ライフサイエンスコーパス: jasmonic acid

1 e regulator of rice root curling mediated by jasmonic acid.

2 ling in response to touch can be reverted by jasmonic acid.

3 the control of GSL levels in the absence of jasmonic acid.

4 ffected root growth sensitivity to exogenous jasmonic acid.

5 LOX4 cDNAs and biochemically with exogenous jasmonic acid.

6 ved in the biosynthesis of the plant hormone jasmonic acid.

7 for cuticular components or the phytohormone jasmonic acid.

8 nse-related phytohormones salicylic acid and jasmonic acid.

9 classic defense hormones salicylic acid and jasmonic acid.

10 alicylic acid content, but not that of trans-jasmonic acid.

11 d cinerolone, that appear to be derived from jasmonic acid.

12 A) and thereby producing 12-O-glucopyranosyl-jasmonic acid (12-O-Glc-JA) is still elusive.

13 le for specifically glycosylating 12-hydroxy-jasmonic acid (12-OH-JA) and thereby producing 12-O-gluc

14 (-2)s(-1)), high temperature (40 degrees C), jasmonic acid (200muM), menadione (120muM) and abscisic

15 3 major growth regulators (auxin, ethylene, jasmonic acid); (4) processing the large amount of carbo

16 AtFAAH overexpressors had lower amounts of jasmonic acid, abscisic acid and both free and conjugate

17 llowing treatment of wheat, separately, with jasmonic acid, abscisic acid or with the avirulent race,

18 Here we show that jasmonic acid also inhibits the plant's responses to rhi

19 ons of biotic elicitors such as chitosan and jasmonic acid also significantly reduced the levels of r

20 onsive pathways including salicylic acid and jasmonic acid also were up-regulated in juvenile primord

21 and concomitant irregular functioning of the jasmonic acid and abscisic acid pathways upon infection.

22 fferent hormones as auxin, gibberellic acid, jasmonic acid and abscisic acid, light, and circadian re

23 t14 does not involve the signaling molecules jasmonic acid and abscisic acid, or autophagy, but assoc

24 water potential stress and for regulation of jasmonic acid and auxin-related gene expression as well

25 establishment, but also for biosynthesis of jasmonic acid and conversion of indole butyric acid to i

26 Induced expression of AdVPE in response to jasmonic acid and ethylene also indicates its involvemen

27 Pharmacological applications of jasmonic acid and ethylene also synergize the induced ac

28 activates de novo synthesis of the hormones jasmonic acid and ethylene and induces the expression of

29 dividual ZmPep-elicited changes in levels of jasmonic acid and ethylene and the magnitude of induced

30 By contrast, several genes in jasmonic acid and ethylene responses were down-regulated

31 A19 may regulate gene expression involved in jasmonic acid and ethylene signaling of pathogen respons

32 AtPMEI expression is strictly regulated by jasmonic acid and ethylene signaling, while only AtPMEI1

33 ndent on salicylic acid signaling and not on jasmonic acid and ethylene signaling.

34 and EIN2 that operate, respectively, in the jasmonic acid and ethylene signalling pathways, do not c

35 lis herbivory, and the synergistic action of jasmonic acid and ethylene.

36 ranscript response but hinted at a link with jasmonic acid and gibberellin signaling pathways.

37 SA, SlSAMT, as well as enzymes that act upon jasmonic acid and indole-3-acetic acid were identified.

38 Jasmonic acid and its derivatives (jasmonates [JAs]) pla

39 Jasmonic acid and its derived metabolites (JAs) orchestr

40 dienoic acid concomitant with an increase of jasmonic acid and jasmonoyl-isoleucine.

41 deficient plants displayed a higher level of jasmonic acid and methyl jasmonate, as well as the oxyli

42 els of these genes implies the importance of jasmonic acid and phenylpropanoid signaling pathways loc

43 y the synthesis, movement, and perception of jasmonic acid and related plant metabolites.

44 d by wounding as well as by the phytohormone jasmonic acid and repressed by ethylene, signals that ar

45 se, most notably genes in the abscisic acid, jasmonic acid and salicylic acid pathways.

46 ms dependent on the plant hormones ethylene, jasmonic acid and salicylic acid to control host defense

47 aling pathways, including those regulated by jasmonic acid and salicylic acid.

