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brassinosteroid signaling

25599 relationships annotated with this phrase. Showing first 500 of 25599.
Source entity Relationship Target entity Species
BR signaling pathway genes (OsBAK1, OsGSK2, OsBSK3, OsBZR1, OsILI1, OsDLT) expression does not significantly differ between WT and lam1-D Oryza sativa
BRASSINOSTEROID ENHANCED EXPRESSION2 (BEE2, AT4G36540) is down-regulated in (VUP1, AT3G21710) OX seedlings Arabidopsis thaliana
(VUP1, AT3G21710) OX down-regulated genes overlap with BR-induced genes Arabidopsis thaliana
OsBRI1 mutations lead to reduced plant height Oryza sativa
Expression of wild-type Arabidopsis BRI1-Flag in bri1-5 mutant led to full rescue Arabidopsis thaliana
OsbHLH92 OE plants are more sensitive to BR Oryza sativa
OsBRI1 mutations lead to more aboveground biomass Oryza sativa
(BRD1, AT1G20670) gene holds responsibility for regulating brassinosteroid pathway Zea mays
BR-dependent increases in expression of PHYTOCHROME B ACTIVATION-TAGGED SUPPRESSOR1 (BAS1, CYP72B1, CYP734A1, AT2G26710) were impaired by Ca2+ channel blocker Arabidopsis thaliana
modified leaf angle via the brassinosteroid pathway is often associated with pleiotropic effects on leaf morphology
uzu1.a standard line BW885 is also present in BW860 (sld1.a + uzu1.a) and BW912 (wst1.c + uzu1.a) Hordeum vulgare
BRASSINOSTEROID-INSENSITIVE2 is negative regulator of brassinosteroid signaling Arabidopsis thaliana
(EIN6, JMJ12, REF6, AT3G48430) interacts with (BES1, BZR2, AT1G19350)
QTL located on chromosome 1 contains (BRD1, AT1G20670) gene Zea mays
lam1-D is more sensitive to brassinosteroid (BR) at concentrations of 10–1000 nM Oryza sativa
LAM1 may participate in BR signal transduction pathway Oryza sativa
cu3 allele of tomato (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) is null allele with extreme dwarf phenotype, aberrant leaf structure, and male sterility Solanum lycopersicum
cu3-abs1 allele is analogous to Arabidopsis bri1-5 Solanum lycopersicum; Arabidopsis thaliana
(ATSERK1, SERK1, AT1G71830) (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) and (ATSERK4, BAK7, BKK1, SERK4, AT2G13790) play a redundant and essential role in brassinosteroid (BR) signaling Arabidopsis thaliana
LAM1 may participate in BR signaling pathway Oryza sativa
upregulated BiPs due to (EBS1, AT4G17680) mutation resulted in even more severe dwarf morphology in (EBS1, AT4G17680) bri1-5 double mutant Arabidopsis thaliana
accumulated BiPs in (AtORM1, ORM1, AT1G01230) amiR-ORM2 plants causing dwarf morphology to persist in progeny lines Arabidopsis thaliana
sequencing of HvBRI1 from BW885, BW860, and BW912 revealed expected single substitution A2612G (His-857 to Arg), known as allele uzu1.a Hordeum vulgare
average culm length of uzu1.a at 14°C was 72% of wild-type length Hordeum vulgare
nonsynonymous amino acid exchange in the (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) kinase domain causes alterations in brassinosteroid signaling Hordeum vulgare
inhibition of BRASSINOSTEROID INSENSITIVE 2 (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) results in dephosphorylation of (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) EMS SUPPRESSOR 1 (BES1, BZR2, AT1G19350)
(ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) mutants are male sterile
(ATWRKY23, WRKY23, AT2G47260) and (NSN1, AT3G07050) act downstream of BR signaling pathways Arabidopsis thaliana
expression of BRI1-Flag with T1049A substitution not only failed to rescue bri1-5 but caused dominant negative effect with phenotypes similar to extreme dwarfism of bri1-1 null allele Arabidopsis thaliana
bes1-1D seedlings exhibit pale green enlarged leaves and abnormally elongated hypocotyls and petioles Arabidopsis thaliana
(ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) tomato activation loop residue Thr-1054 is essential for normal tomato growth and development Solanum lycopersicum
bak1-5 mutation does not affect role of (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) in BR signaling Arabidopsis thaliana
OsbHLH92 KO lines have blocked BR signaling pathway Oryza sativa
RNA interference to downregulate (BIP, BIP2, AT5G42020) transcript levels partially suppressed bri1-5 phenotype Arabidopsis thaliana
brassinosteroids (BRs) play important roles in modulating plant architecture
BR-dependent increases in expression of INDOLE-3-ACETIC ACID-INDUCIBLE1 (AXR5, IAA1, AT4G14560) were impaired by Ca2+ channel blocker Arabidopsis thaliana
Uzu1 gene encodes brassinosteroid hormone receptor Hordeum vulgare
epibrassinolide was unable to complement short-hypocotyl phenotype of ZFP3ox seedlings Arabidopsis thaliana
BL treatment increases OsbHLH91 expression Oryza sativa
change in brassinosteroid signaling caused by the regulation of pectin methylesterase (PME) activity might contribute to changes in germination behavior
OsBU1 expression is significantly increased in lam1-D Oryza sativa
exogenous BR treatment significantly reduces PpTCP4 expression Prunus persica
uzu1.a allele shows sensitivity to elevated temperatures Hordeum vulgare
haplotypes from 'Steptoe' and 'Akashinriki'-derived lines displayed not obvious brassinosteroid phenotype Hordeum vulgare
OsmiR396d is one direct target gene of OsBZR1 Oryza sativa
Phytophthora infestans effector PiAVR2 up-regulates BR-responsive basic helix-loop-helix transcription factor Nicotiana benthamiana
alternatives to the uzu1.a allele of HvBRI1 enable breeding of sturdy and climate-tolerant barley cultivars Hordeum vulgare
leaf-unrolling test differentiates brassinosteroid-signaling mutants from brassinosteroid-biosynthesis mutants Hordeum vulgare
genotyping of original accessions 093AR and ert-ii.79 using 383 Amplified Fragment Length Polymorphism (AFLP) markers found high level of polymorphism (7.6%) throughout genomes, indicating independent mutagenic events Hordeum vulgare
excess unlabeled competitive probe could effectively inhibit biotin probe bound by OsBZR1 Oryza sativa
(VUP1, AT3G21710) OX down-regulated genes overlap with BR-regulated genes Arabidopsis thaliana
brassinosteroid receptor is first protein in the signaling network
uzu1.a allele is found in Northeast Asian short-culm cultivars and landraces such as 'Akashinriki' Hordeum vulgare
steric clashes may affect steroid binding and general positioning of brassinosteroid-binding site Hordeum vulgare
phenotypic characteristics of uzu1.b could be seen in all three genetic backgrounds Hordeum vulgare
Brassinosteroid responsive B-box zinc finger family protein (BBX20, BZS1, STH7, AT4G39070) (HORVU7Hr1G091180) transcript levels were reduced in transgenic compared to wild-type lines Hordeum vulgare
brassinolides promote preferential cell growth along the longitudinal axis Physcomitrella patens
alternatives to the uzu1.a allele of HvBRI1 represent potential genetic building blocks for breeding strategies Hordeum vulgare
uzu1.a mutant has short-awned spikes Hordeum vulgare
phenotypic screen of 160 cv Bowman near-isogenic lines identified sixteen lines with brassinosteroid phenotype Hordeum vulgare
ari-o.297 mutant carries nonsynonymous point mutation in HvBRI1 (T158C, Phe-53 to Ser) Hordeum vulgare
