ライフサイエンスコーパス: phytohormone

1 that mediate physiological responses to this phytohormone.

2 s discovered and it is also the most studied phytohormone.

3 cluding root exudates, biocontrol agents and phytohormones.

4 ylene, abscisic acid, nitric oxid, and other phytohormones.

5 ted following plant treatment with defensive phytohormones.

6 ir genes are responsive to stress-associated phytohormones.

7 ntal signals, including light and endogenous phytohormones.

8 on elaborate signaling networks regulated by phytohormones.

9 abolic processes and complex regulations via phytohormones.

10 ms depends on the interplay between multiple phytohormones.

11 d light-grown seedlings in response to these phytohormones.

12 ns (CKs) are adenine derivatives that act as phytohormones.

13 tance responses in barley in relation to the phytohormone ABA.

14 etween concentrations of the drought-induced phytohormone abscisic acid (ABA) and isoprene; and wheth

15 Here, we show that the phytohormone abscisic acid (ABA) and SA antagonistically

16 ar link between the inhibitory action of the phytohormone abscisic acid (ABA) and the promoting role

17 The phytohormone abscisic acid (ABA) influences the expressi

18 The phytohormone abscisic acid (ABA) is critical to plant de

19 The phytohormone abscisic acid (ABA) is important for growth

20 The phytohormone abscisic acid (ABA) is induced in response

21 Signaling by the stress phytohormone abscisic acid (ABA) is involved in acquired

22 The phytohormone abscisic acid (ABA) plays a key role in the

23 The phytohormone abscisic acid (ABA) plays a major role in t

24 The phytohormone abscisic acid (ABA) plays a role in stresse

25 CAR ABA receptors and PP2C co-receptors, the phytohormone abscisic acid (ABA) prevents premature germ

26 The phytohormone abscisic acid (ABA) promotes stomatal closu

27 Phytohormone abscisic acid (ABA) protects seeds during w

28 that this whole process is regulated by the phytohormone abscisic acid (ABA) through ABSCISIC ACID I

29 Levels of the classical stress phytohormone abscisic acid (ABA) were also mainly enhanc

30 trong a stimulus for stomatal closure as the phytohormone abscisic acid (ABA), but underlying mechani

31 for multiparametric in vivo analyses of the phytohormone abscisic acid (ABA), Ca(2+), protons (H(+))

32 ey player in fern sex differentiation is the phytohormone abscisic acid (ABA), which regulates the se

33 ur, are closed in response to drought by the phytohormone abscisic acid (ABA).

34 cit are not fully elucidated but involve the phytohormone abscisic acid (ABA).

35 f hydration to biochemical regulation by the phytohormone abscisic acid (ABA).

36 ate-limiting step in the biosynthesis of the phytohormone abscisic acid and a component of a major ab

37 biota's capacity to repress responses to the phytohormone abscisic acid in the root.

38 esponses in older rosette leaves through the phytohormone abscisic acid signaling, whereas this antag

39 abscisic aldehyde, which is oxidized to the phytohormone abscisic acid.

40 tA abundance is rapidly downregulated by the phytohormone abscisic acid.

41 s induced by high salinity, drought, and the phytohormone abscisic acid.

42 of suberin deposition and degradation by the phytohormones abscisic acid and ethylene.

43 Production of the phytohormones abscisic and indole acetic acid, and wound

44 Phytohormones act in the integration of growth control a

45 Here, we demonstrate that several additional phytohormones also regulate ACS protein turnover.

46 Phytohormone analysis revealed significantly higher basa

47 4 evolved in seed plants, on top of existing phytohormone and nucleotide-binding-leucine-rich-repeat

48 tifies altered circadian clock networks, and phytohormone and stress response pathways that intersect

49 tails of the evolutionary history of several phytohormone and structural polymer biosynthetic pathway

50 Ethylene is a gaseous phytohormone and the first of this hormone class to be d

51 d conditions were used to compare changes in phytohormone and transcriptome profiles.

