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1 ng pathway that is specifically activated by phytochrome A.
2 uired for normal photosensory specificity of phytochrome A.
3 sion in far-red light is regulated solely by phytochrome A.
4 uction of CHS is mediated almost entirely by phytochrome A.
5 cription factors, and cell receptors such as phytochrome A.
6 on mutant NA (delta7-69) and full-length oat phytochrome A.
7 GSH) pools via a coordinated regulation with phytochrome A.
8 utive photomorphogenic1 (COP1)-Suppressor of phytochrome A-105 (SPA) E3 ubiquitin ligase complex prom
9 Y PHOTOMORPHOGENIC1 (COP1) and SUPPRESSOR OF PHYTOCHROME A-105 (SPA)1 in vitro.
10 is region may be involved in down-regulating phytochrome A activity.
11                            The photoreceptor phytochrome A acts as a light-dependent molecular switch
12 ght photoreceptor for circadian control, and phytochrome A acts under low-intensity red light.
13 ive phytochrome and do not deplete levels of phytochrome A after red-light treatment.
14 light signaling by photoreceptors other than phytochrome A and additively increases ABA insensitivity
15 f the light-labile red/far-red photoreceptor phytochrome A and are photomorphogenic in the dark.
16                                              Phytochrome A and cryptochrome photoreceptors stabilize
17  synergistic signaling mediated through both phytochrome A and cryptochrome1 is required for damping
18  promoted proteasome-mediated degradation of phytochrome A and hypocotyl elongation under far-red lig
19 ed a similar interaction between Arabidopsis phytochrome A and phototropin 1 at the plasma membrane.
20                  Seedlings deficient in both phytochrome A and phytochrome B (phyA phyB), have a grea
21 in far-red and red light required functional phytochrome A and phytochrome B, respectively.
22 responses examined, including proteolysis of phytochrome A and phytochrome-interacting transcription
23 matic radiation, we show that the actions of phytochromes A and B (phyA and phyB) in Arabidopsis thal
24 In Arabidopsis thaliana the participation of phytochromes A and B (phyA and phyB) in the early phase
25 henotypes have established the importance of phytochromes A and B (phyA and phyB) in this development
26 on-photoactive carboxy-terminal fragments of phytochromes A and B and functions in phytochrome signal
27 fically with the photoactivated conformer of phytochromes A and B, suggesting a signaling pathway by
28 20-ox mRNA accumulation is regulated by both phytochromes A and B.
29 re consistent with the demonstrated roles of phytochromes A and B1 during seedling development and le
30 the procedure using monoclonal antibodies to phytochromes A and C (phyA and phyC), which are high- an
31 self is down-regulated by far-red light in a phytochrome A- and PAT1-dependent manner.
32 yA to phyE (phytochrome A holoprotein; PHYA, phytochrome A apoprotein; PHYA, phytochrome A gene; phyA
33       These results implicate leaf-localized phytochrome A as having a unique role in regulating FR-m
34  functional characterization of Avena sativa phytochrome A (AsphyA) as a potential protein kinase.
35 argely regulated by the redundant actions of phytochromes A, B and D.
36  analysis of a quadruple mutant deficient in phytochromes A, B, D, and E, which thus contains only ac
37  tissues, and the percent ratios of the five phytochromes, A:B:C:D:E, are measured as 85:10:2:1.5:1.5
38 /fus mutations are epistatic to mutations in phytochromes, a blue-light photoreceptor, and a downstre
39                           Cryptochrome 1 and phytochrome A both act to transmit low-fluence blue ligh
40 CAT3 mRNA oscillations specifically requires phytochrome A but not phytochrome B and also requires th
41         The data show that the N-terminus of phytochrome A contains two functional domains, one neces
42 e) are two homologous proteins essential for phytochrome A controlled far-red responses in Arabidopsi
43 nduction of all genes tested is blocked in a phytochrome A-deficient mutant, confirming that gene exp
44 howed that this far-red block of greening is phytochrome A dependent and requires an intact downstrea
45 of the tomato aurea mutant demonstrated that phytochrome A-dependent activation of rbcS and chs genes
46 he chromophore-bearing, N-terminal domain of phytochrome A did not induce short hypocotyls in light-g
47                              The Arabidopsis Phytochrome A epiallele, phyA', carries hypermethylation
48                                  Of the five phytochromes-a family of red/far-red light photoreceptor
49 ansduction component that appears to require phytochrome A for function in seedling photomorphogenesi
50  sativum) interact in vitro with recombinant phytochrome A from oat (Avena sativa).
