ライフサイエンスコーパス: brassinosteroid

1 rsor of brassinolide (the most active of the brassinosteroids).

2 factors, such as the phytohormones auxin and brassinosteroid.

3 auxin, strigolactone, gibberellic acid, and brassinosteroids.

4 of responses to the plant hormones auxin and brassinosteroids.

5 5, two defective transmembrane receptors for brassinosteroids.

6 and in alterations in response to auxin and brassinosteroids.

7 into the regulatory mechanisms of bioactive brassinosteroids.

8 critical component of a receptor complex for brassinosteroids.

9 to three brassinosteroid-biosynthesis genes (BRASSINOSTEROID-6-OXIDASE, CONSTITUTIVE PHOTOMORPHOGENIC

10 esponse, thus illuminating one aspect of the brassinosteroid/abscisic acid antagonism.

11 steroids are depleted from the epidermis and brassinosteroids act locally within a leaf.

12 Similar to cytokinin, brassinosteroid acts post-transcriptionally by increasin

13 xplore the mechanism by which cytokinins and brassinosteroids affect ethylene biosynthesis.

14 isic acid (ABA), and hyposensitive to auxin, brassinosteroid and cytokinin, but normally responsive t

15 uxin affected the expression of a few genes; brassinosteroid and gibberellin had only modest effects.

16 tly, TT8 affects stress response, along with brassinosteroid and jasmonic acid biosynthesis, by direc

17 mutant displayed reduced responses to GA and brassinosteroid and showed decreased expression of sever

18 we report evidence that interactions between brassinosteroids and auxin signaling modulate phototropi

19 The remainder appear to be unlinked to brassinosteroids and related to primary and secondary me

20 alyses also suggested an induction of auxin, brassinosteroid, and gibberellin signatures and the invo

21 id, gibberellin, auxin, ethylene, cytokinin, brassinosteroid, and jasmonate.

22 ion of VUP1 represses the expression of many brassinosteroid- and auxin-responsive genes.

23 Moreover, shoot growth is restricted when brassinosteroids are depleted from the epidermis and bra

24 Brassinosteroids are phytohormones involved in plant dev

25 Brassinosteroids are plant steroid hormones that control

26 Brassinosteroids are plant-derived polyhydroxylated deri

27 Brassinosteroids are plant-specific steroid hormones tha

28 OMATIC EMBRYOGENESIS RECEPTOR KINASE (SERK)3/brassinosteroid-associated kinase (BAK)1, a receptor-lik

29 fied a R2R3-MYB transcription factor, BRAVO (BRASSINOSTEROIDS AT VASCULAR AND ORGANIZING CENTER), act

30 ants, steroid hormone action occurs when the brassinosteroids bind a membrane tyrosine kinase recepto

31 Our results demonstrate that brassinosteroids bind directly to the 94 amino acids com

32 id, carotenoid, oxylipin, glucosinolate, and brassinosteroid biosyntheses and have shown that both P4

33 Here, we use dwarf, brassinosteroid biosynthesis and brassinosteroid respons

34 ng sturdy culm, specific for deficiencies in brassinosteroid biosynthesis and signaling in semidwarf

35 e of reduced expression of genes involved in brassinosteroid biosynthesis and signaling.

36 CYP90D2 gene, which encodes an enzyme in the brassinosteroid biosynthesis pathway.

37 1 (DWF1) is responsible for an early step in brassinosteroid biosynthesis that converts 24-methylenec

38 igned more than 20 historic mutants to three brassinosteroid-biosynthesis genes (BRASSINOSTEROID-6-OX

39 ression of the brassinosteroid receptor or a brassinosteroid biosynthetic enzyme in the epidermis, bu

40 studies have demonstrated that cytokinin and brassinosteroid (BR) act as regulatory inputs to elevate

41 to investigate the relationship between the brassinosteroid (BR) and gibberellin (GA) hormones acros

42 A paradigmatic case is the concurrence of brassinosteroid (BR) and gibberellin (GA) signaling in t

43 Brassinosteroid (BR) and glucose (Glc) regulate many com

44 Brassinosteroid (BR) binding activates the receptor kina

45 The brassinosteroid (BR) class of steroid hormones regulates

46 Brassinosteroid (BR) homeostasis and signaling are cruci

47 Brassinosteroid (BR) hormone is shown here to have oppos

48 coding sterol C-22 hydroxylases that control brassinosteroid (BR) hormone levels using a promoter tha

49 Brassinosteroid (BR) hormone signaling controls multiple

50 Brassinosteroid (BR) hormones are primarily perceived at

51 es accumulation of the plant steroid hormone brassinosteroid (BR) in organ boundaries.

