ライフサイエンスコーパス: A. thaliana

1 A. thaliana contains four malic enzymes (NADP-ME 1-4) to

2 Here, through analysis of 1307 A. thaliana accessions, we identify five predominant FLC

3 In 133 A. thaliana accessions, we test for genotype-phenotype a

4 ent in both the 5' and 3' UTRs of these C(3) A. thaliana genes.

5 haracteristic spacing patterns of EEs and 71 A. thaliana promoters containing three EEs.

6 vel of coding sequence and expression across A. thaliana accessions.

7 by restructuring of the organism that adapts A. thaliana to low-elevation Mediterranean climates.

8 F2 are under selective constraint, but among A. thaliana accessions, AtDDF2 has a higher level of non

9 An A. thaliana OS9 loss-of-function line suppresses the sev

10 tic stresses were overrepresented between an A. thaliana autotetraploid and diploid and between two A

11 s arenosa, relatively low (~6.8%) between an A. thaliana diploid and autotetraploid and intermediate

12 In an A. thaliana developmental gene regulatory network, GRACE

13 Here we show that an A. thaliana mutant resistant to the quinolone drug cipro

14 All analyzed A. thaliana S-locus haplotypes belong to the SA, SB, or

15 etic analysis with B-box genes from beet and A. thaliana but only BvCOL1 clustered with CO.

16 nces between P. patens tip-growing cells and A. thaliana pollen tubes and root hairs.

17 inhibit ACCase activity in both E. coli and A. thaliana.

18 eukaryotes tested, including C. elegans and A. thaliana.

19 ross M. truncatula, G. max, L. japonicas and A. thaliana, as well as construction and phylogenetic an

20 lies of heat-responsive TEs in A. lyrata and A. thaliana.

21 r with their relative recovery in potato and A. thaliana.

22 tible systems; N. tabacum 9.8% reduction and A. thaliana 12.3% reduction, but not in the resistant ho

23 enes have been conserved since O. sativa and A. thaliana last shared a common ancestor.

24 r exon, and 0.6695 nucleotide structure) and A. thaliana (0.5808 for CDS, 0.5955 for exon, and 0.8839

25 The yeast and A. thaliana paralogs result from independent gene duplic

26 pression of orthologous genes from yeast and A. thaliana that are coregulated with yeast rei1 or with

27 D was supported by a comparison with another A. thaliana histidine kinase, ETR1.

28 In contrast to allopolyploids, autopolyploid A. thaliana showed the same photosynthetic rate as diplo

29 heir targets within A. thaliana, and between A. thaliana, A. lyrata and C. rubella.

30 el of nucleotide sequence divergence between A. thaliana and A. arenosa MIR172 loci is 15-25%, which

31 In the allotetraploids formed between A. thaliana (At) and Arabidopsis arenosa (Aa), AtCCA1 is

32 Finally, genes affected by A. thaliana histone deacetylase 1 mutation tend to show

33 Production of CH3Cl by A. thaliana paralleled HOL1 expression, as assessed by a

34 e responsible for most of CH3Cl emissions by A. thaliana.

35 ys and X-ray crystallography to characterize A. thaliana PRORP2.

36 In our performance tests on E. coli, A. thaliana and Maylandia zebra data sets, HALC was able

37 though mature miRNA sequences are conserved, A. thaliana and A. arenosa miRNA loci diverge rapidly in

38 s with earlier observations in corresponding A. thaliana mutants.

39 d in BR-deficient and BR signaling-deficient A. thaliana mutants, resulting in clustered stomata.

40 itness among a set of geographically diverse A. thaliana accessions when grown together in a common e

41 We phenotyped multiple homozygous T-DNA A. thaliana mutants at each of two loci (AT1G11060 and A

42 an substitute for ARABIDILLO function during A. thaliana root development and seed germination.

43 Using an engineered A. thaliana line in which a portion of Col-0 chromosome

44 genetics of natural variation by the entire A. thaliana community.

45 Here, we expressed A. thaliana KOR1 as a soluble, enzymatically active prot

46 by the stigma have been maintained in extant A. thaliana.

47 up the positional history of their favorite A. thaliana gene or gene family.

48 ene, MpRKD, which is orthologous to all five A. thaliana RKD genes.

