ライフサイエンスコーパス: tobacco mosaic virus

1 istance protein N that confers resistance to tobacco mosaic virus.

2 expressed in planta using a vector based on Tobacco mosaic virus.

3 plants compromises N-mediated resistance to tobacco mosaic virus.

4 d resistance of NN genotype 6MSAS tobacco to tobacco mosaic virus.

5 ase and also develop increased resistance to tobacco mosaic virus.

6 loped viruses: simian virus 40 and satellite tobacco mosaic virus.

7 -1 gene expression and enhance resistance to tobacco mosaic virus.

8 not susceptible tobacco after infection with tobacco mosaic virus.

9 01, a protein shown to bind the 5' leader of tobacco mosaic virus.

10 ant and to genetically engineered mutants of tobacco mosaic virus.

11 1 proteins and showed enhanced resistance to tobacco mosaic virus.

12 erologous viruses: cucumber mosaic virus and tobacco mosaic virus.

13 ers, demonstrated with a reconstruction of a tobacco mosaic virus.

14 co confers resistance to the viral pathogen, tobacco mosaic virus.

15 ction of in vivo uncoating of the rod-shaped tobacco mosaic virus.

16 icles follows a previous model developed for tobacco mosaic virus.

17 viruses: potato virus Y, potato virus X, and tobacco mosaic virus.

18 by incorporating platinum nanoparticles into tobacco mosaic virus.

19 tracts from the 3' ends of brome mosaic and tobacco mosaic viruses.

20 Here, we show that the tobacco mosaic virus 126-kD protein fused with green flu

21 ta, of the coexpressing transgenic plants by tobacco mosaic virus, alfalfa [correction of alfafa] mos

22 y of multiple systems in nature, such as the tobacco mosaic virus and a cell's cytoskeleton.

23 r-alpha-helix subunits into helical rod of a tobacco mosaic virus and a three-helix fragment of a Ros

24 ng the hypersensitive resistance response to tobacco mosaic virus and after treatment with salicylic

25 bundling dominates the subunit interface in tobacco mosaic virus and conveys rigidity to the rod vir

26 Previous work using Tobacco mosaic virus and Cucumber mosaic virus indicated

27 It is also demonstrated that tobacco mosaic virus and herpes simplex virus can be man

28 both resistance of tobacco to infection with tobacco mosaic virus and induction of defense-related ge

29 ) gene expression and enhanced resistance to tobacco mosaic virus and Pseudomonas syringae pv. tabaci

30 ovalent fusion of similar protein domains in tobacco mosaic virus and to see whether the N-terminal 2

31 pread of two taxonomically distinct viruses, Tobacco mosaic virus and Turnip mosaic virus.

32 le host systems (Nicotiana tabacum with TMV (Tobacco mosaic virus), and Arabidopsis thaliana with TVC

33 IPK is activated in NN tobacco infected with tobacco mosaic virus, and (ii) PVX virus-induced gene si

34 Applications to lumazine synthase, satellite tobacco mosaic virus, and brome mosaic virus show that t

35 sistances to Globodera spp., potato virus Y, tobacco mosaic virus, and tomato spotted wilt virus were

36 We also showed, using tobacco mosaic virus as a model, that a reverse transcri

37 VLPs in Nicotiana benthamiana plants using a Tobacco mosaic virus-based 'launch' vector.

38 Therefore we developed a plant/tobacco mosaic virus-based production system following t

39 cotiana benthamiana by using a deconstructed tobacco mosaic virus-based system that allowed very rapi

40 ts are observed in plant cells infected with tobacco mosaic virus, but the components that modulate t

41 as induced by SA treatment or challenge with Tobacco mosaic virus, but the gene and transcript sequen

42 anic chromophores can be templated using the tobacco mosaic virus coat protein (TMVP).

43 ay studies (2.8-A resolution) on crystals of tobacco mosaic virus coat protein grown from solutions c

44 zed in aliquots of culture medium and of the tobacco mosaic virus coat protein in infected leaves.

45 omophores to cysteine residues introduced on tobacco mosaic virus coat protein monomers.

46 er the control of the subgenomic promoter of tobacco mosaic virus CP in the 30BRz vector.

47 are also compromised for HR mediated by the tobacco mosaic virus defense elicitor p50.

48 RNA by transiently delivering sgRNAs using a Tobacco mosaic virus-derived vector (TRBO) designed with

49 targeted movement of the movement protein of tobacco mosaic virus fused to GFP, P30::GFP.

50 in (MP) is essential for cell-cell spread of tobacco mosaic virus in planta.

51 (MP) is essential for cell-to-cell spread of tobacco mosaic virus in planta.

