| (AtbZIP68, bZIP68, AT1G32150) |
is |
basic region/leucine zipper (AtbZIP, bZIP, AT1G68880) transcription factor |
Arabidopsis thaliana |
| (AtbZIP16, bZIP16, AT2G35530) |
is |
(AtbZIP, bZIP, AT1G68880) protein |
|
| AtBBX20, 21, and 22 |
are identified as |
essential cofactors of AtHY5 |
Arabidopsis thaliana |
| (VQ29, AT4G37710) (PIF1, PIL5, AT2G20180) double mutant |
is pronouncedly shorter than single mutants under |
far-red light/dark cycles or far-red light without Suc supplement |
Arabidopsis thaliana |
| gametangiophores |
are induced by |
supplementing standard growth conditions with continuous FR light |
Marchantia polymorpha |
| certain photomorphogenesis mutants |
have roots that appear green because |
chloroplasts have developed |
Arabidopsis thaliana |
| Ca2+ channel blocker |
affects |
de-etiolation of the seedling hypocotyl |
Arabidopsis thaliana |
| (AtbZIP68, bZIP68, AT1G32150) and (AtGBF1, GBF1, AT4G36730) competing out (AtbZIP16, bZIP16, AT2G35530) |
could induce |
initial expression of PhANGs |
|
| (SMAX1, AT5G57710) (AtMAX2, MAX2, ORE9, PPS, AT2G42620) seedlings |
suppressed longer hypocotyls in |
red light-grown (AtMAX2, MAX2, ORE9, PPS, AT2G42620) seedlings |
Arabidopsis thaliana |
| (AtGBF1, GBF1, AT4G36730) |
acts as negative regulator of |
RBCS expression |
|
| light |
directs |
shade avoidance |
|
| (HLH1, PAR1, AT2G42870) |
functions as |
photomorphogenesis promoting factor |
Arabidopsis thaliana |
| hypocotyl lengths of (HY3, OOP1, PHYB, AT2G18790) |
were longer than |
wild-type and ZFP3ox seedlings |
Arabidopsis thaliana |
| hypocotyls of (HY3, OOP1, PHYB, AT2G18790) /ZFP3ox seedlings |
were gradually shortened by |
increasing fluence rates of red light, similar to wild-type seedlings |
Arabidopsis thaliana |
| dark-grown YHB seedlings |
exhibit unique |
plastid morphology |
Arabidopsis thaliana |
| AtBBX28 and AtBBX29 |
interfere with |
AtHY5 binding to promoters of downstream genes |
Arabidopsis thaliana |
| (FAR1, AT5G22500) (FAR-RED IMPAIRED RESPONSE 1) |
was identified as |
key positive component in the phyA-mediated photomorphogenic pathway |
|
| GR24 |
promote |
responses to light |
Arabidopsis thaliana |
| (SMAX1, AT5G57710) |
fully restores |
cotyledonary petiole angle of (AtMAX2, MAX2, ORE9, PPS, AT2G42620) |
Arabidopsis thaliana |
| intron retention isoforms of B-BOX DOMAIN 22 (BBX22IR) |
have regulatory functions in |
photomorphogenic development |
|
| (AtGBF1, GBF1, AT4G36730) |
is |
basic region/leucine zipper (AtbZIP, bZIP, AT1G68880) transcription factor |
Arabidopsis thaliana |
| delicate interplay between (AtbZIP16, bZIP16, AT2G35530) (AtbZIP68, bZIP68, AT1G32150) and (AtGBF1, GBF1, AT4G36730) |
possibly promotes |
just the right amount of gene expression to avoid photooxidative damage during first light hours |
|
| combined effect of downregulation of other nuclear genes involved in photomorphogenesis |
contributes to |
attenuated expression of plastid encoded genes |
|
| dark-to-light transition |
seedlings face changes in |
redox status |
|
| (VQ29, AT4G37710) expression |
is down-regulated by |
light |
Arabidopsis thaliana |
| (AtMAX2, MAX2, ORE9, PPS, AT2G42620) |
regulates |
photomorphogenesis |
|
| ELONGATED HYPOCOTYL 5 (HY5, TED 5, AT5G11260) |
genetically and physically interacts with |
signaling components |
Arabidopsis thaliana |
| (AtbZIP, bZIP, AT1G68880) triple mutant |
observed downregulated |
LHCB expression compared with WT |
|
| dorsiventral polarity |
is determined by |
illumination, particularly red light |
Marchantia polymorpha |
| extensive transcriptional reprogramming |
drives |
morphological changes necessary to establish a green photosynthetically active seedling |
|
| intron retention isoforms of B-BOX DOMAIN 24 (BBX24IR) |
have regulatory functions in |
photomorphogenic development |
|
| light exposure |
triggers |
photomorphogenic development |
|
| activity of both repressors and activators |
is prerequisite to |
balance and coordinate gene expression between nucleus and plastids |
|
| Decreased Tiller Number 1 (DTN1) |
is required for |
light-induced axillary bud elongation |
|
| (SMAX1, AT5G57710) mutants |
have phenotype of |
enhanced seedling photomorphogenesis |
Arabidopsis thaliana |
| (AtbZIP68, bZIP68, AT1G32150) and (AtGBF1, GBF1, AT4G36730) |
possibly compete out |
(AtbZIP16, bZIP16, AT2G35530) |
|
| COP1-SPA1 heterocomplex |
targets for degradation |
(AtMYB18, LAF1, MYB18, AT4G25560) |
Arabidopsis thaliana |
| (HY3, OOP1, PHYB, AT2G18790) pro:: GUS transcriptional reporter transgene |
displays GUS expression in |
cotyledons, hypocotyls, and roots |
Arabidopsis thaliana |
| (AtBBX32, BBX32, EIP6, AT3G21150) |
represses |
seedling photomorphogenesis |
Arabidopsis thaliana |
| GOLDEN2-LIKE (GLK) |
have diverse roles in |
photomorphogenesis |
|
| (VQ29, AT4G37710) loss-of-function mutant |
exhibits |
decreased hypocotyl elongation under low-intensity far-red light |
Arabidopsis thaliana |
| vq29-1 mutant |
did not affect |
defects of (PIF1, PIL5, AT2G20180) mutant during deetiolation |
Arabidopsis thaliana |
| estradiol-dependent shortening of hypocotyls |
was also observed in |
transgenic seedlings overexpressing (ATZFP1, ZFP1, AT1G80730) (ZFP4, AT1G66140) (ZFP6, AT1G67030) and (ZFP7, AT1G24625) |
Arabidopsis thaliana |
| YHB / phyAphyB transgenic lines |
possess |
open apical hook |
Arabidopsis thaliana |
| smax1-1 max2-8 mutant |
exhibits |
increased cotyledon expansion |
Arabidopsis thaliana |
| pleiotropic photosignaling (AtMAX2, MAX2, ORE9, PPS, AT2G42620) mutant |
exhibits |
decreased light responses |
Arabidopsis thaliana |
| (AtMAX2, MAX2, ORE9, PPS, AT2G42620) mutants |
exhibit |
modified seedling photomorphogenesis |
Arabidopsis thaliana |
| Cotyledons of (SMAX1, AT5G57710) (AtMAX2, MAX2, ORE9, PPS, AT2G42620) seedlings |
are restored to |
wild-type size |
Arabidopsis thaliana |
| inhibition of hypocotyl growth by (HY3, OOP1, PHYB, AT2G18790) during deetiolation of young seedlings |
reaches saturation between |
1 and 10 µmol m–2 s–1 of continuous red light |
|
| (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) negative regulation of photomorphogenesis |
occurs in |
absence of light |
Arabidopsis thaliana |
| (HLH1, PAR1, AT2G42870) and (ADH2, ATGSNOR1, GSNOR, HOT5, PAR2, AT5G43940) overexpression |
promote |
seedling deetiolation |
Arabidopsis thaliana |
| (ZFP3, AT5G25160) overexpression |
could not reduce relative hypocotyl lengths in |
abi5-1 mutant background upon red light illumination |
Arabidopsis thaliana |
| Y276H mutant of (HY3, OOP1, PHYB, AT2G18790) (YHB) |
induces constitutive photomorphogenesis via faithful reconstruction of |
(HY3, OOP1, PHYB, AT2G18790) signaling pathways |
Arabidopsis thaliana |
| light |
directs |
phototropism |
|
| vq29-1 mutant |
did not affect |
seedling greening phenotype |
Arabidopsis thaliana |
| deetiolation of young seedlings |
during which |
PHYTOCHROME B (HY3, OOP1, PHYB, AT2G18790) physiological activity |
|
| hypocotyls of abi5-1/ZFP3ox seedlings |
were only 10% shorter than |
abi5-1 in white light |
Arabidopsis thaliana |
| (ABI5, AtABI5, DPBF1, GIA1, AT2G36270) |
is essential for |
light-dependent function of (ZFP3, AT5G25160) |
Arabidopsis thaliana |
| ein194 mutants in white light conditions |
displayed |
reduced chlorophyll content |
Brassica rapa |
| LONG HYPOCOTYL5 (HY5, TED 5, AT5G11260) |
promotes |
photomorphogenesis |
Arabidopsis thaliana |