52 BES1 functions as a master regulator in the brassinosteroid (BR) pathway that promotes plant growth.

53 onic acid (JA) pathway was induced while the brassinosteroid (BR) pathway was suppressed in infected

54 nase that functions as a coreceptor with the brassinosteroid (BR) receptor BRI1 and the flagellin rec

55 urally defective yet biochemically competent brassinosteroid (BR) receptor BRI1, resulted in identifi

56 urally imperfect yet biochemically competent brassinosteroid (BR) receptor bri1-9, causing its increa

57 EBS1 gene suppressed the growth defects of a brassinosteroid (BR) receptor mutant, bri1-9, in an alle

58 BAK1 is also a coreceptor for the plant brassinosteroid (BR) receptor, the LRR-RK BRI1.

59 In plants, the steroidal hormone brassinosteroid (BR) regulates numerous developmental pr

60 Brassinosteroid (BR) regulates plant development by acti

61 nome-wide screen for mutants showing altered brassinosteroid (BR) sensitivity or bri1-like phenotypes

62 Brassinosteroid (BR) signal transduction research has pr

63 show here that FKBP42/TWD1 is necessary for brassinosteroid (BR) signal transduction.

64 s GSK3-like kinase that negatively regulates brassinosteroid (BR) signaling by phosphorylating BES1 (

65 In this study, we found that brassinosteroid (BR) signaling converges with SUPPRESSOR

66 have been described as positive effectors of brassinosteroid (BR) signaling in plants.

67 Brassinosteroid (BR) signaling is essential for plant gr

68 The brassinosteroid (BR) signaling module is a central regul

69 The brassinosteroid (BR) signaling pathway includes two rece

70 In this study, we show that brassinosteroid (BR) signaling works downstream of Glc i

71 s in plant immunity, cell-death control, and brassinosteroid (BR) signaling, all four functional SERK

72 NSITIVE2 (BIN2), a key negative regulator of brassinosteroid (BR) signaling, can phosphorylate Arabid

73 e pattern; instead, the detailed analysis of brassinosteroid (BR) signaling, innate immunity, and sym

74 PRs of either the negative regulators of the brassinosteroid (BR) signaling, the glycogen synthase ki

75 nown mechanism upon receptor kinase-mediated brassinosteroid (BR) signaling.

76 in many plant signaling processes, including brassinosteroid (BR) signaling.

77 cated a negative regulatory role for BIN2 in brassinosteroid (BR) signaling.

78 hanced early seedling growth due to elevated brassinosteroid (BR) synthesis and/or signalling.

79 fferentially regulates genes associated with brassinosteroid (BR) synthesis during submergence.

80 we show that the activity of two homologous brassinosteroid (BR) transcriptional effectors, BRASSINA

81 enous signals, including light, temperature, brassinosteroid (BR), and gibberellin (GA), regulate cel

82 monal signals, involving light, temperature, brassinosteroid (BR), and gibberellin, that inhibit the

83 coding predicted proteins involved in auxin, brassinosteroid (BR), gibberellic acid (GA), abscisic ac

84 Interestingly, brassinosteroid (BR)-induced gene expression was inhibit

85 nstrating the role of BRAVO in counteracting Brassinosteroid (BR)-mediated cell division in the QC ce

86 pattern (PAMP)-triggered immunity (PTI) and brassinosteroid (BR)-mediated growth was recently report

87 gered immunity (PTI) and the LRR-RLK BRI1 in brassinosteroid (BR)-mediated growth.

