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

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

15 s 1 (NPR1) during N NLR-mediated response to tobacco mosaic virus.

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

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

18 by incorporating platinum nanoparticles into tobacco mosaic virus.

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

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

21 This phenomenon is illustrated with both tobacco mosaic virus (0.6-2.7 MDa) and AAV9 (3.7-4.7 MDa

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

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

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

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

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

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

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

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

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

31 iviral and antibacterial performance against tobacco mosaic virus and influenza A virus, and Escheric

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

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

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

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

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

37 ral analysis of the Phi92 capsid and sheath, tobacco mosaic virus, and bacteriorhodopsin at slightly

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

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

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

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

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

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

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

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

46 complexes using a circular permutant of the tobacco mosaic virus coat protein (cpTMV), which self-as

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

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

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

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

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

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

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

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

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

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

57 6 also permitted efficient multiplication of tobacco mosaic virus in the shoot apices, leading to ser

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

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

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

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

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

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

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

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

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

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

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

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

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

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

72 lies from rigid-solid angle dendrons forming Tobacco Mosaic Virus-like assemblies, columnar organizat

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

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

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

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

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

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

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

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

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

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

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

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

85 ly of MPs (named after the molecular mass of tobacco mosaic virus MP, the classical model of plant vi

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

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

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

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

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

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

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

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

94 lar infectious agent, later determined to be tobacco mosaic virus, paved the way for the field of vir

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

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

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

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

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

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

101 promoter in the presence of the elicitor of tobacco mosaic virus resulted in its increased expressio

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

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

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

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

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

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

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

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

110 the 1058-nucleotide RNA genome of satellite tobacco mosaic virus (STMV), which has been shown to hav

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

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

113 s described in 1898: a plant pathogen called tobacco mosaic virus that infects a wide range of plants

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

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

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

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

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

119 Unrelated Tobacco mosaic virus (TMV) also depends on Hsp70-1 and C

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

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

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

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

124 phage, pepper mild mottle virus (PMMoV), and tobacco mosaic virus (TMV) as indicators of the reductio

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

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

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

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

129 Tobacco mosaic virus (TMV) derivatives that encode movem

130 mber and flexibility was optimized using the tobacco mosaic virus (TMV) display platform.

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

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

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

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

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

136 Tobacco mosaic virus (TMV) forms dense cytoplasmic bodie

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

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

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

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

141 merging class of nano-biotechnology with the Tobacco Mosaic Virus (TMV) having found a wide range of

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

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

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

145 The history of tobacco mosaic virus (TMV) includes many firsts in scien

146 Tobacco mosaic virus (TMV) induces the hypersensitive re

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

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

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

150 of the origin of assembly sequence (OAS) of tobacco mosaic virus (TMV) is necessary for the specific

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

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

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

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

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

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

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

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

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

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

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

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

163 nanosensors capable of selectively detecting tobacco mosaic virus (TMV) viral RNA fragments, which su

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

165 terfacially bridging covalent network within tobacco mosaic virus (TMV) virus-like particles (VLPs).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

184 g on AuNPs is applied to the construction of tobacco mosaic virus (TMV)-AuNP conjugates, and energy t

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

186 further development of the agroinfiltratable Tobacco mosaic virus (TMV)-based overexpression (TRBO) v

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

205 , which is an NLR that confers resistance to Tobacco mosaic virus (TMV).

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

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

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

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

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

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

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

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

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

215 Previously, we used a Tobacco mosaic virus viral vector to express both GFP an

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

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

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

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

220 le to restore the hypersensitive response to tobacco mosaic virus, while B-ca1 and B-ca1ca5 plants fa

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