| hypocotyl shortening in ZFP3ox plants |
was estradiol dependent, indicating that it is the result of |
(ZFP3, AT5G25160) overexpression |
Arabidopsis thaliana |
| ELONGATED HYPOCOTYL 5 (HY5, TED 5, AT5G11260) |
suppresses |
photomorphogenesis |
Arabidopsis thaliana |
| plant photomorphogenesis |
involves |
complex interplay between multiple light-sensing systems including multiple regulatory photoreceptors, photosynthetic pigments, and other photoprotective or photodynamic pigments |
|
| brassinosteroids (BRs) |
may modulate photomorphogenesis through synergetic regulation with |
other hormones |
|
| light-grown deetiolated seedlings |
display |
photosynthetically active chloroplasts |
|
| COP1-SPA1 heterocomplex |
targets for degradation |
(HY5, TED 5, AT5G11260) |
Arabidopsis thaliana |
| (ATZFP1, ZFP1, AT1G80730) |
is implicated in |
photomorphogenic responses |
Arabidopsis thaliana |
| NF-YC |
regulates |
photomorphogenesis |
|
| B-box (BBX) transcription factors |
genetically interact with |
ELONGATED HYPOCOTYL 5 (HY5, TED 5, AT5G11260) |
Arabidopsis thaliana |
| a peroxisome biogenesis protein |
can influence |
photomorphogenesis |
|
| (FHY2, FRE1, HY8, PHYA, AT1G09570) |
contributes to |
hypocotyl growth response in white light |
|
| aberrant vitamin B6 content |
correlates with |
light sensitivity |
Arabidopsis thaliana |
| htl mutants |
show |
retarded leaf expansion |
Arabidopsis thaliana |
| unphosphorylated Long Hypocotyl 5 (HY5, TED 5, AT5G11260) |
is less stable than |
phosphorylated Long Hypocotyl 5 (HY5, TED 5, AT5G11260) |
|
| suppression of (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) expression |
results in longer hypocotyls under |
far-red light |
Arabidopsis thaliana |
| (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) |
does not function in hypocotyls under |
red light |
Arabidopsis thaliana |
| suppressed (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) expression (A- ) |
is insensitive to fluence rates of |
far-red light |
Arabidopsis thaliana |
| (HY5, TED 5, AT5G11260) expression |
is concentrated in |
joint sections between cotyledons and hypocotyls |
Arabidopsis thaliana |
| CONSTITUTIVELY PHOTOMORPHOGENIC 1 (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) |
mediates degradation of |
LONG AFTER FAR-RED LIGHT 1 (AtMYB18, LAF1, MYB18, AT4G25560) |
|
| phytochrome A (FHY2, FRE1, HY8, PHYA, AT1G09570) |
is primary photoreceptor responsible for mediating |
photomorphogenic responses in far-red light |
Arabidopsis thaliana |
| (BBX11, AT2G47890) |
mediates |
seedling development |
|
| (VQ29, AT4G37710) overexpression line |
shows hyposensitive hypocotyl growth to |
hypocotyl elongation inhibition |
Arabidopsis thaliana |
| vq29-1 mutant |
is indistinguishable from wild type in |
hypocotyl length in red or blue light conditions |
Arabidopsis thaliana |
| light-grown deetiolated seedlings |
display |
inhibited hypocotyl elongation |
|
| MORE AXILLARY GROWTH2 (AtMAX2, MAX2, ORE9, PPS, AT2G42620) |
positively regulates |
photomorphogenesis under far-red light |
Arabidopsis thaliana |
| phytochrome-mediated signals concerning the ratio of red to far red light |
adjust |
hypocotyl elongation |
|
| distinct morphology of dark-grown YHB etioplasts |
suggests |
cop phenotype of YHB is distinct from those of (ATDET1, DET1, FUS2, AT4G10180) and (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) mutants |
Arabidopsis thaliana |
| deetiolation |
causes |
cotyledon expansion |
|
| (VQ29, AT4G37710) overexpression |
results in |
hyposensitivity of hypocotyl growth to low-light conditions |
Arabidopsis thaliana |
| (ABI4, ATABI4, GIN6, ISI3, SAN5, SIS5, SUN6, AT2G40220) /ZFP3ox seedlings |
had significantly shorter hypocotyls than |
abi4-101 but longer ones when compared with ZFP3ox seedlings |
Arabidopsis thaliana |
| (AtUVR8, UVR8, AT5G63860) mutant |
was impaired in |
sunfleck-induced reduction of hypocotyl growth |
Arabidopsis thaliana |
| vq29-1 mutant |
has slightly but significantly shorter hypocotyl length than wild type under |
low-intensity white light or low-intensity far-red light |
Arabidopsis thaliana |
| (HLH1, PAR1, AT2G42870) and (ADH2, ATGSNOR1, GSNOR, HOT5, PAR2, AT5G43940) overexpression |
promote |
cotyledon unfolding |
Arabidopsis thaliana |
| gain-of-function phytochrome alleles |
elucidate |
interplay between phytochrome-dependent and phytochrome-independent photomorphogenetic pathways |
Arabidopsis thaliana |
| atTIC55-II expression |
is strongly induced by |
light |
Arabidopsis thaliana |
| (ZFP3, AT5G25160) |
acts additively with |
function of red light receptor |
Arabidopsis thaliana |
| (ZFP3, AT5G25160) |
does not function in |
PhyA- or cryptochrome-dependent signal transduction |
Arabidopsis thaliana |
| overexpression of Arabidopsis (HY3, OOP1, PHYB, AT2G18790) sequence (AtPHYB) |
results in |
stereotypical (HY3, OOP1, PHYB, AT2G18790) overexpression phenotype with short hypocotyls in white light |
Brassica rapa |
| silique length and seed weight phenotypes |
may be regulated by |
other phytochromes encoded in B. rapa genome |
Brassica rapa |
| light- and dark-grown Arabidopsis seedlings |
have distinct changes in gene expression in |
root, hypocotyl, and cotyledon |
Arabidopsis thaliana |
| seed germination and seedling growth |
are highly influenced by |
light intensity |
Arabidopsis thaliana |
| (GUN4, AT3G59400) function |
is obligatorily required for |
light/dark growth conditions |
|
| seedlings |
were illuminated with |
blue or red light for 3 h |
|
| mutation of (ATHD1, ATHDA19, HD1, HDA1, HDA19, HDAC19, RPD3A, AT4G38130) |
produces |
shorter hypocotyl phenotype |
Arabidopsis thaliana |
| light |
inhibits |
hypocotyl extension |
|
| htl-2 mutant |
displays |
long hypocotyl phenotype under blue light |
Arabidopsis thaliana |
| SPINDLY (SPY) and SECRET AGENT (SEC) |
regulate |
light signaling |
|
| DE-ETIOLATED 1 (ATDET1, DET1, FUS2, AT4G10180) |
is part of |
CDD complex (COP10–DET1–CCB1) |
|
| plants |
optimize |
photomorphogenic development |
|
| increased (APRR1, AtTOC1, PRR1, TOC1, AT5G61380) and (APRR5, PRR5, AT5G24470) expression |
possibly leading to suppression of |
hypocotyl growth |
|
| YFP-BBX29 #2 transgenic seedlings |
showed |
similar etiolated phenotypes with Col in the dark |
Arabidopsis thaliana |
| hy5-215 bbx30-2 bbx31-2 triple mutant |
displayed hypocotyls shorter than |
hy5-215 |
Arabidopsis thaliana |
| CONSTITUTIVELY PHOTOMORPHOGENIC1 (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) |
directly interact with |
HECATE 2 (HEC2, AT3G50330) |
Arabidopsis thaliana |
| NF-YC |
regulates photomorphogenesis by |
HDA15-mediated histone acetylation |
|
| brassinolide (BL) treatment |
suppresses |
photomorphogenesis |
|
| light-activated photoreceptors |
transduce |
light signals |
Arabidopsis thaliana |
| strigolactone analog (GR24) |
possibly promotes by inducing |
nuclear exclusion of Constitutive Photomorphogenic1 (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) |
Arabidopsis thaliana |
| ein194 mutant plants |
express |
truncated form of (HY3, OOP1, PHYB, AT2G18790) protein |
Brassica rapa |
| ir-ztl plants |
have increased |
hypocotyl length |
Nicotiana attenuata |
| 67% overlap of early red light-responsive genes with YHB–D SSTF-regulated genes |
represents |
high level of overlap |
Arabidopsis thaliana |
| chy1-10 plants |
are not chilling sensitive in the light |
light |
|
