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1 BMV encodes RNA replication factors 1a, with domains imp
2 BMV genomic RNA1 encodes protein 1a, which contains a me
3 BMV genomic RNAs and subgenomic RNA lacking the TLS fail
4 BMV mutants with decreased positive charges encapsidated
5 BMV purified from barley, wheat, and tobacco have distin
6 BMV replicase proteins 1a did not affect the accumulatio
7 BMV RNA replication compartments are not released from t
8 BMV RNA replication compartments show parallels with mem
9 BMV RNA1 and RNA2 could also traffic throughout the plan
10 BMV RNA3 was found to traffic from the initial site of e
11 BMV RNA3s with mutations in SLC were transfected into ba
12 BMV was distributed throughout the film but was more con
13 BMVs were isolated from male C57BL/6 and PPARalpha null
15 rmed to express BMV replicase proteins and a BMV RNA replication template with the capsid gene replac
16 ense RNA3 templates was copied with either a BMV replicase (RdRp) preparation or recombinant BMV prot
17 Pus4 also prevented the encapsidation of a BMV RNA in plants and the reassembly of BMV virions in v
18 ll-length RNAs, the same mutations abolished BMV RNA synthesis in transfected barley protoplasts.
20 involving the CCA 3' sequence in one or all BMV RNAs still allowed RNA accumulation in barley protop
21 ition of the Cucumber mosaic virus (CMV) and BMV SLCs indicates that the requirements in the BMV SLC
22 We have observed previously that in FHV and BMV, unlike ectopically expressed capsid protein (CP), p
26 termine if 1a had similar effects on another BMV RNA replication template, we constructed a plasmid e
27 ding frames were precisely exchanged between BMV RNA 3 (B3) and FHV RNA 2 (F2), creating chimeric RNA
29 idence that homologous recombination between BMV RNAs more likely occurs during positive- rather than
31 c promoter (sgp) in brome mosaic bromovirus (BMV) RNA3 supports frequent homologous recombination eve
32 stranded trisegment Brome mosaic bromovirus (BMV) was used to analyze the mechanism of homologous RNA
38 been identified that function in controlling BMV translation, selecting BMV RNAs as replication templ
40 amiana leaves expressing replication-derived BMV CP as a green fluorescent protein (GFP) fusion, in c
42 o replicate in yeast, we show that efficient BMV RNA replication requires Lsm1p, a yeast protein rela
44 These results show that the encapsidated BMV RNAs reflect a combination of host effects on the ph
45 entify such host factors, we used engineered BMV derivatives to assay viral RNA replication in each s
48 h deletion strain was transformed to express BMV replicase proteins and a BMV RNA replication templat
52 nfect plants and provide material to extract BMV replicase that can perform template-dependent RNA-de
53 step in RNA replication complex assembly for BMV, and possibly for other positive-strand RNA viruses.
56 d susceptibility and restriction factors for BMV and TBSV have been identified using yeast as a model
62 y the cis- and trans-acting requirements for BMV RNA replication in plants and that significant diffe
66 r constructs, repression of translation from BMV RNA1 and RNA2 was observed, suggesting that the effe
69 d peptides to select a human antibody, 5H/I1-BMV-D5 (D5), that binds to HR1 and inhibits the assembly
71 To better understand the role of P bodies in BMV replication, we examined the subcellular locations o
72 rt here that involvement of DOA4 and BRO1 in BMV RNA replication is not dependent on the MVB pathway'
76 t that in addition to its known functions in BMV RNA synthesis, 1a also regulates viral gene expressi
77 The previously unexpected heterogeneity in BMV should influence the timing of the infection and als
78 of ultrastructural modifications induced in BMV-infected N. benthamiana leaves revealed a reticulove
79 three isoforms of SOD and activity level in BMV on D-0, but these effects were not detected on D-3.
81 ought to examine the role of RNA polarity in BMV recombination by expressing a series of replication-
84 through an intergenic replication signal in BMV genomic RNA3 to stabilize RNA3 and induce RNA3 to as
85 indings suggest that fibrates elevate SOD in BMV through PPARalpha, which contributes to the infarct
87 RNA synthesis are not identical to those in BMV, suggesting that the subgenomic core promoter can in
90 rt and expand the conclusion that 1a-induced BMV RNA stabilization and membrane association reflect e
92 a defective Lsm1p-7p/Pat1p complex inhibits BMV RNA translation primarily by stalling or slowing the
94 urprisingly, virions assembled from TLS-less BMV RNA in the presence of tRNAs or TLS-containing short
102 ate's initiation site on the accumulation of BMV RNA3 genomic minus-strand, genomic plus-strand, and
103 bservations suggest that the accumulation of BMV RNAs in P bodies may be an important step in RNA rep
105 to the perinuclear ER, or colocalization of BMV 2a polymerase, nor did it block spherule formation.
