S-nitrosylation and S-glutathionylation |
Arabidopsis thaliana |
| pathogen infection |
significantly increases |
(ATNPR1, NIM1, NPR1, SAI1, AT1G64280) transcript levels |
Solanum lycopersicum |
| Botrytis cinerea inoculation |
raises SA content by 2.0-fold under ambient [CO2] and 2.7-fold under |
elevated [CO2] |
Solanum lycopersicum |
| pTRV:PI-silenced plants |
do not exhibit altered levels of |
(ATNPR1, NIM1, NPR1, SAI1, AT1G64280) and (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) transcript expression |
Solanum lycopersicum |
| (ATMYB44, ATMYBR1, MYB44, MYBR1, AT5G67300) |
modulates antagonistic interaction by activating |
SA-mediated defenses |
|
| SA |
provides increased resistance to |
Fusarium oxysporum |
Arabidopsis thaliana |
| TaADF7 knock-down plants |
had |
(AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) gene expression significantly reduced when TaADF7 was silenced |
Triticum aestivum |
| impairment of (ATEIN2, CKR1, EIN2, ERA3, ORE2, ORE3, PIR2, AT5G03280) |
left unaffected |
salicylic acid signaling pathway |
Arabidopsis thaliana |
| (ATSPX1, SPX1, AT5G20150) |
mediates crosstalks among |
leaf senescence, Pi starvation and SA signaling pathways |
Arabidopsis thaliana |
| BohLOL1 gene expression |
is upregulated by |
2,6-dichloroisonicotinic acid |
Bambusa oldhamii |
| SA levels |
show no treatment effect between |
control and other treatments |
Phaseolus lunatus |
| benzothiadiazole S-methylester |
is |
potent SA analog |
|
| NPR1-dependent salicylic acid signaling |
controls |
long-distance transport of sodium into shoot |
Arabidopsis thaliana |
| elevated CO2 |
increased expression of |
(AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) |
Solanum lycopersicum |
| (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
is involved in feedback regulation of |
salicylic acid (SA) levels |
Arabidopsis thaliana |
| SA synthesis (OsICS1 and OsPAL1) and signaling (OsPAD4 and OsEDS1) |
was not affected noticeably by |
(MIR319, MIR319B, AT5G41663) /OsTCP21 |
Oryza sativa |
| monomeric NON-EXPRESSOR OF PR GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
migrates to |
nucleus |
Arabidopsis thaliana |
| seeds of the oldest plants |
contained significantly higher |
salicylic acid levels |
Cistus albidus |
| oxidative stress-induced glutathione accumulation prevention in a (CAT2, AT4G35090) (ATECS1, AtGSH1, CAD2, GSH1, GSHA, PAD2, RAX1, RML1, AT4G23100) double mutant |
resulted in |
decreased SA content and (ATICS1, EDS16, ICS1, SID2, AT1G74710) transcript amounts |
Arabidopsis thaliana |
| single (CAT2, AT4G35090) mutant |
accumulated |
substantial levels of SA |
Arabidopsis thaliana |
| pTRV:NPR1-silenced plants |
show significantly lower levels of |
(ATNPR1, NIM1, NPR1, SAI1, AT1G64280) and (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) transcripts |
Solanum lycopersicum |
| salicylic acid (SA)-mediated resistance to aphids |
has been observed on some occasions |
some plant species |
|
| Arabidopsis (BIP, BIP2, AT5G42020) knockout lines |
displayed |
concomitant decrease in (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) gene expression |
Arabidopsis thaliana |
| Arabidopsis nonphenylpropanoid mutants containing increased SA content |
display |
dwarfism |
Arabidopsis thaliana |
| silencing of GmPAD4 |
reduced |
basal salicylic acid accumulation |
Glycine max |
| SA marker genes (PR-1 and (PR-5, PR5, AT1G75040) ) |
are not differentially expressed in |
wat1-1 versus Col-0 |
Arabidopsis thaliana |
| SA induction of NON-EXPRESSOR OF PR GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) -independent genes |
can also be repressed by |
inhibition of kinase activity |
|
| (TOP2, AT5G10540) |
is |
salicylic acid target |