88 through TOR controls the accumulation of the brassinosteroid (BR)-signaling transcription factor BZR1

89 responses to two plant hormones, zeatin and brassinosteroid (BR).

90 controlled by hormones, including auxin and brassinosteroid (BR).

91 uxin, gibberellic acid (GA), cytokinin (CK), brassinosteroids (BR) and peptide hormones are also impl

92 Plant responses to brassinosteroids (BR) are mediated through a plasma memb

93 cient for suppression of immune signaling by brassinosteroids (BR).

94 well as intrinsic signals such as hormones (brassinosteroid [BR], auxin, cytokinin, ethylene) and nu

95 ays a positive role in gibberellin- (GA) and brassinosteroid- (BR) regulated seed germination.

96 es have indicated that CYP734A1 binds active brassinosteroids, brassinolide and castasterone, as well

97 Brassinosteroids (BRs) are a unique class of plant stero

98 Brassinosteroids (BRs) are essential for many physiologi

99 Brassinosteroids (BRs) are essential growth-promoting ho

100 Brassinosteroids (BRs) are essential hormones for plant

101 Brassinosteroids (BRs) are essential phytohormones regul

102 Brassinosteroids (BRs) are growth-promoting plant hormon

103 Brassinosteroids (BRs) are hormones that control many as

104 Brassinosteroids (BRs) are important regulators for plan

105 Brassinosteroids (BRs) are key regulators in plant growt

106 Brassinosteroids (BRs) are phytosteroid hormones control

107 Brassinosteroids (BRs) are plant hormones involved in va

108 Brassinosteroids (BRs) are plant hormones that are perce

109 Brassinosteroids (BRs) are plant hormones that regulate

110 strong evidence that steroid hormones called brassinosteroids (BRs) are required to maintain position

111 Brassinosteroids (BRs) are steroid hormones that are ess

112 Brassinosteroids (BRs) are steroid hormones that are ess

113 Brassinosteroids (BRs) are steroid hormones that control

114 Brassinosteroids (BRs) are steroid hormones that coordin

115 Brassinosteroids (BRs) bind to the extracellular domain

116 Abscisic acid (ABA) and brassinosteroids (BRs) exhibit antagonistic interactions

117 ) is the main ligand-perceiving receptor for brassinosteroids (BRs) in Arabidopsis (Arabidopsis thali

118 to investigate a role for the phytohormones brassinosteroids (BRs) in specifying bristle identity an

119 The plant hormones brassinosteroids (BRs) participate in light-mediated reg

120 Notably, application of brassinosteroids (BRs) partly rescued the stomatal leaf

121 Here we show that brassinosteroids (BRs) play a key role in organ boundary

122 Brassinosteroids (BRs) play an essential role in plant g

123 Brassinosteroids (BRs) play key roles in plant growth an

124 Here, we show that a phytohormone, the brassinosteroids (BRs) promotes pollen and seed developm

125 Brassinosteroids (BRs) regulate a wide range of developm

126 For instance, brassinosteroids (BRs) regulate cell elongation, vascula

127 Brassinosteroids (BRs) regulate multiple aspects of plan

128 Brassinosteroids (BRs) regulate multiple aspects of plan

129 Brassinosteroids (BRs) regulate plant development throug

130 Brassinosteroids (BRs) regulate plant growth and stress

131 Brassinosteroids (BRs) signal through a plasma membrane-

132 Here we show that brassinosteroids (BRs), a class of natural plant hormone

133 Mutants in brassinosteroids (BRs), a class of plant hormones necess

134 at are coordinated by hormones including the brassinosteroids (BRs), a group of steroids with structu

135 Plant sterols and steroid hormones, the brassinosteroids (BRs), are compounds that exert a wide

136 Plant steroid hormones, brassinosteroids (BRs), are of great importance for plan

137 terplay of light and plant hormones, such as brassinosteroids (BRs), in the regulation of plant growt

138 Plant steroid hormones, brassinosteroids (BRs), play essential roles in modulati

139 Plant steroid hormones, brassinosteroids (BRs), play essential roles in plant gr

140 The plant steroid hormones, brassinosteroids (BRs), play important roles in plant gr

141 Plant steroid hormones, brassinosteroids (BRs), play important roles in plants.

142 Plant steroid hormones, brassinosteroids (BRs), regulate essential growth and de

143 Active brassinosteroids (BRs), such as brassinolide (BL) and ca

144 Among these hormones are the brassinosteroids (BRs), the polyhydroxylated steroid hor

145 kinase, BRI1, is a cell-surface receptor for brassinosteroids (BRs), the steroid hormones of plants,

146 regulators including plant steroid hormones, brassinosteroids (BRs).

