ライフサイエンスコーパス: brome

1 stream pseudoknot tracts from the 3' ends of brome mosaic and tobacco mosaic viruses.

2 ecules of the RNA3 segment in the tripartite brome mosaic bromovirus (BMV) RNA genome.

3 vealed that the subgenomic promoter (sgp) in brome mosaic bromovirus (BMV) RNA3 supports frequent hom

4 model system of a single-stranded trisegment Brome mosaic bromovirus (BMV) was used to analyze the me

5 in the RNA3 segment was first described for Brome mosaic bromovirus (BMV), a model tripartite positi

6 Brome mosaic bromovirus (BMV), a positive-stranded RNA v

7 Brome mosaic bromovirus (BMV), a tripartite plus-sense R

8 promoter (sgp) region in the RNA3 segment of brome mosaic bromovirus (BMV), a tripartite plus-strand

9 rich regions during genetic recombination in brome mosaic bromovirus (BMV).

10 We report here that overexpression of the brome mosaic virus (BMV) 1a protein can repress viral RN

11 s that constitute recombination hot spots in Brome mosaic virus (BMV) and retroviruses.

12 ve been performed with plant viruses such as brome mosaic virus (BMV) and tomato bushy stunt virus (T

13 e-like 1a and polymerase-like 2a proteins of brome mosaic virus (BMV) are required for viral RNA repl

14 iously we demonstrated that a 27 nt RNA from brome mosaic virus (BMV) can direct correct initiation o

15 A templates of 33 nucleotides containing the brome mosaic virus (BMV) core subgenomic promoter were u

16 uction, and molecular modeling, we show that brome mosaic virus (BMV) CP can assemble in vivo two rem

17 Low-level expression of the brome mosaic virus (BMV) CP was found to stimulate viral

18 Brome mosaic virus (BMV) encodes two mutually interactin

19 Brome mosaic virus (BMV) encodes two RNA replication fac

20 Brome mosaic virus (BMV) encodes two RNA replication pro

21 strand subgenomic RNAs, the requirements for brome mosaic virus (BMV) genomic plus-strand RNA synthes

22 ructure present at the 3' end of each of the brome mosaic virus (BMV) genomic RNAs is sufficient to d

23 ecruitment to replication of the plant virus brome mosaic virus (BMV) genomic RNAs when replication i

24 ion of wild-type (wt) capsid protein (CP) of Brome mosaic virus (BMV) has an intrinsic property of mo

25 The plant virus brome mosaic virus (BMV) has served as a model for posit

26 Brome mosaic virus (BMV) is a member of the alphavirus-l

27 Brome mosaic virus (BMV) is a model positive-strand RNA

28 Brome mosaic virus (BMV) is a representative positive-st

29 Brome mosaic virus (BMV) is a tripartite positive-strand

30 Brome mosaic virus (BMV) is an RNA virus, and its three

31 For example, the heterologous RNA1 of brome mosaic virus (BMV) is packaged three times more ef

32 Brome mosaic virus (BMV) packages its genomic and subgen

33 dral particles of amino terminally truncated brome mosaic virus (BMV) protein were created by treatme

34 g Nicotiana benthamiana leaves, we show that brome mosaic virus (BMV) replicase is competent to initi

35 Brome mosaic virus (BMV) replicates its RNA in endoplasm

36 her Saccharomyces cerevisiae, which supports brome mosaic virus (BMV) replication, also supports BMV

37 trated that plus-strand RNA synthesis by the brome mosaic virus (BMV) RNA replicase is more efficient

38 Brome mosaic virus (BMV) RNA replication has been examin

39 Brome mosaic virus (BMV) RNA replication is directed by

40 Like many positive-strand RNA viruses, brome mosaic virus (BMV) RNA replication occurs in membr

41 Brome mosaic virus (BMV) RNA replication occurs on the p

42 To facilitate manipulation of brome mosaic virus (BMV) RNA replicons in Saccharomyces

43 The cis-acting elements for Brome mosaic virus (BMV) RNA synthesis have been charact

44 Brome mosaic virus (BMV) RNA synthesis occurs in approxi

45 Brome mosaic virus (BMV) RNA synthesis occurs in vesicul

46 d in these functions, we used the ability of brome mosaic virus (BMV) RNA to replicate in yeast.

47 thin the subgenomic promoter (sgp) region in brome mosaic virus (BMV) RNA3.

