ライフサイエンスコーパス: submergence

1 A-1 impacts multiple pathways of response to submergence.

2 the Sub1A-1 allele are tolerant of prolonged submergence.

3 ia or anoxia, root waterlogging, or complete submergence.

4 (ABA), and gibberellin (GA) signaling during submergence.

5 istematic base and not hindered by prolonged submergence.

6 s of the recurrent parent and is tolerant to submergence.

7 ike genes whose transcripts are regulated by submergence.

8 nscriptionally up-regulated by SUB1A-1 under submergence.

9 roducing the increased TPR during underwater submergence.

10 ) supported by the animal's rugose skin upon submergence.

11 ia responsive genes, enabling adaptations to submergence.

12 ed to terrain that undergoes long periods of submergence.

13 ryza are implicated in tolerance of seawater submergence.

14 es SA accumulation to promote germination in submergence.

15 are mature leaves that do not elongate under submergence.

16 nct hypoxia signaling pathway in rice during submergence.

17 plants have evolved the ability to cope with submergence.

18 esponse is required for the plant to survive submergence.

19 levels remained high above the pot since its submergence.

20 o sense environmental perturbations, such as submergence.

21 ns differing significantly in sensitivity to submergence.

22 nerating processes remained adult-like after submergence.

23 of rice seedlings to the adverse effects of submergence.

24 onses by inducing SLR1 after several days of submergence.

25 esults in restricted shoot elongation during submergence.

26 CEPTOR-LIKE KINASE1 (FRK1) and WRKY53, after submergence.

27 G OF RPW8 4 (HR4) and alters its response to submergence.

28 d with brassinosteroid (BR) synthesis during submergence.

29 evel of induction during the early stages of submergence.

30 determines whether plants survive prolonged submergence.

31 the enhancement of GA responsiveness during submergence.

32 ated with the Sub1A-1-mediated response upon submergence.

33 a major quantitative trait locus designated Submergence 1 (Sub1) near the centromere of chromosome 9

34 Submergence-1 (Sub1), a major quantitative trait locus a

35 Submergence 1A (SUB1A), is an ethylene response factor (

36 crease in epizootic activity (known as viral submergence(3)) is unclear, as is the possibility of re-

37 germination and seedling establishment under submergence(4), is a key trait for the development of tr

38 tiva cultivars die within a week of complete submergence--a major constraint to rice production in so

39 The data define a cohort of conserved submergence-activated genes with signatures of overlappi

40 nt of chromatin accessibility, and degree of submergence activation are more prevalent in the wetland

41 The total extent of submergence along riverbanks and other flow paths was es

42 archless pgm mutant is highly susceptible to submergence and also fails to induce anaerobic genes at

43 ion of OS-ACS1 occurs within 12 h of partial submergence and at low oxygen concentrations.

44 ance and photomorphogenesis genes to outgrow submergence and by priming submerged plants for future l

45 Submergence and drought are major constraints to rice (O

46 mechanism that underpins adaptation to both submergence and drought in soybean.

47 economization of energy reserves under both submergence and drought.

48 cript levels were shown to be upregulated by submergence and ethylene, with the Sub1C allele in M202

49 regulated in a SUB1A-dependent manner during submergence and is involved in modulating the GA signali

50 ouble mutant showed hypersensitivity to both submergence and osmotic stress.

51 -level rise (IPCC RCP 8.5) led to widespread submergence and potential loss of stored C for created m

52 g marsh production is primarily regulated by submergence and the resulting edaphic conditions.

53 found that ago1-27 plants are intolerant to submergence and transcriptome analysis identified genes

54 e rapidly in the intercalary meristem during submergence and treatment with GA before the increase in

55 Submergence and treatment with gibberellin, both of whic

56 ns between cell types and their responses to submergence and/or TOD are driven by expression changes

57 instem are activated by voluntary underwater submergence, and some probably contribute to the sympath

58 In plants, hypoxia can be induced by submergence, and the lack of oxygen impairs mitochondria

59 itative responses of both Rorippa species to submergence appeared roughly similar but differed quanti

60 Acclimation responses to submergence are coordinated by the submergence-inducible

61 haliana) plants require starch for surviving submergence as well as for ensuring the rapid induction

62 to the acute hypoxia experienced upon plant submergence, as well as Little Zipper 2 (ZPR2) and Verna

63 utilized a broad thermal niche and exhibited submergence behaviour, possibly for thermal refuge, when

64 the transcriptomic and hormonal responses to submergence between mature and growing leaves using rice

65 SLR1 protein levels declined under prolonged submergence but were accompanied by an increase in accum

66 s ethylene-promoted GA responsiveness during submergence by augmenting accumulation of the GA signali

67 ant rice maintains viability during complete submergence by limiting underwater elongation until floo

68 Inhibition of PCOs may prepare plants for submergence by promoting upregulation of hypoxia respons

69 creases the threshold RRSLR initiating marsh submergence by up to 60% in the range of forcings explor

70 Plants respond to hypoxia, often caused by submergence, by expressing a specific set of genes that

71 Tolerance to submergence can be activated in the intolerant genotype

72 ate that variation in log size and degree of submergence can be used as a tool to vary habitat suitab

73 Though submergence caused a substantial reconfiguration of the

74 type had higher brassinosteroid levels after submergence compared to the intolerant genotype.

