ライフサイエンスコーパス: cauliflower mosaic virus

1 s under the control of the 35S promoter from cauliflower mosaic virus.

2 SPY under the control of the 35S promoter of Cauliflower mosaic virus.

3 tible to the virulent pathogens Erisyphe and cauliflower mosaic virus.

4 curonidase (GUS) reporter gene driven by the cauliflower mosaic virus 35S (CaMV35S) promoter to stand

5 little effect on activity of the full-length cauliflower mosaic virus 35S and maize ubiquitin promote

6 driven by the strong constitutive promoters, cauliflower mosaic virus 35S and tCUP.

7 ted transformation with a T-DNA that carries cauliflower mosaic virus 35S enhancer sequences at its r

8 , EC 4.3.1.5) gene, modified by inclusion of cauliflower mosaic virus 35S enhancer sequences in its p

9 An activation tagging screen in which the cauliflower mosaic virus 35S enhancer was inserted rando

10 used activation tagging with T-DNA carrying cauliflower mosaic virus 35S enhancers to investigate th

11 onstitutive over-expression of MPL1 from the Cauliflower mosaic virus 35S gene promoter curtailed the

12 ssed constitutively from the promoter of the cauliflower mosaic virus 35S gene.

13 ld-type SHM1 under the control of either the cauliflower mosaic virus 35S or the SHM1 promoter in shm

14 entation upstream or downstream of a minimal cauliflower mosaic virus 35S promoter (-90 to +5).

15 ase (Nia) construct under the control of the cauliflower mosaic virus 35S promoter (35S-Nia2), one cl

16 S1/cad1-3) or ectopically expressed with the cauliflower mosaic virus 35S promoter (35S::TaPCS1/cad1-

17 e-specific detection of a transgene from the Cauliflower Mosaic Virus 35S Promoter (CaMV35S), inserte

18 xin transcribed region (Fed-1) driven by the cauliflower mosaic virus 35S promoter (P35S), light acts

19 nt expression of ACMV-[CM] AC4 driven by the Cauliflower mosaic virus 35S promoter (p35S-AC4) enhance

20 la gene under transcriptional control of the cauliflower mosaic virus 35S promoter accumulated ricino

21 Overexpression of Pto under the cauliflower mosaic virus 35S promoter activates spontane

22 Next, Tag1 was inserted between a cauliflower mosaic virus 35S promoter and a beta-glucuro

23 ctases) were placed under the control of the cauliflower mosaic virus 35S promoter and introduced int

24 When a fusion gene comprising the cauliflower mosaic virus 35S promoter and RF2a cDNA was

25 s (TBSV) cDNA, positioned between a modified cauliflower mosaic virus 35S promoter and the hepatitis

26 This fusion was placed downstream of the cauliflower mosaic virus 35S promoter and upstream of th

27 (Nicotiana tabacum) under the control of the cauliflower mosaic virus 35S promoter caused up to a 4-f

28 Overexpressing Pto under the control of the cauliflower mosaic virus 35S promoter constitutively act

29 ng the osmotin gene under the control of the cauliflower mosaic virus 35S promoter constitutively ove

30 dimer can confer light responsiveness of the cauliflower mosaic virus 35S promoter containing the -92

31 ression of DEK1-MEM under the control of the cauliflower mosaic virus 35S promoter gave a dominant ne

32 expressing UGT707B1 under the control of the cauliflower mosaic virus 35S promoter have been construc

33 e GCR1 under the control of the constitutive cauliflower mosaic virus 35S promoter have reduced sensi

34 the novel WAVE-DAMPENED2 (WVD2) gene by the cauliflower mosaic virus 35S promoter in mutant plants.

35 nsgene under the control of the constitutive cauliflower mosaic virus 35S promoter in order to suppre

36 Expression of des from the cauliflower mosaic virus 35S promoter in the plant speci

37 on of the same gene under the control of the cauliflower mosaic virus 35S promoter in transgenic plan

38 r-expression of F5H under the control of the cauliflower mosaic virus 35S promoter increased lignin s

39 either behind its own promoter or behind the cauliflower mosaic virus 35S promoter into Lotus cornicu

40 Overexpression of AtERF53 driven by the cauliflower mosaic virus 35S promoter resulted in an uns

41 or (LeETR1) under the control of an enhanced cauliflower mosaic virus 35S promoter resulted in some e

42 ants overexpressing CGS under control of the cauliflower mosaic virus 35S promoter show increased sol

43 ntaining a kanamycin resistance marker and a cauliflower mosaic virus 35S promoter to control express

44 ent, the gusA gene that was driven by the 2x Cauliflower mosaic virus 35S promoter was bombarded into

45 pecific unknown seed protein promoter or the Cauliflower mosaic virus 35S promoter were employed.

