ライフサイエンスコーパス: salt stress

1 in Sorghum in response to drought, heat, and salt stress.

2 Pi levels modulate responses of the root to salt stress.

3 s conditions such as nitrogen starvation and salt stress.

4 wer germination capacities under osmotic and salt stress.

5 xpressing miRNVL5 showed hypersensitivity to salt stress.

6 onsible for the cell's ability to respond to salt stress.

7 to investigate and compare their response to salt stress.

8 involved in regulation of plant response to salt stress.

9 dynamic nature of physiological responses to salt stress.

10 and negative control of gene expression upon salt stress.

11 ing dwarfism and hypersensitivity to osmotic/salt stress.

12 ontent, was greater in gr3 than the WT under salt stress.

13 ascular bundles with altered S:G ratio under salt stress.

14 ing molecule regulating adaptive response to salt stress.

15 ndividual isoforms in seed germination under salt stress.

16 ing and result in altered germination during salt stress.

17 ne 3-hydroxylase (CsF3H) encoding gene under salt stress.

18 were responsible for its hypersensitivity to salt stress.

19 nt and photosystem II activity than WT under salt stress.

20 ly unknown how NAD affects plant response to salt stress.

21 rs in the control of seed germination during salt stress.

22 tios in shoots of seedlings grown under mild salt stress.

23 acuoles from young leaves is unchanged under salt stress.

24 membrane ionic permeability under prolonged salt stress.

25 (35S:ERF1) were more tolerant to drought and salt stress.

26 sis but rather its regulation in response to salt stress.

27 ession of OsGR3 but not OsGR1 was induced by salt stress.

28 moderate low water potential (psi(w)) or to salt stress.

29 ic stress conditions such as dehydration and salt stress.

30 well as leaf photosynthetic efficiency under salt stress.

31 o confer inappropriate activation of Kss1 by salt stress.

32 response to stress and are more tolerant to salt stress.

33 fungus, as well as in the growth response to salt stress.

34 d levels of ROS, and enhanced sensitivity to salt stress.

35 SAUSA300_0957 (gene 957) as essential under salt stress.

36 ies accumulation in seedlings in response to salt stress.

37 fungus Botrytis cinerea and less tolerant to salt stress.

38 bility and sensitivity of seeds and roots to salt stress.

39 iR398 was first induced upon 3-4 h of ABA or salt stress.

40 te" impairs the ability of cells to overcome salt stress.

41 nosine 5'-phosphosulfate reductase (APR), by salt stress.

42 ting that the interaction may be enhanced by salt stress.

43 rabidopsis thaliana plants hypersensitive to salt stress.

44 e nucleus in response to alkaline pH but not salt stress.

45 a key role in regulating ion transport under salt stress.

46 , and gpat5 seedlings had lower tolerance to salt stress.

47 increased sensitivity to lower humidity and salt stress.

48 ive oxygen species (ROS), particularly under salt stress.

49 logous genes resulted in hypersensitivity to salt stress.

50 and MtSec61gamma to relieve ER stress during salt stress.

51 ly proteins and was found to be sensitive to salt stress.

52 ene led to abnormal cell-cell adhesion under salt stress.

53 d BiP3 under Tm treatment and sensitivity to salt stress.

54 n phosphatase, increases cotton tolerance to salt stress.

55 o be upregulated by high light intensity and salt stress.

56 he downstream responses to fungal attack and salt stress.

57 differential expression of OsBZ8 gene during salt stress.

58 ting root system architecture in response to salt stress.

59 growing tissues allowing tomato growth under salt stress.

60 a(+) is accompanied by K(+) deficiency under salt stress.

61 use of its high capacity to tolerate extreme salt stress.

62 compared to control plants under drought and salt stress.

63 to be induced by nutrient starvation and/or salt stress.

64 , and this acetylation did not change during salt stress.

65 histone acetylation was observed only during salt stress.

66 pression significantly increases only during salt stress.

