ライフサイエンスコーパス: BMV

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

14 uperimposable upon those of the original T=3 BMV particles.

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.

19 for the replication and transcription of all BMV RNAs.

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

23 However, Mga2p processing and BMV RNA replication are restored by supplementing free u

24 hile higher levels inhibited translation and BMV RNA replication.

25 same transformations were shown by TYMV and BMV RNA, and with heating, the RNA from STMV.

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

28 s in this work demonstrate a linkage between BMV RNA1 translation and replication.

29 idence that homologous recombination between BMV RNAs more likely occurs during positive- rather than

30 t in the tripartite brome mosaic bromovirus (BMV) RNA genome.

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

33 first described for Brome mosaic bromovirus (BMV), a model tripartite positive-sense RNA virus.

34 Brome mosaic bromovirus (BMV), a tripartite plus-sense RNA virus, has been used a

35 the RNA3 segment of brome mosaic bromovirus (BMV), a tripartite plus-strand RNA virus.

36 nst MuV might be protected from infection by BMV.

37 UTR due to end-to-end template switching by BMV replicase during (-)-strand synthesis.

38 been identified that function in controlling BMV translation, selecting BMV RNAs as replication templ

39 was previously shown to severely debilitate BMV RNA replication in plants.

40 amiana leaves expressing replication-derived BMV CP as a green fluorescent protein (GFP) fusion, in c

41 from ER accumulated in the cytoplasm during BMV infection.

42 e stability of the virions that encapsidated BMV RNA2 and RNA3/4.

43 These results show that the encapsidated BMV RNAs reflect a combination of host effects on the ph

44 entify such host factors, we used engineered BMV derivatives to assay viral RNA replication in each s

45 constructed and tested for binding enriched BMV replicase in a template competition assay.

46 Highly enriched BMV present in lysates had a surprising range of sizes,

47 h deletion strain was transformed to express BMV replicase proteins and a BMV RNA replication templat

48 bacterium tumefaciens to transiently express BMV RNAs in Nicotiana benthamiana.

49 emplate, we constructed a plasmid expressing BMV genomic RNA2 in vivo.

50 Yeast strains expressing BMV RNA replication proteins 1a and 2a(pol) were enginee

51 nfect plants and provide material to extract BMV replicase that can perform template-dependent RNA-de

52 step in RNA replication complex assembly for BMV, and possibly for other positive-strand RNA viruses.

53 desaturase gene OLE1, which is essential for BMV RNA replication.

54 d that significant differences can exist for BMV RNA replication in different hosts.

55 d susceptibility and restriction factors for BMV and TBSV have been identified using yeast as a model

56 sequences that contain regulatory motifs for BMV RNA gene expression and replication.

57 sequence near the initiation nucleotide for BMV RNA accumulation in plant cells.

58 is, 2a exhibits a strong cis preference for BMV RNA2.

59 A portion of the promoter for BMV minus-strand RNA synthesis could substitute for the

60 eadenylated mRNA decapping were required for BMV RNA translation.

61 y the cis- and trans-acting requirements for BMV RNA replication in plants and that significant diffe

62 d for 1a to function in cis and in trans for BMV RNA accumulation.

63 We also expressed the four BMV-encoded proteins from nonreplicating RNAs and analyz

64 t carries the AU-rich hot spot sequence from BMV.

65 r constructs, repression of translation from BMV RNA1 and RNA2 was observed, suggesting that the effe

66 esting that 1a may regulate translation from BMV RNAs.

67 steps that lead to assembly of a functional BMV RNA replication complex.

68 d peptides to select a human antibody, 5H/I1-BMV-D5 (D5), that binds to HR1 and inhibits the assembly

69 In BMV and FHV, genome packaging is coupled to replication,

70 To better understand the role of P bodies in BMV replication, we examined the subcellular locations o

71 rt here that involvement of DOA4 and BRO1 in BMV RNA replication is not dependent on the MVB pathway'

72 nternal termination and that encapsidates in BMV virions.

73 tion and characterization of host factors in BMV RNA replication.

74 e genes were shown previously to function in BMV replication, validating the approach.

75 t that in addition to its known functions in BMV RNA synthesis, 1a also regulates viral gene expressi

76 The previously unexpected heterogeneity in BMV should influence the timing of the infection and als

77 of ultrastructural modifications induced in BMV-infected N. benthamiana leaves revealed a reticulove

78 three isoforms of SOD and activity level in BMV on D-0, but these effects were not detected on D-3.

