ライフサイエンスコーパス: dicot

1 in modulating seed vigor in a monocot and a dicot.

2 out in Arabidopsis (Arabidopsis thaliana), a dicot.

3 single species of phylogenetically unrelated dicots.

4 ily following the divergence of monocots and dicots.

5 compound leafed species across monocots and dicots.

6 of other plants, including both monocots and dicots.

7 od zones but are limited to a few percent in dicots.

8 sponse may be conserved between monocots and dicots.

9 ast partially conserved between monocots and dicots.

10 that preceded the divergence of monocots and dicots.

11 ates the divergence of Arabidopsis from most dicots.

12 rectly predict gene function in monocots and dicots.

13 in biosynthetic pathway in both monocots and dicots.

14 verged before the divergence of monocots and dicots.

15 y was the ancestral state in the majority of dicots.

16 but prior to the separation of monocots and dicots.

17 scular pattern similar to that found in most dicots.

18 , as well as for comparisons of monocots and dicots.

19 ng mechanism is present in both monocots and dicots.

20 igh levels in the roots of both monocots and dicots.

21 lies, similar to those found in monocots and dicots.

22 ratios of the AS types between monocots and dicots.

23 ze and various homologs in other grasses and dicots.

24 mparison of NAC genes from both monocots and dicots.

25 ly predicted greater aridity favoring native dicots.

26 Thus, phasiRNAs show tremendous diversity in dicots.

27 achypodium, but only one chloroplastic GR in dicots.

28 basal monocot, whereas TAS4 is only found in dicots.

29 Like most dicots, A. thaliana microsporocytes undergo simultaneous

30 t a site that prevents aminoacylation by the dicot alanyl-tRNA synthetase, indicating that features i

31 d with monocot ryegrass (Lolium perenne) and dicot alfalfa (Medicago sativa) COMTs.

32 ly angiosperm radiation, the organs of woody dicots already were exploited in intricate and modern wa

33 cture to the members of the non-TIR class of dicots, although many do not code for a coiled-coil doma

34 5'- and 3'-UTRs of AhRbcS1 mRNA from the C4 dicot amaranth were linked to a gusA reporter gene.

35 s contrast with those found for another C(4) dicot, Amaranthus hypochondriacus, in which light was no

36 e frequency of stomatal development in model dicot and basal land plant species.

37 Using examples from several dicot and monocot genomes, we outline some pitfalls and

38 cycle, must therefore have originated before dicot and monocot lineages separated.

39 mechanisms underlying junction formation in dicot and monocot plants transformed using different pro

40 nnot be ascribed solely to divergence of the dicot and monocot protein sequences.

41 that MFP1 is conserved in a large number of dicot and monocot species.

42 olyclonal antibodies detect homologs in both dicot and monocot species.

43 ring for isoflavone production in non-legume dicot and monocot tissues.

44 -ZIP genetic module seems to be conserved in dicot and monocotyledonous species to prevent branching

45 uding 71, 220 and 14 promoters from monocot, dicot and other plants, respectively.

46 Positive products were obtained for 6 dicots and 31 monocots of 54 plant species tested.

47 nts in the xylan synthesis machinery in both dicots and grasses.

48 matic analysis revealed MIR828 homologues in dicots and gymnosperms, but only in one basal monocot, w

49 Homologs of SIM were detected in other dicots and in monocots but not in mammals or fungi.

50 Homologs of GBP were found in other dicots and in the monocot rice (Oryza sativa), as well.

51 d genes that have been identified to date in dicots and monocots along with their putative orthologs

52 e similarly large families suggest that both dicots and monocots have evolved with a large preexistin

53 The presence of linear cyclotides in both dicots and monocots suggests their ancient origin and ex

54 ealed that their composition is different in dicots and monocots, as well as for TATA and TATA-less p

55 lose homologues in other plant species, both dicots and monocots, but is not found in other kingdoms.

56 bins (Hbs) are found in different tissues of dicots and monocots, very little is known about hb genes

57 al conservation of BOP gene function between dicots and monocots, while phylogenetic analyses highlig

58 comparative study of four divergent taxa, in dicots and monocots, whose genomes have already been com

59 nscriptional activation applications in both dicots and monocots.

