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 A. thaliana mutants disrupted in the biosynthesis of the

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

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

5 from genome-wide association studies of 199 A. thaliana accessions.

6 ion model led to the identification of 1,220 A. thaliana genes with previously unknown functions, eac

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

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

9 NA methylation are highly variable among 725 A. thaliana accessions.

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

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

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

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

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

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

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

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

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

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

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

21 ated A. thaliana iron transporter (IRT1) and A. thaliana ferritin (FER1) accumulated iron levels 7-18

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

23 species Arabidopsis arenosa, A. lyrata, and A. thaliana, and show that AGL36-like genes are imprinte

24 n XI that is conserved between P. patens and A. thaliana.

25 rowth is conserved between M. polymorpha and A. thaliana, suggesting that it was active in the common

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

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

28 ospora rootlets, S. moellendorffii roots and A. thaliana roots compared to the leaves of each respect

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

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

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

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

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

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

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

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

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

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

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

40 SMX was intensively metabolized by A. thaliana, with only 1.1% of SMX in plant tissues pres

41 ab-E and myosin XI phenotypes are rescued by A. thaliana's Rab-E1c and myosin XI-K/E, respectively.

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

43 Choosing A. thaliana for further analysis, the defensin pathway w

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

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

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

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

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

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

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

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

52 all compositional changes in 4E02 expressing A. thaliana lines.

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

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

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

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

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

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

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

60 ClpB disaggregase, in particular, ClpB3 from A. thaliana.

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

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

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

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

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

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

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

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

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

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

71 In A. thaliana therefore, KAI2 and MAX2 act to limit root s

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

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

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

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

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

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

78 l growth rate and metabolite accumulation in A. thaliana and P. trichocarpa accessions as the outcome

79 esis of 12-O-glucopyranosyl-jasmonic acid in A. thaliana.

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

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

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

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

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

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

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

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

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

89 ds to the opposite phenotype as described in A. thaliana Mathematical modeling helps to explain how t

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

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

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

93 2 in regions of higher sequence diversity in A. thaliana.

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

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

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

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

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

99 Thus, our findings in A. thaliana uncover a potentially general link between c

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

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

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

103 Overexpression of this gene in A. thaliana promotes androecium development.

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

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

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

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

108 onally redundant in terms of plant growth in A. thaliana.

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

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

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

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

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

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

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

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

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

118 found most trichome mutant classes known in A. thaliana We identified orthologous genes of the relev

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

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

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

122 f biased transmission of genetic material in A. thaliana, and serve as a springboard for future studi

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

124 ey features of C. hirsuta leaf morphology in A. thaliana.

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

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

127 oybean trichomes, similar to observations in A. thaliana.

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

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

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

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

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

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

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

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

136 pparent species-wide (nonhost) resistance in A. thaliana is due to natural pyramiding of multiple Res

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

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

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

140 with increased neighborhood mutation risk in A. thaliana and rice.

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

142 Our results show increased sensitivity in A. thaliana when using the PAREameters inferred criteria

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

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

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

146 as the main transformation pathway of SMX in A. thaliana plants, with N(4)-glycosyl-SMX accounting fo

147 ccumulation, translocation and speciation in A. thaliana.

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

149 at LuTFL1 is a functional homolog of TFL1 in A. thaliana capable of changing both flowering time and

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

151 corolla tube expresses several genes that in A. thaliana are associated with the distal petal region.

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

153 levels of AtPARK13 confer thermotolerance in A. thaliana.

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

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

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

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

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

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

160 expression of a cytosolic HMGL35 version in A. thaliana delays germination and leads to rapid wiltin

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

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

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

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

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

166 validate the implication of these genes into A. thaliana growth, six of them were further studied by

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

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

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

170 d by distinct NLR-encoding genes in multiple A. thaliana accessions provides species-wide resistance

171 imentally validated interactions in multiple A. thaliana datasets.

172 Plants engineered to coexpress a mutated A. thaliana iron transporter (IRT1) and A. thaliana ferr

173 southern end of Europe, putting many native A. thaliana populations at evolutionary risk.

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

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

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

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

178 nalization that contributes to adaptation of A. thaliana.

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

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

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

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

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

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

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

186 redundant in plant growth and development of A. thaliana.

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

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

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

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

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

192 Whereas growth of A. thaliana at standard temperature (ST; 23 degrees C) i

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

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

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

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

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

198 i were overexpressed in a transgenic line of A. thaliana producing C18-HFA, respectively.

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

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

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

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

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

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

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

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

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

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

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

210 tic architecture of quantitative response of A. thaliana to a naturally occurring virus in a field en

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

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

213 the Zn homeostasis gene network in roots of A. thaliana.

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

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

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

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

218 (14, 50, and 200 nm) into the root system of A. thaliana.

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

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

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

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

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

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 identified orthologous genes of the relevant A. thaliana genes by sequence similarity and synteny and

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

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

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 two-hybrid analyses showed that 4E02 targets A. thaliana vacuolar papain-like cysteine protease (PLCP

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

237 These results provide evidence that A. thaliana's germination niche and correlated life-hist

238 -ray scattering solution studies reveal that A. thaliana meso-diaminopimelate decarboxylase adopts a

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

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

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

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

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

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

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

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

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

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

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 s, significantly improving annotation of the A. thaliana genome.

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

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

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

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

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

266 We demonstrate that the complexity of the A. thaliana transcriptomes has been substantially under-

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

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

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

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

271 r iron-mobilizing coumarins in sculpting the A. thaliana root bacterial community by inhibiting the p

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

273 In summary, the A. thaliana gene loci At3g14390 and At5g11880 encode fun

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

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

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

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

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

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

280 In contrast to A. thaliana, P. patens has more robust CHH methylation,

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

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

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

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

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

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

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

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

289 fagin inferred over half the "Unknown" A. thaliana query genes, and about 20% for S. cerevisiae

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

291 Future work could incorporate FISH utilizing A. thaliana mapped BAC clones to allow the chromosomes o

292 a limited number of experimentally validated A. thaliana interactions and were adapted to fit these s

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