79 or RNA recruitment by 1a have been mapped in BMV genomic RNA2 and RNA3.

80 ought to examine the role of RNA polarity in BMV recombination by expressing a series of replication-

81 induce vesicles similar to those present in BMV infections.

82 we have studied homologous recombination in BMV RNA1 and RNA2 components during infection.

83 through an intergenic replication signal in BMV genomic RNA3 to stabilize RNA3 and induce RNA3 to as

84 indings suggest that fibrates elevate SOD in BMV through PPARalpha, which contributes to the infarct

85 the intercistronic recombination hot spot in BMV RNA3.

86 RNA synthesis are not identical to those in BMV, suggesting that the subgenomic core promoter can in

87 Deletion of the oligo(A) tract in BMV RNA3 inhibited synthesis of sgRNA3a during infection

88 flexible N-terminal arm of the CP increased BMV RNA replication and virion production.

89 rt and expand the conclusion that 1a-induced BMV RNA stabilization and membrane association reflect e

90 RNA accumulation, but dramatically inhibited BMV systemic spread in plants.

91 a defective Lsm1p-7p/Pat1p complex inhibits BMV RNA translation primarily by stalling or slowing the

92 Efficient incorporation into BMV virions of nonviral RNA chimeras containing NE and t

93 urprisingly, virions assembled from TLS-less BMV RNA in the presence of tRNAs or TLS-containing short

94 ring demands on their respective lifecycles: BMV must package separately each of several different RN

95 tase (SOD) levels in the brain microvessels (BMVs).

96 that phosphorylation of the capsid modulates BMV infection.

97 Moreover, BMV RNA replication templates were still recovered from

98 ane invaginations induced by multifunctional BMV protein 1a.

99 n the ssRNA organization in the multipartite BMV viral capsid and the monopartite bacteriophages MS2

100 plasts transfected with wild-type and mutant BMV transcripts.

101 Mass spectrometry shows that in native BMV virions, a significant fraction of the amino-termina

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

104 the known pH-dependent swelling behavior of BMV virions.

105 to the perinuclear ER, or colocalization of BMV 2a polymerase, nor did it block spherule formation.

106 , overlapping, nonreplicating derivatives of BMV genomic RNA3.

107 g residues severely reduced encapsidation of BMV RNA1 without affecting the encapsidation of RNA2.

108 ted defects in the specific encapsidation of BMV RNA4.

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

112 Inhibition of BMV RNA translation was selective, with no effect on gen

113 rom peripheral ER tubules to the interior of BMV-induced RNA replication compartments on perinuclear

114 on, we examined the subcellular locations of BMV RNAs in yeast cells.

115 ement the defective cell-to-cell movement of BMV.

116 a series of replication-defective mutants of BMV RNA3 in (+) or (-) polarity.

117 nsequence of the nonpolyadenylated nature of BMV RNAs but also involved the combined effects of the v

118 Pairs of BMV RNA3 variants carrying marker mutations at different

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

121 encapsidation was due to the purification of BMV particles to homogeneity.

122 of a BMV RNA in plants and the reassembly of BMV virions in vitro.

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

129 The role of BMV RNA1 in increased repair was examined.

130 n this work, we describe a novel 5' sgRNA of BMV (sgRNA3a) that we propose arises by premature intern

131 busvirus can use the recombination signal of BMV.

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

136 ovement protein increased the trafficking of BMV RNAs.

137 on the pH-dependent structural transition of BMV has also been investigated.

138 ly different dynamics for the three types of BMV virions, suggest that the different RNA genes they c

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

141 -strand synthesis had only modest effects on BMV replication in barley protoplasts.

142 plicating RNAs and analyzed their effects on BMV RNA accumulation.

143 Alterations of CCA to GGA in only BMV RNA3 also allowed RNA accumulation at wild-type leve

144 inserts through modification of the original BMV vector RNA sequence.

145 d sequencing revealed that, unlike any other BMV RNA segment, sgRNA3a carries a 3' oligo(A) tail, in

146 the BMV 2a polymerase does not require other BMV proteins to initiate RNA synthesis but that the 1a h

147 ding regions, most likely due to error-prone BMV RNA replication.

148 le into virions when incubated with purified BMV coat protein.

149 replicase (RdRp) preparation or recombinant BMV protein 2a.

150 e yeast LSM1 gene is required for recruiting BMV RNA from translation to replication.

151 1a also recruits BMV replication templates such as genomic RNA3.

