ライフサイエンスコーパス: RNA polymerase III

1 h a subset are not suggestive of stalling by RNA polymerase III.

2 nscription of the 5 S rRNA and tRNA genes by RNA polymerase III.

3 POLR3A and POLR3C encode subunits of RNA polymerase III.

4 , U2), whereas the U6 gene is transcribed by RNA polymerase III.

5 r TFIIIB plays key roles in transcription by RNA polymerase III.

6 occurs in the internal promoter regions for RNA polymerase III.

7 elocation to the nucleus, where it represses RNA polymerase III.

8 biogenesis of noncoding RNAs transcribed by RNA polymerase III.

9 rase II promoter rather than from ubiquitous RNA polymerase III.

10 es at the transcription initiation region of RNA polymerase III.

11 the up-stream region of genes transcribed by RNA polymerase III.

12 nent in basal and regulated transcription by RNA polymerase III.

13 plasmid DNA by the function of the cellular RNA polymerase III.

14 g and accurately initiating transcription by RNA polymerase III.

15 ion initiation sites of genes transcribed by RNA polymerase III.

16 mid-borne 5S and U6 RNA genes transcribed by RNA polymerase III.

17 achieve in the case of genes transcribed by RNA polymerase III.

18 efective transcription of SNR6 (U6 snRNA) by RNA polymerase III.

19 ation/reinitiation of transcription by human RNA polymerase III.

20 n and tagetitoxin, suggesting involvement of RNA polymerase III.

21 factors that mediate promoter selectivity by RNA polymerase III.

22 ion initiation sites of genes transcribed by RNA polymerase III.

23 h DNA binding factors, and directly recruits RNA polymerase III.

24 ession of transcription that is dependent on RNA polymerase III.

25 ly promotes SINE expression and occupancy by RNA polymerase III.

26 ubunit factors required for transcription by RNA polymerase III.

27 ements is transcribed into non-coding RNA by RNA polymerase III.

28 late methylation impedes U6 transcription by RNA polymerase III.

29 hed at telomeres and at genes transcribed by RNA polymerase III.

30 ion initiation sites of genes transcribed by RNA polymerase III.

31 ter is critical for optimal transcription by RNA polymerase III.

32 tRNAs, and other transcripts synthesized by RNA polymerase III and facilitates their maturation, whi

33 ong type I IFN (IFN-I) response triggered by RNA polymerase III and melanoma differentiation-associat

34 unit is critical for proper functionality of RNA Polymerase III and normal plant development.

35 RNA polymerase III and Pol II were found to co-localize

36 proteins, initiation factors of translation, RNA polymerase III and ribosomal DNA.

37 results provide a characterization of human RNA polymerase III and show that the RPC5 subunit is ess

38 e of thymines, which is the pause signal for RNA polymerase III and thus could potentially reduce tra

39 recognition particle (SRP) is transcribed by RNA polymerase III, and most steps in SRP biogenesis occ

40 The BFV pri-miRNA is transcribed by RNA polymerase III, and the three resultant mature miRNA

41 ry in infected cells limits transcription by RNA polymerase III, and vice versa.

42 was also associated with the absence of anti-RNA polymerase III antibodies and presence of anti-U1 RN

43 demonstrate strong associations between anti-RNA polymerase III antibodies and SRC.

44 Testing for anti-RNA polymerase III antibodies should be incorporated int

45 New associations include anti-RNA polymerase III antibodies with gastric antral vascul

46 on was observed with anticentromere and anti-RNA polymerase III antibodies.

47 a temporal association between SSc onset and RNA polymerase III antibodies.

48 trongly been associated with the presence of RNA polymerase III antibody.

49 al in that they are initially transcribed by RNA polymerase III as a single, approximately 122-nt pri

50 tein include all nascent transcripts made by RNA polymerase III as well as certain small RNAs synthes

51 and other nascent transcripts synthesized by RNA polymerase III as well as other noncoding RNAs.

