ライフサイエンスコーパス: plant gene

1 s to downregulate the expression of a target plant gene.

2 e that houses intron and exon information of plant genes.

3 higher degree of expansion compared to other plant genes.

4 efficient method for targeted mutagenesis of plant genes.

5 technique for characterizing the function of plant genes.

6 assessing and characterizing the function of plant genes.

7 ted shared high sequence similarity to known plant genes.

8 high salinity induce the expression of many plant genes.

9 high salinity induce the expression of many plant genes.

10 ler understanding of the number and types of plant genes.

11 fy and isolate deletion mutants for targeted plant genes.

12 mber, small size, and close association with plant genes.

13 hat are correlated with circadian control of plant genes.

14 s names for plant-wide families of sequenced plant genes.

15 flanking regions of other nitrate-inducible plant genes.

16 (MITEs) recently found to be associated with plant genes.

17 limited on the role of MARs associated with plant genes.

18 quently found in and flanking many wild-type plant genes.

19 ffect of avr genes on the expression of such plant genes.

20 ctional conservation between these human and plant genes.

21 erage a "functional map-space" of homologous plant genes.

22 make targeted sequence changes in endogenous plant genes.

23 y temperature-sensitive alleles of essential plant genes.

24 s reveals the evolution of the expression of plant genes after speciation and whole genome duplicatio

25 the global regulation of hundreds of higher-plant genes, an event that is linked to the macroevoluti

26 We present a new WWW-based tool for plant gene analysis, the Arabidopsis Co-Expression Tool

27 e genome's average and is the highest of any plant gene analyzed to date.

28 n the euchromatinization and activation of a plant gene and expand the evidence for histone code cons

29 For these reasons, understanding plant gene and genome evolution is only possible if we c

30 biquitous in plants and play a major role in plant gene and genome evolution.

31 ed to the discovery of hundreds of imprinted plant genes and confirmed DNA and histone methylation as

32 or 1 (FAC1) is one of the earliest expressed plant genes and encodes an AMP deaminase (AMPD), which i

33 ferred from the analysis of intron phases of plant genes and from the comparison of two functionally

34 i) is widely used for functional analysis of plant genes and is achieved via generating stable transf

35 re created to apply controlled annotation to plant genes and plant ESTs: Mendel-GFDb is a database of

36 edge currently exists regarding the roles of plant genes and proteins in the Agrobacterium tumefacien

37 Relatively little is known about the role plant genes and proteins play in this process.

38 enes: the SURE (sucrose response element) of plant genes and the ChoRE (carbohydrate response element

39 evidence for a specific affinity between the plant genes and their cyanobacterial homologues.

40 sequences have been identified in endogenous plant genes and there are no reports of animal virus der

41 on-coding regions that are typical of higher-plant genes and use of highly conserved gene family-spec

42 ogether, which TFs work together to regulate plant genes, and how the combinations of these TFs are s

43 ntal approaches for functional validation of plant genes, and propose haploid strategies to reduce th

44 on of the Arabidopsis CAB2, as well as other plant genes; and (3) aspects of the physiological role o

45 rning we used coding and intron sequences of plant genes annotated in the GenBank.

46 infection in whole plants and that different plant genes are involved in eliciting the HR and the loc

47 Many plant genes are known to be involved in the development

48 ethods to generate targeted modifications in plant genes are not currently available.

49 However, many plant genes are organised in multigene families that exh

50 ical roles of the vast majority of imprinted plant genes are unknown, and the evolutionary forces sha

51 In plants, genes are imprinted primarily in the endosperm,

52 anscriptomics approach to identify parasitic plant genes associated with host factor recognition and

53 a view of the evolutionary history of every plant gene at the level of sequence, gene structure, gen

54 Here we characterize a plant gene, Atwbc19, the gene that encodes an Arabidopsi

55 erefore, are associated with both animal and plant genes, but the identity of these elements is strik

56 n, this gene cluster has been assembled from plant genes by gene duplication, neofunctionalization, a

57 tion overlap in the regulation of endogenous plant genes by monitoring changes in expression of appro

58 RNA silencing of endogenous plant genes can be achieved by virus-mediated, transient

59 Understanding the functions encoded by plant genes can be facilitated by reducing transcript le

60 Selectable markers derived from plant genes circumvent the potential risk of antibiotic/

61 is sp. PCC 6803 strain that expresses higher plant genes coding for a light-harvesting complex II pro

62 The plant gene complements the K. aerogenes ureG mutation, d

63 A newly identified plant gene confers partial resistance to a fungal pathog

64 posable elements, and it is likely that most plant genes contain legacies of multiple transposable el

65 Plant genes controlling the delivery of border cells and

66 n shuffling in two important nucleus-encoded plant genes: cytosolic glyceraldehyde-3-phosphate dehydr

67 Phytome serves as a glue between disparate plant gene databases both by identifying the evolutionar

68 ut also that the regulation of this class of plant genes dates back more than 400 million years.