Arabidopsis thaliana |
| plant-specific factors |
may modulate |
TOP2–SA interaction |
Arabidopsis thaliana |
| salicylic acid (SA) |
is |
important resistance pathway against biotrophs |
|
| salicylic acid treatment of uninfected (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) lines |
did not cause |
necrosis |
Arabidopsis thaliana |
| 35S pro::NahG transgenic line |
is |
derivative of Col-0 |
Arabidopsis thaliana |
| PtrWRKY89 |
is |
induced by SA at early stage |
Populus trichocarpa |
| Constitutive overexpression of CaPAL1 in Arabidopsis |
conferred |
induction of (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) expression |
Arabidopsis thaliana |
| CaPAL1 silencing |
significantly compromised |
induction of SA accumulation |
Capsicum annuum |
| whole-transcriptome approach to investigate SA involvement in A. thaliana response to compatible viruses |
is |
unique study of SA role in Arabidopsis thaliana viral response |
Arabidopsis thaliana |
| endogenous salicylic acid (SA) signaling cascades |
participates in |
plant responses to salt stress |
Arabidopsis thaliana |
| more SA and SAG accumulation in HGLs |
correlated with |
stronger HR reaction |
|
| SA-inducible genes |
are not constitutively expressed in |
quadruple-DELLA mutant |
Arabidopsis thaliana |
| salicylic acid (SA) |
regulates |
many aspects of plant immunity in distal non-infected tissues |
Arabidopsis thaliana |
| ZmMPK17 transcript |
increases during treatment with |
salicylic acid |
Zea mays |
| expression levels of (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) (AtBG2, AtPR2, BG2, BGL2, GNS2, PR-2, PR2, AT3G57260) and (PR-5, PR5, AT1G75040) |
are similar to those in |
TRV:00 plants |
Gossypium barbadense |
| npr4-4D mutant protein |
no longer responds to |
salicylic acid (SA) treatment |
Arabidopsis thaliana |
| CaRBP1 silencing |
significantly compromised |
SA accumulation |
Capsicum annuum |
| OsPP18 |
is transiently induced by |
salicylic acid (SA) treatment |
Oryza sativa |
| ENHANCED DISEASE SUSCEPTIBILITY 1a (GmEDS1a) and ENHANCED DISEASE SUSCEPTIBILITY 1b (GmEDS1b) genes |
only partially rescued |
defect in pathogen-responsive salicylic acid accumulation |
Arabidopsis thaliana |
| reducing the SA accumulation in HCT-reduced plants |
alleviated |
dwarfism |
Arabidopsis thaliana |
| (CBP60G, AT5G26920) |
contributes to plant immunity through |
modulation of salicylic acid levels |
|
| SIE141 |
modulates |
salicylic acid (SA) signaling |
Arabidopsis thaliana |
| salicylate levels |
show no significant changes in |
mock-inoculated leaves |
Solanum tuberosum |
| TMV inoculation |
raises SA content by 3.5-fold under ambient [CO2] and 18.6-fold under |
elevated [CO2] |
Solanum lycopersicum |
| SIE141 |
affects |
salicylic acid (SA) signaling |
Arabidopsis thaliana |
| (ATMAPK3, ATMPK3, MPK3, AT3G45640) mutant |
showed no differential expression in genes involved in |
salicylic acid (SA) biosynthesis and signalling |
Arabidopsis thaliana |
| (ATCIPK14, ATSR1, CIPK14, PKS24, SnRK3.15, SR1, AT5G01820) (CAMTA3, SR1, AT2G22300) |
contributes to plant immunity through |
modulation of salicylic acid levels |
|
| 558 upregulated genes in 35S::AtSPX1/WT |
are significantly enriched in |
SA signaling pathways |
Arabidopsis thaliana |
| NON-EXPRESSOR OF PR GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
is |
master regulator of salicylic acid (SA) signaling |
Arabidopsis |
| partial rescue of bak1-4 bkk1-1 by NahG |
suggested |
cell-death phenotype in the double mutant was likely SA-dependent |
Arabidopsis thaliana |
| up-regulation of (ATGDU3, GDU3, LSB1, AT5G57685) |
increases expression of |
Cell wall-associated kinase 1 (AtWAK1, PRO25, WAK1, AT1G21250) |
Arabidopsis thaliana |
| salicylic acid (SA) |