152 to endoplasmic reticulum membranes, recruits BMV 2a polymerase and viral RNA templates, and forms mem

153 ctin Patch Protein 1 (App1) modestly reduced BMV genomic plus-strand RNA accumulation, but dramatical

154 Others are needed to co-regulate BMV RNA translation and recruitment of BMV RNAs from tra

155 d, membrane-associated compartments, require BMV replication factors 1a and 2a, and use negative-stra

156 on in controlling BMV translation, selecting BMV RNAs as replication templates, activating the replic

157 genes whose absence inhibited or stimulated BMV RNA replication and/or gene expression by 3- to >25-

158 ng a functional GFP-2a fusion that supported BMV RNA replication and subgenomic mRNA transcription.

159 osaic virus (BMV) replication, also supports BMV RNA recombination.

160 These results demonstrate that BMV RNAs can use a replication-independent mechanism to

161 tive-strand promoters and demonstrating that BMV can give rise to subgenomic RNA replicons.

162 found by ectopic expression experiments that BMV CP itself has the intrinsic property of modifying ER

163 In protoplasts, we found that BMV RNA3s with their SLCs replaced with two different CM

164 We observed that BMV genomic RNA2 and RNA3 accumulated in P bodies in a m

165 Our results also show that BMV RNA replication depends on additional Mga2p-regulate

166 We show that BMV RNA replication is inhibited 80-90% by deleting the

167 We show that BMV RNA replication is severely inhibited by a mutation

168 Prior results show that BMV RNA replication is severely inhibited by deletion of

169 eletion and medium supplementation show that BMV RNA replication requires unsaturated fatty acids, no

170 We previously showed that BMV RNA replication in yeast is severely inhibited prior

171 The BMV CP has also been shown to preferentially bind to an

172 The BMV model contains amino acid residues 41-189 for the pe

173 The BMV particle, with a maximum diameter of 195 A, is made

174 The BMV replicase enzyme supported a lower recombination fre

175 inct interactions between the capsid and the BMV genomic RNAs.

176 RNA into a template for RNA synthesis by the BMV replicase in vitro.

177 ition of the subgenomic core promoter by the BMV replicase.

178 In transiently transfected human cells, the BMV polymerase 2a activated signaling by the innate immu

179 n RNA3 trafficked into leaves containing the BMV replication enzymes, RNA replication, transcription,

180 d by addition of a 201-nt RNA containing the BMV TLS.

181 e Virus (CCMV) could also substitute for the BMV subgenomic core promoter.

182 Consistent with a critical role for the BMV TLS in virion assembly, mutations in the BMV genomic

183 These results better define how the BMV CP can interact with RNA and regulate different vira

184 ge number of modified lysine residues in the BMV capsid protein increases from 6 to 12, correlating w

185 BMV TLS in virion assembly, mutations in the BMV genomic RNAs that were designed to disrupt the foldi

186 Moreover, when copied in the BMV replicase in vitro reaction, the minus-strand RNA3 t

187 The only viral component in the BMV RNA replication complex that localizes independently

188 SLCs indicates that the requirements in the BMV SLC are highly specific.

189 results indicate that key nucleotides in the BMV subgenomic core promoter direct replicase recognitio

190 germ and yeast were similarly active in the BMV virion assembly reaction, but ribosomal RNA and poly

191 that distinct capsid-RNA interactions in the BMV virions allow different rates of viral RNA release.

192 the subgenomic core promoter can induce the BMV replicase in interactions needed for subgenomic RNA

193 esponding with the process of infection, the BMV replicases extracted from plants at different times

194 ed RIG-I activation, and coexpression of the BMV 1a protein stimulated 2a activity.

195 The crystallographic structure of the BMV capsid shows four trypsin cleavage sites (K(65), R(1

196 deletion of the first eight residues of the BMV coat protein (CP) resulted in the RNA1-containing pa

197 periments showed that phosphorylation of the BMV CP can impact binding to RNAs in the virions, includ

198 entical to those from the 5' sequence of the BMV genomic RNA2 and RNA3.

199 me coat protein (CP) encapsidate each of the BMV genomic RNAs.