introduction of charged Lys-573 to hydrophobic active site is expected to prevent brassinosteroid binding Hordeum vulgare
barley uzu1.a mutant is known to have alterations in brassinosteroid signaling Hordeum vulgare
(ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) EMS SUPPRESSOR 1 (BES1, BZR2, AT1G19350) binds to corresponding regulatory sequences
BY-2 cells treated with 24-epibrassinolide (BL) Nicotiana tabacum
(PP2A, AT1G69960) protein phosphatase dephosphorylates (BZR1, AT1G75080) and (BES1, BZR2, AT1G19350) Arabidopsis thaliana
HDA703 overexpressing rice plants overexpression promotes mesocotyl elongation Oryza sativa
plant height is regulated by brassinosteroids
BRASSINOSTEROID INSENSITIVE1 (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) is receptor for brassinosteroids
(BSL1, AT4G03080) is positive regulator of growth and development controlled by BR signaling cascade
(ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) (LRR X subfamily member) interacts with SERK1II/ (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) (LRR II subfamily member)
ari.256 mutant carries mutation in HvBRI1 (A1733T) Hordeum vulgare
sequencing of HvBRI1 from brassinosteroid-insensitive mutant isolated among 950 M2 plants revealed novel HvBRI1 allele (G2171A substitution) Hordeum vulgare
cell elongation is regulated by brassinosteroids
GROWTH REGULATING FACTOR 6 (14-3-3lambda, AFT1, GRF6, AT5G10450) was not directly involved in brassinosteroid (BR) signaling Oryza sativa
activation-tagging approach identified (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) SUPPRESSOR 1 (BRS1, SCPL24, AT4G30610)
atbs2-D phenotype is unlikely to be caused by (ATDET2, DET2, DWF6, AT2G38050) overexpression Arabidopsis thaliana
(ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) is also involved in brassinosteroid (BR) responses Arabidopsis thaliana
miROE8 had leaf angle increased more efficiently than ZH10 when exogenous 24-eBL was applied Oryza sativa
leaf angle of BZR1R/miROE8 was increased compared with BZR1R or ZH10 Oryza sativa
Phytophthora infestans effector PiAVR2 activates brassinosteroid (BR) pathway Nicotiana benthamiana
(LRX2, AT1G62440) is regulated by BL treatment Arabidopsis thaliana
chemical or mutational blockage of ethylene signaling did not change enhanced BR responsiveness seen for fer-2 light-grown hypocotyls
FERONIA-mediated brassinosteroid signaling promotes hypocotyl elongation Arabidopsis thaliana
downstream components include GSK3-like kinase (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710)
(AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) is negative regulator of brassinolide signaling Arabidopsis thaliana
UVR8-BES1/ (BIM1, AT5G08130) interaction inhibits BR-responsive gene expression
BR-deficient mutant det2-1 produces fewer ovules and seeds Arabidopsis thaliana
exchange of nonpolar Val-282 to negatively charged Asp in uzu1.301 will result in formation of salt bridge between Asp-282 and Lys-302 Hordeum vulgare
plants moved from 26°C to 14°C resulted in already developed tillers remained short but new tillers grew taller Hordeum vulgare
exchanges of amino acid residues instead affect interactions with other proteins of the signaling cascade, such as CONSTITUTIVE DIFFERENTIAL GROWTH1 or BRASSINOSTEROID-SIGNALING KINASEs
OsDLT1 was up-regulated in miROEs Oryza sativa
OsMIR396d expression was decreased in BR-signal reduced OsBZR1 RNAi line (BZR1R) Oryza sativa
constitutive overexpression of VASCULAR-RELATED UNKNOWN PROTEIN1 (VUP1, AT3G21710) resembles brassinosteroid-deficient mutants Arabidopsis thaliana
Mutations in the three genes show almost identical visible phenotypes Hordeum vulgare
overexpression of AtPMEI5 caused strong phenotypes that could be suppressed when a brassinosteroid receptor was mutated in the overexpressor Arabidopsis thaliana
uzu1.a allele of HvBRI1 is highly temperature-sensitive Hordeum vulgare
steric clashes with neighboring residues are likely to occur in both cases Hordeum vulgare
novel HvBRI1 allele was named uzu1.c Hordeum vulgare
transcription factor OsBZR1 binds to CGTGT/CG element Oryza sativa
OsmiR396d was involved in BR signal regulated leaf angle development process Oryza sativa
brassinosteroid (BR) is perceived by BRI1-associated receptor kinase 1 Oryza sativa; Arabidopsis thaliana
(ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) is important positive regulator of brassinosteroid (BR) responses
ert-ii.79 mutation was identified earlier in uzu1 mutant 093AR (uzu1.b) Hordeum vulgare
clear brassinosteroid phenotypes in crosses and different genetic backgrounds strongly suggest brassinosteroid phenotypes are identifiable in mutant populations of most barley cultivars Hordeum vulgare
temperature-sensitive phenotype is not associated with brassinosteroid or HvBRI1 mutations in general Hordeum vulgare
BRASSINOSTEROID INSENSITIVE1 (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) -Associated Receptor Kinase (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) is involved in the perception of phytohormone brassinosteroid (BR)
BRASSINOSTEROID INSENSITIVE1 (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) increasing endosomal localization of enhances downstream response Arabidopsis thaliana
brassinosteroid signaling is largely unaffected by C-terminal tags on (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) or (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400)
ari-o.297 mutant was renamed uzu1.297 Hordeum vulgare
dephosphorylation of GSK3/SHAGGY-like Kinase (OsGSK2) releases suppression on LEAF AND TILLER ANGLE INCREASED CONTROLLER (OsLIC) Oryza sativa
OsMIR396d expression was up-regulated in BR-signal enhanced OsLIC antisense line (LIC-AS) Oryza sativa
(ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) is involved in perception of the plant hormone brassinosteroid
increased leaf angle and semidwarf phenotypes of miROE plants are similar to phenotypes of BR signal-enhanced rice plants Oryza sativa
function of OsBZR1 might be partially dependent on OsmiR396d Oryza sativa
Uzu1 gene is orthologous to BRASSINOSTEROID-INSENSITIVE1 (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) Hordeum vulgare; Arabidopsis thaliana
lamina inclination is often caused by proliferation or expansion of collar adaxial cells Oryza sativa
ARABIDOPSIS THALIANA BRASSINOSTEROID-INSENSITIVE2 inhibits MBW activity Arabidopsis thaliana
BR signaling mutants share round and dark green rosette leaves
BRASSINAZOLE RESISTANT 1 (BZR1, AT1G75080) binds to corresponding regulatory sequences
yeast two-hybrid screen coupled with reverse genetics identified (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430)
bri1-9 mutant is caused by ER retention of mutated BR receptor
P (NPC3, AT3G03520) :GUS shows enhanced GUS activity in response to BL treatment Arabidopsis thaliana
fer-2 etiolated seedlings are partially brassinosteroid insensitive with regard to promotion of hypocotyl elongation Arabidopsis thaliana
(BZR1, AT1G75080) and (BES1, BZR2, AT1G19350) act together to regulate expression of brassinosteroid-inducible genes Arabidopsis thaliana
