ライフサイエンスコーパス: turnip

1 ochrome f is much more acidic than that from turnip.

2 nt to trigger the hypersensitive response in turnip.

3 C), found abundantly in garlic, cabbage, and turnips.

4 ca species, including crops such as cabbage, turnip and oilseed, display enormous phenotypic variatio

5 ome may evolve from the ancestor of European turnip and the C subgenome may evolve from the common an

6 ntiation among three crop morphotypes (leaf, turnip, and oilseed) and for correlated evolution of cir

7 e domestication of the tuberous morphotypes, turnip (B. rapa) and kohlrabi (B. oleracea).

8 blackradish (Raphanus sativus L.) (TBR) and Turnip (Brassica rapa L.) using a simple and effective s

9 TURNIP comprises a suite of Perl scripts and modules tha

10 5' and 3' untranslated regions (UTRs) of the turnip crinkle carmovirus (TCV) genomic RNA (4 kb) as we

11 hanisms of RNA recombination were studied in turnip crinkle carmovirus (TCV), which has a uniquely hi

12 e used either a purified recombinant RdRp of Turnip crinkle carmovirus or a partially purified RdRp p

13 RNA C (a small parasitic RNA associated with turnip crinkle carmovirus) are repaired to the wild-type

14 ogenetically conserved RSE of the carmovirus Turnip crinkle virus (TCV) adopts an alternative, smalle

15 pots for recombination in the genomic RNA of turnip crinkle virus (TCV) and satellite (sat)-RNA C, a

16 nucleotides (nt) immediately upstream of the Turnip crinkle virus (TCV) coat protein (CP) open readin

17 Turnip crinkle virus (TCV) contains a structured 3' regi

18 ancer in the 3' untranslated region (UTR) of Turnip crinkle virus (TCV) contains an internal T-shaped

19 In Arabidopsis, resistance to Turnip Crinkle Virus (TCV) depends on the resistance (R)

20 rresponds to the last 283 nucleotides of the turnip crinkle virus (TCV) genome and hence is designate

21 The 3(') untranslated region (3(') UTR) of turnip crinkle virus (TCV) genomic RNA contains a cap-in

22 Resistance to Turnip Crinkle Virus (TCV) in Arabidopsis ecotype Dijon

23 rees C) that permits rigorous replication of Turnip crinkle virus (TCV) in Arabidopsis, plants contai

24 Turnip crinkle virus (TCV) inoculation onto TCV-resistan

25 Inoculation of turnip crinkle virus (TCV) into a (TCV)-resistant line o

26 The capsid protein (CP) of Turnip crinkle virus (TCV) is a multifunctional protein

27 Turnip crinkle virus (TCV) is a small, plus-sense, singl

28 The 356-nucleotide satC of Turnip crinkle virus (TCV) is unusual in that its 3'-hal

29 Inoculation of turnip crinkle virus (TCV) on the resistant Arabidopsis

30 Inoculation of turnip crinkle virus (TCV) on the resistant Arabidopsis

31 h in an untranslated satellite RNA (satC) of Turnip crinkle virus (TCV) regulates initiation of minus

32 We report here that the coat protein (CP) of Turnip crinkle virus (TCV) strongly suppresses PTGS.

33 y and tertiary elements within the 3' end of Turnip crinkle virus (TCV) that are required for viral a

34 specifically with the capsid protein (CP) of turnip crinkle virus (TCV) through yeast two-hybrid scre

35 60S subunits, and 80S ribosomes, whereas the Turnip crinkle virus (TCV) TSS binds only to 60S subunit

36 ority of the 3' untranslated region (UTR) of Turnip crinkle virus (TCV) was previously identified as

37 satC, a satellite RNA associated with Turnip crinkle virus (TCV), enhances the ability of the

38 The 3' ends of RNAs associated with turnip crinkle virus (TCV), including subviral satellite

39 All RNAs associated with turnip crinkle virus (TCV), including the genomic RNA (4

40 uctures of both native and expanded forms of turnip crinkle virus (TCV), using cryo-electron microsco

41 Sat-RNA C, associated with turnip crinkle virus (TCV), was previously found to inte

42 viously showed that a sat-RNA (sat-RNA C) of turnip crinkle virus (TCV), which normally intensifies s

43 if1-hairpin (M1H), located on (-)-strands of Turnip Crinkle Virus (TCV)-associated satellite RNA C (s

44 A Turnip crinkle virus (TCV)-based system was devised to d

45 diG) intensify the symptoms of their helper, turnip crinkle virus (TCV).

