ライフサイエンスコーパス: Brassicaceae

1 lier, inbreeding, colonizer Cakile edentula (Brassicaceae).

2 selenium (Se) hyperaccumulation in Stanleya (Brassicaceae).

3 using the perennial plant Boechera stricta (Brassicaceae).

4 wild population of Erysimum mediohispanicum (Brassicaceae).

5 curred specifically in the Camelineae tribe (Brassicaceae).

6 ) preceded the diversification of crucifers (Brassicaceae).

7 species, Plutella xylostella, which feeds on Brassicaceae.

8 vestigate triterpene biosynthesis across the Brassicaceae.

9 rgoing tandem duplication in the ancestor of Brassicaceae.

10 n vivo investigation of the roles of MatR in Brassicaceae.

11 unction for a VRN2-like VEFS gene beyond the Brassicaceae.

12 ound composition, and of a distantly related Brassicaceae.

13 ay does not show cross-reactivity with other Brassicaceae.

14 obscured by the loss of the SoPIN1 clade in Brassicaceae.

15 m segmental and tandem duplication events in Brassicaceae.

16 ly of cytochrome P450 enzymes is specific to Brassicaceae.

17 have marked the evolutionary history of the Brassicaceae.

18 and signaling events that underlie SI in the Brassicaceae.

19 tbreeding mode of sexual reproduction in the Brassicaceae.

20 Cleomaceae is the family closest to Brassicaceae.

21 imary dormancy induction mechanism(s) in the Brassicaceae.

22 he self-pollen rejection response within the Brassicaceae.

23 the second intron of AG orthologs throughout Brassicaceae.

24 era stricta, but not in less closely related Brassicaceae.

25 belongs to one such group, the plant family Brassicaceae.

26 giosperm lineages, including the Poaceae and Brassicaceae.

27 some that are specific to Arabidopsis or the Brassicaceae.

28 in the self-incompatibility response of the Brassicaceae.

29 death and defense across the Solanaceae and Brassicaceae.

30 the diversification of plant architecture in Brassicaceae.

31 lyses indicated that the BPEPs are unique to Brassicaceae.

32 romosome regions in 21 species of the family Brassicaceae.

33 in Arabidopsis and some other members of the Brassicaceae.

34 nent of the extracellular pollen coat in the Brassicaceae.

35 ated in Arabidopsis and other members of the Brassicaceae.

36 ng oleosin-like proteins is described in the Brassicaceae.

37 hock on genomic components of Brassica nigra Brassicaceae.

38 e been conserved during the evolution of the Brassicaceae.

39 fter divergence of Aethionema from the other Brassicaceae.

40 immune signaling in most plants, except the Brassicaceae.

41 at distinguish simple from complex leaves in Brassicaceae.

42 rmed successive sister groups to the rest of Brassicaceae.

43 y explain fruit-shape diversification in the Brassicaceae.

44 and conserved in SARD1 orthologs within the Brassicaceae.

45 fferent degrees of diploidization across the Brassicaceae.

46 large sesterterpene repertoire in the wider Brassicaceae.

47 y contribute to reproductive barriers in the Brassicaceae.

48 n that differs from the ancestral one in the Brassicaceae.

49 activity between members of the Poaceae and Brassicaceae.

50 the different composition of the seed oil in Brassicaceae.

51 of new LD organelles, such as tapetosomes in Brassicaceae.

52 udied POLYCOMB REPRESSIVE COMPLEX2 (PRC2) in Brassicaceae.

53 c), the causal agent of black rot disease of Brassicaceae.

54 nctional divergence of the PRC2 complexes in Brassicaceae.

55 ration of seed dormancy functions across the Brassicaceae.

56 lready present early in the evolution of the Brassicaceae.

57 (Brassicaceae), a diverse genus of flowering plants nativ

58 logy, and ecophysiology in Boechera stricta (Brassicaceae), a perennial forb native to the Rocky Moun

59 d with leaves and roots of Boechera stricta (Brassicaceae), a perennial wild mustard.

60 rphic chemical defences in Boechera stricta (Brassicaceae), a short-lived perennial wildflower.

61 We propose that during early evolution of Brassicaceae, a duplicate oleosin gene mutated from expr

62 the largest variation in floral structure in Brassicaceae, a family in which the floral ground plan i

63 In Brassicaceae, a tandem oleosin gene cluster of five to n

64 al species, including various members of the Brassicaceae and Apiaceae family.