unphosphorylated (BZR1, AT1G75080) and (BES1, BZR2, AT1G19350) in the nucleus regulate expression of BR-responsive genes
suppressed expression of (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) is consistent with altered brassinosteroid responses to light in (HY5, TED 5, AT5G11260) and (HYH, AT3G17609) mutants Arabidopsis thaliana
BRZ treatment represses HDA703 overexpressing rice mesocotyl elongation Oryza sativa
five near-isogenic lines with short-culm phenotypes lack unique combination of brassinosteroid features Hordeum vulgare
ARABIDOPSIS THALIANA BRASSINOSTEROID-INSENSITIVE2 phosphorylates (AtEGL3, ATMYC-2, EGL1, EGL3, AT1G63650) and AtGL3 Arabidopsis thaliana
activation-tagging approach identified BRI1-5 ENHANCED 1 (ATMIN7, BEN1, BIG5, MIN7, AT3G43300)
feronia knockout mutant has altered responsiveness to brassinosteroids Arabidopsis thaliana
FERONIA is required for brassinosteroid response in etiolated seedlings Arabidopsis thaliana
cross-phosphorylation between (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) and (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) is believed to be critical for activation of the receptor complex
(ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) protein level can be regulated by BR signal Arabidopsis
BR perception can activate BSKs Arabidopsis
overexpression of VASCULAR-RELATED UNKNOWN PROTEIN1 (VUP1, AT3G21710) represses expression of brassinosteroid-responsive genes Arabidopsis thaliana
Arabidopsis bak1-5 mutant is not impaired in BR signaling Arabidopsis thaliana
dephosphorylation of GSK3/SHAGGY-like Kinase (OsGSK2) releases suppression on DWARF AND LOW-TILLERING (OsDLT) Oryza sativa
uzu1.a mutant has unaltered stem diameter Hordeum vulgare
leaf lamina inclination assay was adopted to barley Hordeum vulgare
OsBZR1 bound promoter of OsMIR396d in vivo Oryza sativa
(ANAC072, ANAC72, AtRD26, RD26, AT4G27410) represses brassinosteroid signaling Arabidopsis thaliana
(ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) is able to interact with (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) Arabidopsis thaliana
(ATBS1, bHLH135, BS1, PRE3, TMO7, AT1G74500) may be (ATBS1, bHLH135, BS1, PRE3, TMO7, AT1G74500) (activation-tagged (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) suppressor 1) gene Arabidopsis thaliana
24-epibrassinolide (EBL) causes reduction in hypocotyl length Arabidopsis thaliana
bin2-1 mutant shows dramatic dwarf phenotype Arabidopsis
(BSU1, AT1G03445) may directly dephosphorylate conserved phosphorylation site pY200 of (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) Arabidopsis
PIF transcription factors are central nodes impinged upon by brassinosteroid (BR) signaling pathway
BR signaling is transduced through dimerization
brassinosteroids (BRs) modulate agronomic traits Oryza sativa
(BES1, BZR2, AT1G19350) acts as TF that targets downstream gene promoters by binding to BRRE (CGTGT/CG) and E-box (CACGTG/CACTTG) elements Arabidopsis thaliana
Brassinosteroids (BRs) perception initiates phosphorylation-mediated signaling
brassinosteroids (BRs) directly bind extracellular leucine-rich repeat domain of (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400)
(BZR1, AT1G75080) inhibits expression of GATA
(AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) plays negative regulatory role in BR signaling
(AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) interaction with extracellular region of (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) enhances (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) endocytosis
OsBZR1 represses Ghd7 expression Oryza sativa
other phytohormones cannot restore dwarf phenotype to wild-type
(BZR1, AT1G75080) inhibits expression of (BBX20, BZS1, STH7, AT4G39070)
(HY5, TED 5, AT5G11260) (HYH, AT3G17609) mutants show altered brassinosteroid responses to light Arabidopsis thaliana
(BES1, BZR2, AT1G19350) is basic helix–loop–helix protein family transcription factor Arabidopsis thaliana
24-Epibrassinolide (EBL) application increases nuclear-localised signal of BES1-GFP Arabidopsis thaliana
fer-2 light-grown seedlings have increased BR response Arabidopsis thaliana
phosphorylation status of OsBZR1 determines protein stability of OsBZR1 Oryza sativa
suppressor screens for mutations resistant to BR biosynthesis inhibitor identified (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430)
(BZR1, AT1G75080) phosphorylation results in (BZR1, AT1G75080) degradation Arabidopsis thaliana
(BZR1, AT1G75080) translocates to nucleus Arabidopsis thaliana
(ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) mainly phosphorylates (BES1, BZR2, AT1G19350) (BZR1, AT1G75080) Arabidopsis
inactivation of (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) results in activation of downstream transcription factors Arabidopsis
brassinosteroids (BRs) are important for cell elongation
BRASSINAZOLE RESISTANT 1 (BZR1, AT1G75080) is BR signaling transcription factor Oryza sativa
HDA703 is involved in BR signaling Oryza sativa
HDA703 directly interacts with OsBZR1 Oryza sativa
(BZR1, AT1G75080) is basic helix–loop–helix protein family transcription factor Arabidopsis thaliana
(BES1, BZR2, AT1G19350) protein abundance on promoter regulatory elements of XTH19 and XTH23 detected by ChIP-qPCR analysis Arabidopsis thaliana
bri1-5 mutant is weak BR receptor mutant
(ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) signaling removes inhibition of (BZR1, AT1G75080) Arabidopsis thaliana
(ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) and (BKI1, AT5G42750) interaction is inhibitory to BR signaling
(AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) interaction with extracellular region of (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) suppresses BR signaling
OsBZR1 strictly controls HDA703 expression Oryza sativa
low levels of exogenous brassinosteroids reverses phenotype of brassinosteroid-deficient dwarf mutants
etiolated fer-2 seedlings are partially BR-insensitive Arabidopsis thaliana
non-phosphorylated (BES1, BZR2, AT1G19350) can trigger downstream brassinosteroid-related transcription network Arabidopsis thaliana
brassinosteroids (BRs) do not affect ability of BES1 to bind (AtBRC1, ATTCP18, BRC1, TCP18, AT3G18550) promoter Arabidopsis thaliana
brassinosteroids (BRs) do not modulate BRANCHED1 (AtBRC1, ATTCP18, BRC1, TCP18, AT3G18550) expression Arabidopsis thaliana
lower levels of EBL (10 nM) stimulate hypocotyl shortening Arabidopsis thaliana
(ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) kinase domain identifies substrate via (ALNS, TTL, AT5G58220)
brassinosteroid-regulated phosphorylation status of OsBZR1 determines transduction of brassinosteroid signals by OsBZR1 Oryza sativa
(ATXTH19, XTH19, AT4G30290) and (XTH23, XTR6, AT4G25810) were probably downstream target genes of (BES1, BZR2, AT1G19350) Arabidopsis thaliana
(ATSERK1, SERK1, AT1G71830) and (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) ( (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) ASSOCIATED KINASE 1 [ ]) are co-receptors for (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400)
epidermal expression of (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) (BR receptor) in mutants fully rescues leaf length and width