67 metabolites and ions conferring tolerance to salt stress.

68 a critical role for OsOTS1 SUMO protease in salt stress.

69 were associated with altered sensitivity to salt stress.

70 nd uncovered a potential role for this TF in salt stress.

71 o required for optimal responses to cold and salt stresses.

72 ze plants subjected to prolonged drought and salt stresses.

73 o demonstrated more tolerance to drought and salt stresses.

74 e and promote plant tolerance to drought and salt stresses.

75 otic stresses and is tolerant to drought and salt stresses.

76 n the control wheat plants under drought and salt stresses.

77 Exposure to a high salt stress (150 mM NaCl) triggered a rapid repression o

78 harvested at control (0 mM NaCl) and severe salt stress (300 mM NaCl) in P. indica-colonized and non

79 Under salt stress (50-400 mM NaCl), miRNVL5 expression was rep

80 ow Pi dampened the inhibiting effect of mild salt stress (75 mm) on all measured RSA components.

81 1 is unable to accumulate anthocyanins under salt stress, a key phenotype of sos3-1 under high NaCl l

82 alsa to be enriched in genes contributing to salt stress acclimatization, nutrient solubilization and

83 h rapid and gradual increases of ethanol and salt stress across the genome.

84 The salt stress activated the sucrose biosynthetic pathway m

85 ecotype Columbia-0 accession of Arabidopsis, salt stress affected MR elongation more severely than LR

86 gh levels of SUMO-conjugated proteins during salt stress and are highly salt sensitive; however, in n

87 ut the possible roles of functional OsGR3 in salt stress and biotic stress tolerance.

88 of SR45 resulted in enhanced sensitivity to salt stress and changes in expression and splicing of ge

89 ealed the involvement of WxL operons in bile salt stress and endocarditis pathogenesis.

90 quired for a fast MT disassembly response to salt stress and for salt stress tolerance.

91 verexpression of CsF3H provided tolerance to salt stress and fungus A. solani infection to transgenic

92 -3-ols in tobacco and conferred tolerance to salt stress and fungus Alternaria solani infection.

93 Salt stress and high light intensity accelerated biosynt

94 coordinating changes in ion transport during salt stress and in promoting salt tolerance.

95 alters plant development and improves plant salt stress and nitrogen (N) deficiency tolerance.

96 sos6-1 plants are hypersensitive to salt stress and osmotic stress imposed by mannitol or po

97 analysis indicates a role for PIAL1 and 2 in salt stress and osmotic stress responses, whereas under

98 s stability is substantially increased under salt stress and other ionic and dehydration stresses.

99 is thaliana tno1 mutant is hypersensitive to salt stress and partially mislocalizes vacuolar proteins

100 S2242 plays important roles in adaptation to salt stress and pathogenesis; however, its biological fu

101 as putative factors integrating responses to salt stress and Pi starvation.

102 nCaK does not impair growth under osmotic or salt stress and that SynCaK is not involved in the regul

103 pes, the expression of OsPCF2 in roots under salt stress and the OsNIN-like4 in roots subjected to PE

104 K cascade signal during the initial phase of salt stress and translates the salt-induced signal into

105 ction of the two pigmented antibiotics under salt-stressed and normal conditions in submerged cultiva

106 hosts, stimulating their growth, alleviating salt stress, and inducing local and systemic resistance

107 tion, more severe water loss in shoots under salt stress, and slower removal of Na(+) from the root a

108 its representative target, CSD1, by ABA and salt stresses, and raise the possibility that regulation

109 also indispensable for the establishment of salt stress- and leaf age-dependent phyllosphere bacteri

110 on, we undertook a transcriptional screen of salt stressed Arabidopsis (Arabidopsis thaliana) roots.

111 During salt stress, Arabidopsis plants arrest growth through de

112 ory responses to different carbon sources or salt stresses are more moderate, but we find numerous di

113 ous stress treatments, including drought and salt stress, are able to induce stromule formation in th

114 biomass production and increased yield under salt stress as compared to wild type plants.