60 conserved within growing organs and between dicots and monocots.

61 resent in the most recent common ancestor of dicots and monocots.

62 ctionally distinct ATP synthase complexes in dicots and mosses.

63 ccharides found in the primary cell walls of dicots and nongraminaceous monocots, where they are thou

64 resenting a unique composition distinct from dicots and other monocots.

65 ediating cytokinin signaling in monocots and dicots and reveal how phytohormones can impact cytokinin

66 is and Medicago, with no correlation between dicots and rice.

67 dates the evolutionary split of monocots and dicots and that these proteins show conserved and novel

68 o AS landscapes conserved among monocots and dicots and uncovered AS events in plant defense-related

69 herbaceous dicots; and arborescent monocots, dicots, and conifers.

70 rent extensins from representative monocots, dicots, and gymnosperms, the pl 4.6 isozyme cross-linked

71 s that include one lower vascular plant, two dicots, and three monocots.

72 ic ferns; aquatic and terrestrial herbaceous dicots; and arborescent monocots, dicots, and conifers.

73 ized to date, the lower eudicot and magnolid dicot AP3 homologs contain distinctly different motifs f

74 The Mediterranean plant Thapsia garganica (dicot, Apiaceae), also known as deadly carrot, produces

75 the previously annotated plant genomes, the dicot Arabidopsis thaliana and the monocot Oryza sativa,

76 ajor angiosperm subclasses, specifically the dicot Arabidopsis thaliana and the monocot Oryza sativa,

77 Studies in the model dicot Arabidopsis thaliana have identified key transcrip

78 e, in which case genes cloned from the model dicot Arabidopsis thaliana provide an alternative route.

79 originate from several monocot species, the dicot Arabidopsis thaliana, and the moss Ceratodon purpu

80 manol biosynthesis has been dissected in the dicot Arabidopsis thaliana, which has green, photosynthe

81 ute approximately 90% of the IAA pool in the dicot Arabidopsis, whereas ester-linked conjugates and f

82 indices, and the entire genomes of the model dicot, Arabidopsis thaliana, and the model monocot and c

83 In the dicot, Arabidopsis thaliana, two catalase (CAT) genes, C

84 s, we show that RDN1 and RDN2 orthologs from dicots as well as a related RDN gene from rice (Oryza sa

85 that predate the divergence of monocots and dicots; at least three have been maintained in both line

86 In both dicots, blue light and UV-A radiation were the major sig

87 In dicots, both peroxidases and laccases are known to parti

88 max, Lupinus alba and Vicia faba, nonlegume dicots Brassica napus and Helianthus annus, and nonlegum

89 lar phenomenon has been described in several dicots, but in no other monocots.

90 Narea for agricultural legumes and nonlegume dicots, but not for cereal crops.

91 cted mutagenesis allows full comparison with dicot CADs and elucidates the potential signature sequen

92 s share many functional characteristics with dicot CBFs, including a general primary domain structure

93 Pectins, major components of dicot cell walls, are synthesized in a heavily methylest

94 he cross-species ESTs from within monocot or dicot class are a valuable source of evidence for gene p

95 tified CNSs were integrated in the PLAZA 3.0 Dicots comparative genomics platform together with new f

96 owering plants), including both monocots and dicots, contain small catalase gene families.

97 Interestingly, several dicots contained genes homologous to At2g28780 and a cog

98 cestral catalase gene common to monocots and dicots contained seven introns.

99 HvCBFs specifically bound monocot and dicot cor gene CRT elements in vitro under both warm and

100 t induces systemic disease resistance in the dicot cotton (Gossypium hirsutum).

101 these genes share conserved roles with their dicot counterparts in flower and inflorescence patternin

102 to correspond to the localizations of their dicot counterparts.

103 a sativa), the impact of retrotransposons on dicot crop genomes is not well documented.

104 Soybean is an important dicot crop producing edible oil and protein.

105 en reported from studies of both monocot and dicot crops, their wild relatives, and the plant model,

106 ding 2,4-D, with utility in both monocot and dicot crops.