147 3 double mutant roots are insensitive toward brassinosteroids but have a phenotype different from bri

148 the largely differing response to zeatin and brassinosteroid by the metabolic pathways in chloroplast

149 Brassinosteroids cause the rapid dissociation of BKI1-ye

150 How the endogenous brassinosteroids change in response to environmental sti

151 nts show that the minimal binding domain for brassinosteroids consists of a 70-amino acid island doma

152 Treatment with auxin or brassinosteroids could enhance binding of either transcr

153 ctivities of downstream MAPKs are reduced in brassinosteroid-deficient mutants but increased by treat

154 , and altered photomorphogenesis, resembling brassinosteroid-deficient mutants.

155 BAK1 is involved in brassinosteroid-dependent growth and development, innate

156 iption and integrate the auxin response to a brassinosteroid-dependent molecular circuit that promote

157 nthesis of structural sterols from signaling brassinosteroid derivatives and are highly regulated.

158 A15 (SAUR15), a well-characterized auxin and brassinosteroid early response gene in Arabidopsis (Arab

159 the mechanism by which another phytohormone, brassinosteroid, elevates ethylene biosynthesis in etiol

160 Overexpression of the HBI1-related bHLHs brassinosteroid enhanced expression2 (BEE2) and cryptoch

161 helix (bHLH) transcription factor homolog of brassinosteroid enhanced expression2 interacting with IB

162 binding of either transcription factor, and brassinosteroid enhancement of MP/ARF5 binding required

163 osynthesis of plant hormones (e.g. ethylene, brassinosteroid, gibberellic acid) were significantly ch

164 growth-regulating signals, including auxin, brassinosteroid, gibberellin, light, and temperature.

165 tential to fine-tune the levels of different brassinosteroid hormones throughout plant growth and dev

166 date the putative cellular targets for plant brassinosteroids in mammals.

167 , abscisic acid (ABA), cytokinins (CKs), and brassinosteroids in molding plant-pathogen interactions.

168 and CYP72C1 in Arabidopsis diverge more than brassinosteroid inactivating P450s in other plants, this

169 YP734A1 and CYP72C1, have been identified as brassinosteroid-inactivating enzymes important for stero

170 onsible for regulating the levels of several brassinosteroids, including typhasterol, castasterone an

171 PAT inhibition by CMMC occurs in a brassinosteroid-independent manner.

172 Our results indicate that brassinosteroid inhibits stomatal development by allevia

173 s capability to specifically suppress a weak brassinosteroid insensitive 1 (bri1) allele, bri1-5, whe

174 Recently, two Arabidopsis receptor kinases--BRASSINOSTEROID INSENSITIVE 1 (BRI1) and BRI1-ASSOCIATED

175 ntaining two transmembrane receptor kinases, BRASSINOSTEROID INSENSITIVE 1 (BRI1) and BRI1-ASSOCIATED

176 The brassinosteroid receptor brassinosteroid insensitive 1 (BRI1) is a member of the

177 ity of the dual-specificity receptor kinase, brassinosteroid insensitive 1 (BRI1), reflects the balan

178 ed in BR perception and signal transduction: brassinosteroid insensitive 1 (BRI1), which is the BR re

179 using the membrane-integral receptor kinase BRASSINOSTEROID INSENSITIVE 1 (BRI1).

180 sphorylation of the Arabidopsis RD RLK BRI1 (brassinosteroid insensitive 1).