46 d antisense HEMA1 mRNA from the constitutive cauliflower mosaic virus 35S promoter were generated.

47 of antisense mRNA (under the control of the cauliflower mosaic virus 35S promoter) markedly retards

48 e was overexpressed under the control of the cauliflower mosaic virus 35S promoter, a guaiacyl-rich,

49 in Arabidopsis thaliana under control of the cauliflower mosaic virus 35S promoter, and the transcrip

50 essing DWF4 (AOD4) were generated, using the cauliflower mosaic virus 35S promoter, and their phenoty

51 lase promoter, but not the commonly employed cauliflower mosaic virus 35S promoter, generates a ligni

52 lation; when expressed from the constitutive cauliflower mosaic virus 35S promoter, IRT1 protein accu

53 and the other CYCA1;2/TAM-GFP driven by the cauliflower mosaic virus 35S promoter, the largest diffe

54 l line under the control of the constitutive cauliflower mosaic virus 35S promoter, was introduced in

55 The cauliflower mosaic virus 35S promoter-directed expressio

56 xpression of GFP-fusions was controlled by a cauliflower mosaic virus 35S promoter.

57 bidopsis lines expressing CCX3 driven by the cauliflower mosaic virus 35S promoter.

58 transketolase cDNA under the control of the cauliflower mosaic virus 35S promoter.

59 72a-1 (35S::MIR172) under the control of the cauliflower mosaic virus 35S promoter.

60 ith PHOT expression constructs driven by the cauliflower mosaic virus 35S promoter.

61 P)-4 in antisense conformation driven by the cauliflower mosaic virus 35S promoter.

62 tation (PGbetaS-AS) under the control of the cauliflower mosaic virus 35S promoter.

63 is plants with AtWRKY18 under control of the cauliflower mosaic virus 35S promoter.

64 ta-galactosidase 4 (TBG4) cDNA driven by the cauliflower mosaic virus 35S promoter.

65 gal introns) clone, regulated by an enhanced cauliflower mosaic virus 35S promoter.

66 isoform, in leaf tissue under control of the cauliflower mosaic virus 35S promoter.

67 cDNAs under the control of the constitutive cauliflower mosaic virus 35S promoter.

68 rame is transcribed under the control of the cauliflower mosaic virus 35S promoter.

69 To address this question, we introduced a Cauliflower mosaic virus 35S promoter:HSFA2 construct in

70 quence in the antisense orientation, and the cauliflower mosaic virus 35S RNA gene terminator.

71 ucted an expression cassette composed of the Cauliflower Mosaic Virus 35S RNA promoter, the A. thalia

72 Overexpression plants were generated using cauliflower mosaic virus 35S, and protein levels in the

73 compared with other commonly used promoters (cauliflower mosaic virus 35S, mas2', and maize ubiquitin

74 the WRINKLED1 cDNA under the control of the cauliflower mosaic virus 35S-promoter led to increased s

75 This was true for the autonomous element in cauliflower mosaic virus 35S-Tag1-beta-glucuronidase con

76 Surprisingly, cauliflower mosaic virus 35S::GL1 try plants contain a s

77 1-like homeobox gene, SHOOT MERISTEMLESS, in cauliflower mosaic virus 35S::KNAT1 transformants.

78 f three transgenic tomato lines carrying the cauliflower mosaic virus 35S::Pto transgene exhibited mi

79 In plants with a cauliflower mosaic virus 35S:HF-RPL18 transgene immunopu

80 ing So KAS III when under the control of the cauliflower mosaic virus-35S promoter and in Arabidopsis

81 PDH45 overexpression driven by constitutive cauliflower mosaic virus-35S promoter in rice transgenic

82 sgenic pea lines (in a lele background) with cauliflower mosaic virus-35S-driven expression of PsGA3o

83 nce, in front of a minimal 35S promoter from cauliflower mosaic virus (-46 to +4), conferred specific

84 rnip mosaic virus, cucumber mosaic virus and cauliflower mosaic virus as well as to the fungus Botryt

85 timerized transcriptional enhancers from the cauliflower mosaic virus (CaMV) 35S gene has been applie

86 Gene constructs consisting of the cauliflower mosaic virus (CaMV) 35S promoter driving a c

87 UGT1 antisense mRNA under the control of the cauliflower mosaic virus (CaMV) 35S promoter exhibited d

88 y expressing KAN under the regulation of the cauliflower mosaic virus (CAMV) 35S promoter indicate th