49 growth in the availability of omics data for A. thaliana as well as improvements in data analysis met

50 Patterns of expression for A. thaliana show that GlsA/ZFR genes are strongly expres

51 nt an updated co-functional gene network for A. thaliana, AraNet v2, which covers approximately 84% o

52 f a genome-scale functional gene network for A. thaliana, AraNet, which was constructed by integratin

53 , which generates functional predictions for A. thaliana and 27 nonmodel plant species using an ortho

54 -A resolution crystal structure of APSR from A. thaliana (AtAPSK) in complex with beta,gamma-imidoade

55 h we have co-immunopurified with AtMSI4 from A. thaliana suspension culture cells and identified by l

56 , we compare the 24-nt siRNA complement from A. thaliana and a closely related congener with a two- t

57 CYP76Cs from A. thaliana. thus provide a first example of promiscuous

58 tion of an unprecedented amount of data from A. thaliana, which has facilitated data-driven approache

59 member of the B-box zinc finger family from A. thaliana and contains a single conserved Zn(2+)-bindi

60 Prediction models from A. thaliana could also be applied to predict Oryza sativ

61 ) transporter, similar to the known one from A. thaliana, is likely absent and could even be harmful

62 report the crystal structure of PRORP1 from A. thaliana at 1.75 A resolution, revealing a prototypic

63 Transient expression of seven TPSs from A. thaliana, Capsella rubella, and Brassica oleracea in

64 transcriptional analyses in loss of function A. thaliana and P. patens mutants suggest that the trans

65 ion of the defective mutants with functional A. thaliana SWEET1 inhibited glucose transport, indicati

66 d during adaptation of TEV to its novel host A. thaliana To assess the effect that host species may h

67 Currently, only 11 imprinted A. thaliana genes are known.

68 In A. thaliana ecotype Columbia (Col-0), AtAAS expression w

69 Targeted gene silencing of BADC isoform 1 in A. thaliana significantly increased seed oil content whe

70 icted tRNA-specific adenosine deaminase 2 in A. thaliana.

71 out 50% in B. distachyon and by about 35% in A. thaliana.

72 n vertebrates, 3 in D. melanogaster and 4 in A. thaliana; a 9% update in total).

73 the unique distribution pattern of m(6)A in A. thaliana is associated with plant-specific pathways i

74 Distinct from mammals, m(6)A in A. thaliana is enriched not only around the stop codon a

75 The substitution of amino acids in A. thaliana natural strains is heavily constrained and i

76 or the existence of supercoiling activity in A. thaliana and that the plant is sensitive to quinolone

77 b in B. napus and their promoter activity in A. thaliana showed differences in the induction of the p

78 ly-transmitted deletion in a repeat array in A. thaliana.

79 ription for moss stomatal development, as in A. thaliana(7).

80 Overexpression of both EcGBF3 and AtGBF3 in A. thaliana resulted in improved tolerance to osmotic st

81 ively regulating the expression of AtLRL3 in A. thaliana, LRL genes promote rhizoid development indep

82 opment independently of AtRHD6 and AtRSL1 in A. thaliana but the regulatory interactions between auxi

83 e extensive tools and resources available in A. thaliana for analysis of SI signaling.

84 at enhanced activation of SA biosynthesis in A. thaliana hybrids may contribute to their increased re

85 Formation of the disulfide bond in A. thaliana APSK (AtAPSK) inverts the binding affinities

86 available maps with gene expression data in A. thaliana, Arabidopsis arenosa, and allotetraploids.

87 not sufficient for root hair development in A. thaliana, it suggests that there are differences in t

88 ion for anthocyanin content was dissected in A. thaliana and shown to be affected by a common regulat

89 shaped patterns of methylation diversity in A. thaliana natural populations over evolutionary timesc

90 recursors were processed more efficiently in A. thaliana than in resynthesized allotetraploids, sugge

91 senic hyperaccumulation can be engineered in A. thaliana by knocking out the HAC1 gene and expressing

92 the active sites of the BBE-like enzymes in A. thaliana suggested that 14 out of 28 members of the f

93 The overall response to Ga exposure in A. thaliana is highly similar to that with aluminum stre

94 also exhibit parentally biased expression in A. thaliana, suggesting that there is evolutionary conse

95 c expression of the entire protein family in A. thaliana.

96 ific to the suite of glucosinolates found in A. thaliana, with other combinations of glucosinolates b

97 Moreover, CAX1 loss of function in A. thaliana led to higher Cd sensitivity at low concentr

98 bilization or limited translocation of Ga in A. thaliana.

