ライフサイエンスコーパス: RNA polymerase I

1 hat form a TFIIF-related subcomplex in yeast RNA polymerase I.

2 that BLM interacts with RPA194, a subunit of RNA polymerase I.

3 the TATA-binding protein in transcription by RNA polymerase I.

4 e of the essential transcription factors for RNA polymerase I.

5 lar mechanisms that control transcription by RNA polymerase I.

6 at the rDNA because of a barrier imposed by RNA polymerase I.

7 segment analogue from a plasmid is driven by RNA polymerase I.

8 sically associated with Fob1 and subunits of RNA polymerase I.

9 not capable of forming a stable complex with RNA polymerase I.

10 out 0.5 microM CX-5461 (CX), an inhibitor of RNA polymerase I.

11 sites (BESs) by virtue of a multifunctional RNA polymerase I.

12 ng by Rrn3 is essential for transcription by RNA polymerase I.

13 o multicopy tandem arrays and transcribed by RNA polymerase I.

14 The optimal temperature for Syn5 RNA polymerase is 24 degrees C, much lower than that for

15 RNA polymerase is a central macromolecular machine contr

16 Bacterial RNA polymerase is a common target for many antibiotics.

17 Transcription by RNA polymerase is a highly dynamic process involving mul

18 Promoter recognition by RNA polymerase is a key point in gene expression and a t

19 HCV RNA polymerase is a key target for the development of di

20 The PB2 subunit of the influenza virus RNA polymerase is a major determinant of viral pathogeni

21 The PB2 subunit of the influenza virus RNA polymerase is a major virulence determinant of influ

22 The vaccinia virus RNA polymerase is a multi-subunit enzyme that contains e

23 RNA polymerase is a ratchet machine that oscillates betw

24 RNA polymerase is a target for numerous regulatory event

25 he primary sigma subunit of Escherichia coli RNA polymerase, is a negatively charged domain that affe

26 Prokaryotic primase, a DNA-dependent RNA polymerase, is a target of interest for the developm

27 tif A that is conserved in all RNA-dependent RNA polymerases, is a key determinant of polymerase fide

28 rRNA transcription requires, in addition to RNA polymerase I, a single DNA-binding factor, transcrip

29 A polymerases: in particular two subunits of RNA polymerase I (A14 and A43) display genetic and bioch

30 ammalian homologues of two subunits of yeast RNA polymerase I, A34.5 and A49, that form a TFIIF-relat

31 Bacterial RNA polymerase is able to initiate transcription with ad

32 aramutation1), which encodes a RNA-dependent RNA polymerase, is absolutely required for establishing

33 s a protein closely related to RNA-dependent RNA polymerases, is absolutely required for paramutation

34 eotide incorporation during transcription by RNA polymerase is accompanied by pyrophosphate formation

35 Incorporation of such compounds in RNA by RNA polymerase is accompanied by release of di- and trip

36 otein that participates in the regulation of RNA polymerase I activity and rRNA synthesis and therefo

37 nd Src can successfully rescue the defective RNA polymerase I activity induced by the loss of kindlin

38 We present evidence that RNA polymerase I activity inhibits the ability of Utp22

39 To fully define the factors that control RNA polymerase I activity, biochemical analyses using pu

40 me biogenesis, which is under the control of RNA polymerase I activity.

41 tream binding factor (UBF) 1, a regulator of RNA polymerase I activity.

42 RNA polymerase II transcription, but not on RNA polymerase I activity.

43 sigma(28) RNA polymerase is an alternative RNA polymerase that has

44 sigma(28) RNA polymerase is an alternative RNA polymerase that has

45 eterotrimeric viral PA/PB1/PB2 RNA-dependent RNA polymerase is an attractive target for a challenging

46 The NS5B RNA-dependent RNA polymerase is an attractive target for the developme

47 In this regard, the viral RNA polymerase is an attractive target that allows the d

48 Transcriptional pausing by RNA polymerase is an underlying event in the regulation

49 in the synthesis of RPs and complements the RNA polymerase I and III systems.

