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1 rub canopy and with and without the invasive brome.
2 s; 2n = 4x = 28) and Bromus diandrus (ripgut brome; 2n = 8x = 56), have evolved resistance to glyphos
3 strongly suggests that plant species such as brome can undermine the positive and stabilizing effects
6 vealed that the subgenomic promoter (sgp) in brome mosaic bromovirus (BMV) RNA3 supports frequent hom
7 model system of a single-stranded trisegment Brome mosaic bromovirus (BMV) was used to analyze the me
8 in the RNA3 segment was first described for Brome mosaic bromovirus (BMV), a model tripartite positi
11 promoter (sgp) region in the RNA3 segment of brome mosaic bromovirus (BMV), a tripartite plus-strand
13 We report here that overexpression of the brome mosaic virus (BMV) 1a protein can repress viral RN
15 ve been performed with plant viruses such as brome mosaic virus (BMV) and tomato bushy stunt virus (T
16 e-like 1a and polymerase-like 2a proteins of brome mosaic virus (BMV) are required for viral RNA repl
17 iously we demonstrated that a 27 nt RNA from brome mosaic virus (BMV) can direct correct initiation o
18 A templates of 33 nucleotides containing the brome mosaic virus (BMV) core subgenomic promoter were u
19 uction, and molecular modeling, we show that brome mosaic virus (BMV) CP can assemble in vivo two rem
24 strand subgenomic RNAs, the requirements for brome mosaic virus (BMV) genomic plus-strand RNA synthes
25 ructure present at the 3' end of each of the brome mosaic virus (BMV) genomic RNAs is sufficient to d
26 ecruitment to replication of the plant virus brome mosaic virus (BMV) genomic RNAs when replication i
27 ion of wild-type (wt) capsid protein (CP) of Brome mosaic virus (BMV) has an intrinsic property of mo
34 ication-derived four-molecule RNA progeny of Brome mosaic virus (BMV) is packaged by a single capsid
37 dral particles of amino terminally truncated brome mosaic virus (BMV) protein were created by treatme
38 g Nicotiana benthamiana leaves, we show that brome mosaic virus (BMV) replicase is competent to initi
40 her Saccharomyces cerevisiae, which supports brome mosaic virus (BMV) replication, also supports BMV
41 trated that plus-strand RNA synthesis by the brome mosaic virus (BMV) RNA replicase is more efficient
54 leotides (-17, -14, -13, and -11) within the brome mosaic virus (BMV) subgenomic core promoter are re
55 ave been proposed for the recognition of the brome mosaic virus (BMV) subgenomic core promoter by the
57 higher eukaryotic positive-strand RNA virus brome mosaic virus (BMV) to replicate in yeast to show t
58 e three subsets of virions that comprise the Brome mosaic virus (BMV) were previously thought to be i
59 tions of genome segments from the tripartite Brome mosaic virus (BMV) were transiently expressed in l
63 A CAM is required for the replication of Brome Mosaic Virus (BMV), a plant-infecting RNA virus th
64 he multidomain RNA replication protein 1a of brome mosaic virus (BMV), a positive-strand RNA virus in
70 ultifunctional RNA replication protein 1a of brome mosaic virus (BMV), a positive-strand RNA virus, l
72 s form homologous recombination hot spots in brome mosaic virus (BMV), a tripartite positive-stranded
73 three genomic and a single subgenomic RNA of brome mosaic virus (BMV), an RNA virus infecting plants,
74 nd -3) and a single subgenomic RNA (RNA4) of Brome mosaic virus (BMV), an RNA virus pathogenic to pla
75 ral replication features with the tripartite brome mosaic virus (BMV), an RNA virus that infects plan
76 a previously undescribed role for the TLS of brome mosaic virus (BMV), and potentially for cellular t
77 liovirus, turnip yellow mosaic virus (TYMV), brome mosaic virus (BMV), and satellite tobacco mosaic v
78 , namely, Cowpea chlorotic mottle (CCMV) and Brome mosaic virus (BMV), are modulated by the host and
81 e movement of alfalfa mosaic virus (AMV) and brome mosaic virus (BMV), its precise function is not fu
83 ens reveals that the replication of TBSV and brome mosaic virus (BMV), which belongs to a different s
85 ics of more than 500 individual particles of brome mosaic virus (BMV)-for which RNA-protein interacti
93 nts, and among these, the tripartite viruses Brome mosaic virus and Cucumber mosaic virus have been s
94 the structures of several VLPs obtained from brome mosaic virus capsid proteins and gold nanoparticle
96 ously known: one pair involves the 3' end of brome mosaic virus genomic RNA (PKB134) and the alternat
97 work, folding dynamics for the TLS domain of Brome Mosaic Virus have been investigated using single-m
98 or the retrotransposition of Ty elements and brome mosaic virus in yeast cells, we assessed the role
99 ibition of rabbit reticulocyte expression by Brome mosaic virus mRNA, suggesting that inhibition of i
101 ting the relative levels and interactions of brome mosaic virus replication factors 1a and 2a polymer
103 l acetyltransferase) RNA or naturally capped brome mosaic virus RNA, however, was not affected by the
105 nitiation of subgenomic RNA synthesis by the brome mosaic virus RNA-dependent RNA polymerase (RdRp),
107 that Ded1p is also required for translating brome mosaic virus RNA2 in yeast thus raise the intrigui
109 ynthase, satellite tobacco mosaic virus, and brome mosaic virus show that the spherical elastic model
110 These results identify base moieties in the brome mosaic virus subgenomic promoter required for effi
115 fer RNA (tRNA)-like structure (TLS) from the brome mosaic virus, which affects replication, translati
116 egulated proteins in both 1 SL and 2 SL by a brome mosaic virus-based gene silencing vector in maize