ライフサイエンスコーパス: abiotic stress

1 response against herbivores, pathogens, and abiotic stress.

2 morphogenesis and defense against biotic and abiotic stress.

3 lant development and responses to biotic and abiotic stress.

4 the plants to protect them against biotic or abiotic stress.

5 athways that control responses to biotic and abiotic stress.

6 s for their protective action in response to abiotic stress.

7 egulation in ABA biosynthesis in response to abiotic stress.

8 and are involved in responses to biotic and abiotic stress.

9 and development as well as plant response to abiotic stress.

10 lization, pathogen defense, and responses to abiotic stress.

11 o quickly regulate cellulose synthesis under abiotic stress.

12 velopment, and in defense against biotic and abiotic stress.

13 enes encoding photosynthetic proteins during abiotic stress.

14 n of the IAA5 and IAA19 genes in response to abiotic stress.

15 d in responses to hormones and to biotic and abiotic stress.

16 s about secondary wall gene regulation under abiotic stress.

17 s almost certainly important in tolerance to abiotic stress.

18 sive perennial weed after episodes of severe abiotic stress.

19 -overexpressing lines conferred tolerance to abiotic stress.

20 , defense against pathogens, and response to abiotic stress.

21 role in the acclimation process of plants to abiotic stress.

22 ne organization and protein structure during abiotic stress.

23 gulating stomatal aperture during biotic and abiotic stress.

24 onditions, demonstrating a role for auxin in abiotic stress.

25 nd oxygen levels, is characteristic for this abiotic stress.

26 longation, seed germination, and response to abiotic stress.

27 in mediating rapid systemic signaling during abiotic stress.

28 s implicated in pathogen defense, biotic and abiotic stress.

29 ted molecular patterns (MAMPs) or with other abiotic stresses.

30 plays a critical role in plant tolerance to abiotic stresses.

31 responsible for maize molecular response to abiotic stresses.

32 lopmental stages and tolerance of biotic and abiotic stresses.

33 th, development, and responses to biotic and abiotic stresses.

34 ically confronted by simultaneous biotic and abiotic stresses.

35 global interest because of its tolerance to abiotic stresses.

36 nt are continuously challenged by biotic and abiotic stresses.

37 scence, and in plant responses to biotic and abiotic stresses.

38 as increase in tolerance against biotic and abiotic stresses.

39 insights into the functional consequences of abiotic stresses.

40 va is especially vulnerable to pathogens and abiotic stresses.

41 tive stress, thus mitigating a wide range of abiotic stresses.

42 acquisition and helping plants to withstand abiotic stresses.

43 expression levels and adaptation to multiple abiotic stresses.

44 fits and protecting hosts against biotic and abiotic stresses.

45 , as well as responses to certain biotic and abiotic stresses.

46 3 and 8 were majorly regulated in biotic and abiotic stresses.

47 gnaling in the plant response to a number of abiotic stresses.

48 ortant functions in plant protection against abiotic stresses.

49 s a key regulatory hub in plant responses to abiotic stresses.

50 role in the response of plants to different abiotic stresses.

51 t signals including pathogens, wounding, and abiotic stresses.

52 dehydration protein) family, to combat these abiotic stresses.

53 hormone cross talk and redox signaling under abiotic stresses.

54 nutrition and plant resistance to biotic and abiotic stresses.

55 ecules and protect plants against biotic and abiotic stresses.

56 and activates its expression under different abiotic stresses.

57 ferences, compared to stomatal regulation by abiotic stresses.

58 athway regulates plant responses to multiple abiotic stresses.

59 ess regulator TSPO is transiently induced by abiotic stresses.

60 defense mechanism of plants under biotic and abiotic stresses.

61 bnetwork structures in response to different abiotic stresses.

62 l-demonstrated roles of SACPDs in biotic and abiotic stresses.

63 pal regulators of plant responses to several abiotic stresses.

