ライフサイエンスコーパス: nodulation

1 aintenance of rhizobial endosymbiosis during nodulation.

2 led to increased NF induction of ENOD11 and nodulation.

3 positive and negative roles in M. truncatula nodulation.

4 cesses, and for comparative analysis of stem nodulation.

5 encode key transcription factors involved in nodulation.

6 creased sensitivity to nitrate inhibition of nodulation.

7 in cortical cells during the early stages of nodulation.

8 rotein complex are involved in regulation of nodulation.

9 of arbuscular mycorrhizal (AM) symbiosis and nodulation.

10 sential signal molecules that trigger legume nodulation.

11 the presence of an additional signal during nodulation.

12 aluate the role of G-protein subunits during nodulation.

13 red for years to be specifically involved in nodulation.

14 view of transcriptional reprogramming during nodulation.

15 ck loop involving auxin and cytokinin during nodulation.

16 onal NFP2-orthologous receptor to LCO-driven nodulation.

17 d infection thread development during legume nodulation.

18 rotransposon in the bHLH gene led to reduced nodulation.

19 s, appear to play essential roles in soybean nodulation.

20 ve epidermal infection events uncoupled from nodulation.

21 he importance of GS52 enzymatic activity for nodulation.

22 also required for rhizobial colonization and nodulation.

23 des, is critical for rhizobial infection and nodulation.

24 ecially traits associated with symbiosis and nodulation.

25 signal to shoot tissues to suppress further nodulation.

26 state and affects the growth parameters and nodulation.

27 uggest a role for CND in controlling soybean nodulation.

28 ar adenosine diphosphate is important during nodulation.

29 ght act as auxin transport regulators during nodulation.

30 ing flavonoid compounds are also critical to nodulation.

31 whereas flavone-deficient roots had reduced nodulation.

32 f S. meliloti nod genes, completely restored nodulation.

33 itical role for the GS52 ecto-apyrase during nodulation.

34 he level of rhizobial infection and enhanced nodulation.

35 predating and coinciding with the origin of nodulation.

36 to the origin of LCO receptors essential for nodulation.

37 g a shared evolutionary origin of LCO-driven nodulation.

38 runcatula) and determinate (Lotus japonicus) nodulation.

39 mportant for infection thread initiation and nodulation.

40 , ectomycorrhizal associations, or Rhizobium nodulation.

41 creased lateral root emergence and decreased nodulation.

42 RFs) are signal molecules that modulate host nodulation.

43 ting these targets with CRISPR-Cas9 promotes nodulation.

44 e undergone expansions and play key roles in nodulation.

45 l to regulate root nitrogen-fixing symbiotic nodulation.

46 rs independent of the LjLhk1 receptor during nodulation.

47 ine the precise stage at which SLs influence nodulation.

48 ers involved in vascular differentiation and nodulation.

49 ecause Micromonospora itself does not induce nodulation.

50 the future detailed investigation of soybean nodulation.

51 X/LAX family of auxin influx transporters in nodulation.

52 ides are also involved in controlling legume nodulation.

53 in acclimation to nutrient deficiencies and nodulation.

54 uding the CRE1 receptor essential to promote nodulation.

55 MtDELLA1 can bind the ERN1 (ERF required for nodulation 1) promoter and positively transactivate its

56 (for Ethylene Responsive factor required for Nodulation), a direct target gene of MtNF-YA1 and MtNF-Y

57 lls in three different development stages of nodulation after rhizobium infection.

58 Nodulation and arbuscular mycorrhization require the act

59 ial infection, increased expression of early nodulation and autoregulation of nodulation genes, and i

60 of a putative heavy-metal efflux-resistance nodulation and division type copper efflux system (encod

61 Knockdown mutants were impaired for nodulation and early root hair deformation responses wer

62 vidence supports a passive bacterial role in nodulation and infection after the microsymbiont has tri

63 Tight control of nodulation and infection is required to maintain the mut

64 temically from shoots to positively regulate nodulation and is required for the activity of carboxyl-

65 tCEP1 and its likely receptor, CRA2, mediate nodulation and lateral root development through differen

66 in2b are required for negative regulation of nodulation and Ljein2a Ljein2b double mutants are hypern

67 unctions at the earliest stage of the common nodulation and mycorrhization symbiosis signaling pathwa

68 s, suggesting common infection mechanisms in nodulation and mycorrhization.