181 LLIN-SENSING 2 (FLS2) with their co-receptor BRASSINOSTEROID INSENSITIVE 1-ASSOCIATED KINASE 1 (BAK1)

182 atic embryogenesis receptor kinase 3 (SERK3)/brassinosteroid insensitive 1-associated kinase 1 (BAK1)

183 brane-resident RLKs, flagellin-sensing 2 and brassinosteroid insensitive 1-associated kinase 1 (BAK1)

184 ll death was shown to require N. benthamiana Brassinosteroid insensitive 1-Associated Kinase 1 (NbBAK

185 However, in Brassinosteroid insensitive 1-Associated Kinase 1 (SERK3

186 Arabidopsis thaliana BRASSINOSTEROID INSENSITIVE 1-associated receptor kinase

187 ense responses required the known coreceptor BRASSINOSTEROID INSENSITIVE 1-ASSOCIATED RECEPTOR KINASE

188 ctivation of the Arabidopsis thaliana kinase BRASSINOSTEROID INSENSITIVE 1-ASSOCIATED RECEPTOR-LIKE K

189 They include a BRASSINOSTEROID INSENSITIVE 2 (BIN2) interaction domain,

190 Brassinosteroids Insensitive 1 (BRI1) is required for BR

191 tion and ERAD of a brassinosteroid receptor, BRASSINOSTEROID-INSENSITIVE 1 (BR1).

192 Arabidopsis thaliana receptor-like kinases, brassinosteroid-insensitive 1 (BRI1) and BRI1-associated

193 growth and development and require an active BRASSINOSTEROID-INSENSITIVE 1 (BRI1) receptor serine/thr

194 gh plasma membrane-localized receptor kinase brassinosteroid-insensitive 1 (BRI1), BRI1-associated re

195 Brassinosteroid-INsensitive 2 (BIN2) is an Arabidopsis G

196 lycogen synthase kinase 3 (GSK3)-like kinase brassinosteroid-insensitive 2 (BIN2), which has been wel

197 LYCOGEN SYNTHASE KINASE 3)-like kinase BIN2 (BRASSINOSTEROID-INSENSITIVE 2), a well established negat

198 The cell surface receptor kinase BRASSINOSTEROID-INSENSITIVE-1 (BRI1) is the major recept

199 ifferent ligand-perceiving receptors such as BRASSINOSTEROID INSENSITIVE1 (BRI1) and FLAGELLIN-SENSIT

200 BRASSINOSTEROID INSENSITIVE1 (BRI1) is a BR receptor, an

201 Brassinosteroid insensitive1 (BRI1) is epistatic to HXK1

202 The BRASSINOSTEROID INSENSITIVE1 (BRI1) receptor kinase has

203 bidopsis thaliana), BRs are perceived by the BRASSINOSTEROID INSENSITIVE1 (BRI1) receptor.

204 plasma membrane through the receptor kinase BRASSINOSTEROID INSENSITIVE1 (BRI1) together with co-rec

205 of the leucine-rich repeat receptor kinase, brassinosteroid insensitive1 (BRI1), was shown to depend

206 tor in Arabidopsis (Arabidopsis thaliana) is BRASSINOSTEROID INSENSITIVE1 (BRI1).

207 the leucine-rich repeat receptor-like kinase brassinosteroid insensitive1 (BRI1).

208 surface by a membrane-bound receptor kinase, BRASSINOSTEROID INSENSITIVE1 (BRI1).

209 avily glycosylated brassinosteroid receptor, BRASSINOSTEROID INSENSITIVE1, while MNS1 to MNS3 appear

210 IOS1 also associated with BRASSINOSTEROID INSENSITIVE1-ASSOCIATED KINASE1 (BAK1) i

211 exes between the membrane-localized IOS1 and BRASSINOSTEROID INSENSITIVE1-ASSOCIATED KINASE1 (BAK1)-d

212 the leucine-rich repeat receptor-like kinase BRASSINOSTEROID INSENSITIVE1-ASSOCIATED KINASE1 (BAK1)/S

213 flagellin sensing2 and its signaling partner brassinosteroid insensitive1-associated kinase1 is obser

214 production that was partially independent of BRASSINOSTEROID INSENSITIVE1-ASSOCIATED KINASE1.