brassinolide (BL) was studied for effects on phenotype of npc3-1, npc3-2, npc4-1, and npc4-2 knockouts Arabidopsis thaliana
(ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) heterodimerizes with (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) Arabidopsis thaliana
brassinosteroids at high levels lead to inhibition of hypocotyl elongation Arabidopsis thaliana
(BKI1, AT5G42750) overexpression causes bri1-like dwarf phenotype
myristoylated (BKI1, AT5G42750) leads to further enhanced dwarf plant phenotype
BRASSINAZOLE-RESISTANT 1 (BZR1, AT1G75080) directly targets APETALA2 (AP2, AtAP2, FL1, FLO2, AT4G36920) Arabidopsis thaliana
forward genetic screens for BR-insensitive dwarf mutants identified loss-of-function alleles of (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400)
bri1-301 mutant is weakest known (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) mutant
BL treatment enhances GUS activity in leaf margins and tips of developing young leaves Arabidopsis thaliana
brassinosteroid signaling mainly controls phosphorylation status of BRI1-EMS SUPPRESSOR1 (BES1, BZR2, AT1G19350) Arabidopsis thaliana
(ATXTH19, XTH19, AT4G30290) and (XTH23, XTR6, AT4G25810) are downstream of BR-responsive genes Arabidopsis thaliana
(BRL3, AT3G13380) encodes brassinosteroid receptor
(ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) levels are regulated in Arabidopsis Arabidopsis thaliana
rice SVP-group genes act as negative regulators of BR responses Oryza sativa
fer-2 hypocotyls treated with EBL across increasing concentrations are significantly less responsive than Col-0 wt hypocotyls treated with EBL across increasing concentrations Arabidopsis thaliana
10 nM 24-epibrassinolide (EBL) treatment causes reduction in hypocotyl length independent of increased ethylene production Arabidopsis thaliana
(ATOFP3, OFP3, AT5G58360) overexpression enhanced phenotypes of BR-deficient mutants Oryza sativa
OsD2 and OsD11 expression is increased in hda703 mutant Oryza sativa
bri1-5 mutant has ER retention of mutated BR receptor
brassinosteroid-dependent increases in ethylene production and magnitude of ethylene response results in hypocotyl shortening in etiolated seedlings following treatment with near saturating concentrations of brassinosteroids
brassinosteroid receptor BRASSENOSTERIOD INSENSITIVE1 (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) localizes to distinct membrane microdomains
HDA703 interacts with OsBZR1 Oryza sativa
inhibition of BRASSINOSTEROID INSENSITIVE 2 (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) results in dephosphorylation of BRASSINAZOLE RESISTANT 1 (BZR1, AT1G75080)
Micro-Tom cultivar is brassinosteroid-deficient Solanum lycopersicum
BR perception can activate (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) Arabidopsis
(CBB3, CPD, CYP90, CYP90A, CYP90A1, DWF3, AT5G05690) mutant feeding with BRs restores dwarf phenotype to wild-type
BR receptor (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) mediates brassinosteroid regulation of (BES1, BZR2, AT1G19350) (BZR1, AT1G75080) family Arabidopsis thaliana
(ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) phosphorylates (ARF11, ARF19, IAA22, AT1G19220) Arabidopsis thaliana
yeast two-hybrid screen coupled with reverse genetics identified (BES1, BZR2, AT1G19350)
atbs-D mutants will be excellent tools in studying BR signaling process Arabidopsis thaliana
brassinosteroid signaling is required for cell expansion
eBL treatment largely restores hypocotyl elongation in Col-0 wt hypocotyls Arabidopsis thaliana
bin2-1 mutant protein possesses significantly higher kinase activity than wild-type (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) protein Arabidopsis
(AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) may be involved in regulation of photomorphogenesis through modulating BR signaling by interacting with BRASSINOSTEROID INSENSITIVE 1-ASSOCIATED KINASE 1 (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) Arabidopsis thaliana
BRASSINAZOLE-RESISTANT 1 (BZR1, AT1G75080) directly targets AINTEGUMENTA (ANT) Arabidopsis thaliana
(BES1, BZR2, AT1G19350) and (BZR1, AT1G75080) play a redundant role in brassinosteroid signaling Arabidopsis thaliana
(ATXTH19, XTH19, AT4G30290) and (XTH23, XTR6, AT4G25810) play an important role in brassinosteroid-induced gene expression Arabidopsis thaliana
Gly989Ile mutation in bri1-301 completely inhibits in vitro kinase activity of (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) fusion kinase
dephosphorylation of conserved phosphorylation site pY200 of (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) inhibits kinase activity of (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) Arabidopsis
(AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) interaction with BRASSINOSTEROID INSENSITIVE 1-ASSOCIATED KINASE 1 (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) suppresses brassinosteroid signaling Arabidopsis thaliana
(ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) SUBSTRATE KINASES (BSKs) and CONSTITUTIVE DIFFERENTIAL GROWTH 1 (CDG1, AT3G26940) phosphorylate (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) SUPPRESSOR 1 (BSU1, AT1G03445)
fer-2 hypocotyls are significantly less responsive to complete range of EBL concentrations Arabidopsis thaliana
brassinosteroids promote cell expansion Arabidopsis thaliana
(ALNS, TTL, AT5G58220) strongly interacts with kinase-active (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400)
(ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) (Brassinolide Insensitive 2) represses through phosphorylation and degradation (AtPIF4, PIF4, SRL2, AT2G43010)
(AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) plays negative regulatory role in cell elongation
brassinosteroid (BR) signaling components upstream of (BES1, BZR2, AT1G19350) have no effect on (AtBRC1, ATTCP18, BRC1, TCP18, AT3G18550) expression Arabidopsis thaliana
EBR treatment resulted in reduced GFP-RGA levels Arabidopsis thaliana
HDA703 overexpression in d61-2 background show shorter mesocotyls Oryza sativa
(ATHD1, ATHDA19, HD1, HDA1, HDA19, HDAC19, RPD3A, AT4G38130) associates with (BZR1, AT1G75080) Arabidopsis thaliana
Leucine-Rich Repeat Receptor-Like Kinases (LRR–RLKs) belong to BRASSINOSTEROID INSENSITIVE 1 (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) family
steroid-related signals may have been functional early in evolution of land plants
CYP90D is regulated by BL treatment Arabidopsis thaliana
Phosphorylated (BSK1, AT4G35230) and (BSU1, AT1G03445) interaction promotes dephosphorylation of a conserved phosphor-tyrosine residue in (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710)
BSKs interact with (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400)
(ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) negatively controls BR signaling Arabidopsis
(BSU1, AT1G03445) overexpression cannot rescue dwarf phenotype of bin2-1 Arabidopsis
uzu1.a mutant has more erect plant architecture Hordeum vulgare
substitution of Arg-710 to Lys causes mild brassinosteroid phenotype Hordeum vulgare
