ライフサイエンスコーパス: gibberellin

1 s flowering downstream from the phytohormone gibberellin.

2 egulated by sugar starvation and the hormone gibberellin.

3 nd mediated by hormones such as auxin and/or gibberellin.

4 ng overshoots after the removal of exogenous gibberellin.

5 esocotyl appears predominantly controlled by gibberellin.

6 nts exhibit reduced growth responsiveness to gibberellin.

7 the foolish-seedling disease of rice, makes gibberellin.

8 t the juvenile phase and have high levels of gibberellin.

9 production of the diterpenoid plant hormone gibberellin.

10 s mutants and in the presence of suppressive gibberellin.

11 and the phytohormones auxin, cytokinin, and gibberellin.

12 by antagonizing the phytohormones auxin and gibberellin.

13 teractions among glucose, abscisic acid, and gibberellins.

14 ids and to contribute to the biosynthesis of gibberellins.

15 oducing ent-kaurene, which is a precursor of gibberellins.

16 sed levels of chlorophylls, carotenoids, and gibberellins.

17 f ga1-3 (RGA), and have altered responses to gibberellins.

18 IS, the regulation of trichome initiation by gibberellins.

19 eved by blocking the action or production of gibberellins.

20 hormones, including auxins, jasmonates, and gibberellins.

21 ed operon that may lead to the production of gibberellins.

22 ctors to control plant growth in response to gibberellin (1) .

23 ly regulate the acetylation level of the C19-GIBBERELLIN 2-OXIDASE2 (GA2ox2) locus and repress the ex

24 strate that the gibberellin-degrading enzyme GIBBERELLIN 2-OXIDASE6 is transcriptionally induced by E

25 ed significantly increased levels of ABA and gibberellin, 2- and 5-fold, respectively.

26 genome-wide transcriptome data and show that GIBBERELLIN 20 OXIDASE 2, which encodes an enzyme requir

27 mutations at GA locus 5 (GA5), which encodes gibberellin 20-oxidase 1 (GA20ox1) involved in the last

28 genes have low expression there is enhanced GIBBERELLIN 3 BETA-HYDROXYLASE 1 (GA3ox1) expression, ex

29 Gibberellin 3-oxidase (GA3ox) catalyzes the final step i

30 Gibberellin 3-oxidase in Arabidopsis is encoded by a mul

31 ranscriptional activation of GID1 and GA3ox (GIBBERELLIN 3-OXIDASE) genes controlling GA perception a

32 degradation is promoted by the phytohormone gibberellin [4].

33 Imbibition on gibberellin(4 + 7) did not ameliorate germination percen

34 and percentage on both water and 100 microM gibberellin(4 + 7) were recovered.

35 ccurately predicts the response to exogenous gibberellin after a number of chemical and genetic pertu

36 Gibberellin and ABA therefore act antagonistically to re

37 gene interaction partners, and also modulate gibberellin and abscisic acid signaling to regulate dive

38 in seed dormancy, mediated by alteration of gibberellin and abscisic acid signalling.

39 sheath1, possibly correlated with changes in gibberellin and auxin signaling.

40 k between the growth-promoting plant hormone gibberellin and cortical microtubule organization.

41 s, we predict how these perturbations affect gibberellin and DELLA levels and thereby provide insight

42 ation and leaf growth by a process involving gibberellin and DELLA signaling.

43 Moreover, genes related to auxin, gibberellin and ethylene biosynthesis were significantly

44 n of genes encoding regulated enzymes in the gibberellin and ethylene biosynthetic pathways (LsGA3ox1

45 e in both modulating the level of endogenous gibberellin and generating overshoots after the removal

46 Last, we found that gibberellin and jasmonic acid had a synergistic effect o

47 sponse element (RE), two heat shock REs, one gibberellin and two auxin REs, and five sugar REs.

48 e integration of photoperiod, vernalization, gibberellin and/or autonomous signaling pathways by regu

49 ranscript and selective hormone profiling of gibberellins and abscisic acid revealed changes only in

50 sis of unsaturated fatty acids, eicosanoids, gibberellins and carotenoids.

51 otype is associated with increased levels of gibberellins and certain flavonoid compounds in roots.