65 BSU1-type genes are exclusively found in the Brassicaceae and display a remarkable sequence divergenc

66 e that is one of the most widespread GSLs in Brassicaceae and has also been associated with growth in

67 at RPM1 evolved before the divergence of the Brassicaceae and has been deleted independently in the B

68 rsely, AtPOT1b and other POT1b homologs from Brassicaceae and its sister family, Cleomaceae, naturall

69 ast two important SI systems employed in the Brassicaceae and Papaveraceae.

70 mic data elucidate early genome evolution in Brassicaceae and pave the way for future whole-genome se

71 y of SINEs, named BoS, that is widespread in Brassicaceae and present at approximately 2000 copies in

72 fication and characterization of RGAs in the Brassicaceae and provides a framework for further studie

73 They occur in the Brassicaceae and related families.

74 ervation of inherited resistance in both the Brassicaceae and Solanaceae suggests that this trait may

75 ibuted flowering plant families (Asteraceae, Brassicaceae and Solanaceae).

76 arious time periods through the evolution of Brassicaceae and that active elements may still reside i

77 n response in Sisymbrium irio (Lineage II of Brassicaceae) and tobacco, indicating that activity of t

78 gens of diverse plant species, primarily the Brassicaceae, and cause infections that suppress host im

79 plants of the Poaceae, Fabaceae, Asteraceae, Brassicaceae, and Cucurbitaceae that were given l-(35)S-

80 ht into the conservation of ABI1 function in Brassicaceae, and understand better its regulatory effec

81 this short conserved sequence, including the Brassicaceae, and we propose an evolutionary scenario to

82 chitectures of the endosperms of two related Brassicaceae, Arabidopsis (Arabidopsis thaliana) and the

83 The Brassicaceae are also outliers in the sense that they ha

84 T oleosins in Brassicaceae are encoded by rapidly evolved multitandem

85 y dated major splits within the evolution of Brassicaceae are essential.

86 Initial pollen-pistil interactions in the Brassicaceae are regulated by rapid communication betwee

87 or the oleic and eicosenoic substrates among Brassicaceae, as well as their incorporation to triacylg

88 n domain in A. thaliana and other members of Brassicaceae but Kin17 domain in G.hirsutum.

89 in the Se hyperaccumulator Stanleya pinnata (Brassicaceae) by comparing it with the related secondary

90 (parsley and carrot), Asteraceae (lettuce), Brassicaceae (cabbage and broccoli), and Solanaceae (tom

91 microgreens species/subspecies representing Brassicaceae, Chenopodiaceae, Lamiaceae, Malvaceae and A

92 The Brassicaceae consists of a wide range of species, includ

93 a indicate that oilseed plants in the family Brassicaceae contain at least one to three seed-up-regul

94 The angiosperm family Brassicaceae contains both the research model Arabidopsi

95 or for enhancing root defense systems of non-Brassicaceae crops.

96 Diversification of the Brassicaceae crown group started at the Eocene-to-Oligoc

97 The clade diverged from other Brassicaceae crown-group clades during the Oligocene, fo

98 zed analyses of comparative genomics data in Brassicaceae (crucifer) plants.

99 The Brassicaceae (Cruciferae) family, owing to its remarkabl

100 , or the Hesperis clade, is one of the major Brassicaceae (Crucifereae) clades, comprising some 48 ge

101 In self-incompatible members of the Brassicaceae (crucifers), the inhibition of "self"-polle

102 the beta- and alpha-WGD events shared by all Brassicaceae, cytogenetic and transcriptome analyses rev

103 , which are typical of the > 3000 species of Brassicaceae, develop from a gynoecium that consists of

104 Brassicaceae display extensive variation in the mixture

105 ith other exocyst subunits, functions in the Brassicaceae dry stigma to deliver cargo-bearing secreto

106 Four varieties of Brassicaceae (Duchy, Scots Kale, Kale, Kalorama) and Pru

107 ology and phenology in Arabidopsis thaliana (Brassicaceae) due to contemporary climate change.