69 ence on the evolutionary relatedness between nodulation and mycorrhization.

70 living Bradyrhizobium isolates, lacking both nodulation and nitrogen fixation genes, to have their ge

71 identify a role for cytokinin in regulating nodulation and nitrogen fixation in response to nitrate

72 m host cells that is critically required for nodulation and nitrogen fixation is not fully understood

73 Previously, we isolated >100 nodulation and nitrogen fixation mutants from a populati

74 otypes, deletion mutants exhibited wild-type nodulation and nitrogen fixation when they were inoculat

75 were delineated, including known factors for nodulation and nitrogen fixation, and candidates with pr

76 regulation of nodulation genes, and improved nodulation and nitrogen fixation.

77 p between the molecular mechanisms governing nodulation and NLS formation.

78 ial and complex lipid metabolism for soybean nodulation and nodule development, laying the foundation

79 embrane lipid biosynthesis are essential for nodulation and rhizobia-soybean symbioses.

80 nstruct or mutations in ARGONAUTE7, enhances nodulation and rhizobial infection, alters the spatial d

81 nip/latd mutants have pleiotropic defects in nodulation and root architecture.

82 As part of the transcriptional machinery for nodulation and symbiosis across a range of Rhizobium, No

83 role of NolR in the regulation of different nodulation and symbiosis genes are proposed.

84 A sequences from diverse rhizobial genes for nodulation and symbiosis.

85 ula ecotype R108 was screened for defects in nodulation and symbiotic nitrogen fixation.

86 the two developmental pathways required for nodulation and that activation of the pathway involving

87 The link between nodulation and the biosynthesis of nitrogen-containing a

88 in signaling in these cells led to increased nodulation and, as a consequence, to higher nitrogen fix

89 e expression patterns of genes implicated in nodulation, and also transcription factors, using both t

90 E INFECTIONS3 (DMI3/CCaMK), ERF REQUIRED FOR NODULATION, and SUPERNUMERARY NODULES (SUNN).

91 t the operon is selectively expressed during nodulation, and the scattered distribution of the operon

92 t development and systemic autoregulation of nodulation (AON) integrated with nitrogen (N) signaling

93 l meristem, is involved in autoregulation of nodulation (AON), a mechanism that systemically controls

94 Autoregulation of nodulation (AON), a systemic signaling pathway in legume

95 esses in plants, including autoregulation of nodulation (AON), which allows legumes to limit the numb

96 The effects of light on nodulation are dependent on a functional lov gene.

97 The early stages of nodulation are governed by a few well-defined functions,

98 cess and some of them display a profuse stem nodulation as exemplified in the African Aeschynomene af

99 S344D was shown to suppress the spontaneous nodulation associated with a gain-of-function mutant of

100 ifying lineage-specific expansions (LSEs) of nodulation-associated genes can be a strategy to discove

101 tokinin and had attenuated expression of key nodulation-associated transcription factors known to be

102 ed beds displays various patterns, including nodulation, banding and scallops and fingers.

103 might also have a direct role in regulating nodulation because overexpression of their phospho-mimic

104 - Fix-), one mutant with delayed and reduced nodulation but effective in nitrogen fixation (dNod+/- F

105 on test indicates that Os-POLLUX can restore nodulation, but not rhizobial infection, to a Medicago t

106 ulation of legume-specific processes such as nodulation, but the lack of genetic data from a legumino

107 Mechanisms inhibiting legume nodulation by low soil pH, although highly prevalent and

108 ene in soybeans (Glycine max) that restricts nodulation by many strains of Bradyrhizobium elkanii.