107 enes at 137 MYA, and divergence of grass and dicot cytosolic PGK genes at 155 MYA.

108 ation of floral organ identity in the higher dicots depends on the function of a limited set of homeo

109 A function is conserved between monocots and dicots, despite their different stomatal morphologies, w

110 ant P450 families existed before the monocot-dicot divergence that occurred approximately 200 million

111 cestor of angiosperms but before the monocot-dicot divergence, there was a change in the selective co

112 within the nsLTP family predated the monocot/dicot divergence.

113 events in each species following the monocot/dicot divergence.

114 lasses of plant MTs that predate the monocot-dicot divergence.

115 s that these genes diverged prior to monocot/dicot divergence.

116 genetics of apomixis in monocots as well as dicots during the past 15 years.

117 EGaseA and weaker evidence for selection on dicot EGases and Glycine EGaseB.

118 In the dicot epidermis, cell lineage is an important factor in

119 Many angiosperm plants, including basal dicots, eudicots, and monocots, emit (E,E)-4,8,12-trimet

120 and are often conserved across crucifers and dicots, even though they are not under higher levels of

121 HDACs suggests a duplication event early in dicot evolution, followed by further diversification in

122 Arabidopsis reveals more synteny with other dicots (exemplified by cotton), and that additional, mor

123 Over 3 million public domain cereal and dicot expressed sequence tags were mapped onto the compl

124 lies is the ancestor of approximately 75% of dicot families, our results indicate that RNase-based se

125 ically important dioecious tree in the basal dicot family Lauraceae used in food and drugs and in the

126 CO(2) to Rubisco, was used to transform the dicot Flaveria bidentis.

127 ssion patterns in transgenic lines of the C4 dicot Flaveria bidentis.

128 isolated a second monocot gene (mPex2) and a dicot gene (tPex).

129 na, Capsicum, Datura, Trigonella, and Vigna, dicot genera that readily regenerate plants from mesophy

130 e nucleus, and chimaeric, half-monocot, half-dicot genes.

131 5-fold lower than in the best characterized dicot genome of Arabidopsis but 6- to 10-fold higher tha

132 nt to which Arabidopsis is representative of dicot genomes and also the degree to which gene loss and

133 rgeted, specific modification of monocot and dicot genomes using a variety of genome engineering appr

134 opsis is broadly representative of the other dicot genomes, there seems to be substantial variation e

135 Dicot glucuronoxylan consists of a linear backbone of be

136 occurred prior to the split of monocots and dicots >or=200 MYA.

137 ers are found in non-grass species (monocot, dicot, gymnosperm, and moss species) including Arabidops

138 Surprisingly, all HKT homologues known from dicots have a serine at the filter position in P-loop A,

139 lower GC content at the third position have dicot homologs but the high GC content transcripts tend

140 red for cell-to-cell movement in monocot and dicot hosts.

141 ost range isolate infecting both monocot and dicot hosts.

142 icates a conserved mechanism in monocots and dicots in responding to Zn deficiency.

143 pertoire of grasses has changed from that of dicots in their independent evolution since the two grou

144 erved intronic regions among angiosperms and dicots, in particular, correspond to alternatively-splic

145 Seed development in dicots includes early endosperm proliferation followed b

146 much as 10% on a dry weight basis while most dicots, including Arabidopsis, will accumulate less than

147 in seed-specific promoters from monocots and dicots indicates that organ and temporal specification b

148 Dicot-infecting geminiviruses carry genes that encode mu

149 Most dicot-infecting geminiviruses encode a replication enhan

150 the important role played by AU sequences in dicot intron recognition.

151 xyloglucan (XyG) found in the cell walls of dicots is a fucogalactoXyG with an XXXG core motif, wher

152 tive action of safeners between monocots and dicots is not known.

153 evolutionary divergence between monocots and dicots is responsible for distinctions in ISA function.

154 evolutionary divergence between monocots and dicots is responsible for the distinctions in ISA1 funct

155 ated and functionally characterized from the dicot larkspur (Consolida orientalis) the benzoxazinoid-

156 hting fundamental differences in monocot and dicot leaf development programs.