52 gnaling is highly integrated with the light, gibberellin, and auxin pathways through both direct inte

53 red the expression of genes involved in ABA, gibberellin, and ethylene biosynthesis and signaling pat

54 ndole acetic acid, active cytokinins, active gibberellin, and salicylic acid were detected in the roo

55 nd response of phytohormones, such as auxin, gibberellins, and strigolactone, were differentially exp

56 We distinguished single and double bonds in gibberellins, and we enantioselectively crystallized rac

57 ient carbon metabolism and the plant hormone gibberellin are required to guarantee optimal plant grow

58 Gibberellins are a class of tetracyclic plant hormones t

59 apart from the circumstantial evidence that gibberellins are somehow involved in the expression of L

60 of seven hormones, including abscisic acid, gibberellin, auxin, ethylene, cytokinin, brassinosteroid

61 Gibberellin binds its receptor, GID1, to form a complex

62 , including carotenoid, brassinosteroid, and gibberellin biosyntheses have been added from the litera

63 served as a histidine in enzymes involved in gibberellin biosynthesis and as an arginine in those ded

64 heir Mg(2+) cofactor, with those involved in gibberellin biosynthesis being more sensitive to such in

65 nt of the pickle (pkl) mutant, inhibition of gibberellin biosynthesis during germination induces embr

66 prominent role than the embryo in auxin and gibberellin biosynthesis for fruit set.

67 lases and as a novel, selective inhibitor of gibberellin biosynthesis in plants.

68 erved after biotic stress treatments and the gibberellin biosynthesis inhibitor paclobutrazol.

69 , which encodes ent-kaurene oxidase 2 of the gibberellin biosynthesis pathway, is down-regulated in O

70 n which LsERF1 acts through the promotion of gibberellin biosynthesis to counter the inhibitory effec

71 te-dependent dioxygenase 2-ODD2, involved in gibberellin biosynthesis was significantly increased at

72 isic acid and paclobutrazol (an inhibitor of gibberellin biosynthesis) on seed germination.

73 se 1 (GA20ox1) involved in the last steps of gibberellin biosynthesis, are found in different populat

74 biochemical regulatory mechanism in limiting gibberellin biosynthesis, but the importance of its rele

75 o changes in transcripts encoding enzymes of gibberellin biosynthesis.

76 rding ent-kaurenoic acid from ent-kaurene in gibberellin biosynthesis.

77 germinate on paclobutrazol, an inhibitor of gibberellin biosynthesis.

78 ys, which is transduced into a daily rate of gibberellin biosynthesis.

79 rosettes, probably through the activation of gibberellin biosynthetic genes.

80 genes associated with the abscisic acid and gibberellin biosynthetic pathways and results of biosynt

81 ic acid catabolic pathway (via CYP707A2) and gibberellins biosynthetic pathway (via GA20ox1) in seeds

82 unted growth of the mutant is not rescued by gibberellin, brassinosteroid, or indoleacetic acid appli

83 s) participate in electron transport chains; gibberellins (C20), brassinosteroids (C30) and abscisic

84 ds and sterols are derived from FPP, whereas gibberellins, carotenoids, casbenes, taxenes, and others

85 ription factor LEAFY induces expression of a gibberellin catabolism gene; consequently, increased LEA

86 complexity from methanol to plant hormones (gibberellins, containing eight stereocenters), were crys

87 ng pathway and was associated with increased gibberellin content and reduced abscisic acid sensitivit

88 The signals auxin, cytokinin and gibberellin control the balance between cell division an

89 ed significantly increased amounts of active gibberellins, cytokinins, salicylic acid, and jasmonate

90 Gibberellin-deficient (gib-1) seeds maintained LeGOLS-1

91 overexpression line, we demonstrate that the gibberellin-degrading enzyme GIBBERELLIN 2-OXIDASE6 is t

92 e oxygen species (ROS) associated with early gibberellin-dependent flowering and abscisic acid hypers

93 regulating tubulin subunit availability in a gibberellin-dependent manner.

94 bberellin signaling network, we simulate how gibberellin dilution affects the downstream components,

95 as identified, and the activity of DTA1 as a gibberellin (GA) 2-oxidase was confirmed.

96 Gibberellin (GA) 3-oxidase, a class of 2-oxoglutarate-de

97 GAI) and Repressor of GAI-Like, which affect gibberellin (GA) action, and the GA catabolic gene, GA 2

98 The aim of this study was to investigate how gibberellin (GA) and abscisic acid (ABA) regulate conver

99 studying the regulation of transcription by gibberellin (GA) and abscisic acid (ABA).