108 Two Brassicaceae (Eruca sativa, Brassica oleracea var. sabau

109 ploidy, and lineage separation events during Brassicaceae evolution are clustered in time around epoc

110 A number of species within the Brassicaceae express sporophytic self-incompatibility, u

111 ombined into four databases to represent the Brassicaceae, Fabaceae, Gramineae and Solanaceae familie

112 sponse to eMax seems to be restricted to the Brassicaceae family and also varied among different acce

113 Weeds from Brassicaceae family are a major threat in many crops inc

114 The Brassicaceae family comprises c. 4000 species including

115 Although the Brassicaceae family evolved from other eudicots at the b

116 xtending this method to other species in the Brassicaceae family identified centromere-linked clones

117 The Brassicaceae family includes the most important plant mo

118 of T. goesingense SAT in the nonaccumulator Brassicaceae family member Arabidopsis was found to caus

119 e-step hydrothermal method using a series of Brassicaceae family members (i.e. radish, cabbage, brocc

120 Of these, almost one-quarter are Brassicaceae family members, including numerous Thlaspi

121 y of biennial and perennial plants including Brassicaceae family plants.

122 RCO evolved in the Brassicaceae family through gene duplication and was los

123 (a member of the Brassicaceae family) via a transesterification procedure

124 racterize the flowers of most species in the Brassicaceae family, and this phenotype is generally rob

125 ficinale (watercress), a wild species of the Brassicaceae family, in which submergence enhances stem

126 Members of the Brassicaceae family, including Arabidopsis thaliana and

127 vy metal hyperaccumulator model plant in the Brassicaceae family, is a morphologically and phenotypic

128 aria blight continues to infect crops in the Brassicaceae family, leading to yield losses in Brassica

129 In members of the Brassicaceae family, such as Arabidopsis (Arabidopsis th

130 ning process activated in plants outside the Brassicaceae family, where SSP orthologs are absent?

131 thogen entry and are lineage specific to the Brassicaceae family.

132 latory changes in fruit evolution within the Brassicaceae family.

133 ng issues in the evolution of species in the Brassicaceae family.

134 rring in all the vegetables belonging to the Brassicaceae family.

135 a, a globally cultivated oilseed crop of the Brassicaceae family.

136 log expression dominance relationships among Brassicaceae genomes have contributed to selection respo

137 Systematic analysis of 13 sequenced Brassicaceae genomes was performed to identify all OSC g

138 alyses with preset karyotype patterns of the Brassicaceae genomes.

139 Comparative genomics in the Brassicaceae has largely focused on direct comparisons b

140 The Brassicaceae have reduced CHG methylation levels and als

141 ances the water storage capacity of infected Brassicaceae host plants.

142 gical races that each specialize on distinct Brassicaceae host species.

143 cillium longisporum invades the roots of its Brassicaceae hosts and proliferates in the plant vascula

144 go maydis is the only smut fungus adapted to Brassicaceae hosts.

145 Despite its crucial role in Brassicaceae hybridization, the structural basis of this

146 ults give a detailed anatomic description of Brassicaceae hydathodes and highlight the efficient use

147 ing a number of A. thaliana relatives within Brassicaceae identified a clear phylogenetic co-occurren

148 ize species survival in Aethionema arabicum (Brassicaceae) in which external and endogenous triggers

149 elf-incompatibility system characteristic of Brassicaceae, in which complicated dominance interaction

150 The Brassicaceae include several major crop plants and numer

151 a small gene family in most plant taxa, the Brassicaceae, including Arabidopsis (Arabidopsis thalian

152 resent in all sampled angiosperms except for Brassicaceae, including Arabidopsis.

153 in all available genome annotations from the Brassicaceae, including multiple genome assemblies of th

154 psis ind mutant suggesting a general role of Brassicaceae IND genes in preventing valve margin cells

155 Our combined analyses of genomic data for Brassicaceae indicate that extant chromosome number vari

156 bserved for YCF1 function in a member of the Brassicaceae is also true for, e.g., algal and noncanoni

157 The self-incompatibility (SI) system of the Brassicaceae is based on allele-specific interactions am

158 ion of self-pollination in self-incompatible Brassicaceae is based on allele-specific trans-activatio

159 he self-incompatibility (SI) response of the Brassicaceae is mediated by allele-specific interaction