dephosphorylation of GSK3/SHAGGY-like Kinase (OsGSK2) releases suppression on REDUCED LEAF ANGLE1 Oryza sativa
leaf angles in progenies of miROE8/d61 were significantly increased compared with parents Oryza sativa
(ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) loses kinase activity fails to phosphorylate CYC U4;1
BL binding to (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) induces fixation of the island domain
genetic studies and yeast one/two-hybrid screens coupled with microarray and chromatin immunoprecipitation experiments revealed new roles of key regulatory transcription factors Arabidopsis thaliana; Oryza sativa
activation-tagging approach identified (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430)
(BZR1, AT1G75080) and (BES1, BZR2, AT1G19350) binding to BR-responsive gene promoters regulates expression of BR-responsive genes
dephosphorylation of (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) may lead to inactivation of (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710)
brassinosteroids (BRs) play essential roles in plant growth and development
HDA703 is probably a positive regulator of BR signaling Oryza sativa
boron (B) deficiency reduces nuclear-localised signal of BES1-GFP Arabidopsis thaliana
softening in epidermis allows inner tissues to expand
Compound 5141662 has reduced effect on bzr1-1D mutant plants
wild-type plants grown on 40 μM BRP in the dark for 3 d then transferred to MS medium have longer hypocotyls than wild-type plants grown on 1 μM BRZ in the dark for 3 d then transferred to MS medium Arabidopsis thaliana
BRASSINOSTEROID-INSENSITIVE 2 (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) is inhibited in response to BR perception at the cell surface Arabidopsis thaliana
(ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) phosphorylation of (BES1, BZR2, AT1G19350) and (BZR1, AT1G75080) promotes protein degradation of (BES1, BZR2, AT1G19350) and (BZR1, AT1G75080) Arabidopsis thaliana
(ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) activation may lead to phosphorylation of BSKs
BR-perceptional mutants display dramatically dwarfed phenotypes Arabidopsis thaliana
bri1-9 mutant is weak allele of (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400)
BRASSINOSTEROID INSENSITIVE 1 (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) forms complex with (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430)
(ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) directly associates with (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) Kinase Inhibitor (BKI1, AT5G42750)
(BSU1, AT1G03445) overexpression can partially suppress dwarf phenotype of heterozygous bin2-1 Arabidopsis
BRs can restore dwarf phenotype to wild-type
(ATOFP3, OFP3, AT5G58360) (OVATE FAMILY PROTEIN 3) interacts with DLT Oryza sativa
inhibitors of signaling components are used for chemical biology approaches to understand brassinosteroid mode of action
LOB regulates BR catabolic gene (BAS1, CYP72B1, CYP734A1, AT2G26710)
Arabidopsis mutants with altered brassinosteroid signalling had changes in growth orientation and cell shape in RAM Arabidopsis thaliana
genetic and biochemical studies identified two key transcription factors and interacting partners
BRASSINAZOLE RESISTANT1 (BZR1, AT1G75080) is positive regulator of BR signaling
EBR treatment after Brz treatment completely blocks Brz-induced expression of (ATBR6OX, BR6OX, BR6OX1, CYP85A1, AT5G38970) Cucumis sativus
suppressor screens for mutations that revert the dwarf phenotype identified (BES1, BZR2, AT1G19350)
mutant with profound increase in ethylene signaling displays loss of key control mechanism required for modulation of response to brassinosteroids Arabidopsis thaliana
FERONIA is required for normal promotion of brassinosteroid response in dark-grown hypocotyls Arabidopsis thaliana
(ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) phosphorylates (BZR1, AT1G75080)
bri1-EMS SUPPRESSOR1 (BES1, BZR2, AT1G19350) was originally identified as integral component of brassinosteroid signaling pathway Arabidopsis thaliana
hda703 mutant show typical BR loss-of-function phenotype Oryza sativa
HDA703 and OsBZR1 interaction and transcriptional regulation could be underlying mechanisms contributing to HDA703-mediated roles in rice BR signaling Oryza sativa
(BES1, BZR2, AT1G19350) targets (ATXTH19, XTH19, AT4G30290) and (XTH23, XTR6, AT4G25810) in vivo Arabidopsis thaliana
application of brassinosteroid inhibitors decreased leaf angles (LAs) in rice Oryza sativa
OsMED25 interaction with OsBZR1 regulate brassinosteroid (BR) signaling Oryza sativa
(ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) KINASE INHIBITOR 1 (BKI1, AT5G42750) inhibits interaction between kinase domains of (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) and SERK
brassinosteroid has perception and signal transduction mechanisms
Arabidopsis root allowed detailed characterization of BR perception at the cell membrane Arabidopsis thaliana
brassinosteroids (BRs) are proposed to promote cell growth in the root meristem by loosening cell walls in the epidermis and endodermis
brassinosteroids (BRs) are perceived at plasma membrane
BRASSINOSTEROID INSENSITIVE 1 (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) engages SERK3 as coreceptor for perceiving brassinosteroids (BRs)
brassinosteroid analogs provide knowledge on recognition of the hormone and signaling initiation
(ANAC054, ATNAC1, CUC1, AT3G15170) is alleviated from (BZR1, AT1G75080) repression
(BRL2, VH1, AT2G01950) does not behave as functional BR receptor
understanding vascular and cell-specific BRL receptors will help shed light on membrane signaling and cell communication in plants
genes related to BRs are expressed in all layers
brassinosteroids regulate cell division, elongation, differentiation, and reproductive development
brassinosteroids (BRs) play crucial roles in regulation of lamina inclination
Arabidopsis thaliana seedlings treated with 24-epi-brassinolide (BL) Arabidopsis thaliana
mutations negatively affecting FERONIA function lead to reduced BR response Arabidopsis thaliana
eBL treatment induces increased cotyledon size Arabidopsis thaliana
brassinosteroids (BRs) control ovule number by effects of BZR1 on expression of ovule development genes Arabidopsis thaliana
rescue of leaf length and width by epidermal (CBB3, CPD, CYP90, CYP90A, CYP90A1, DWF3, AT5G05690) or (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) expression affects not only epidermal cell size but also mesophyll cells
phosphorylated (BSU1, AT1G03445) can inactivate BRASSINOSTEROID INSENSITIVE 2 (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710)
loss of function of rice OsBRI1 displayed erect leaves Oryza sativa
prevention of (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) phosphorylation of (BZR1, AT1G75080) (BES1, BZR2, AT1G19350) activates BRASSINAZOLE RESISTANT 1 (BZR1, AT1G75080) and BRI1-EMS-SUPPRESSOR 1 (BES1, BZR2, AT1G19350)
BR signaling is relatively well-understood signaling mechanisms mediated by brassinosteroids plants
(ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) is regulated by proteasome-mediated protein degradation mechanism Arabidopsis thaliana