215 dent on the regulatory receptor-like kinases brassinosteroid insensitive1-associated receptor kinase1

216 seedling lethal and cell death phenotypes of BRASSINOSTEROID INSENSITIVE1-associated receptor kinase1

217 The membrane-bound Brassinosteroid insensitive1-associated receptor kinase1

218 th these findings, the transcription factors BRASSINOSTEROID INSENSITIVE1-EMS SUPPESSOR1 and MONOPTER

219 A BRASSINOSTEROID INSENSITIVE1-ETHYL METHANESULFONATE-SUPP

220 ffectors, BRASSINAZOLE RESISTANT1 (BZR1) and BRASSINOSTEROID INSENSITIVE1-ETHYL METHANESULFONATE-SUPP

221 growth and development and require an active BRASSINOSTEROID-INSENSITIVE1 (BRI1) and BRI1-ASSOCIATED

222 The leucine-rich repeat receptor-like kinase BRASSINOSTEROID-INSENSITIVE1 (BRI1) is the main ligand-p

223 UTO) and one brassinosteroid-signaling gene (BRASSINOSTEROID-INSENSITIVE1 [HvBRI1]).

224 al transduction cascade, as is the case with BRASSINOSTEROID-INSENSITIVE1 Associated Kinase1 and CPK5

225 The PEPR coreceptor BRASSINOSTEROID-INSENSITIVE1 Associated Kinase1 contribu

226 ologs in Arabidopsis (Arabidopsis thaliana), brassinosteroid-insensitive1 suppressor (BSU1).

227 ffect mutant variants of the receptor kinase BRASSINOSTEROID-INSENSITIVE1.

228 Here, we demonstrate that the protein kinase BRASSINOSTEROID INSENSITIVE2 (BIN2), a key negative regu

229 of which carry gain-of-function mutations in BRASSINOSTEROID-INSENSITIVE2 (BIN2), one of the three me

230 In addition, auxin, cytokinin, ethylene, brassinosteroids, jasmonates, and salicylic acid also co

231 pression data, the SUB1A genotype had higher brassinosteroid levels after submergence compared to the

232 ably involved in a new mechanism to regulate brassinosteroid levels.

233 uctase (BAN), BEN1 is probably involved in a brassinosteroid metabolic pathway.

234 tants but increased by treatment with either brassinosteroid or GSK3-kinase inhibitor.

235 of the mutant is not rescued by gibberellin, brassinosteroid, or indoleacetic acid application and is

236 These data indicate that the brassinosteroid pathway promotes high vein density in th

237 xin transcriptional response on a functional brassinosteroid pathway.

238 vity of the locally acting, growth-promoting brassinosteroid pathway.

239 haracterized roles in stamen development and brassinosteroid perception, SERK1 plays a unique role in

240 1) is tyrosine phosphorylated in response to brassinosteroid perception.

241 BAK1/SERK3, a receptor kinase implicated in brassinosteroid perception.

242 iterpenoids, which include membrane sterols, brassinosteroid phytohormones, and non-steroidal triterp

243 Brassinosteroids play important roles in regulating root

244 Analyses of brassinosteroid profiles demonstrated that BEN1 is indee

245 erols but without significant alterations to brassinosteroid profiles.

246 The brassinosteroid receptor brassinosteroid insensitive 1 (

247 The brassinosteroid receptor BRI1 and KAPP are shown to asso

248 he auxin translocators PIN2 and AUX1 and the brassinosteroid receptor BRI1 into distinct endomembrane

249 d cell-death control by interacting with the brassinosteroid receptor BRI1, immune receptors, such as

250 ession of phenotypes caused by the defective brassinosteroid receptor bri1-9 strongly suggest that th

251 t plants, which harbour mutated forms of the brassinosteroid receptor BRI1.

252 160, which turned out to be identical to the brassinosteroid receptor BRI1.

253 tation also hampered vacuolar sorting of the brassinosteroid receptor BRI1.

254 bri1-5 is a weak mutant allele of the brassinosteroid receptor gene, BRI1.

255 is mutant caused by retention of a defective brassinosteroid receptor in the ER.