89 Frequently, the cauliflower mosaic virus (CaMV) 35S promoter is used to

90 n of chimeric gene constructs containing the cauliflower mosaic virus (CaMV) 35S promoter required th

91 six expression constructs, two utilized the cauliflower mosaic virus (CaMV) 35S promoter with duplic

92 thin the AGAMOUS second intron (AGI) and the Cauliflower Mosaic Virus (CaMV) 35S promoter, respective

93 nsgenic tobacco plants that express either a cauliflower mosaic virus (CaMV) 35S promoter-TTS2 transg

94 the GFP fusion proteins expressed under the cauliflower mosaic virus (CaMV) 35S promoter.

95 novel Arabidopsis cDNA library driven by the cauliflower mosaic virus (CaMV) 35S promoter.

96 anscribed at moderate levels compared to the cauliflower mosaic virus (CaMV) 35S promoter.

97 he amount of CP produced by the constitutive cauliflower mosaic virus (CaMV) double 35S promoter.

98 Gene I of cauliflower mosaic virus (CaMV) encodes a protein that i

99 rtions of the large intergenic region of the Cauliflower mosaic virus (CaMV) genome for promoter acti

100 Cauliflower mosaic virus (CaMV) is a double-stranded DNA

101 The gene VI product (P6) of Cauliflower mosaic virus (CaMV) is a multifunctional pro

102 Cauliflower mosaic virus (CaMV) is aphid-transmitted, wi

103 The P6 protein of Cauliflower mosaic virus (CaMV) is responsible for the f

104 Here, we show that cauliflower mosaic virus (CaMV) MP contains three tyrosi

105 experiments directed towards development of cauliflower mosaic virus (CaMV) replicons for propagatio

106 r three defense pathways during infection by Cauliflower mosaic virus (CaMV), a compatible pathogen o

107 f autophagy in the compatible interaction of cauliflower mosaic virus (CaMV), a double-stranded DNA p

108 rotein P6 is the main symptom determinant of cauliflower mosaic virus (CaMV), and transgene-mediated

109 T1;5, play important roles in infection with Cauliflower mosaic virus (CaMV).

110 plify sequences flanking 35S transgenes from cauliflower mosaic virus (CaMV).

111 MPs of turnip vein clearing virus (TVCV) and cauliflower mosaic virus (CaMV).

112 3 under the control of the 35S promoter from cauliflower mosaic virus consist of two outer whorls of

113 orescent protein (GFP) or with a similar 35S-cauliflower mosaic virus constitutive promoter construct

114 s clone of CMV RNA3 (LS strain) fused to the cauliflower mosaic virus-derived 35S promoter.

115 Two regions of cauliflower mosaic virus DNA were designed as markers to

116 es a Dissociation (Ds) element containing 4x cauliflower mosaic virus enhancers along with the Activa

117 Others have suggested that Cauliflower mosaic virus evolved in this manner and our

118 of the viral genome, it is possible that the Cauliflower mosaic virus genome is composed of genes fro

119 Transcription from the as-1 element of the cauliflower mosaic virus is induced by salicylic acid (S

120 on was examined for the seven genes of eight Cauliflower mosaic virus isolates.

121 shunting has only been observed to date on a cauliflower mosaic virus mRNA.

122 the response because systemic infection with cauliflower mosaic virus or cucumber mosaic virus did no

123 th overexpression (using the 35S promoter of Cauliflower mosaic virus) or suppression (using double-s

124 placed by either the C.fasciculata or by the cauliflower mosaic virus ORF VI sequence.

125 gene under the enhanced 355 promoter of the cauliflower mosaic virus produced green fluorescence tha

126 These were constitutively transcribed from a cauliflower mosaic virus promoter and assayed for posttr

127 Overexpression of AtPAP15 with the 35S cauliflower mosaic virus promoter produced mutants with

128 includes the bZIP motif to a minimal -50 35S cauliflower mosaic virus promoter, enhanced expression i

129 omato prosystemin gene, regulated by the 35S cauliflower mosaic virus promoter, resulted in constitut

130 omparable in strength of the full-length 35S cauliflower mosaic virus promoter.

131 of an internal control with an enhanced 35S cauliflower mosaic virus promoter.

132 echnology, studying the molecular biology of Cauliflower mosaic virus, rice tungro viruses, and Banan

133 l to those required for ribosome shunting in cauliflower mosaic virus RNA and are well conserved in c

134 pe) to systemic infection with the DNA virus cauliflower mosaic virus was shown to result in enhancem