one target of BRP is involved in BR action
many major components of BR signalling pathway have been identified BR signaling pathway
kinase domains of (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) and SERK adopt correct orientation to remove inhibition by (BKI1, AT5G42750)
brassinosteroids are essential for plant development and growth
BRL receptor signaling operates under specific spatiotemporal constraints
(AtIAA17, AXR3, IAA17, AT1G04250) mutant shows significant resistance to brassinosteroids Arabidopsis thaliana
brassinosteroids regulate growth in dark-grown hypocotyls
brassinosteroid (BR) signaling regulates phosphorylation status of OsBZR1 Oryza sativa
OsBZR1 and (BES1, BZR2, AT1G19350) differentially regulate shoot branching based on specific integration of brassinosteroid signals Oryza sativa; Arabidopsis thaliana
salt treatment and IAA treatment induction effects reduced significantly in (AtDWF4, CLM, CYP90B1, DWF4, PSC1, SAV1, SNP2, AT3G50660) mutant and BES1-RNAi transgenic plant roots Arabidopsis thaliana
(BES1, BZR2, AT1G19350) is homologue of (BZR1, AT1G75080) Arabidopsis thaliana
activation of (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) and its co-receptor (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) results in inhibition of (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) Arabidopsis thaliana
bzr1-1D mutant plants used to rescue wild-type plants not rescued by BR application Arabidopsis thaliana
reduction in BR action can be suppressed by activating the BR pathway through stabilization of (BES1, BZR2, AT1G19350) by the -D mutation Arabidopsis thaliana
steady-state level of (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) is specifically regulated by plant steroid hormone Arabidopsis thaliana
BSKs may inactivate GSK3-like protein kinase (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710)
(ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) is negative regulator
WRKY DNA-BINDING PROTEIN 70 (ATWRKY70, WRKY70, AT3G56400) is involved in brassinosteroid-regulated growth Arabidopsis thaliana
(ERF115, AT5G07310) is activated by downstream signaling of brassinosteroids (BL) Arabidopsis thaliana
(ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) phosphorylation of (BES1, BZR2, AT1G19350) and (BZR1, AT1G75080) blocks transduction of plant steroid signal into nucleus Arabidopsis thaliana
rice 14-3-3 proteins directly regulate OsBZR1 function in BR signalling Oryza sativa
wild-type plants show greater sensitivity to BRP Arabidopsis thaliana
brassinosteroids (BRs) are critical for plant growth and development
BRP causes inhibition of hypocotyl length Arabidopsis thaliana
(ELF6, AT5G04240) and (EIN6, JMJ12, REF6, AT3G48430) are recruited by (BES1, BZR2, AT1G19350) Arabidopsis thaliana
BR-deficient mutants display dramatically dwarfed phenotypes Arabidopsis thaliana
brassinosteroids (BRs) largely rely on transcription factors to regulate plant physiological and developmental processes
additional transcription factors and other nuclear proteins are involved in regulating nuclear activities of BR signaling Arabidopsis thaliana; Oryza sativa
lithium is specific inhibitor of GSK3 kinase
BR-activated transcriptional factor (BES1, BZR2, AT1G19350) can bind to promoter regions of nine CESA genes Arabidopsis thaliana
naturally occurring self-compatible long homostyle Turnera species carry inactivating mutations of BAHD Turnera
bzr1-1D bes1-D double mutant were resistant to BRZ (brassinazole) in hypocotyl length and apical hook formation Arabidopsis thaliana
(ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) or (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) was not able to interact directly with or phosphorylate (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) Arabidopsis thaliana
(ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) receptor mediates BL-induced (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) depletion Arabidopsis thaliana
Mutation of 14-3-3-binding site in OsBZR1 protein resulted in increased nuclear distribution of OsBZR1 Oryza sativa
brassinopride (BRP) treatment can be reversed by co-treatment with brassinolide Arabidopsis thaliana
(AtRAV1, EDF4, RAV1, AT1G13260) is down-regulated by brassinosteroid Arabidopsis thaliana
TRX-y transcript levels shows no significant change in dim mutant plants compared with CR plants Solanum lycopersicum
ethylene effect on apical hook is consequence of downstream BR signaling Arabidopsis thaliana
BR action on the hypocotyl is not mediated by ethylene Arabidopsis thaliana
gBIN2:GFP transgenic seedlings were used in immuno-kinase assay
proper BR synthesis and signaling appear necessary for maintaining a straight hypocotyl in the presence of ethylene Arabidopsis thaliana
BL-induced (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) depletion requires functional BR receptor Arabidopsis thaliana
(CDG1, AT3G26940) is involved in brassinosteroid-mediated regulation of growth Arabidopsis thaliana
Mutation of 14-3-3-binding site in OsBZR1 protein abolished interaction between OsBZR1 and 14-3-3 proteins Oryza sativa
auxin potentially increases plant sensitivity to brassinosteroids
brassinopride (BRP) inhibits BR action
bri1-116;bzr1-1D double mutant has no BR receptor for perception of BR gradient Arabidopsis thaliana
plant growth hormones exogenous application revealed (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) depletion is specifically induced by BR Arabidopsis thaliana
(BRL1, AT1G55610) and (BRL3, AT3G13380) function as BR receptors
brassinosteroid (BR) signaling increases nuclear accumulation of (BES1, BZR2, AT1G19350) Arabidopsis thaliana
small molecules will continue to provide opportunities for unraveling the dynamic and highly interconnected signaling
BRI1-ASSOCIATED RECEPTOR KINASE (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) and BOTRYTIS-INDUCED KINASE1 (BIK1, AT2G39660) are shared by brassinosteroid (BR) signal mediated by BRASSINOSTEROID INSENSITIVE 1 (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400)
(BRL1, AT1G55610) behaves as functional BR receptor
understanding vascular and cell-specific BRL receptors opens up novel possibilities to improve stress adaptation without penalizing growth
CPD::GUS transgenic line contains BR-repressed (CBB3, CPD, CYP90, CYP90A, CYP90A1, DWF3, AT5G05690) promoter driving expression of β-glucuronidase Arabidopsis thaliana
brassinopride (BRP) activates expression of CPD::GUS reporter gene Arabidopsis thaliana
BRP analog a6 seems to have reduced effect on BR action
BL treatment causes significant reduction in (BZR1, AT1G75080) phosphorylation activity
(AtRAV1, EDF4, RAV1, AT1G13260) is down-regulated by brassinosteroids Arabidopsis thaliana
(ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) kinase can phosphorylate and inhibit class of plant-specific transcription factors, (BES1, BZR2, AT1G19350) (BZR1, AT1G75080)
BR-treated S-morph flowers develop long styles with L-morph like incompatibility type Primula
BRP inhibits BR action
(ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) is Arabidopsis GSK3 kinase Arabidopsis thaliana