107 g residues severely reduced encapsidation of BMV RNA1 without affecting the encapsidation of RNA2.
109 dditional restraints in the encapsidation of BMV RNAs, which could be applicable to other viruses.
110 nt MuV bearing the F and HN glycoproteins of BMV (rMuVJL5-F/HNBMV) virus and rMuVJL5 were demonstrate
111 virus bearing the F and HN glycoproteins of BMV in the background of a recombinant JL5 genome (rMuVJ
113 rom peripheral ER tubules to the interior of BMV-induced RNA replication compartments on perinuclear
117 nsequence of the nonpolyadenylated nature of BMV RNAs but also involved the combined effects of the v
119 e determined by coinoculations with pairs of BMV RNA3 variants that carried a duplicated sgp region f
120 expressed from the nontranslated portions of BMV RNA1 and RNA2, suggesting that 1a may regulate trans
123 ulate BMV RNA translation and recruitment of BMV RNAs from translation to viral RNA replication compl
124 ion, and both translation and recruitment of BMV RNAs to viral RNA replication are regulated by a cel
125 rted at the modified 3' noncoding regions of BMV RNA3 and RNA2 in either positive or negative orienta
126 All eight mapped to noncoding regions of BMV RNAs, and the positions of seven localized to sequen
127 he mechanism for the differential release of BMV RNAs from virions is unknown, since 180 copies of th
128 nts in the 3' untranslated region of RNA1 of BMV purified from barley and wheat, but not from tobacco
130 n this work, we describe a novel 5' sgRNA of BMV (sgRNA3a) that we propose arises by premature intern
132 lthough the subcellular localization site of BMV replication has been identified, that of the capsid
133 ated replication complex that is the site of BMV-specific RNA-dependent RNA synthesis in plant and ye
134 orce microscopy showed that the stiffness of BMV virions with different RNAs varied by a range that i
135 ombinants generated by template switching of BMV replicase with a nascent UTR from WT RNA1 or RNA2 du
139 tion studies clearly revealed that uptake of BMV was higher from hydrophobic FFS than that from the m
140 n the presence of MCT, the overall uptake of BMV was increased and provides the basis for further opt
146 d sequencing revealed that, unlike any other BMV RNA segment, sgRNA3a carries a 3' oligo(A) tail, in
147 the BMV 2a polymerase does not require other BMV proteins to initiate RNA synthesis but that the 1a h
153 to endoplasmic reticulum membranes, recruits BMV 2a polymerase and viral RNA templates, and forms mem
154 ctin Patch Protein 1 (App1) modestly reduced BMV genomic plus-strand RNA accumulation, but dramatical
156 d, membrane-associated compartments, require BMV replication factors 1a and 2a, and use negative-stra
157 on in controlling BMV translation, selecting BMV RNAs as replication templates, activating the replic
158 genes whose absence inhibited or stimulated BMV RNA replication and/or gene expression by 3- to >25-
159 ng a functional GFP-2a fusion that supported BMV RNA replication and subgenomic mRNA transcription.
164 found by ectopic expression experiments that BMV CP itself has the intrinsic property of modifying ER
171 eletion and medium supplementation show that BMV RNA replication requires unsaturated fatty acids, no
180 In transiently transfected human cells, the BMV polymerase 2a activated signaling by the innate immu
181 n RNA3 trafficked into leaves containing the BMV replication enzymes, RNA replication, transcription,
185 Consistent with a critical role for the BMV TLS in virion assembly, mutations in the BMV genomic
187 ge number of modified lysine residues in the BMV capsid protein increases from 6 to 12, correlating w
188 BMV TLS in virion assembly, mutations in the BMV genomic RNAs that were designed to disrupt the foldi
192 results indicate that key nucleotides in the BMV subgenomic core promoter direct replicase recognitio
193 germ and yeast were similarly active in the BMV virion assembly reaction, but ribosomal RNA and poly
194 that distinct capsid-RNA interactions in the BMV virions allow different rates of viral RNA release.