99 Essential genes in A. thaliana are often single copy or derived from older

100 d 34 maternally expressed imprinted genes in A. thaliana endosperm that are regulated by the DNA-deme

101 TFBSs in the promoter sequences of genes in A. thaliana.

102 the utility and power of haploid genetics in A. thaliana.

103 PYK10, the most abundant beta-glucosidase in A. thaliana root ER bodies, hydrolyzes indole glucosinol

104 ough the deamination of guanosine by GSDA in A. thaliana, excluding other possible sources like the d

105 Web-based application for conducting GWAS in A. thaliana.

106 press genes encoding microbial hydrolases in A. thaliana, and target the hydrolases to the apoplast c

107 ext of mechanisms of S-locus inactivation in A. thaliana.

108 t for reconstituting self-incompatibility in A. thaliana and uncovered an important role for ARC1 in

109 trategy for studying self-incompatibility in A. thaliana, we offer our perspective on what constitute

110 de molecular profile of mutations induced in A. thaliana by FN irradiation and are particularly infor

111 ter cells are able to initiate infections in A. thaliana and in C. elegans albeit, with lower mortali

112 cells are not able to initiate infections in A. thaliana and present significantly reduced virulence

113 and trans-regulation and GxE interactions in A. thaliana, laying the ground for mechanistic investiga

114 y induce deletions longer than a kilobase in A. thaliana.

115 these, LATE ELONGATED HYPOCOTYL, is known in A. thaliana to regulate many stress-response genes that

116 leucine-rich repeat (NLR)-encoding locus in A. thaliana.

117 ge and a very recent observable gene loss in A. thaliana.

118 ily through gene duplication and was lost in A. thaliana, contributing to leaf simplification in this

119 an I sub-populations and their modulation in A. thaliana organs.

120 Through site-directed mutagenesis in A. thaliana, we show that IME signals can be inserted or

121 Loss- and gain-of-function mutants in A. thaliana were studied.

122 shoots, mimicking lfy ap1 double mutants in A. thaliana.

123 how different from the situation observed in A. thaliana mainly producing housekeeping isoprenoid met

124 n MIR164A/CUC and AS1 that does not occur in A. thaliana.

125 nd characterization of genes and pathways in A. thaliana responsible for hybrid lethality in the A. t

126 a new model for ground tissue patterning in A. thaliana in which the ability to form a functional en

127 and glutamine, and further with peptides, in A. thaliana cells.

128 and stable self-incompatibility phenotype in A. thaliana and how this should be investigated and repo

129 romoted an approach herkogamous phenotype in A. thaliana flowers.

130 odel suggest that the R gene polymorphism in A. thaliana may not be maintained through a tightly coup

131 d the pattern of historical recombination in A. thaliana and observed an enrichment of hotspots in it

132 ervation that the ACR2 arsenate reductase in A. thaliana plays no detectable role in arsenic metaboli

133 Our results in A. thaliana are consistent with a mechanism by which the

134 gene bodies, mirroring our recent results in A. thaliana.

135 d maintenance of robust circadian rhythms in A. thaliana, demonstrating that metabolism has a crucial

136 pendent and -independent PTI against RKNs in A. thaliana, suggesting the existence of diverse nematod

137 eletions and insertions still segregating in A. thaliana indicates that the process of DNA loss is on

138 of Exo70A1 neither abolish nor weaken SI in A. thaliana SRK-SCR plants.

139 BBX32 (AtBBX32) represses light signaling in A. thaliana and that expression of AtBBX32 in soybean in

140 e SHR proteins function as mobile signals in A. thaliana and all of the SHR homologs physically inter

141 o required for variant-specific silencing in A. thaliana, but SUVH5 [SU(VAR)3-9 HOMOLOG 5] and SUVH6,

142 ccumulation, translocation and speciation in A. thaliana.

143 Using a reverse genetic strategy in A. thaliana, we identified PRR2 as a positive regulator

144 omote evolutionary and functional studies in A. thaliana, especially the MAGIC genetic reference popu

145 l and leaf development in C. hirsuta than in A. thaliana.

146 expressed at low levels relative to that in A. thaliana, which is associated with hypermethylation o

147 levels of AtPARK13 confer thermotolerance in A. thaliana.