160 Aethionema arabicum (Brassicaceae) is a dimorphic annual species that is hypo

161 The worldwide-distributed genus Lepidium (Brassicaceae) is well suited for cross-species compariso

162 FP) from field-penny cress, Thlaspi arvense (Brassicaceae), is a representative of specifier proteins

163 Clubroot, a destructive disease of Brassicaceae, is caused by the soilborne, biotrophic pro

164 dent way, the stability and reactivity of 12 Brassicaceae isothiocyanates during aqueous heating at 1

165 germination in three species of Lineage I of Brassicaceae, it did not induce a germination response i

166 Brassicaceae leaves were also moderate dietary sources o

167 een identified in several species across the Brassicaceae, less is known about the conservation of th

168 erate new biosynthetic pathways in different Brassicaceae lineages by shuffling the genes encoding a

169 ed to modulate stress responses in different Brassicaceae lineages.

170 in the dimorphic annual Aethionema arabicum (Brassicaceae), linking fruit biomechanics, dispersal aer

171 sion shift identified here suggests that the Brassicaceae may have evolved unique pattern-recognition

172 hat the colocalized PT-TPS gene pairs in the Brassicaceae may have originated from a common ancestral

173 arotenoid content and composition changes in Brassicaceae microgreens.

174 Here we show the feasibility of three Brassicaceae oilseeds crambe, camelina, and carinata, no

175 ar-weight (SH; angiosperms), and tapetum (T; Brassicaceae) oleosins.

176 ina Pajares, a model perennial member of the Brassicaceae, only undergoes floral induction during ver

177 green genotypes, belonging to Asteraceae and Brassicaceae: P, S, K, Ca, Cl, Mn, Fe, Ni, Cu, Zn, Br, R

178 Here, we inferred a Brassicaceae phylogeny using newly generated targeted en

179 Broccoli belongs to the Brassicaceae plant family consisting of widely eaten veg

180 ciated with explosive pod shatter across the Brassicaceae plant family.

181 of selenate in pakchoi was similar to other Brassicaceae plants such as kale and broccoli.

182 ins of many major clades (e.g., angiosperms, Brassicaceae, Poaceae), suggesting that polyploidy drive

183 RGHs were analyzed, primarily from Fabaceae, Brassicaceae, Poaceae, and Solanaceae species, but also

184 genomes of bacterial isolates from roots of Brassicaceae, poplar, and maize.

185 While most eudicot families including the Brassicaceae possess a single gene that is closely relat

186 Brassicaceae present a great heterogeneity of seed oil a

187 result of the phenylpropanoid pathway, many Brassicaceae produce considerable amounts of soluble hyd

188 Plants in the speciose genus Erysimum (Brassicaceae) produce both ancestral glucosinolates and

189 eviously undescribed family of proteins, the Brassicaceae PSV-embedded proteins (BPEPs), associated w

190 These results demonstrate that Brassicaceae PSVs contain internalized membranes, and ra

191 the tobacco endosperm that are absent in the Brassicaceae representatives are major tissue asymmetrie

192 In the case of the Brassicaceae representatives, the structurally homogeneo

193 The genus Boechera (Brassicaceae) represents an ideal model to test the rela

194 tors controlling self-incompatibility in the Brassicaceae, research in this field has focused on unde

195 phyD, are restricted to flowering plants and Brassicaceae, respectively.

196 ts of paralogs (Lal2, SCRL) of the canonical Brassicaceae S locus genes (SRK, SCR), and is situated i

197 -scale seed production from hybrid plants in Brassicaceae seed crops and, more generally, for inhibit

198 ibitor expression play a crucial role during Brassicaceae seed germination.

199 6 (NPC6) promotes seed oil production in the Brassicaceae seed oil species Arabidopsis, Camelina and

200 In the Brassicaceae, self-incompatibility (SI) is a spectacular

201 An investigation of CTPS orthologs in Brassicaceae showed CTPS2 is a member of an ancient line

202 rohabitat data for 37 streptanthoid species (Brassicaceae), soil analyses, and competition experiment

203 well-studied eudicot families including the Brassicaceae, Solanaceae and Fabaceae, our work in eudic

204 Leaf samples from five Brassicaceae species (Brassica carinata, Brassica olerac

205 et-hedging strategy of plants, in the annual Brassicaceae species Aethionema arabicum Our results ind

206 ted the extent of balancing selection in two Brassicaceae species and highlighted its importance for

207 llen tube penetration from distantly related Brassicaceae species and resulting in interspecific/inte

208 and confer vernalization requirement in the Brassicaceae species Arabidopsis thaliana and Arabis alp

209 Moreover, conserved noncoding regions among Brassicaceae species are enriched around PRR binding sit

210 romosomes is difficult, since many non-model Brassicaceae species are lacking genetic and/or physical

211 s were shown to be conserved in 17 of the 29 Brassicaceae species by phylogenetic footprinting.

