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

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

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

8 TURNIP comprises a suite of Perl scripts and modules tha

9 5' and 3' untranslated regions (UTRs) of the turnip crinkle carmovirus (TCV) genomic RNA (4 kb) as we

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

33 60S subunits, and 80S ribosomes, whereas the Turnip crinkle virus (TCV) TSS binds only to 60S subunit

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

70 Soluble turnip cytochrome f has been purified from the periplasm

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

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

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

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

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

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

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

78 available at http://www.ncyc.co.uk/software/turnip.html.

79 plastocyanin] to cytochrome f purified from turnip leaves.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

100 ocal and systemic antiviral activity against Turnip mosaic virus.

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

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

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

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

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

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

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

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

109 12.49mM and 4.055EU/mL, respectively for the Turnip-POD.

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

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

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

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

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

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

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

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

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

119 The TURNIP source code, results files and online help are av

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

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

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

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

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

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

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

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

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

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

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

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

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

133 TURNIP was originally developed for the Saccharomyces Ge

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

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

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

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

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

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

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

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

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

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

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

145 The turnip yellow mosaic virus genomic RNA terminates at its

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

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

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

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

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