148 le of GBF3 in imparting drought tolerance in A. thaliana and indicate the conserved role of this gene

149 erance and root-to-shoot As translocation in A. thaliana, with PvACR3 being localized to the plasma m

150 However, unlike in A. thaliana, rice endosperm sRNA populations are dominat

151 Unlike in A. thaliana, the maternal allele of many A. lyrata PEGs

152 ic loci responsible for natural variation in A. thaliana.

153 ar to that underpinning natural variation in A. thaliana.

154 i primarily tracked dawn or dusk, whereas in A. thaliana, a wider range of responses were observed, c

155 as been studied in several species including A. thaliana, tobacco (Nicotiana tabacum), N. benthamiana

156 eleted in self-compatible species, including A. thaliana.

157 also significantly reduced in virus infected A. thaliana by 19.6% but not in N. tabacum or the resist

158 Interestingly, A. thaliana was discovered to have a recognition system

159 RNAs with specificity similar to that of its A. thaliana counterpart.

160 FAP knockout A. thaliana plants show elevated alpha-linolenic acid le

161 protein consisting of annotated full-length A. thaliana OEP80 with an N-terminal hexahistidine tag (

162 and high methylation variability across many A. thaliana strains at that site are the strongest predi

163 S. cerevisiae, H. sapiens, D. melanogaster, A. thaliana, and E. coli, and confirm significant and co

164 sis of mutant phenotypes from FN-mutagenized A. thaliana populations.

165 eraction in a background in which the native A. thaliana CENH3 is replaced with CENH3s from distant s

166 and annotation of the genomes of 18 natural A. thaliana accessions, and their transcriptomes.

167 An analogous phenomenon occurs in nonhybrid A. thaliana, in which specific classes of rRNA gene vari

168 f this community differs among accessions of A. thaliana.

169 stable SI phenotype in several accessions of A. thaliana.

170 nalization that contributes to adaptation of A. thaliana.

171 on influencing the evolution and adaption of A. thaliana.

172 tional role in the evolution and adaption of A. thaliana.

173 ional modeling and spectroscopic analyses of A. thaliana GrxS14-BolA1 holo-heterodimer (BolA_H), we p

174 r controlled environmental conditions and of A. thaliana and C. hirsuta in two natural habitats.

175 brane and this is true of Formin1 (AtFH1) of A. thaliana.

176 oping anther tissues of young floral buds of A. thaliana, principally in developing pollen grains of

177 s in chromatin modification in root cells of A. thaliana.

178 l-like transcriptome in sporophytic cells of A. thaliana.

179 Based on comparison of A. thaliana and R. raphanistrum ortholog floral expressi

180 a by targeting the starch-binding domains of A. thaliana starch synthase III to this structure.

181 Ecotypes of A. thaliana were tested for their ability to produce liv

182 YFP) and expression in developing embryos of A. thaliana.

183 examined green plants with the exception of A. thaliana.

184 cross-regulation among the five RKD genes of A. thaliana [10].

185 The much smaller 125-Mb genome of A. thaliana, which diverged from A. lyrata 10 million ye

186 current knowledge of the natural history of A. thaliana from the perspective of the most closely rel

187 tion has also brought the natural history of A. thaliana into the limelight.

188 ed sequence variation in the complete IGS of A. thaliana WT plants and provide the reference/consensu

189 carboxyl carrier protein (BCCP) isoforms of A. thaliana ACCase.

190 We show that lack of A. thaliana respiratory burst oxidase protein F (AtrbohF

191 We sequenced 180 lines of A. thaliana from Sweden to obtain as complete a picture

192 Manipulation of A. thaliana RFO content by overexpressing ZmGOLS2, ZmRS,

193 s confirmed using fluorescence microscopy of A. thaliana protoplasts transiently expressing the N-ter

194 e metabolite profiling utilizing a number of A. thaliana relatives within Brassicaceae identified a c

195 ed haplotypes in the worldwide population of A. thaliana Moreover, we found 105 single-copy genes, wh

196 ive dimerization/oligomerization property of A. thaliana Cryptochrome 2 (Cry2).

197 tide polymorphisms in individual proteins of A. thaliana based on the reference genome Col-0.

198 cation), and gene expression (by RT-qPCR) of A. thaliana orthologue genes were performed across diffe

199 d to infer the evolutionary relationships of A. thaliana.

200 bidopsis arenosa, an outcrossing relative of A. thaliana.

201 ed from self-incompatible close relatives of A. thaliana restore robust SI in several accessions that

202 s in outcrossing A. arenosa or repression of A. thaliana alleles.