100 analyses involving mutants in the long-day, gibberellin (GA) and phyB flowering pathways indicated t

101 oss talk with signaling pathways mediated by gibberellin (GA) and SPINDLY (SPY), a GA response inhibi

102 We show here that exogenous gibberellin (GA) application accelerates spike developme

103 ntially sensitive to abscisic acid (ABA) and gibberellin (GA) at elevated temperatures.

104 The gibberellin (GA) biosynthesis inhibitor paclobutrazol ca

105 Gibberellin (GA) biosynthesis is necessary for normal pl

106 barley elf3 mutant are strongly dependent on gibberellin (GA) biosynthesis.

107 s transcriptional regulation of key genes of gibberellin (GA) biosynthesis.

108 on of GIBBERELLIC ACID3-OXIDASE2, encoding a gibberellin (GA) biosynthetic enzyme, and the levels of

109 The activity of the gibberellin (GA) biosynthetic enzymes GA 20-oxidases (GA

110 Transcripts of the gibberellin (GA) biosynthetic gene EaGA3ox1 and GA-respo

111 Levels of intermediates in the gibberellin (GA) biosynthetic pathway were altered, and

112 is induced not only by sugar starvation and gibberellin (GA) but also by O2 deficiency.

113 Conversely, the hormone gibberellin (GA) can antagonise the effects of KNOX over

114 in the biosynthesis or signaling pathways of gibberellin (GA) can cause dwarfing phenotypes in plants

115 The diterpenoid phytohormone gibberellin (GA) controls diverse developmental processe

116 gs were demonstrated to be non-responsive to gibberellin (GA) for cell elongation, hypersensitive to

117 The phytohormone gibberellin (GA) has long been known to regulate the gro

118 e pathway or through proteolysis-independent gibberellin (GA) hormone signaling.

119 ionship between the brassinosteroid (BR) and gibberellin (GA) hormones across both stages of photomor

120 Gibberellin (GA) involvement in the reproductive events

121 The phytohormone gibberellin (GA) is a key regulator of plant growth and

122 The hormone gibberellin (GA) is a key regulator of plant growth.

123 The plant growth hormone gibberellin (GA) is important for many aspects of plant

124 duced levels of the growth-promoting hormone gibberellin (GA) lead to increased tolerance to water de

125 ner alone increased tuber yields by lowering gibberellin (GA) levels and increasing cytokinins.

126 is poorly understood, although a decrease in gibberellin (GA) levels is known to be required.

127 Gibberellin (GA) levels were investigated because it is

128 s rescued either by exogenous application of gibberellin (GA) or by introducing della quadruple mutan

129 t cases the homologs must participate in non-gibberellin (GA) pathways.

130 a) produces ent-copalyl diphosphate for both gibberellin (GA) phytohormone and defensive phytoalexin

131 P450 (CYP) 701 family member is required for gibberellin (GA) phytohormone biosynthesis.

132 The gibberellin (GA) phytohormones play important roles in p

133 the response of plants to application of the gibberellin (GA) precursors ent-kaurenoic acid and GA12

134 The phytohormone gibberellin (GA) promotes growth by inducing degradation

135 The phytohormone gibberellin (GA) promotes plant growth by stimulating ce

136 The hormone gibberellin (GA) regulates Arabidopsis root growth by co

137 Gibberellin (GA) regulates plant development primarily b

138 The application of bioactive gibberellin (GA) restored the runnering phenotype in the

139 olved in oxidative cytokinin degradation and gibberellin (GA) signal transduction, respectively, to s

140 oteins are the master negative regulators in gibberellin (GA) signaling acting in the nucleus as tran

141 ration of ethylene, abscisic acid (ABA), and gibberellin (GA) signaling during submergence.

142 We explore the roles of gibberellin (GA) signaling genes SLEEPY1 (SLY1) and RGA-

143 (SLY1) F-box gene is a positive regulator of gibberellin (GA) signaling in Arabidopsis (Arabidopsis t

144 ve) are negative regulators of plant hormone gibberellin (GA) signaling in Arabidopsis.

145 s are highly conserved repressors of hormone gibberellin (GA) signaling in plants.

146 ressors in plants by inhibiting phytohormone gibberellin (GA) signaling in response to developmental

147 the concurrence of brassinosteroid (BR) and gibberellin (GA) signaling in the control of cell expans

148 ate the crosstalk of abscisic acid (ABA) and gibberellin (GA) signaling in wheat (Triticum aestivum),

149 e presents evidence that DELLA repression of gibberellin (GA) signaling is relieved both by proteolys

150 he gene encoding SlDELLA, a repressor in the gibberellin (GA) signaling pathway.