50 s that influence transcription elongation by RNA polymerase I and its regulation.

51 DEXH/D-box protein shown to function in both RNA polymerase I and polymerase II transcript metabolism

52 in Saccharomyces cerevisiae is performed by RNA polymerase I and regulated by changes in growth cond

53 titers in embryonated chicken eggs, between RNA polymerase I and RNA polymerase II transcription uni

54 was to bring together the world's experts on RNA polymerase I and RNA polymerase III to highlight and

55 ly, rDNA silencing required transcription by RNA polymerase I and the direction of spreading was cont

56 l is that Rrn3 functions as a bridge between RNA polymerase I and the transcription factors bound to

57 phosphorylation facilitates transcription by RNA polymerases I and II and has an unanticipated functi

58 f c-Myc target genes that are transcribed by RNA polymerases I and II.

59 ubunits of Arabidopsis thaliana multisubunit RNA polymerases I and III (abbreviated as Pol I and Pol

60 e Ninth International Biennial Conference on RNA Polymerases I and III (the "OddPols") was held on Ju

61 Eighth International Biennial Conference on RNA polymerases I and III (the 'Odd Pols') was held June

62 xpanding the usual topics on the advances in RNA polymerases I and III research to include presentati

63 Expression of RNA polymerases I and III was evaluated by immunohistoch

64 noncoding sequences and genes transcribed by RNA polymerases I and III.

65 min organization does not detectably inhibit RNA polymerases I and III.

66 ich was remedied by the addition of purified RNA polymerase I, and an anti-p31 serum completely block

67 Nevertheless, p31 cosedimented with purified RNA polymerase I, and RNA interferance-mediated silencin

68 Rrn3 interacts with the rpa43 subunit of RNA polymerase I, and treatment with cycloheximide inhib

69 onuclin deficiency in oocytes perturbed both RNA polymerase I- and II-mediated transcription, and ooc

70 High levels of rRNA synthesis by RNA polymerase I are important for cell growth and proli

71 Microscopy studies indicated that RNA polymerase I assembles near its promoter.

72 se Ibeta complex and interacts directly with RNA polymerase I-associated transcription factor RRN3, w

73 The human homologue of yeast Rrn3 is an RNA polymerase I-associated transcription factor that is

74 verexpressed in some cancers, interacts with RNA Polymerase I, associates with active ribosomal RNA g

75 l domain of the alpha subunit (alpha-CTD) of RNA polymerase is at least partially dispensable for Rha

76 nuclease activity of influenza RNA-dependent RNA polymerase is attractive for the development of new

77 the synthesis of rRNA by inactivation of the RNA polymerase I basal transcription factor RRN3/TIF-IA.

78 the fact that the vast majority of sigma(70)-RNA polymerase is bound by 6S RNA during stationary phas

79 romatin containing rRNA genes transcribed by RNA polymerase I but not with genes transcribed by RNA p

80 s inactivated Rrn3 not only dissociates from RNA polymerase I, but is not capable of forming a stable

81 These data reveal that activation of RNA polymerase I by L-Myc and other MYC family proteins

82 observations suggest that treacle might link RNA polymerase I-catalyzed transcription and post-transc

83 (DSB) occurs and either a DNA polymerase or RNA polymerase is coming along, how do we save the train

84 red that Mybbp1a is associated with both the RNA polymerase I complex and the ribosome biogenesis mac

85 us recessive mutations in TAF1A, encoding an RNA polymerase I complex protein, were associated with m

86 , a DNA-binding protein and component of the RNA polymerase I complex regulating RNA synthesis.

87 ous study showed that during optimal growth, RNA polymerase is concentrated into transcription foci o

88 chanism of substrate loading in multisubunit RNA polymerase is crucial for understanding the general

89 uncover a role for topoisomerase IIalpha in RNA polymerase I-directed ribosomal RNA gene transcripti

90 box RNA helicase in the multistep process of RNA polymerase I-directed transcription of the ribosomal

91 plication of the NTD in its interaction with RNA polymerase is discussed.