51 ifs (GT1-bx, GT2-bx, and GT3-bx) in the rice phytochrome A gene (PHYA) promoter.
52 essed epi-allele of the Arabidopsis thaliana phytochrome A gene (PHYA) termed phyA' that shows methyl
53 , phytochrome A gene; phyA, mutant allele of phytochrome A gene), on immunoblots and have used them t
54 otein; PHYA, phytochrome A apoprotein; PHYA, phytochrome A gene; phyA, mutant allele of phytochrome A
55 n elements have been described for different phytochromes, a generalized understanding of signal proc
56 five Arabidopsis phytochromes, phyA to phyE (phytochrome A holoprotein; PHYA, phytochrome A apoprotei
57 rome polypeptides, we have overexpressed oat phytochrome A in Arabidopsis thaliana.
58    We show that transgenic overproduction of phytochrome A in tobacco suppresses shade avoidance, cau
59 s-IAA4 are phosphorylated by recombinant oat phytochrome A in vitro.
60 of the chromophore-binding module of soybean phytochrome A, including ~2.2 angstrom XFEL structures o
61  far-red light perceived by the light-labile phytochrome A, irrespective of whether they involve phot
62                                          Oat phytochrome A is a phosphoprotein.
63                            The N-terminus of phytochrome A is important for the structural integrity
64                                              Phytochrome A is the primary photoreceptor for mediating
65                             One phytochrome, phytochrome A, is highly light labile.
66 x transcription factor, is required for both phytochrome A-mediated far-red and cryptochrome 1-mediat
67 t that FIN219 may define a critical link for phytochrome A-mediated far-red inactivation of COP1 and
68                                 Furthermore, phytochrome A-mediated induction of CHS by red light is
69 he RSF1 gene strongly suggests that numerous phytochrome A-mediated responses require a bHLH class tr
70                       SPA1 is a repressor of phytochrome A-mediated responses to far-red light.
71               One likely explanation is that phytochrome A mediates the responses of these genes to c
72          Northern analysis demonstrated that phytochrome A mRNA in fruit accumulates 11.4-fold during
73 of deetiolation, in the wild type and not in phytochrome A mutant upon prolonged low R/FR.
74 hose products are required for light-induced phytochrome A nuclear accumulation and subsequent light
75 nal is similar in potato plants deficient in phytochrome A or PHYB and wild-type plants.
76      This light response, mediated by either phytochrome A or phytochrome B, represents a prime examp
77  Deletion analysis of Ps-IAA4 indicates that phytochrome A phosphorylation occurs on the N-terminal h
78 by temperature-dependent redundancy with the phytochrome A photoreceptor.
79 ns resembling chromophore-binding domains of phytochrome, a photoreceptor in plants.
80                                              Phytochrome A photoreceptors accumulate in shade and int
81  phytochrome B (PHYB(Y276H)) and Arabidopsis phytochrome A (PHYA(Y242H)) in transgenic Arabidopsis pl
82 ther Box II/-90GUS or Unit I/-46GUS with oat phytochrome A (phyA) and GTP gamma S, an activator of he
83 nly enhances light sensitivity downstream of phytochrome A (phyA) and modulates phyB function.
