ライフサイエンスコーパス: petunia

1 assembly is not conserved between tomato and petunia.

2 ORISMATE MUTASE (PhCM1 and PhCM2) cDNAs from petunia.

3 t, and the economically important ornamental petunia.

4 sponsible for synthesis of methylbenzoate in petunia.

5 40 h in snapdragon and approximately 32 h in petunia.

6 es the flavonols required for germination in petunia.

7 eens of pollen/pollen tube cDNA libraries of petunia.

8 required for pollen germination in maize and petunia.

9 element may have utility for gene tagging in petunia.

10 ome of different inbred lines and species of Petunia.

11 ODO1 and other FVBP genes to the evening in Petunia.

12 igated in plants of the South American genus Petunia.

13 l in leaves but not flowers of nontransgenic petunias.

14 A-CoA) have previously been characterized in petunia, a plant with flowers rich in phenylpropanoid/be

15 Similarly, petunia acylsugars lack an acyl group at the R3' positio

16 Of the three identified petunia ADTs, expression of ADT1 was the highest in petu

17 such as tomato, pepper, tobacco, potato, and Petunia, all belonging to the Solanaceae family.

18 Like PH3, TTG2 can bind to petunia AN11 and the Arabidopsis homolog TTG1, complemen

19 f sequences of floral MADS-box proteins from petunia and found that the rate differences for 14 pairs

20 ontrolling crop timing and quality traits in Petunia and highlight the power of using multiple inters

21 attempted bulk isolation from protoplasts of Petunia and oat (Avena sativa).

22 logy to restorers in distantly related taxa (petunia and rice) than to PPRs elsewhere in the Mimulus

23 Petunia and snapdragon both synthesize methylbenzoate fr

24 n shown to enhance expression variegation in petunia and tobacco and to carry a hot spot for de novo

25 y increases zeatin levels, Sho expression in petunia and tobacco especially enhances the levels of ce

26 s resembling those of the Solanaceae species petunia and tobacco.

27 fingers similar to zinc finger proteins from petunia and wheat.

28 a, and Proliferating cell factor) genes from petunia, and have identified that these TCP-type transcr

29 , a regulator of anthocyanin biosynthesis in petunia, and more distantly related to those of the beta

30 Arabidopsis homolog TTG1, complement ph3 in petunia, and reactivate the PH3 target gene PH5.

31 d define aleurain homologues in Arabidopsis, Petunia, and tobacco cell extracts.

32 teins ANTHOCYANIN11 (AN11) (Petunia hybrida [petunia]) and TRANSPARENT TESTA GLABRA1 (TTG1) (Arabidop

33 nown to regulate anthocyanin accumulation in petunia anthers.

34 Genetically, the comparable step in the petunia anthocyanin pathway is controlled by the Anthocy

35 In turn, we demonstrate that the petunia AP2-type REPRESSOR OF B-FUNCTION (ROB) genes rep

36 s regulatory network in the Asterid model of petunia are similar to those in the Rosid model of Arabi

37 y genome sequences will enhance the value of Petunia as a model system for research on unique biologi

38 In Petunia, as in tobacco, fed radioactive Spd is bound to

39 a emit mostly benzaldehyde, while flowers of Petunia axillaris subsp. axillaris emit a mixture of vol

40 in a natural population of self-incompatible Petunia axillaris subsp. axillaris, and found that all t

41 ce suppression of Ph-4CL1 did not affect the petunia benzenoid scent profile, whereas downregulation

42 In petunia, both the nuclear Rf gene and mitochondrial CMS-

43 s are similar to a pollen-expressed RLK from petunia, but they are expressed later during pollen deve

44 s involved transformation of tomato with the Petunia chi-a gene encoding chalcone isomerase.

45 In Petunia, constitutive expression of PhLHY depressed the

46 te and phenylethyl benzoate, both present in petunia corollas, with similar catalytic efficiencies.

47 s for post-pollination ethylene synthesis in petunia corollas.

48 esis and sensitivity and ABA accumulation in petunia corollas.

49 no acid identity and are highly expressed in petunia corollas.

