ライフサイエンスコーパス: desiccation

1 lent conditions of temperature, salinity and desiccation).

2 le for trehalose in protecting cells against desiccation).

3 nther growth delays dehiscence by prolonging desiccation.

4 s potentially novel mechanisms for surviving desiccation.

5 esistance to antibiotics, disinfectants, and desiccation.

6 ve a remarkable array of stresses, including desiccation.

7 and embryos acquire the ability to withstand desiccation.

8 s, a related species with tolerance to rapid desiccation.

9 ich widespread fire activity depends on fuel desiccation.

10 um during dehydration and upon recovery from desiccation.

11 gly induced in response to osmotic stress or desiccation.

12 es subjected to drought and seeds undergoing desiccation.

13 moist conditions is recommended followed by desiccation.

14 tant role in determining pollen folding upon desiccation.

15 rrier function, which protects the body from desiccation.

16 maltose at conferring tolerance to long-term desiccation.

17 se is essential for survival after long-term desiccation.

18 anisms to tolerate external hypertonicity or desiccation.

19 halose during short-term, but not long-term, desiccation.

20 utant pollen collapsed at the time of anther desiccation.

21 tage of GC-rich DNA during cell freezing and desiccation.

22 alose is essential for survival to long-term desiccation.

23 ommonly used to prevent corneal exposure and desiccation.

24 area shrinkage between full turgor and oven desiccation.

25 escent spores that are resistant to heat and desiccation.

26 g seeds during embryogenesis, maturation and desiccation.

27 tentials and experienced less shrinkage upon desiccation.

28 loplast membranes is increased during kernel desiccation.

29 water to maintain water balance and prevent desiccation.

30 cover physiological functions after complete desiccation.

31 low, serves to replace this water to prevent desiccation.

32 ormation but before the progressive onset of desiccation.

33 WSCP as interacting with RD21 (responsive to desiccation 21), a granulin domain-containing cysteine p

34 cysteine protease dubbed RD21 (RESPONSIVE TO DESICCATION-21).

35 Acute desiccation activates stress signaling pathways in the o

36 We found that during desiccation, all three species increased expression of c

37 ed upon UV treatment, alkylation damage, and desiccation, also in a RecA-mediated manner.

38 d Ranunculus bulbosus was less vulnerable to desiccation (analyzed via loss of kleaf and turgor loss

39 tion by increasing adhesion and tolerance to desiccation and antibiotics.

40 nfer resistance to stress conditions such as desiccation and antibiotics.

41 resting study on bacteria, which can survive desiccation and at the same time undergo the B-A-B trans

42 ogalacturonan was less methylesterified upon desiccation and changes were also demonstrated in the de

43 chanisms to cope with photo-oxidation during desiccation and cold events, while additional metabolic

44 physiological mechanism during recovery from desiccation and cold stress.

45 opeptide gene and its encoded peptides alter desiccation and cold tolerance.

46 Cysts are resistant to desiccation and divide when water and nutrients are avai

47 LK and DILP levels in neurons in response to desiccation and drinking.

48 anisms underpinning multistress tolerance to desiccation and freezing, we conducted an exhaustive sea

49 nergy but also protects the mosquito against desiccation and heat stresses.

50 ophile, offers novel insights into surviving desiccation and heat.

51 Common responses to desiccation and low temperature involved chloroplast pro

52 tes in the capa-expressing Va neurons during desiccation and nonlethal cold stress but is not release

53 ynthesis of the moss cuticle, which prevents desiccation and organ fusion.

54 evaporation-condensation processes and thus desiccation and osmolarity changes.

55 comial, opportunistic pathogen that survives desiccation and quickly acquires resistance to multiple

56 osing cells or not to Mars-related stresses (desiccation and radiation).

57 ts reconcile MSC events and demonstrate that desiccation and refilling were timed by the interplay be

58 scopy to characterize the dynamics of tissue desiccation and rehydration in petioles (stipes) of inta

59 fied unique stipe traits that may facilitate desiccation and resurrection of the vascular system, inc

60 l dynamics of water movement observed during desiccation and resurrection.