| (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) |
is involved in negative regulation of |
photomorphogenesis |
Arabidopsis thaliana |
| phyB-GFP fusion protein |
shows dynamics of cellular localization during |
de-etiolation |
Arabidopsis thaliana |
| light-grown deetiolated seedlings |
display |
expanded cotyledons |
|
| seedling deetiolation |
is |
one of the best-studied photomorphogenesis events |
|
| CONSTITUTIVE PHOTOMORPHOGENIC 1 (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) |
is |
key suppressor of photomorphogenesis |
Arabidopsis thaliana |
| light |
participates in complicated network with |
hormone signaling |
|
| vq29-1 mutant |
exhibited reduced hypocotyl elongation under |
low white light and different intensities of far-red light without Suc supplement |
Arabidopsis thaliana |
| (HY3, OOP1, PHYB, AT2G18790) |
has |
unique as well as partially redundant or antagonistic roles in different photomorphogenic responses |
Arabidopsis thaliana |
| effect of red light on relative hypocotyl lengths |
was comparable in |
abi2-1 and Col-0 seedlings |
Arabidopsis thaliana |
| Woodson et al. (2015) |
reported |
molecular mechanism of deetiolation defect of Arabidopsis fc mutants |
Arabidopsis thaliana |
| complex regulatory network |
interconnects |
tetrapyrrole metabolism, photoreceptor, and G-protein signaling pathways |
Arabidopsis thaliana |
| sunflecks |
reduced |
hypocotyl growth |
Arabidopsis thaliana |
| phototropins |
regulate |
rapid inhibition of the growth of etiolated hypocotyls |
|
| (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) |
targets for ubiquitination and degradation |
(FBI1, HFR1, REP1, RSF1, AT1G02340) |
Arabidopsis thaliana |
| ZFP3ox plants |
produced shorter hypocotyls than |
wild-type plants, both in dark and in white light |
Arabidopsis thaliana |
| (HY3, OOP1, PHYB, AT2G18790) protein |
was expressed in |
all three organs of white light-grown B. rapa seedlings |
Brassica rapa |
| light |
directs |
seedling deetiolation |
|
| (FHY2, FRE1, HY8, PHYA, AT1G09570) |
has |
unique as well as partially redundant or antagonistic roles in different photomorphogenic responses |
Arabidopsis thaliana |
| COP1-mediated degradation |
promotes |
skotomorphogenesis |
Arabidopsis thaliana |
| barley plants greenhouse-grown under artificial illumination supplemented with daily sunlight |
with day/night cycle of |
16/8 h |
Hordeum vulgare |
| the dominant (ATPEX2, PEX2, TED3, AT1G79810) mutation in a peroxisomal protein |
suppresses |
the pleiotropic de-etiolated mutant phenotypes of (ATDET1, DET1, FUS2, AT4G10180) and (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) |
|
| (AtSOD2, CSD2, CZSOD2, SOD2, AT2G28190) knockdown line |
has |
severe and light-dependent phenotype |
Arabidopsis thaliana |
| (ZFP3, AT5G25160) |
is implicated in red light signaling independent of |
(HY3, OOP1, PHYB, AT2G18790) |
Arabidopsis thaliana |
| inhibition of hypocotyl elongation in abi4-101 |
was less sensitive to red light, especially at |
lower fluence rates |
Arabidopsis thaliana |
| light-grown deetiolated seedlings |
display |
unfolding of apical hooks |
|
| ein194 mutants in white light conditions |
displayed |
dramatically elongated stature |
Brassica rapa |
| digestion of entire chloroplasts |
has been observed during |
greening of etiolated seedlings |
Arabidopsis thaliana |
| continuous red light (Rc) |
regulates approximately 80% of genes also |
Y276H mutant of (HY3, OOP1, PHYB, AT2G18790) (YHB)-regulated genes |
Arabidopsis thaliana |
| SNAP-LITE LED lighting system |
was used for |
red light (662 ± 10 nm) illumination |
Arabidopsis thaliana |
| (FHY2, FRE1, HY8, PHYA, AT1G09570) |
has dual action (positive and negative) on |
de-etiolation of seedlings |
Arabidopsis thaliana |
| limited overlap |
is consistent with |
light-dependent developmental differences |
Arabidopsis thaliana |
| hypocotyl elongation inhibition |
is dependent on |
fluence rate |
Arabidopsis thaliana |
| phy (phytochrome) |
works together with CRY to regulate |
photomorphogenesis |
|
| (FHY2, FRE1, HY8, PHYA, AT1G09570) (HY3, OOP1, PHYB, AT2G18790) double mutant |
shows reduced |
chlorophyll accumulation |
|
| photoactivated phytochrome |
interacts directly with |
basic helix-loop-helix (bHLH) transcription factors |
Arabidopsis thaliana |
| (PIF1, PIL5, AT2G20180) (PAP3, PIF3, POC1, AT1G09530) (AtPIF4, PIF4, SRL2, AT2G43010) and (A-PUT2, bHLHb1, PIF5, PIL6, AT3G59060) |
act as |
constitutive repressors of photomorphogenesis in the dark |
Arabidopsis thaliana |
| CRYPTOCHROME 1 (ATCRY1, BLU1, CRY1, HY4, OOP2, AT4G08920) |
mainly mediates |
de-etiolation in high light |
Arabidopsis thaliana |
| htl-1 mutant |
exhibits |
long hypocotyl phenotype under blue light |
Arabidopsis thaliana |
| genome-wide comparison of gene expression between dark-grown wild-type seedling and BR biosynthesis mutant (ATDET2, DET2, DWF6, AT2G38050) seedling treated with light or light and exogenous brassinolide (BL) |
confirmed |
negative role of BR in photomorphogenesis |
Arabidopsis thaliana |
| (HY5, TED 5, AT5G11260) protein accumulation |
is detected under |
blue light |
Arabidopsis thaliana |
| (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) expression |
suppresses |
hypocotyl elongation |
Arabidopsis thaliana |
| CONSTITUTIVELY PHOTOMORPHOGENIC 1 (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) |
mediates degradation of |
LONG HYPOCOTYL IN FAR-RED (FBI1, HFR1, REP1, RSF1, AT1G02340) |
|
| MIR gene expression level |
determines |
miRNA expression levels |
|
| CONSTITUTIVELY PHOTOMORPHOGENIC 1 (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) /SUPPRESSOR OF PHYA-105 (SPA) E3 ubiquitin ligase complex |
ubiquitinates |
ELONGATED HYPOCOTYL 5 (HY5, TED 5, AT5G11260) |
Arabidopsis thaliana |
| hec mutants |
partially suppress photomorphogenic phenotypes of |
pifq mutants |
Arabidopsis thaliana |
| cop1-6pif1hec1hec2 higher-order mutant |
exhibits |
hypocotyl length phenotype |
Arabidopsis thaliana |
| VQ29-OE PIF1-OE double transgenic plants |
display much longer hypocotyls than parent single overexpression lines and wild type under |
low light conditions |
Arabidopsis thaliana |
| CONSTITUTIVE PHOTOMORPHOGENIC 1 (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) |
targets for degradation |
ELONGATED HYPOCOTYL 5 (HY5, TED 5, AT5G11260) |
Arabidopsis thaliana |
| Arabidopsis fc mutants |
show |
deetiolation defect when exposed to light |
Arabidopsis thaliana |
| Y276H mutant of (HY3, OOP1, PHYB, AT2G18790) (YHB) |
induces constitutive photomorphogenesis in |
light-independent fashion |
Arabidopsis thaliana |
| YHB seedlings |
are significantly shorter than |
wild type |
Arabidopsis thaliana |
| haf2-1 mutants |
do not display |
long hypocotyl phenotype |
Arabidopsis thaliana |
| pCOR28:YFP-COR28 |
complements |
cor27-2 cor28-2 mutant phenotype |
Arabidopsis thaliana |
| hy5-215 bbx28-4 bbx29-2 triple mutant seedlings |
displayed hypocotyl length shorter than |
hy5-215 |
Arabidopsis thaliana |
| deetiolation |
causes |
chlorophyll development |
|
| B. rapa FPsc (HY3, OOP1, PHYB, AT2G18790) protein (Bra022192) |
is more than 90% identical to |
Arabidopsis (HY3, OOP1, PHYB, AT2G18790) protein |
Brassica rapa; Arabidopsis thaliana |
| PHYTOCHROME E (PHYE, AT4G18130) |
previously linked to |
shade avoidance, germination, seedling de-etiolation, and flowering time |
Arabidopsis thaliana |
| YHB-regulated gene expression pattern |