151 INDLY (SPY) protein negatively regulates the gibberellin (GA) signaling pathway.

152 reviously been established in both light and gibberellin (GA) signaling, through interactions with ph

153 1) and SNEEZY (SNE), in Arabidopsis thaliana gibberellin (GA) signaling.

154 sis SLY1 (SLEEPY1) gene positively regulates gibberellin (GA) signaling.

155 Here we show that gibberellin (GA) signalling mediated by DELLA proteins i

156 Abscisic acid (ABA) and gibberellin (GA) signalling responds rapidly following b

157 Excessive gibberellin (GA) signalling, mediated through the DELLA

158 KN1 negatively modulates the accumulation of gibberellin (GA) through the control of ga2ox1, which co

159 tative CHD3 chromatin remodeling factor, and gibberellin (GA), a plant growth regulator.

160 eurone cells responded to nitric oxide (NO), gibberellin (GA), and abscisic acid, with NO being upstr

161 cence downstream from auxin, cytokinin (CK), gibberellin (GA), and light signaling.

162 red for biosynthesis of the growth regulator gibberellin (GA), is upregulated in svp mutants.

163 ight, temperature, brassinosteroid (BR), and gibberellin (GA), regulate cell elongation largely by in

164 ed by a limited response to the phytohormone gibberellin (GA), resulting in improved resistance to st

165 cap enzyme endo-beta-mannanase is induced by gibberellin (GA), which is thought to be the major hormo

166 oss-talk between the phytohormones auxin and gibberellin (GA), which partly control overlapping proce

167 In gibberellin (GA)-deficient mutant (gib-1) seeds, express

168 n seeds that had completed germination or in gibberellin (GA)-deficient seeds stimulated to germinate

169 a quiescence survival strategy that inhibits gibberellin (GA)-induced carbohydrate consumption and el

170 l known that abscisic acid (ABA) antagonizes gibberellin (GA)-promoted seed germination.

171 e found that DOG1 inhibits the expression of gibberellin (GA)-regulated genes encoding cell-wall remo

172 nes encoding the DELLAs, a family of nuclear gibberellin (GA)-regulated growth-repressing proteins.

173 phenotype is suppressed by the phytohormone gibberellin (GA).

174 pkl seedlings by the plant growth regulator gibberellin (GA).

175 pment are both regulated by the phytohormone gibberellin (GA).

176 ylene, N-1-naphthylphthalamic acid (NPA) and gibberellin (GA).

177 ally acting hormones abscisic acid (ABA) and gibberellin (GA).

178 LLA, GhSLR1, repressor of the growth hormone gibberellin (GA).

179 Gibberellins (GA) and cytokinins act antagonistically in

180 To study the role of abscisic acid (ABA) and gibberellins (GA) in pre-maturity alpha-amylase (PMA) fo

181 Gibberellins (GA) promote while abscisic acid (ABA) inhi

182 indicate that GCR1 plays a positive role in gibberellin- (GA) and brassinosteroid- (BR) regulated se

183 GA19, the immediate precursor of the active gibberellin, GA1, by UV-B in this zone, which is regulat

184 growth was partially restored by the active gibberellin GA3 or the functional analog of jasmonoyl-is

185 Light and gibberellins (GAs) antagonistically regulate hypocotyl e

186 Gibberellins (GAs) are a class of plant hormones involve

187 The gibberellins (GAs) are a group of endogenous compounds t

188 Bioactive gibberellins (GAs) are diterpene phytohormones that modu

189 Gibberellins (GAs) are key modulators of plant growth an

190 Bioactive gibberellins (GAs) are phytohormones that regulate growt

191 Gibberellins (GAs) are plant hormones involved in the re

192 Gibberellins (GAs) are plant hormones that affect plant

193 Gibberellins (GAs) are plant hormones that promote a wid

194 Gibberellins (GAs) are plant hormones that regulate most

195 Previous work has shown that 13-hydroxylated gibberellins (GAs) are predominant in the long-day (LD)

196 actor for the induction of dormancy, whereas gibberellins (GAs) are required for germination.

197 Degradation of active C(19)-gibberellins (GAs) by dioxygenases through 2beta-hydroxy

198 Abscisic acid (ABA) and gibberellins (GAs) control several developmental process

199 trichome formation, a process controlled by gibberellins (GAs) in Arabidopsis rosette leaves.