115 LH112 that is up-regulated under drought and salt stresses, as indicated by previous microarray data

116 Expression of several known salt stress-associated genes, including SALT OVERLY SENS

117 HsfB2b function is important during heat and salt stress because HsfB2b overexpression sustains circa

118 ect in anthocyanin production in response to salt stress but not to other stresses such as high light

119 OI expression was enhanced by B. cinerea and salt stress but repressed by the plant hormone gibberell

120 n ompU deletion mutant was sensitive to bile salt stress but resistant to polymyxin B stress, indicat

121 n of ion homeostasis or cell expansion under salt stress, but do not play a major role in plant toler

122 and partially rescue its hypersensitivity to salt stress, but not affect NAD concentration.

123 eloped fewer and shorter lateral roots under salt stress, but not in control conditions.

124 plant cell wall is an important response to salt stress, but relatively little is known about the bi

125 n thought to be involved in the detection of salt stress, but the molecular components of the sensing

126 me cellular responses are common to heat and salt stresses, but pretreatment with mild heat did not p

127 s, and NAD participates in plant response to salt stress by affecting stress-induced accumulation of

128 1 SnRK2s function in root development under salt stress by affecting the transcript levels of aquapo

129 on of reactive oxygen species resulting from salt stress by participating in a new salt tolerance pat

130 tGSTU17 in adaptive responses to drought and salt stresses by functioning as a negative component of

131 ise mechanism, our findings demonstrate that salt stress can regulate the phage lysis-lysogeny switch

132 ts deficient for SERF1 are more sensitive to salt stress compared with the wild type, while constitut

133 ed, plants were more tolerant to drought and salt stresses compared with wild-type plants.

134 nowledge on gene expression regulation under salt stress condition.

135 elongatus UTEX 2973 to produce sucrose under salt stress conditions and investigated if the high effi

136 pplication of CBNs to crops cultivated under salt stress conditions improved the desired phenotypical

137 hannel internalization act in concert during salt stress conditions to modulate aquaporin activity, t

138 t Arabidopsis accessions in control and mild salt stress conditions, different strategies for regulat

139 09 significantly enhanced plant growth under salt stress conditions, doubling fresh weight levels whe

140 Under salt stress conditions, miRNA161 and miRNA173 were stabi

141 % when compared to uninoculated plants under salt stress conditions, suggesting that these salt toler

142 Under salt stress conditions, the N-terminal fragment of AtbZI

143 ranscription factors grown under control and salt stress conditions, we experimentally validated 141

144 n levels of many miRNAs were regulated under salt stress conditions.

145 d regulates Na(+) and K(+) homeostasis under salt stress conditions.

146 c efficiency and lower membrane damage under salt stress conditions.

147 ion and electrolyte leakage under drought or salt stress conditions.

148 gs were grown on agar plates under different salt stress conditions.

149 to a substantial recovery in LR growth under salt stress conditions.

150 ynthetic genes such as F3H, F3'H and LDOX in salt stress conditions.

151 e for dynamic instability in the response to salt stress conditions.

152 st productivity of 1.9 g L(-1) day(-1) under salt stress conditions.

153 -3-ols on pectin methyl esterification under salt stressed conditions was further validated through i

154 ity in roots and leaves under unstressed and salt stressed conditions.

155 eum vegetative development under control and salt-stress conditions, and then compared the metabolic

156 Under both normal and salt-stress conditions, total GR activity was decreased

157 isrupted mitochondrial stress response under salt-stress conditions.