61 ave a limited shelf life, due to postharvest desiccation and senescence, which limits their global di

62 Insect cuticular hydrocarbons (CHCs) prevent desiccation and serve as chemical signals that mediate s

63 They protect terrestrial insects against desiccation and serve as signaling molecules in a wide v

64 e pivotal dual traits for adaptation to both desiccation and signaling have contributed to the consid

65 m corneum serves to protect the body against desiccation and simultaneously limits the passage of dru

66 ed by high temporal persistence, severe soil desiccation and thick dry layers; all of which suggested

67 f a balance of trehalose stockpiled prior to desiccation and trehalose degradation by trehalases in d

68 tive propagules and provided protection from desiccation and UV-B radiation.

69 e hygrosensation (humidity sensing) to avoid desiccation and, in vectors such as mosquitoes, to locat

70 cts as a barrier against pathogen attack and desiccation, and as such is covered by a cuticle, compos

71 es: physical damage to hindwings, predation, desiccation, and cold shock.

72 of cellular protection mechanisms induced by desiccation, and how vegetative desiccation tolerance ci

73 lies and monitored food intake, responses to desiccation, and peptide expression levels.

74 AAs) also contributes to alternative energy, desiccation, and seed vigor; thus, manipulating FAA leve

75 icle that provides essential protection from desiccation, and so its evolution is believed to have be

76 -crystalline amorphous solids (vitrify) upon desiccation, and this vitrified state mirrors their prot

77 the capability (capa) neuropeptide gene is a desiccation- and cold stress-responsive gene in diverse

78 core set of mechanisms to protect them from desiccation- and rehydration-induced damage.

79 s that facilitate plastic responses to avoid desiccation are unclear.

80 transcript abundance of genomic 'clusters of desiccation-associated genes' (CoDAGs), reflecting the c

81 so been proposed as stress effectors against desiccation because they were found in nearly all anhydr

82 ecies from all kingdoms of life, can survive desiccation by entering a state with no detectable metab

83 Dehydration can be due to desiccation caused by a lack of environmental water or t

84 on cells from an exponential culture survive desiccation compared with one in five cells in stationar

85 Desiccation costs are high for harvester ants foraging i

86 bination of intense solar radiation and soil desiccation creates a short circuit in the biogeochemica

87 um cell junctions in each anther locule, and desiccation creates mechanical forces that open the locu

88 upply (upward growth) with avoidance of root desiccation (downward growth).

89 e for insects because they might suffer from desiccation during hot summer days.

90 Experimental desiccation enabled dehiscence of miR167-deficient anthe

91 As desiccation extends, the activities of the protein chape

92 of the cellular structure during wheat grain desiccation facilitates access to lutein-promoting trans

93 t a variety of external stressors including: desiccation, freeze/thaw, exposure to high temperatures,

94 This review explores how desiccation generates cell damage and how tolerant cells

95 A-sensitive COLD REGULATED and RESISTANCE TO DESICCATION genes was diminished in Arabidopsis during i

96 How tardigrades survive desiccation has remained a mystery for more than 250 yea

97 the form of spores were highly resistant to desiccation, heat, and UV light.

98 o extreme environments including exposure to desiccation, heavy metals, UV and Gamma irradiation.

99 During desiccation, homoiochlorophyllous resurrection plants re

100 rmal melanism hypothesis (TMH), the melanism-desiccation hypothesis (MDH) and the photo-protection hy

101 The transcriptomic response to desiccation identified four structural clusters of novel

102 g environmental constraints such as seasonal desiccation imposed by living on land.