52 border cells corresponded to differences in phytohormone and volatile levels compared with adjacent

53 The capacity of chloroplasts to synthesize phytohormones and a diverse range of secondary metabolit

54 are shedding light on the mode of action of phytohormones and are opening up a new avenue of researc

55 ression through the production of inhibitory phytohormones and by reducing sugar levels and energy ba

56 PDR1 expression is regulated by phytohormones and by the soil phosphate abundance, and t

57 w the current knowledge of interplay between phytohormones and control of sulfur metabolism and discu

58 or MYB72 in the onset of ISR and the role of phytohormones and defense regulatory proteins in the exp

59 ete biosynthetic pathway for brassinosteroid phytohormones and enzymes for brassinosteroid inactivati

60 merging relationship between the function of phytohormones and epigenetic modifications.

61 as precursors in the biosynthesis of several phytohormones and proposed regulatory signals.

62 ated by complex signaling networks involving phytohormones and reactive oxygen species (ROS).

63 ittle is known about the interaction between phytohormones and regulation of sulfur metabolism.

64 hat Xa21 triggered redistribution of energy, phytohormones and resources among essential cellular act

65 nt enrichment of transcripts associated with phytohormones and secondary cell wall (SCW) metabolism,

66 Phytohormones and the primary plant cell wall play major

67 he levels of phenolic acids and carboxylated phytohormones and their glucoconjugates.

68 rature that describes signalling components, phytohormones and transcription factors that interact wi

69 signaling processes that act in concert with phytohormones and transcription factors to regulate sene

70 Carotenoids and apocarotenoids act as phytohormones and volatile precursors that influence pla

71 ts into crosstalk between ethylene and other phytohormones, and a novel regulatory mechanism that con

72 scripts related to floral organ development, phytohormones, and cell cycle regulation.

73 The results support the hypothesis that phytohormones are acting in concert to regulate the onse

74 h as Arabidopsis thaliana have revealed that phytohormones are central regulators of plant defense.

75 r, downstream signaling pathways for the key phytohormones are distinct.

76 Interactions among phytohormones are essential for providing tolerance of s

77 Phytohormones are involved in diverse aspects of plant l

78 Thereby we hypothesize that phytohormones are key players for BS induction and suppr

79 Phytohormones are plant growth regulators that are invol

80 newly discovered class of carotenoid-derived phytohormones, are essential for developmental processes

81 d are opening up a new avenue of research on phytohormones as well as on the mechanisms regulating ep

82 type tightly controls the relationship among phytohormones, as well as provide significant insights i

83 between melatonin and the stress-associated phytohormones at molecular and metabolic levels.

84 The phytohormone auxin (indole-3-acetic acid, IAA) is a smal

85 Tight homeostatic regulation of the phytohormone auxin [indole-3-acetic acid (IAA)] is essen

86 led to altered distribution patterns of the phytohormone auxin and associated auxin transport-relate

87 g the tooth growth process, responses to the phytohormone auxin are maintained at tips of the teeth t

88 The phytohormone auxin controls plant growth and development

89 1 to motivate long-distance transport of the phytohormone auxin from the shoot to root apex.

90 The phytohormone auxin governs crucial developmental decisio

91 The transport network of the phytohormone auxin has been proposed to mediate this sys

92 The phytohormone auxin has been shown to be of pivotal impor

93 Here, we reveal that the phytohormone auxin impacts on the shape of the biggest p

94 mation, and recent findings suggest that the phytohormone auxin inhibits nodule formation.