69 The plant gene defines an ORF of 1,218 bp that, when the pro

70 Plants genes differ from those of animals in many ways,

71 nchor genome for the grasses will accelerate plant gene discovery in many important crops (e.g., corn

72 dopsis genes can provide a powerful tool for plant gene discovery, functional analysis and elucidatio

73 he development of biotechnological tools for plant gene disruption and repair have lagged behind the

74 he first analysis of small RNA expression in plant gene dosage variants.

75 These plant gene duplicates are mostly derived from whole geno

76 erization of amino acid substitutions in the plant gene eIF4E to evaluate the performance of these me

77 Over one-quarter of all plant genes encode proteins of unknown function that can

78 The KNOTTED class of plant genes encodes homeodomain proteins.

79 We report the characterization of a plant gene encoding a member of the BET subgroup of brom

80 tification and biotechnological utility of a plant gene encoding the tocopherol (vitamin E) biosynthe

81 ave identified three symbiotically regulated plant genes encoding a beta,1-3 endoglucanase (MtBGLU1),

82 strategy, we identified approximately 13,000 plant genes encoding peptides with common features: (i)

83 Unlike most other plant genes encoding small HSPs, expression of the RTM2

84 Plant genes encoding the subsequent steps in L-fucose sy

85 Two newly identified plant genes establish a novel signaling feedback from th

86 tion clusters have contributed profoundly to plant gene evolution.

87 The best-characterized plant gene exhibiting a complex antisense transcript pat

88 Most plant genes express certain isoforms at a significantly

89 version pathway could be reconstituted using plant genes expressed in Escherichia coli.

90 nown to produce a wide variety of changes in plant gene expression and function.

91 is an important mechanism for regulation of plant gene expression and virus-plant interactions.

92 tion, suggesting that this feature regulates plant gene expression at multiple levels.

93 The phytochrome photoreceptor family directs plant gene expression by switching between biologically

94 set of full-length cDNAs from Salk/Stanford/Plant Gene Expression Center/RIKEN.

95 Finally, the public Plant Gene Expression Database was developed as part of

96 ng new model for both the RNA processing and plant gene expression fields.

97 ch may be a ubiquitous mechanism to regulate plant gene expression in response to environmental stres

98 ibility and specificity of transmission, and plant gene expression in response to phytoplasmal infect

99 To characterize plant gene expression in the establishment of the symbio

100 basis for broad-based predictive modeling of plant gene expression in the field.

101 esponses include redox-controlled changes in plant gene expression in the nucleus and organelles.

102 Plant gene expression induced by oral secretions reveale

103 Controlled down-regulation of endogenous plant gene expression is a useful tool, but antisense an

104 n that differs from traditional views of how plant gene expression is controlled.

105 ver, the global influence of this feature on plant gene expression is still largely unclear.

106 The level of DNA methylation controls plant gene expression on a global level.

107 port describes an early divergence in global plant gene expression responses caused by a rhizobial de

108 We describe a chemically inducible plant gene expression system, with negligible background

109 and Drosophila, Gal4 is not ideal for use in plant gene expression technology.

110 ified a new regulatory mechanism controlling plant gene expression that is probably generally used, w

111 he contributions by transcription factors to plant gene expression will require increasing knowledge

112 To devise a general strategy for controlling plant gene expression with artificial transcription fact

113 The regulation of plant gene expression, necessary for development and ada

114 erstand the regulatory networks that control plant gene expression, tools are needed to systematicall

115 ion process that can be used to downregulate plant gene expression.

116 gnate binding elements in the engineering of plant gene expression.

117 ion and serve as a tool to decrease specific plant gene expression.

118 onal activators that can be used to regulate plant gene expression.

119 ental stimuli are transduced into changes in plant gene expression.

120 anslational regulation plays a major role in plant gene expression.

121 ce, suggesting a regulatory role of m(6)A in plant gene expression.

122 RNA-binding proteins are key regulators of plant gene expression.

123 d the prevalence of circadian oscillation in plant gene expression.

124 as well as provide insights about endogenous plant gene-expression mechanisms.

125 This is one of the largest plant gene families that has been sequenced from a singl

126 molecular evolutionary characteristics of 25 plant gene families, with the goal of better understandi

127 functional divergence of the FtsZ1 and FtsZ2 plant gene families.