103 s underlying adaptations to seasonal habitat desiccation in African killifishes, identifying the gene

104 LIPs are universally highly expressed during desiccation in all surveyed resurrection plants and may

105 adly, the patterns of deformation induced by desiccation in both mesophyll and xylem suggest that cel

106 Tolerance to desiccation in cultures of Saccharomyces cerevisiae is i

107 en identified whose expression is induced by desiccation in diverse, desiccation-tolerant (DT) taxa,

108 ications, and expression dynamics related to desiccation in E. nindensis It was previously hypothesiz

109 e of protective genes is up-regulated during desiccation in even more distantly related DT green alga

110 (RFOs) accumulate in seeds during maturation desiccation in many plant species.

111 y expressed at high levels or induced during desiccation in multiple tardigrade species.

112 lient plants, and some can survive prolonged desiccation in semiarid regions with seasonal rainfall.

113 croclimates in winter and greater host plant desiccation in summer.

114 the human host, losing infectivity following desiccation in the environment.

115 y experiences high osmolarity as a result of desiccation in the soil.

116 foraging activity is stronger as the risk of desiccation increases.

117 y reduced carotenoid degradation during seed desiccation, increasing beta-carotene content 8.4-fold r

118 gly protects cells against disinfectants and desiccation, indicating its potential significance for l

119 o make dividing yeast tolerant to short-term desiccation, indicating that other disaccharides have st

120 ufficiency of trehalose as an antagonizer of desiccation-induced damage in yeast emphasizes its poten

121 nearly all anhydrobiotes, and could mitigate desiccation-induced damage to model proteins and membran

122 These results show that desiccation-induced up-regulation of expression of prote

123 We show that desiccation induces protein misfolding/aggregation of cy

124 ance in two of the species, contrasting with desiccation intolerance in the third.

125 ty was sufficient for complementation of the desiccation intolerant seed phenotype of abi3.

126 by knockout mutants and overexpression in a desiccation-intolerant mutant background to play an impo

127 on is unique to DT algae or also occurs in a desiccation-intolerant relative.

128 is widespread downshift did not occur in the desiccation-intolerant taxon.

129 ility to survive dehydration to the point of desiccation is a key adaptive trait enabling terrestrial

130 survive the dry daytime on leaves and avoid desiccation is not well understood.

131 Rapid water loss, or desiccation, is a universal threat for terrestrial plant

132 e regions of pollen elastic parameters where desiccation leads to a regular, complete closing of all

133 ies showed increased frond temperature, high desiccation levels and reduced photophysiological perfor

134 the strong correlation between sunlight and desiccation, light is probably an important external sig

135 However, most organisms are sensitive to desiccation, likely due to an assortment of different st

136 AAs) in seeds play an important role in seed desiccation, longevity, and germination.

137 eason for a better fungal adaptation to soil desiccation may be hydraulic redistribution of water by

138 graphy), biophysical (evapotranspiration and desiccation of invertebrates) and ecological (food chain

139 uted low CH4 oxidation rates in dry soils to desiccation of MOB, we present several lines of evidence

140 Desiccation of plants is often lethal but is tolerated b

141 However, we demonstrate that the final desiccation of the Bodele Basin occurred around 1 ka.

142 We show that desiccation of the corneal surface due to nerve damage a

143 s an extended history of hydrogen escape and desiccation of the planet.

144 The desiccation of upper soil horizons is a common phenomeno

145 unction with other findings on the impact of desiccation on arthropods and fungal growth, suggest tha

146 ided with protective mechanisms to cope with desiccation or cold stress.

147 protein-loaded material without the need for desiccation or freeze-drying.

148 r days, which especially endanger insects of desiccation or prey visibility.

149 ny inland waters exhibit complete or partial desiccation, or have vanished due to global change, expo

150 esized that transcriptional rewiring of seed desiccation pathways confers vegetative desiccation tole

151 ically protected from degradation during the desiccation period and conserved in dry seeds to allow i

152 throughout the year, excluding a reversible desiccation period.

153 tion is a response trait that influences the desiccation phenotype by increasing survivorship, shifti

154 itical during preparation of worms for harsh desiccation (preconditioning) and during the entry of ye

155 lopment while their expression ceases during desiccation, presenting a comprehensive map of peanut li

156 pidly accumulated before the seed begins the desiccation process.