48 ating tripartite interactions, one involving jasmonic acid and the other salicylic acid.

49 ession of AtERF4 can be induced by ethylene, jasmonic acid, and abscisic acid (ABA).

50 Levels of salicylic acid (SA), jasmonic acid, and abscisic acid increased in rust-infec

51 ed phytohormones (salicylates, auxins, trans-jasmonic acid, and abscisic acid) and the transcript lev

52 he stress hormones salicylic acid, ethylene, jasmonic acid, and abscisic acid.

53 The plant hormones, salicylic acid (SA), jasmonic acid, and ethylene have emerged as key players

54 signaling pathways involving salicylic acid, jasmonic acid, and ethylene to defend against pathogen a

55 Levels of 12-oxo-phytodienoic acid, jasmonic acid, and its isoleucine derivative increased i

56 scisic acid, auxin, gibberellic acid, methyl jasmonic acid, and salicylic acid differentially regulat

57 hat are simultaneously depleted of ethylene, jasmonic acid, and salicylic acid signaling.

58 of two defense hormones: salicylic acid and jasmonic acid, and show increased resistance to the bact

59 ohormones, salicylic acid, abscisic acid and jasmonic acid, and the bacterial virulence factor, coron

60 ion was associated with notable induction of jasmonic acid- and green leaf volatile-biosynthetic gene

61 opropanecarboxylic acid), salicylic acid and jasmonic acid (applied as methyl jasmonate).

62 carriers, and sugar transporters), ethylene, jasmonic acid, auxin, gibberellic acid, and abscisic aci

63 Our studies of lox3 lox4 as well as other jasmonic acid biosynthesis and perception mutants show t

64 athways (e.g., metabolism, redox regulation, jasmonic acid biosynthesis and stress responses).

65 witch coincided with increased expression of jasmonic acid biosynthesis genes and large-scale activat

66 ver, ECB saliva induced genes present in the jasmonic acid biosynthesis pathway in both tomato and ma

67 12-oxo-phytodienoic acid, a precursor in the jasmonic acid biosynthesis pathway, in the sorghum SCA-t

68 ess response, along with brassinosteroid and jasmonic acid biosynthesis, by directly binding to the p

69 ss signals conferred in part by promotion of jasmonic acid biosynthesis.

70 t SA binds to CATALASE2 to inhibit auxin and jasmonic acid biosynthetic enzymes as a means to strengt

71 scence-associated genes (SAGs), ethylene and jasmonic acid biosynthetic genes, APETALA2, ethylene-res

72 Ethylene and jasmonic acid both act to regulate the plant's responsiv

73 ciated with plant defense and growth such as jasmonic acid, brassinosteroids, cytokinins, auxin and s

74 r mechanical wounding nor the application of jasmonic acid, but infestation by sucking insects, induc

75 ones such as gibberellins, abscisic acid and jasmonic acid, but surprisingly, not auxin.

76 ed basil (especially elicited with 100microM jasmonic acid) can be recommended for food technologists

77 xygenase activity was missing and endogenous jasmonic acid concentrations were reduced in developing

78 At 1 d infestion, the jasmonic acid content in leaves noninfested and in leave

79 ell abscisic acid content and an increase in jasmonic acid content.

80 e nifH mutant nodules had elevated levels of jasmonic acid, correlating with signs of nitrogen depriv

81 more, exogenous application of OPDA on maize jasmonic acid-deficient plants caused enhanced callose a

82 primordia; indeed, exogenous application of jasmonic acid delayed both the appearance of adult trait

83 associated with transgenerational priming of jasmonic acid-dependent defense responses in both specie

84 JAZh plants deregulated a specific branch of jasmonic acid-dependent direct and indirect defenses: ir

85 acid, jasmonoyl-isoleucine accumulation, and jasmonic acid-dependent gene expression in Atdpl1-1 muta

86 cell wall modification, salicylic acid- and jasmonic acid-dependent pathways, redox homeostasis, str

87 Herbivory generates a jasmonic acid-dependent reduction in seed dormancy, medi

88 and a strong disturbance of the turnover of jasmonic acid derivatives.