157 Dicot leaf primordia initiate at the flanks of the shoot

158 Dicot leaves are composed of a heterogeneous mosaic of j

159 vities decline in these osmotically stressed dicot leaves, while spermidine and spermine titers incre

160 tivity in barrel medic (Medicago truncatula, dicot, Leguminosae), poplar (Populus deltoides, dicot, S

161 rved in simple leafed species of monocot and dicot lineages and constitutes a potential key determina

162 with positive selection in both Glycine and dicot lineages and the proximity of rapidly evolving sit

163 s, predate the divergence of the monocot and dicot lineages, suggesting that they were a determinant

164 parate duplication events in the monocot and dicot lineages.

165 mitochondrial ALDH genes in the monocot and dicot lineages.

166 d prior to the divergence of the monocot and dicot lineages.

167 velopment have been demonstrated in numerous dicots, little is known about the function of these meri

168 accepted monolignol biosynthesis pathway in dicots may have functionally redundant paralogues in swi

169 D- and/or L-Ins(3,4,6) P(3), suggesting that dicots may share pathways of InsP(6) biosynthesis and br

170 des, of which three contain both monocot and dicot members, while two indicate class-specific diversi

171 uses complete male sterility, but not in the dicot model Arabidopsis (Arabidopsis thaliana) ecotype L

172 he flowering plant Arabidopsis thaliana is a dicot model organism for research in many aspects of pla

173 sistent with the evolution of TAS4 since the dicot-monocot divergence.

174 As opposed to the classically assumed dicot/monocot dichotomy, we found continuous variations

175 genome and have often been generalized as a dicot/monocot dichotomy.

176 somal processing proteases of higher plants (dicots, monocots) but not present in orthologs of animal

177 are present in diverse plant taxa, including dicots, monocots, lycophytes, and microalgae.

178 715 binding sites for 501 genes conserved in dicots, monocots, mosses, and green algae.

179 angiosperms, the context of the AUG codon in dicot mRNAs is aaA(A/C)aAUGGCu which is similar to the h

180 in contrast to studied cereals and nonlegume dicots, Narea was positively related to photosynthesis i

181 S lineage was recently reported from a basal dicot, no representative sequences have yet been found i

182 While routinely used in some dicots, no VIGS system was known for monocot plants unti

183 Endosperm proliferation in dicots not only provides nutrient supplies for subsequen

184 f collectively define 5'intron boundaries in dicot nuclei.

185 h in Solanaceae but not in other families of dicots or monocots.

186 cations after the divergence of monocots and dicots or that independent gene conversion-like events h

187 ith this observation, PAP1, PAP2, and MYB113 dicot paralogs show peptide and nucleotide footprints fo

188 iva), and wheat (Triticum aestivum); but the dicots pea (Pisum sativum), soybean (Glycine max Merr.),

189 from Arabidopsis phyC, the only full-length dicot phyC sequence available.

190 ntify introns in the genome of the reference dicot plant Arabidopsis thaliana and we demonstrate the

191 gradient is not observed in the genes of the dicot plant Arabidopsis.

192 One of the key events in dicot plant embryogenesis is the emergence of the two co

193 tical for 5' and 3' splice site selection in dicot plant nuclei and development of a model for pre-mR

194 . thaliana IRX10 and with a homolog from the dicot plant Plantago ovata, showing that xylan xylosyltr

195 Transcripts of typical dicot plant plastid genes undergo C-->U RNA editing at a

196 onal status of a wide variety of monocot and dicot plant species and helps them, whether directly or

197 Most monocot and dicot plant species preferentially expressed NLRs in roo

198 r in Arabidopsis thaliana than in most other dicot plant species that have been studied.

199 l expression of the Cas9/sgRNA system in two dicot plant species, Arabidopsis and tobacco, and two mo

200 encing (VIGS), has been demonstrated only in dicot plant species, where it has become an important to

201 has been used on tissues of both monocot and dicot plant species.

202 are unable to provide herbicide tolerance to dicot plant species.

