ライフサイエンスコーパス: TATA-binding protein

1 nd the eukaryotic transcriptional regulator, TATA binding protein.

2 e promoters to facilitate recruitment of the TATA-binding protein.

3 involves recruitment of the SAGA complex and TATA-binding protein.

4 mounts of these two purified factors but not TATA-binding protein.

5 nhibited the ability of IE2/IEP86 to bind to TATA-binding protein.

6 r, chromatin remodeling SWI/SNF complex, and TATA-binding protein.

7 s initiated with at least partially TAF-free TATA-binding protein.

8 erization interface of the full-length yeast TATA-binding protein.

9 and uracil DNA glycosylase, as well as with TATA-binding protein.

10 in the presence of TFIIIB subunits Brf1 and TATA-binding protein.

11 antibodies to dsDNA, histones H1 and H4, and TATA-binding protein.

12 basal transcription that interacts with the TATA-binding protein.

13 ained gene expression and the recruitment of TATA-binding protein.

14 allele of MOT1, which encodes a regulator of TATA-binding protein.

15 and a unique T-rich module interacting with TATA-binding proteins.

16 rase II-dependent transcription involves the TATA binding protein, a component of the basal transcrip

17 ugh mutation of RTF1 suppresses mutations in TATA-binding protein, alters transcriptional start sites

18 the human TAF1L protein can bind directly to TATA-binding protein, an essential component of TFIID.

19 ecting away from its extended interface with TATA-binding protein anchoring Bdp1 binding.

20 riptional repression and displacement of the TATA binding protein and RNA polymerase II (RNA Pol II).

21 Like TATA binding protein and RNA polymerase II (RNAPII), Spn

22 pical general transcription factors, such as TATA binding protein and TFII B, have not yet been ident

23 f the ANK-1 gene and disrupts the binding of TATA binding protein and TFIID, components of the preini

24 recruitment of FoxA1, RNA polymerase II and TATA binding protein and their subsequent interactions a

25 ract with the general transcription factors, TATA binding protein and transcription factor IIB, which

26 IID sets the mRNA start site and consists of TATA-binding protein and associated factors (TAF(II)s),

27 complex, disrupting the association between TATA-binding protein and Brf1.

28 U6-7, U6-8 and U6-9) since they are bound by TATA-binding protein and enriched in acetylated histone

29 lso necessary for the optimal recruitment of TATA-binding protein and Pol II to the GAL1 promoter.

30 TATA-binding protein and TAF1.TAF2 heterodimers are the

31 erivatives having weakened interactions with TATA-binding protein and TFIIB exhibit a strong dependen

32 that are homologues of the RNA polymerase II TATA-binding protein and TFIIB.

33 ruitment of the essential initiation factors TATA-binding protein and transcription factor B, respect

34 only M. thermoautotrophicum RNA polymerase, TATA-binding protein and transcription factor B.

35 gly, slipping at this juncture is induced by TATA-binding protein and transcription factor IIB and re

36 PIAS1-KLF5 complex was co-localized with the TATA-binding protein and was enriched in RNA polymerase

37 gene that harbors putative binding sites for TATA-binding proteins and the transcriptional activator

38 IB, a complex formed by Brf1 (or Brf2), TBP (TATA-binding protein), and Bdp1.

39 to reduce recruitment of SAGA, Srb mediator, TATA binding protein, and RNA polymerase II to the ARG1

40 ubunits Spt8p and Spt3p, which interact with TATA-binding protein, and for a gene-specific transcript

41 d and mismatched sequences, the detection of TATA-binding protein, and sequence-selective DNA hybridi

42 d promoter association of RNA polymerase II, TATA-binding protein, and TFIIB of the general transcrip

43 systems (containing only RNA polymerase II, TATA-binding protein, and TFIIB) and in a complex system

44 TAF9 is a TATA-binding protein associated factor (TAF) conserved f

45 11 and the histone acetyltransferase TAF1, a TATA-binding protein Associated Factor (TAF) of the RNA

46 -binding factor Zeste and with numerous TBP (TATA-binding-protein)-associated factors that are compon

47 A specific TATA binding protein-associated factor (TAF), dTAF(II)11

48 We find that EKLF interacts with TATA binding protein-associated factor 9 (TAF9), which l

49 istone acetyltransferase (HAT) domain of the TATA binding protein-associated factor TAF1 induces ts13

50 eTAFH domain, which is homologous to several TATA binding protein-associated factors (TAFs) and inter

51 TATA binding protein-associated factors 1 and 7 (TAF1 an

52 e TFIID complex through interaction with its TATA-binding protein-associated factor (Taf) subunits Ta

53 TATA-binding protein-associated factor 1 (TAF1) is an es

54 A polymerase II binding, in association with TATA-binding protein-associated factor 1, was increased;

55 e we identified the missing factor of RLC as TATA-binding protein-associated factor 11 (TAF11) by gen

56 t by a novel TRF3/TAF3 (TBP-related factor 3/TATA-binding protein-associated factor 3) complex.