95 The uptake of the phytohormone auxin into cells is known to be crucial for

96 The directional distribution of the phytohormone auxin is essential for plant development.

97 The phytohormone auxin is implied in steering various develo

98 The phytohormone auxin is well known to play an important ro

99 keleton shows proximity to vacuoles, and the phytohormone auxin not only controls the organization of

100 The metabolism and redistribution of the phytohormone auxin play pivotal roles in establishing ac

101 The phytohormone auxin plays crucial roles in nearly every a

102 The phytohormone auxin promotes the growth of plant shoots b

103 The phytohormone auxin regulates virtually every aspect of p

104 The directional transport of the phytohormone auxin represents a key, plant-specific mech

105 , we identify a link between the UPR and the phytohormone auxin, a master regulator of plant physiolo

106 A local maximum of the phytohormone auxin, and consequent expression of CLASS I

107 negative regulators of the transport of the phytohormone auxin, by which they influence auxin distri

108 nts depends on the intercellular flow of the phytohormone auxin, of which the directional signaling i

109 t the small GTPase ROP2, if activated by the phytohormone auxin, promotes activation of TOR, and thus

110 l processes that are largely governed by the phytohormone auxin, suggesting that auxin regulates resp

111 dopsis has been shown to be regulated by the phytohormone auxin, via the expression of the auxin infl

112 Here we found that, phytohormone auxin-induced, sterol-dependent nanocluster

113 late transcriptional events modulated by the phytohormone auxin.

114 by synthesis and proper distribution of the phytohormone auxin.

115 and implicated in cellular responses to the phytohormone auxin.

116 t on the photoreceptor phytochrome B and the phytohormone auxin.

117 lated by modeling the polar transport of the phytohormone auxin.

118 as thermomorphogenesis and is induced by the phytohormone auxin.

119 stimuli and endogenous factors, such as the phytohormones auxin and brassinosteroid.

120 The phytohormones auxin and cytokinin interact to regulate m

121 nce for the signaling cross-talk between the phytohormones auxin and gibberellin (GA), which partly c

122 in Arabidopsis thaliana by antagonizing the phytohormones auxin and gibberellin.

123 h regulatory signals including light and the phytohormones auxin, cytokinin, and gibberellin.

124 Transcriptome analysis revealed that various phytohormone (auxin and salicylic acid) response genes a

125 gs to cellular functions (calcium and MAPK), phytohormones (auxin, gibberellins, abscisic acid, JA an

126 Phytohormone binding inactivates the phosphatase activit

127 he tricarboxylic acid cycle, carbon balance, phytohormone biosynthesis and redox homeostasis.

128 The circadian clock regulates phytohormone biosynthesis and signaling pathways to gene

129 with specific regulatory programs, including phytohormone biosynthesis, signaling, and response, whic

130 e of CPSs in all land plants for gibberellin phytohormone biosynthesis, such plasticity presumably un

131 e processes including embryo development and phytohormones biosynthesis.

132 Phytohormone brassinosteroids (BRs) are essential for pl

133 etaria viridis to investigate a role for the phytohormones brassinosteroids (BRs) in specifying brist

134 Herein we investigated the phytohormone composition throughout grape berry ripening

135 triggered immunity, phenotype and changes in phytohormone content by high-performance liquid chromato

136 Although it is well established that phytohormones contribute to antixenotic- and antibiotic-

137 Auxin phytohormones control most aspects of plant development

138 Strigolactones (SLs) are a class of phytohormones controlling shoot branching.

139 Thus, HopBB1 fine-tunes host phytohormone crosstalk by precisely manipulating part of

140 Here, we reveal an alternative phytohormone crosstalk mechanism, revealing that BR sign

141 controlled by regulatory loops involving the phytohormone cytokinin and stem cell identity genes.

142 The phytohormone cytokinin influences many aspects of plant

143 The phytohormone cytokinin is a regulator of numerous proces

144 The phytohormone cytokinin promotes nodule formation, and re

145 The phytohormone cytokinin regulates diverse aspects of plan

146 which is transcriptionally regulated by the phytohormone cytokinin, is necessary for the ability of

147 erse processes, such as the signaling of the phytohormone cytokinin.

148 ana) mutants involved in the response to the phytohormone cytokinin.

149 tial resolution, we show here that two major phytohormones, cytokinin and auxin, display different ye

150 The interaction of two phytohormones, cytokinin and auxin, is fundamental in co

151 lso increase cellular oxidation and activate phytohormone defense pathways.