212 coding the largest subunit of Pol IV, in the Brassicaceae species Capsella (Capsella rubella), caused

213 The Brassicaceae species have a similar cell wall architectu

214 es of A. thaliana with polyploid and diploid Brassicaceae species have suggested that rapid genome ev

215 ay does not show cross-reactivity with other Brassicaceae species including broccoli, cauliflower, ra

216 e compared pericentromere sequence from four Brassicaceae species separated by <15 million years (Myr

217 Phylogenetic analysis of CEK orthologs in Brassicaceae species showed evolutionary divergence betw

218 The synchronized diversification of Brassicaceae species suggests that polyploid events may

219 me of wild radish (Raphanus raphanistrum), a Brassicaceae species that experienced a whole-genome tri

220 s in several recently sequenced genomes from Brassicaceae species that had diversified approximately

221 reciprocal gene-swapping experiments between Brassicaceae species we show that the DOG1-mediated dorm

222 oes not show any cross-reactivity with other Brassicaceae species with the exception of white mustard

223 del species Arabidopsis thaliana and related Brassicaceae species, and great advances have been made

224 ns from A. thaliana, and from two additional Brassicaceae species, Arabidopsis lyrata and Brassica ol

225 ired for self-incompatibility in two diverse Brassicaceae species, Brassica napus and A. lyrata, and

226 In contrast, Brassicaceae species, including oilseed rape (Brassica n

227 Two Brassicaceae species, Physaria fendleri and Camelina sat

228 lucosinolates, naturally produced by several Brassicaceae species, play an important role in human he

229 dopsis transcriptomes, along with four other Brassicaceae species, revealed a high level of global se

230 Among 29 Brassicaceae species, several other motifs, but not the

231 RBs are always present with the exception of Brassicaceae species, that do not possess member of the

232 y account for the variety of shapes in other Brassicaceae species, thus providing a simplified framew

233 d glucosinolate profiles was observed in the Brassicaceae species, with the total amounts ranging fro

234 within their long terminal repeats in seven Brassicaceae species.

235 ed on whole-chloroplast sequence data for 29 Brassicaceae species.

236 isualized comparative genomics approaches in Brassicaceae species.

237 r scaffolds based on available karyotypes of Brassicaceae species.

238 ing the active stage of pollen maturation in Brassicaceae species.

239 nelles in tapetum cells of floral anthers in Brassicaceae species.

240 in the adaptive divergence between these two Brassicaceae species.

241 their CArG-boxes were widely conserved among Brassicaceae species.

242 etic analysis of the Alyssum serpyllifolium (Brassicaceae) species complex that includes populations

243 al and petal identity) gene is thought to be Brassicaceae specific.

244 One Brassicaceae-specific clade of GH3 proteins was predicte

245 The reaction is catalyzed by the Brassicaceae-specific cytochrome P450 monooxygenase CYP7

246 k identifies EIF4E1B/EIF4E1C-type genes as a Brassicaceae-specific diverged form of EIF4E.

247 In addition, the Brassicaceae-specific FIS-PRC2 complex modified the regu

248 FIS2) and MEDEA (MEA), which function in the Brassicaceae-specific FIS-PRC2 complex that regulates se

249 27 MS5 homologs and found that they define a Brassicaceae-specific gene family that has expanded part

250 SSP is a recently diverged, Brassicaceae-specific member of the BRASSINOSTEROID SIGN

251 In summary, BnMS5 belongs to a Brassicaceae-specific new gene family, and has gained a

252 we specifically show that MEcPP promotes two Brassicaceae-specific traits, namely endoplasmic reticul

253 f the glucosinolate-myrosinase system of the Brassicaceae, specifier proteins determine the profile o

254 nt from eIFiso4G1 and is present only in the Brassicaceae, suggesting a recent evolution.