89 Jasmonic acid did not confer any apparent defense respon

90 l induction of defense-related phytohormones jasmonic acid, E, and salicylic acid at 30, 120, and 240

91 ORA59 is the master regulator of the jasmonic acid-ET-induced defense program.

92 molecule impacts signaling in tomato via the jasmonic acid, ethylene, and auxin pathways; (2) CMA doe

93 ol per leaf, ZmPep3 stimulates production of jasmonic acid, ethylene, and increased expression of gen

94 st necrotrophic attackers by suppressing the jasmonic acid-ethylene (ET) defense response.

95 ts reveal transcriptional changes resembling jasmonic acid/ethylene (JA/ET) signalling in the presenc

96 nes regulated by both the salicylic acid and jasmonic acid/ethylene pathways is reduced in ups1 compa

97 ease in central metabolism, induction of the jasmonic acid/ethylene pathways, and emission of volatil

98 nents and H2A.Z also resulted in compromised jasmonic acid/ethylene-mediated immunity.

99 Furthermore, although jasmonic acid genes were repressed and salicylic acid-re

100 1/Cullin/F-box-type ubiquitin ligase: auxin, jasmonic acid, gibberellic acid, and strigolactone.

101 ubtle transient aberration of salicylic acid-jasmonic acid homeostasis during development.

102 d we demonstrate that they act by modulating jasmonic acid homeostasis.

103 proteins in the regulation of salicylic and jasmonic acid host defense responses as well as virus-sp

104 und-induced synthesis of 12-O-glucopyranosyl-jasmonic acid in A. thaliana.

105 nhanced induction of the key defense hormone jasmonic acid in exposed plants after herbivory.

106 and ts2 inflorescences, revealing a role for jasmonic acid in male flower development in maize.

107 te, a repellent derived from the nonvolatile jasmonic acid in the signaling pathway of plant defenses

108 by engineering seed-specific accumulation of jasmonic acid in transgenic plants.

109 e been shown to adenylate the plant hormones jasmonic acid, indole acetic acid and salicylic acid (SA

110 rmones including abscisic acid, gibberellin, jasmonic acid, indole-3-acetic acid, etc.

111 ly induced after wounding, likely owing to a jasmonic acid-induced cell wall invertase, and is limite

112 tifs required to repress salicylic acid- and jasmonic acid-induced gene transcription in planta.

113 ccumulated the phytoalexin sakuranetin after jasmonic acid induction, only very low amounts accumulat

114 comparative proteomic analysis using tomato jasmonic acid insensitive1 ( jai1), the receptor mutant

115 uch delayed compared with development on the jasmonic acid-insensitive1 (jai1) mutant.

116 This effect of jasmonic acid is amplified in the ethylene-insensitive m

117 opsidis and to P. syringae pv tomato whereas jasmonic acid is essential for the resistance to B. cine

118 atine, a toxin that mimics the plant hormone jasmonic acid isoleucine and promotes opening of stomata

119 al herbivory resulted in the accumulation of jasmonic acid-isoleucine and loss of dormancy in seeds o

120 efenses that depend on signaling via (1) the jasmonic acid-isoleucine conjugate (JA-Ile) and (2) othe

121 The plant hormone jasmonic acid (JA) activates host defense responses agai

122 L.) leaves induced by arachidonic acid (AA), jasmonic acid (JA) and beta-aminobutyric acid (BABA).

123 s of the elicitors: methyl jasmonate (MeJA), jasmonic acid (JA) and DL-methionine (MET), in order to

124 s that are regulated by salicylic acid (SA), jasmonic acid (JA) and ethylene (ET) pathways.

125 Furthermore, transcripts involved in jasmonic acid (JA) and ethylene (ET) signaling pathways

126 ling pathways involving salicylic acid (SA), jasmonic acid (JA) and ethylene has shown that these thr

127 W; Lissorhoptrus oryzophilus), and how plant jasmonic acid (JA) and GA regulate this tripartite inter

128 ng with altered balance of the phytohormones jasmonic acid (JA) and gibberellic acid (GA).