157 These changes imply that stronger desiccation processes occur during seed development.

158 Further, transgenic plants grown until desiccation produced more seed protein and starch, as we

159 majority of Cupressaceae species, uses leaf desiccation rather than high ABA levels to close stomata

160 t Shock Proteins, aquaporins, expansins, and desiccation related proteins (DRPs), which are highly di

161 expansion at 6 Ma coincident with major MSC desiccation; relative sea-level modelling indicates a pr

162 (mbCHCs) are a dual trait that affects both desiccation resistance and mate choice in Drosophila ser

163 produce cuticular hydrocarbons required for desiccation resistance and pheromonal communication.

164 phila lipid metabolism promotes lifespan and desiccation resistance in adults and suppresses hallmark

165 fruit are astomatous and a major target for desiccation resistance to enhance shelf life.

166 neurons diminished LK expression, increased desiccation resistance, and diminished food intake.

167 cular hydrocarbons have been shown to confer desiccation resistance.

168 ssociated with venation features that affect desiccation resistance.

169 Its eggs are desiccation resistant, and the larvae develop rapidly in

170 The formation of a highly desiccation-resistant endospore might serve as a logical

171 erature is an important cue for developing a desiccation-resistant phenotype and might act as a relia

172 serve mass and coat mass were similar across desiccation responses, desiccation-sensitive seeds alloc

173 pecies and compared the patterns across seed desiccation responses.

174 n the potential roles of sncRNA in mediating desiccation-responsive pathways in early land plants.

175 Preventing corneal desiccation results in a milder and more transient HSK w

176 serve water with a more cautious response to desiccation risk.

177 t grass Eragrostis nindensis and the related desiccation-sensitive cereal Eragrostis tef to identify

178 genomes of P. vanderplanki and a congeneric desiccation-sensitive midge P. nubifer.

179 The exact stress(es) that cause lethality in desiccation-sensitive organisms and how the lethal stres

180 that may act as protective compartments for desiccation-sensitive proteins.

181 s were similar across desiccation responses, desiccation-sensitive seeds allocated more and evolved f

182 lls that produce CHCs) of a closely related, desiccation-sensitive species, D. birchii, due in part t

183 dition to affecting survival or behaviour of desiccation-sensitive species, lower rainfall may indire

184 surrection plant genomes and no expansion in desiccation-sensitive species.

185 vances the understanding of the evolution of desiccation sensitivity in seeds.

186 t from the media converts yeast from extreme desiccation sensitivity to a high level of desiccation t

187 ecies provides evidence for the existence of desiccation-specific gene expression systems in P. vande

188 now allow pathogenic enterococci to survive desiccation, starvation, and disinfection in the modern

189 accumulation and has a reduced tolerance of desiccation stress compared with the wild type.

190 nstream targets of OsHOX24 under control and desiccation stress conditions via chromatin immunoprecip

191 hese findings indicate that OsHOX24-mediated desiccation stress regulation involves modulation of a p

192 OsHOX24 mediates regulation of desiccation stress response via complex regulatory netwo

193 l in response to temperature, oxidative, and desiccation stress.

194 This approach has broad use in desiccation studies to carefully investigate the relatio

195 emes of physical and biological stress (e.g. desiccation, temperature, UV radiation and microbial inf

196 Diverse organisms capable of surviving desiccation, termed anhydrobiotes, include species from

197 Desiccation tests showed that foragers of colonies that

198 re less sensitive and better adapted to soil desiccation than bacterial-based food webs.

199 hen the same groups of cells were exposed to desiccation, the aggregates survived better, and the com

200 with diverse metabolic processes during the desiccation time course, suggesting a switch from active

201 enudation of the right femoral artery by air desiccation to induce an atherosclerotic-like lesion and

202 yperosmotic barrier presenting the threat of desiccation to reach a source of food odor.