64 ons and in protecting plants from biotic and abiotic stresses.

65 ssue development and responses to biotic and abiotic stresses.

66 lant development and responses to biotic and abiotic stresses.

67 tus and providing protection from biotic and abiotic stresses.

68 mone transport or defense against biotic and abiotic stresses.

69 l to engineer plants against both biotic and abiotic stresses.

70 ion in the alleviation of diverse biotic and abiotic stresses.

71 pensates for growth rate reduction caused by abiotic stresses.

72 a protective barrier against many biotic and abiotic stresses.

73 cotiana benthamiana and confers tolerance to abiotic stresses.

74 ion productivity and tolerance of biotic and abiotic stresses.

75 impending challenges from specific biotic or abiotic stresses.

76 fits and protecting hosts against biotic and abiotic stresses.

77 have suggested roles mainly in tolerance to abiotic stresses.

78 proteins perceive and respond to biotic and abiotic stresses.

79 seed coat permeability and susceptibility to abiotic stresses.

80 tained due to a trade-off between biotic and abiotic stress adaptation.

81 plant defense, and tolerance/sensitivity to abiotic stress all point to a fundamental role of splici

82 High soil salinity constitutes a major abiotic stress and an important limiting factor in culti

83 and systemic tissues of plants subjected to abiotic stress and attempt to propose a model for the in

84 lated categories of holm oak are enriched in abiotic stress and chromatin assembly.

85 teractions can buffer plant communities from abiotic stress and consumer pressure caused by climatic

86 al interactions occurring under simultaneous abiotic stress and herbivory.

87 Both abiotic stress and species interactions can limit popula

88 could occur within seconds of initiation of abiotic stress and that this response could invoke known

89 ing a putative regulatory connection between abiotic stress and the circadian clock.

90 te, no systematic screening of lncRNAs under abiotic stress and their regulatory roles in cassava has

91 nly used to study the responses of plants to abiotic stress and to assess stress tolerance.

92 onal cross-talk modulates plant responses to abiotic stresses and defenses against insect herbivores

93 showed unequal contributions in response to abiotic stresses and development, which may aid wheat ad

94 nts are less responsive to growth-inhibiting abiotic stresses and have elevated expression of stress

95 e constantly subjected to various biotic and abiotic stresses and have evolved complex strategies to

96 majority of the rest were down-regulated in abiotic stresses and up-regulated in biotic stresses.

97 in various organs, as well as in response to abiotic stresses and various hormone treatments.

98 sociated with leaf expansion, independent of abiotic stress, and another that is drought induced.

99 abundance was increased significantly during abiotic stress, and characterization of mutant lines rev

100 t a positive species interaction ameliorates abiotic stress, and has a profound effect on a species'

101 plants are activated by developmental cues, abiotic stress, and pathogen infection.

102 s in plant tissues in response to biotic and abiotic stress, and regulates plant growth.

103 otect host plants against diverse biotic and abiotic stresses, and promote biodegradation of various

104 genes respond differentially to a variety of abiotic stresses, and that proteins encoded by these gen

105 Crops resistant to abiotic stresses are a long-term goal of many research p

106 Plant responses to biotic and abiotic stresses are often very specific, but signal tra

107 Traditional evaluation of crop biotic and abiotic stresses are time-consuming and labor-intensive

108 espiration or as a consequence of biotic and abiotic stress as well as in the initiation of senescenc

109 fect on the expression of well-characterized abiotic stress-associated transcriptional regulatory net

110 duction and response to different biotic and abiotic stresses at the post-transcriptional levels.

111 ply for protection of spores from biotic and abiotic stresses but also for spore structural developme

112 d much to clarify the signalling pathways of abiotic stress, but guard cell signalling in response to

113 ctively defend themselves against biotic and abiotic stresses by synthesizing diverse secondary metab

114 Abiotic stress can release the transcription of epigenet

115 Abiotic stresses cause accumulation of reactive oxygen s

116 insects and numerous microbial pathogens and abiotic stresses caused by adverse climatic conditions.