203 rs in monocot plants and in Arabidopsis as a dicot plant, as a guide to efforts toward improving salt

204 Here, we identified several dicot plants (Euphorbiaceae and Cleomaceae) that produce

205 nd their acyclic variants were isolated from dicot plants of the Rubiaceae, Violaceae, Cucurbitaceae,

206 These results also suggest that monocot and dicot plants share a conserved signal transduction pathw

207 stigate the architecture of telomeres in the dicot plants Silene latifolia and Arabidopsis thaliana u

208 hey are best known for their cytotoxicity in dicot plants that leads to the induction of rapid tissue

209 ions preserved, at least between monocot and dicot plants(6,7).

210 s and other mammals, and between monocot and dicot plants, as well as providing evidence for similari

211 We show that similar to dicot plants, colonization of maize roots by T. virens i

212 information on hormone-mediated immunity in dicot plants, little information is available on monocot

213 ults demonstrate a role, in both monocot and dicot plants, of hemicellulose and pectin acetylation in

214 In most dicot plants, the SYP13II transcript is alternatively sp

215 facilitated group II splicing in monocot and dicot plants, we examined the mutant phenotypes associat

216 ocot genes can be alternatively processed in dicot plants, we have investigated both the efficiency o

217 pproach for the identification of CNSs in 10 dicot plants, yielding 1,032,291 CNSs associated with 24

218 at different stages during the evolution of dicot plants.

219 lcohol in the seed coats of both monocot and dicot plants.

220 trons prior to the divergence of monocot and dicot plants.

221 been shown to promote viral recombination in dicot plants.

222 t known whether this is a general pattern in dicot plants.

223 of CCoAOMT expression with lignification in dicot plants.

224 esis during normal growth and development in dicot plants.

225 d and used for immunolocalization in several dicot plants.

226 architectural variation of both monocot and dicot plants.

227 nserved noncoding sequences (CNSs) across 12 dicot plants.

228 of transcription factors in both monocot and dicot plants.

229 hol in the seed coats of several monocot and dicot plants.

230 rganelle marker lines have been generated in dicot plants; however, useful and reliable fluorescent o

231 occurred at 129 MYA, divergence of grass and dicot plastid PGK genes at 137 MYA, and divergence of gr

232 two decades; however, the mean trend for 18 dicot populations was -5.8% per year, but only -0.4% per

233 d leaves of C4 monocots (maize, sorghum) and dicots (Portulaca oleracea) in the dark or light, comple

234 Additionally, A. thaliana and other dicots possess a second E2, which contains two lipoyl do

235 n important hemicellulosic polysaccharide in dicot primary cell walls.

236 Evolutionary divergence between monocots and dicots probably explains the ability of ISA1 to function

237 een the model organism Arabidopsis and other dicots, providing areas of focus for further research.

238 ded soil cultivated with monocot (Wheat) and dicot (Rape) crop species.

239 transcripts and showed that, in contrast to dicots, root zeaxanthin epoxidase transcripts were uncha

240 ent were identified in Arabidopsis, but this dicot's developmental pattern and stomatal morphology re

241 ot, Leguminosae), poplar (Populus deltoides, dicot, Salicaceae), and switchgrass (Panicum virgatum, m

242 In grasses and in dicot secondary cell walls, the major hemicellulose is a

243 PRF1, PRF2, PRF3, and a distant dicot sequence formed a separate novel class, suggesting

244 A second group contained monocot and dicot sequences, including the known resistance genes, R

245 sistance gene Bs4 suggests that monocots and dicots share an ancient or convergently evolved mechanis

246 diverged in expression between monocots and dicots since their divergence.

247 d animals, made possible by the cloning of a dicot (soybean) ferritin gene presented here and the rec

248 5 sequences of Musa, a monocot, and Ixora, a dicot species (Rubiaceae).