84           Here, we show that light-activated phytochrome A (phyA) and phytochrome B (phyB) interact w
85                   The far-red light receptor phytochrome A (phyA) and the bZIP transcription factor H
86 endent response of cryptochrome 2 (cry2) and phytochrome A (phyA) and their role as day-length sensor
87 ng protein by using the C-terminal domain of phytochrome A (PhyA) as the bait in yeast two-hybrid scr
88 ss multiple phytochrome photoreceptors, with phytochrome A (phyA) being light labile and other member
89   Photoconversion of the plant photoreceptor phytochrome A (phyA) from its inactive Pr form to its bi
90 ith arsenic tolerance and is inserted in the Phytochrome A (PHYA) gene, strongly reducing the express
91                                              Phytochrome A (phyA) is a photoreceptor of higher plants
92                                              Phytochrome A (phyA) is a red/far-red (FR) light photore
93                                              Phytochrome A (phyA) is crucial to initiate the early st
94                                              Phytochrome A (PHYA) is essential for the far-red (FR) h
95                                              Phytochrome A (phyA) is expected to be the only active p
96                           We identified that phytochrome A (phyA) is required for the morning FT expr
97                                  Among them, phytochrome A (PHYA) is responsible for the far-red high
98                                              Phytochrome A (phyA) is the major photoreceptor of deeti
99                                              Phytochrome A (phyA) is the photolabile plant light rece
100                                              Phytochrome A (phyA) is the primary photoreceptor for me
101                              In Arabidopsis, phytochrome A (phyA) is the primary photoreceptor mediat
102                                              Phytochrome A (phyA) is the primary photoreceptor respon
103                                              Phytochrome A (phyA) is the primary photoreceptor that r
104                                              Phytochrome A (phyA) is the single dominant photorecepto
105                            The photoreceptor phytochrome A (phyA) mediates various far-red light-indu
106 aracterization of a strong dominant-negative phytochrome A (phyA) mutation (phyA-300D) in Arabidopsis
107 ted for red-light-induced enhancement in the phytochrome A (phyA) null mutant, the phytochrome B- (ph
108 measure expression profiles in wild-type and phytochrome A (phyA) null-mutant Arabidopsis seedlings,
109                      Light signaling via the phytochrome A (phyA) photoreceptor controls basic plant
110                       These mutants lack the phytochrome A (phyA) photoreceptor.
111 nstream of the far-red (FR) light-responsive phytochrome A (PHYA) photoreceptor.
112 e five phytochromes in Arabidopsis thaliana, phytochrome A (phyA) plays a major role in seedling deet
113                                              Phytochrome A (phyA) plays a primary role in initiating
114                                              Phytochrome A (phyA) possesses two spatially different s
115  is due to a single amino-acid change in the phytochrome A (PHYA) protein.
116 red nuclear translocation, the photoreceptor phytochrome A (phyA) regulates gene expression under con
117                                  Arabidopsis phytochrome A (phyA) regulates not only seed germination
118  suggesting a locus likely to be involved in phytochrome A (phyA) signal transduction.
119    Consistent with a role of SPA proteins in phytochrome A (phyA) signaling, a phyA mutant had enhanc
120  in deep canopy shade can, together, trigger phytochrome A (phyA) signaling, inhibiting shade avoidan
121 lone from sorghum (Sorghum bicolor) encoding phytochrome A (PHYA) was fully sequenced, revealing 16 o
122                           In this study, oat phytochrome A (phyA), Arabidopsis phytochrome B (phyB) o
123 that CKI1 expression is under the control of phytochrome A (phyA), functioning as a dual (both positi
124  light, a response that is also modulated by phytochrome A (phyA), representing a classical example o
125 tic digest of the iodoacetamide-modified oat phytochrome A (phyA), the molecular surface topography o
126 ctive in signaling intermediates specific to phytochrome A (phyA), we screened for extragenic mutatio
127 dopsis genes, transcriptionally regulated by phytochrome A (phyA), were previously identified using a
128 nduced deetiolation is mediated primarily by phytochrome A (phyA), whereas red-light-induced deetiola
129  that phototropic enhancement is primarily a phytochrome A (phyA)-dependent red/far-red-reversible lo
130  result in dominant negative interference of phytochrome A (phyA)-mediated hypocotyl growth inhibitio
131    Moreover, imb1 seeds are deficient in the phytochrome A (phyA)-mediated very-low-fluence response
132  far-red light and therefore specific to the phytochrome A (phyA)-signaling pathway.