50 ated in snapdragon cv Maryland True Pink and petunia cv Mitchell flowers using a volatile ester, meth

51 ethanol benzoyltransferase was isolated from petunia cv Mitchell using a functional genomic approach.

52 Transcripts for petunia cyclotides and acyclotides encode the shortest k

53 rsor structure, their sequences suggest that petunia cyclotides mature via the same biosynthetic rout

54 which is moderately to highly repetitive in petunia, does not predominantly localise to constitutive

55 RNA is spatially and temporally regulated in petunia during plant development.

56 ly (snapdragon) and nocturnally (tobacco and petunia) emitting plants.

57 We recently reported the identification of a petunia enzyme, isoeugenol synthase 1 (PhIGS1) that cata

58 acid sequence is most similar to that of the petunia Epf1 protein, they possess an interfinger linker

59 g that Pszf1 may be the pea homologue of the petunia Epf1 zinc finger gene.

60 cide resistance by stable integration of the petunia EPSPS gene into the tobacco chloroplast genome u

61 In petunia, expression of the gene responsible for methylbe

62 in addition to 29-32 kDa aleurain homologs, Petunia extracts contain a protein of approximately 50 k

63 nd PhPHB2, sequences that we identified in a petunia floral expressed sequence tag (EST) database, sh

64 R (BEN) confines the C-function to the inner petunia floral whorls, in parallel with the microRNA BLI

65 Petunia flower petals emit large amounts of isoeugenol,

66 Interestingly, ODO1-silenced transgenic petunia flowers accumulated higher EOBI transcript level

67 ntrations of supplied phenylalanine (Phe) in petunia flowers and capture flux redistributions caused

68 We also found that petunia flowers contain an enzyme, PhEGS1, that is highl

69 plant system, we simultaneously decreased in petunia flowers expression of all three Phe ammonia lyas

70 Down-regulation of PhCHD expression in petunia flowers resulted in reduced CHD enzyme activity,

71 sotope labeling, and transient expression in petunia flowers reveal that BALDH is capable of oxidizin

72 near least squares optimization of data from petunia flowers supplied with either 75 or 150 mm(2)H(5)

73 e to the formation of benzenoid compounds in petunia flowers.

74 entification and characterization of a novel petunia gene encoding an enzyme belonging to the BAHD ac

75 onal genomics approach, we have identified a petunia gene encoding cinnamoyl-CoA hydratase-dehydrogen

76 with TRV containing CHS and a fragment of a petunia gene encoding for 1-aminocyclopropane-1-carboxyl

77 acco rattle virus (TRV) bearing fragments of Petunia genes resulted in systemic infection and virus-i

78 The petunia genome contains a gene encoding a 9,10(9',10') c

79 ry and differential screening to identify 22 petunia germinating pollen clones.

80 cific glycine-rich proteins (GRP) related to petunia GRP1 (ptGRP1) was examined in three species of m

81 Simple leaves, such as those of petunia, have a single unit of blade, whereas compound l

82 in regulatory proteins ANTHOCYANIN11 (AN11) (Petunia hybrida [petunia]) and TRANSPARENT TESTA GLABRA1

83 By characterization of a Petunia hybrida adenosine triphosphate-binding cassette

84 ML2 and two MIXTA-related genes, PhMYB1 from Petunia hybrida and AtMYB16 from Arabidopsis thaliana, i

85 nalyses of CCRs from Medicago truncatula and Petunia hybrida and of an atypical CAD (CAD2) from M. tr

86 SBP1 from Petunia hybrida and Solanum chacoense is a putative E3 u

87 We have isolated and characterized Petunia hybrida cv. Mitchell phenylacetaldehyde synthase

88 Petunia (Petunia hybrida cv. Mitchell) flowers, which emit large

89 The Sho gene from Petunia hybrida encodes an enzyme responsible for the sy

90 t a mixture of eugenol and isoeugenol, while Petunia hybrida flowers emit mostly isoeugenol with smal