256 We show that expression of the brassinosteroid receptor or a brassinosteroid biosynthet

257 sfolded variants of the heavily glycosylated brassinosteroid receptor, BRASSINOSTEROID INSENSITIVE1,

258 ich are caused by ER retention and ERAD of a brassinosteroid receptor, BRASSINOSTEROID-INSENSITIVE 1

259 Here, we report that a mutated brassinosteroid receptor, bri1-5, that carries a Cys69Ty

260 rmation with a second receptor kinase termed brassinosteroid receptor1 associated kinase1 (BAK1).

261 o bacterial pathogens, but have no effect on brassinosteroid-regulated growth.

262 Genetic analysis demonstrated that brassinosteroid-regulated root epidermal cell patterning

263 Here we demonstrate in Arabidopsis that brassinosteroid regulates stomatal development by activa

264 tudy provides insights into the mechanism of brassinosteroid regulation of root hair patterning.

265 In silico mapping of brassinosteroid-related genes in the barley genome in co

266 barley plant architecture and sturdiness by brassinosteroid-related genes.

267 tematically examined root hair phenotypes in brassinosteroid-related mutants, and found that brassino

268 use dwarf, brassinosteroid biosynthesis and brassinosteroid response mutants in conjunction with tis

269 teroid signaling components to attenuate the brassinosteroid response, thus illuminating one aspect o

270 nation is an important control mechanism for brassinosteroid responses in plants.

271 sic acid, gibberellin, methyl jasmonic acid, brassinosteroid, salicylic acid), chemicals (clofibrate,

272 xpression of genes involved in GA, auxin and brassinosteroid signaling as well as cell elongation/exp

273 ein in rice directly interacts with critical brassinosteroid signaling components to attenuate the br

274 d gene expression demonstrate that auxin and brassinosteroid signaling function interdependently.

275 ssinosteroid-related mutants, and found that brassinosteroid signaling inhibits root hair formation t

276 phosphorylation of the downstream substrate brassinosteroid signaling kinase 1 (BSK1).

277 Sterols are also the precursors to the brassinosteroid signaling molecules.

278 Its biological role in the brassinosteroid signaling pathway was first established

279 A brassinosteroid signaling pathway was predicted to be in

280 m of BES1, a transcriptional effector of the brassinosteroid signaling pathway.

281 are key regulators in light, jasmonate, and brassinosteroid signaling pathways, respectively.

282 s associated with cell wall modification and brassinosteroid signaling were induced under enriched FR

283 We found that with enhanced brassinosteroid signaling, GL2, a cell fate marker for n

284 olved in auxin, abscisic acid, ethylene, and brassinosteroid signaling, peroxisome function, disease

285 rt through regulation of auxin transport and brassinosteroid signaling, two processes that are crucia

286 , impaired BRI1 endocytosis and enhanced the brassinosteroid signaling.

287 tein, BKI1, which is a negative regulator of brassinosteroid signaling.

288 About half of these are related to brassinosteroid signaling.

289 HOTOMORPHOGENIC DWARF, and DIMINUTO) and one brassinosteroid-signaling gene (BRASSINOSTEROID-INSENSIT

290 The brassinosteroid-signaling protein BZR1 is one of the tar

291 regulated transcription factor PIF4, and the brassinosteroid-signaling transcription factor BZR1, int

292 Brassinosteroid signalling from the epidermis is not suf

293 lyses indicate that receptor kinase-mediated brassinosteroid signalling inhibits stomatal development

294 Brassinosteroids, the steroid hormones of plants, are pe

295 members of the CYP734A subfamily inactivate brassinosteroids through C-26 hydroxylation, the biochem

296 ant MAPKKK to its upstream regulators and of brassinosteroid to a specific developmental output.

297 first evidence for direct binding of active brassinosteroids to BRI1 using a biotin-tagged photoaffi

298 ide the nucleus occurs from plants that make brassinosteroids to higher metazoans (primates).

299 Reporter response to brassinosteroid treatment relied on the same two element

300 ASE1 (BAK1), the receptor and coreceptor for brassinosteroids--were shown to autophosphorylate on tyr