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1 ith the key signaling protein constitutively photomorphogenic 1 (COP1) and induction of UV-B-protecti
2 is study, we identify mammalian constitutive photomorphogenic 1 (COP1) as a novel E3 ubiquitin ligase
3 n dark-grown wild-type roots by constitutive photomorphogenic 1 (COP1) E3 ligase and 26S proteasome a
4 8(C231S,C335S) interacts with CONSTITUTIVELY PHOTOMORPHOGENIC 1 (COP1) in plants to initiate photomor
5                                 Constitutive photomorphogenic 1 (COP1) is a p53-targeting E3 ubiquiti
6                               CONSTITUTIVELY PHOTOMORPHOGENIC 1 (COP1) is an E3 ligase for a number o
7                     Arabidopsis constitutive photomorphogenic 1 (COP1) is an E3 ubiquitin ligase that
8            Here, we show that CONSTITUTIVELY PHOTOMORPHOGENIC 1 (COP1) is required for UV-B-induced n
9                             The constitutive photomorphogenic 1 (COP1) protein of Arabidopsis functio
10            E3 ubiquitin ligase, Constitutive Photomorphogenic 1 (COP1) regulates turnover of Adipose
11  followed by interaction with CONSTITUTIVELY PHOTOMORPHOGENIC 1 (COP1), a major factor in UV-B signal
12 on with the E3 ubiquitin ligase CONSTITUTIVE PHOTOMORPHOGENIC 1 (COP1), a master regulator of plant g
13                               Constitutively photomorphogenic 1 (COP1), a RING finger ubiquitin ligas
14  and their positive regulator CONSTITUTIVELY PHOTOMORPHOGENIC 1 (COP1), promotes hypocotyl growth to
15  by suppressing the activity of CONSTITUTIVE PHOTOMORPHOGENIC 1 (COP1), resulting in activation of th
16 th B-BOX PROTEIN 24 (BBX24) and CONSTITUTIVE PHOTOMORPHOGENIC 1 (COP1), which inhibit the transcripti
17 rphogenesis involves UVR8 and CONSTITUTIVELY PHOTOMORPHOGENIC 1 (COP1)-mediated repression of PIF4 tr
18 INTERACTING FACTOR 1 (PIF1) and CONSTITUTIVE PHOTOMORPHOGENIC 1 (COP1).
19      CAM7 works in concert with CONSTITUTIVE PHOTOMORPHOGENIC 1 and ELONGATED HYPOCOTYL 5, and plays
20  integrators DE-ETIOLATED 1 and CONSTITUTIVE PHOTOMORPHOGENIC 1 maintain heterochromatin in a deconde
21                         COP1 (constitutively photomorphogenic 1) is a RING-finger-containing protein
22 ulated development, the COP1 (constitutively photomorphogenic 1) protein is characterized by a RING-f
23 or of photomorphogenesis, COP1 (constitutive photomorphogenic 1), is not a chief regulator of the ear
24 attenuating the activity of the CONSTITUTIVE PHOTOMORPHOGENIC 1-SUPPRESSOR OF PHYA-105 1 (COP1-SPA1)
25 ds in etiolated roots of cop (constitutively photomorphogenic)1, cop9, and det (de-etiolated)1 mutant
26 ator of Cullins-1 (ROC1), and constitutively photomorphogenic-1.
27 s the smallest subunit of the constitutively photomorphogenic 9 (COP9) signalosome (CSN), which consi
28 rpins against subunits of the COnstitutively Photomorphogenic-9- (COP9-) signalosome (CSN) in somatic
29 reduced chlorophyll in leaves and additional photomorphogenic abnormalities when the seedlings are gr
30 r AtZFP1 in shoot development, downstream of photomorphogenic activation.
31                     We found that GI acts in photomorphogenic and circadian blue light signaling path
32 cial environmental signal that controls many photomorphogenic and circadian responses in plants.
33 part through downregulation of BNQ-dependent photomorphogenic and developmental signaling pathways.
34 a plant photoreceptor protein that regulates photomorphogenic and protective responses to UV light.
35  opposing in cis the promoting effect of the photomorphogenic and thermomorphogenic regulator Phytoch
36           Mutants of COP1 are constitutively photomorphogenic, and this has been attributed to their
37 lecular basis of translational regulation in photomorphogenic Arabidopsis thaliana, we adopted a ribo
38 mutant seedlings also display characteristic photomorphogenic cellular differentiation and elevated e
39 iate signal transduction pathways leading to photomorphogenic changes in development.