91 Here, we used Petunia hybrida flowers, which are rich in Phe-derived v

92 A repetitive DNA sequence (RPS) from Petunia hybrida had previously been shown to enhance exp

93 The Petunia hybrida HAIRY MERISTEM (HAM) gene, a member of t

94 Petunia hybrida is a popular bedding plant that has a lo

95 ic expression of a MYB transcription factor, Petunia hybrida ODORANT1, to alter Phe and phenylpropano

96 ith high homology to the recently identified Petunia hybrida phenylacetaldehyde synthase involved in

97 Here, a gene encoding a Petunia hybrida plastidial cationic amino-acid transport

98 ation of a spontaneous mutable Hf1 allele in Petunia hybrida provided an opportunity to isolate and c

99 ind with a high degree of specificity to the Petunia hybrida S-ribonuclease.

100 ding Protein1 (Pi SBP1), almost identical to Petunia hybrida SBP1, which interacts with Pi SLFs, S-RN

101 with 59 to 61% sequence identity to petunia (Petunia hybrida) and potato (Solanum tuberosum) FLS.

102 proteins ANTHOCYANIN11 (AN11) from petunia (Petunia hybrida) and TRANSPARENT TESTA GLABRA1 (TTG1) fr

103 Using petunia (Petunia hybrida) as a model for vegetative branching, we

104 We show that the petunia (Petunia hybrida) C-clade genes PETUNIA MADS BOX GENE3 an

105 s tested by RNAi suppression of the petunia (Petunia hybrida) cinnamoyl-CoA reductase 1 (PhCCR1), whi

106 vestigate the metabolic pathways in petunia (Petunia hybrida) cv Mitchell leading from Phe to benzeno

107 ropenes (isoeugenol and eugenol) in petunia (Petunia hybrida) flowers have the precursor 4-coumaryl c

108 nalysis of the benzenoid network in petunia (Petunia hybrida) flowers revealed that both pathways yie

109 olated in a genetic mutant screen a petunia (Petunia hybrida) Gibberellic Acid Insensitive, Repressor

110 regulates anthocyanin synthesis in petunia (Petunia hybrida) has been characterized.

111 he AIS1 protein is 59% identical to petunia (Petunia hybrida) isoeugenol synthase 1 and displays appa

112 We have isolated a cDNA from petunia (Petunia hybrida) leaves encoding a putative protein of 2

113 fied two potential CoA-ligases from petunia (Petunia hybrida) petal-specific cDNA libraries.

114 Agrobacterium-mediated infection of petunia (Petunia hybrida) plants with tobacco rattle virus (TRV)

115 Experiments with germinating petunia (Petunia hybrida) pollen and boronate-affinity chromatogr

116 Petunia (Petunia hybrida) pollen requires flavonols (Fl) to germi

117 xpression of VvMYB4a and VvMYB4b in petunia (Petunia hybrida) repressed general phenylpropanoid biosy

118 is a glutathione S-transferase from petunia (Petunia hybrida) required for efficient anthocyanin expo

119 s, tobacco (Nicotiana tabacum), and petunia (Petunia hybrida) resulted in plants with GA deficiency a

120 we show that in the asterid species petunia (Petunia hybrida), AP2B/BLIND ENHANCER (BEN) confines the

121 In petunia (Petunia hybrida), EMISSION OF BENZENOIDS II (EOBII) cont

122 snapdragon (Antirrhinum majus), and petunia (Petunia hybrida).

123 ragrance in many flowers, including petunia (Petunia hybrida).

124 Flowers of the artificial hybrid Petunia hybrida, a cross between P. integrifolia and P.

125 ajus, Epilobium hirsutum, Nicotiana tabacum, Petunia hybrida, and the cereal crop Setaria italica to

126 lyses of genomic DNA from the progenitors of Petunia hybrida, as well as from Nicotiana tabacum, indi

127 repetitive hypermethylated DNA fragment from Petunia hybrida, attracts DNA methylation when transferr

128 In Petunia hybrida, SL transport within the plant and towar

129 In Petunia hybrida, volatile emissions are dominated by pro

130 s to be the orthologous gene of PhEOBII from Petunia hybrida, which contributes to the regulation of

131 ed in estolide biosynthesis in the stigma of Petunia hybrida.