interacted more strongly with |
full-length (OOP, TOP1, AT5G65620) |
Arabidopsis thaliana |
| (BAH1, NLA, SYG1, AT1G02860) mutant plants |
show further increase in |
salicylic acid (SA) levels upon pathogen infection |
Arabidopsis thaliana |
| (SAUR19, AT5G18010) overexpression |
rescues |
SA-induced (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) phenotypes in the dark |
|
| (AP-3 beta, PAT2, WAT1, AT3G55480) roots |
contain more |
SA |
Arabidopsis thaliana |
| repression of SA-inducible kinases |
brings about |
severe inhibition of SA-responsive transcription in low R:FR |
Arabidopsis thaliana |
| salicylic acid (SA) |
activates |
SIPK |
Nicotiana tabacum |
| (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) transcript levels in control plants |
are induced to similar levels after |
salicylic acid treatment |
Arabidopsis thaliana |
| 13-HOT treatment in barley leaves |
induces expression usually activated after |
salicylic acid treatment |
|
| (AtBRN1, AtRBP-DR1, BRN1, RBP-DR1, AT4G03110) |
activates |
SA-mediated immunity |
Arabidopsis thaliana |
| genes responsive to salicylic acid |
were upregulated in |
tko plants |
Arabidopsis thaliana |
| (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) and (AtBG2, AtPR2, BG2, BGL2, GNS2, PR-2, PR2, AT3G57260) messenger RNA (mRNA) levels |
are not elevated in noninfected |
quadruple-DELLA mutant compared to La-er plants |
Arabidopsis thaliana |
| NON-EXPRESSOR OF PATHOGENESIS-RELATED GENE 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
is |
master gene for SA signaling transduction |
|
| salicylic acid (SA) treatment |
induces |
PATHOGENESIS-RELATED 1 (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) accumulation |
|
| (ATMPK4, MAPK4, MPK4, AT4G01370) mutant |
displays |
constitutive activation of the salicylic acid (SA) pathway |
Arabidopsis thaliana |
| (AtNUDT7, GFG1, NUDT7, AT4G12720) mutant |
has constitutively expressed |
NPR1-dependent salicylic acid signaling pathway |
Arabidopsis thaliana |
| SA |
is |
salicylic acid |
|
| CRYPTOCHROME 1 (ATCRY1, BLU1, CRY1, HY4, OOP2, AT4G08920) |
enhances |
salicylic acid (SA)-induced PR-1 expression |
Arabidopsis thaliana |
| acarbose infiltration with Pseudomonas syringae |
results in higher induction of |
salicylic acid (SA) levels |
Arabidopsis thaliana |
| W box |
is |
wounding, salicylic acid and stress response element |
|
| NON-EXPRESSOR OF PR GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
interacts with |
TGA family transcription factors |
|
| Pst (avrPtoB S335D) infection |
had PR1 transcript levels similar to |
Pst (ΔavrPtoB) infection |
Arabidopsis thaliana |
| high light |
1O2 enhances |
salicylate levels in leaves |
Arabidopsis thaliana |
| nahG-ox plants |
have significantly lower |
endogenous salicylic acid (SA) levels |
Brachipodium distachyon |
| presence of the NahG transgene |
partially rescues |
bak1-4 bkk1-1 double-mutant phenotype |
Arabidopsis thaliana |
| salicylic acid |
is used for |
salicylic acid signaling assays |
Arabidopsis thaliana |
| KD-GmBIR1 samples |
had higher level of |
SA |
Glycine max |
| exogenous application of salicylic acid (SA) |
induced |
N-rich protein (NRP, NRP1, AT5G42050) -mediated cell death signaling |
Glycine max |
| phb3-3 plants |
respond normally to |
exogenous SA treatment |
Arabidopsis thaliana |
| CA-MPK4 transgenic plants |
accumulate less |
salicylic acid following pathogen infection |
Arabidopsis thaliana |
| salicylic acid (SA) pathway |
is major contributor to |
defense against Pseudomonas syringae |
Arabidopsis thaliana |
| NPR1–TGAs interactions |
is used to validate |
efficiency of Gateway-compatible Gal4-AD–TF library |
Arabidopsis thaliana |
| cpr22 double mutants with (ATEDS1, EDS1, AT3G48090) |