128 acid substitution, we analyzed embryophyte (plant) gene families from TAED (The Adaptive Evolution D

129 The PlantTribes database is a plant gene family database based on the inferred proteom

130 of better understanding general processes in plant gene family evolution.

131 frequencies under continent-island models of plant gene flow to the data.

132 we present the first large-scale analysis of plant genes for CNSs.

133 In this survey of 5074 plant genes for their AUG context sequences, purines are

134 ch create opportunities for basic studies of plant gene function and agricultural trait manipulation

135 for comparative analysis of the evolution of plant gene function and development.

136 king, thereby frustrating efforts to dissect plant gene function and engineer crop plants that better

137 They are ideal vectors for understanding plant gene function because of their ability to cause sy

138 , adding a significant tool for the study of plant gene function.

139 es a valuable approach for new insights into plant gene functions.

140 aking directed DNA sequence modifications to plant genes (gene targeting) is at present lacking, ther

141 olecular isolation of economically important plant genes has been facilitated by the construction and

142 Several plant genes have been cloned that encode members of the

143 Although retrotransposons associated with plant genes have been identified, little is known about

144 e to dehydration' (ERD) genes are a group of plant genes having functional roles in plant stress tole

145 have been characterized as first examples of plant genes homologous to the animal trithorax genes.

146 d the avrPto-mediated signal induce a common plant gene in the elicitation of the HR.

147 flora, but little is known about the role of plant genes in establishing such associations.

148 s a powerful tool for functional analysis of plant genes in moss.

149 e recent molecular characterization of three plant genes in which mutations cause phenotypes that mim

150 plication of ancestral angiosperm (flowering plant) genes in elite cottons (Gossypium hirsutum and Go

151 set, the Institute for Genomic Research's 33 plant gene indices, and the entire genomes of the model

152 This study investigates the plant genes induced by harpins and the effect of avr gen

153 olves cloning a short sequence of a targeted plant gene into a viral delivery vector.

154 have identified, and are now characterizing, plant genes involved in 2,4,6-trinitrotoluene detoxifica

155 Recent studies that identified several plant genes involved in Agrobacterium-mediated transform

156 As a result, most plant genes involved in antiviral silencing were identif

157 osslinking of the cell wall, induces several plant genes involved in cellular protection and defence,

158 Plant genes involved in developmental reprogramming, wou

159 lationships and molecular interactions among plant genes involved in F. virguliforme resistance.

160 about the T-DNA integration process, and no plant genes involved in integration have yet been identi

161 active state of transgenes and of endogenous plant genes involved in physiological processes, includi

162 tional upregulation of several rhizobial and plant genes involved in S-assimilation, highlight the fu

163 gene silencing, we further demonstrate that plant genes involved in SA biosynthesis and signaling ar

164 Fewer than 20 plant genes involved in the nodulation process have been

165 n in symbiosis of a repertoire of fungal and plant genes involved in the transport and metabolism of

166 mutant, Deltayap1, was employed to identify plant genes involved in tolerance of oxidative stress.

167 ere, we show that aTI in Polgamma2 and other plant genes involves ribosome scanning dependent on sequ

168 Functional identification of plant genes is generally achieved by a combination of cr

169 tants in order to understand the function of plant genes is not well documented.

170 a comprehensive insight into the function of plant genes, it is crucial to assess their functionaliti

171 In plants gene knock-outs and targeted mutational analyses

172 (K27/H3) nucleosome methylation patterns of plant genes may be gene-, tissue- or development-regulat

173 In plants, genes may sustain extensive pleiotropic function

174 By screening for plant genes mediating metal tolerance we identified a wh

175 nvestigate the function of potentially every plant gene, methods to dissect virtually any aspect of t

176 ZFN-stimulated gene targeting at endogenous plant genes, namely the tobacco acetolactate synthase ge

177 dicates that Agrobacterium infection induces plant genes necessary for the transformation process whi

178 ve either been approved by the Commission on Plant Gene Nomenclature (CPGN), an organization of the I

179 ion is reflected by the absence in all three plant genes of the IRE, a highly conserved, noncoding se

180 In plants, genes of the GLUTAMATE RECEPTOR-LIKE (GLR) famil

181 nitiation sites appear to operate in several plant genes, often to expand protein targeting.

182 ng an orthology-based projection of nonmodel plant genes on the A. thaliana gene network.

183 e not found in any other previously reported plant genes or transposons, except for apple.

184 ay be the products of transgenes, endogenous plant genes or viral RNAs.