132 ity with the flavonoid-3',5'-hydroxylases of Petunia hybrida.

133 anum lycopersicum; SlpreproHypSys), petunia (Petunia hybrida; PhpreproHypSys), potato (Solanum tubero

134 extensions, faba bean [Vicia faba], petunia [Petunia hybrida], and tobacco [Nicotiana tabacum]).

135 rt Mosaic Virus promoter was introduced into petunia in the sense and antisense orientations using Ag

136 erization of PiSLF, an S-locus F-box gene of Petunia inflata (Solanaceae).

137 d genetic and physical map of the S locus of Petunia inflata and identify any additional genes locate

138 sed S2 -SLF1 (SLF1 with an S2 -haplotype) of Petunia inflata for co-immunoprecipitation (Co-IP) and m

139 19 S haplotypes from a natural population of Petunia inflata in Argentina, used reverse transcriptase

140 Here, we show that SLF1 of Petunia inflata is itself subject to degradation via the

141 y of the 20 lysine residues in S(3)-RNase of Petunia inflata might be targets for ubiquitination.

142 Petunia inflata possesses S-RNase-based self-incompatibi

143 Petunia inflata S-locus F-box (Pi SLF) is thought to fun

144 ng that non-self interactions between PiSLF (Petunia inflata SLF) and S-RNase are stronger than self-

145 on and characterization of PiORP1, an ORP of Petunia inflata that interacts with the cytoplasmic kina

146 lination-induced petal senescence process in Petunia inflata using a number of cell performance marke

147 n-expressed receptor-like kinase of petunia (Petunia inflata), named PRK1, and we have shown by the a

148 calmodulin-like domain protein kinases from Petunia inflata, CALMODULIN-LIKE DOMAIN PROTEIN KINASE1

149 tdInsP2)-cleaving phospholipase C (PLC) from Petunia inflata, named Pet PLC1.

150 To identify the pollen S gene of Petunia inflata, we had previously used mRNA differentia

151 ity) locus regulates self-incompatibility in Petunia inflata; the S-RNase regulates pistil specificit

152 Flowers of Petunia integrifolia emit mostly benzaldehyde, while flo

153 total FVBP emission in PhCM1 RNAi knockdown petunias is reduced by approximately 60-70%, and total c

154 spatial distribution of cyclotides within a petunia leaf section by MALDI imaging and observed that

155 tion tagging experiment we have identified a petunia line that showed CK-specific effects including e

156 The genomes reveal that the Petunia lineage has experienced at least two rounds of h

157 ounts of unedited RPS12 protein in different petunia lines correlate with the abundance of unedited t

158 Conversely, transgenic petunia lines expressing VvMYBC2-L1 and VvMYBC2-L3 showe

159 Additionally, in the Petunia lines in which PhLHY expression was reduced, the

160 Different petunia lines were found vary in the extent of rps12 tra

161 ionone synthesis in the corollas of selected petunia lines, indicating a significant role for this en

162 In petunia, loss-of-function nam mutants result in embryos

163 the petunia (Petunia hybrida) C-clade genes PETUNIA MADS BOX GENE3 and FLORAL BINDING PROTEIN6 (FBP6

164 aditional model systems such as Arabidopsis, Petunia, maize or rice.

165 Petunia may have evolved at least two types of SLF prote

166 GS) approach to knock down PH4 expression in petunia, measured volatile emission and internal pool si

167 (PhCCoAOMT1) from the petals of the fragrant petunia 'Mitchell'.

168 iple forms of RPS12 proteins are produced in petunia mitochondria as a result of partial editing, we

169 ibosomal protein S12 are partially edited in petunia mitochondria.

170 nedited-specific antibodies are present in a petunia mitochondrial ribosome fraction.

171 osttranscriptional C-repression mechanism in petunia, most likely not existing in Arabidopsis.

172 Both maize and petunia mutants are self-sterile due to a failure to pro

173 tivity has a pleiotropic effect in maize and petunia mutants: pollen fertility as well as flavonoid s

174 Here, we reveal the involvement of PH4, a petunia MYB-R2R3 transcription factor previously studied

175 This gene is a member of the NAC domain [petunia NAM (no apical meristem) and Arabidopsis ATAF1,

176 main transcription factor, homologous to the Petunia NAM and Arabidopsis CUC proteins.