109 MtCEP1 increases nodulation by promoting rhizobial infections, the develo

110 When tested for nodulation by Sinorhizobium meliloti, flavonoid-deficien

111 Nodulation by succinoglycan-defective strains was achiev

112 flux pump is the archetype of the resistance nodulation cell division (RND) exporters from Gram-negat

113 y-metal resistance is mediated by resistance nodulation cell division (RND)-based efflux pumps compos

114 ripartite efflux complexes in the resistance-nodulation-cell division (RND) family to expel various t

115 embrane proteins belonging to the resistance-nodulation-cell division (RND) superfamily play signific

116 pumps belonging to the ubiquitous resistance-nodulation-cell division (RND) superfamily transport sub

117 Transporters of the resistance-nodulation-cell division (RND) superfamily typically ass

118 Here we identified six putative resistance-nodulation-cell division (RND) type factors.

119 Resistance-nodulation-cell division efflux pumps are integral membr

120 TMs 2-13 exhibit a typical resistance-nodulation-cell division fold, among which TMs 3-7 const

121 One mechanism involves an RND (resistance-nodulation-cell division protein family)-driven triparti

122 mphiphile efflux subfamily, these resistance-nodulation-cell division proteins largely form trimeric

123 We investigated the role of the resistance-nodulation-cell division superfamily (RND) efflux system

124 d multidrug efflux pumps from the resistance-nodulation-cell division superfamily (vexB and vexD [her

125 sidual activity provided by other resistance-nodulation-cell division superfamily-type efflux pumps,

126 ite efflux pumps belonging to the resistance-nodulation-cell division superfamily.

127 d transporters that belong to the resistance-nodulation-cell division superfamily.

128 tite efflux complexes in the RND (resistance-nodulation-cell division) family to expel diverse toxic

129 divergently transcribed putative resistance-nodulation-cell-division (RND) efflux pump, encoded by z

130 Rhizobial nodulation competitiveness and effectiveness at N(2) fix

131 The pooled correlation between rhizobium nodulation competitiveness and plant aboveground biomass

132 g of the innate mechanisms regulating legume nodulation control under acidic conditions, which could

133 initial inoculum, plant population size and nodulation cycle length.

134 minated by non-fixing bacteria during serial nodulation cycles with a probability that is function of

135 -1 for root architecture defects but not for nodulation defects.

136 grafting studies using an autoregulation-of-nodulation-deficient mutant line, altered in the autoreg

137 efflux pump, which belongs to the resistance nodulation division (RND) family, recognizes and extrude

138 Resistance nodulation division efflux systems have a major role in

139 Efflux pumps of the resistance-nodulation division superfamily, such as AcrB, make a ma

140 l G288D substitution in AcrB, the resistance-nodulation division transporter in the AcrAB-TolC tripar

141 enes encoding the VexAB and VexGH resistance-nodulation-division (RND) efflux systems and their cogna

142 ia infections, and members of the resistance-nodulation-division (RND) family of efflux pumps have be

143 pecially those that belong to the resistance-nodulation-division (RND) family, often show very broad

144 g efflux systems belonging to the resistance-nodulation-division (RND) superfamily are ubiquitous in

145 is enabled by efflux pumps of the Resistance-Nodulation-Division (RND) superfamily of proteins creati

146 ems (a P1B-ATPase, a porin, and a resistance-nodulation-division (RND) system) and of a putative Cu(+

147 Resistance-nodulation-division (RND) type multidrug efflux pumps ha

148 Resistance-nodulation-division efflux pumps play a key role in inhe

149 uctural features of an MFP in the resistance-nodulation-division efflux system and provide direct evi

150 tite efflux complex CusCBA of the resistance-nodulation-division family that is essential for bacteri

151 efflux complexes belonging to the resistance-nodulation-division family to expel diverse toxic compou

152 hese products is mediated by RND (resistance-nodulation-division) family efflux systems.

153 RND (resistance-nodulation-division) family transporters in Gram-negativ

154 trimeric transporters of the RND (resistance-nodulation-division) superfamily, which often conduct ef

155 negatively regulates rhizobial infection and nodulation during the nitrogen-fixing root nodule symbio

156 nhibitor 2,3,5,-triiodobenzoic acid, rescued nodulation efficiency in cre1 mutants and allowed auxin

157 teraction and may pave the way for enhancing nodulation efficiency in legumes.

158 signalling control rhizobial infections and nodulation efficiency.

159 h competitive inhibition of ERF Required for Nodulation (ERN1).