52 ults reveal an unexpected role for tDNAs and RNA polymerase III-associated proteins in establishment

53 of polyglutamine, MOAG-2/LIR-3 regulates the RNA polymerase III-associated transcription of small non

54 ons have demonstrated an association between RNA polymerase III autoantibodies and a close temporal r

55 TFIIIA is essential for RNA polymerase III-based transcription of 5S rRNA in euk

56 ternal DNA scaffold is needed for TFIIIB and RNA polymerase III binding, and that productive initiati

57 rate that L11 suppresses c-Myc-dependent and RNA polymerase III-catalyzed transcription of 5 S rRNA a

58 We have purified an RNA polymerase III complex and identified its components

59 elements, or in extragenic loci that inhibit RNA polymerase III complex assembly, reduce barrier acti

60 have partially purified and characterized a RNA polymerase III complex that can direct transcription

61 ting a hierarchy that favors assembly of the RNA polymerase III complex versus assembly of adjacent a

62 RNA polymerase III demonstrated a robust nucleolar stain

63 The products of RNA Pol III (RNA polymerase III) dependent genes are elevated in both

64 by transfection, activated the pathway in an RNA polymerase III-dependent fashion.

65 levels coincided with hypoxic inhibition of RNA polymerase III-dependent MYC target genes, which MYC

66 Here we show that Maf1, a repressor of RNA polymerase III-dependent tRNA transcription, is an i

67 ncing, SINE-seq), which selectively profiles RNA Polymerase III-derived SINE RNA, thereby identifying

68 Like RNA polymerase III driven short hairpin RNA vectors, the

69 lso concurrently occupies a U6 promoter with RNA polymerase III during repression.

70 Thus, this region of the RNA polymerase III E2E promoter contains a B box sequenc

71 evidence suggests that genes transcribed by RNA polymerase III exhibit multiple functions within a c

72 A unique nucleolar RNA polymerase III expression pattern has been identifie

73 snaR-A is transcribed by RNA polymerase III from an intragenic promoter, turns ov

74 omplexes including RNA splicing proteins and RNA polymerase III from yeast, have been undertaken.

75 of reactions in response to partial loss of RNA Polymerase III function.

76 High levels of RNA polymerase III gene transcription are achieved by fa

77 ative DNA binding with another member of the RNA polymerase III general transcription machinery, TFII

78 s is the synthesis of RNA molecules, certain RNA polymerase III genes also function as genomic landma

79 We first used STAGE in yeast to confirm that RNA polymerase III genes are the most prominent targets

80 resenting the first quantitative analysis of RNA polymerase III genes in situ by electron microscopy.

81 IIIB generally required for transcription of RNA polymerase III genes, and the second is hBRFU, one o

82 A longtime interest in eukaryotic RNA polymerase III has centered on yeast and on the enum

83 romyces cerevisiae RNA polymerase III, human RNA polymerase III has not been entirely characterized.

84 vitro transcription of the rat vRNA gene by RNA polymerase III has previously been shown to be depen

85 Unlike Saccharomyces cerevisiae RNA polymerase III, human RNA polymerase III has not bee

86 encoding a putative RPC5-like subunit of the RNA Polymerase III in a model species Nicotiana benthami

87 ctly involved in transcription initiation by RNA polymerase III in eukaryotes.

88 the founding members of those recognized by RNA polymerase III in which all control elements for ini

89 ence that methylated SINE DNA is occupied by RNA polymerase III, including the use of high-throughput

90 ocked in RAW 264.7 cells pretreated with the RNA polymerase III inhibitor ML60218.

91 The RNA polymerase III initiation factor TFIIIB is assembled

92 limiting step in the ordered assembly of the RNA polymerase III initiation factor TFIIIB.

93 eri and Maraia (2015) demonstrate that yeast RNA polymerase III integrates inputs from both strands o

94 positive-sense genome and is transcribed by RNA polymerase III into a noncoding RNA of 140 nt.

95 We have found that the synthesis of tRNA by RNA polymerase III is also inhibited in response to ARF.

96 RNA polymerase III is essential for the transcription of

97 In eukaryotic cells, RNA polymerase III is highly conserved and transcribes h

98 integration upstream of tRNA genes, but that RNA polymerase III is not required.

99 ether the general transcription machinery or RNA polymerase III is preferentially phosphorylated.

100 tween DNA replication forks and transcribing RNA polymerase III machinery at NPCs.

101 The results suggest RNA polymerase III-mediated transcription of TARE may be

102 d polyuridine sequence of viral and cellular RNA polymerase III non-coding transcripts is critical fo

103 peaks within the domains occur frequently at RNA-polymerase-III-occupied transfer RNA (tRNA) genes, w

104 In contrast, transcription by RNA polymerase III of purified, circularized cloned DNAs

105 th TFIIIC to promote accurate termination by RNA polymerase III on a C-tailed VA1 template.

106 ranscription factor occurs in the absence of RNA polymerase III or polymerase II but requires specifi

107 the previously described sensors TLR9, DAI, RNA polymerase-III or IFI16/p204.