52 6 also permitted efficient multiplication of tobacco mosaic virus in the shoot apices, leading to ser

53 struct the N-mediated resistance response to tobacco mosaic virus in tomato demonstrates the utility

54 different from the four-helix-bundle fold of tobacco mosaic virus in which helix bundling dominates t

55 colocalization with the movement protein of Tobacco mosaic virus indicated an association of Hsp70h

56 that are differentially regulated during the tobacco mosaic virus-induced hypersensitive response in

57 ion was observed in response to ethylene- or tobacco mosaic virus-induced senescence.

58 P2 expression suppressed local resistance to tobacco mosaic virus, induction of pathogenesis-related

59 and stresses, such as drought, wounding and tobacco mosaic virus infection did not enhance nicotine

60 re responsive to salicylic acid treatment or tobacco mosaic virus infection.

61 In tobacco mosaic virus-inoculated tobacco leaves, newly sy

62 Cell-to-cell spread of tobacco mosaic virus is facilitated by the virus-encoded

63 The coat protein of tobacco mosaic virus is known to form three different cl

64 Tobacco mosaic virus is used as a probe to measure surfa

65 Studies on structure of tobacco mosaic virus led to our investigating an ultrace

66 We found that 2a can function as part of a tobacco mosaic virus-like 1a-2a fusion and that a 2a seg

67 mbly dynamics and the biosensing efficacy of Tobacco mosaic virus-like particle (TMV VLP) sensing pro

68 cle thin filament structure, and the mass of tobacco mosaic virus (mass standard) was within 5% of th

69 Resistance against tobacco mosaic virus mediated by tobacco N, a TIR-NBS-LR

70 In this study, we followed the dynamics of tobacco mosaic virus movement protein (MP) distribution

71 Cell-to-cell tobacco mosaic virus movement protein (TMV MP) mediates

72 ly phosphorylates the C-terminal residues of tobacco mosaic virus movement protein (TMV MP); this pos

73 estingly, plasmodesmatal localization of the Tobacco mosaic virus movement protein and Arabidopsis pr

74 nd map functionally important regions of the tobacco mosaic virus movement protein, deletions of thre

75 es leads to reduced movement of GFP fused to tobacco mosaic virus movement protein.

76 ntercellular movement of a GFP fusion to the tobacco mosaic virus movement protein.

77 drugs interfered with the PD localization of Tobacco mosaic virus movement protein.

78 of MTs in the intracellular distribution of tobacco mosaic virus MP is discussed.

79 onally indispensable alternative exon in the tobacco mosaic virus N resistance gene.

80 Substitution of the efficiently translated tobacco mosaic virus Omega 5' untranslated region result

81 rabidopsis (Arabidopsis thaliana) and either tobacco mosaic virus or potato X virus infecting Nicotia

82 c and transgenic plants expressing the MP of tobacco mosaic virus or red clover necrotic mosaic virus

83 microtubules or perturbations in the case of tobacco mosaic virus or the bacterial flagellar filament

84 we studied image contrast using ice-embedded tobacco mosaic virus particles as test samples at 20-80

85 of the spontaneous reconstitution of rodlike tobacco mosaic virus particles in solutions containing t

86 ging the (1)H spin density within individual tobacco mosaic virus particles sitting on a nanometer-th

87 nic lines expressing PAPII were resistant to tobacco mosaic virus, potato virus X and the fungal path

88 A containing the 5'-leader (called Omega) of tobacco mosaic virus preferentially uses eIF4G in wheat

89 The stacked disk aggregate of tobacco mosaic virus protein is an intriguing object due

90 Like many other viruses, Tobacco mosaic virus replicates in association with the

91 stance against potato virus X and N-mediated tobacco mosaic virus resistance.

92 resistant, but not susceptible, tobacco with tobacco mosaic virus resulted in enhanced NO synthase (N

93 The molecular structure of satellite tobacco mosaic virus (STMV) has been refined to 1.8 A re

94 Satellite tobacco mosaic virus (STMV) is a small, spherical ssRNA

95 Satellite tobacco mosaic virus (STMV) is a T = 1 icosahedral virus

96 we demonstrate that replication of Satellite tobacco mosaic virus (STMV) is controlled by the coopera

97 crystallographic structure of the satellite tobacco mosaic virus (STMV) particle reveals 30 helices

98 rand RNA genome of the icosahedral satellite tobacco mosaic virus (STMV) using nucleotide-resolution

99 Satellite tobacco mosaic virus (STMV) was probed using a variety o

100 MV), brome mosaic virus (BMV), and satellite tobacco mosaic virus (STMV)) along with the RNA from the

101 red for N gene-mediated HR and resistance to Tobacco Mosaic Virus, suggesting that it is an important

102 a lesser inhibitory effect on the unrelated Tobacco mosaic virus, suggesting that various viruses sh

103 When infected by tobacco mosaic virus, these transgenic plants accumulate

104 nteraction within the helicase domain of the Tobacco mosaic virus (TMV) 126- and 183-kDa replicase pr

105 In this study, the helicase domain of the Tobacco mosaic virus (TMV) 126- and/or 183-kDa replicase

106 teraction between the helicase domain of the Tobacco mosaic virus (TMV) 126-/183-kDa replicase protei

107 ates and coordinates these activities is the Tobacco mosaic virus (TMV) 30-kDa protein (MP(TMV)).