57 One gene identified by the method encodes TATA-binding protein-associated factor 7 (TAF7), which f

58 PU.1 gene transcription via deacetylation of TATA-binding protein-associated factor 9 (TAF9), a compo

59 e carboxyl halves of the VP16 AD, VP16C, and TATA-binding protein-associated factor 9 (TAF9).

60 vo interactions with other Sp1 molecules and TATA-binding protein-associated factor II 110.

61 gulate Sp1-mediated transcription (i.e., the TATA-binding protein-associated factor TAF(II)250 and cy

62 To investigate how the TAF (TATA-binding protein-associated factor) subunits of TFII

63 e N-terminal 163 amino acids of Homo sapiens TATA-binding protein-associated factor-1 (hsTAF1), causi

64 uence changes in TAF1, the gene that encodes TATA-binding protein-associated factor-1, which appear t

65 r (TF) IID- and TFTC/SAGA-related complexes, TATA-binding protein-associated factors (TAF(II)s) are i

66 gene encoding TAF(II)250, the largest of the TATA-binding protein-associated factors (TAFs) in TFIID.

67 on and action of testis-specific homologs of TATA-binding protein-associated factors (tTAFs).

68 ranscription factors such as Mot1p and TAFs (TATA-binding protein-associated factors).

69 ins, the Gcn5 acetyltransferase, a subset of TATA-binding-protein-associated factors (TAF(II)s), and

70 However, its ability to complex with TATA-binding protein at a model promoter is equivalent t

71 not likely to be due to a difference in TBP (TATA-binding protein) binding efficiency because protein

72 esting that targeted acetylation occurs when TATA-binding protein binds to the TATA box or at a later

73 moter region, and we showed that p53 and the TATA binding protein bound to the bcl-2 TATA sequence.

74 Furthermore, recruitment of the TFIID/TATA-binding protein complex and the large subunit of RN

75 In vitro, Mot1 can disrupt TATA-binding protein-DNA complexes in an ATP-dependent r

76 y Mot1, consistent with Mot1's ATP-dependent TATA-binding protein-DNA dissociating activity.

77 s that interact with each other and with the TATA binding protein/DNA complex.

78 fused dTAF(II)110 (amino acid 1-308) to the TATA binding protein domain of the yeast scaffolding TAF

79 lex with heat shock transcription factor and TATA-binding protein during laccase induction.

80 4, C/ebp-homology protein (Chop), Pol II and TATA-binding protein exhibited enhanced recruitment to t

81 hnRNP K binds the TATA-binding protein, explaining how the 4EBE might repl

82 ent SAGA-like complexes (PCAF complex, TFTC [TATA-binding-protein-free TAF(II)-containing complex], a

83 The amino-terminal domain of yeast TATA-binding protein has been proposed to play a crucial

84 contrast, association of RNA polymerase II, TATA-binding protein, histone acetyltransferases (p300 a

85 reduced promoter association of Mediator and TATA-binding protein in a Pol II (rpb1-1) mutant, indica

86 oIN)-EGFP fusion protein associates with the TATA-binding protein in cells.

87 ween two opposing models for the role of the TATA-binding protein in transcription by RNA polymerase

88 0 also mediates an association with TIP120B (TATA-binding protein-interacting protein 120B), a putati

89 nhibitory function involving a nonproductive TATA-binding protein interaction mediated by the Spt3 an

90 s undergoing oncogenic transformation by the TATA-binding protein or c-Myc display enhanced RNA pol I

91 The TATA binding protein, p53, histone deacetylase-1 and mSi

92 activating protein complex (SNAP(c)) and the TATA-binding protein related factor 4 (TRF4) have been i

93 Recently, TATA-binding protein-related factor 2 (TRF2) rather than

94 The discovery of TATA-binding protein-related factors (TRFs) has suggeste

95 s required for general transcription such as TATA-binding protein, RNA polymerase II, and TFIIH are n

96 It also showed that a TATA-binding protein specifically bound to the TATA box

97 resentatives of the SAGA pathway include the TATA binding protein, Spt3, and Mot1.