46 lation of subviral sat-RNA C associated with turnip crinkle virus (TCV).

47 iably examine the viral RNA encapsidation of turnip crinkle virus (TCV).

48 is produced by the replication machinery of turnip crinkle virus (TCV).

49 similar to the TSS 3'CITE of the carmovirus Turnip crinkle virus (TCV).

50 (TSS) similar to the ribosome-binding TSS of Turnip crinkle virus (TCV).

51 rgeted by some VSRs, such as that encoded by Turnip crinkle virus (TCV).

52 the R protein HRT, and thereby resistance to Turnip Crinkle virus (TCV).

53 were screened for antiviral activity towards Turnip crinkle virus (TCV, Tombusviridae).

54 n of the hp to the 3' untranslated region of Turnip crinkle virus (TCV-hp) and co-transfection of the

55 he replicase proteins of the closely related Turnip crinkle virus and distantly related Hepatitis C v

56 The mutation frequency of Turnip crinkle virus can increase 12-fold without induci

57 Turnip crinkle virus contains a T-shaped, ribosome-bindi

58 ritical 3' UTR hairpin in the genomic RNA of turnip crinkle virus did not directly interact with the

59 In contrast, symptom enhancement by satC of Turnip crinkle virus is due to satC interference with vi

60 ior of a subviral RNA (satC) associated with Turnip crinkle virus is required for fitness and that it

61 jected them to infections with CPB-CC-PDS, a turnip crinkle virus mutant capable of inducing silencin

62 liana mutants compromised for recognition of turnip crinkle virus previously identified CRT1, a membe

63 Comparison of the symptoms caused by turnip crinkle virus strain M (TCV-M) and TCV-B infectio

64 haliana CRT1 (compromised for recognition of Turnip Crinkle Virus) was previously shown to be require

65 vement-defective viruses, Potato virus X and Turnip crinkle virus, and an agroinfiltration assay, we

66 reated plants were resistant to infection by turnip crinkle virus, Pseudomonas syringae pv 'tomato' D

67 e or defective interfering RNAs (DI-RNAs) of Turnip crinkle virus, Tomato bushy stunt virus, Cucumber

68 d colleagues discovered that P38, the VSR of Turnip crinkle virus, uses its glycine/tryptophane (GW)

69 virus, carnation Italian ringspot virus, and turnip crinkle virus-associated RNA; the insect plus-str

70 scovered in satC, a replicon associated with turnip crinkle virus.

71 as we exemplify with the orthologous p38 of turnip crinkle virus.

72 idopsis thaliana) Compromised Recognition of Turnip Crinkle Virus1 subfamily of microrchidia Gyrase,

73 based on crystal structures of poplar PC and turnip cyt f at pH 7 and a variety of ionic strengths.

74 n has been examined in vitro with mutants of turnip cytochrome f and mutants of pea and spinach plast

75 acement using the coordinates of a truncated turnip cytochrome f as a model.

76 Soluble turnip cytochrome f has been purified from the periplasm

77 of the small subunit of Rubisco fused to the turnip cytochrome f precursor.

78 The 1.96 A structure of turnip cytochrome f revealed a linear internal chain of

79 tners to these differences, the reactions of turnip cytochrome f with P. laminosum plastocyanin and P

80 atomic structure of the lumen-side domain of turnip cytochrome f, consisting of Arg209 and Lys187, 58

81 the active lumen-side C-terminal fragment of turnip cytochrome f, containing the conserved Lys58,65,6

82 ys the same folding and detailed features as turnip cytochrome f, including (a) an unusual heme Fe li

83 crucifers such as Brassica spp., radish, and turnip, delivers XopP, a highly conserved core-effector

84 ntified by Mikhail Woronin in 1875 and named turnip disease in England.

85 configurational sampling by the Daughter of Turnip (DOT) docking program resulted in the computation

86 plastocyanin] to cytochrome f purified from turnip leaves.

87 sis mutants with decreased susceptibility to Turnip mosaic potyvirus (TuMV) were isolated.