117 Frost stress is one of the major abiotic stresses causing seedling death and yield reduct

118 tworks related to defense against biotic and abiotic stress, cell cycle growth and division in Arabid

119 cold, salinity and heat, or any of the major abiotic stresses combined with pathogen infection.

120 distinct from nitrogen starvation and other abiotic stresses commonly used to induce oil accumulatio

121 s a key phytohormone produced in response to abiotic stress conditions and is an activator of abiotic

122 ed by an ethylene treatment and that several abiotic stress conditions could stimulate cell elongatio

123 ioides) plants were subjected to four common abiotic stress conditions individually: high soil salini

124 that auxin-mediated growth inhibition under abiotic stress conditions is one of the developmental an

125 Under abiotic stress conditions the yield losses are often eve

126 the cell-surface expression of PIP2;7 during abiotic stress conditions through protein-protein intera

127 es and prominent differences between various abiotic stress conditions, such as salt, cold, ultraviol

128 e tested in roots and leaves under different abiotic stress conditions.

129 ly expressed under both biotic challenge and abiotic stress conditions.

130 that promotes anthocyanin accumulation under abiotic stress conditions.

131 in the production of aliphatic suberin under abiotic stress conditions.

132 arding their gene expression under different abiotic stress conditions.

133 accretion of reactive oxygen species during abiotic stress conditions.

134 d gene could improve plant performance under abiotic stress conditions.

135 2-Ln levels significantly rose under several abiotic-stress conditions such as wounding or exposure t

136 in plant defense response against different abiotic-stress conditions, mainly by inducing heat shock

137 Drought is the main abiotic stress constraining sugarcane production.

138 9 biological processes, including biotic and abiotic stresses, development, flavonoid biosynthesis, t

139 A, auxin, ethylene, GA, and JA), response to abiotic stress (DREB1A/2A, RD22) and light (PIF3), phosp

140 criptionally differentially regulated during abiotic stresses during Botrytis cinerea infection or af

141 produce are exposed to pre- and postharvest abiotic stresses during the production chain.

142 Chlamydomonas reinhardtii cells exposed to abiotic stresses (e.g. nitrogen, zinc, or phosphorus def

143 xify ROS, ROS is beneficial to plants during abiotic stress enabling them to adjust their metabolism

144 genes also occurs during different types of abiotic stress (environmentally-equivalent conditions of

145 s and mitomycin C, but not to other forms of abiotic stress, established a specific role for TAF1 in

146 and apply this method to reanalyze a set of abiotic stress expression data in Arabidopsis thaliana.

147 can be affected by drought stress, a common abiotic stress for tomato.

148 We present an abiotic stress gene regulatory network of 200,014 intera

149 ry mechanism of cellulose biosynthesis under abiotic stress has not been well explored.

150 ainst pathogen infections, pest attacks, and abiotic stresses has advanced, the exact mechanism(s) by

151 ealize that the roles of B vitamins in plant abiotic stress have had minimal attention in the literat

152 d in photosynthesis, starch accumulation and abiotic stresses have been positively selected, whereas

153 veness, acclimation, and memory of plants to abiotic stress holds substantive potential for improving

154 Abiotic stresses impact negatively on plant growth, prof

155 ubstrate relations, regulate the response to abiotic stress in Arabidopsis thaliana.

156 between the circadian clock and responses to abiotic stress in model plants, little is known of the c

157 review recent studies on the role of ROS in abiotic stress in plants, and propose that different abi

158 Epmbf1 was induced by a number of abiotic stresses in E. pusillum and transgenic yeast, an

159 f ARFs in conferring tolerance to biotic and abiotic stresses in plant species.

160 portance of systemic acquired acclimation to abiotic stresses in plants and identified several differ

161 mic methylation is variable under biotic and abiotic stresses in plants.

