ライフサイエンスコーパス: jasmonic acid

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

2 ffected root growth sensitivity to exogenous jasmonic acid.

3 LOX4 cDNAs and biochemically with exogenous jasmonic acid.

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

5 for cuticular components or the phytohormone jasmonic acid.

6 nse-related phytohormones salicylic acid and jasmonic acid.

7 independent of SA and NPR1, but dependent on jasmonic acid.

8 d 90% for salicylic acid and 90 and 100% for jasmonic acid.

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

10 classic defense hormones salicylic acid and jasmonic acid.

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

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

13 RSH gene expression following treatment with jasmonic acid; 2) bona fide ppGpp synthesis activity of

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

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

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

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

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

27 The expression of jasmonic acid and ethylene regulated PATHOGENESIS-RELATE

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

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

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

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

32 ferent set of defense responses activated by jasmonic acid and ethylene signaling.

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

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

35 ernaria brassicicola, and the plant hormones jasmonic acid and ethylene.

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

37 Jasmonic acid and indole-3-acetic acid levels were also

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

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

40 Jasmonic acid and its derived metabolites (JAs) orchestr

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

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

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

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

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

46 Jasmonic acid and salicylic acid represent important sig

47 es were linear over a range of 5-1000 ng for jasmonic acid and salicylic acid.

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

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

50 t defensin (PDF)1.2 following treatment with jasmonic acid and/or ethylene.

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

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

53 5PTase11 gene is regulated by abscisic acid, jasmonic acid, and auxin, suggesting a role for phosphoi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

72 tic acid, abscisic acid, gibberellin, methyl jasmonic acid, brassinosteroid, salicylic acid), chemica

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

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

75 id carboxyl methyltransferase), and JMT (SAM:jasmonic acid carboxyl methyltransferase).

76 Artificial damage and jasmonic acid caused significant increases in trichome p

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

80 ed accumulation of proteinase inhibitors was jasmonic acid dependent.

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

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

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

84 suggest that a prosystemin independent- but jasmonic acid-dependent pathway is utilized for proteina

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

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

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

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

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

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

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

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

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

94 gnaling through either the salicylic acid or jasmonic acid/ethylene defense pathways, suggesting resi

95 ctive oxygen species-and PDF1.2-a marker for jasmonic acid/ethylene defense signaling-was detectable

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

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

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

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

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

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

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

107 ic changes in salicylic acid, cinnamic acid, jasmonic acid, indole-3-acetic acid, abscisic acid, unsa

108 The chemical analysis of salicylic acid, jasmonic acid, indole-3-acetic acid, and abscisic acid i

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

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

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

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

113 racterization of a sterile mutant of tomato (jasmonic acid-insensitive1 [jai1]) that is defective in

114 ion of LeARG2 was not observed in the tomato jasmonic acid-insensitive1 mutant, indicating that this

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

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

117 asmonic acid, suggesting that adenylation of jasmonic acid is not necessary.

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 undamaged corn seedlings to rapidly produce jasmonic acid (JA) and emit sesquiterpenes.

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 st to previous reports, no major increase in jasmonic acid (JA) and methyl jasmonate (MJ) was detecte

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

150 defense responses, our understanding of how jasmonic acid (JA) functions at the biochemical level is

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

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

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

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

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

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

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

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

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

160 Jasmonic acid (JA) is a fatty acid-derived signaling mol

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

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

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

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

165 Jasmonic acid (JA) measurements and JA feeding experimen

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

181 In addition, suppression of jasmonic acid (JA) signaling component COI1 ortholog aff

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

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

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

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

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

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

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

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

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

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

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

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

194 d in response to wounding and treatment with jasmonic acid (JA), a potent signal for plant defense re

195 he different effects of salicylic acid (SA), jasmonic acid (JA), abscisic acid (ABA), and auxin on th

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

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

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

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

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

201 ng the signal molecules salicylic acid (SA), jasmonic acid (JA), and ethylene (ET).

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

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

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

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

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

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

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

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

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

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

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

213 aminum), sorghum (Sorghum bicolor) activates jasmonic acid (JA)- and salicylic acid (SA)-regulated ge

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

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

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

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

218 es the Arabidopsis phytoalexin camalexin and jasmonic acid (JA)-dependent signaling, respectively.

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

220 The Arabidopsis gene COI1 is required for jasmonic acid (JA)-induced growth inhibition, resistance

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

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

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

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

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

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

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

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

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

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

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

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

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

234 s found for genes linked to the phytohormone jasmonic acid (JA).

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

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

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

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

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

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

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

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

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

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

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

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

247 As jasmonic acid-mediated lignification is a typical reacti

248 ydrogenase restores both salicylic acid- and jasmonic acid-mediated phenotypes of ssi2 plants.

249 al for the regulation of salicylic acid- and jasmonic acid-mediated signaling pathways.

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

251 coronafacic acid (CFA), an analog of methyl jasmonic acid (MeJA), and coronamic acid (CMA), which re

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

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

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

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

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

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

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

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

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

261 nals which differ from those on the systemin/jasmonic acid pathway typical of well-characterised woun

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

263 However, ssi2-triggered defects in the jasmonic acid pathway, morphology, and cell death phenot

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

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

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

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

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

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

270 ied were known sugar-, auxin-, wounding- and jasmonic acid-related genes, suggesting the existence of

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

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

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

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

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

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

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

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

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

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

281 Salicylic acid and jasmonic acid signaling pathway components are dispensab

282 s, indicating that DC3000 required an intact jasmonic acid signaling pathway in the plant to suppress

283 albeit independent of the salicylic acid or jasmonic acid signaling pathways.

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

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

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

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

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

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

290 ction and consistently reduced the effect of jasmonic acid, suggesting negative cross-talk between th

291 trichome induction following treatment with jasmonic acid, suggesting that adenylation of jasmonic a

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

293 ed constitutive SA signaling, the ability of jasmonic acid to activate PDF1.2 expression is reinstate

294 Application of jasmonic acid to developing inflorescences rescued stame

295 stitutive activation of bHLH05 and mimicking jasmonic acid treatment.

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

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

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

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