40         rfd3 and rfd4 belong to the group of photomorphogenic cop/det/fus mutants.
41 alizes in nuclear bodies with CONSTITUTIVELY PHOTOMORPHOGENIC (COP) 1, a RING motif-containing E3 lig
42                            This constitutive photomorphogenic (COP) phenotype was not observed for mu
43                 The pleiotropic CONSTITUTIVE PHOTOMORPHOGENIC (COP), DEETIOLATED (DET), and FUSCA (FU
44 the dark, N282 expression led to pleiotropic photomorphogenic cotyledon development, including cellul
45                 The pleiotropic constitutive photomorphogenic/deetiolated/fusca (cop/det/fus) mutants
46 duce the transition from skotomorphogenic to photomorphogenic development (deetiolation) in dark-germ
47 ance of COP1, a transcriptional repressor of photomorphogenic development [1] [2].
48 e-mediated blue light regulation of seedling photomorphogenic development and genome expression profi
49 ncluding shoot and root growth, vascular and photomorphogenic development and leaf senescence.
50 ithin the nucleus as a repressor of seedling photomorphogenic development and that high inactivation
51 ifically as a light-inactivable repressor of photomorphogenic development and to elucidate the functi
52 omponent mechanism in the broader control of photomorphogenic development by phytochrome and cryptoch
53 downstream regulators, dictate the extent of photomorphogenic development in a quantitative manner.
54 chanism between PIFs and HFR1 that underlies photomorphogenic development in Arabidopsis thaliana.
55 F3, and PIF4/5 as an underlying mechanism of photomorphogenic development in Arabidopsis thaliana.
56  complex initially defined as a repressor of photomorphogenic development in Arabidopsis.
57 gy is the collective repression of premature photomorphogenic development in dark-grown seedlings by
58 t abolish the complex result in constitutive photomorphogenic development in darkness and pleiotropic
59 etic screens, one for mutations resulting in photomorphogenic development in darkness and the other f
60 ys a key role in the repression of the plant photomorphogenic development in darkness.
61 ECs contributes to the coordination of skoto/photomorphogenic development in plants.
62 -box protein, positively regulates facets of photomorphogenic development in response to light.
63           Plant photoreceptors that regulate photomorphogenic development include red/far-red-light-a
64       Under conditions which induce or mimic photomorphogenic development including growth in the lig
65 e ability to switch from skotomorphogenic to photomorphogenic development is essential for seedling s
66 rs, allowing their accumulation and inducing photomorphogenic development of plants.
67 aliana seedlings grown under light display a photomorphogenic development pattern, showing short hypo
68               PIFs are central regulators of photomorphogenic development that act to promote stem gr
69 ochrome B (phyB) is the dominant receptor of photomorphogenic development under red light.
70 icotyledon seedling undergoes organ-specific photomorphogenic development when exposed to light.
71 Y5 is directly correlated with the extent of photomorphogenic development, and that the COP1-HY5 inte
72 y-photoreceptor system to induce appropriate photomorphogenic development, but at excessive levels, s
73 OP1 acts as a light-inactivable repressor of photomorphogenic development, but its molecular mode of
74      COP1 acts within the nucleus to repress photomorphogenic development, but light inactivates COP1
75 emitted by dysfunctional chloroplasts impact photomorphogenic development, but the molecular link bet
76  originally identified as a key regulator of photomorphogenic development.
77 ce of COP1 for the appropriate regulation of photomorphogenic development.
78 negatively regulate COP1, a key repressor of photomorphogenic development.
79 ucible genes, promoting their expression and photomorphogenic development.
80 ngs transitioning from dark to light undergo photomorphogenic development.
81 th intact WD-40 repeats are able to suppress photomorphogenic development.
82 , a bZIP protein and a positive regulator of photomorphogenic development.
83 anism for its control of gene expression and photomorphogenic development.
84 undance of COP1, an established repressor of photomorphogenic development.
85 s genes that are necessary for repression of photomorphogenic development.
86 sisting in etioplast development, and normal photomorphogenic development.