160 ht not play a critical role in M. truncatula nodulation, even though they are the most abundant root

161 s chitin, peptidoglycan (PGN), and rhizobial nodulation factor (NF), that induce immune or symbiotic

162 proteins directly interact with the soybean nodulation factor receptors NFR1alpha and NFR1beta, sugg

163 t, indicating that MtCBS1 acts downstream of nodulation factor signaling.

164 S. meliloti nodulation factor treatments of MtROP9i led to deformed

165 Nodulation factor-induced Ca(2+) responses were observed

166 Rhizobial nodulation factors (NFs) activate a specific signaling p

167 Large reductions in nodulation frequency, plant growth, and significant shif

168 er to accurately and efficiently reconstruct nodulation gene network, a crowdsourcing platform, Crowd

169 ing based on the observations that the early nodulation gene NODULE INCEPTION was not induced and tha

170 We also identified that some key nodulation genes were not expressed in rice roots during

171 on of early nodulation and autoregulation of nodulation genes, and improved nodulation and nitrogen f

172 bial infection, and the induction of two key nodulation genes, Nodulation Signaling Pathway1 (NSP1) a

173 ctor coordinates the expression of key early nodulation genes.

174 measuring transcript numbers of known early nodulation genes.

175 ompanied by reduced expression of some early nodulation genes.

176 sponse Factor Required for Nodulation1 early nodulation genes.

177 e contrasted genomic properties and the stem-nodulation habit of its parental lineages (4x).

178 The effect of nitrogen on nodulation has been extensively investigated, but the ef

179 ular and morphological characters, including nodulation, have led to major changes in our understandi

180 and polysomal mRNAs for 15 genes involved in nodulation identified a group of transcripts with slight

181 involved in the long-distance regulation of nodulation in actinorhizal symbioses.

182 K, SYMRK, and HK1 are required for efficient nodulation in Aeschynomene evenia.

183 However, the same treatment did not restore nodulation in flavonoid-deficient roots, suggesting that

184 eated S. meliloti cells, completely restored nodulation in flavonoid-deficient roots.

185 iry roots, which may account for the reduced nodulation in GmLEC2a-OE hairy roots but increased nodul

186 tion in GmLEC2a-OE hairy roots but increased nodulation in GmWRI1b-OE hairy roots.

187 y rhizobial signals which initiate infection/nodulation in host legume species, the identity of the e

188 Nitrogen-fixing root nodulation in legumes challenged with nitrogen-limiting

189 Nodulation in legumes involves the coordination of epide

190 Nodulation in legumes requires the recognition of rhizob

191 conserved NF-Y protein complexes to control nodulation in leguminous plants.

192 show that antisense inhibition of LNP blocks nodulation in Lotus japonicus.

193 e role of the WOX5 transcription factor upon nodulation in Medicago truncatula and pea (Pisum sativum

194 nin accumulation is tightly regulated during nodulation in order to balance the requirement for cell

195 ntified four LysM-type receptors controlling nodulation in P. andersonii: PanLYK1, PanLYK3, PanNFP1,

196 CRE1-dependent CK pathway to regulate early nodulation in response to both NF and CK signals critica

197 in regulation of the G-protein cycle during nodulation in soybean.

198 our companion study, we found inhibition of nodulation in the ENM but not in the bulk/dissolved trea

199 ents, our results suggest that inhibition of nodulation in the ENM treatment was primarily due to phy

200 In contrast with the sunn-1 mutant, nodulation in the lss mutant is more extensive and is le

201 K-kd was 6-fold higher than rhizobia-induced nodulation in TR25/SYMRK roots.

202 Spontaneous nodulation in TR25/SYMRK-kd was 6-fold higher than rhizo

203 cate that elements specifically required for nodulation include NIN and possibly related gene network

204 hrough processes not previously connected to nodulation, including phosphorous supply and salicylic a

205 SLs appear to influence nodulation independently of ethylene action, as SL-defic

206 rdingly, MtCEP1 counteracts the reduction in nodulation induced by increasing ethylene precursor conc

207 sis indicated that ckx3 mutants have reduced nodulation, infection thread formation and root growth.

208 formed, indicating a function of this RRB in nodulation initiation.