158 sunflower diversity panel under control and salt-stressed conditions and measured a suite of morphol

159 r HDA19 levels led to increased tolerance to salt stress corresponding to the increased ABA sensitivi

160 etr1 and etr2 loss-of-function mutants under salt stress could not be explained by differences in the

161 Salt-stress damage, a common occurrence in delta and coa

162 s, ompD, ompF, and ompC, were higher in bile salts-stressed DeltacspE and correlated with higher intr

163 ABA in root growth and survival tests and to salt stress during germination and at the vegetative sta

164 ze sucrose as an osmoprotectant to cope with salt stress environments.

165 proteins was demonstrated by nutritional and salt stress experiments.

166 In the Deltafgk3 mutant, cold, heat, and salt stresses failed to induce the expression of the str

167 During salt stress, for instance, Na(+) and Cl(-) are sequester

168 Earlier studies found that salt stress from increased tidal flooding prevented tree

169 ation to the nucleus and the upregulation of salt stress genes.

170 rice genotypes with contrasting response to salt stress, genomic resequencing in diverse genetic mat

171 at in dual transgenics, ROS generated during salt stress gets converted into H2O2 by SOD and its opti

172 ulation of anthocyanins in plants exposed to salt stress has been largely documented.

173 r conditions of light stress, osmotic shock, salt stress, heat stress, and recovery from heat stress.

174 under multiple stress conditions, including salt stress; however, factors regulating this process ar

175 alt-sensitive mutant named hypersensitive to salt stress (hss) from an ethyl methanesulfonate-induced

176 s transcriptionally regulated in response to salt stress in a salt-tolerant rice genotype (Hasawi), a

177 R isoforms, showing that APR is regulated by salt stress in an ABA-independent manner.

178 ion of HSFA4A results in hypersensitivity to salt stress in Arabidopsis (Arabidopsis thaliana).

179 hibition of endoreplication and tolerance to salt stress in Arabidopsis (Arabidopsis thaliana).

180 psdmt could enhance tolerance to drought and salt stress in Arabidopsis.

181 en shown to be involved in tolerance to mild salt stress in glycophytes such as Arabidopsis, wheat an

182 sis indicated a whole system response during salt stress in I. imperati, which included four metaboli

183 ys essential roles in the response of ER and salt stress in Medicago.

184 lic pathway may be one of the ways to combat salt stress in plants.

185 nic (wild) tobacco seedlings were exposed to salt stress in presence of flavan-3-ols, epicatechin and

186 22920, and AT3G49200), which were induced by salt stress in wild-type but repressed in miRNVL5-expres

187 al conditions and in response to drought and salt stresses in the staple plant Oryza sativa.

188 nsive alterations in the transcriptome under salt stress, including several genes such as ASCORBATE P

189 ed plant sensitivity toward osmotic and high-salt stress, indicating that NatB is required for tolera

190 e restored the response of the hss mutant to salt stress, indicating that the decreased NAD contents

191 We found that salt stress induced a single Ca(2+) elevation that was m

192 In the wild type, salt stress induced the snRNA-to-snR-DPG switch, which w

193 Transcriptome analysis revealed that salt stress-induced genes are highly correlated with chi

194 d protein SPIRAL1 (SPR1) plays a key role in salt stress-induced MT disassembly.

195 in a salt-tolerant rice genotype (Hasawi), a salt-stress-induced cDNA expression library was construc

196 Thus, salt stress induces a signaling cascade involving the pr

197 We report that salt stress induces an extended quiescent phase in poste

198 Salt stress induces GhANN8b phosphorylation, which is su

199 We found that salt stress induces the accumulation of beta-1,4-galacta

200 Instead, our evidence suggests that salt stress induces this lysogenic bacteriophage by inte

201 lt 1 (RAS1), revealed that it is an ABA- and salt stress-inducible gene and encodes a previously unde

202 The salt stress induction required both JA and ET signaling

203 he finely tuned transcriptional control upon salt stress is dependent on physiological functions of t

204 fruticosa plants response to soil water and salt stress is essential for water irrigation management

205 eased SUMO conjugation in rice plants during salt stress is in part achieved by down-regulation of OT

206 tion through V1-V(o) assembly in response to salt stress is strongly dependent on PI(3,5)P2 synthesis

207 Early detection of salt stress is vital for plant survival and growth.

208 previously that acquired osmotolerance after salt stress is widespread among Arabidopsis thaliana acc

209 In response to salt stress, it was found that myc-tagged AtbZIP17 was c

210 increase in quaternary ammonium compounds in salt-stressed leaves of G lines, presumably due to the a

211 ein is lacking in growth-inhibited leaves of salt-stressed maize.