98 RF2a and TBP (TATA-binding protein) synergistically activate transcrip

99 esentatives of the TFIID pathway include the TATA binding protein, TAF1, and Bdf1.

100 p68/p72 proteins impaired recruitment of the TATA binding protein TBP; RNA polymerase II; and the cat

101 ates RNA polymerase II transcription via the TATA-binding protein TBP and that Nhp6 functions in the

102 TFIIIB, an essential complex comprising the TATA-binding protein TBP and the TAF subunits Brf1 and B

103 uence-specific transcription factors and the TATA-binding protein TBP.

104 TFIID is comprised of the TATA binding protein (TBP) and 12-15 TBP-associated fact

105 IID as a 15-subunit complex comprised of the TATA binding protein (TBP) and 14 distinct TBP-associate

106 ruitment of RNA polymerase II (polII) or the TATA binding protein (TBP) and acetylations of histones

107 TFIID is composed of TATA binding protein (TBP) and approximately a dozen TBP

108 mbinant full-length Saccharomyces cerevisiae TATA binding protein (TBP) and its isolated C-terminal c

109 Prior to induction, TNF exhibited pre-bound TATA Binding Protein (TBP) and paused RNA Polymerase II

110 ive histone marks, along with the binding of TATA binding protein (TBP) and POLR2E to the CDKN1A prom

111 Srb mediator, which stimulate recruitment of TATA binding protein (TBP) and polymerase II to target p

112 these coactivators reduce the recruitment of TATA binding protein (TBP) and RNA polymerase II (Pol II

113 At promoters, ATX1 is required for TATA binding protein (TBP) and RNA Polymerase II (Pol II

114 ed2Delta mutation impairs the recruitment of TATA binding protein (TBP) and RNA polymerase II to the

115 IA interacts with TFIID via association with TATA binding protein (TBP) and TBP-associated factor 11

116 IA is known to stabilize the binding of both TATA binding protein (TBP) and TFIID to the TATA box of

117 minal domain of the Saccharomyces cerevisiae TATA binding protein (TBP) and the single tryptophan loc

118 TATA binding protein (TBP) and transcription factor IIB

119 plemented in vitro by additional recombinant TATA binding protein (TBP) at only the TATA-containing p

120 The TATA binding protein (TBP) binds to TATA boxes in core p

121 IP49a, previously shown to interact with the TATA binding protein (TBP) complex and to modulate c-myc

122 munoprecipitation assay, we demonstrate that TATA binding protein (TBP) does not detectably interact

123 sidues in monomeric Saccharomyces cerevisiae TATA binding protein (TBP) free in solution and in the T

124 ed ATPase that uses ATP hydrolysis to remove TATA binding protein (TBP) from DNA.

125 The roles of three TATA binding protein (TBP) homologs (TBP1, TBP2, and TBP

126 substantially reduced the level of cellular TATA binding protein (TBP) in both normal human fibrobla

127 eceptor-ligand interactions, and apply it to TATA binding protein (TBP) interactions with oligonucleo

128 The TATA binding protein (TBP) is a central component of the

129 TATA binding protein (TBP) is a central transcription fa

130 TATA binding protein (TBP) is a key component of the euk

131 The TATA binding protein (TBP) is an essential component of

132 his period, the general transcription factor TATA binding protein (TBP) is replaced by its paralogue,

133 The TATA binding protein (TBP) is required for the expressio

134 The human TATA binding protein (TBP) locus consists of a functiona

135 e structures and dynamics of the full-length TATA binding protein (TBP) of Saccharomyces cerevisiae a

136 y caused by combining an spt16 mutation with TATA binding protein (TBP) or TFIIA defects.

137 TATA binding protein (TBP) plays a central role in trans

138 We confirm the roles of Mediator and SAGA in TATA binding protein (TBP) recruitment and demonstrate t

139 The recruitment of TATA binding protein (TBP) to gene promoters is a critic

140 Importantly, among the PIC components, Tata Binding Protein (TBP) was the most resistant to evi

141 formation of sequence-specific complexes of TATA binding protein (TBP) with the minor groove of DNA

142 TATA binding protein (TBP), a universal transcription fa

143 oans have evolved multiple paralogues of the TATA binding protein (TBP), adding another tunable level

144 wed that reduced intracellular levels of the TATA binding protein (TBP), brought about by tbp heteroz

145 stomatitis viruses, both of which target the TATA binding protein (TBP), RVFV appears to target the b

146 ing that Y544 is critical for binding to the TATA binding protein (TBP), suggesting that this interac

147 ing a series of heteroduplex HIS4 promoters, TATA binding protein (TBP), TFIIB, and Pol II.