162 in fruit development as well as responses to abiotic stresses in strawberry.

163 offers tolerance against oxidative and other abiotic stresses in the alr1105 transformed Escherichia

164 ermore, when subjected to various biotic and abiotic stresses in the dark, the singlet oxygen-specifi

165 s of peanut (Arachis hypogaea) to biotic and abiotic stresses include the synthesis of prenylated sti

166 ave emerged as central regulator of numerous abiotic stresses including HMs.

167 Because of the focus on abiotic stress-induced elRs in recent decades, biotic st

168 FINGER OF ARABIDOPSIS THALIANA12 (ZAT12), an abiotic stress-induced transcription factor.

169 in addition to tolerance against a range of abiotic stress inducers.

170 We assessed whether different abiotic stresses induction have an impact on MP levels i

171 Plant's response and adaptation to abiotic stresses involve sophisticated genetic and epige

172 notyping pipeline for the genetic studies of abiotic stress iron deficiency chlorosis (IDC) of soybea

173 Its accumulation in ssadh mutants and during abiotic stresses is a response to avoid the SSA induced

174 molecular mechanisms underlying tolerance to abiotic stresses is important in crop breeding.

175 ENPs) and trace elements (a common source of abiotic stress) is critical to gaining insights into the

176 Under most instances of moderate abiotic stress levels, increased isoprenoid emission rat

177 Biotic and abiotic stresses limit agricultural yields, and plants a

178 During abiotic stress, MG levels accumulate to toxic levels in

179 e report for the first time that, similar to abiotic stresses, MG levels increase during biotic stres

180 However, the mechanisms of abiotic stress mitigation by isoprene are still under de

181 We provide a valuable resource of 572 abiotic stress modules of coregulated genes with functio

182 ated at the transcription level by different abiotic stresses, namely salt and drought stress, until

183 eins that control the response to biotic and abiotic stresses, namely the immune receptor XA21, which

184 Predisposition results from abiotic stresses occurring prior to infection that affec

185 heir specialized metabolites in responses to abiotic stress or biotic stress factors like pathogens a

186 Adaptive plant responses to specific abiotic stresses or biotic agents are fine-tuned by a ne

187 eta-Glucosidases are known to play a role in abiotic stresses, particularly dehydration through absci

188 erone OsNAPL6 may serve a regulatory role in abiotic stress physiology possibly via modulating nucleo

189 Manipulation of a single abiotic stress-related gene could improve plant performa

190 While the abiotic stress-related hormone abscisic acid (ABA) is kn

191 as a possible target for the engineering of abiotic stress-resilient crops.

192 loit genetic diversity to improve biotic and abiotic stress resistance and oil production, while also

193 tic stress conditions and is an activator of abiotic stress resistance mechanisms and a regulator dur

194 quantitative trait loci for both biotic and abiotic stress resistance, our results identify a unique

195 al of manipulating miR528 in improving plant abiotic stress resistance.

196 protein structure and function of biotic and abiotic stress-resistance genes, and QTLs could shed lig

197 The development of abiotic stress-resistant cultivars is of premium importa

198 ics, the role of plant histone chaperones in abiotic stress response and adaptation remains elusive.

199 al processes, yet it has also been linked to abiotic stress response in a less defined manner.

200 The abiotic stress response in plants is complex and tightly

201 unknown link between histone chaperones and abiotic stress response in plants.

202 the most significant molecular mechanisms of abiotic stress response in plants.

203 In addition to the well-described abiotic stress response pathway initiated by the hormone

204 h control plants are associated to biotic or abiotic stress response.

205 mRNA isoforms is an important feature of the abiotic stress response.

206 volved in the plant defense response and the abiotic stress response.

207 nowledge on how hormonal signaling regulates abiotic stress responses and defenses against insects, a

208 The biotic and abiotic stress responses are conferred by series of gene

209 f cv Semillon berries by inducing biotic and abiotic stress responses as well as ripening processes.