203 In seeds, desiccation tolerance (DT) and the ability to survive th

204 Desiccation tolerance (DT) is a remarkable process that

205 plants, with dehydration tolerance (DhT) and desiccation tolerance (DT) representing some of the most

206 A6 (AWM11684) in insect cells improves their desiccation tolerance and a fraction of the protein is s

207 chaperones, explaining its important role in desiccation tolerance and emphasizing the translational

208 that there is an inverse correlation between desiccation tolerance and growth rate in glucose-, ammon

209 atures underlying the recurrent evolution of desiccation tolerance are unknown.

210 g support for the hypothesis that vegetative desiccation tolerance arose by redirection of genetic in

211 Knockdown of the capa gene increases desiccation tolerance but lengthens chill coma recovery

212 We suggest that AfrLEA6 promotes desiccation tolerance by engaging in two distinct molecu

213 nch of the TOR and Ras-cAMP pathway inhibits desiccation tolerance by inhibiting the stress response

214 s induced by desiccation, and how vegetative desiccation tolerance circumvents destructive, stress-in

215 The time frame for maintaining long-term desiccation tolerance consists of a balance of trehalose

216 In extant land plants, desiccation tolerance depends on the action of the hormo

217 Loss of the GS dramatically decreased desiccation tolerance in both organisms.

218 observations support convergent evolution of desiccation tolerance in land plants through tandem gene

219 nderstanding the networks that regulate seed desiccation tolerance in model plant systems would provi

220 spectives for understanding the evolution of desiccation tolerance in plants.

221 ion of transcripts typically associated with desiccation tolerance in seeds and involvement of orthol

222 ulate reserve accumulation, dormancy, and/or desiccation tolerance in seeds in a gene-specific or red

223 nedesmaceae and capitalized on extraordinary desiccation tolerance in two of the species, contrasting

224 Here, we summarize in vivo studies of desiccation tolerance in worms, yeast, and tardigrades.

225 Vegetative desiccation tolerance in X. viscosa was found to be unco

226 Desiccation tolerance is also associated with colony rep

227 Desiccation tolerance is an ancient trait, lost from veg

228 We found that induction of desiccation tolerance is cell autonomous and that there

229 Among green plants, desiccation tolerance is common in seeds and spores but

230 Desiccation tolerance is common in seeds and various oth

231 The data also suggest that desiccation tolerance may require induced protective mec

232 Desiccation tolerance of anhydrobiotes provides an unusu

233 geneous nature of dryland landscapes and the desiccation tolerance of biocrusts, which leaves them fr

234 yed a stable expression, suggesting that the desiccation tolerance of T. gelatinosa mostly relies on

235 a conserved metabolic rewiring that confers desiccation tolerance on organisms as diverse as worm an

236 tresses that could be induced by water loss, desiccation tolerance seemed likely to require many esta

237 pecialization of individual hydrophilins for desiccation tolerance suggests that other hydrophilins m

238 in yeast emphasizes its potential to confer desiccation tolerance to otherwise sensitive organisms.

239 ccharide trehalose is a major determinant of desiccation tolerance via unresolved mechanisms.

240 Desiccation tolerance was a critical adaptation for the

241 nhanced relative to pro and a defect in seed desiccation tolerance was uncovered.

242 , and these genes are sufficient to increase desiccation tolerance when expressed in heterologous sys

243 tion targets involved in reserve storage and desiccation tolerance, and repression of photosynthesis

244 TDPs are required for tardigrade desiccation tolerance, and these genes are sufficient to

245 he maturation programs, such as dormancy and desiccation tolerance, are also found in non-seed plants

246 reflect the role of ABI3 in seed maturation, desiccation tolerance, entry into a quiescent state and

247 s TDPs as functional mediators of tardigrade desiccation tolerance, expanding our knowledge of the ro

248 n host-derived substrates and is involved in desiccation tolerance, implying that CsrA controls key f

249 r and genetic mechanisms enabling vegetative desiccation tolerance, we produced a high-quality whole-

250 examining the genomic background of extreme desiccation tolerance, which is exclusively found in lar

251 d range of carbon sources, including several desiccation tolerance-promoting sugars and unusually lar

252 ydrophilins as the major stress effectors of desiccation tolerance.

