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 pyogenes Cas9 (SpCas9) under the control of Cauliflower mosaic virus 35S (35S), S. lycopersicum ribo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

37 th GIG1 cDNA under the constitutively active cauliflower mosaic virus 35S promoter in the gig1 backgr

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

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

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

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

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

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

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

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

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

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

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

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

50 ed on the detection of a specific GM (P-35S (Cauliflower mosaic virus 35S promoter)) and non-GM DNA m

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

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

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

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

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

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

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

58 The cauliflower mosaic virus 35S promoter-directed expressio

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

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

61 72a-1 (35S::MIR172) under the control of the cauliflower mosaic virus 35S promoter.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

80 1-like homeobox gene, SHOOT MERISTEMLESS, in cauliflower mosaic virus 35S::KNAT1 transformants.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

97 ne (LUC) driven by CREB fused with a minimal cauliflower mosaic virus (CaMV) 35S promoter.

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

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

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

101 ransactivator/viroplasmin (TAV) protein from Cauliflower mosaic virus (CaMV) can function as a suppre

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

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

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

105 the role of Arabidopsis thaliana PBs during Cauliflower mosaic virus (CaMV) infection.

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

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

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

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

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

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

112 dy, we report the first crystal structure of cauliflower mosaic virus (CaMV) RT in complex with a dup

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

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

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

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

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

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

119 3 under the control of the 35S promoter from cauliflower mosaic virus consist of two outer whorls of

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

139 Cauliflower mosaic virus replication complexes are conde

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

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

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