203 The transcriptomic response of A. thaliana to 2,5-dichlorobiphenyl (2,5-DCB), and its O

204 le for these molecules in the SI response of A. thaliana.

205 nhibition of self pollen or for reversion of A. thaliana to its fully self-incompatible ancestral sta

206 he conserved correlations point to a role of A. thaliana REIL proteins in the maturation of the eukar

207 on of this gene increased the sensitivity of A. thaliana plants to drought stress.

208 esent multiple data to show that the size of A. thaliana OEP80 is smaller than previously estimated.

209 ic datasets for sequenced natural strains of A. thaliana.

210 sent a 2.6 A resolution crystal structure of A. thaliana PRMT 10 (AtPRMT10) in complex with a reactio

211 Recent studies of A. thaliana population structure, using thousands of acc

212 different fields of research in the study of A. thaliana has made a large contribution to our molecul

213 A subset of A. thaliana GTFs have also expanded in number, indicatin

214 (14, 50, and 200 nm) into the root system of A. thaliana.

215 analyses of the natural genetic variation of A. thaliana have involved small numbers of individual pl

216 In this study, we modified the cell wall of A. thaliana by targeting the starch-binding domains of A

217 ess miR172 expression in the outer whorls of A. thaliana flowers.

218 We briefly relate our findings on A. thaliana cryptochrome to photoreaction pathways in an

219 upon outcrossing, show a binding pattern on A. thaliana centromere repeats that is indistinguishable

220 ow frequencies in P. syringae populations on A. thaliana.

221 onfers a virulence benefit to P. syringae on A. thaliana.

222 ed transgenic B. napus plants overexpressing A. thaliana ABI1.

223 and function of proteins in the model plant A. thaliana.

224 racy across diverse populations of the plant A. thaliana.

225 allopolyploid as in the maternal progenitor A. thaliana and significantly more expressed than in the

226 sion/purification of the quinolone-resistant A. thaliana gyrase yields active enzyme that is resistan

227 in Rosids (but apparently lost in the Rosid A. thaliana) for which we propose the name RDR7.

228 SP protein level and ESP activity from seven A. thaliana ecotypes showed a positive correlation betwe

229 The present study identified a family of six A. thaliana genes that share five limited regions of seq

230 Here, we show that hybrids between some A. thaliana accessions show increased resistance to the

231 japonicus plus two reference plant species, A. thaliana and Populus trichocarpa, with annotations ba

232 tionship among four closely related species, A. thaliana, A. lyrata, Capsella rubella and Brassica ra

233 f ARC1 in reconstructing a strong and stable A. thaliana self-incompatibility phenotype, in the conte

234 Surprisingly, A. thaliana and related species express two distinct AC4

235 uction in seedlings of Arabidopsis thaliana (A. thaliana).

236 Furthermore, we show that A. thaliana ARABIDILLOs function similarly during seed g

237 wild-type Arabidopsis thaliana We show that A. thaliana CENH3-containing nucleosomes exhibit a stron

238 hese experiments now show unequivocally that A. thaliana encodes an organelle-targeted DNA gyrase tha

239 The A. thaliana REIL paralogs are required specifically in t

240 Seven QTLs affecting the A. thaliana component of this hybrid incompatibility wer

241 dopsis thaliana and Arabidopsis arenosa, the A. thaliana-derived rRNA genes are selectively silenced.

242 uantitative trait loci (QTLs) encoded by the A. thaliana genome that affect the frequency of postzygo

243 functional KOR1 G429R mutant encoded by the A. thaliana rsw2-1 allele displayed only oligomannosidic

244 otetraploids were primarily derived from the A. thaliana MIR172b locus.

245 Furthermore, the A. thaliana HI can be used to produce haploids from a re

246 s antibody recognized a 70-kD protein in the A. thaliana chloroplast membrane fraction which migrated

247 hat of the 12 predicted GGPPS encoded in the A. thaliana genome 10 are functional proteins that can s

248 that FCA and FPA play important roles in the A. thaliana genome in RNA 3' processing and transcriptio

249 esent some of the youngest duplicates in the A. thaliana genome.

250 For comparison, average speed in the A. thaliana hypocotyl expressing GFP-AtCESA6 was 184 +/-

251 An analysis of all known sequences in the A. thaliana kinome found that alphaC helix disorder may

252 ive walls comparable to that observed in the A. thaliana ms2 mutant, and extremely compromised germin

253 alyzed transfer DNA insertion mutants in the A. thaliana orthologs of THL1 and THL2.