48 The four brome mosaic virus (BMV) RNAs (RNA1 to RNA4) are encapsi

49 The 3' portions of plus-strand brome mosaic virus (BMV) RNAs mimic cellular tRNAs.

50 leotides (-17, -14, -13, and -11) within the brome mosaic virus (BMV) subgenomic core promoter are re

51 ave been proposed for the recognition of the brome mosaic virus (BMV) subgenomic core promoter by the

52 The brome mosaic virus (BMV) system has been characterized e

53 higher eukaryotic positive-strand RNA virus brome mosaic virus (BMV) to replicate in yeast to show t

54 e three subsets of virions that comprise the Brome mosaic virus (BMV) were previously thought to be i

55 tions of genome segments from the tripartite Brome mosaic virus (BMV) were transiently expressed in l

56 Brome mosaic virus (BMV), a member of the alphavirus-lik

57 Genome packaging in the plant-infecting Brome mosaic virus (BMV), a member of the alphavirus-lik

58 Brome mosaic virus (BMV), a member of the alphavirus-lik

59 A CAM is required for the replication of Brome Mosaic Virus (BMV), a plant-infecting RNA virus th

60 he multidomain RNA replication protein 1a of brome mosaic virus (BMV), a positive-strand RNA virus in

61 Brome mosaic virus (BMV), a positive-strand RNA virus in

62 Brome mosaic virus (BMV), a positive-strand RNA virus in

63 Brome mosaic virus (BMV), a positive-strand RNA virus in

64 Brome mosaic virus (BMV), a positive-strand RNA virus in

65 Brome mosaic virus (BMV), a positive-strand RNA virus, e

66 ultifunctional RNA replication protein 1a of brome mosaic virus (BMV), a positive-strand RNA virus, l

67 In Brome mosaic virus (BMV), a stem-loop structure named C

68 s form homologous recombination hot spots in brome mosaic virus (BMV), a tripartite positive-stranded

69 three genomic and a single subgenomic RNA of brome mosaic virus (BMV), an RNA virus infecting plants,

70 ral replication features with the tripartite brome mosaic virus (BMV), an RNA virus that infects plan

71 a previously undescribed role for the TLS of brome mosaic virus (BMV), and potentially for cellular t

72 liovirus, turnip yellow mosaic virus (TYMV), brome mosaic virus (BMV), and satellite tobacco mosaic v

73 For brome mosaic virus (BMV), both processes occur in virus-

74 In Brome mosaic virus (BMV), genomic RNA1 (gB1) and RNA2 (g

75 The structure of brome mosaic virus (BMV), the type member of the bromovi

76 ens reveals that the replication of TBSV and brome mosaic virus (BMV), which belongs to a different s

77 Here, we report the development of a Brome mosaic virus (BMV)-based vector that better mainta

78 Using enriched replicase from brome mosaic virus (BMV)-infected plants and variants of

79 The RNA replicase extracted from Brome mosaic virus (BMV)-infected plants has been used t

80 and amount of RNA packaged in the tripartite Brome Mosaic Virus (BMV).

81 o the pH-dependent structural transitions of brome mosaic virus (BMV).

82 The four encapsidated RNAs of brome mosaic virus (BMV; B1, B2, B3, and B4) contain a h

83 sects (Flock house virus [FHV]), and plants (Brome mosaic virus [BMV]).

84 nts, and among these, the tripartite viruses Brome mosaic virus and Cucumber mosaic virus have been s

85 the structures of several VLPs obtained from brome mosaic virus capsid proteins and gold nanoparticle

86 The 3'-end region of the genomic RNA of brome mosaic virus forms a tRNA-like structure that is c

87 ously known: one pair involves the 3' end of brome mosaic virus genomic RNA (PKB134) and the alternat

88 work, folding dynamics for the TLS domain of Brome Mosaic Virus have been investigated using single-m

89 or the retrotransposition of Ty elements and brome mosaic virus in yeast cells, we assessed the role

90 ibition of rabbit reticulocyte expression by Brome mosaic virus mRNA, suggesting that inhibition of i

91 We examined RNA synthesis by the brome mosaic virus RdRp on DNA, RNA, and hybrid template

92 ting the relative levels and interactions of brome mosaic virus replication factors 1a and 2a polymer

93 In addition, the inhibition of brome mosaic virus RNA in vitro translation in wheat ger

94 l acetyltransferase) RNA or naturally capped brome mosaic virus RNA, however, was not affected by the

95 For the brome mosaic virus RNA-dependent RNA polymerase (RdRp),

96 nitiation of subgenomic RNA synthesis by the brome mosaic virus RNA-dependent RNA polymerase (RdRp),

97 c by competitive binding assay with tRNA and brome mosaic virus RNA.

98 that Ded1p is also required for translating brome mosaic virus RNA2 in yeast thus raise the intrigui

99 tructs resembling the minimal TLS element of brome mosaic virus RNA3.

100 ynthase, satellite tobacco mosaic virus, and brome mosaic virus show that the spherical elastic model

101 These results identify base moieties in the brome mosaic virus subgenomic promoter required for effi

102 In the divided genome of Brome mosaic virus system, both inter- and intrasegmenta

103 Brome mosaic virus, a tripartite positive-stranded RNA v

104 essing, all-atom modelling and validation of brome mosaic virus, an RNA virus.

105 For brome mosaic virus, we previously showed that such spher

106 egulated proteins in both 1 SL and 2 SL by a brome mosaic virus-based gene silencing vector in maize

107 genomic core promoter of the closely related brome mosaic virus.

108 and increase virion stability of a mutant of brome mosaic virus.