133 TRATE TRANSPORTER 1 (NRT1.1), and light, via PHYTOCHROME A (PHYA).
134  dawn, activates plant antiviral defense via phytochrome A (phyA).
135 tion in far-red light, which is perceived by phytochrome A (phyA).
136 romotion of greening, acting in part through phytochrome A (phyA).
137 t perceived through cryptochrome 2 (cry2) or phytochrome A (phyA).
138 chrome 1 (cry1) or cryptochrome 2 (cry2) and phytochrome A (phyA).
139 tors, especially the far-red light-absorbing phytochrome A, play a crucial role in early seedling dev
140 ght-dependent manner, with the photoreceptor phytochrome A playing a major role.
141 oring the biological activity of mutagenized phytochrome A polypeptides.
142 tional role of single protomer activation in phytochromes, a property that might correlate with the n
143 type of Arabidopsis seedlings overexpressing phytochrome A provides a simple visual assay for rapidly
144                              As anticipated, phytochrome A-regulated, nuclear-encoded transcripts wer
145          In this report, we have studied the phytochrome A regulation of a gene that is down-regulate
146 ions, SCL5 acts redundantly with the related PHYTOCHROME A SIGNAL TRANSDUCTION 1 (PAT1) and SCL21 tra
147 th SCL21 and PAT1 are positive regulators of phytochrome A signal transduction for several high-irrad
148 s deficient in a downstream component of the phytochrome A signal transduction pathway.
149         Thus, fhy1 defines a branch point in phytochrome A signal transduction pathways for gene expr
150 ve identified a new Arabidopsis mutant, pat (phytochrome A signal transduction)1-1, which shows stron
151 1 (PAT1), which are specifically involved in phytochrome A signal transduction.
152 psis thaliana), SCARECROW-LIKE21 (SCL21) and PHYTOCHROME A SIGNAL TRANSDUCTION1 (PAT1), which are spe
153  the positive clones encodes a member of the Phytochrome A Signal Transduction1 subfamily of GRAS (fo
154 transcription factors, are key components in phytochrome A signaling and the circadian clock.
155 d that FIN219 interacts closely with another phytochrome A signaling component, FHY1.
156 ed fin219, suggested that it defines a novel phytochrome A signaling component.
157 ing that although FHY1 is a component of the phytochrome A signaling pathway, it is not a component o
158 ein may act only on a discrete branch of the phytochrome A signaling pathway.
159               Several positive regulators of phytochrome A signaling--e.g., LAF1, HFR1, and HY5--oper
160            Upon activation by far-red light, phytochrome A signals are transduced through several pat
161    One way plants sense light is through the phytochromes, a small family of diverse photochromic pro
162                 COP1 acts with SUppressor of phytochrome A (SPA) proteins.
163 e nucleus, suggesting a possible function in phytochrome A-specific regulation of gene expression.
164 es are very similar to those of higher plant phytochrome A, supporting the conclusion that this speci
165 studies indicate that, with the exception of phytochrome A, the family of phytochrome photoreceptors
166                          As in the canonical phytochromes, a unique motif of the second GAF domain, t
167                      The plant photoreceptor phytochrome A utilizes three signal transduction pathway
168 region, a series of smaller deletions of oat phytochrome A were created, designated NB (delta49-62),
169 TYL IN FAR RED1/SLENDER IN CANOPY SHADE1 and phytochrome A, which function largely independently to n

 
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