254 chloromethane dehalogenase cmuA gene in the A. thaliana phyllosphere correlated with HOL1 genotype,

255 underlying stem-cell niche patterning in the A. thaliana root in terms of some of the key dynamic tra

256 ent the spontaneous activation of SRK in the A. thaliana stigma.

257 iana responsible for hybrid lethality in the A. thaliana x A. arenosa interspecific cross.

258 have simple leaves, whereas others like the A. thaliana relative Cardamine hirsuta bear complex leav

259 These arrays make up 5 % of the A. thaliana genome.

260 Our data expands the knowledge of the A. thaliana IGS sequence arrangement and variability, wh

261 We have assembled 117 Mb of the A. thaliana Landsberg erecta (Ler) genome into five chro

262 ock-outs of a putative moss homologue of the A. thaliana MS2 gene, which is highly expressed in the m

263 cluding those from the northern limit of the A. thaliana range.

264 e, which is the functional equivalent of the A. thaliana SC haplotype.

265 We previously reported on the A. thaliana gene EDM2, which is required for several dev

266 ed projection of nonmodel plant genes on the A. thaliana gene network.

267 was not required for the E. coli YidC or the A. thaliana Alb3 to functionally complement the E. coli

268 uliflower Mosaic Virus 35S RNA promoter, the A. thaliana beta-expansin signal peptide, and the fluore

269 sely, the moss MS2 gene could not rescue the A. thaliana ms2 phenotype.

270 or the DNA repair factor DDB2 in shaping the A. thaliana DNA methylation landscape in the absence of

271 We show that the A. thaliana ARC1 ortholog is a highly decayed pseudogene

272 to or less than 5 % and are specific to the A. thaliana lineage; thus, they predictably represent so

273 abulary terms, and maintains and updates the A. thaliana genome assembly and annotation.

274 Finally, studies using the A. thaliana copt6-1 mutant and plants overexpressing COP

275 ot possible at that time to show whether the A. thaliana genes encoded an active gyrase enzyme, nor w

276 eases (TAIR8, TAIR9 and TAIR10) in which the A. thaliana assembly was updated, pseudogenes and transp

277 te that is inherently less stable within the A. thaliana species.

278 the three Arabidopsis species than the three A. thaliana ecotypes.

279 wisted "S"-shaped conformation when bound to A. thaliana AHAS (AtAHAS) with the pyrimidinyl group ins

280 ong the phylogenetic lineage from cassava to A. thaliana, suggests that alterations in the electrogen

281 In contrast to A. thaliana, auxin promotes rhizoid development by posit

282 pendent on LFY in C. hirsuta, by contrast to A. thaliana.

283 as based on the highest sequence identity to A. thaliana enzyme.

284 EcGBF3 transgenic A. thaliana results also suggest that drought tolerance

285 Exposing transgenic A. thaliana pollen to recombinant Papaver PrsS protein t

286 Self-incompatible transgenic A. thaliana plants have proved to be valuable for analys

287 he viability of creating a set of transgenic A. thaliana plants with modified cell walls to use as a

288 ddition, a decrease in the expression of two A. thaliana Expansin genes (AtEXP5 and AtEXP8) was obser

289 pression is regulated differently in the two A. thaliana ecotypes.

290 In wild-type A. thaliana, stomatal distribution follows the one-cell

291 ll mutant plants were crossed with wild-type A. thaliana.

292 f 22 methionine-derived glucosinolates using A. thaliana accessions from across Europe.

293 cible xylan xylosyltransferase activity with A. thaliana IRX10 and with a homolog from the dicot plan

294 846 have conserved genomic arrangements with A. thaliana and candidate target jacalins, similar prima

295 in vernalization response is associated with A. thaliana accessions collected from different geograph

296 folding in N- and C-lobes is conserved with A. thaliana IP5 2-K.

297 dual RFO amounts, positively correlated with A. thaliana seed vigor, to which stachyose and verbascos

298 t (LRR) protein that directly interacts with A. thaliana PNP, AtPNP-A.

299 that are coregulated with yeast rei1 or with A. thaliana REIL2, respectively.

300 variation in miRNAs and their targets within A. thaliana, and between A. thaliana, A. lyrata and C. r