129 nses in rst1 correlate with higher levels of jasmonic acid (JA) and increased basal and B. cinerea-in

130 Jasmonic acid (JA) and its biologically active derivativ

131 nd abiotic stress lead to elevated levels of jasmonic acid (JA) and its derivatives and activation of

132 lipin pathway, responsible for production of jasmonic acid (JA) and its precursor 12-oxo-phytodienoic

133 ation that included enhanced accumulation of jasmonic acid (JA) and JA-Ile, elevated expression of ov

134 Jasmonates, including jasmonic acid (JA) and methyl jasmonate, induced the for

135 nts of endogenous phytohormonal signaling of jasmonic acid (JA) and salicylic acid (SA) compared with

136 es, including abscisic acid (ABA), ethylene, jasmonic acid (JA) and salicylic acid.

137 signaling, biosynthesis of the phytohormone jasmonic acid (JA) and the elicitation of volatile organ

138 signaling, biosynthesis of the phytohormone jasmonic acid (JA) and the elicitation of volatile organ

139 dy, we report that saliva elicits a burst of jasmonic acid (JA) and the induction of late responding

140 ersicum) plants grown from seed treated with jasmonic acid (JA) and/or beta-aminobutryric acid (BABA)

141 Activated forms of jasmonic acid (JA) are central signals coordinating plan

142 ic defence hormones, salicylic acid (SA) and jasmonic acid (JA) associated with defence against biotr

143 abidopsis thaliana) most mutants affected in jasmonic acid (JA) biosynthesis and signaling are male s

144 ic acid (SA) has been proposed to antagonize jasmonic acid (JA) biosynthesis and signaling.

145 pression analysis of salicylic acid (SA) and jasmonic acid (JA) biosynthesis genes and exogenous meth

146 er jasmonate levels and lower transcripts of jasmonic acid (JA) biosynthesis genes.

147 ctivity of LIPOXYGENASE3, a gene involved in jasmonic acid (JA) biosynthesis in N. attenuata.

148 Most interestingly, the jasmonic acid (JA) biosynthesis pathway was significantl

149 Cu deficiency upregulates the expression of jasmonic acid (JA) biosynthetic genes in flowers and inc

150 ative transcriptomic analysis shows that the jasmonic acid (JA) biosynthetic pathway plays an importa

151 accumulation of leaf abscisic acid (ABA) and jasmonic acid (JA) concentrations, and activate Ca(2+) ,

152 COR is a structural mimic of active jasmonic acid (JA) conjugates.

153 Jasmonic acid (JA) did not complement the wound-signalin

154 though crosstalk between ABA and the hormone Jasmonic Acid (JA) has been shown, the molecular entitie

155 transcriptionally repressing a subset of the jasmonic acid (JA) hormone signaling outputs.

156 pal defense hormones salicylic acid (SA) and jasmonic acid (JA) in Arabidopsis, we demonstrate that t

157 previously unknown role of the plant hormone jasmonic acid (JA) in determining rice (Oryza sativa) sp

158 bit reduced sensitivity to the plant hormone jasmonic acid (JA) in JA-dependent root inhibition assay

159 Here, multiple functions of jasmonic acid (JA) in maize (Zea mays) are revealed by c

160 role of MYC transcription factors (TFs) and jasmonic acid (JA) in photomorphogenic growth.

161 The functions of jasmonic acid (JA) in plant defense and development are

162 The biosynthesis of jasmonic acid (JA) in plant peroxisomes requires the act

163 Jasmonic acid (JA) is a critical hormonal regulator of p

164 Jasmonic acid (JA) is a lipid-derived signal that regula

165 Jasmonic acid (JA) is a lipid-derived signal that regula

166 The phytohormone jasmonic acid (JA) is vital in plant defense and develop

167 In contrast, jasmonic acid (JA) level in the SV-treated plants remain

168 Jasmonic acid (JA) measurements and JA feeding experimen

169 . tomato DC3000 produces coronatine (COR), a jasmonic acid (JA) mimic.

170 he effect of addition of basil elicited with jasmonic acid (JA) on the biological properties, oxidati

171 The effect of elicitation with jasmonic acid (JA) on the plant yield, the production an

172 emically, in Arabidopsis mutants impaired in jasmonic acid (JA) or salicylic acid (SA) signaling.

173 domonas fluorescens, or by the phytohormones jasmonic acid (JA) or salicylic acid (SA).