212 acidification by feeding detached leaves of salt-stressed mutants with glucose or sucrose supported

213 lel purification of samples from control and salt-stressed NTAP-SOS2/sos2-2 plants demonstrated that

214 a model system to investigate the effects of salt stress on allantoin metabolism and to know whether

215 ng plants showed higher tolerance to ABA and salt stress on plates and in soil, accumulating lower le

216 e Pi deprivation response prevailed over the salt stress only for lateral root elongation.

217 noid pathway flux is required, such as under salt stress or upon sudden light intensity changes.

218 erance to environmental challenges including salt stress, osmotic stress and water deficit.

219 l, the molecular processes controlling early salt stress perception and signaling are not fully under

220 bundant in NTAP-SOS2 complexes isolated from salt-stressed plants, suggesting that the interaction ma

221 Changes in CYP79B2 expression in salt stress positively correlated with lateral root deve

222 d appears to have protective effects against salt stress potentially linked to its sodium transport a

223 Ups5 knockout plants under salt stress presented a susceptible phenotype and altere

224 cted 89 candidates out of the 1784 predicted salt stress-related genes with available SALK T-DNA muta

225 The mechanism by which plants cope with salt stress remains poorly understood.

226 Improved salt stress resistance is associated with increased wate

227 d CATs reveals a point of cross talk between salt stress response and other signaling factors includi

228 ase, has emerged as an important mediator of salt stress response and stress signaling through its in

229 redundant functions in the regulation of the salt stress response but opposite functions to control f

230 , makes it an ideal candidate for studies on salt stress response caused by a particular gene.

231 rectly upregulated the expression of several salt stress response genes, including the homeodomain tr

232 The salt stress response in Arabidopsis requires a subtilisi

233 t of transporters putatively involved in the salt stress response in Picochlorum SE3.

234 urther suggests that OsEREBP2 is involved in salt stress response in rice.

235 The salt stress response includes a rapid depolymerization o

236 e suggests that ERF1 might be related to the salt stress response through ethylene signaling.

237 alization of SYP61, which is involved in the salt stress response, was disrupted in the tno1 mutant.

238 a previously uncharacterized role for SR1 in salt stress response.

239 by abscisic acid signaling compared with the salt stress response.

240 and splicing of genes involved in regulating salt stress response.

241 tion pathways and is itself regulated by the salt-stress response signalling machinery.

242 e describe a signaling pathway that mediates salt stress responses in Arabidopsis.

243 kinase described as a negative regulator of salt stress responses in rice.

244 and temporal resolution of our knowledge of salt stress responses, (c) discovering and considering c

245 Previously, we showed that salt-stress-responsive GR3 is a functional protein local

246 Salt-stressed seedlings showed decreased uptake and tran

247 Salt stress sensitive rice variety IR64 was used for dev

248 sults suggest that MusaPIP2;6 is involved in salt stress signaling and tolerance in banana.

249 aporin gene, MusaPIP2;6 which is involved in salt stress signaling in banana.

250 re important components of early osmotic and salt stress signaling pathways in plants.

251 ng TFIIIA transgenic lines under osmotic and salt stress, strong accordance between phenotypic and mo

252 did not hyperaccumulate H2O2 in response to salt stress, suggesting that it is altered signaling rat

253 agos tomatoes displayed greater tolerance to salt stress than the commercial lines and showed substan

254 s showed that SR1 mutant is more tolerant to salt stress than the wild type and complemented line.