200 The role of gibberellins (GAs) in regulation of lateral root develop

201 Because gibberellins (GAs) increase internode length by affectin

202 Light and gibberellins (GAs) mediate many essential and partially

203 Gibberellins (GAs) or gibberellic acids are ubiquitous d

204 Gibberellins (GAs) play a critical role in fruit-set and

205 Gibberellins (GAs) play a key role in these adaptive res

206 Gibberellins (GAs) regulate many aspects of plant develo

207 e show that BRs regulate the biosynthesis of gibberellins (GAs), another class of growth-promoting ho

208 sis of several hormones, including auxin and gibberellins (GAs), which stimulate fruit set.

209 thaliana) in relation to the availability of gibberellins (GAs).

210 the final step in the synthesis of bioactive gibberellins (GAs).

211 t catalyze formation of the methyl esters of gibberellins (GAs).

212 ant hormones, including cytokinins (CKs) and gibberellins (GAs).

213 pression of a few genes; brassinosteroid and gibberellin had only modest effects.

214 ng, in addition, indicated a modification of gibberellin homeostasis and a strong disturbance of the

215 hylene and the upregulation of cytokinin and gibberellin hormonal responses were also characteristic

216 To examine the role of gibberellin hormones (GAs) in tolerance to apical merist

217 by regulating the synthesis of cytokinin and gibberellin hormones--mobile molecules more usually asso

218 investigate the distribution of the hormone gibberellin in the root elongation zone.

219 , TATCCA box, and CAREs box, implicating the gibberellins in regulation of many rhizome-specific gene

220 ic acid-3 (GA3), consistent with the role of gibberellins in trichome development.

221 r, the role of abscisic acid and diterpenes (gibberellins) in germination assumed much greater import

222 ir DNA-binding activities are blocked by the gibberellin-inactivated repressor RGA.

223 lt stress but repressed by the plant hormone gibberellin, indicating a complex regulation of BOI gene

224 ct on another hormone-regulated process, the gibberellin-induced and ABA-suppressed expression of alp

225 idopsis (Arabidopsis thaliana) DELLA protein GIBBERELLIN INSENSITIVE and screened a collection of con

226 f the gibberellin signal transduction [e.g., GIBBERELLIN INSENSITIVE DWARF 1 (GID1) and DELLA], biosy

227 s, three functionally redundant GA receptors GIBBERELLIN INSENSITIVE DWARF1 (GID1a, b, and c), and th

228 thesis and catabolism enzymes, GA receptors (GIBBERELLIN INSENSITIVE DWARF1, GID1) and early GA signa

229 pitation indicates that the interaction with GIBBERELLIN INSENSITIVE impairs the activity of RELATED

230 RGA (repressor of ga1-3) and GAI (gibberellin insensitive) are negative regulators of plan

231 ELLA-dependent transcriptional activation of GIBBERELLIN-INSENSITIVE DWARF1 (GID1) GA receptor genes.

232 GA binding to the GIBBERELLIN-INSENSITIVE DWARF1 (GID1) GA receptors stimu

233 This response requires GIBBERELLIN-INSENSITIVE DWARF1-mediated GA perception an

234 Gibberellin is perceived by its nuclear receptors GA INS

235 ther, we simulate perturbed systems in which gibberellin levels are reduced, considering both genetic

236 s response is absent in mutants with altered gibberellin levels or DELLA activity.

237 ose metabolism and altered abscisic acid and gibberellin levels.

238 o dilute, creating a significant gradient in gibberellin levels.

239 tly, increased LEAFY activity causes reduced gibberellin levels.

240 g signals, including auxin, brassinosteroid, gibberellin, light, and temperature.

241 The two opposing functions of gibberellin may facilitate evolutionary and environmenta

242 (five ERFs); and (3) negative regulation of gibberellin-mediated shoot elongation (four ERFs).

243 synthase activity relevant to the ancestral gibberellin metabolic function.

244 xpression of GA2ox2, HDT1/2 likely fine-tune gibberellin metabolism and they are crucial for regulati

245 Osmotic stress induces changes in gibberellin metabolism, resulting in the stabilization o

246 monofunctional enzymes (TPS-c and TPS-e) of gibberellin metabolism.

247 tially contribute to light regulation of the gibberellin metabolism.

248 icity indicates the ease with which primary (gibberellin) metabolism can be subverted to secondary bi

249 rmones (indole-3-acetic acid, abscisic acid, gibberellin, methyl jasmonic acid, brassinosteroid, sali

250 e synthesis of ent-kaurene, the precursor of gibberellins, no other tomato TPS genes could be demonst

251 l damage, jasmonic acid, salicylic acid, and gibberellin on induction of trichomes in Arabidopsis.