accurately reflects |
process of photomorphogenesis in wild-type Arabidopsis |
Arabidopsis thaliana |
| BR deficiency |
stimulates |
photomorphogenesis |
|
| phytochrome-interacting factors (PIFs) |
function as |
negative factors in darkness or under FR, R, and B light |
Arabidopsis thaliana |
| deetiolated (HY5, TED 5, AT5G11260) null mutant seedlings |
exhibit |
reduced anthocyanin accumulation |
Arabidopsis thaliana |
| abi5-1 |
prevents |
ZFP3-promoted hypocotyl shortening |
Arabidopsis thaliana |
| complex regulatory network |
reacts to |
change in light intensity |
Arabidopsis thaliana |
| dark-grown YHB seedlings |
exhibit |
cop mutant phenotype |
Arabidopsis thaliana |
| brassinosteroids (BRs) |
regulates |
plant growth and development |
|
| genes involved in BR and light signaling pathway |
will help elucidate |
molecular mechanism of plant photomorphogenesis |
|
| light |
regulates |
chloroplast movement |
|
| COP1-mediated ubiquitination and degradation |
mediates the regulation of |
photomorphogenic development |
Arabidopsis thaliana |
| photomorphogenesis phenotype |
includes |
expanded cotyledons |
|
| hypocotyl length in darkness |
is slightly promoted before inhibition by |
blue light (BL) treatment |
Arabidopsis thaliana |
| distinct developmental programs of cotyledons and hypocotyls |
include |
promotion of cotyledon expansion |
|
| distinct developmental programs of cotyledons and hypocotyls |
include |
inhibition of hypocotyl elongation |
|
| (ATCOL3, BBX4, COL3, AT2G24790) |
mediates |
seedling development |
|
| BBX proteins |
control photomorphogenic development with |
distinct molecular mechanisms |
|
| ethylene-independent severe alterations in seedling morphology |
prevents |
apical hook formation |
Arabidopsis thaliana |
| silencing of GATA |
suppresses |
photomorphogenesis |
|
| brassinosteroid (BR) signaling |
represses expression of |
key positive regulators of light response |
|
| DELLA proteins |
interact with |
(AtPIF4, PIF4, SRL2, AT2G43010) |
|
| (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) |
regulates |
cell elongation in hypocotyls |
Arabidopsis thaliana |
| microprocessor components |
could be differently regulated during |
photoperiodic changes |
|
| Cryptochromes (CRYs) |
mediate |
blue light regulation of development |
|
| red light |
induces |
stomatal opening |
Arabidopsis thaliana |
| (AtBBX32, BBX32, EIP6, AT3G21150) |
mediates |
seedling development |
|
| multiple BBX members |
mediate seedling development either positively or negatively |
seedling development |
|
| hec1hec2 double mutant |
partially suppressed |
photomorphogenic effect of cop1-6 and cop1-6pif1 double mutants |
Arabidopsis thaliana |
| The four SPA proteins |
form stable complex with |
(ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) |
Arabidopsis thaliana |
| (AtbZIP, bZIP, AT1G68880) protein (HY5, TED 5, AT5G11260) (ELONGATED HYPOCOTYL5) |
is proposed to function as |
high hierarchical regulator of transcriptional cascade controlling photomorphogenesis |
Arabidopsis thaliana |
| AtOEP16 |
has role in |
de-etiolation |
Arabidopsis thaliana |
| htl-1 mutant |
displays |
long hypocotyl phenotype under blue light |
Arabidopsis thaliana |
| htl-1 and htl-2 mutants |
have |
very similar hypocotyl phenotype |
Arabidopsis thaliana |
| light |
regulates |
plant development |
|
| (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) expression |
enhances |
blue light (BL) sensitivity |
Arabidopsis thaliana |
| (COR27, AT5G42900) VP-AAox and (COR28, HUP41, AT4G33980) VP-AAox lines |
show hyposensitivity to |
red light |
Arabidopsis thaliana |
| (AtBBX21, BBX21, LHUS, STH2, AT1G75540) (BBX22, DBB3, LZF1, STH3, AT1G78600) (bbx23, AT4G10240) (BBX24, STO, AT1G06040) (BBX25, STH, AT2G31380) and (BBX28, AT4G27310) |
modulate transcriptional activation activity in regulation of |
photomorphogenic development |
|
| cop1-6 mutant |
displayed |
opened cotyledons in the dark |
Arabidopsis thaliana |
| (BBX28, AT4G27310) /29 and (BBX30, miP1b, AT4G15248) (BBX31, miP1a, AT3G21890) |
may function additively in |
promoting hypocotyl elongation |
Arabidopsis thaliana |
| hec1hec2 double mutant |
significantly suppressed |
constitutive photomorphogenic phenotypes of pifQ |
Arabidopsis thaliana |
| hypocotyl growth inhibition |
depends on |
nuclear (HY3, OOP1, PHYB, AT2G18790) |
|
| light signal |
regulates |
plant growth and development |
|
| continuous cool-white light |
was provided at |
approximately 100 ± 10 μmol m−2 s−1 |
Arabidopsis thaliana |
| HTL overexpression |
causes |
short hypocotyl phenotype under red light |
Arabidopsis thaliana |
| htl mutants |
show |
elongated petioles |
Arabidopsis thaliana |
| (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) expression in hypocotyls |
is elevated in |
white light |
Arabidopsis thaliana |
| (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) expression in hypocotyls |
is significantly elevated by |
far-red light |
Arabidopsis thaliana |
| (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) transcript |
is down-regulated in hypocotyls of |
(HY5, TED 5, AT5G11260) mutants |
Arabidopsis thaliana |
| suppressed (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) expression |
causes hypersensitive response only under |
far-red, blue, and white light conditions |
|
| miP-DCL1 seedlings |
show delay in |
cotyledon opening |
|
| phytochromes |
are essential for |
plant growth and development |
|
| (AtHMAC6, AtHMP38, HMA6, PAA1, PCH1, AT4G33520) and pch1pchl seedlings |
failed to inhibit |
hypocotyl elongation in short day conditions |
Arabidopsis thaliana |
| phytochromes and cryptochromes |
promote |
photomorphogenesis |
|
| light |
plays important roles in control of |
seedling development |
|
| LBD genes |
function in |
photomorphogenesis |
|
| short day photoperiod |
has |
one point of photoinduction each day |
|
| (HY3, OOP1, PHYB, AT2G18790) |
works redundantly with phyA in regulating |
hook opening |
Arabidopsis thaliana |
| htl-2 mutant |
displays |
long hypocotyl phenotype under far-red light |
Arabidopsis thaliana |
| htl-1 mutant |
exhibits |
long hypocotyl phenotype under far-red light |
Arabidopsis thaliana |
| htl-1 young seedlings |
exhibits |
smaller cotyledon |
Arabidopsis thaliana |
| blue light (BL) |
inhibits |
hypocotyl elongation in darkness |
|
| abscisic acid (ABA) |
plays important roles in control of |
seedling development |
|
| UV RESISTANCE LOCUS 8 (AtUVR8, UVR8, AT5G63860) and CONSTITUTIVELY PHOTOMORPHOGENIC 1 (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) interaction |
promotes |
UV-B-induced photomorphogenesis |
Arabidopsis thaliana |
| plants |
modulate |
light responses |
|
| (COR27, AT5G42900) and (COR28, HUP41, AT4G33980) |
act redundantly in |
red light-dependent hypocotyl growth inhibition |
Arabidopsis thaliana |
| (ASK1, ATSKP1, SKP1, SKP1A, UIP1, AT1G75950) seedlings grown under red and far-red light |
had hypocotyl length significantly shorter than |
WT seedlings |
Arabidopsis thaliana |
| short-day (SD) light conditions |
provided by |
white light (120 μmol m −2 s −1 ) |
Arabidopsis thaliana |
| light |
triggers |
multiple signaling pathways involving almost all plant hormones |
|
| (BBX28, AT4G27310) |
mediates |
seedling development |
|
| feedback regulatory loop of (BBX28, AT4G27310) /29, (HY5, TED 5, AT5G11260) and (BBX30, miP1b, AT4G15248) /31 |
fine-tunes |