185 ery both the public and private databases of plant genes, over 50% of the sequences flanking these Hb

186 We also explore the prediction of plant gene-phenotype associations, as for the Arabidopsi

187 y focus is to display sets of highly curated plant genes predicted to encode proteins associated with

188 Sequence comparison between the plant gene product and the yeast lysine-forming and glut

189 Understanding plant gene promoter architecture has long been a challen

190 erful tool for the in vitro determination of plant gene regulation mechanisms.

191 These results have broad implications for plant gene regulation, where intron retention is widespr

192 ps one of the best examples of combinatorial plant gene regulation.

193 ng RNAs (siRNAs), are critical components of plant gene regulation.

194 An understanding of plant gene regulatory mechanisms at a systems level requ

195 d at deciphering the overall architecture of plant gene regulatory networks are starting to realize t

196 ower genes, clear cases of exon shuffling in plant genes remain to be uncovered.

197 To identify plant genes required for successful symbiotic infection,

198 The plant genes required for the growth and reproduction of

199 Several of the plant genes required for transduction of rhizobial signa

200 2-phenylethanol to flavor and fragrance, the plant genes responsible for its synthesis have not been

201 Our studies of plant genes reveal novel transcriptional regulation duri

202 Other related plant gene sequences in maize, rice, and Arabidopsis wer

203 Using a large set of plant gene sequences we compared individual introns to t

204 vidence, the Gramene pipeline can generate a plant gene set that is comparable in quality to the huma

205 nce and expression data for large numbers of plant genes should make it possible to dissect this and

206 Plant gene silencing was originally thought to be a quir

207 t homeotic genes are negatively regulated by plant genes similar to the repressors from the animal Pc

208 e a convenient and flexible means to disrupt plant genes, so allowing their function to be assessed.

209 synthesis, using the ecdysone receptor-based plant gene switch system and the ligand methoxyfenozide.

210 Our previous study using the plant gene switch system, a chemically induced gene expr

211 r-increasing number of alternatively spliced plant gene systems.

212 ost range transposable element available for plant gene tagging.

213 ould potentially boost their application for plant gene targeting.

214 Hence, altering a plant gene that critically facilitates compatibility cou

215 fic degradation of mRNAs from the endogenous plant gene that is targeted for silencing.

216 and DNA macroarrays, we identified numerous plant genes that are differentially expressed during ear

217 ay Dundee and allows rapid identification of plant genes that are up- or down-regulated by multiple t

218 Plant genes that contain the G-box in their promoters ar

219 Elucidating how allelic diversity within plant genes that function to detect pathogens (resistanc

220 The proportion of plant genes that have one or more alternative transcript

221 We enumerate plant genes that impart nonhost resistance and the bacte

222 orhizobium meliloti would identify regulated plant genes that likely condition key events in nodule i

223 ating regulatory variability for a subset of plant genes that may ultimately lead to evolutionary div

224 Several previously identified plant genes that play a role in immunity were found to a

225 are a viable tool for the identification of plant genes that regulate cell death.

226 Many plant genes that respond to environmental and developmen

227 agated between these elements and endogenous plant genes that share sequence homology.

228 Unlike many plant genes that undergo duplication, GalAK occurs as a

229 To facilitate the characterization of plant genes, the Cre-loxP site-specific recombination sy

230 otic stress activates the expression of many plant genes through ABA-dependent as well as ABA-indepen

231 effective system for functional analysis of plant genes through gene silencing.

232 w temperature induces the expression of many plant genes through undefined signaling pathways.

233 ses also activate the expression of numerous plant genes through undefined signaling pathways.

234 ion of AtNHX1 by NaCl and the ability of the plant gene to suppress the yeast nhx1 mutant suggest tha

235 The response of some plant genes to glucose analogues 3-O-methylglucose (3OMG

236 es (VEGF-A, HoxB13, and CFTR), an endogenous plant gene (tobacco SuRA), and a chromosomally integrate

237 n, regulates its own expression, and induces plant gene transcription.

238 s engineered to carry sequences derived from plant gene transcripts activate the host's sequence-spec

239 growth of the fungal symbiont; however, the plant genes underlying this process are largely unknown.

240 trons have been inserted into vertebrate and plant genes, whereas, in other lineages, intron gain was

241 re providing knowledge about the function of plant genes with an unprecedented clarity and quantity.

242 a genuine plant photolyase gene and that the plant genes with homology to type I photolyases (the cry

243 ne of Arabidopsis is a member of a family of plant genes with similarities to bacterial membrane tran

244 In plants, genes within small duplications (<100 kb) often