252 ce of exogenous auxin and sugars, but not by gibberellin or abscisic acid, and is antagonized by cyto

253 P3b is not involved in flowering promoted by gibberellin or vernalization.

254 resistant to sirtinol and auxin, but not to gibberellins or brassinolide.

255 he production of or sensitivity to ethylene, gibberellin, or cytokinin.

256 ssinolide but cannot be recovered by auxins, gibberellins, or cytokinins.

257 enes interact with the cytokinin, auxin, and gibberellin pathways.

258 ast, we engineered an optogenetic biosensor, GIBBERELLIN PERCEPTION SENSOR 1 (GPS1), that senses nano

259 of the diterpene synthase genes required for gibberellin phytohormone biosynthesis provided an early

260 ene synthases found in all higher plants for gibberellin phytohormone biosynthesis to the production

261 site presence of CPSs in all land plants for gibberellin phytohormone biosynthesis, such plasticity p

262 phate synthases found in all seed plants for gibberellin phytohormone metabolism, by a larger aromati

263 rpenoid as a virulence factor, potentially a gibberellin phytohormone, which is antagonistic to JA, c

264 ich presumably limits flux toward the potent gibberellin phytohormones.

265 tural products, which includes the important gibberellin plant hormones.

266 gi produce ent-kaurene as a precursor to the gibberellin plant hormones.

267 to ent-kaurene, the olefin precursor to the gibberellin plant hormones.

268 In contrast, similar diterpenes of gibberellin primary (i.e. general) metabolism are produc

269 Although gibberellin promotes termination of vegetative developme

270 Abscisic acid (ABA) inhibits, whereas gibberellin promotes, germination and early seedling dev

271 and cytokinin treatments, while darkness and gibberellin reduce expression.

272 sociated with stress, manganese binding, and gibberellin-regulated transcription factor were common i

273 However, gibberellin regulates expression of GID1, GA20ox, and GA

274 Control of abscisic acid- and gibberellin-related gene expression in seeds requires no

275 In this way, gibberellin relieves DELLA-dependent growth repression.

276 henotype seems to be a partial or incomplete gibberellin response emerging from a strongly altered ho

277 and in vivo data on the expression levels of gibberellin-responsive genes.

278 This allows accumulation of gibberellin-sensitive DELLA proteins.

279 Many of the components of the gibberellin signal transduction [e.g., GIBBERELLIN INSEN

280 c transferase (OGT) SPINDLY (SPY) suppresses gibberellin signaling and promotes cytokinin (CK) respon

281 While SPY has been shown to suppress gibberellin signaling and to promote cytokinin (CK) resp

282 SPINDLY (SPY) is a negative regulator of gibberellin signaling in Arabidopsis thaliana that also

283 We identified roles for auxin and gibberellin signaling in Suc-induced hypocotyl elongatio

284 By incorporating the gibberellin signaling network, we simulate how gibberell

285 Fourteen of them are up-regulated by the gibberellin signaling pathway during pollen development,

286 but hinted at a link with jasmonic acid and gibberellin signaling pathways.

287 how these feedback loops interact to control gibberellin signaling.

288 te the role of the various feedback loops in gibberellin signaling.

289 ay between symbiosis, nutrient, and hormone (gibberellin) signaling.

290 e we provide genetic evidence that the light/gibberellin-signaling pathway affects the properties of

291 smitted via CCaMK and CYCLOPS) and hormonal (gibberellin) signals.

292 an induction of auxin, brassinosteroid, and gibberellin signatures and the involvement of several ca

293 aurene synthase, a key regulatory enzyme for gibberellin synthesis, the following day.

294 the interplay between carbon metabolism and gibberellins that modulates plant growth.

295 ight, temperature, brassinosteroid (BR), and gibberellin, that inhibit the atypical basic helix-loop-

296 l quantifies how rapid cell expansion causes gibberellin to dilute, creating a significant gradient i

297 that dual opposite roles of the phytohormone gibberellin underpin this phenomenon in Arabidopsis.

298 ated diterpenoid, although the production of gibberellins was not observed.

299 mounts after imbibition unless supplied with gibberellin, whereas abscisic acid (ABA) did not prevent

300 ssion, and that AG activates biosynthesis of gibberellin, which has been proposed to promote the shif