photomorphogenic development |
|
| (FHY2, FRE1, HY8, PHYA, AT1G09570) |
works redundantly with phyB in regulating |
cotyledon unfolding |
Arabidopsis thaliana |
| light signals |
regulate |
plant growth and development |
|
| DELLA proteins |
interact with |
(PAP3, PIF3, POC1, AT1G09530) |
|
| blue light (BL) treatment |
triggers |
hypocotyl length variation |
|
| HY5-HOMOLOG (HYH, AT3G17609) |
directly binds to GATA-box of promoter of |
(AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) |
Arabidopsis thaliana |
| pifq mutant |
shows |
short hypocotyls under both −UV-B and +UV-B |
Arabidopsis thaliana |
| gi mutants |
display |
elongated hypocotyls under blue light |
Arabidopsis thaliana |
| cop1-6 mutant |
displayed |
dramatically shortened hypocotyls |
Arabidopsis thaliana |
| kanamycin resistant seedlings |
were grown for 6 days under light |
light conditions |
|
| ambient light |
has profound effects on |
early seedling de-etiolation |
Arabidopsis thaliana |
| light-grown phenotype |
includes |
development of true leaves |
|
| phyB-overexpressing lines |
demonstrated that light sensitivity of phyB-mediated photomorphogenic responses is |
dose-dependent |
Arabidopsis thaliana |
| mathematical modeling |
confirmed |
good correlation between absolute Pfr levels and physiological activity |
Arabidopsis thaliana |
| phytochrome-interacting factors (PIFs) |
repress |
seedling photomorphogenesis |
|
| htl mutants |
show attenuated expression of |
chalcone synthase (ATCHS, CHS, TT4, AT5G13930) |
Arabidopsis thaliana |
| light sensing |
triggers adjustment of |
energy distribution |
|
| LONG HYPOCOTYL 5 (HY5, TED 5, AT5G11260) |
is required for |
hypocotyl growth inhibition in lighted conditions |
|
| brassinosteroids (BRs) |
are closely related to |
photomorphogenesis |
|
| (HY5, TED 5, AT5G11260) mutants |
showed irregular hypocotyl length promotion in response to |
elevated blue light (BL) treatment |
|
| BR-responsive gene expression inhibition |
promotes |
UV-B-induced photomorphogenesis |
|
| GIGANTEA (GI) |
physically interacts with |
phytochrome B (HY3, OOP1, PHYB, AT2G18790) |
Arabidopsis thaliana |
| HA-YFP-COR27 or -COR28 overexpression lines |
have shorter hypocotyls than wildtype when grown in |
R light |
|
| root hair elongation under control conditions |
is sensitive to |
light |
|
| (FHY2, FRE1, HY8, PHYA, AT1G09570) |
works redundantly with phyB in regulating |
hypocotyl growth inhibition |
Arabidopsis thaliana |
| htl mutants |
show |
retarded cotyledon expansion |
Arabidopsis thaliana |
| BR biosynthesis-defective mutants ( (ATDET2, DET2, DWF6, AT2G38050) (AtDWF4, CLM, CYP90B1, DWF4, PSC1, SAV1, SNP2, AT3G50660) (CBB3, CPD, CYP90, CYP90A, CYP90A1, DWF3, AT5G05690) (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) ) |
display |
photomorphogenesis phenotype |
Arabidopsis thaliana |
| BR biosynthesis-defective mutants ( (ATDET2, DET2, DWF6, AT2G38050) (AtDWF4, CLM, CYP90B1, DWF4, PSC1, SAV1, SNP2, AT3G50660) (CBB3, CPD, CYP90, CYP90A, CYP90A1, DWF3, AT5G05690) (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) ) |
display photomorphogenesis phenotype when grown in |
darkness |
Arabidopsis thaliana |
| photomorphogenesis phenotype |
includes |
short hypocotyls |
|
| (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) |
does not function in hypocotyls under |
dark |
Arabidopsis thaliana |
| (HY5, TED 5, AT5G11260) protein accumulation |
is similar to |
(AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) expression |
Arabidopsis thaliana |
| (HY5, TED 5, AT5G11260) (HYH, AT3G17609) double mutant |
displays strong phenotype |
(HY5, TED 5, AT5G11260) and (HYH, AT3G17609) function in photomorphogenesis |
Arabidopsis thaliana |
| mutations in hec genes |
partially suppress |
photomorphogenic phenotypes of cop1-6pif1 and pifQ mutant seedlings growing in the dark |
Arabidopsis thaliana |
| exposure to total darkness for 2 h |
results in reduction in |
(DDA1, AT5G41560) transcript abundance in wild-type seedlings |
Arabidopsis thaliana |
| (DDA1, AT5G41560) |
functions as |
transcriptional activator to repress hypocotyl elongation in the light |
Arabidopsis thaliana |
| phytochromes |
mediate |
light-regulated pathways |
|
| transgenic plants with suppressed (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) expression |
exhibits |
elongated hypocotyls under darkness |
|
| blue light (BL) |
induces |
hypocotyl elongation under light |
|
| phytochromes and cryptochromes |
are known to repress |
CONSTITUTIVE PHOTOMORPHOGENESIS 1 (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) activity |
|
| UV-B light |
antagonizes |
thermomorphogenesis |
|
| COLD-REGULATED GENE 28 (COR28, HUP41, AT4G33980) |
represses |
early seedling development in red light |
|
| phytochrome-interacting factors (PIFs) |
includes |
(PIF1, PIL5, AT2G20180) (PAP3, PIF3, POC1, AT1G09530) (AtPIF4, PIF4, SRL2, AT2G43010) and (A-PUT2, bHLHb1, PIF5, PIL6, AT3G59060) |
|
| (AtBBX21, BBX21, LHUS, STH2, AT1G75540) |
mediates |
seedling development |
|
| CONSTITUTIVELY PHOTOMORPHOGENIC1 (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) |
directly interact with |
HECATE 2 (HEC2, AT3G50330) |
Arabidopsis thaliana |
| htl-1 mutant |
displays |
long hypocotyl phenotype under red light |
Arabidopsis thaliana |
| (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) transcript in (HY5, TED 5, AT5G11260) (HYH, AT3G17609) mutant |
is down-regulated compared to |
wild-type plants |
Arabidopsis thaliana |
| miRNA-biogenetic inconsistency |
could be essential for |
seedlings buried deep in soil |
|
| increase in ELONGATED HYPOCOTYL 5 (HY5, TED 5, AT5G11260) abundance |
triggers |
photomorphogenesis |
|
| light |
regulates |
seedling de-etiolation |
|
| (APRR1, AtTOC1, PRR1, TOC1, AT5G61380) mutant |
is hyposensitive to R light with regard to |
inhibition of hypocotyl growth |
|
| SUPPRESSOR OF (FHY2, FRE1, HY8, PHYA, AT1G09570) (SPA) proteins and CONSTITUTIVELY PHOTOMORPHOGENIC1 (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) complex |
suppress |
plant photomorphogenesis |
Arabidopsis thaliana |
| plates |
kept under corresponding light conditions for 1 week for |
hypocotyl measurement |
Arabidopsis thaliana |
| htl-2 mutant |
shows |
phenotypic spectrum similar to htl-1 |
Arabidopsis thaliana |
| (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) expression in hypocotyls |
is elevated in |
blue light |
Arabidopsis thaliana |
| (HY5, TED 5, AT5G11260) (HYH, AT3G17609) mutants |
curve peak shifts left to |
10 or 100 μM blue light (BL) concentration |
|
| (AtHMAC6, AtHMP38, HMA6, PAA1, PCH1, AT4G33520) and PCHL |
result in |
enhanced light sensitivity |
|
| PIF transcription factors |
are |
central regulators of seedling de-etiolation |
|
| cor27-2 cor28-2 phyB-9 triple mutant |
is almost completely insensitive to red light, similar to |
phyB-9 single mutant |
Arabidopsis thaliana |
| CaM7-light-induced photomorphogenesis |
requires |
an additional factor or modification |
Arabidopsis thaliana |
| double mutations of haf2-1 and hy5-1 |
have synergistic effect on |
photomorphogenic traits |
Arabidopsis thaliana |
| htl-1 young seedlings |
exhibits |
longer petioles |
Arabidopsis thaliana |
| (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) expression in hypocotyls |
is elevated in |
far-red light |
Arabidopsis thaliana |