87 nes (BRASSINOSTEROID-6-OXIDASE, CONSTITUTIVE PHOTOMORPHOGENIC DWARF, and DIMINUTO) and one brassinost
88 upregulated under low N include CONSTITUTIVE PHOTOMORPHOGENIC DWARF, DWF4, and BRASSINOSTEROID-6-OXID
89 ar data support that SCF(EBF1/2) function as photomorphogenic E3s during seedling development.
90 yB double mutants were less sensitive to the photomorphogenic effects of UV-B.
91 le to unequivocally associate several of the photomorphogenic effects seen in phyB mutants with phyto
92   The light-induced stabilization of HFR1, a photomorphogenic factor targeted for degradation by COP1
93 ng pathways, also plays an important role in photomorphogenic growth and light-regulated gene express
94 omplex, which targets positive regulators of photomorphogenic growth for degradation by the proteasom
95 rapid differential growth through unilateral photomorphogenic growth inhibition.
96                     In dark-grown seedlings, photomorphogenic growth is suppressed by the action of t
97 same TFs that activate defence responses are photomorphogenic growth regulators.
98 rs have been implicated in the regulation of photomorphogenic growth, chlorophyll biosynthesis, chlor
99  HYPOCOTYL 5 (HY5), a critical regulator for photomorphogenic growth, is present in inner mesophyll c
100 5 work in an antagonistic manner to regulate photomorphogenic growth.
101 tion factors (TFs) and jasmonic acid (JA) in photomorphogenic growth.
102  triggering the transition from etiolated to photomorphogenic growth.
103 ortant roles than HYH in blue light-mediated photomorphogenic growth.
104 cting cellular GA distribution in skoto- and photomorphogenic hypocotyls, respectively.
105 actors (PIF1, 3, 4, and 5) is constitutively photomorphogenic in darkness establishes that these fact
106 d red or white light, phyA mutants are hyper-photomorphogenic in many respects.
107 /far-red photoreceptor phytochrome A and are photomorphogenic in the dark.
108 tubule dynamics for hours without triggering photomorphogenic inhibition of growth, we used Arabidops
109                           The root-perceived photomorphogenic inhibition of shoot greening demonstrat
110 ants that define four additional pleiotropic photomorphogenic loci and a null mutant allele of the pr
111 h arm of chromosome 4, and is not allelic to photomorphogenic loci identified previously.
112  which, cin4, is allelic to the constitutive photomorphogenic mutant fus9/cop10.
113            Through positional cloning of the photomorphogenic mutant hy1, the Arabidopsis HO (designa
114 niscent of the previously characterised dark-photomorphogenic mutant, de-etiolated 3 (det3); conseque
115       We report that a previously identified photomorphogenic mutant, hypersensitive to red and blue
116                        We report here that a photomorphogenic mutant, red and far-red insensitive 2-1
117            We have identified an Arabidopsis photomorphogenic mutant, sub1, which exhibits hypersensi
118 analysis, the data show that red1 is a novel photomorphogenic mutant.
119  the previously characterized constitutively photomorphogenic mutants (cop, det, fus, and shy).
120 tum) yg-2 and Nicotiana plumbaginifolia pew1 photomorphogenic mutants are defective in specific HO ge
121                             The constitutive photomorphogenic mutants cop1 and det1 did not show sign
122 nd the elg mutation acts additively with the photomorphogenic mutants phyB, hy1 and hy2.
123  chromosome 2, distinct from any other known photomorphogenic mutants.
124 toreceptor deficient plants and constitutive photomorphogenic mutants.
125 nd1-1 mutant displays a partial constitutive photomorphogenic phenotype and has defects in HY5 degrad
126  had the same ectopic lignification and dark-photomorphogenic phenotype as that of the det3 mutant.
127  compared to pif1, indicating that the hyper-photomorphogenic phenotype of phyA requires PIF1.
128 YHB-YFP plants, including their constitutive photomorphogenic phenotype, red light-regulated thermomo
129 at YHB(G767R) elicits selective constitutive photomorphogenic phenotypes in dark-grown phyABCDE null
130 ated based on their deetiolated/constitutive photomorphogenic phenotypes in the dark.
131 truncated form of PIF1 causes constitutively photomorphogenic phenotypes in the dark.
132                                          The photomorphogenic phenotypes of ATAF2 loss- and gain-of-f
133 ith this, the hec mutants partially suppress photomorphogenic phenotypes of both cop1 and pifQ mutant
134 mutant partially suppresses the constitutive photomorphogenic phenotypes of cop1-6 pif1 and of the qu
135 o explain the ectopic lignification and dark-photomorphogenic phenotypes of the det3 mutant.