152 Moreover, the phytochrome and phytohormone-dependent transmission of ROS waves is cent

153 l showing the relationship between KNOX1 and phytohormones during storage root initiation.

154 r, extensive cross talk occurs among all the phytohormones during stress events, and the challenge is

155 (EIN2), a master signaling regulator of the phytohormone ethylene (ET), lowers sensitivity to both e

156 f the leaf petiole and involves the volatile phytohormone ethylene (ET).

157 well-characterized signaling pathway of the phytohormone ethylene and plant-optimized genome-wide ri

158 The phytohormone ethylene has numerous effects on plant grow

159 The phytohormone ethylene is widely involved in many develop

160 The phytohormone ethylene modulates plant growth and develop

161 The gaseous phytohormone ethylene plays an important role in spike d

162 The phytohormone ethylene regulates plant growth and develop

163 nmental conditions and can be induced by the phytohormone ethylene.

164 Signaling networks among multiple phytohormones fine-tune plant defense responses to insec

165 Abscisic acid is a phytohormone found in fruits and vegetables and is endog

166 The phytohormone gibberellin (GA) is a key regulator of plan

167 er growth repressors in plants by inhibiting phytohormone gibberellin (GA) signaling in response to d

168 We show that dual opposite roles of the phytohormone gibberellin underpin this phenomenon in Ara

169 ng and repress flowering downstream from the phytohormone gibberellin.

170 regulated by several factors, including the phytohormones gibberellin and abscisic acid, through con

171 ignalling pathways underlying the effects of phytohormones have been elucidated by genetic screens an

172 Furthermore, some phytohormones have been shown to affect epigenetic modif

173 in stress response networks and an important phytohormone in plant-microbe interactions with systemic

174 le knowledge to further decipher the role of phytohormones in BS induction and BS symptom development

175 sis and the synthesis or response to several phytohormones in leaves as well as an altered expression

176 Despite the crucial roles of phytohormones in plant development, comparison of the ex

177 The action of phytohormones in plants requires the spatiotemporal regu

178 Detection of phytohormones in situ has gained significant attention d

179 effect, solely or in combination with other phytohormones, in the morphology of potato plants and al

180 esponse to drought stress and treatment with phytohormones, including abscisic acid, ethephon, methyl

181 Several phytohormones, including methyl jasmonate, ethylene, and

182 Active pools of phytohormones, including those involved in plant stress

183 acetaldehyde dehydrogenase to synthesize the phytohormone indole-3-acetic acid to elude host response

184 death are driven by the bacterially-produced phytohormone indole-3-acetic acid.

185 Multiple phytohormones interact to control root growth, including

186 Overall, an improved understanding of phytohormone intervention strategies employed by pests a

187 Auxin is a phytohormone involved in cell elongation and division.

188 Abscisic acid (ABA) is a phytohormone involved in pivotal physiological functions

189 n this review, we provide an overview of the phytohormones involved in immunity and the ways pathogen

190 Brassinosteroids are phytohormones involved in plant development and physiolo

191 Crosstalk among phytohormones is crucial for balancing plant growth and

192 s cancelled by exogenous applications of the phytohormone jasmonate.

193 pecies-specific biosynthetic pathways by the phytohormone jasmonate.

194 The phytohormone jasmonic acid (JA) is vital in plant defens

195 uced up-regulation of the defence signalling phytohormone jasmonic acid were all significantly reduce

196 ants, coinciding with altered balance of the phytohormones jasmonic acid (JA) and gibberellic acid (G

197 bacteria Pseudomonas fluorescens, or by the phytohormones jasmonic acid (JA) or salicylic acid (SA).

198 The lipid-derived phytohormone jasmonoyl-isoleucine regulates plant immuni

199 T operate in parallel to gibberellic acid, a phytohormone known to regulate these same three transiti

200 s emerged as a critical player in regulating phytohormone levels and their activity.

201 We analyzed and compared phytohormone levels with their precursors produced in ch

202 to disease through pathogen manipulation of phytohormone levels, which otherwise regulate developmen

203 mmune output through rheostat-like tuning of phytohormone levels.