92 the evolution and function of the organellar RNA polymerases is discussed.

93 sigma(D) RNA polymerase is dispensable for transcription of this

94 Upon the addition of rifampicin, RNA polymerase is distributed among >500 functional prom

95 ectly to the housekeeping holoenzyme form of RNA polymerase (i.e. sigma70-RNA polymerase in E. coli).

96 del that Spt4/5 may contribute to pausing of RNA polymerase I early during transcription elongation b

97 Thus, RNA polymerase I, elongation factors, and rRNA sequence

98 e transcription fidelity by Escherichia coli RNA polymerase: (i) enhanced suppression of nucleotide m

99 I find that RNA polymerase is error-prone, and these errors can resu

100 We argue that translocation of RNA polymerase is essential and that translocation of th

101 osition DksA in the secondary channel of the RNA polymerase is essential for the resistance of Salmon

102 by the nuclear-encoded mitochondrial poly(A) RNA polymerase, is essential for maintaining mitochondri

103 ation of transcription mediated by all three RNA polymerases is essential for c-Myc-driven proliferat

104 in the number of colocalizing telomeric and RNA polymerase I foci in the nucleus.

105 c subunit RPB6z and tandem affinity purified RNA polymerase I from crude extract.

106 Promoter escape efficiency of E. coli RNA polymerase is guided by both the core promoter and t

107 The initiation of transcription by RNA polymerase I has been implicated as a regulatory tar

108 The elongation phase of transcription by RNA polymerase is highly regulated and modulated.

109 This core consists of the RNA polymerase (I, II, or III), the TATA box-binding pro

110 r with his presentation "Conservation of the RNA polymerase I, II and III transcription initiation ma

111 Human nuclei contain three RNA polymerases (I, II and III) that transcribe differen

112 DNA locus containing transcription units of RNA polymerases I, II or III or an autonomous replicatio

113 did high levels of actinomycin D (to inhibit RNA polymerases I, II, and III) or alpha-amanitin (to in

114 s found in basal transcription machinery for RNA polymerases I, II, and III, pol II transcriptional e

115 ion in the shared Rpb6 subunit, assembled in RNA polymerases I, II, and III, that illuminated a new r

116 In addition to RNA polymerases I, II, and III, the essential RNA polyme

117 haebacterial RNA polymerases, the eukaryotic RNA polymerases I, II, and III, the nuclear-cytoplasmic

118 tic genomes is carried out by three distinct RNA polymerases I, II, and III, whereby each polymerase

119 in addition to the well-known DNA-dependent RNA polymerases I, II, and III.

120 ribosomal biogenesis through upregulation of RNA polymerases I-, II-, and III-dependent transcription

121 level, through the coordinate regulation of RNA polymerases I-III and downstream in the coordinate r

122 Anti-RNA polymerase I/III (anti-RNAP I/III) antibodies are cl

123 ies against topoisomerase I, centromere, and RNA polymerase I/III by immunoprecipitation and/or enzym

124 antly between groups (-1.2 years in the anti-RNA polymerase I/III group, +13.4 years in the anti-topo

125 Six patients tested positive for anti-RNA polymerase I/III, 5 for anti-topoisomerase I, and 8

126 d scleroderma in patients with antibodies to RNA polymerase I/III, which is distinct from scleroderma

127 able tumors from patients with antibodies to RNA polymerase I/III.

128 he possibility that cross-regulation between RNA polymerases is important in maintaining normal cell

129 The active VSG is transcribed by RNA polymerase I in one of approximately 15 telomeric VS

130 initiated research on rRNA transcription by RNA polymerase I in the yeast Saccharomyces cerevisiae.