210 lly redundant functions in the regulation of abiotic stress responses but have opposite functions to

211 iated lincRNAs play important roles in plant abiotic stress responses but lincRNAs and TE-lincRNAs mi

212 heir possible roles in mediating hormone and abiotic stress responses in cassava.

213 l processes and a key mediator of biotic and abiotic stress responses in plants.

214 However, PEN3 also functions in abiotic stress responses to cadmium and indole-3-butyric

215 Furthermore, we show that ERFVIIs enhance abiotic stress responses via physical and genetic intera

216 division and cell cycle activity, biotic and abiotic stress responses, and proteolysis.

217 lants, G-proteins affect multiple biotic and abiotic stress responses, as well as many developmental

218 promoting plant hormones that play a role in abiotic stress responses, but molecular modes that enabl

219 sticated pool at target loci associated with abiotic stress responses, flowering time, and morphology

220 isregulation of genes involved in biotic and abiotic stress responses, the most prominent one being t

221 is and photosynthesis, and (3) activation of abiotic stress responses.

222 toperiodic control of flowering, growth, and abiotic stress responses.

223 alysis to extrapolate their precise roles in abiotic stress responses.

224 eproduction, as well as governing biotic and abiotic stress responses.

225 es plant growth and development and mediates abiotic stress responses.

226 acid (ABA) is an essential molecule in plant abiotic stress responses.

227 ars to control both cell fate regulators and abiotic stress responses.

228 enriched in proteins involved in biotic and abiotic stress responses.

229 e plays vital roles in plant development and abiotic stress responses; however, little is known about

230 a, genome-wide expression of many biotic and abiotic stress-responsive genes is diurnally repressed a

231 the variability in transcriptome response to abiotic stress, RNA sequencing was performed using 14-da

232 p previously shown to be involved in ABA and abiotic stress signaling in other plant species.

233 e outcome of interactions between biotic and abiotic stress signaling is often plant and/or insect sp

234 circadian clock as an integrator of ambient abiotic stress signals important for the growth and fitn

235 s in the defense mechanism against different abiotic-stress situations.

236 As sessile organisms, plants must cope with abiotic stress such as soil salinity, drought, and extre

237 Furthermore, abiotic stresses such as dark and ultraviolet C irradiat

238 s may require novel approaches to overcoming abiotic stresses such as drought and salinity as well as

239 est attack and exhibit enhanced tolerance to abiotic stresses such as drought, low temperature, or me

240 stress in plants, and propose that different abiotic stresses, such as drought, heat, salinity and hi

241 tal role in plant response and adaptation to abiotic stresses, such as drought, high salinity and low

242 Abiotic stresses, such as salinity, cause global yield l

243 and its uptake by plants is affected by many abiotic stresses, such as salinity, cold, heat, and drou

244 el for the study of higher plant response to abiotic stresses, survive in the desert ecosystem charac

245 Low temperature is a seasonal abiotic stress that restricts native plant ranges and cr

246 Plants are exposed to recurring biotic and abiotic stresses that can, in extreme situations, lead t

247 traits to tolerate both herbivore attack and abiotic stress, the climatic niche of a species should b

248 the potential to regulate plant responses to abiotic stresses, their role in such responses remains p

249 characterized the effects of three types of abiotic stress (thermal, oxidative and hyperosmotic) on

250 nents, invading pathogens, wound signals, or abiotic stress, they often switch to a primed state of e

251 Plants respond to abiotic stress through a variety of physiological, bioch

252 characterization of CsBGlu12 and its role in abiotic stress through ROS scavenging.

253 Plants need to cope with biotic and abiotic stress through well-coordinated cell-to-cell com

254 nes orchestrate crosstalk between biotic and abiotic stresses through a variety of mechanisms, includ

255 We propose that plants sense multiple abiotic stresses through the Cys-Arg/N-end rule pathway

256 bscisic acid (ABA) is induced in response to abiotic stress to mediate plant acclimation to environme

257 To test this, we used abiotic stresses to manipulate the availability of reduc

258 rior crop cultivars with enhanced biotic and abiotic stress tolerance and increased biomass yields.