148 on is associated with decreased occupancy by TATA binding protein (TBP), the Swi/Snf nucleosome-remod

149 a protein-protein contact between TFIIB and TATA binding protein (TBP), while the other (K272I) disr

150 chicken DT40 cells containing a conditional TATA binding protein (TBP)-associated factor 9 allele (T

151 rgently transcribed promoters from the human TATA binding protein (TBP)-proteasome component-B1 (PSMB

152 machinery through direct recruitment of the TATA binding protein (TBP).

153 yet nearly all Pol II transcription requires TATA binding protein (TBP).

154 f photoswitching in previous FRAP studies of TATA binding proteins (TBP) and also as a tool to minimi

155 the physical half-life or residence time for TATA-binding protein (TBP) across the yeast genome from

156 TATA-binding protein (TBP) affinity alone does not deter

157 IID is a megadalton-sized complex comprising TATA-binding protein (TBP) and 13 TBP-associated factors

158 TFIID comprises the TATA-binding protein (TBP) and 13 TBP-associated factors

159 n-sized multiprotein complex composed of the TATA-binding protein (TBP) and 13 TBP-associated factors

160 on factor TFIID is a multisubunit complex of TATA-binding protein (TBP) and 14 distinct TBP-associate

161 ranscription factor TFIID is composed of the TATA-binding protein (TBP) and 14 TBP-associated factors

162 ucleated by TFIID, a complex composed of the TATA-binding protein (TBP) and a series of TBP-associate

163 The TATA-binding protein (TBP) and a transcription factor (T

164 with two other Pol I initiation factors, the TATA-binding protein (TBP) and core factor (CF).

165 effects of TFIIA on the interaction between TATA-binding protein (TBP) and DNA.

166 TIF-IB is a multimeric protein that contains TATA-binding protein (TBP) and four TBP-associated facto

167 50, is specific for these promoters, whereas TATA-binding protein (TBP) and hB" are required for pol

168 tive acting general factor that contacts the TATA-binding protein (TBP) and mediates an activator-ind

169 histone fold module that interacts with the TATA-binding protein (TBP) and negatively regulates tran

170 ake stable protein-protein interactions with TATA-binding protein (TBP) and place it on the promoter-

171 charomyces cerevisiae protein that binds the TATA-binding protein (TBP) and removes TBP from DNA usin

172 ents of the transcription machinery, such as TATA-binding protein (TBP) and RNA polymerase II (RNAPII

173 Human TFIID contains the TATA-binding protein (TBP) and several TBP-associated fa

174 uman transcription factor TFIID contains the TATA-binding protein (TBP) and several TBP-associated fa

175 s did not enhance E2 responsiveness, whereas TATA-binding protein (TBP) and SNURF cooperatively coact

176 The latter's TATA-binding protein (TBP) and TAFs photocross-link to t

177 The TFIID complex is composed of the TATA-binding protein (TBP) and TBP-associated factors (T

178 TFIID-a complex of TATA-binding protein (TBP) and TBP-associated factors (T

179 TFIID, a multiprotein complex comprising the TATA-binding protein (TBP) and TBP-associated factors (T

180 onent BRG-1, and basal transcription factors TATA-binding protein (TBP) and TFIIB, as well as hyperac

181 ilization and exhibited defective binding of TATA-binding protein (TBP) and TFIID complex formation.

182 ll as two general transcription factors, the TATA-binding protein (TBP) and the eukaryotic TFIIB orth

183 he archaeal transcription initiation factors TATA-binding protein (TBP) and transcription factor B (T

184 In srb5(-) cells, recruitment of TATA-binding protein (TBP) and transcription factor IIB

185 inery recognizing the core promoter includes TATA-binding protein (TBP) and two TBP-related factors.

186 TFIIA and TATA-binding protein (TBP) associate directly at the TAT

187 transcription factor, TFIID, consists of the TATA-binding protein (TBP) associated with a series of T

188 studies have implicated Nhp6 in facilitating TATA-binding protein (TBP) binding to some Pol II promot

189 in of replication led us to hypothesize that TATA-binding protein (TBP) could affect HPV replication.

190 nscriptional regulator in vivo by modulating TATA-binding protein (TBP) DNA-binding activity.