131 We then used an RNA polymerase I inhibitor to target rRNA synthesis in a

132 of RNA-DNA hybrid sequence by multi-subunit RNA polymerases is involved in transcription regulation

133 Transcription of ribosomal DNA by RNA polymerase I is a central feature of eukaryotic ribo

134 n that transcription of the ribosomal DNA by RNA polymerase I is a major target for cellular regulati

135 e data suggest that transcription of rRNA by RNA polymerase I is linked to rRNA processing and matura

136 ption and that its ability to associate with RNA polymerase I is lost upon transcription.

137 T7 RNA polymerase is known to induce bending of its promote

138 ition, overexpression of the protein reduces RNA polymerase I loading on endogenous rRNA genes as rev

139 We show that components of the RNA polymerase I machinery are brought to ribosomal gene

140 absence of CRP, suggesting that contact with RNA polymerase is maintained throughout the transcriptio

141 In bacteria, promoter identification by RNA polymerase is mediated by a dissociable sigma factor

142 R2rp1, controls DNA repair and repression of RNA polymerase I-mediated expression immediately adjacen

143 nd to the nucleolus of the cell, the site of RNA polymerase I-mediated ribosomal RNA (rRNA) transcrip

144 studies, the signaling pathways that control RNA polymerase I-mediated rRNA production are not well u

145 RNA polymerase I-mediated rRNA production is a key deter

146 ociation with RNA polymerase I to facilitate RNA polymerase I-mediated rRNA transcription.

147 We report that nucleolar BLM facilitates RNA polymerase I-mediated rRNA transcription.

148 e of BLM nucleolar localization upon ongoing RNA polymerase I-mediated rRNA transcription.

149 I, and an anti-p31 serum completely blocked RNA polymerase I-mediated transcription.

150 and PAF53 copurify with that fraction of the RNA polymerase I molecules that can function in transcri

151 Syn5 RNA polymerase is more efficient in utilizing low concen

152 nted that the binding of Fin and sigma(F) to RNA polymerase is mutually exclusive.

153 nt mutation in the second largest subunit of RNA polymerase I near the active center of the enzyme th

154 The Rc alpha Ec beta beta' RNA polymerase is not activated by RcNtrC.

155 at the PB2 627 domain of the influenza virus RNA polymerase is not involved in core catalytic functio

156 We show that RNA polymerase is not trapped at repressed promoters.

157 ed by the single subunit viral RNA-dependent RNA polymerases is not yet understood.

158 RNA polymerase I occupancy of the genes remains normal,

159 of both promoter-proximal RNA abundance and RNA polymerase I occupancy.

160 The influence of temperature on RNA polymerase is of particular interest because its tra

161 lpha subunit (alpha CTD) of Escherichia coli RNA polymerase is often involved in transcriptional regu

162 contrast to mRNAs, rRNAs are transcribed by RNA polymerase I or III and are not believed to be polya

163 ion in nucleotide levels or the depletion of RNA polymerase I or III subunits generates a cell cycle

164 ted that the phosphorylation of either yeast RNA polymerase I or mammalian Rrn3 regulates the formati

165 temporally coincides with the repression of RNA polymerase I (Pol I) activity.

166 rRNA, but instead leads to an inhibition of RNA Polymerase I (Pol I) activity.

167 ar termination of transcription catalyzed by RNA polymerase I (pol I) and arrest of replication forks

168 Although rRNA transcriptional control by RNA polymerase I (Pol I) and associated factors is well

169 Notably, RNA polymerase I (Pol I) and Pol II recover from shallow

170 e rRNA genes (rDNA), where it interacts with RNA polymerase I (Pol I) as well as with histones.