200 Second, subsets of the BMV particles separated by density gradients into a pool

201 None of the BMV proteins or RNA could efficiently suppress posttrans

202 esting that the effect on translation of the BMV RNA replication proteins is responsible for the decr

203 Modification of the BMV RNA3 sequence yielded a vector, BMVCP5, that better

204 fy the replicase-binding sites in all of the BMV RNAs and suggest that the recognition of RNA3 is dif

205 ns 1a did not affect the accumulation of the BMV RNAs in the absence of RNA replication, unlike the s

206 However, the relative amounts of the BMV RNAs that accumulated in barley and wheat are simila

207 ements, nested fragments of all three of the BMV RNAs, both plus- and minus-sense fragments, were con

208 psidated RNA and the release of three of the BMV RNAs.

209 A comparison of the BMV T=1 particles was made with the reassembled T=1 part

210 ural classes identified by inspection of the BMV virion crystal structure.

211 Knowledge of the structures of the BMV wild-type and T=1 particles now permit us to propose

212 o perinuclear ER membranes and recruited the BMV 2a(pol) polymerase.

213 al fluorescence microscopy revealed that the BMV 1a and 2a colocalized to perinuclear region in human

214 These results show that the BMV 2a polymerase does not require other BMV proteins to

215 Using mass spectrometry, we found that the BMV CP contains a complex pattern of posttranslational m

216 ance of CP-mediated vesicle induction to the BMV infection cycle in planta.

217 ion in trans to replicate and transcribe the BMV RNAs.

218 In vitro results generated with the BMV replicase and minimal-length RNAs generally agreed w

219 In plant protoplasts replicating all three BMV genomic RNAs, mutations blocking sgRNA transcription

220 However, substitutions in all three BMV RNAs severely reduced RNA accumulation, demonstratin

221 All three BMV RNAs trafficked bidirectionally to sink leaves near

222 Thus, BMV replication vesicle formation and RNA replication de

223 Thus, BMV subgenomic and genomic RNA syntheses mutually interf

224 ned whether these requirements also apply to BMV replication in barley protoplasts.

225 ver, topical NF-kappaB Decoy, in contrast to BMV, restores compromised stratum corneum integrity and

226 g complex were also required for translating BMV RNAs.

227 However, the extra RNAs included truncated BMV RNAs, an additional copy of RNA4, potential cellular

228 Synchronized coexpression of wild-type BMV and FHV genome components in plant cells resulted in

229 Furthermore, wild-type BMV RNA1 was required for the repair and replication of

230 However, unlike BMV or retroviruses, where recombination usually occurre

231 d transcription, in the present work we used BMV RNA3 constructs that carried altered sgp repeats.

232 box in the 5'-untranslated region (5' UTR); BMV RNA3 that lacks a B box in its 5' UTR is not subject

233 vitro release of betamethasone-17-valerate (BMV), a representative dermatological drug, was determin

234 Unlike betamethasone valerate (BMV), long-term NF-kappaB Decoy treatment does not induc

235 at overexpression of the brome mosaic virus (BMV) 1a protein can repress viral RNA replication in a d

236 combination hot spots in Brome mosaic virus (BMV) and retroviruses.

237 th plant viruses such as brome mosaic virus (BMV) and tomato bushy stunt virus (TBSV).

238 -level expression of the brome mosaic virus (BMV) CP was found to stimulate viral RNA accumulation, w

239 Brome mosaic virus (BMV) encodes two RNA replication factors: 1a has a C-ter

240 ation of the plant virus brome mosaic virus (BMV) genomic RNAs when replication is reproduced in yeas

241 ) capsid protein (CP) of Brome mosaic virus (BMV) has an intrinsic property of modifying the endoplas

242 The plant virus brome mosaic virus (BMV) has served as a model for positive-strand RNA virus

243 Brome mosaic virus (BMV) is a model positive-strand RNA virus whose replicat

244 Brome mosaic virus (BMV) is a representative positive-strand RNA virus whose

245 Brome mosaic virus (BMV) is a tripartite positive-strand RNA virus used to s

246 Brome mosaic virus (BMV) is an RNA virus, and its three genomic RNAs are enc

247 -molecule RNA progeny of Brome mosaic virus (BMV) is packaged by a single capsid protein (CP) into th

248 the heterologous RNA1 of brome mosaic virus (BMV) is packaged three times more efficiently by CCMV CP

249 Brome mosaic virus (BMV) packages its genomic and subgenomic RNAs into three

250 ino terminally truncated brome mosaic virus (BMV) protein were created by treatment of the wild-type

251 ana leaves, we show that brome mosaic virus (BMV) replicase is competent to initiate positive-strand

252 Brome mosaic virus (BMV) replicates its RNA in endoplasmic reticulum (ER)-as

253 revisiae, which supports brome mosaic virus (BMV) replication, also supports BMV RNA recombination.