204 howed induced expression upon application of phytohormones like salicylic acid which might be the key

205 -DEPENDENT PROTEIN KINASE CPK28 in balancing phytohormone-mediated development in Arabidopsis thalian

206 hate-deficient conditions, diacetyl enhances phytohormone-mediated immunity and consequently causes p

207 t's phosphate-starvation response system and phytohormone-mediated immunity.

208 and modulates responsiveness to peptide and phytohormone-mediated intercellular communication.

209 oxidative signals arising from metabolism or phytohormone-mediated processes control almost every asp

210 Salicylic acid (SA) is an important phytohormone mediating both local and systemic defense r

211 ses found in all seed plants for gibberellin phytohormone metabolism, by a larger aromatic residue le

212 hotosynthesis, carbohydrate, amino acid, and phytohormone metabolism.

213 evolutionary progenitors traced to conserved phytohormone metabolism.

214 tive indolic molecules, generating potential phytohormone mimics.

215 We address phytohormone modulation of immunity and surmise how chlo

216 Exogeneous treatment of phytohormones N (6) -benzylaminopurine and 1-Naphthalene

217 Cross talk between phytohormones, nitric oxide (NO), and auxin has been imp

218 bation of GA signaling, the ABA antagonistic phytohormone, nor through interference with the DELLA pr

219 ensive understanding of the roles of various phytohormones on ACS protein stability, which brings new

220 While the effects of phytohormones on plant gene expression have been well ch

221 The effects of phytohormones on SVT regeneration were investigated by a

222 nt recognition of opposing effects for these phytohormones on the microbial defense response.

223 ranscription factors and genes responding to phytohormones or modulating hormone levels in the regula

224 s pathways such as cold and light signaling, phytohormone pathways and plant metabolisms.

225 lating the redox status of the leaves, other phytohormone pathways and/or important PCD components.

226 portant in the control of growth mediated by phytohormone pathways.

227 and the transcriptional induction of several phytohormone pathways.

228 nematodes use multiple tactics to influence phytohormone physiology and alter plant developmental pr

229 Phytohormones play an important role in development and

230 Phytohormones play important roles during flower and fru

231 The gibberellin (GA) phytohormones play important roles in plant growth and d

232 The jasmonate family of phytohormones plays central roles in plant development a

233 (a common toxic pollutant) and ethylene (the phytohormone primarily responsible for fruit ripening) s

234 Abscisic acid is a key phytohormone produced in response to abiotic stress cond

235 lomics and RNAseq data describe two distinct phytohormone profiles in BS berries, differing between p

236 Abscisic acid (ABA) is a key phytohormone promoting abiotic stress tolerance as well

237 terpenoid compounds with roles that include phytohormones, protein modification reagents, anti-oxida

238 d molecules known as effectors, which target phytohormone receptors, transcriptional activators and r

239 Phytohormones regulate many aspects of plant life by act

240 Phytohormones regulate plant growth from cell division t

241 However, how phytohormones regulate SVT regeneration is still unknown

242 sma, or symbiotic bacteria to intervene with phytohormone-regulated defenses.

243 adopted innovative strategies to manipulate phytohormone-regulated defenses.

244 Salicylic acid (SA) is a phytohormone regulating immune responses against pathoge

245 Abscisic acid is a phytohormone regulating plant growth, development and st

246 ar responses to cytokinin and auxin, two key phytohormones regulating cell behaviour.

247 Cytokinins are a major group of phytohormones regulating plant growth, development and s

248 Jasmonates are important phytohormones regulating reproductive development.

249 lar embryo, which revealed the importance of phytohormone-related genes and a suite of transcription

250 TF were differentially expressed; therefore, phytohormone-related genes were assembled into a network

251 root branching and differentially regulated phytohormone-related genes.

252 tion factors (TF) indicated that a number of phytohormone-related TF were differentially expressed; t

253 tory sequence conservation and applied it to phytohormone REs in 45 angiosperms.

254 cis-regulatory elements primarily related to phytohormone responsiveness.