OsMADS22 / OsMADS47 / OsMADS55 triple RNAi plants manifest dramatic brassinosteroid responses with regard to senescence Oryza sativa
(BZR1, AT1G75080) (BES1, BZR2, AT1G19350) undergoes degradation or nuclear exclusion of phosphorylated (BZR1, AT1G75080) in the absence of BR
brassinolide-induced heterodimerization of (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) and SERK brings into close proximity transmembrane helices
(ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) inactivation prevents (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) phosphorylation of transcription factors
structural data on the brassinosteroid receptor complex provides insights into recognition of the hormone and signaling initiation
wild-type plants grown on medium containing chemicals and BR rescued by BR Arabidopsis thaliana
gbin2-1:GFP transgenic line is BL-insensitive Arabidopsis thaliana
(AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) is involved in BR signaling
14-3-3 proteins mediate brassinosteroid (BR) signal transduction Arabidopsis thaliana
BR signal induces dissociation of negative regulator (BKI1, AT5G42750) from the plasma membrane
Somatic Embryogenesis Receptor Kinase 3 (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) BRI1-associated Kinase 1 physically interacts with BR insensitive 1 (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400)
dephosphorylated (BES1, BZR2, AT1G19350) turns on BR-responsive transcription
(ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) phosphorylation of CYC U4;1 under low BR concentration generates erect leaf leaves
low nitrogen (N) upregulates expression of BRASSINOSTEROID INSENSITIVE 1-ASSOCIATED RECEPTOR KINASE 1 Arabidopsis thaliana
chloroplastic TRX-f plays a role in EBR-induced increase in CO2 assimilation Solanum lycopersicum
polar auxin transport works further downstream to brassinosteroid (BR) signalling Arabidopsis thaliana
S-locus gene jointly controls style length and female incompatibility Primula; Turnera subulata
(BES1, BZR2, AT1G19350) ( ) were identified as dominant gain-of-function mutants resistant to brassinazole
BRs enable epidermis to plastically expand (grow) under the tension imposed by inner tissues
brassinosteroid signaling-triggered transcription may regulate callose accumulation in response to high brassinosteroid levels Arabidopsis thaliana
auxin application influences brassinosteroid sensitivity
brassinosteroids (BRs) are involved in plant growth and development
bzr1-1D mutant plants is resistant to effects of Compound 5141662
BL treatment had little effect on gbin2-1:GFP seedlings Arabidopsis thaliana
cyp734a50 mutants develop long styles with L-morph like incompatibility type Primula
(ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) has established brassinolide (BL)-dependent role in development
(OPS, AT3G09070) overexpression rescues sterile phenotype of bri1-116 and bin2-1D Arabidopsis thaliana
hypermorphic bzr1-1D mutation suppressed elongation defect of (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) Arabidopsis thaliana
restricted (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) expression in outer tissue layers could partially rescue growth defects of (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) mutants Arabidopsis thaliana
(UBC13A, UBC35, AT1G78870) (AtUBC36, UBC13B, UBC36, AT1G16890) double mutant shows enhanced induction of BR-induced (BAS1, CYP72B1, CYP734A1, AT2G26710) gene Arabidopsis thaliana
signaling cascade involves de-phosphorylation and nuclear translocation of (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) EMS-SUPRESSOR 1 (BES1, BZR2, AT1G19350)
longer coleoptiles, curly roots, erect leaves and smaller seeds phenotypes indicate that BRs may be involved in xiao phenotype Oryza sativa
0.01 μm epi-BL treatment caused root curling to be just visible in wild-type plants Oryza sativa
OsMADS55 RNAi plants display weak brassinosteroid responses in lamina joint Oryza sativa
(BSK1, AT4G35230) serves as essential component of BRI1-BAK1 receptor complex in BR signaling
(ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) (BR Insensitive 2) is inactivated by (BSU1, AT1G03445) ( (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) SUPPRESSOR 1) phosphatase Arabidopsis thaliana
ops-2 mutant displays transcript levels of SAURAC1 and DWF4 similar to wild-type (WT) plants Arabidopsis thaliana
(OPS, AT3G09070) overexpression suppresses dwarf seedling phenotype of bri1-116 Arabidopsis thaliana
OPS-GFP presence causes mCherry-BIN2 depletion from nuclei Nicotiana benthamiana
BRI1-LIKE 1 (BRL1, AT1G55610) is expressed in growing plant tissues Arabidopsis thaliana
paracrine, mobile signal can substitute for absence of brassinosteroid perception in other tissues in the bri 3- RESCUED scenario
data cannot exclude that signal is a composite of various non-canonical (and canonical) brassinosteroid signaling outputs
CLASP modulates BRI1-mediated signaling Arabidopsis thaliana
brassinosteroids (BRs) modulate seed development
bzr1-D mutant has estimated parameters δ bzb = 0.3 Arabidopsis thaliana
parameter θ is inversely scaled with (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) levels
change in electrophoretic mobility of MpBES1 occurs upon treatments with BL or LiCl Arabidopsis thaliana
dephosphorylated (active) (BES1, BZR2, AT1G19350) form was detected at higher levels in roc1-1D mutant Arabidopsis thaliana
eight genes have expression levels negatively related to partially dephosphorylated form of (BES1, BZR2, AT1G19350) Arabidopsis thaliana
roc1-1D, roc1-2 and roc1-3 mutants have increased sensitivity to exogenous 24-epiBL and to brassinazole under blue light but not in the dark Arabidopsis thaliana
brassinosteroids (BRs) play prominent roles in gene expression
(ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) localizes to nucleus and cytoplasm
(THE1, AT5G54380) is down-regulated in bri1-5 mutant Arabidopsis thaliana
(HERK1, AT3G46290) is up-regulated in bes1-D mutant Arabidopsis thaliana
(BEE1, AT1G18400) (BEE2, AT4G36540) and (BEE3, AT1G73830) are functionally redundant positive regulators of BR signalling
binding of BR to its receptor (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) leads to activation of (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) and its co-receptor (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) Arabidopsis thaliana
inhibition of BR action causes increased expression of BR-repressed genes
bzr1-1D bes1-D double mutant were resistant to BRZ (brassinazole) Arabidopsis thaliana
gain-of-function (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) mutations or overexpression of wild-type gene result in morphological phenotype resembling BR-deficient or BR-signaling mutants Arabidopsis thaliana
(BES1, BZR2, AT1G19350) and (ELF6, AT5G04240) (EIN6, JMJ12, REF6, AT3G48430) regulates target gene expression Arabidopsis thaliana
DWARF4 (AtDWF4, CLM, CYP90B1, DWF4, PSC1, SAV1, SNP2, AT3G50660) is brassinosteroid (BR)-downregulated gene Arabidopsis thaliana
BRs-deficient dim plants show decreased TRX-x transcripts Solanum lycopersicum