209 ing to nodule development, autoregulation of nodulation, intracellular accommodation of bacteria, nod

210 Soybean nodulation is a highly controlled process that involves

211 e still many gaps to be filled before legume nodulation is sufficiently understood to be managed for

212 Nodulation is the result of a mutualistic interaction be

213 Nodulation is the result of a symbiosis between legumes

214 N, required for N-mediated autoregulation of nodulation, is not involved.

215 e underlying molecular mechanisms leading to nodulation, many efforts are underway to identify nodula

216 nes are associated with nitrogen metabolism, nodulation, metal homeostasis, and stress responses.

217 Analyses of nodulation mutants showed that perception of Nod factor

218 mNARK is critical for systemic regulation of nodulation (new organ made on the root through symbiosis

219 We investigated how chitin and nodulation (Nod) factor receptors of Lotus japonicus ini

220 Rhizobial nodulation (Nod) factors activate both nodule morphogene

221 induced in roots and root hairs by rhizobial nodulation (Nod) factors via activation of the nodulatio

222 nd dependent on host perception of bacterial nodulation (Nod) factors.

223 transcriptional regulators (LTTRs), mediates nodulation (nod) gene expression in the soil bacterium S

224 the question of how flavonoids affected root nodulation of faba bean in a wheat and faba bean intercr

225 the rooting of cuttings, and facilitate the nodulation of legumes.

226 id (1-NOA) and 2-NOA, which we found reduced nodulation of Medicago truncatula.

227 Nodulation of soybean (Glycine max) root hairs by the ni

228 LA1 protein can partially rescue the reduced nodulation of the cre1 mutant and triggers the formation

229 extensively investigated, but the effects of nodulation on plant nitrogen responses remain largely un

230 nin alfalfa is a direct result of changes in nodulation or nitrogen fixation efficiency.

231 ions locally and has no apparent function in nodulation or root development.

232 ntified a previously unsuspected role of the nodulation pathway in the establishment of different bac

233 We found that a functional autoregulation of nodulation pathway is required for roots to perceive, ta

234 Here we identify a Lotus japonicus nodulation pectate lyase gene (LjNPL), which is induced

235 ted shoot growth, and show that the aberrant nodulation phenotype caused by LORE1 insertions in the A

236 re we show that ern2 mutants exhibit a later nodulation phenotype than ern1, being able to form nodul

237 atula displayed a shoot controlled increased nodulation phenotype, similar to the clv2 mutants of pea

238 ene inhibitor treatment counteracts the cra2 nodulation phenotype.

239 s reported previously, str shows a wild-type nodulation phenotype.

240 and triple-knockout lines showed dissimilar nodulation phenotypes but coincided in upregulation of a

241 We performed a screen for aberrant nodulation phenotypes using the Lotus japonicus LORE1 in

242 ications were shown to alter root growth and nodulation phenotypes, revealing additional regulators o

243 Fewer than 20 plant genes involved in the nodulation process have been functionally characterized.

244 duced by rhizobial bacteria that trigger the nodulation process in legumes, and by some fungi that al

245 tion, precisely how this protein impacts the nodulation process remains undetermined.

246 utant line, altered in the autoregulation-of-nodulation receptor kinase GmNARK, determined that a sys

247 The symbiotic receptor-like kinases nodulation receptor-like kinase (NORK) and lysin motif d

248 nitiate spontaneous nodule organogenesis and nodulation-related gene expression in the absence of rhi

249 The method predicted a soybean nodulation-related gene regulatory network consisting of

250 ation, many efforts are underway to identify nodulation-related genes and determine how these genes i

251 dentified 533 miRNA targets, including three nodulation-related genes and eight nodule-specific genes

252 me, become a comprehensive knowledge base of nodulation-related pathways.