259 acid (ABA) is a plant hormone that mediates abiotic stress tolerance and regulates growth and develo

260 The roles of Tre6P in abiotic stress tolerance and stomatal regulation are als

261 c acid (ABA) is a key phytohormone promoting abiotic stress tolerance as well as developmental proces

262 st time, show that the BjERD4 is involved in abiotic stress tolerance besides offering new clues abou

263 ifying capabilities, confers dual biotic and abiotic stress tolerance in model plant Nicotiana tabacu

264 erved role of this gene in drought and other abiotic stress tolerance in several plant species.

265 The enhanced abiotic stress tolerance in transgenic plants is related

266 the ERF-VII protein family) by examining the abiotic stress tolerance of an ERF74 overexpression line

267 Our analyses indicate an important abiotic stress tolerance strategy in several eudicots, w

268 2 phosphorylation plays an important role in abiotic stress tolerance that likely serves as a univers

269 evelopment, hormone signaling and biotic and abiotic stress tolerance through coordination of transcr

270 e fungal endophytes often confers biotic and abiotic stress tolerance to their hosts.

271 und produced by some plant species, enhances abiotic stress tolerance under current atmospheric CO2 c

272 ncing plant growth, nutrient use efficiency, abiotic stress tolerance, and disease resistance-into ag

273 eness of the role of the phytobiome in plant abiotic stress tolerance, led us to sequence the transcr

274 astid MSH1 depletion results in variegation, abiotic stress tolerance, variable growth rate, and dela

275 se, and this is often linked to immunity and abiotic stress tolerance.

276 tropical hybrids selected to exhibit diverse abiotic stress tolerance.

277 elopment and were recently shown to regulate abiotic stress tolerance.

278 protein arginine methyltransferase vital to abiotic stress tolerance.

279 ential metabolic markers for the breeding of abiotic stress-tolerant maize.

280 er on many areas of plant biology, including abiotic stress, transcriptional regulation, light percep

281 es, plant immunity, signaling in response to abiotic stress, transporters, biosynthesis of cells wall

282 creased expression in response to biotic and abiotic stress treatments suggestive of a role in adapta

283 observed in various tissues when undergoing abiotic stress treatments, implying that each CAF1 gene

284 Abiotic stress triggers an ABA signal transduction casca

285 The early response to abiotic stress typically involves induction of genes inv

286 Abiotic stress unbalances cell ion homeostasis, and plan

287 e that miR319 plays in the plant response to abiotic stress using transgenic creeping bentgrass (Agro

288 genes, common to singlet oxygen, biotic and abiotic stresses was defined and confirmed to be activat

289 on of GHB in Arabidopsis plants subjected to abiotic stresses was described as a way of avoiding SSA

290 oxes but not DRE elements; conversely, under abiotic stress, we observed specific binding of ERF1 to

291 ific features in transcriptional response to abiotic stress were detected.

292 of genes involved in responses to biotic and abiotic stresses were found to be differentially express

293 ilies in B. distachyon, wheat and rice under abiotic stresses were investigated by next-generation se

294 Ps accumulation in seeded fruits during both abiotic stresses, whereas no association was found in pa

295 Drought and salinity are the major abiotic stresses which adversely affect the growth and p

296 critical role for SP1 in plant responses to abiotic stress, which is a major and increasing cause of

297 altered levels of expression in response to abiotic stress, which requires concerted action of both

298 promote plant growth and confer tolerance to abiotic stress, which suggests common principles underpi

299 ellular transcriptional response pathways to abiotic stress, while reducing the dimensions in gene-or

300 e primed state, plants respond to biotic and abiotic stress with faster and stronger activation of de