ライフサイエンスコーパス: submergence

1 roducing the increased TPR during underwater submergence.

2 ns differing significantly in sensitivity to submergence.

3 nerating processes remained adult-like after submergence.

4 of rice seedlings to the adverse effects of submergence.

5 onses by inducing SLR1 after several days of submergence.

6 esults in restricted shoot elongation during submergence.

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

8 d with brassinosteroid (BR) synthesis during submergence.

9 evel of induction during the early stages of submergence.

10 determines whether plants survive prolonged submergence.

11 the enhancement of GA responsiveness during submergence.

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

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

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

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

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

17 istematic base and not hindered by prolonged submergence.

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

19 ike genes whose transcripts are regulated by submergence.

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

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

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

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

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

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

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

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

28 Submergence and drought are major constraints to rice (O

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

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

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

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

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

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

35 Submergence and treatment with gibberellin, both of whic

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

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

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

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

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

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

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

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

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

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

46 Tolerance to submergence can be activated in the intolerant genotype

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

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

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

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

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

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

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

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

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

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

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

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

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

60 Submergence-induced hypoxia in plants results in stabili

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

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

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

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

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

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

67 Submergence of plant organs perturbs homeostasis by limi

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

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

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

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

72 Underwater submergence produces a complex autonomic response that i

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

74 Complete submergence represses photosynthesis and aerobic respira

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

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

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

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

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

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

81 Submergence resulted in the induction of genes involved

82 The submergence-stimulated decrease in ABA content was Sub1A

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

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

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

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

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

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

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

90 Aquatic submergence, therefore, removes environmental pressures

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

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

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

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

95 Submergence tolerance in lowland rice is conferred by a

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

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

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

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

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

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

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

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

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

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

106 Submergence-tolerant rice maintains viability during com

107 Furthermore, prior submergence treatment conferred higher resistance to the

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

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

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

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

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

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

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

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