171 Transcription initiation by RNA Polymerase I (Pol I) depends on the Core Factor (CF)

172 sted that after each round of transcription, RNA polymerase I (Pol I) dissociates into subunits that

173 ological change is accompanied by release of RNA polymerase I (Pol I) from the nucleolus and inhibiti

174 WI/SNF also plays a role in transcription by RNA polymerase I (Pol I) in Saccharomyces cerevisiae.

175 FA), which is essential for transcription by RNA polymerase I (Pol I) in the parasite Trypanosoma bru

176 hosphatase activity of Cdc14 is required for RNA polymerase I (Pol I) inhibition in vitro and in vivo

177 RNA polymerase I (Pol I) is a dedicated polymerase that

178 roliferation; thus, transcription of rRNA by RNA polymerase I (Pol I) is an important target for the

179 Ribosomal RNA gene transcription by RNA polymerase I (Pol I) is the driving force behind rib

180 Here, we identify a Drosophila RNA polymerase I (Pol I) regulatory complex composed of

181 isiae's Upstream Activating Factor (UAF), an RNA polymerase I (pol I) specific transcription stimulat

182 somal RNA (rRNA) is transcribed from rDNA by RNA polymerase I (Pol I) to produce the 45S precursor of

183 ribosomal RNA (rRNA) synthesis by tethering RNA polymerase I (Pol I) to the rDNA promoter.

184 genes (TCOF1, POLR1C and POLR1D) involved in RNA polymerase I (Pol I) transcription account for more

185 Regulation of RNA polymerase I (Pol I) transcription is critical for c

186 a nucleolar protein that associates with the RNA polymerase I (Pol I) transcription machinery to supp

187 oximal unique sequence located downstream of RNA polymerase I (Pol I) transcription, but fails to ent

188 tudy reveals that the selective inhibitor of RNA polymerase I (Pol I) transcription, CX-5461, effecti

189 NA genes, and potently and rapidly represses RNA polymerase I (Pol I) transcription.

190 iption of the large ribosomal RNA repeats by RNA polymerase I (pol I) within the nucleolus.

191 the rDNA promoter through interactions with RNA polymerase I (Pol I), and to a pair of DNA replicati

192 rRNA transcription, catalyzed by RNA polymerase I (Pol I), plays a critical role in ribos

193 laboratory demonstrated the critical role of RNA polymerase I (Pol I)-associated factor PAF53 in mamm

194 We have established a human RNA polymerase I (pol I)-driven influenza virus reverse

195 ucleolar DEAD/DEAH-box helicases involved in RNA polymerase I (Pol I)-mediated transcriptional activi

196 d UBF) is thought to function exclusively in RNA polymerase I (Pol I)-specific transcription of the r

197 To study the effect of CpG methylation on RNA polymerase I (pol I)-transcribed rRNA genes, we cons

198 can sleeping sickness, TbISWI down-regulates RNA polymerase I (Pol I)-transcribed variant surface gly

199 rowth requires synthesis of ribosomal RNA by RNA polymerase I (Pol I).

200 ribed from the ribosomal DNA (rDNA) genes by RNA polymerase I (Pol I).

201 is of rRNA (building blocks of ribosomes) by RNA Polymerase I (Pol I).

202 ion of ribosomal DNA (rDNA) transcription by RNA polymerase I (Pol I).

203 role for Mot1 in regulating transcription by RNA polymerase I (Pol I).

204 complex positively affects transcription by RNA polymerase I (Pol I).

205 n sites (ESs) in a monoallelic fashion using RNA polymerase I (Pol I).

206 Transcription by RNA polymerase I (Pol-I) is the main driving force behin

207 These bloodstream parasites use RNA polymerase-I (pol-I) to transcribe just one telomeri

208 luciferase reporter RNA driven by the canine RNA polymerase I promoter.

209 The RNA polymerase I promoters of reactivated T. porrifolius

210 contrast, nascent pre-mRNA synthesized by T7 RNA polymerase is quantitatively assembled into the nons

211 In contrast, RNA polymerase is recruited to the melAB promoter only i

212 ation, functioning in core promoter binding, RNA polymerase I recruitment, and UBF stabilization and

213 trate that the association of SigH with core RNA polymerase is reduced under these conditions.