254 and RNA synthesis by the brome mosaic virus (BMV) RNA replicase is more efficient if the template con

255 Brome mosaic virus (BMV) RNA replication has been examined in a number of sy

256 tive-strand RNA viruses, brome mosaic virus (BMV) RNA replication occurs in membrane-invaginated vesi

257 Brome mosaic virus (BMV) RNA replication occurs on the perinuclear region of

258 cis-acting elements for Brome mosaic virus (BMV) RNA synthesis have been characterized primarily for

259 Brome mosaic virus (BMV) RNA synthesis occurs in approximately 70 nm, negati

260 Brome mosaic virus (BMV) RNA synthesis occurs in vesicular endoplasmic retic

261 promoter (sgp) region in brome mosaic virus (BMV) RNA3.

262 The four brome mosaic virus (BMV) RNAs (RNA1 to RNA4) are encapsidated in three disti

263 portions of plus-strand brome mosaic virus (BMV) RNAs mimic cellular tRNAs.

264 r the recognition of the brome mosaic virus (BMV) subgenomic core promoter by the replicase.

265 ositive-strand RNA virus brome mosaic virus (BMV) to replicate in yeast to show that the yeast LSM1 g

266 irions that comprise the Brome mosaic virus (BMV) were previously thought to be indistinguishable.

267 ents from the tripartite Brome mosaic virus (BMV) were transiently expressed in leaves of Nicotiana b

268 g in the plant-infecting Brome mosaic virus (BMV), a member of the alphavirus-like superfamily, as we

269 d for the replication of Brome Mosaic Virus (BMV), a plant-infecting RNA virus that can replicate in

270 eplication protein 1a of brome mosaic virus (BMV), a positive-strand RNA virus in the alphavirus-like

271 Brome mosaic virus (BMV), a positive-strand RNA virus in the alphavirus-like

272 Brome mosaic virus (BMV), a positive-strand RNA virus in the alphavirus-like

273 eplication protein 1a of brome mosaic virus (BMV), a positive-strand RNA virus, localizes to the cyto

274 tranded DNA viruses, and Bromo Mosaic Virus (BMV), a T = 3 single stranded RNA virus.

275 single subgenomic RNA of brome mosaic virus (BMV), an RNA virus infecting plants, are packaged by a s

276 subgenomic RNA (RNA4) of Brome mosaic virus (BMV), an RNA virus pathogenic to plants, are distributed

277 ures with the tripartite brome mosaic virus (BMV), an RNA virus that infects plants and is a member o

278 ibed role for the TLS of brome mosaic virus (BMV), and potentially for cellular tRNA, in mediating th

279 low mosaic virus (TYMV), brome mosaic virus (BMV), and satellite tobacco mosaic virus (STMV)) along w

280 For brome mosaic virus (BMV), both processes occur in virus-induced, membrane-as

281 In Brome mosaic virus (BMV), genomic RNA1 (gB1) and RNA2 (gB2), encoding the re

282 The structure of brome mosaic virus (BMV), the type member of the bromoviridae family, has be

283 replication of TBSV and brome mosaic virus (BMV), which belongs to a different supergroup among plus

284 ort the development of a Brome mosaic virus (BMV)-based vector that better maintains inserts through

285 enriched replicase from brome mosaic virus (BMV)-infected plants and variants of the promoter templa

286 replicase extracted from Brome mosaic virus (BMV)-infected plants has been used to characterize the c

287 multipartite RNA virus, brome mosaic virus (BMV).

288 ckaged in the tripartite Brome Mosaic Virus (BMV).

289 tructural transitions of brome mosaic virus (BMV).

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),

292 irus [FHV]), and plants (Brome mosaic virus [BMV]).

293 RNAs generally agreed with those of in vivo BMV RNA replication.

294 onse in rats, returning bone mineral volume (BMV) [corrected], to intact levels in the distal femur i

295 cowpea chlorotic mottle virus (CCMV), which BMV closely resembles.

296 Furthermore, while BMV dissolved better into the hydrophobic films, it was

297 localized UFA depletion helps to explain why BMV RNA replication is more sensitive than cell growth t

298 Similar to the situation with BMV, most of the recombination junction sites in the DI

299 nthamiana and N. clevelandii coexpressing wt BMV and Cucumber mosaic virus (CMV) showed that despite

300 duce vesicles similar to those present in wt BMV infection.