195 the subgenomic core promoter can induce the BMV replicase in interactions needed for subgenomic RNA
196 esponding with the process of infection, the BMV replicases extracted from plants at different times
198 deletion of the first eight residues of the BMV coat protein (CP) resulted in the RNA1-containing pa
199 periments showed that phosphorylation of the BMV CP can impact binding to RNAs in the virions, includ
204 esting that the effect on translation of the BMV RNA replication proteins is responsible for the decr
206 fy the replicase-binding sites in all of the BMV RNAs and suggest that the recognition of RNA3 is dif
207 ns 1a did not affect the accumulation of the BMV RNAs in the absence of RNA replication, unlike the s
209 ements, nested fragments of all three of the BMV RNAs, both plus- and minus-sense fragments, were con
215 al fluorescence microscopy revealed that the BMV 1a and 2a colocalized to perinuclear region in human
217 Using mass spectrometry, we found that the BMV CP contains a complex pattern of posttranslational m
221 In plant protoplasts replicating all three BMV genomic RNAs, mutations blocking sgRNA transcription
227 ver, topical NF-kappaB Decoy, in contrast to BMV, restores compromised stratum corneum integrity and
229 However, the extra RNAs included truncated BMV RNAs, an additional copy of RNA4, potential cellular
234 d transcription, in the present work we used BMV RNA3 constructs that carried altered sgp repeats.
235 box in the 5'-untranslated region (5' UTR); BMV RNA3 that lacks a B box in its 5' UTR is not subject
236 vitro release of betamethasone-17-valerate (BMV), a representative dermatological drug, was determin
238 at overexpression of the brome mosaic virus (BMV) 1a protein can repress viral RNA replication in a d
241 -level expression of the brome mosaic virus (BMV) CP was found to stimulate viral RNA accumulation, w
243 ation of the plant virus brome mosaic virus (BMV) genomic RNAs when replication is reproduced in yeas
244 ) capsid protein (CP) of Brome mosaic virus (BMV) has an intrinsic property of modifying the endoplas
250 the heterologous RNA1 of brome mosaic virus (BMV) is packaged three times more efficiently by CCMV CP
252 ino terminally truncated brome mosaic virus (BMV) protein were created by treatment of the wild-type
253 ana leaves, we show that brome mosaic virus (BMV) replicase is competent to initiate positive-strand
255 revisiae, which supports brome mosaic virus (BMV) replication, also supports BMV RNA recombination.
256 and RNA synthesis by the brome mosaic virus (BMV) RNA replicase is more efficient if the template con
258 tive-strand RNA viruses, brome mosaic virus (BMV) RNA replication occurs in membrane-invaginated vesi
260 cis-acting elements for Brome mosaic virus (BMV) RNA synthesis have been characterized primarily for
268 ositive-strand RNA virus brome mosaic virus (BMV) to replicate in yeast to show that the yeast LSM1 g
269 irions that comprise the Brome mosaic virus (BMV) were previously thought to be indistinguishable.
270 ents from the tripartite Brome mosaic virus (BMV) were transiently expressed in leaves of Nicotiana b
271 g in the plant-infecting Brome mosaic virus (BMV), a member of the alphavirus-like superfamily, as we
272 d for the replication of Brome Mosaic Virus (BMV), a plant-infecting RNA virus that can replicate in
273 eplication protein 1a of brome mosaic virus (BMV), a positive-strand RNA virus in the alphavirus-like
276 eplication protein 1a of brome mosaic virus (BMV), a positive-strand RNA virus, localizes to the cyto
277 single subgenomic RNA of brome mosaic virus (BMV), an RNA virus infecting plants, are packaged by a s
278 ures with the tripartite brome mosaic virus (BMV), an RNA virus that infects plants and is a member o
279 ibed role for the TLS of brome mosaic virus (BMV), and potentially for cellular tRNA, in mediating th
280 low mosaic virus (TYMV), brome mosaic virus (BMV), and satellite tobacco mosaic virus (STMV)) along w
284 replication of TBSV and brome mosaic virus (BMV), which belongs to a different supergroup among plus
285 ort the development of a Brome mosaic virus (BMV)-based vector that better maintains inserts through
286 enriched replicase from brome mosaic virus (BMV)-infected plants and variants of the promoter templa
287 replicase extracted from Brome mosaic virus (BMV)-infected plants has been used to characterize the c
290 our encapsidated RNAs of brome mosaic virus (BMV; B1, B2, B3, and B4) contain a highly conserved 3' 2
291 igenic relationship between bat mumps virus (BMV) and the JL5 vaccine strain of mumps virus (MuVJL5),
294 onse in rats, returning bone mineral volume (BMV) [corrected], to intact levels in the distal femur i
297 localized UFA depletion helps to explain why BMV RNA replication is more sensitive than cell growth t
299 nthamiana and N. clevelandii coexpressing wt BMV and Cucumber mosaic virus (CMV) showed that despite
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