75 ng the angle of attack and the dimensionless submergence depth which lead to ice breaking are predict

76 nder, which is only dependent on the initial submergence depth, is introduced and used in classificat

77 fic transcriptomic and hormonal responses to submergence, drought and recovery from these stresses in

78 ociated genes, all of which can occur during submergence, drought, and constant darkness.

79 ontribute to the enhancement of tolerance to submergence, drought, and oxidative stress.

80 To avoid submergence during sea-level rise, coastal wetlands buil

81 n and gibberellic acid responsiveness during submergence, economizing carbohydrate reserves and signi

82 species of the Brassicaceae family, in which submergence enhances stem elongation and suppresses peti

83 ing cells that attenuate DNA synthesis under submergence; genes involved in auxin signaling, the circ

84 The GAC was converted to a cathode by submergence in a high ionic strength solution and connec

85 s study, we report that MPK3 is activated by submergence in a SUB1A-dependent manner.

86 family was rapidly and strongly induced upon submergence in Arabidopsis thaliana, and this induction

87 Is has been linked to improved survival post-submergence in Arabidopsis, rice (Oryza sativa) and barl

88 ses that sequentially occur during and after submergence in Arabidopsis.

89 trait locus affecting tolerance to complete submergence in lowland rice (Oryza sativa), contains two

90 contribute to distinct adaptive responses to submergence in mature and growing rice leaves.

91 We propose that BR limits GA levels during submergence in the SUB1A rice through a GA catabolic enz

92 s aerial exposure, rapid flushing and longer submergence in turbid waters.

93 Submergence induced changes in levels of the microRNAs m

94 ptional regulation encompassed darkness- and submergence-induced alternative splicing of transcripts

95 In mature leaves, submergence-induced auxin accumulation was suppressed by

96 Here we show that extant bryophytes exhibit submergence-induced developmental plasticity, suggesting

97 Submergence-induced hypoxia in plants results in stabili

98 The submergence-induced hypoxic condition negatively affects

99 of temperature shift experiments showed that submergence-induced inhibition of stomatal development i

100 Two submergence-induced peroxisomal Oryza sativa cinnamate:C

101 ce OS-ACS1 and OS-ACS2 and show that partial submergence induces expression of OS-ACS1 and suppresses

102 ponses to submergence are coordinated by the submergence-inducible Sub1A, which encodes an ethylene-r

103 In the submergence-intolerant japonica cultivar M202, this locu

104 ed GA responsiveness and shoot elongation in submergence-intolerant lines.

105 Overexpression of Sub1A-1 in a submergence-intolerant O. sativa ssp. japonica conferred

106 ure to improve the underwater germination of submergence-intolerant rice varieties.

107 re used to explore how the wood position and submergence level (discharge) affect wake structure, and

108 ed with increasing log length and decreasing submergence level.

109 d marsh vertical accretion, increasing tidal submergence of marsh surfaces, particularly where creeks

110 thylene, and nitric oxide, change during the submergence of plant organs in water.

111 Submergence of plant organs perturbs homeostasis by limi

112 requires a large volume along with repeated submergence of the dosage form within the disintegration

113 Submergence of the GAC in water and use of the GAC as th

114 ation and tectonic evidence suggest complete submergence of the island during the latest Cretaceous t

115 ncentrations, and transcriptome responses to submergence of two species, Rorippa sylvestris and Rorip

116 , we assessed the causal impact of rice crop submergence on yield losses from 1980 to 2015.

117 xygen stress (hypoxia), such as during shoot submergence or root waterlogging, includes increasing th

118 rant and survive up to two weeks of complete submergence owing to a major quantitative trait locus de

119 Underwater submergence produces a complex autonomic response that i

120 the role for the miR775-GALT9 module in post-submergence recovery through a crosstalk between the eth

121 the role of the miR775-GALT9 module in post-submergence recovery.

122 A typical adaptive response to submergence regulated by SUB1A, the ethylene-responsive

123 embers in a phylogenetic context resolved 12 submergence-regulated AP2/ERFs into three putative funct

124 Complete submergence represses photosynthesis and aerobic respira

125 A core submergence response included hormonal regulation and me

126 show that a major component of the bryophyte submergence response is controlled by the phytohormone e

127 ming pathways, similar to the low-oxygen and submergence response of Arabidopsis and rice (Oryza sati

128 ranscriptome analyses comparing the temporal submergence response of Sub1A-1-containing tolerant M202

129 ed developmental plasticity, suggesting that submergence responses evolved relatively early in the ev

130 ontrol plays an important role in regulating submergence responses in plants.