108 endent activator of IFN regulatory factor 3, RNA polymerase III, or high-mobility group boxes.

109 e upon the stability and accumulation of its RNA polymerase III (Pol III) directed transcripts was de

110 transcription regulation that involves both RNA polymerase III (Pol III) elements and CCCTC binding

111 The C53 and C37 subunits of RNA polymerase III (pol III) form a subassembly that is

112 BocaSR is transcribed by RNA polymerase III (Pol III) from an intragenic promoter

113 TFIIIB is required for transcription of all RNA polymerase III (pol III) genes.

114 tivators that regulate the activity of human RNA polymerase III (Pol III) in the context of chromatin

115 sents a limiting step in the assembly of the RNA polymerase III (pol III) initiation factor TFIIIB.

116 RNA polymerase III (pol III) is involved in the generati

117 RNA polymerase III (Pol III) is one of three eukaryotic

118 Nielsen et al. characterized their RNA polymerase III (Pol III) preparation and concluded t

119 Termination by RNA polymerase III (Pol III) produces RNAs whose 3' olig

120 Short hairpin RNAs (shRNAs) transcribed by RNA polymerase III (Pol III) promoters can trigger seque

121 by the use of expression cassettes driven by RNA polymerase III (pol III) promoters.

122 h the sweet orange MAF1 (CsMAF1) protein, an RNA polymerase III (Pol III) repressor that controls rib

123 s or oncogenes, directly associates with the RNA polymerase III (pol III) subunit RPC32 and enhances

124 RNA polymerase III (Pol III) synthesizes short noncoding

125 RNA polymerase III (Pol III) synthesizes tRNAs and other

126 e chromatin immunoprecipitation assay in the RNA polymerase III (pol III) system that allowed us to m

127 A genes and regulates their transcription by RNA polymerase III (pol III) through direct binding and

128 RNA polymerase III (pol III) transcribes many essential,

129 RNA polymerase III (Pol III) transcribes medium-sized no

130 RNA polymerase III (Pol III) transcribes small untransla

131 Deregulation of RNA polymerase III (Pol III) transcription enhances cell

132 Deregulation of RNA polymerase III (Pol III) transcription enhances cell

133 es cerevisiae gene BDP1 encodes a subunit of RNA polymerase III (Pol III) transcription factor (TFIII

134 e chromosomal locations bound in vivo by the RNA polymerase III (Pol III) transcription factor III C

135 The binding of the RNA polymerase III (pol III) transcription factor TFIIIC

136 RNA polymerase III (pol III) transcription from the huma

137 vation and various stress conditions repress RNA polymerase III (Pol III) transcription in S. cerevis

138 Maf1 is the 'master' repressor of RNA polymerase III (Pol III) transcription in yeast, and

139 hat allow productive binding in vitro of the RNA polymerase III (Pol III) transcription initiation fa

140 RNA polymerase III (Pol III) transcription of tRNA genes

141 minal repeat retrotransposon Ty3 is found at RNA polymerase III (Pol III) transcription start sites o

142 osphopeptide from Maf1, a known repressor of RNA polymerase III (Pol III) transcription.

143 Canonical RNA polymerase III (pol III) type 2 promoters contain a

144 evisiae U6 RNA gene, SNR6, is transcribed by RNA polymerase III (Pol III), but lacks the intragenic B

145 anscription of small non-coding RNA genes by RNA polymerase III (Pol III), but the precise role of th

146 ns and a subset of small RNAs transcribed by RNA polymerase III (pol III), including the signal recog

147 e central transcription initiation factor of RNA polymerase III (pol III), is composed of three subun

148 integration upstream of genes transcribed by RNA polymerase III (pol III), mainly tRNA genes.

149 ituted with recombinant factors and purified RNA polymerase III (pol III), pol III must be treated wi

150 about the initial phase of transcription by RNA polymerase III (Pol III), the enzyme that synthesize

151 In fission yeast, we demonstrated that RNA polymerase III (Pol III)-transcribed genes such as t

152 The association of RNA polymerase III (Pol III)-transcribed genes with nucl

153 charomyces cerevisiae integrates upstream of RNA polymerase III (Pol III)-transcribed genes, yet the

154 out chromatin-modifying activities acting on RNA polymerase III (Pol III)-transcribed genes.

155 o evidence of the production of noncanonical RNA polymerase III (Pol III)-transcribed viral microRNAs

156 ferentially upstream of genes transcribed by RNA polymerase III (Pol III).