108 The tobacco N gene confers resistance to tobacco mosaic virus (TMV) and encodes a Toll-interleuki

109 The tobacco N gene confers resistance to Tobacco mosaic virus (TMV) and encodes a toll-interleuki

110 teraction between the replication protein of tobacco mosaic virus (TMV) and phloem-specific auxin/ind

111 ave made improvements to this approach using Tobacco Mosaic Virus (TMV) as a test specimen and obtain

112 istinct Cabbage leaf curl virus (CaLCuV) and Tobacco mosaic virus (TMV) cell-to-cell movement protein

113 structural and biophysical properties of the Tobacco mosaic virus (TMV) coat protein (CP) are address

114 Expression of tobacco mosaic virus (TMV) coat protein (CP) in plants c

115 Constitutive expression of a gene encoding tobacco mosaic virus (TMV) coat protein (CP) in transgen

116 Tobacco mosaic virus (TMV) derivatives that encode movem

117 The replicase protein of Tobacco mosaic virus (TMV) disrupts the localization and

118 The genome of tobacco mosaic virus (TMV) encodes replicase protein(s),

119 Tobacco mosaic virus (TMV) entry into minor, major and t

120 was examined in expanding infection sites of tobacco mosaic virus (TMV) expressing a fusion between t

121 The movement protein (MP) of tobacco mosaic virus (TMV) facilitates the cell-to-cell

122 Tobacco mosaic virus (TMV) forms dense cytoplasmic bodie

123 ts echo when I later tackled the assembly of Tobacco mosaic virus (TMV) from its constituent RNA and

124 The 5'-leader sequence (called Omega) of tobacco mosaic virus (TMV) functions as a translational

125 Virus expression vectors based on the tobacco mosaic virus (TMV) genome are powerful tools for

126 Tobacco mosaic virus (TMV) has had an illustrious histor

127 ate the role of BRs in plant defense against Tobacco Mosaic Virus (TMV) in Nicotiana benthamiana.

128 virus (GRV) ORF3 protein was expressed from Tobacco mosaic virus (TMV) in place of the TMV CP [TMV(O

129 ed significant inhibitory activities against tobacco mosaic virus (TMV) in vivo and in vitro.

130 Tobacco mosaic virus (TMV) induces the hypersensitive re

131 is more prevalent before and for 3 hr after tobacco mosaic virus (TMV) infection.

132 Tobacco mosaic virus (TMV) is a positive-sense, single-s

133 f tobacco plants (genotype NN) infected with tobacco mosaic virus (TMV) is accompanied by the inducti

134 The tobacco mosaic virus (TMV) movement protein (MP) facilit

135 The protein shell of the tobacco mosaic virus (TMV) provides a robust and practic

136 on between STMV CP and the helper virus (HV) Tobacco mosaic virus (TMV) replicase.

137 The dominant tobacco mosaic virus (TMV) resistance gene N induces a h

138 hin 2min; and cross-selectivity studies with tobacco mosaic virus (TMV) showed an excellent specifici

139 By taking advantage of a deconstructed tobacco mosaic virus (TMV) system, where the capsid prot

140 Using tobacco mosaic virus (TMV) tagged with green fluorescent

141 cognizes the 50 kDa helicase (p50) domain of Tobacco mosaic virus (TMV) through its TIR domain.

142 Cell-to-cell spread of tobacco mosaic virus (TMV) through plant intercellular c

143 protein (MP) mediates cell-to-cell spread of tobacco mosaic virus (TMV) through plant intercellular c

144 us cDNA-derived coat protein (CP) mutants of tobacco mosaic virus (TMV) to invade vascular cells in m

145 bridization to visualize the distribution of tobacco mosaic virus (TMV) viral RNA (vRNA) in infected

146 report the engineering of the surface of the tobacco mosaic virus (TMV) virion with a mosquito decape

147 As the first discovered virus, tobacco mosaic virus (TMV) was at the center of virus re

148 btained with viral RNA when the 30-kDa MP of tobacco mosaic virus (TMV) was coinjected with TMV TOTO-