174 plants experiencing Pi deficiency induce the jasmonic acid (JA) pathway and enhance their defense aga

175 is accompanied by early up-regulation of the jasmonic acid (JA) pathway and simultaneous down-regulat

176 RESPONSE FACTOR (AP2/ERF) family genes, and jasmonic acid (JA) pathway genes.

177 expression of defense genes regulated by the jasmonic acid (JA) pathway is suppressed and larval perf

178 Our results revealed that the jasmonic acid (JA) pathway was induced while the brassin

179 ling with a focus on salicylic acid (SA) and jasmonic acid (JA) pathways in response to A. solani.

180 In these responses, salicylic acid (SA) and jasmonic acid (JA) play important signaling roles.

181 the defense hormones salicylic acid (SA) and jasmonic acid (JA) plays a central role in the modulatio

182 The plant hormone jasmonic acid (JA) plays a pivotal role in plant-insect

183 one-third of the antiherbivore phytohormone jasmonic acid (JA) produced by unparasitized plants.

184 ight provide precursors for pathogen-induced jasmonic acid (JA) production.

185 le genes were higher, but those inducible by jasmonic acid (JA) showed lower expression in PLDbeta1 m

186 a so far unrecognized link between AOP2 and jasmonic acid (JA) signaling independent of MYB28 and MY

187 spray to simulate rain, we demonstrate that jasmonic acid (JA) signaling plays a key role in early g

188 , a microProtein that acts as a modulator of jasmonic acid (JA) signaling.

189 the relative strength of salicylic acid and jasmonic acid (JA) signaling.

190 kinases MKK4 and MKK5 but is independent of jasmonic acid (JA) signaling.

191 Arabidopsis thaliana) that displays impaired jasmonic acid (JA) synthesis in specific cell types and

192 Genes of the octadecanoic acid pathway of jasmonic acid (JA) synthesis were induced by SA as well

193 pression is also induced by the phytohormone jasmonic acid (JA) through the established pathway requi

194 JAs derive from jasmonic acid (JA) through various enzymatic modificatio

195 ed that OsJAR1 encoded an enzyme conjugating jasmonic acid (JA) to at least Ile, Leu, Met, Phe, Trp a

196 ect effects and intergenerational effects of jasmonic acid (JA) treatment, which is involved in herbi

197 al for Nod-factor-induced ENOD11 expression, jasmonic acid (JA) was added to reduce the rate of Nod-f

198 Unexpectedly, jasmonic acid (JA) was not involved, as the JA-deficient

199 synergistic combination of ethylene (ET) and jasmonic acid (JA) was required for accumulation of the

200 Levels of jasmonic acid (JA) were elevated and levels of salicylic

201 (UV-C) irradiation, salicylic acid (SA) and jasmonic acid (JA) were investigated in three sfr6 mutan

202 n of genes involved in flavonoid, terpenoid, jasmonic acid (JA), and abscisic acid (ABA) biosynthesis

203 t chemical elicitors: arachidonic acid (AA), jasmonic acid (JA), and abscisic acid (ABA).

204 hormones salicylic acid (SA), ethylene (ET), jasmonic acid (JA), and abscisic acid (ABA).

205 (ERF1)] clustered into salicylic acid (SA), jasmonic acid (JA), and ethylene (ET) pathways suggest t

206 interactions focused on salicylic acid (SA), jasmonic acid (JA), and ethylene (ET).

207 results in activation of MAPKs, synthesis of jasmonic acid (JA), and expression of defense genes.

208 ohormone production, including ethylene (E), jasmonic acid (JA), and salicylic acid, in a range of pl

209 rapid accumulation of phytohormones, such as jasmonic acid (JA), and the induced defense metabolites

210 Some of these oxylipins, for example jasmonic acid (JA), are important signal molecules in pl

211 lants corresponded with reduced synthesis of jasmonic acid (JA), but levels of salicylic acid (SA) we

212 ck the receptor of the plant defense hormone jasmonic acid (JA), CORONATINE INSENSITIVE1 (COI1).