157 II (Pol II), but U6 snRNA is synthesized by RNA polymerase III (Pol III).

158 transcription factor TFIIIC complex without RNA polymerase III (Pol III).

159 the initiation sites of genes transcribed by RNA polymerase III (pol III).

160 ranscription from small nuclear RNA genes by RNA polymerase III (pol III).

161 short abundant transcripts that are made by RNA polymerase III (Pol III).

162 is a class of retrotransposon transcribed by RNA polymerase III (Pol III).

163 ed cluster of miRNAs that are transcribed by RNA polymerase III (pol III).

164 n led to the identification of DNA-dependent RNA polymerase III (Pol-III) as the enzyme responsible f

165 molecular epitope spreading in patients with RNA polymerase III (POLR3) and the minor spliceosome spe

166 dontia and Hypogonadotropic Hypogonadism) or RNA polymerase III (POLR3)-related leukodystrophy cases

167 c La proteins, p43 does not bind strongly to RNA polymerase III precursor transcripts and does not ex

168 ities such as processing and/or transport of RNA polymerase III precursor transcripts and translation

169 itiation complexes on U1 to U5 promoters but RNA polymerase III preinitiation complexes on U6 promote

170 Its activity in mice is correlated with its RNA polymerase III promoter activity and its orientation

171 RNA sequence has two elements which fit the RNA polymerase III promoter consensus sequence, and show

172 arrying silencing cassettes consisting of an RNA polymerase III promoter expressing short hairpin RNA

173 ng achieved with an shRNAi expressed from an RNA polymerase III promoter in transient transfection wa

174 ts of breaks in the individual strands of an RNA polymerase III promoter on initiation of transcripti

175 se data establish that RNA polymerase II and RNA polymerase III promoter sequences are superimposed f

176 ptional control region contains an efficient RNA polymerase III promoter, in addition to the well cha

177 ion of a loxP-flanked neomycin cassette into RNA polymerase III promoter, which controls a vector-bas

178 randed oligonucleotides or plasmids encoding RNA polymerase III promoter-driven small hairpin RNA.

179 lizing an adenoviral vector employing the H1 RNA polymerase III promoter.

180 s first provided by the properties of TFIIIB-RNA polymerase III-promoter complexes assembled with del

181 Our data indicate that first, RNA polymerase III promoters are the most prominent bind

182 Thus, in fruit flies, different classes of RNA polymerase III promoters differentially utilize TBP

183 s) for CRISPR-TFs can only be expressed from RNA polymerase III promoters in human cells, limiting th

184 sized exogenously or can be transcribed from RNA polymerase III promoters in vivo, thus permitting th

185 cifically, MHV68 miRNAs are transcribed from RNA polymerase III promoters located within adjacent vir

186 Transcription initiation at RNA polymerase III promoters requires transcription fact

187 gene and up to four sgRNAs from independent RNA polymerase III promoters that are incorporated into

188 Use of weaker RNA polymerase III promoters to minimize shRNA expressio

189 kbones expressing various RIG-I ligands from RNA polymerase III promoters were screened in a cell cul

190 anscription of both TATA-less and snRNA-type RNA polymerase III promoters, and a factor equally relat

191 tor IIIB (TFIIIB), an activity that binds to RNA polymerase III promoters, generally through protein-

192 with specificities for different classes of RNA polymerase III promoters, have evolved in human cell

193 mutations as gRNAs expressed from individual RNA polymerase III promoters.

194 synthetic short hairpin RNAs, typically from RNA polymerase III promoters.

195 ically required for transcription of U6-type RNA polymerase III promoters.

196 l nuclear RNA (snRNA)-type, TATA-containing, RNA polymerase III promoters.

197 lly required for transcription of snRNA-type RNA polymerase III promoters.

198 ress viral miRNAs by using embedded proviral RNA polymerase III promoters.

199 nced mating loci, and regions transcribed by RNA polymerase III, providing evidence that the enzymati

200 RNA polymerase III recognizes and pauses at its terminat

201 ranscription at critical steps subsequent to RNA polymerase III recruitment.

202 n the transcription of tRNA and 5 S genes by RNA polymerase III, recruitment of the transcription fac

203 cipitation directly linking these factors to RNA polymerase III regulation.