177 The petunia NAM and ArabidopsisATAF1 and CUC2 genes define t

178 cyclic peptides we called "acyclotides" from petunia of the agronomically important Solanaceae plant

179 tracts DNA methylation when transferred into Petunia or other species.

180 gene, STENOFOLIA (STF), and its orthologs in Petunia, pea, and Nicotiana sylvestris are required for

181 ADTs, expression of ADT1 was the highest in petunia petals and positively correlated with endogenous

182 s synthesized predominantly via arogenate in petunia petals and uncover a novel posttranscriptional r

183 ADT1 suppression via RNA interference in petunia petals significantly reduced ADT activity, level

184 In petunia petals, AN11 and the bHLH protein AN1 activate,

185 ed Phe ((2)H(5)-Phe) was supplied to excised petunia petals.

186 alcohol, for which activity was detected in petunia petals.

187 Petunia (Petunia hybrida cv. Mitchell) flowers, which em

188 protein with 59 to 61% sequence identity to petunia (Petunia hybrida) and potato (Solanum tuberosum)

189 The WD40 proteins ANTHOCYANIN11 (AN11) from petunia (Petunia hybrida) and TRANSPARENT TESTA GLABRA1

190 Using petunia (Petunia hybrida) as a model for vegetative bran

191 We show that the petunia (Petunia hybrida) C-clade genes PETUNIA MADS BOX

192 thesis was tested by RNAi suppression of the petunia (Petunia hybrida) cinnamoyl-CoA reductase 1 (PhC

193 sed to investigate the metabolic pathways in petunia (Petunia hybrida) cv Mitchell leading from Phe t

194 e phenylpropenes (isoeugenol and eugenol) in petunia (Petunia hybrida) flowers have the precursor 4-c

195 ic flux analysis of the benzenoid network in petunia (Petunia hybrida) flowers revealed that both pat

196 e have isolated in a genetic mutant screen a petunia (Petunia hybrida) Gibberellic Acid Insensitive,

197 work that regulates anthocyanin synthesis in petunia (Petunia hybrida) has been characterized.

198 The AIS1 protein is 59% identical to petunia (Petunia hybrida) isoeugenol synthase 1 and disp

199 We have isolated a cDNA from petunia (Petunia hybrida) leaves encoding a putative pro

200 we identified two potential CoA-ligases from petunia (Petunia hybrida) petal-specific cDNA libraries.

201 Agrobacterium-mediated infection of petunia (Petunia hybrida) plants with tobacco rattle vir

202 Experiments with germinating petunia (Petunia hybrida) pollen and boronate-affinity c

203 Petunia (Petunia hybrida) pollen requires flavonols (Fl)

204 itutive expression of VvMYB4a and VvMYB4b in petunia (Petunia hybrida) repressed general phenylpropan

205 AN9 is a glutathione S-transferase from petunia (Petunia hybrida) required for efficient anthocy

206 rabidopsis, tobacco (Nicotiana tabacum), and petunia (Petunia hybrida) resulted in plants with GA def

207 Here, we show that in the asterid species petunia (Petunia hybrida), AP2B/BLIND ENHANCER (BEN) con

208 In petunia (Petunia hybrida), EMISSION OF BENZENOIDS II (EO

209 haliana, snapdragon (Antirrhinum majus), and petunia (Petunia hybrida).

210 tant to fragrance in many flowers, including petunia (Petunia hybrida).

211 mato (Solanum lycopersicum; SlpreproHypSys), petunia (Petunia hybrida; PhpreproHypSys), potato (Solan

212 tly pollen-expressed receptor-like kinase of petunia (Petunia inflata), named PRK1, and we have shown

213 To gain a better understanding of EIN2, a petunia (Petunia x hybrida cv Mitchell Diploid [MD]) hom

214 sion of alpha-Gal was modified in transgenic petunia (Petunia x hybrida cv Mitchell).