255 endogenous contents of the stress-associated phytohormones (salicylates, auxins, trans-jasmonic acid,

256 rapidly induced by exogenous application of phytohormone salicylic acid (SA), methyl jasmonate (MeJA

257 d signaling dependent on, the foliar defense phytohormone salicylic acid is required to assemble a no

258 at, ER stress-inducing chemical tunicamycin, phytohormone salicylic acid, and pathogen infection.

259 y PBS3, a signaling component of the defense phytohormone salicylic acid.

260 proceeds via signaling networks that include phytohormones, secondary metabolites, and transcription

261 Strigolactones (SLs) are carotenoid-derived phytohormones shaping plant architecture and inducing th

262 In addition, absolute quantification of phytohormones showed that jasmonic acid (JA), jasmonoyl-

263 otein interactions have an important role in phytohormone signal integration.

264 owledge about molecular components mediating phytohormone signaling and cross talk with available gen

265 tors and repressors, and other components of phytohormone signaling in the host plant.

266 nes encoding novel biochemical pathways, new phytohormone signaling pathways (notably auxin), expande

267 The intricate network of phytohormone signaling pathways enables plants to activa

268 Three additional phytohormone signaling pathways have also been shown to

269 Many phytohormone signaling pathways rely on the ubiquitin (U

270 The timing of the evolution of most phytohormone signaling pathways seems to coincide with t

271 cyst nematodes successfully exploit various phytohormone signaling pathways to establish a new hormo

272 is phenomenon, we examined the role of three phytohormone signaling pathways, jasmonic acid, salicyli

273 genes associated with epigenetic regulation, phytohormone signaling, cell wall architecture, signal t

274 in their offspring, along with the roles of phytohormone signalling in regulating maternal effects.

275 rated a systems-level map of the Arabidopsis phytohormone signalling network, consisting of more than

276 Pathogens target phytohormone signalling pathways to promote disease.

277 tors of photosynthesis, the circadian clock, phytohormone signalling, growth and response to the envi

278 gen-activated protein kinase, involvement of phytohormone signals, and the existence of transcription

279 d by assessing changes in defense-associated phytohormones, specialized metabolites and global gene e

280 een hypothesized that altered homeostasis of phytohormones such as auxin and strigolactone is at leas

281 l and energy metabolisms and many related to phytohormones such as cytokinin, suggesting that Xa21 tr

282 lopmental transition influenced by light and phytohormones such as ethylene.

283 These include pathways regulating phytohormones such as gibberellins, abscisic acid and ja

284 to biosynthesis, transport, and response of phytohormones, such as auxin, gibberellins, and strigola

285 processes are regulated in interaction with phytohormones, such as auxin.

286 Cytokinin is a phytohormone that is well known for its roles in numerou

287 Abscisic acid (ABA) is a key phytohormone that mediates environmental stress response

288 Jasmonoyl-isoleucine (JA-Ile) is a phytohormone that orchestrates plant defenses in respons

289 Ethylene is an important phytohormone that promotes the ripening of fruits and se

290 Auxin is an important phytohormone that regulates response, differentiation, a

291 Strigolactones (SLs) are phytohormones that play a central role in regulating sho

292 Here, we show that a phytohormone, the brassinosteroids (BRs) promotes pollen

293 Plants employ diverse responses mediated by phytohormones to defend themselves against pathogens and

294 le, root attack induces different changes in phytohormones to those in damaged leaves, including a lo

295 us conditions (i.e. nutrient deprivation and phytohormone treatments) allowed the identification of 1

296 c reporters that instantaneously convert the phytohormone-triggered interaction of ABA receptors with

297 vestigate these oxylipins as well as related phytohormones using a quadrupole-time-of-flight (Q-TOF)

298 On the other hand, the stress-related phytohormones were generally more abundant in the bark c

299 virulence factor, potentially a gibberellin phytohormone, which is antagonistic to JA, consistent wi

300 of complex pathways for production of the GA phytohormones, which were actually first isolated from t