did not affect |
SA levels |
|
| BdWRKY38 |
mediates |
salicylic acid (SA) signaling |
Brachypodium distachyon |
| BdWRKY38 |
is |
major modulator of the salicylic acid (SA) signaling pathway |
Brachipodium distachyon |
| (ATRBOHD, DELT1, RBOHD, AT5G47910) expression |
close to the limit of quantification in |
NahG plants |
Solanum tuberosum |
| DEGs |
revealed enrichment in |
SA biosynthesis and signaling |
Arabidopsis thaliana |
| NON-EXPRESSOR OF PR GENES 3 (ATNPR3, NPR3, AT5G45110) |
binds |
salicylic acid (SA) |
Arabidopsis thaliana |
| R419 residue in (ATNPR4, NPR4, AT4G19660) |
is essential for |
SA-binding activity of (ATNPR4, NPR4, AT4G19660) |
Arabidopsis thaliana |
| salicylhydroxamic acid and azide |
inhibits |
SA-dependent reactive oxygen species (ROS) production |
Arabidopsis thaliana |
| low red:far-red light ratio (R:FR) |
causes strong reduction in regulation of |
SA-responsive genes |
Arabidopsis thaliana |
| SA accumulation |
results in |
induction of basal resistance |
Arabidopsis thaliana |
| KD-GmBIR1 overexpression |
has significantly higher levels of |
SA (salicylic acid) |
Glycine max |
| ITPA loss-of-function |
causes |
salicylic acid (SA) accumulation |
Arabidopsis thaliana |
| WT-GmBIR1 samples |
had significantly lower level of |
SA |
Glycine max |
| (ATCNGC2, CNGC2, DND1, AT5G15410) mutant |
displays elevated levels of |
salicylic acid (SA) |
Arabidopsis thaliana |
| enhanced resistance phenotype in (ATCNGC2, CNGC2, DND1, AT5G15410) (ATCNGC4, CNGC4, DND2, HLM1, AT5G54250) , and cpr22 mutants |
is |
SA dependent |
Arabidopsis thaliana |
| T–DNA insertion lines |
tested for |
SA response phenotype |
Arabidopsis thaliana |
| Pseudomonas spp. infection |
induced |
faster and stronger (PR-5, PR5, AT1G75040) gene expression in 35S::BiP4 inoculated leaves |
Glycine max |
| BiP-mediated positive modulation of N-rich protein (NRP, NRP1, AT5G42050) cell death signaling |
occurs through |
yet undefined mechanism activated by salicylic acid (SA) signaling |
Glycine max |
| various defense responses |
include production and accumulation of |
salicylic acid |
|
| silencing of GmEDS1 gene |
affects |
pathogen-induced salicylic acid (SA) accumulation |
Glycine max |
| SA-dependent defense response |
contributed to |
resistance phenotype of KD-GmBIR1 plants |
Glycine max |
| salicylic acid (SA) |
is involved in positive control of |
hypersensitive response (HR) |
Arabidopsis thaliana |
| synthesis of PR proteins |
is under control of |
salicylic acid (SA) signaling pathway |
|
| Pst (ΔavrPtoB) complemented with AvrPtoB WT or AvrPtoB S335A infection |
had PR1 transcript levels similar to |
Pst infection |
Arabidopsis thaliana |
| feedback loop |
indicating the role of |
(ATRBOHD, DELT1, RBOHD, AT5G47910) in the spatial regulation of salicylic acid (SA) accumulation |
Solanum tuberosum |
| (ATNPR3, NPR3, AT5G45110) |
is |
one of the SA biosynthesis and signaling genes |
Arabidopsis thaliana |
| (CHR3, SYD, AT2G28290) and (ATBRM, BRM, CHA2, CHR2, FFO3, AT2G46020) |
may play opposing roles in regulating |
salicylic acid signaling |
Arabidopsis thaliana |
| cngc2-3 mutant |
has significantly higher |
total salicylic acid levels compared to Columbia wild-type |
Arabidopsis thaliana |
| MdPR5 |
is |
SA-regulated gene |
Malus domestica |
| increased level of SA in KD-GmBIR1 |
activated |
SA-dependent defense response |
Glycine max |
| (LCR77, PDF1.2, PDF1.2A, AT5G44420) |
is highly induced when |
SA-associated pathways are impaired in (ATCNGC2, CNGC2, DND1, AT5G15410) mutant |
Arabidopsis thaliana |
| (CAMTA3, SR1, AT2G22300) |
is a key regulator in the expression of |
(ATEDS1, EDS1, AT3G48090) (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) and salicylic acid-mediated plant immunity |