204 ll nuclear RNA (snRNA) gene transcription by RNA polymerase III requires cooperative promoter binding

205 mplex transition.Transcription initiation by RNA polymerase III requires TFIIIB, a complex formed by

206 n U6 small nuclear RNA gene transcription by RNA polymerase III requires the general transcription fa

207 RNA polymerase III (RNA pol III) transcribes structural

208 ity of viral microRNAs (miRNAs) derived from RNA polymerase III (RNAP III) transcribed precursors.

209 RNA polymerase III (RNAP III) type III promoters (U6 or

210 nd on common host transcripts transcribed by RNA polymerase III (RNAP III), yet how these transcripts

211 RNA) genes (tDNAs), which are transcribed by RNA polymerase III (RNAPIII) and encode RNA molecules re

212 RNA polymerase III (RNAPIII) components, including Rpc53

213 osons evolutionarily derived from endogenous RNA Polymerase III RNAs.

214 IIIC transcription factor but do not recruit RNA polymerase III, show specific intranuclear positioni

215 an activator of snRNA promoters, and in the RNA polymerase III snRNA promoters, with TATA-binding pr

216 haromyces cerevisiae tau55, a subunit of the RNA polymerase III-specific general transcription factor

217 d promoter elements define the assembly of a RNA polymerase III-specific preinitiation complex.

218 itions +2 and +62 on E2E transcription in an RNA polymerase III-specific, in vitro system.

219 In contrast, nucleolar RNA polymerase III staining was not detected in any of 4

220 ereupon it primes the phosphorylation of the RNA polymerase III subunit Rpc53 by a specific GSK-3 fam

221 Orthologues of the yeast RNA polymerase III subunits C128 and C37 remain unidenti

222 f a concerted mechanism involving TFIIIB and RNA polymerase III subunits for the closed to open pre-i

223 We found that two RNA polymerase III subunits, referred to as RPC8 and RPC

224 ition and the properties of E2E RNAs made by RNA polymerase III suggest that the function of this vir

225 ieve recruitment of Saccharomyces cerevisiae RNA polymerase III, TBP is associated with two additiona

226 expressed human vRNA genes even though a new RNA polymerase III termination sequence has evolved betw

227 ' unique end after the A-tail and before the RNA polymerase III terminator, and random mutations foun

228 icipates in two steps of promoter opening by RNA polymerase III that are comparable to the successive

229 of retrotransposons that are transcribed by RNA polymerase III, thus generating exclusively noncodin

230 he bovine leukemia virus, a retrovirus, uses RNA polymerase III to directly transcribe the pre-miRNA

231 the world's experts on RNA polymerase I and RNA polymerase III to highlight and share their latest r

232 region, and the U1 PSE is unable to recruit RNA polymerase III to transcribe the U6 gene.

233 TBP recruits condensin onto RNA polymerase III-transcribed (Pol III) genes and highl

234 s the EBV latent replication origin OriP and RNA polymerase III-transcribed EBV-encoded RNA genes.

235 We show that condensin frequently associates RNA polymerase III-transcribed genes (tRNA and 5S rRNA)

236 However, RNA polymerase III-transcribed genes exhibit diverse pro

237 se results suggest that different classes of RNA polymerase III-transcribed genes have distinct gener

238 tRNAs are encoded by RNA polymerase III-transcribed genes that reside at seem

239 show that RB represses different classes of RNA polymerase III-transcribed genes via distinct mechan

240 nstructs with known 5' flanking sequences of RNA polymerase III-transcribed genes.

241 on of both RNA polymerase II-transcribed and RNA polymerase III-transcribed snRNA genes and is recogn

242 t ER was associated with a large fraction of RNA polymerase III-transcribed tRNA genes, independent o

243 e majority RNA polymerase II transcript; the RNA polymerase III-transcribed U1 small nuclear RNA has

244 A) is a perfect match to the TATA box of the RNA polymerase III-transcribed U6 small nuclear RNA (SNR

245 BC1 RNA, a noncoding RNA polymerase III transcript that is targeted to dendri

246 The major human species, snaR-A, is an RNA polymerase III transcript with restricted tissue dis

247 icellular organisms beyond the regulation of RNA polymerase III transcription and suggest that Maf1 p

248 The retinoblastoma protein (RB) represses RNA polymerase III transcription effectively both in viv

249 integrase targeted by a synthetic fusion of RNA polymerase III transcription factor IIIB subunits, B

250 the N terminus of Bdp1p, a component of the RNA polymerase III transcription factor TFIIIB, is requi

251 tes map to tRNA and other genes bound by the RNA polymerase III transcription factor TFIIIC, and ribo

252 e key glycolytic enzyme, and La protein, the RNA polymerase III transcription factor, with the cis-ac

253 n physically associates with a subcomplex of RNA polymerase III transcription factors on the tRNA gen

254 TFIIIA is required to activate RNA polymerase III transcription from 5S RNA genes.

255 ctor TRF1 rather than TBP is responsible for RNA polymerase III transcription in Drosophila.