249 ator [RUA]) that is conserved in monocot and dicot species and suggested that the -10 element plays o

250 The differences between the two C(4) dicot species in cotyledon cell differentiation may aris

251 tochondrial response across both monocot and dicot species indicate that the dual-functioning nature

252 xpressed sequence-tag collections from other dicot species provides an opportunity to assess gene con

253 precipitated OTC activity in all monocot and dicot species tested, and sodium dodecyl sulfate polyacr

254 d-plasmid junctions in plants comes from the dicot species tobacco and Arabidopsis.

255 n have been described in some detail for one dicot species, Arabidopsis, in which three paralogous bH

256 models shows differences between monocot and dicot species, but also suggests GC intron-specific bias

257 Interestingly, PtrCESA6 from aspen, a dicot species, shares maximum identity of 81-84% with th

258 ericentromeric heterochromatin in this model dicot species.

259 sses of MBD proteins are only represented in dicot species.

260 y but have little effect on weedy monocot or dicot species.

261 wall-related CesA member from Arabidopsis, a dicot species.

262 nents, Tic110 and Toc75, in both monocot and dicot species.

263 er and inflorescence morphology from that of dicot species.

264 nomics and proteomic research in monocot and dicot species.

265 udicot and eleven lower eudicot and magnolid dicot species.

266 d pollen-specific profilins from monocot and dicot species.

267 PuORF) that is present in varied monocot and dicot species.

268 ding survival strategies of two related wild dicot species: Rumex palustris and Rumex acetosa.

269 nstructed from a monocot specific isolate, a dicot specific isolate and broad host range isolate infe

270 wide, angiosperm specific, monocot specific, dicot specific, and those that were species specific.

271 al must have been evolved before the monocot-dicot split took place approximately 150 million years a

272 s that likely occurred following the monocot/dicot split.

273 xtension of isolated cell walls from various dicot stems and the leaves of amaryllidaceous monocots,

274 runcatula represent sister clades within the dicot subclass Rosidae.

275 ariation in seed carotenoids in monocots and dicots suggests a surprising overlap in the genetic arch

276 ry to the situation observed in heterologous dicot systems, efficient Ds excision in barley, a hetero

277 In the dicots, targets of those phasiRNAs include several large

278 e than 10% of the contigs from each of three dicot test species have no detectable homologue in Arabi

279 psis, specifically by identifying genes from dicot test species that are absent from Arabidopsis.

280 ene in maize, Sus3, which is more similar to dicot than to monocot SuSys.

281 ignol homodehydrodimerization as they are in dicots that have similar syringyl-guaiacyl compositions.

282 Unlike in Arabidopsis and other dicots, the class of NBS-LRR genes coding for a Toll and

283 In dicots, the xylan backbone of beta-(1,4)-linked xylosyl

284 enes was reconstructed using 74 loci from 15 dicot, three monocot, and one conifer species.

285 nomics approach and to tie them to the other dicots through the fully sequenced genome of Arabidopsis

286 t AtEFR can be transferred successfully from dicot to monocot species, further revealing that immune

287 ous gradient progressing from gymnosperms to dicots to monocots.

288 Bombardment of a highly expressed dicot tRNA(ala)(GAC) gene into Zea mays bz-E2 or bz-E5 c

289 identified for expression and utilization of dicot tRNAs also function in monocots.

290 The primitive RIPs evolved to the dicot type 1 related RIPs (like those from Caryophyllale

291 ne from a clade composed of both monocot and dicot type-B OsRRs complemented an Arabidopsis type-B re

292 s conserved across diverse taxa (monocots to dicots), unlike tomato, banana ripening requires at leas

293 In foliar organs of dicots, veins are arranged in a highly branched or retic

294 xtension of a variety of grass walls but not dicot walls.

295 rs should be functional in both monocots and dicots, we suggest that the native MuDR promoter be used

296 ons of auxin flows in vascular patterning in dicots, while two types of vascular pattern alterations

297 and tools for all crops, whether monocots or dicots, will be gained through an initiative, and each c

298 h, syringyl-guaiacyl lignin typical of other dicots, with prominent beta-aryl ether (beta-O-4), pheny

299 cing of GlcA residues in the major domain of dicot xylan might allow the xylan backbone to fold as a

300 In contrast to dicots, xylan in grasses is extensively modified by alph