255 ss treatment; under sub-lethal conditions of salt stress, the ratios of their seed germination and se

256 Although roots are the primary targets of salt stress, the signaling networks that facilitate meta

257 Under the salt stress, the T3 of RNAi plants showed significant hi

258 response is essential for the adaptation to salt stress, the underlying molecular mechanism has rema

259 stark differences in adaptations to extreme salt stresses, the genomes of S. parvula and Arabidopsis

260 es cerevisiae cells treated with and without salt stress to explore population variation and identify

261 In the case of local salt stress to the Arabidopsis thaliana root, Ca(2+) wav

262 aled the importance of the Ara metabolism in salt stress tolerance and also provides new insights int

263 ensitive (SOS) pathway is critical for plant salt stress tolerance and has a key role in regulating i

264 echanisms that can aid in plant breeding for salt stress tolerance are therefore of great importance

265 expression of GhCHR in Arabidopsis conferred salt stress tolerance by reducing Na(+) accumulation in

266 s reveal that GR3 plays an important role in salt stress tolerance by regulating the GSH redox state

267 Halophytes are rich sources of salt stress tolerance genes which have often been utiliz

268 ent of these different metabolic pathways in salt stress tolerance is discussed.

269 that allantoin accumulation is essential for salt stress tolerance.

270 ed as an important regulator of ABA-mediated salt stress tolerance.

271 we show that ATI1 is involved in Arabidopsis salt stress tolerance.

272 t a negative role of AtGSTU17 in drought and salt stress tolerance.

273 disassembly response to salt stress and for salt stress tolerance.

274 the role of SR45 and its splice variants in salt stress tolerance.

275 s that are crucial for Na(+) homeostasis and salt stress tolerance.

276 new insights into the function of SlCBL10 in salt stress tolerance.

277 To learn more about the role of GR3 in salt-stress tolerance, we investigated the response to 1

278 ng an appropriate defense response to confer salt-stress tolerance.

279 ctors binding to the promoter of OsNHX1 in a salt stress tolerant rice genotype (Hasawi).

280 ctors binding to the promoter of OsNHX1 in a salt stress tolerant rice genotype (Hasawi).

281 reased the tolerance of transgenic plants to salt stress treatment; under sub-lethal conditions of sa

282 Darkness and salt stress triggered BPM1 degradation, whereas elevated

283 Salt stress triggers a simultaneous transcriptional repr

284 this cassette, were not improved in cold or salt stress under the conditions tested.

285 dance of those proteins was analyzed against salt stress using gel-based two-dimensional proteomics a

286 ared the transcriptomes of I. imperati under salt stress vs. control to identify candidate genes and

287 Response to salt stress was also investigated in 8 day-old seedlings

288 Upregulation of these genes by salt stress was blocked by T-DNA insertion mutations in

289 ast, such dynamic regulation of miR398 under salt stress was completely absent in Arabidopsis, in whi

290 regulation of miR398 in response to ABA and salt stress was more dynamic in plants than previously r

291 xpression analysis of genes expressed during salt stress was performed using a novel multiplexed quan

292 ticular gene families related to response to salt stress, water transport, growth, and defense respon

293 n, which is known to be highly induced under salt stress, we have used a Y1H system to screen a salt

294 blish which RSA parameters are responsive to salt stress, we performed a detailed time course experim

295 plants exposed to repetitive heat, cold, or salt stress were more resistant to virulent bacteria tha

296 d in Nonabokra plants even in the absence of salt stress, whereas in IR64, the expression significant

297 of active removal of KOR1 from the PM during salt stress, which otherwise interfered with stress accl

298 ncrease in the ability to survive drought or salt stresses, which are similar to freezing in their in

299 ted resistance to necrotrophic infection and salt stress, while the pad2-1 mutant was sensitive.

300 ibited enhanced tolerance to dehydration and salt stresses, while the knockdown lines were susceptibl