Arabidopsis thaliana |
| PRR2-like proteins in vascular plants |
have distinct functions in |
fruit ripening and SA responses |
|
| (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) mutants |
fail to raise |
SA response |
|
| top lines |
are similar to |
(NRP, NRP1, AT5G42050) mutants |
Arabidopsis thaliana |
| SA accumulation |
results in |
PR gene expression |
Arabidopsis thaliana |
| SUNA1 expression |
is impaired in |
SA biosynthesis-defective mutant (ATICS1, EDS16, ICS1, SID2, AT1G74710) |
Arabidopsis thaliana |
| (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) mutant |
shows no significant difference in pathogen population density between |
Chlorella fusca-treated and BG11 medium-treated leaves |
Arabidopsis thaliana |
| salicylic acid (SA) responsive genes |
encode |
BdWRKY38 and BdWRKY44 |
Brachypodium distachyon |
| salicylic acid (SA) |
induces |
transcriptional changes |
Arabidopsis thaliana |
| (ATCNGC2, CNGC2, DND1, AT5G15410) (ATCNGC4, CNGC4, DND2, HLM1, AT5G54250) double mutants with (ATPAD4, PAD4, AT3G52430) |
did not affect |
SA levels |
|
| triple mutant (ATPSKR1, PSKR1, AT2G02220) (AtPSKR2, PSKR2, AT5G53890) (PSY1R, AT1G72300) plants |
show delayed |
SA accumulation |
Arabidopsis thaliana |
| drought stress |
induces expression of |
SA-responsive genes |
Arabidopsis thaliana |
| two NON-EXPRESSOR OF PR GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) cysteine mutants |
had |
enhanced (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) expression in the absence of elevated SA |
|
| (AFB1, ATGRH1, GRH1, AT4G03190) overexpression |
led to suppression of |
SA levels |
|
| plant-produced (OOP, TOP1, AT5G65620) |
bound |
salicylic acid (SA) |
Arabidopsis thaliana |
| salicylic acid (SA) signaling |
is not required for |
elevated CO2-induced heat stress tolerance |
Arabidopsis thaliana |
| (CPR5, HYS1, OLD1, AT5G64930) mutant |
exhibits |
drought tolerance |
Arabidopsis thaliana |
| SA levels in pskr1-3 mutant plants |
are about 1.6-fold higher than in |
wild-type plants at 12 and 24 h post-inoculation |
Arabidopsis thaliana |
| drought stress |
induces expression of |
(AtBG2, AtPR2, BG2, BGL2, GNS2, PR-2, PR2, AT3G57260) |
Arabidopsis thaliana |
| (ACD6, DEG16, AT4G14400) mutant |
exhibits |
drought tolerance |
Arabidopsis thaliana |
| wild type plants under non-infection conditions |
show |
baseline levels of salicylic acid (SA) |
Arabidopsis thaliana |
| salicylic acid receptor mutant npr1-2 |
did not show increased bacterial colonization |
Xcc8004 ΔxopAC Tn5:lux |
Arabidopsis thaliana |
| plant defenses |
are induced via |
NPR1-dependent signaling process |
|
| full-length (OOP, TOP1, AT5G65620) |
was more sensitive to SA than |
truncated (OOP, TOP1, AT5G65620) |
Arabidopsis thaliana |
| top lines |
exhibit |
SA resistance |
Arabidopsis thaliana |
| bacterial SA hydroxylase (nahG gene) |
metabolizes |
salicylic acid (SA) |
Oryza sativa |
| NONEXPRESSOR OF PATHOGENESIS-RELATED GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
mitigates |
SA-induced inhibition of hypocotyl elongation |
Arabidopsis thaliana |
| (AHBP-1B, AtTGA2, TGA2, AT5G06950) |
binds to |
(CBP60G, AT5G26920) promoter region |
Arabidopsis thaliana |
| (ATMYB44, ATMYBR1, MYB44, MYBR1, AT5G67300) over-expression |
causes up-regulated PR1 phenotype that is reversed by |
SA depletion |
|
| pskr1-3 mutant |
showed higher induction of |
(AtBG2, AtPR2, BG2, BGL2, GNS2, PR-2, PR2, AT3G57260) |
Arabidopsis thaliana |
| up-regulation of (ATGDU3, GDU3, LSB1, AT5G57685) |
increases expression of |
upstream regulator (ACD6, DEG16, AT4G14400) |
Arabidopsis thaliana |
| SA-repressed ETHYLENE RESPONSE FACTORS (ERF) |
are upregulated in |
F1 hybrid |
Brassica napus |