256 the properties of the small E2E RNAs and E2E RNA polymerase III transcription in more detail.

257 We selected the BRF1 gene, which encodes an RNA polymerase III transcription initiation factor subun

258 ts contribute to the definition of the basal RNA polymerase III transcription machinery and show that

259 gesting that the complex is recruited by the RNA polymerase III transcription machinery.

260 In adenovirus type 5-infected cells, RNA polymerase III transcription of a gene superimposed

261 retinoblastoma (RB) protein represses global RNA polymerase III transcription of genes that encode no

262 Protein kinase CK2 regulates RNA polymerase III transcription of human U6 small nucle

263 itors reduce PNC prevalence in parallel with RNA polymerase III transcription reduction, and a subset

264 The RNA polymerase III transcription terminator is flexibly

265 MAF1 is a global repressor of RNA polymerase III transcription that regulates the expr

266 III suggest that the function of this viral RNA polymerase III transcription unit is unusual.

267 Transfer RNA (tRNA) genes and other RNA polymerase III transcription units are dispersed in

268 sequence, and shows homology with dispersed RNA polymerase III transcription units in mammals.

269 In the fruit fly Drosophila melanogaster, RNA polymerase III transcription was found to be depende

270 that tDNAs associate with NPCs to coordinate RNA polymerase III transcription with the nuclear export

271 In the case of RNA polymerase III transcription, this is due to phospho

272 better understanding of the function of this RNA polymerase III transcription, we have examined the p

273 or inhibits the growth-promoting activity of RNA polymerase III transcription.

274 er activity requires sequences necessary for RNA polymerase III transcription.

275 e yeast BRF, is not universally required for RNA polymerase III transcription.

276 CK2 is likely to modulate its activation of RNA polymerase III transcription.

277 pact and yet powerful promoters that support RNA polymerase III transcription.

278 condary effects on RNA polymerase I, but not RNA polymerase III, transcription.

279 that components of the RNA polymerase II and RNA polymerase III transcriptional machines compete for

280 These noncoding RNA polymerase III transcripts are normally complexed wi

281 protects the UUU(OH) 3' terminii of nascent RNA polymerase III transcripts from exonuclease digestio

282 Although the RNA polymerase III transcripts were present at significa

283 iated with precursor tRNAs and other nascent RNA polymerase III transcripts while nonphosphorylated (

284 cleolar localization of Misu is dependent on RNA polymerase III transcripts, and knockdown of Misu de

285 functions commonly associated with the core RNA Polymerase III transcripts, but also more diverse ce

286 The association of Lhp1p with larger RNA polymerase III transcripts, pre-RNase P RNA and the

287 novel downstream Myc target that methylates RNA polymerase III transcripts.

288 3' uridylates found in all newly synthesized RNA polymerase III transcripts.

289 La autoantigen, functioning in maturation of RNA polymerase III transcripts.

290 one binding to 3' UUUOH sequences of nascent RNA polymerase III transcripts.

291 cursor and processed tRNAs, as well as other RNA polymerase III transcripts.

292 und on both the RNA polymerase II U1 and the RNA polymerase III U6 promoters as determined by chromat

293 es by either RNA polymerase II (U1 to U5) or RNA polymerase III (U6) is dependent upon a proximal seq

294 NAs by RNA polymerase II (U1, U2, U4, U5) or RNA polymerase III (U6) is dependent upon a unique, posi

295 est that to terminate transcription in vivo, RNA polymerase III uses a mechanism other than hairpin-d

296 t hairpin siRNAs or siRNAs expressed from an RNA polymerase III vector based on the mouse U6 RNA prom

297 ut the period examined, E2E transcription by RNA polymerase III was found to be at least as efficient

298 , ribosome-EF-Tu complex, 20S proteasome and RNA polymerase III, we illustrate how local sharpening c

299 o provides the first nascentome analysis for RNA polymerase III, which indicates that transcription o

300 Bdp1 subunit of the Brf2-TFIIIB complex, and RNA polymerase III, with negative and positive outcomes