88 We evolved turnip mosaic potyvirus in well-watered and drought cond

89 experiments demonstrate accurate tracking of turnip mosaic potyvirus infecting Arabidopsis (Arabidops

90 g tobamovirus, potato virus X potexvirus, or turnip mosaic potyvirus.

91 s (PlAMV) triple gene block 3 (TGB3) and the Turnip mosaic virus (TuMV) 6K2 proteins activate alterna

92 ettle on Nicotiana benthamiana infected with Turnip mosaic virus (TuMV) and fecundity on virus-infect

93 t broad-spectrum resistance to the potyvirus Turnip mosaic virus (TuMV) due to a natural mechanism ba

94 The approximately 10-kb RNA genome of Turnip mosaic virus (TuMV) encodes a membrane protein, k

95 ogenic recessive resistance to the Potyvirus Turnip mosaic virus (TuMV) has been found in a number of

96 Infection of Arabidopsis by Turnip mosaic virus (TuMV) induces a number of developme

97 Like other positive-strand RNA viruses, the Turnip mosaic virus (TuMV) infection leads to the format

98 Previously, we demonstrated that Turnip mosaic virus (TuMV) infection suppresses callose

99 sensitive, as are plants over-expressing the Turnip mosaic virus (TuMV) P1/HC-Pro viral protein that

100 Turnip mosaic virus (TuMV) reorganizes the endomembrane

101 ntiviral pathway during plant infection with turnip mosaic virus (TuMV), a positive-stranded RNA poty

102 o PD-localized potyviral proteins encoded by Turnip mosaic virus (TuMV), in the intercellular movemen

103 for three members of the family Potyviridae: Turnip mosaic virus (TuMV), Papaya ringspot virus (PRSV)

104 nd -adapted isolates of the natural pathogen turnip mosaic virus (TuMV).

105 accessions were inoculated with its natural Turnip mosaic virus (TuMV).

106 nip yellow mosaic virus (TYMV) and HC-Pro of turnip mosaic virus (TuMV).

107 The interaction between VPg of turnip mosaic virus and wheat germ eukaryotic translatio

108 rious RNAs, the interactions between PAP and turnip mosaic virus genome-linked protein (VPg) were inv

109 It confers immunity to plum pox virus and turnip mosaic virus in both Solanaceae and Brassicaceae

110 these helicases in the nuclei decreases upon Turnip mosaic virus infections, which couples with the d

111 omologues of an aphid transmitted potyvirus (Turnip mosaic virus), a rymovirus (Agropyron mosaic viru

112 viously, we demonstrated that infection with Turnip mosaic virus, a member of one of the largest fami

113 role in restricting compatible infection by turnip mosaic virus, a member of the largest plant RNA v

114 e also inserted ATR13 into the genome of the turnip mosaic virus, a single-stranded RNA virus.

115 d in InsP6 and were hypersusceptible to TMV, turnip mosaic virus, cucumber mosaic virus and cauliflow

116 abiotic stress factors significantly altered turnip mosaic virus-specific signaling networks, which l

117 ocal and systemic antiviral activity against Turnip mosaic virus.

118 ceptibility to cucumber mosaic virus but not turnip mosaic virus.

119 y distinct viruses, Tobacco mosaic virus and Turnip mosaic virus.

120 and can be isolated in gram quantities from turnip or Chinese cabbage inexpensively.

121 er risk, although subjects reporting greater turnip (P for trend < 0.001) and Chinese cabbage (P for

122 ilayer nanofiber mats based on potato starch-turnip peel extract (PS-TPE) and guar gum-cinnamaldehyde

123 purification factors for the TBR-POD and the Turnip-POD were 40.3-fold (with a yield of 10.6%) and 26

124 The molecular masses of the TBR-POD and Turnip-POD were approximately 67.3 and 65.8kDa, respecti

125 TBR-POD and as 4.09mM and 0.797EU/mL for the Turnip-POD.

126 e a non-competitive inhibitor of TBR-POD and Turnip-POD.

127 12.49mM and 4.055EU/mL, respectively for the Turnip-POD.