253 olution and gene duplication associated with desiccation tolerance.

254 disordered proteins (TDPs) are essential for desiccation tolerance.

255 a few angiosperm species possess vegetative desiccation tolerance.

256 ng as a model system for studying vegetative desiccation tolerance.

257 of growth that allows for the expression of desiccation tolerance.

258 esting that they could potentially influence desiccation tolerance.

259 e desiccation sensitivity to a high level of desiccation tolerance.

260 ydrobiotes has been strongly correlated with desiccation tolerance.

261 rty of trehalose is directly responsible for desiccation tolerance.

262 sordered proteins, which play major roles in desiccation tolerance.

263 ragrostis tef to identify changes underlying desiccation tolerance.

264 ssential role in seed maturation, conferring desiccation tolerance.

265 at shock and nutrient deprivation, increases desiccation tolerance.

266 seed desiccation pathways confers vegetative desiccation tolerance.

267 be necessary but is not sufficient to confer desiccation tolerance.

268 o control a preexisting PP2C-SnRK2-dependent desiccation-tolerance pathway enabled transition from an

269 ranscriptomes in B. argenteum to establish a desiccation-tolerance transcriptomic atlas.

270 Here, we report measurements of thermal and desiccation tolerances and safety margins across a gradi

271 ctive power, but the potential importance of desiccation tolerances have been less explored in some s

272 We also found significant differences in desiccation tolerances, measured as critical water conte

273 restrial green algae and all its species are desiccation tolerant (DT).

274 The desiccation tolerant bryophyte Bryum argenteum is an imp

275 Remarkably, desiccation tolerant organisms can survive years without

276 We identify that desiccation tolerant seeds exhibit a striking transcript

277 ions that facilitated efficient dispersal of desiccation tolerant spores, evolved in the ancestral la

278 Diverse organisms across taxa are desiccation tolerant, capable of surviving extreme water

279 Desiccation-tolerant (DT) plants can dry past -100 MPa a

280 ession is induced by desiccation in diverse, desiccation-tolerant (DT) taxa, including, e.g., late em

281 imilar expression patterns in leaves of both desiccation-tolerant and -sensitive species.

282 Craterostigma plantagineum belongs to the desiccation-tolerant angiosperm plants.

283 aged comparative genomic approaches with the desiccation-tolerant grass Eragrostis nindensis and the

284 whole-genome sequencing and assembly of the desiccation-tolerant grass Oropetium thomaeum.

285 Experiments on the desiccation-tolerant moss Syntrichia ruralis assessed th

286 and how the lethal stresses are mitigated in desiccation-tolerant organisms remain poorly understood.

287 ic reprogramming occurred in these naturally desiccation-tolerant organs.

288 Cells of all desiccation-tolerant plants and seeds must possess a cor

289 set of crucial genes specifically induced in desiccation-tolerant plants.

290 eversible recovery of hydraulic conductance, desiccation-tolerant seeds, or rhizomes may allow them t

291 e by redirection of genetic information from desiccation-tolerant seeds.

292 re and evolved faster in reserve compared to desiccation-tolerant seeds.

293 d these ancestral protective mechanisms, and desiccation-tolerant species are dispersed across the la

294 elated orthologs with expression specific to desiccation-tolerant species.

295 low temperature in buds and leaves, whereas desiccation treatment induces PpeS6PDH in buds and repre

296 cines, including additives, temperature, and desiccation, were determined and their protective effica

297 igins to colonise land, they needed to avoid desiccation while still enabling gas and water exchange

298 nts and secondary metabolic routes rose upon desiccation, while putrescine, proline and a variety of

299 Sweat bees were the least sensitive to desiccation, with the lowest CWC (51.7%), followed by bu

300 During desiccation, xylem conduits in stipes embolized before c