213 were still observed in mutants deficient in jasmonic acid (JA), ethylene (ET) and salicylic acid (SA

214 quantification of phytohormones showed that jasmonic acid (JA), jasmonoyl-Ile, salicylic acid, absci

215 esponsive to multiple stress stimuli such as jasmonic acid (JA), salicylic acid (SA), H(2)O(2), xenob

216 me polyphenol oxidase and genes regulated by jasmonic acid (JA), whereas the salicylic acid (SA)-resp

217 sponse to biotic and abiotic stimuli through jasmonic acid (JA)- and abscisic acid (ABA)-mediated pat

218 In contrast, jasmonic acid (JA)- and ethylene-dependent RNAs (PDF1.2,

219 e attack are modulated by cross-talk between jasmonic acid (JA)- and salicylic acid (SA)-signaling pa

220 post infection and in the down-regulation of jasmonic acid (JA)-associated responses at later stages.

221 ced increases in mRNA levels of ethylene- or jasmonic acid (JA)-biosynthesis and -inducible genes in

222 hile necrotrophic pathogens are sensitive to jasmonic acid (JA)-dependent resistance, biotrophic path

223 host protein PtJAZ6, a negative regulator of jasmonic acid (JA)-induced gene regulation in Populus.

224 ic acid (SA)-mediated responses and inhibits jasmonic acid (JA)-inducible defenses, resulting in enha

225 was associated with repressed sensitivity of jasmonic acid (JA)-inducible gene expression.

226 progeny displayed reduced responsiveness of jasmonic acid (JA)-inducible genes and enhanced suscepti

227 n the alteration of salicylic acid (SA)- and jasmonic acid (JA)-mediated defense responses.

228 rong changes in reactive oxygen species- and jasmonic acid (JA)-related gene expression.

229 The jasmonic acid (JA)-responsive AP2/ERF transcription fact

230 AS2, and attenuates expression of selective jasmonic acid (JA)-responsive gene.

231 yperactivated transcript accumulation of the jasmonic acid (JA)-responsive genes VSP2 and Thi2.1 upon

232 mutants, phloem cap cells were lignified and jasmonic acid (JA)-responsive genes were highly upregula

233 nse response, most directly that mediated by jasmonic acid (JA).

234 Nicotiana tabacum L.) is highly regulated by jasmonic acid (JA).

235 lipids provide fatty acids for synthesis of jasmonic acid (JA).

236 nal and structural mimic of the phytohormone jasmonic acid (JA).

237 h convert linolenic acid to the phytohormone jasmonic acid (JA).

238 noterpenoid acid and an alcohol derived from jasmonic acid (JA).

239 by Bt tolerant caterpillars, or treated with jasmonic acid (JA).

240 AE) that includes transient accumulations of jasmonic acid (JA).

241 lcium/calmodulin-mediated defense signaling, jasmonic acid (JA)/ethylene (ET) and sialic acid (SA)-in

242 t antagonism between salicylic acid (SA) and jasmonic acid (JA)/ethylene (ET) signalling resulting in

243 However, how Elongator functions in jasmonic acid (JA)/ethylene (ET)-mediated defense is unk

244 ns in MED16 blocked the induction of several jasmonic acid (JA)/ethylene (ET)-responsive genes and co

245 s includes the isoleucine (Ile) conjugate of jasmonic acid (JA-Ile) and its biosynthetic precursor 12

246 ctivity of the tryptophan (Trp) conjugate of jasmonic acid (JA-Trp) in Arabidopsis (Arabidopsis thali

247 nfection with both pathogens triggers higher jasmonic acid, jasmonoyl-isoleucine accumulation, and ja

248 ame rate, but, after 4 h of desiccation, the jasmonic acid level was much higher in mutant than WT le

249 leaf streak pathogen, serving to reduce the jasmonic acid-mediated defense response.

250 r the regulation of salicylic acid (SA)- and jasmonic acid-mediated defense signaling in the plant.

251 tein kinases, as well as salicylic acid- and jasmonic acid-mediated defense signalling pathways.

252 As jasmonic acid-mediated lignification is a typical reacti

253 In addition, acd6-1 shows ethylene- and jasmonic acid-mediated signaling that is antagonized and

254 d levels were triggered in EV samples, while jasmonic acid metabolism and signaling were drastically

255 benzothiadiazole, local applications of the jasmonic acid methyl ester or abscisic acid triggered sy

256 However, unlike ethylene, jasmonic acid not only inhibits spiking but also suppres

257 The rapidity of the effects of ethylene and jasmonic acid on Nod factor signaling suggests direct cr

258 e effect of elicitation with arachidonic and jasmonic acids on the production of phenolic compounds a

259 ntation, but not by exogenous application of jasmonic acid or indole acetic acid.