| (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) suppression of brassinosteroid signaling and ELONGATED HYPOCOTYL 5 (HY5, TED 5, AT5G11260) and -HOMOLOG (HYH, AT3G17609) activation of |
synergistically regulate |
cell elongation of hypocotyls |
Arabidopsis thaliana |
| bbx28-4 bbx29-2 mutant |
showed |
similar hypocotyl phenotypes to Col when grown in the dark |
Arabidopsis thaliana |
| (HY5, TED 5, AT5G11260) protein accumulation |
suggests a possible link between |
(AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) and (HY5, TED 5, AT5G11260) |
Arabidopsis thaliana |
| (HY5, TED 5, AT5G11260) mutant |
exhibits |
elongated hypocotyls under darkness |
|
| UV-B light |
antagonizes |
shade avoidance |
|
| elongated hypocotyl of gi mutants |
suggests |
repressive role in photoreceptor mediated growth inhibition |
Arabidopsis thaliana |
| COLD-REGULATED GENE 27 (COR27, AT5G42900) |
represses |
early seedling development in far-red light |
|
| COLD-REGULATED GENE 28 (COR28, HUP41, AT4G33980) |
represses |
early seedling development in blue light |
|
| bbx30-2 bbx31-2 double mutant seedlings |
displayed shortened hypocotyls compared with Col |
light conditions |
Arabidopsis thaliana |
| PHYTOCHROME-INTERACTING FACTOR 1 (PIF1, PIL5, AT2G20180) |
directly interact with |
HECATE 2 (HEC2, AT3G50330) |
Arabidopsis thaliana |
| haf2-1 mutants |
can enhance |
long hypocotyl phenotype of blue light receptor mutants (hy4-1) |
Arabidopsis thaliana |
| CRYPTOCHROME 1 (ATCRY1, BLU1, CRY1, HY4, OOP2, AT4G08920) |
regulates |
photomorphogenesis under continuous light (CL) or short-day (SD) illuminated by white light (WL-CL or WL-SD) or blue light (BL-CL or BL-SD) |
Arabidopsis thaliana |
| light |
is |
one of the most informative environmental signals for plant growth, development, and survival |
|
| mature chloroplasts |
are required for |
photosynthesis |
|
| tissue-specific expression pattern of (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) |
is similar to |
tissue-specific expression pattern of (HY5, TED 5, AT5G11260) |
Arabidopsis thaliana |
| (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) transcript |
is elevated in |
(ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) mutant |
Arabidopsis thaliana |
| (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) overexpression |
causes |
hyposensitive response to exogenous blue light (BL) in light types |
|
| ELONGATED HYPOCOTYL 5 (HY5, TED 5, AT5G11260) |
is |
extensively studied for importance in photomorphogenesis |
Arabidopsis thaliana |
| strong overexpression of HA-YFP-COR27 and -COR28 in COR27ox-1 and COR28ox-1 |
leads to hypersensitive response to |
red light |
Arabidopsis thaliana |
| bbx28-4 bbx29-2 double mutant seedlings |
displayed shortened hypocotyls compared with Col |
light conditions |
Arabidopsis thaliana |
| phytochrome-interacting factors (PIFs) |
are |
group of repressors |
|
| htl seedling photomorphogenesis phenotype |
points to existence of |
endogenous ligand |
Arabidopsis thaliana |
| (ATPHO1, PHO1, AT3G23430) ;H4 (SHORT HYPOCOTYL UNDER BLUE1 (SHB1, AT4G25350) ) |
has regulatory role in |
hypocotyl elongation under blue light |
Arabidopsis thaliana |
| 24-epibrassinolide (EBL) treatment |
promotes |
apical hook formation |
Arabidopsis thaliana |
| photomorphogenesis |
occurs during |
dark-light transition |
Arabidopsis thaliana |
| strong overexpression of wildtype (COR27, AT5G42900) and (COR28, HUP41, AT4G33980) in COR27ox-1 and COR28ox-1 |
might lead to antagonistic effects on |
(COR27, AT5G42900) and (COR28, HUP41, AT4G33980) function |
Arabidopsis thaliana |
| pifq mutant hypocotyl elongation arrest |
is similar to |
PhyB-overexpressing transgenic seedlings |
Arabidopsis thaliana |
| HECATE proteins ( (HEC1, AT5G67060) 2 and 3) |
act as |
positive regulators of photomorphogenesis |
|
| HISTONE DEACETYLASE 15 (ATHDA15, HDA15, AT3G18520) |
positively regulates |
photomorphogenesis |
|
| PAR-RNAi seedlings |
exhibit |
hyperetiolation phenotypes |
Arabidopsis thaliana |
| (ZFP3, AT5G25160) |
suggests role for ZFP3 in |
amplification of red light signals |
Arabidopsis thaliana |
| redundant role between the many PIFs |
may explain |
absence of (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) mutant-like phenotype in (PAP3, PIF3, POC1, AT1G09530) (AtPIF4, PIF4, SRL2, AT2G43010) double mutant |
Arabidopsis thaliana |
| (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) |
expression in hypocotyls is up-regulated by |
light |
Arabidopsis thaliana |
| peak shifts |
were not observed in |
darkness |
|
| red light (λ max 680 nm) |
supplied by |
LED light sources (Qiding Photo Electric Shanghai Co., (GDC1, LTD, AT1G50900) Shanghai, China) |
Arabidopsis thaliana |
| GATA protein |
is stabilized in |
light |
|
| phosphorylation state of the (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) interaction site |
is mediated by |
casein kinase II (CKII) |
|
| (HY5, TED 5, AT5G11260) and HYH-mediated (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) regulation |
may serve as bridge linking |
brassinosteroid signaling and photomorphogenesis |
Arabidopsis thaliana |
| 4-day etiolated PCH1OE and PCHLOE seedlings |
showed delayed |
cotyledon greening |
Arabidopsis thaliana |
| UV-B light perception and signal transduction |
benefits plants by inducing |
photomorphogenic development |
|
| weak (COR27, AT5G42900) overexpression line |
has longer hypocotyls than wildtype when grown in |
R light |
|
| photomorphogenesis (de-etiolation) |
is |
critical for enabling germinated seed to become healthy seedling |
|
| feedback loop consisting of (BBX28, AT4G27310) (BBX29, AT5G54470) (BBX30, miP1b, AT4G15248) (BBX31, miP1a, AT3G21890) and (HY5, TED 5, AT5G11260) |
regulates |
photomorphogenesis |
|
| bbx29-1 and bbx29-2 mutants |
displayed significantly shortened hypocotyls compared with Col when grown in |
white (W), blue (B), red (R) and far-red (FR) light conditions |
Arabidopsis thaliana |
| (BBX29, AT5G54470) |
promotes |
hypocotyl elongation |
Arabidopsis thaliana |
| four of the up-regulated chloroplast proteins |
have also been shown to be up-regulated during |
light-induced photomorphogenesis |
Arabidopsis thaliana |
| HTL overexpression |
causes |
short hypocotyl phenotype under far-red light |
Arabidopsis thaliana |
| (HY5, TED 5, AT5G11260) expression |
is concentrated in |
cotyledons |
Arabidopsis thaliana |
| (HY5, TED 5, AT5G11260) protein accumulation |
is detected under |
white light |
Arabidopsis thaliana |
| low expression of (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) |
results in stimulation of |
cell elongation |
Arabidopsis thaliana |
| Ultraviolet-B (UV-B) light at low intensities |
can promote |
photomorphogenesis |
Arabidopsis thaliana |
| (HY3, OOP1, PHYB, AT2G18790) |
is |
key factor for seedling establishment |
|
| HECATE 2 (HEC2, AT3G50330) |
is degraded in the dark and is stabilized by light at |
seedling stage |
Arabidopsis thaliana |
| (GUN1, AT2G31400) mutant |
is defective in |
greening after transfer from dark to light |
Arabidopsis thaliana |
| internode elongation |
is regulated by |
phytochromes |
Arabidopsis thaliana |
| deetiolation |
occurs during |
underground seedlings emergence to light |
Arabidopsis thaliana |
| complex molecular cascades |
reprogram seedlings for |
photomorphogenesis |
Arabidopsis thaliana |
| (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) and the four partially redundant SPA proteins |
work together to repress |