inhibition of a full (ATRALF1, RALF1, RALFL1, AT1G02900) response in (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) plants treated with His and brassinolide (BL) could mean that brassinolide is perhaps inhibiting (ATRALF1, RALF1, RALFL1, AT1G02900) through one of the other brassinolide receptors Arabidopsis thaliana
overexpression of (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) is able to suppress weak (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) allele, -5 Arabidopsis thaliana
24-epibrassinolide (BR) exerted root directional defects at very low concentration (10nM) Arabidopsis thaliana
bim123 hypocotyls are hypersensitive to brassinosteroids (BRs) Arabidopsis thaliana
OsMADS22 / OsMADS55 double RNAi lines show notably reduced stem elongation Oryza sativa
(BZR1, AT1G75080) (BES1, BZR2, AT1G19350) undergoes nuclear accumulation of dephosphorylated (BZR1, AT1G75080) in the presence of BR
(AtMYB103, ATMYB80, MS188, MYB103, MYB80, AT5G56110) is involved in brassinosteroids Arabidopsis thaliana
brassinosteroid (BR) signaling requires functional BR receptor Arabidopsis thaliana
BR signal can activate preformed homodimer of (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400)
brassinosteroids (BRs) activate kinase function of (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) (BRASSINOSTEROID INSENSITIVE 1)
(ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) (BR-insensitive 2) controls phosphorylation states of (BES1, BZR2, AT1G19350) ( (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) EMS Suppressor 1)
brassinosteroids (BRs) are perceived by receptor-like kinase (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400)
interaction of (ATSERK4, BAK7, BKK1, SERK4, AT2G13790) and (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) was greatly enhanced by exogenously applied BL Arabidopsis thaliana
depletion of endogenous BRs by treatment with brassinazole (BRZ) showed basal levels of threonine phosphorylation on both (ATSERK4, BAK7, BKK1, SERK4, AT2G13790) and (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) Arabidopsis thaliana
(ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) and (ATSERK4, BAK7, BKK1, SERK4, AT2G13790) are not only involved in a BRI1-mediated pathway Arabidopsis thaliana
BR signaling in the epidermis is sufficient for promoting root growth
CLASP is targeted by brassinosteroid pathway Arabidopsis thaliana
BR signaling regulates CLASP expression Arabidopsis thaliana
(BZR1, AT1G75080) protein accumulation in nucleus occurs during BR signaling Arabidopsis thaliana
brassinazole treatment affects seedling hypocotyl length Arabidopsis thaliana
AtBES1 is orthologous to AtBZR1 Arabidopsis thaliana
High nuclear (BES1, BZR2, AT1G19350) signal reflects high BR signaling intensity Arabidopsis thaliana
(UBC13A, UBC35, AT1G78870) (AtUBC36, UBC13B, UBC36, AT1G16890) double mutant shows increased transcriptional inhibition of BR-repressed (AtDWF4, CLM, CYP90B1, DWF4, PSC1, SAV1, SNP2, AT3G50660) gene Arabidopsis thaliana
effect of (ATRALF23, RALF23, AT3G16570) on BR signaling may involve BRI1-like receptors
(FER, AT3G51550) regulates BRI1-BAK1 complex formation and signaling
loss of function of XIAO tissue-specifically enhances BR response by regulating transcription of OsMDP1, OsLIC and BU1 Oryza sativa
Arabidopsis thaliana SOMATIC EMBRYOGENESIS RECEPTOR KINASE 1 and Arabidopsis thaliana SOMATIC EMBRYOGENESIS RECEPTOR KINASE 2 ( (ATSERK1, SERK1, AT1G71830) and (ATSERK2, SERK2, AT1G34210) ) play important roles in brassinosteroid (BR)-dependent signalling pathways Arabidopsis thaliana
OsMADS55 is involved in negative regulation of brassinosteroid responses Oryza sativa
brassinosteroids (BRs) play prominent roles in photosynthesis
phosphorylated (BES1, BZR2, AT1G19350) and 14-3-3 protein complex is exported to cytoplasm
modified leaf angle via the brassinosteroid pathway is often associated with pleiotropic effects on plant height
(BES1, BZR2, AT1G19350) is substrate of (AtUBP12, UBP12, AT5G06600) /13 Arabidopsis thaliana
SlBRI1-Flag(T1054A) failed to rescue cu3-abs1 mutant and enhanced dwarfism and altered leaf phenotype in dominant negative effect Solanum lycopersicum
dwarf plants phenotype in sdg725 mutant is similar to phenotypes in mutants of BR-relative genes Oryza sativa
mutations that impair the BR phosphorelay cascade did not much affect BR-dependent expression of INDOLE-3-ACETIC ACID-INDUCIBLE1 (AXR5, IAA1, AT4G14560) and PHYTOCHROME B ACTIVATION-TAGGED SUPPRESSOR1 (BAS1, CYP72B1, CYP734A1, AT2G26710) Arabidopsis thaliana
(UGT73C6, AT2G36790) is preferentially regulated by (ATHSFA2, HSFA2, AT2G26150) Arabidopsis thaliana
TRX-m2 transcript levels reduced by 30-40% in dim mutant plants compared with CR plants Solanum lycopersicum
TRX-x transcript levels reduced by 30-40% in dim mutant plants compared with CR plants Solanum lycopersicum
DWARF4 (AtDWF4, CLM, CYP90B1, DWF4, PSC1, SAV1, SNP2, AT3G50660) is regulated by (BES1, BZR2, AT1G19350) (BRI1-EMS-SUPPRESSOR 1) and (BZR1, AT1G75080) (BRASSINAZOLE-RESISTANT 1) Arabidopsis thaliana
constitutive brassinosteroid (BR) signaling in OPS-OE can be consequence of increased brassinosteroid (BR) biosynthesis Arabidopsis thaliana
brassinazole (BRZ) treatment reduces hypocotyl length in wild-type (WT) plants in darkness Arabidopsis thaliana
OPS-OE plants are almost insensitive to brassinazole (BRZ) treatment Arabidopsis thaliana
brassinosteroids (BRs) binding causes recruitment of (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) (BRI1-associated kinase 1)
loss of (FER, AT3G51550) leads to increase in BR signaling Arabidopsis thaliana
gain-of-function mutations at (BZR1, AT1G75080) abolished roc1-1D and/or roc1-2 phenotypes Arabidopsis thaliana
(ATRBX1, HRT1, RBX1, ROC1, AT5G20570) and -1D mutants showed (BES1, BZR2, AT1G19350) phosphorylation phenotypes Arabidopsis thaliana
(BSU1, AT1G03445) localizes to nucleus
lam1-D shows stronger inhibition by 2,4-eBL treatment Oryza sativa
bes1-D mutant acts positively in brassinosteroid signalling Arabidopsis thaliana
(DREB26, AT1G21910) gene shows expression promoted by application of brassinosteroids Arabidopsis thaliana
auxin treatment triggers production of brassinosteroid receptor Oryza sativa
DR5::GUS is brassinosteroid-responsive
(BES1, BZR2, AT1G19350) and (BZR1, AT1G75080) are able to dimerize with each other (BES1, BZR2, AT1G19350) and (BZR1, AT1G75080) dimers
intracellular segment of (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) and (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) are critical for interaction and for brassinosteroid signaling
(ATHM1, ATM1, THM1, TRX-M1, AT1G03680) /4 is involved in BRs-induced changes in CO2 assimilation Solanum lycopersicum
(ARL, AT2G44080) (ARGOS-like) is involved in brassinosteroid (BR) pathway Arabidopsis thaliana
enhancement of BR signaling pathway automatically reduced its antagonistic pathway Arabidopsis thaliana
brassinosteroid-dependent growth was driven by brassinosteroid perception or synthesis in epidermis Arabidopsis thaliana
BU1 is primary brassinosteroid-responsive gene Oryza sativa
BU1 RNAi plants did not show dwarf phenotype Oryza sativa