214 Although UBF1 has been shown to activate RNA polymerase I-regulated genes, the function of UBF2 h

215 th RNA polymerase II (with beta-catenin) and RNA polymerase I-regulated promoters suggest an explanat

216 A levels were measured along with markers of RNA polymerase I regulatory factors and regulators of pr

217 also displayed a down-regulation of several RNA polymerase I- related factors, consistent with termi

218 during mitotic growth and G0 entry, and (ii) RNA polymerase I release prevents heterochromatin format

219 longation into the gene body is overcome and RNA polymerase is released to produce osmY mRNA.

220 Ribosomal RNA transcription mediated by RNA polymerase I represents the rate-limiting step in ri

221 The dissociable sigma subunit of bacterial RNA polymerase is required for the promoter-specific ini

222 Its interaction with the alpha-subunit of RNA polymerase is required for transcriptional induction

223 terminal domain (ATD) of yeast mitochondrial RNA polymerase is required to couple transcription to tr

224 The RNA-dependent RNA polymerase is responsible for genome replication of

225 The sigma subunit of procaryotic RNA polymerases is responsible for specific promoter rec

226 ntly related member of the T7-like family of RNA polymerases, is responsible for transcription of the

227 e demonstrate a link between the dynamics of RNA polymerase I (RNA Pol I) assembly and transcriptiona

228 regulate transcription of the large rRNAs by RNA polymerase I (RNA Pol I) was investigated.

229 R-loops accumulate in nucleoli during RNA polymerase I (RNAP I) transcription.

230 stronically transcribed by a multifunctional RNA polymerase I (RNAPI) from a short promoter that is l

231 Here we show that the stability of RNA polymerase I (RNAPI) is tightly coupled to zinc avai

232 or mammalian Rrn3 regulates the formation of RNA polymerase I.Rrn3 complexes that can interact with t

233 f the polymerase I and SL1 complexes and the RNA polymerase I-specific transcription initiation facto

234 the DFC of the nucleolus, as defined by the RNA polymerase I-specific upstream binding factor and th

235 excision repair (NER) that is triggered when RNA polymerase is stalled by DNA damage.

236 tailed pattern of the blockage suggests that RNA polymerase is sterically hindered by H-DNA and has d

237 hown to occur cotranscriptionally, while the RNA polymerase is still actively engaged with the chroma

238 The sigma subunit of bacterial RNA polymerase is strictly required for promoter recogni

239 s helicases, DNA polymerase/exonuclease, and RNA polymerase is studied in detail.

240 etween the locus encoding the second largest RNA polymerase I subunit and a lysine tRNA gene [i.e., R

241 mplicated two genes, one of which encodes an RNA polymerase I subunit.

242 cleolar disassembly started with the loss of RNA polymerase I subunits from the fibrillar centers.

243 hSpagh also bound the free RPA194 subunit of RNA polymerase I, suggesting a general role in assemblin

244 this novel functional component of T. brucei RNA polymerase I TbRPA31.

245 only known eukaryote with a multifunctional RNA polymerase I that, in addition to ribosomal genes, t

246 Bacteriophage T7 RNA polymerase is the best-characterized member of a wid

247 The twisting of DNA due to the movement of RNA polymerases is the basis of numerous classic experim

248 Gene transcription by the enzyme RNA polymerase is tightly regulated.

249 odulates rDNA structures in association with RNA polymerase I to facilitate RNA polymerase I-mediated

250 The rDNA genes are transcribed by RNA polymerase I to make structural RNAs for ribosomes.

251 TIF-IA), a GTP-binding protein that recruits RNA polymerase I to the ribosomal DNA promoter.

252 important function of nucleolin is to permit RNA polymerase I to transcribe nucleolar chromatin.

253 ved in the transcriptional regulation of the RNA polymerase I transcribed variant surface glycoprotei

254 Thus, transcription-coupled repair occurs in RNA polymerase I-transcribed genes in yeast.

255 h a variety of cellular processes, including RNA polymerase I transcription and cell cycle progressio

256 reates a chromatin environment permissive to RNA polymerase I transcription and nascent rRNA processi

257 localization of this complex requires active RNA polymerase I transcription and the small ubiquitin-l

258 a reverse genetics system in which the eight RNA polymerase I transcription cassettes for viral RNA s

259 olus and normally inhibit progression of the RNA polymerase I transcription complex.