253 ioinformatic tools, we identified 13 LSEs of nodulation-related secreted protein families, each uniqu

254 site (RRBS) in their promoters, we found the nodulation-related Type-A RR Mt RR4 and the Nodulation S

255 Nodulation requires the reprogramming of the plant cell,

256 hat the MtCEP1 peptide-dependent increase in nodulation requires the symbiotic signaling pathway and

257 thylene production is an early and sustained nodulation response that acts at multiple stages to regu

258 nosuppression was characterized by a reduced nodulation response, which was associated with a signifi

259 inal domain of MtEIN2 is sufficient to block nodulation responses, consistent with previous reports i

260 d signaling, 240 nutrient-responsive and 365 nodulation-responsive Signaling-SSPs were identified, gr

261 standing the molecular basis of Rj4-mediated nodulation restriction and facilitates the development o

262 e control of genotype-specific infection and nodulation reveals a common recognition mechanism underl

263 During nodulation, rhizobia are entrapped within curled root ha

264 nvestigate the role of SGF14c during soybean nodulation, RNA interference was employed to silence SGF

265 lts together revealed that autoregulation of nodulation, root development, and the location of nitrog

266 ction marker, and of the cytokinin-regulated Nodulation Signaling Pathway 2 (Mt NSP2) gene.

267 nodulation-related Type-A RR Mt RR4 and the Nodulation Signaling Pathway 2 (NSP2) TF.

268 dulation (Nod) factors via activation of the nodulation signaling pathway and the NIN transcription f

269 Activation of the nodulation signaling pathway in spontaneously nodulating

270 d the induction of two key nodulation genes, Nodulation Signaling Pathway1 (NSP1) and NSP2 Accordingl

271 the following genes: DMI1, DMI2, DMI3, NIN, NODULATION SIGNALING PATHWAY1 (NSP1), NSP2, SUNN, and SI

272 hairs that involves the complex interplay of Nodulation Signaling Pathway1 (NSP1)/NSP2 GRAS and Ethyl

273 gnaling genes as well as of the CK-regulated Nodulation Signaling Pathway2 and Ethylene Response Fact

274 gets the key nodulation transcription factor Nodulation Signaling Pathway2, correlates with bacterial

275 ms that DELLA proteins can interact with the nodulation signalling pathway 2 (NSP2) and nuclear facto

276 protein, named Scarecrow-like13 Involved in Nodulation (SIN1), localizes both to the nucleus and the

277 mbiosis-signaling pathway has parallels with nodulation-specific signaling and functions to promote m

278 tative lipid-binding BON (bacterial OsmY and nodulation) superfamily, and a C domain (residues 201-32

279 This includes orthologues of nodulation-suppressing CLE peptides and AtCLE40 that con

280 Rhizobium and Ensifer: this was confirmed by nodulation tests.

281 ogress made in plant genetic control of root nodulation that occurs in non-legume actinorhizal plant

282 s, the developmental competency of roots for nodulation, the formation of fused nodules, and an incre

283 We also show that during nodulation, the G-protein cycle is regulated by the acti

284 During the course of nodulation, there is a nodule-specific redirection of Mt

285 NIN) allows induction of this program during nodulation through activation of LBD16 that promotes aux

286 . elkanii strains are highly competitive for nodulation; thus, cultivars harboring an Rj4 allele are

287 Cytokinin hormones are critical for early nodulation to coordinate root nodule organogenesis and t

288 the nitrogen-fixing clade indicated that the nodulation trait has a shared evolutionary origin in all

289 omic comparative analyses indicated that the nodulation traits of legumes, Parasponia spp., as well a

290 ion, maturity, morphology, pigmentation, and nodulation traits.

291 onical miR171 isoform, which targets the key nodulation transcription factor Nodulation Signaling Pat

292 This absence of nodulation was due to a defect in Nod factor signaling b

293 When the CND gene was silenced, nodulation was reduced.

294 To test the role of auxin influx in nodulation we used the auxin influx inhibitors 1-naphtho

295 further investigate the role of GS52 during nodulation, we used RNA interference to silence GS52 exp

296 oles of the metabolic pathway during soybean nodulation were further supported by analysis of transge

297 n the cortex is necessary and sufficient for nodulation, whereas cytokinin is antagonistic to lateral

298 -deficient roots had a near complete loss of nodulation, whereas flavone-deficient roots had reduced

299 Analysis of temporal WOX5 expression during nodulation with quantitative reverse transcription-polym

300 two soybean genes Rj2 and Rfg1 that restrict nodulation with specific strains of Bradyrhizobium japon