136                                       Severe photomorphogenic phenotypes, including the defect of phy
137  blue light, and are compromised in multiple photomorphogenic processes, including seed germination,
138 or, and increases expression of constitutive photomorphogenic protein (COP)1.
139 ubiquitination by the E3 ligase constitutive photomorphogenic protein (COP1).
140 ouse double minute 2 (Mdm2) and constitutive photomorphogenic protein 1 (COP1).
141 on with the E3 ubiquitin ligase constitutive photomorphogenic protein 1 (COP1).
142                                              Photomorphogenic remodelling of seedling growth is a key
143  The subcellular localization of COP1, a key photomorphogenic repressor, is regulated by light in Ara
144  this transition, plants must rapidly remove photomorphogenic repressors accumulated in the dark.
145 gly inhibits hypocotyl elongation during the photomorphogenic response known as de-etiolation, the tr
146 uces the phosphorylation of cry2, triggering photomorphogenic responses and eventually degradation of
147 elatively little is known about the types of photomorphogenic responses and signal transduction pathw
148 notype, elg seedlings retain a full range of photomorphogenic responses and the elg mutation acts add
149                         Here, we examine two photomorphogenic responses in maize: inhibition of mesoc
150 w doses of UV-B light (280 to 315 nm) elicit photomorphogenic responses in plants that modify biochem
151 me blue light photoreceptors mediate various photomorphogenic responses in plants, including hypocoty
152 or ultraviolet-B (UV-B) light that initiates photomorphogenic responses in plants.
153 r specifically for UV-B light that initiates photomorphogenic responses in plants.
154                         UV-B light initiates photomorphogenic responses in plants.
155     The photoreceptor UVR8 mediates numerous photomorphogenic responses of plants to UV-B wavelengths
156 but not damage, occurs at low doses of UV-B, photomorphogenic responses of UV-B sensitive mutants wer
157 hotoreception, W233, W285, and W337, impairs photomorphogenic responses to different extents.
158 s a photoreceptor that specifically mediates photomorphogenic responses to ultraviolet (UV)-B in plan
159         UV RESISTANCE LOCUS8 (UVR8) mediates photomorphogenic responses to UV-B by regulating transcr
160 ceptor UV RESISTANCE LOCUS 8 (UVR8) mediates photomorphogenic responses to UV-B in Arabidopsis throug
161 ISTANCE LOCUS 8 (UVR8) specifically mediates photomorphogenic responses to UV-B wavelengths.
162 TOMORPHOGENIC 1 (COP1) in plants to initiate photomorphogenic responses to UV-B, although the interac
163                                              Photomorphogenic responses triggered by low fluence rate
164 UVR8) is a UV-B photoreceptor that initiates photomorphogenic responses underlying acclimation and UV
165                                      Whereas photomorphogenic responses were observed at low doses, h
166 K1 and LNK2 genes control circadian rhythms, photomorphogenic responses, and photoperiodic dependent
167 and degradation of PIFs triggers a series of photomorphogenic responses.
168 ceptors in plants and often regulate similar photomorphogenic responses.
169 nteractions to control pre-mRNA splicing and photomorphogenic responses.
170  tightly regulate gene expression to control photomorphogenic responses.
171 ribes a genetic tool for the manipulation of photomorphogenic responses.
172 zation of UVR8 are required for UV-B-induced photomorphogenic responses.
173 ate into the nucleus in red light to mediate photomorphogenic responses.
174 C80 motif and signal transduction to trigger photomorphogenic responses.
175 udies of phytochrome C (phyC) have suggested photomorphogenic roles for this receptor, conclusive evi
176 tigate which genes are involved in the early photomorphogenic root development of dark grown roots.
177 sting global effects not directly related to photomorphogenic signaling; and 12 (37%) lines displayed
178     Altogether, our results pinpoint MYCs as photomorphogenic TFs that control phytochrome responses
179 henotypes are intimately associated with the photomorphogenic transition in an organ-specific manner.
180 (COP1), which functions with UVR8 to control photomorphogenic UV-B responses.
181 ion; understanding the mechanisms underlying photomorphogenic variation is therefore of significant i

 
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