131 molecular resolution of genetic variation in submergence responses involving interactions between dar

132 Submergence-responsive transcriptome analysis revealed r

133 Submergence resulted in the induction of genes involved

134 wever, how plants detect and transduce early submergence signals remains elusive.

135 be a signaling component that distinguishes submergence-specific regulation of the stress response.

136 esses, whereas stimulated auxin response was submergence-specific.

137 The submergence-stimulated decrease in ABA content was Sub1A

138 5 (miR775-Oe) confers enhanced recovery from submergence stress and reduced accumulation of RBOHD and

139 ression in a positive regulatory loop during submergence stress signaling.

140 orchestrates a plethora of responses during submergence stress tolerance in rice (Oryza sativa).

141 rice possess variable levels of tolerance to submergence stress, but gene discovery and utilization o

142 However, the molecular function of submergence stress-induced miRNAs in physiological or de

143 on is inversely affected at 24 h of complete submergence stress.

144 on factor, SUB1A, which confers tolerance to submergence stress.

145 nted novel stress/tissue conditions, such as submergence-stressed flowers, which enabled the identifi

146 stronger transcriptional response to promote submergence survival.

147 We employed new deep submergence technologies during an International Polar Y

148 During submergence the RAP2.12, RAP2.2 and RAP2.3 are stabilize

149 During submergence, the tolerant M202(Sub1) displayed restraine

150 Aquatic submergence, therefore, removes environmental pressures

151 senescence via ethylene accumulation during submergence (three ERFs); (2) negative regulation of eth

152 ted metabolic and developmental responses to submergence through differential expression of Sub1A and

153 Here we show that plants can rapidly detect submergence through passive ethylene entrapment and use

154 for rapid internode elongation upon partial submergence to maintain its foliage above the rising flo

155 development during stress, hormone-regulated submergence tolerance and stomatal movements.

156 e substrates, including ERF-VIIs, to enhance submergence tolerance in agriculture.

157 Submergence tolerance in lowland rice is conferred by a

158 ethylene response factor (ERF) that confers submergence tolerance in rice (Oryza sativa) via limitin

159 SUB1A-1, a major determinant of submergence tolerance in rice, was shown not to be a sub

160 sults provide a mechanistic understanding of submergence tolerance in rice.

161 nnection between MAPK signaling cascades and submergence tolerance is currently unknown.

162 found between the Sub1 allelic variation and submergence tolerance probably due to low minor allele f

163 Here, we evaluated the influence of the submergence tolerance regulator, SUBMERGENCE1A (SUB1A),

164 riggered ethylene-mediated induction confers submergence tolerance through a quiescence survival stra

165 The PCOs are potential targets for improving submergence tolerance through enzyme engineering or chem

166 tolerant genotypes and sufficient to confer submergence tolerance to intolerant accessions.

167 fied 18 cultivars with non-Sub1A-1 source of submergence tolerance which after further mapping and va

168 aracterized genetic variants associated with submergence tolerance, seed shattering and plant archite

169 Therefore, in addition to providing robust submergence tolerance, SUB1A improves survival of rapid

170 available metabolic pathway data identified submergence tolerance-associated pathways governing anae

171 ing that Sub1A-1 is a primary determinant of submergence tolerance.

172 ion of anaerobic survival genes and enhanced submergence tolerance.

173 179 rice genotypes and its association with submergence tolerance.

174 Submergence-tolerant rice maintains viability during com

175 Furthermore, prior submergence treatment conferred higher resistance to the

176 g of roots of young plants exposed to a 24-h submergence treatment or air.

177 The presence of SUB1A-1 and its strong submergence-triggered ethylene-mediated induction confer

178 place ethylene as a central regulator of the submergence-triggered inhibition of stomatal development

179 for the molecular physiological basis of the submergence-triggered inhibition of stomatal development

180 In conclusion, we propose that submergence triggers innate immunity in Arabidopsis via

181 sed by roots becoming waterlogged or foliage submergence, triggers changes in gene transcription and

182 and chromatin accessibility associated with submergence up-regulation.

183 -end rule pathway mutants ged1 and prt6-1 to submergence was studied in more detail to understand pre

184 ion in gene regulatory networks activated by submergence, we conducted a high-resolution analysis of

185 responses to the compound stress imposed by submergence, we investigated transcriptomic adjustments

186 on conditions, such as prolonged darkness or submergence, which was partially associated with carbohy

187 Both Rorippa species could tolerate deep submergence, with R. sylvestris surviving much longer th