| (ATMED14, MED14, SWP, AT3G04740) mutation |
reduces |
SA responsiveness |
Arabidopsis thaliana |
| (ATNPR4, NPR4, AT4G19660) |
functions together with |
(AHBP-1B, AtTGA2, TGA2, AT5G06950) (OBF5, TGA5, AT5G06960) (BZIP45, TGA6, AT3G12250) |
Arabidopsis thaliana |
| npr1-1 npr4-4D double mutant |
shows completely blocked induction of |
SYSTEMIC ACQUIRED RESISTANCE DEFICIENT 1 (SARD1, AT1G73805) |
Arabidopsis thaliana |
| PtrWRKY80 |
could be only involved in |
SA signalling pathway |
Populus trichocarpa |
| expression of (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) in HGLs |
was barely affected in |
HGLs in the absence of pathogen challenge |
Nicotiana tabacum |
| elevated [CO2] |
increases transcript level of |
(ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
Solanum lycopersicum |
| salicylic acid (SA) |
enhances interaction between |
(ATNPR3, NPR3, AT5G45110) (ATNPR4, NPR4, AT4G19660) and (AHBP-1B, AtTGA2, TGA2, AT5G06950) |
Arabidopsis thaliana |
| TOPs |
are |
SA-binding proteins |
Arabidopsis thaliana |
| NPR1-dependent salicylic acid (SA) signaling |
is not involved in |
elevated CO2-induced heat stress tolerance |
Arabidopsis thaliana |
| (AP-3 beta, PAT2, WAT1, AT3G55480) mutation |
is not accompanied by changes in expression of |
SA marker genes PR-1 and (PR-5, PR5, AT1G75040) |
Arabidopsis thaliana |
| (ATSIZ1, SIZ1, AT5G60410) |
negatively affects |
drought tolerance |
Arabidopsis thaliana |
| Col-0 plants infected with H. arabidopsidis and pre-treated with DNQX |
examined expression of |
defense genes involved in SA-related pathway |
Arabidopsis thaliana |
| PpWRKY31 overexpression |
enhanced |
expression of genes associated with salicylic acid |
Pyrus pyrifolia |
| salicylic acid (SA) |
modulates |
circadian rhythms |
Arabidopsis |
| SIE141-triggered resistance activation |
was accompanied by |
salicylic acid (SA) accumulation in the roots |
Arabidopsis thaliana |
| total salicylic acid (SA) levels |
is increased in |
GmPLDα1KD hairy roots compared to GUS hairy roots |
Glycine max |
| phosphorylation at Ser11/Ser15 |
activates |
NON-EXPRESSOR OF PR GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
|
| SA concentration in systemic tissue |
is high enough to disrupt |
NPR4–NPR1 interaction |
|
| nahG (ATSIZ1, SIZ1, AT5G60410) double mutant |
suppresses |
drought tolerance phenotype of (ATSIZ1, SIZ1, AT5G60410) |
Arabidopsis thaliana |
| 35S:YUC1 plants |
did not exhibit significant suppression of |
SA-responsive gene expression |
|
| exogenous auxin treatment |
can suppress |
SA-mediated defense gene expression |
|
| (ATGDU3, GDU3, LSB1, AT5G57685) mutant |
activates |
salicylic acid (SA) pathway |
Arabidopsis thaliana |
| PpWRKY31-PpRPL12 regulatory module |
indirectly influences |
salicylic acid pathway |
Pyrus pyrifolia |
| SA-NPR1-SUNA1 signaling cascade |
represents |
antibacterial translation regulatory mechanism |
Arabidopsis thaliana |
| pathogen challenge |
generates |
SA gradient |
|
| (LGO, SMR1, AT3G10525) |
is required for |
elevated SA |
Arabidopsis thaliana |
| (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) mutant |
was complemented by |
MpNPR |
Arabidopsis thaliana; Marchantia polymorpha |
| (04C11, ATPEN1, PEN1, AT4G15340) mutation |
is linked to |
accumulation of SA |
Arabidopsis thaliana |
| N-terminal domain of (TGA3, AT1G22070) |
is sufficient for interaction with |
full-length (ATWRKY53, WRKY53, AT4G23810) |
Arabidopsis thaliana |
| SUNA1 expression |
is dependent on |
NON-EXPRESSOR OF PR GENES 1 (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
Arabidopsis thaliana |
| (BIP, BIP2, AT5G42020) |
antagonistically modulates |
salicylic acid (SA)-mediated induction of pathogenesis-related (PR) genes |
Glycine max |