260 oduced greater concentrations of the hormone jasmonic acid or its precursor 12- oxo-phytodienoic acid

261 gs with mediators of plant stress responses (jasmonic acid or salicylic acid) increased seedling MDA

262 duced by fungal infection and treatment with jasmonic acid or ZmPep1.

263 knockout line implied the involvement of the jasmonic acid pathway in symptom mitigation.

264 , those associated with indirect defense and jasmonic acid pathway were clearly over-represented, ind

265 ated resistance to CLA is independent of the jasmonic acid pathway.

266 d induction of a set of genes related to the jasmonic acid pathway.

267 ylpropanoid, hydroxycinnamic acid (HCAA) and jasmonic acid pathways, and their biosynthetic genes.

268 including those in auxin, abscisic acid, and jasmonic acid pathways.

269 th jasmonic acid-related gene expression and jasmonic acid precursors specifically accumulated in pao

270 ) accumulation], and 35S-LOX2- (defective in jasmonic acid production and hyper-accumulator of SA), a

271 lic acid-regulated PATHOGENESIS-RELATED1 and jasmonic acid-regulated PDF1.2.

272 ous correlation with the salicylic acid- and jasmonic acid-related defense signaling pathways.

273 hway intermediates, i.e. pheophorbide a Both jasmonic acid-related gene expression and jasmonic acid

274 ling to regulate ALMT1 is salicylic acid and JASMONIC ACID RESISTANT1 (JAR1)/JASMONATE INSENSITIVE1 (

275 H oxidase) mutant seedlings but increased in jasmonic acid resistant1 (jar1-1) mutant seedlings.

276 some are involved in lignin biogenesis, and jasmonic acid response genes, and phloroglucinol stainin

277 Significantly enhanced expression of jasmonic acid-responsive genes in the knockout line impl

278 molecules including abscisic acid, ethylene, jasmonic acid, salicylic acid and yeast extract; and str

279 le of three phytohormone signaling pathways, jasmonic acid, salicylic acid, and ethylene (ET), in TuM

280 ted by the plant hormones indoleacetic acid, jasmonic acid, salicylic acid, and gibberellic acid or b

281 activities, defense, and response to (methyl)jasmonic acid, salicylic acid, or ethylene.

282 only a subset of induced programs, including jasmonic acid signaling and biosynthesis of indole gluco

283 proteins function as negative regulators of jasmonic acid signaling in plants.

284 Salicylic acid and jasmonic acid signaling pathway components are dispensab

285 ted roles for increased oxidative stress and jasmonic acid signaling responses during weed stress.

286 response factor, but not the MYC2 branch of jasmonic acid signaling, contributed to induction of PME

287 or ethylene signaling, but was dependent on jasmonic acid signaling.

288 lvement of TPL/TPR corepressors in auxin and jasmonic acid signaling.

289 d signaling, but independent of ethylene and jasmonic acid signaling.

290 s accession Col-0 and ein2/jar1, an ethylene/jasmonic acid-signaling deficient mutant that exhibits e

291 cific Arabidopsis thaliana AtGH3.12/PBS3 and jasmonic acid-specific AtGH3.11/JAR1.

292 scisic acid, ethylene, gibberellic acid, and jasmonic acid, suggesting these central regulators affec

293 Application of jasmonic acid to developing inflorescences rescued stame

294 stitutive activation of bHLH05 and mimicking jasmonic acid treatment.

295 ation of the defence signalling phytohormone jasmonic acid were all significantly reduced under inbre

296 Basal levels of jasmonic acid were substantially higher in the EV compar

297 the defense phytohoromes salicylic acid and jasmonic acid were unable to restore SAR in gl1 plants.

298 sis leads to a deficiency in accumulation of jasmonic acids, which results in impaired expression of

299 d we enantioselectively crystallized racemic jasmonic acid, whose absolute configuration had only bee

300 stain critical levels of nitric oxide and/or jasmonic acid, whose biosynthesis both depend on NADPH p