255 udicots and ERS2 homologs appear only in the Brassicaceae, suggesting it is the most recent receptor

256 rates of CYP76C gene duplication and loss in Brassicaceae, suggesting the association of the CYP76C s

257 The appearance of ERS2 in the Brassicaceae suggests ongoing evolution of the ethylene

258 Conservation of the WRKY70 binding among the Brassicaceae suggests that WRKY70 repression of SARD1 is

259 y extendable dataset for further advances in Brassicaceae systematics and a timely higher-level phylo

260 s of plant chemical defense in Streptanthus (Brassicaceae), tested for evolutionary escalation of def

261 rabicum is an annual plant and member of the Brassicaceae that grows in environments characterized by

262 amily in Arabidopsis lyrata, a member of the Brassicaceae that has a sporophytic self-incompatibility

263 GLSs) are secondary metabolites found in the Brassicaceae that protect plants from herbivory and path

264 In Brassicaceae, the dry stigmatic papillary cells control

265 In Arabidopsis and other Brassicaceae, the enzyme myrosinase (beta-thioglucoside

266 As a unique feature for Brassicaceae, the genome of each member is composed of 2

267 ttle obvious sequence similarity outside the Brassicaceae, the intron from cucumber AG has at least p

268 est crucifer tribe, Arabideae (~550 species; Brassicaceae, the mustard family), diversified into seve

269 s found in the pollen coat of members of the Brassicaceae, the pollen coat proteins (PCPs), are emerg

270 In seeds of the family Brassicaceae, the PSVs lack visible crystalloids and hav

271 In the Brassicaceae, the requirement for vernalization is confe

272 In all tested self-incompatible Brassicaceae, the S haplotype encompasses two linked gen

273 In the Brassicaceae, the self-incompatibility system is mediate

274 s for two very different fruit shapes in the Brassicaceae: the heart-shaped Capsella rubella silicle

275 Within the Brassicaceae, these outcrossing systems are the evolutio

276 a feature characteristic of FLC in perennial Brassicaceae This analysis identifies an additional phas

277 ifornia shield leaf (Streptanthus tortuosus; Brassicaceae) tissue cultures, recognizes an antigen in

278 ate that ZAR1 function is conserved from the Brassicaceae to the Solanaceae.

279 ema arabicum is an important model plant for Brassicaceae trait evolution, particularly of seed (deve

280 Sixteen species representing 10 Brassicaceae tribes were analyzed by comparative chromos

281 presenting 50 of the 52 currently recognized Brassicaceae tribes.

282 s type; II-Acanthus sp; III-Celastraceae; IV-Brassicaceae; V-Anacardiaceae and Astragalus type; VI-As

283 not differ significantly between Prunus vs. Brassicaceae varieties, but xanthophyll was higher than

284 f-mining specialist on plants in the family (Brassicaceae), was not attracted to yeast volatiles in a

285 o facilitate comparative genomics across the Brassicaceae we recently outlined a system of 24 conserv

286 e with the ecological model system Boechera (Brassicaceae), we discuss advancements possible through

287 servation is tetradynamy in the large family Brassicaceae, where the four medial stamens are longer t

288 Erysimum cheiranthoides (Brassicaceae), which produces both ancestral glucosinola

289 umber of genes in Ae. arabicum than in other Brassicaceae, which could be partially explained by loss

290 ber of plant families, but not in the family Brassicaceae, which includes Arabidopsis.

291 il bomb" is a major defense mechanism in the Brassicaceae, which includes crops such as canola and th

292 as been lost in some plant lineages like the Brassicaceae, which raises the question of what alternat

293 a natural population of Arabidopsis lyrata (Brassicaceae), whose SSI system has recently been descri

294 tibility system (SSI) in cruciferous plants (Brassicaceae), whose structure is unknown.

295 odeling of PIN dynamics in plants outside of Brassicaceae will offer insights into auxin-driven patte

296 Arabidopsis rpl mutant correlated across the Brassicaceae with a point mutation in a conserved cis-el

297 diversification rates on the branch uniting Brassicaceae with its sister families.

298 sociated fungal microbiome of Arabis alpina (Brassicaceae) with the hypothesis that some of its compo

299 psella belong to the tribe Camelineae in the Brassicaceae, with Capsella rubella serving as an outgro

300 er-soluble chlorophyll binding proteins from Brassicaceae (WSCPs).