photomorphogenesis |
Arabidopsis thaliana |
| (HY5, TED 5, AT5G11260) HOMOLOG (HYH, AT3G17609) |
is predominantly involved in |
blue light-mediated development |
|
| light-grown seedlings of miP-DCL1 |
have defects in |
flowering time |
|
| phytochromes |
are |
red/far-red reversible photoreceptors |
|
| (SAUR27, AT3G03840) (SAUR28, AT3G03830) and (SAUR66, AT1G29500) expression |
is required for |
cotyledon expansion |
Arabidopsis thaliana |
| cor27-2 cor28-2 double mutant |
shows strongly reduced hypocotyl growth compared with wildtype in |
red light |
Arabidopsis thaliana |
| (BBX31, miP1a, AT3G21890) |
mediates |
seedling development |
|
| YFP-BBX29 cop1-6 #2 transgenic line |
was indistinguishable from |
Col and YFP-BBX29 #2 grown in the dark |
Arabidopsis thaliana |
| HECATEs (HECs) |
directly interact with and antagonize |
phytochrome-interacting factors (PIFs) |
|
| tobacco cell lines VBI-0 and BY-2 |
lack |
light response |
Nicotiana tabacum |
| NPA inhibition of hypocotyl elongation |
has |
wavelength dependency the same as found for division synchrony in VBI-3 |
Arabidopsis thaliana |
| blue light |
triggers responses through |
range of mechanisms at molecular, cellular, and organ levels |
|
| darkness |
promotes activity of |
E3 ubiquitin ligase (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) /SPA |
|
| liquid-liquid phase separation (LLPS) |
influences |
photomorphogenesis |
|
| pentuple DELLA knockout mutants |
show only slightly altered elongation in |
red light |
|
| blue light |
decreases yielding properties of |
cell walls |
|
| efo mutant |
does not exhibit |
constitutive photomorphogenesis |
Arabidopsis thaliana |
| two major classes of photoreceptors |
mediate |
seedling de-etiolation |
Arabidopsis thaliana |
| continuous red light |
had little impact on |
NPA inhibition of hypocotyl elongation |
Arabidopsis thaliana |
| blue light |
is known to trigger |
large variety of photomorphogenic responses |
|
| ted5-1 mutant hypocotyls |
are longer than |
dda1-1 hypocotyls |
Arabidopsis thaliana |
| phytochrome |
mediates |
developmental responses to light stimuli |
|
| E3 ubiquitin ligase (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) /SPA |
is |
key repressor of photomorphogenesis |
|
| (JK224, NPH1, PHOT1, RPT1, AT3G45780) LOV2-kinase expression in -5phot2-1 mutant |
is fully functional in restoring |
leaf expansion |
Arabidopsis thaliana |
| continuous far-red light and blue light |
were most effective |
NPA inhibition of hypocotyl elongation |
Arabidopsis thaliana |
| (FHY2, FRE1, HY8, PHYA, AT1G09570) |
works redundantly with phyB in regulating |
chlorophyll content |
Arabidopsis thaliana |
| (ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) |
shows correlation between expression and |
light sensitivity |
Arabidopsis thaliana |
| cryptochromes |
mediate |
light-regulated pathways |
|
| light-related transcription factors |
stimulate |
photomorphogenesis |
|
| (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) expression in hypocotyls |
is significantly elevated by |
blue light |
Arabidopsis thaliana |
| (HY5, TED 5, AT5G11260) and (HYH, AT3G17609) mutants |
exhibit dark-like hypocotyls in light |
dark-like hypocotyl phenotype |
Arabidopsis thaliana |
| homeostasis of (FHY1, FRY1, PAT3, AT2G37678) |
ensures |
proper photomorphogenic development under changing light conditions |
|
| absence of miRNA-biogenetic inconsistency mechanism |
could result in |
internal conflicts between miRNAs and light-responsive transcripts |
|
| (HY3, OOP1, PHYB, AT2G18790) |
is most important in mediating |
physiological responses |
Arabidopsis thaliana |
| cor27-2 cor28-2 |
hypocotyl growth is reduced compared with |
wildtype |
|
| (APRR5, PRR5, AT5G24470) mutant |
is hyposensitive to R light with regard to |
inhibition of hypocotyl growth |
|
| lincomycin-induced retrograde signaling |
occurs via |
GUN1-independent pathway |
|
| apocarotenoid signal (ACS) |
alters |
nuclear photomorphogenetic gene expression, including PhANGs |
|
| shading |
causes conversion of PfrB into |
inactive isoform (PrB) |
|
| photomorphogenic development |
is accompanied by |
developed chloroplasts |
|
| (AtbZIP, bZIP, AT1G68880) gene (HY5, TED 5, AT5G11260) |
is a positive regulator of |
photomorphogenic responses |
Arabidopsis thaliana |
| pifQhec1hec2 sextuple mutant |
exhibits |
hypocotyl length phenotype |
Arabidopsis thaliana |
| hypocotyl growth-inhibition response |
requires |
continuous irradiation over 3 d |
Arabidopsis thaliana |
| hy5-1 seedlings |
show significantly reduced |
(DDA1, AT5G41560) transcript levels |
Arabidopsis thaliana |
| (JK224, NPH1, PHOT1, RPT1, AT3G45780) |
acts as blue light receptor in |
rapid inhibition of hypocotyl elongation |
Arabidopsis thaliana |
| plant development |
responds to |
environmental cues |
|
| light induction of chloroplastic GS |
is mediated by |
phytochrome |
Arabidopsis thaliana |
| DOWN IN DARK AND AUXIN1 (DDA1, AT5G41560) |
functions in |
aspects of photomorphogenesis |
Arabidopsis thaliana |
| transcriptional cascades |
lead to |
subsequent photomorphogenic development |
Arabidopsis thaliana |
| GUN1-dependent plastid signals |
repressed |
cotyledon expansion in low fluence blue light |
Arabidopsis thaliana |
| photoreactivation experiment |
provides evidence that |
inhibition of hypocotyl growth in etiolated seedlings is a consequence of photodimer formation |
Arabidopsis thaliana |
| ELONGATED HYPOCOTYL 5 (HY5, TED 5, AT5G11260) |
is involved in |
photomorphogenesis |
Arabidopsis thaliana |
| cryptochrome |
acts in |
much slower response to hypocotyl elongation inhibition |
Arabidopsis thaliana |
| light |
is a major environmental determinant of |
plant morphology |
|
| dda1-1 ted5-1 double-mutant hypocotyls |
are similar to |
ted5-1 single mutant hypocotyls |
Arabidopsis thaliana |
| Arabidopsis cryptochromes |
regulate gene expression to affect |
developmental responses |
Arabidopsis thaliana |
| (AtMAX2, MAX2, ORE9, PPS, AT2G42620) mutant |
have longer hypocotyls and slightly smaller cotyledons under continuous red, far-red, and blue light compared with |
wild-type (WT) seedlings |
Arabidopsis thaliana |
| dark-grown dda1-1/+ seedlings |
produced hypocotyls intermediate in length between |
Col wild type and dda1-1 homozygotes |
Arabidopsis thaliana |
| bkk1-1 mutant |
did not show |
de-etiolated phenotypes |
Arabidopsis thaliana |
| differences in hypocotyl length |
are light dependent |
light |
|
| synergism between phytochrome B (HY3, OOP1, PHYB, AT2G18790) and cryptochrome 1 (ATCRY1, BLU1, CRY1, HY4, OOP2, AT4G08920) |
generates |
hysteresis in gene expression |
Arabidopsis thaliana |
| induction of (SPA1, AT2G46340) (SPA4, AT1G53090) (HY5, TED 5, AT5G11260) and (HYH, AT3G17609) genes |
showed no synergism between |
phytochrome B (HY3, OOP1, PHYB, AT2G18790) and cryptochrome 1 (ATCRY1, BLU1, CRY1, HY4, OOP2, AT4G08920) |
Arabidopsis thaliana |
| (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) /SPA complexes |
may modulate |
(AtERF#092, ERF1, ERF1B, AT3G23240) protein stability |
|
| blue light |
induces inhibition of |
hypocotyl elongation |
|
| (FHY2, FRE1, HY8, PHYA, AT1G09570) as light antenna |
enables rapid promotion of |
de-etiolation upon soil emergence |
|
| responses of leaves to unnatural environments |
provides the possibility to unravel |
complex developmental and functional interactions that normally occur in the natural light environment |