260 RNA polymerase I transcription constraints lead to persi

261 miniscent of that proposed for the mammalian RNA polymerase I transcription factor UBF.

262 how that nucleolar SmgGDS interacts with the RNA polymerase I transcription factor upstream binding f

263 this location and colocalizes with UBF, the RNA polymerase I transcription factor.

264 n initiation factor IA (TIF-IA), a conserved RNA polymerase I transcription factor.

265 we evaluate the exchange kinetics of several RNA polymerase I transcription factors and nucleosome co

266 and second, coevolution of IGS sequence with RNA polymerase I transcription factors may lead to speci

267 All have been reported to stimulate RNA polymerase I transcription from an adjacent gene pro

268 ransduction, while a just-published study of RNA polymerase I transcription has implicated polymeric

269 RNA polymerase I transcription in human cells requires S

270 than yeast-derived core factor in assays for RNA polymerase I transcription in vitro.

271 ng a putative Rrn11p homolog, SpRrn11h, bear RNA polymerase I transcription initiation factor activit

272 Knowledge of the role of components of the RNA polymerase I transcription machinery is paramount to

273 O1 has been implicated as a component of the RNA polymerase I transcription machinery.

274 ase I, we demonstrated that nucleolin allows RNA polymerase I transcription of chromatin templates in

275 related to nucleolar chromatin structure and RNA polymerase I transcription regulation, rRNA processi

276 cleophosmin (NPM/B23), RNA helicase DDX5 and RNA polymerase I transcription termination factor (TTF-I

277 pose that topoisomerase IIalpha functions in RNA polymerase I transcription to produce topological ch

278 The coordination of RNA polymerase I transcription with pre-rRNA processing,

279 In mammalian RNA polymerase I transcription, SL1, an assembly of TBP

280 er (IGS) play an important role in enhancing RNA polymerase I transcription.

281 erference resulted in specific inhibition of RNA polymerase I transcription.

282 onent of the nucleolus dependently on active RNA polymerase I transcription.

283 role of integrin signaling in regulation of RNA polymerase I transcriptional activity and shed light

284 re we provide original evidence showing that RNA polymerase I transcriptional activity is tightly con

285 r-DNA complexes that precede the assembly of RNA polymerases is unclear.

286 inhibits a subset of metalloenzymes and that RNA polymerase is unlikely to be the primary target.

287 ion of the same set of genes by two types of RNA polymerases is unprecedented for a bacteriophage.

288 RpoS, the sigma S subunit of RNA polymerase, is vital during the growth and survival

289 In contrast, RNA polymerase I was marginally affected.

290 cleolin localizes primarily to nucleoli with RNA polymerase I, we demonstrated that nucleolin allows

291 hat promoter recognition by this alternative RNA polymerase is well conserved among bacteria.

292 site Trypanosoma brucei is a multifunctional RNA polymerase I which, in addition to synthesizing rRNA

293 in a complex that regulates the activity of RNA polymerase I, which controls the rate of ribosomal R

294 NA synthesis by promoting the association of RNA polymerase I with rDNA loci.

295 tion of a TCOF1-NOLC1 platform that connects RNA polymerase I with ribosome modification enzymes and

296 genes (PAGs), these being co-transcribed by RNA polymerase I with the procyclin surface antigen gene

297 ion assays, we found that the association of RNA polymerase I with the promoter and the coding region

298 NuMA coimmunoprecipitates with RNA polymerase I, with ribosomal proteins RPL26 and RPL2

299 aptamers were transcribed at high levels by RNA polymerase I without any additional promoter being i

300 Since Nac activation via sigma(S) -RNA polymerase is without precedent, transcription with