128 ed rape (Brassica napus subsp. oleifera) and turnip rape (B. rapa subsp. oleifera), having similar oi

129 (Phl p 7), alder (Aln g 4), birch (Bet v 4), turnip rape (Bra r 1), lamb's quarter (Che a 3) and oliv

130 important oilseed rape (Brassica napus) and turnip rape (Brassica rapa) were investigated with (1)H

131 f 9,12,15-octadecatrienoic acid (18:3n-3) in turnip rape and short day treatment decreased the total

132 commonly react to seeds of oilseed rape and turnip rape in skin prick tests (SPT) and open food chal

133 n sensitized or allergic to oilseed rape and turnip rape seeds reacted to these proteins from cold-pr

134 or allergen in the seeds of oilseed rape and turnip rape, and cruciferin (an 11S globulin), a new pot

135 ted fatty acids and sucrose were observed in turnip rape, while the overall oil content and sinapine

136 More generally, the TURNIP software ascertains degrees of variation between

137 and maize) and five species of dicots (rape, turnip, soybean, crabapple and tomato).

138 from vegetable phantoms such as potatoes and turnips suggest the technique may be capable of detectin

139 The turnip (tnp) mutant was identified in a screen for modif

140 d phenethyl isothiocyanates were detected in turnip varieties and, in addition, 3-butenyl isothiocyan

141 by a recently discovered crucifer-infecting turnip vein clearing tobamovirus (TVCV).

142 saic cucumovirus, oil seed rape tobamovirus, turnip vein clearing tobamovirus, potato virus X potexvi

143 s to that of the viral movement protein from turnip vein clearing tobamovirus.

144 ition to TMV MP, PME is recognized by MPs of turnip vein clearing virus (TVCV) and cauliflower mosaic

145 As TMV poorly infects Arabidopsis thaliana, Turnip vein clearing virus (TVCV) is the tobamovirus of

146 dmium was used to inhibit systemic spread of turnip vein clearing virus (TVCV), a tobamovirus, in tob

147 m completely blocked viral disease caused by turnip vein clearing virus.

148 Surprisingly, turnip vein-clearing virus (TVCV), a virus from the same

149 virus), and Arabidopsis thaliana with TVCV (Turnip vein-clearing virus)), but not in resistant host

150 istant to infection by Tobacco mosaic virus, Turnip vein-clearing virus, and Sunn hemp mosaic virus (

151 TURNIP was originally developed for the Saccharomyces Ge

152 Turnip yellow mosaic (TYMV) and kennedya yellow mosaic v

153 In addition, a recently identified vOTU from turnip yellow mosaic tymovirus was evaluated to elucidat

154 oding two gene silencing suppressors, P69 of turnip yellow mosaic virus (TYMV) and HC-Pro of turnip m

155 he crystal structures of such a PRO/DUB from Turnip yellow mosaic virus (TYMV) and of its complex wit

156 Turnip yellow mosaic virus (TYMV) contains a tRNA-like s

157 Five highly infectious turnip yellow mosaic virus (TYMV) genomes with sequence

158 Turnip yellow mosaic virus (TYMV) is an icosahedral plan

159 Previously, we have found that the 3'-UTR of Turnip yellow mosaic virus (TYMV) RNA enhances translati

160 B4) participate in the antiviral response to Turnip yellow mosaic virus (TYMV), and that both protein

161 s from four icosahedral viruses (poliovirus, turnip yellow mosaic virus (TYMV), brome mosaic virus (B

162 e structure (TLS) found at the 3' end of the turnip yellow mosaic virus (TYMV).

163 NA-like structure (TLS) at the 3' end of the turnip yellow mosaic virus genome was replaced with hete

164 The turnip yellow mosaic virus genomic RNA terminates at its

165 ence in adenine riboswitches, as well as the turnip yellow mosaic virus ribosome sensor.

166 The results indicate that amplification of turnip yellow mosaic virus RNA requires aminoacylation,

167 A valylated 3'-fragment of turnip yellow mosaic virus RNA, which has a pseudoknotte

168 gene expression is not the major role of the turnip yellow mosaic virus TLS.

169 de backbone is nearly identical with that of turnip yellow mosaic virus, as is the arrangement of sub

170 In turnip yellow mosaic virus, those from the B and C subun

171 ctures of the (N)RTDs from the poleroviruses turnip yellow virus (TuYV) and potato leafroll virus (PL

172 P0 from Turnip yellows virus (TuYV) is a VSR that was previously