|
| stomatal responses to blue light |
could play a key role in |
photomorphogenetic mechanisms |
Festuca arundinacea |
| gain-of-function Cape Verde Islands QTL allele of the (AT-PHH1, ATCRY2, CRY2, FHA, PHH1, AT1G04400) gene ( -Cvi) |
was found to enhance |
cotyledon unfolding in the absence of blue light |
Arabidopsis thaliana |
| cry1cry2 mutant |
shows hypocotyl elongation indistinguishable from |
wild-type seedlings |
Arabidopsis thaliana |
| col-4 and cry1cry2 seedlings |
grown under |
continuous red light |
Arabidopsis thaliana |
| (ATPIN1, PIN1, AT1G73590) |
is crucial for |
photomorphogenesis |
Arabidopsis thaliana |
| hypocotyl elongation |
is under control of |
gibberellins |
Arabidopsis thaliana |
| phyE-1 mutant plants |
display |
internode growth between rosette leaves and early flowering |
Arabidopsis thaliana |
| HR and resistance to TCV conditioned by the R gene (HRT, RCY1, RPP8, AT5G43470) |
is independent of |
phytochromes A and B |
|
| (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) |
may play a role in |
plant photomorphogenesis |
Arabidopsis thaliana |
| photomorphogenic signals |
are sensed by |
photoreceptors |
|
| high irradiance |
results in |
short hypocotyls with expanded leaves in dicotyledonous seedlings |
|
| (HY5, TED 5, AT5G11260) |
is targeted for |
degradation in the dark |
Arabidopsis thaliana |
| photomorphogenic development |
is accompanied by |
photosynthetic gene expression |
|
| (ELF3, PYK20, AT2G25930) |
has phyB-dependent and -independent effects on |
hypocotyl growth |
Arabidopsis thaliana |
| CK and light signalling pathways |
operate independently and converge at regulation of |
stability of ELONGATED HYPOCOTYL 5 (HY5, TED 5, AT5G11260) |
Arabidopsis thaliana |
| brassinosteroids |
show opposite action to |
photomorphogenesis |
|
| plant development and physiology |
are strongly influenced by |
light spectrum of the growth environment |
|
| dark-induced transcript regulation |
is not apparent in |
dda1-1 ted5-1 double mutants |
Arabidopsis thaliana |
| (HY5, TED 5, AT5G11260) |
is absent in |
dark conditions |
Arabidopsis thaliana |
| novel cytokinin (CK)-regulated proteins |
role in |
initiation and/or execution of photomorphogenetic programme |
Arabidopsis thaliana |
| seedlings crossing litter layer of forest |
after which |
photomorphogenesis rules prevail |
Hymenaea courbaril |
| light-grown Arabidopsis seedlings |
exhibit |
open and expanded cotyledons |
Arabidopsis thaliana |
| light |
induces |
chloroplast differentiation |
|
| adventitious root formation |
requires |
light |
Arabidopsis thaliana |
| addition of blue light |
strongly inhibits |
hypocotyl growth |
|
| dda1-1 plants |
displayed aberrant hypocotyl elongation in |
dark |
|
| altered definitions of short days |
associated with |
different photomorphogenetic and circadian phenotypes |
Arabidopsis thaliana |
| (AGY1, AtcpSecA, SECA1, AT4G01800) transcript |
steadily accumulated, accompanying |
greening process of 4-d-old etiolated wild-type seedlings |
Arabidopsis thaliana |
| cryptochromes |
regulate |
development in plants |
|
| phytochrome B |
is most abundant in |
light-grown plants |
|
| (COI1, AT2G39940) |
is possible to be regulated directly or indirectly by |
light |
Arabidopsis thaliana |
| (DDA1, AT5G41560) |
negatively regulates |
hypocotyl elongation during photomorphogenesis |
Arabidopsis thaliana |
| Arabidopsis seeds |
were grown under |
white light at 50 μmol m−2 s−1 |
Arabidopsis thaliana |
| (HY5, TED 5, AT5G11260) activity |
contributes to |
(DDA1, AT5G41560) regulation |
Arabidopsis thaliana |
| irradiance |
can significantly modify |
mesophyll structure |
|
| light source (neon tubes) with prevailing far-red-to-orange light spectrum |
could be the cause of |
differing behaviour of stomata and mesophyll |
|
| guard cells |
could be more sensitive to far-red light than |
mesophyll receptors |
|
| increased endogenous cytokinin (CK) levels |
induces |
partial cotyledon opening |
Arabidopsis thaliana |
| conversion of etioplasts to chloroplasts |
occurs during |
de-etiolation |
|
| cryptochromes ( (ATCRY1, BLU1, CRY1, HY4, OOP2, AT4G08920) and (AT-PHH1, ATCRY2, CRY2, FHA, PHH1, AT1G04400) ) and red/far-red light receptor phytochromes |
regulate |
photomorphogenic responses |
Arabidopsis thaliana |
| variations in light quality |
act as |
photomorphogenic signals |
|
| dark-grown seedlings |
show nearly abolished |
GUS activity |
Arabidopsis thaliana |
| (ATDET1, DET1, FUS2, AT4G10180) (C22) |
controls the transcription of |
multiple genes involved in photomorphogenesis |
|
| spt-10 mutant |
displays |
large cotyledon phenotype |
Arabidopsis thaliana |
| CRYPTOCHROME (CRY) |
could enhance expression of |
(HY5, TED 5, AT5G11260) (HYH, AT3G17609) (SPA1, AT2G46340) and (SPA4, AT1G53090) |
Arabidopsis thaliana |
| lux-4 LUX-CRES lines |
complemented |
hypocotyl growth defect of lux-4 |
Arabidopsis thaliana |
| PHYTOCHROME RAPIDLY REGULATED1 (HLH1, PAR1, AT2G42870) |
is |
light-regulated transcript de-regulated in only one of (ATDET1, DET1, FUS2, AT4G10180) and pifq mutants |
Arabidopsis thaliana |
| (ATHY2, GUN3, HY2, AT3G09150) mutant |
is |
NASC resource |
Arabidopsis thaliana |
| (HY5, TED 5, AT5G11260) mutants |
exhibit |
long hypocotyl in light |
Arabidopsis thaliana |
| changes in Pc |
correlated with |
altered hypocotyl elongation phenotypes in the light |
|
| retrograde signal |
acts in |
signal-responsive cells |
Arabidopsis thaliana |
| COP1oe overexpression line |
is similar to |
(AT-PHH1, ATCRY2, CRY2, FHA, PHH1, AT1G04400) and UBP13oe seedlings |
Arabidopsis thaliana |
| (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) mutant |
has |
shorter hypocotyl |
Arabidopsis thaliana |
| photomorphogenesis |
is controlled by |
CRYPTOCHROME 2 (AT-PHH1, ATCRY2, CRY2, FHA, PHH1, AT1G04400) |
Arabidopsis thaliana |
| cotyledonary node |
is |
anatomically correct terminus |
Arabidopsis thaliana |
| CRLs |
regulate |
photomorphogenesis |
Arabidopsis thaliana |
| partial loss-of-function (ATRBX1, HRT1, RBX1, ROC1, AT5G20570) alleles |
showed |
long hypocotyls under blue, far-red and red light |
Arabidopsis thaliana |
| exogenously applied cytokinin (CK) |
causes |
reductions in hypocotyl elongation and leaf primordia initiation |
Arabidopsis thaliana |
| (GUN1, AT2G31400) seedlings |
show differences in hypocotyl elongation compared to |
wild-type seedlings |
Arabidopsis thaliana |
| DDB1 |
is directly linked to |
seedling photomorphogenesis |
Solanum lycopersicum |
| light signaling pathway |
converges with |
auxin signaling pathway |
Arabidopsis thaliana |
| Hymenaea courbaril |
exhibits |
shade tolerance |
Hymenaea courbaril |
| light |
induces |
photomorphogenesis |
|
| clonal descendants of the VBI-0 line |
were screened for |
auxin-autonomous growth and responsiveness to light manifested by chlorophyll synthesis |
Nicotiana tabacum |
| (HY5, TED 5, AT5G11260) |
is a key player in |
promotion of photomorphogenesis |
Arabidopsis thaliana |
| more than half of identified chloroplast proteins |
are up-regulated at the transcript level during |
light-induced photomorphogenesis |
Arabidopsis thaliana |
| developmental changes in photomorphogenesis |
depend on |
colour, intensity, direction, or photoperiod of light source |
|
| phyABDE quadruple mutant |
exhibited |
reduced cotyledon-expansion phenotype compared to wild-type |
Arabidopsis thaliana |