215 We transformed petunia (Petunia x hybrida cv V26) with P(SAG12)-IPT.

216 nsitive tomato (Lycopersicon esculentum) and petunia (Petunia x hybrida) plants were conducted to det

217 In many flowering plants, such as petunia (Petunia x hybrida), ethylene produced in floral

218 e sheath extensions, faba bean [Vicia faba], petunia [Petunia hybrida], and tobacco [Nicotiana tabacu

219 The basil and petunia phenylpropene-forming enzymes belong to a struct

220 ction of chalcone synthase A transgenes into petunia plants can result in degradation of chalcone syn

221 action of PPR genes, we generated transgenic petunia plants expressing a functional tagged version of

222 red to wild-type MD and ethylene-insensitive petunia plants expressing the Arabidopsis etr1-1 gene fo

223 was validated using flowers from transgenic petunia plants in which benzyl CoA:benzyl alcohol/phenyl

224 est this hypothesis, we generated transgenic petunia plants in which the expression of BPBT, the gene

225 Transgenic petunia plants with reduced PhEIN2 expression were compa

226 vity also affected the overall morphology of petunia plants, resulting in larger flowers and leaves,

227 observed in ethylene-insensitive transgenic petunia plants.

228 ower abscission when expressed in tomato and petunia plants.

229 peptide fragments of F3GalTase purified from petunia pollen were used to isolate a full-length cDNA c

230 Petunia possesses self-incompatibility, by which pistils

231 e polymorphisms (SNPs) for the interspecific Petunia recombinant inbred line (RIL) population - P. ax

232 D APICAL DOMINANCE 1 (DAD1) genes of pea and petunia, respectively, are orthologous to MAX4 and funct

233 The Petunia restorer of fertility gene product is a mitochon

234 Down-regulating alpha-Gal in petunia results in an increase in freezing tolerance at

235 later during pollen development than is the petunia RLK.

236 using a cross-species method by hybridizing petunia samples to a 4 x 44 K Agilent tomato array.

237 pressed Cullin1 gene with high similarity to Petunia SI factors interacts genetically with a gene at

238 Reciprocal transfer of traits between Petunia species now shows that colour and scent are equa

239 The element is named Petunia Spm-like (Psl).

240 Petunia spp. synthesize acylsugars that are structurally

241 ermination-inducing constituent in wild-type petunia stigma extracts.

242 cylglycerol-based estolide polyesters in the petunia stigma.

243 The peptides were active in a petunia suspension culture bioassay at nanomolar concent

244 ene insensitive (44568) and Mitchell Diploid petunias, that multiple components of emission of volati

245 In Petunia, the polymorphic S-locus determines self/non-sel

246 ps of ASATs are predicted between tomato and petunia, these are not supported by biochemical assays.

247 way, have been isolated and characterized in petunia through reverse genetic and biochemical approach

248 lcone synthase (chs) co-suppression among 47 Petunia transformants.

249 topic labeling experiments were performed in petunia transgenic lines.

250 ty in the regulatory circuitry that controls petunia vacuolar acidification and Arabidopsis hair deve

251 SV), Tobacco vein clearing virus (TVCV), and Petunia vein clearing virus (PVCV), can generate episoma

252 oate emission, with minimal changes in other petunia VOCs.

253 d to the Trans Proteomic Pipeline project's 'Petunia' web interface, but can also be run as a command

254 n a better understanding of EIN2, a petunia (Petunia x hybrida cv Mitchell Diploid [MD]) homolog of t

255 lpha-Gal was modified in transgenic petunia (Petunia x hybrida cv Mitchell).

256 We transformed petunia (Petunia x hybrida cv V26) with P(SAG12)-IPT.

257 In Petunia x hybrida cv. 'Mitchell Diploid' floral fragranc

258 to the synthesis of FVBPs in the corolla of Petunia x hybrida cv. 'Mitchell Diploid'.

259 Recently an R2R3-MYB was identified in Petunia x hybrida line P720 to have a role in the transc

260 omato (Lycopersicon esculentum) and petunia (Petunia x hybrida) plants were conducted to determine if

261 In many flowering plants, such as petunia (Petunia x hybrida), ethylene produced in floral organs a