149 In contrast, susceptibility to tobacco mosaic virus (TMV) was not altered in CSN-silenc

150 Recombinant tobacco mosaic virus (TMV) was used as an affinity matri

151 Hybrids of tobacco mosaic virus (TMV) were constructed with the use

152 cially constructed defective RNAs (dRNAs) of Tobacco mosaic virus (TMV) were examined in planta with

153 (STMV)) along with the RNA from the helical tobacco mosaic virus (TMV) were extracted using phenol/c

154 suspensions of mixtures of the rodlike virus tobacco mosaic virus (TMV) with globular macromolecules

155 es, the tobacco N gene confers resistance to tobacco mosaic virus (TMV), and leads to induction of st

156 and viruses such as filamentous phage fd and tobacco mosaic virus (TMV), as well as intermediate fila

157 rein, we show how a robust protein template, tobacco mosaic virus (TMV), can be used to regulate the

158 of three related Sindbis-like plant viruses, Tobacco mosaic virus (TMV), Cucumber mosaic virus (CMV),

159 involved in local, cell-to-cell movement of tobacco mosaic virus (TMV), is also required for the sys

160 ike and spherical viruses is highlighted for tobacco mosaic virus (TMV), M13 bacteriophage, cowpea ch

161 mpared with a standard of known MPL, such as Tobacco Mosaic Virus (TMV), MPL of the fibrils in questi

162 r movement of viruses from different genera [tobacco mosaic virus (TMV), potato virus X (PVX), tomato

163 nylalanine ammonialyase (PAL) reduces SAR to tobacco mosaic virus (TMV), whereas overexpression of PA

164 Infection with Tobacco mosaic virus (TMV), which is known to activate t

165 o leaves undergoing the HR was cloned into a tobacco mosaic virus (TMV)-based expression vector.

166 Tobacco mosaic virus (TMV)-based transient expression ve

167 ene encoding the coat protein of AlMV into a tobacco mosaic virus (TMV)-based vector Av.

168 A tobacco mosaic virus (TMV)-based vector carrying such in

169 athway, we have isolated and characterized a tobacco mosaic virus (TMV)-inducible myb oncogene homolo

170 ive in planta at blocking SAR development in tobacco mosaic virus (TMV)-infected tobacco and Pseudomo

171 al screening of a cDNA library prepared from tobacco mosaic virus (TMV)-infected tobacco leaves.

172 te of this pathway, was found in healthy and tobacco mosaic virus (TMV)-inoculated tobacco (Nicotiana

173 resistant tobacco plants after infection by tobacco mosaic virus (TMV).

174 ted leaves of tobacco resisting infection by tobacco mosaic virus (TMV).

175 sistance (R) genes and confers resistance to tobacco mosaic virus (TMV).

176 were developing HR following infection with tobacco mosaic virus (TMV).

177 the disassembly of simple viruses, including tobacco mosaic virus (TMV).

178 activated in tobacco resisting infection by tobacco mosaic virus (TMV).

179 was introduced into a genomic cDNA clone of tobacco mosaic virus (TMV).

180 inant virus vector based on the plant virus, tobacco mosaic virus (TMV).

181 or N from tobacco that confers resistance to tobacco mosaic virus (TMV).

182 t-nucleotide sequences in the genomic RNA of tobacco mosaic virus (TMV).

183 gen potato virus Y and the virulent pathogen tobacco mosaic virus (TMV).

184 tems; specifically, this work focuses on the tobacco mosaic virus (TMV).

185 acum L. cv Xanthi-nc) leaves inoculated with tobacco mosaic virus (TMV).

186 resistance (R) genes, confers resistance to tobacco mosaic virus (TMV).

187 ated scrambled Ebola RNA sequences inside of tobacco mosaic virus to create a biomimicry that is non-

188 sensitive response and effectively localizes tobacco mosaic virus to sites of inoculation in transgen

189 owed that single-stranded RNA from satellite tobacco mosaic virus transforms from a conformationally

190 uncatula were more resistant to infection by Tobacco mosaic virus, Turnip vein-clearing virus, and Su

191 This analysis, demonstrated here with tobacco mosaic virus U2, a bacteriophage MS2, and equine

192 cotiana benthamiana plants transduced with a tobacco mosaic virus vector expressing GRFT.

193 ead of virus replication complexes (VRCs) of tobacco mosaic virus was followed in intact leaf tissue

194 Furthermore, tobacco mosaic virus was recently shown to replicate in

195 Inspired by natural tobacco mosaic virus, we present the use of a rigid-rod

196 ncy was observed in HR cell death induced by tobacco mosaic virus, which is known to activate the sam

197 ion at PD with the viral movement protein of Tobacco mosaic virus, while superresolution imaging (thr