191 nsferase) complex facilitates the binding of TATA-binding protein (TBP) during transcriptional activa

192 Recently, it was reported that TATA-binding protein (TBP) enhances (6-4) photoproduct f

193 d essential Swi2/Snf2 ATPase that can remove TATA-binding protein (TBP) from DNA using ATP hydrolysis

194 gulator that uses ATP hydrolysis to displace TATA-binding protein (TBP) from DNA.

195 Little is known about TATA-binding protein (TBP) functions after recruitment t

196 Despite the central role of TATA-binding protein (TBP) in transcription, changes in

197 with full-length or the C-terminal domain of TATA-binding protein (TBP) in vitro.

198 The TATA-binding protein (TBP) is a critical general transcr

199 The TATA-binding protein (TBP) is a general factor that is i

200 The TATA-binding protein (TBP) is a key component of the arc

201 TATA-binding protein (TBP) is a key general transcriptio

202 TATA box recognition by TATA-binding protein (TBP) is a key step in transcriptio

203 The TATA-binding protein (TBP) is critical for transcription

204 TATA-binding protein (TBP) is essential for eukaryotic g

205 Surprisingly, giardial TATA-binding protein (TBP) is highly divergent with resp

206 eraction between the SAGA component Spt3 and TATA-binding protein (TBP) is important for TBP binding

207 The TATA-binding protein (TBP) is involved in all nuclear tr

208 The TATA-binding protein (TBP) is one target for transcripti

209 Recruitment of TATA-binding protein (TBP) is severely compromised in th

210 The TATA-binding protein (TBP) nucleates the assembly and de

211 TATA-binding protein (TBP) nucleates the assembly of the

212 increased Pol II density, transcription, and TATA-binding protein (TBP) occupancy in the 3' portion o

213 The TATA-binding protein (TBP) plays a central role in assem

214 The TATA-binding protein (TBP) plays a crucial role in cellu

215 ngly, we found that all or nearly all of the TATA-binding protein (TBP) population is highly mobile i

216 The TATA-binding protein (TBP) recognizes the TATA box eleme

217 Although the TATA-binding protein (TBP) subunit of TFIID is necessary

218 Intriguingly, the unusual trypanosome TATA-binding protein (TBP) tightly associates with tSNAP

219 a transcriptional repressor, it binds to the TATA-binding protein (TBP) to form the HMG-1/TBP/TATA co

220 Binding of the TATA-binding protein (TBP) to promoter DNA bearing the T

221 h TFIID and SAGA, two complexes that deliver TATA-binding protein (TBP) to promoters.

222 t that these factors regulate binding of the TATA-binding protein (TBP) to the promoter.

223 complex acts as a coactivator to recruit the TATA-binding protein (TBP) to the TATA box, a critical s

224 IB plays an important role in recruiting the TATA-binding protein (TBP) to the up-stream region of ge

225 As observed in yeast cells, the TATA-binding protein (TBP) typically displays rapid turn

226 Cytosolic TATA-binding protein (TBP) was found to bind the stress-

227 tein-related factor 2 (TRF2) rather than the TATA-binding protein (TBP) was found to function in tran

228 nction of Mediator-P.5 was not impaired when TATA-binding protein (TBP) was used in place of TFIID, b

229 Association of the TATA-binding protein (TBP) with its cognate site within

230 The association of TATA-binding protein (TBP) with promoter DNA is central

231 We examined the interaction of the TATA-binding protein (TBP) with the NTD of the progester

232 s composed of three subunits, Bdp1, Brf1 and TATA-binding protein (TBP), all essential for normal fun

233 sion of the transcription initiation factor, TATA-binding protein (TBP), alter cellular growth proper

234 Mot1 stably associates with the TATA-binding protein (TBP), and it can dissociate TBP fr

235 t upon replacement of the TFIID complex with TATA-binding protein (TBP), and PRO-seq experiments reve

236 binding of herpes simplex virus type 1 ICP4, TATA-binding protein (TBP), and RNA polymerase II (polII

237 n interactions with DNA-bound activators and TATA-binding protein (TBP), as well as enzymes for histo

238 extensively characterized; NC2 binds to the TATA-binding protein (TBP), blocking the recruitment of

239 To elucidate the roles of the TATA-binding protein (TBP), p300, and the CREB-binding p

240 ents of the general transcription machinery [TATA-binding protein (TBP), TAF4, and TAF6] as well as t

241 The TATA-binding protein (TBP), TFIIA, and TFIIB interact wi

242 ional activity for in vitro interaction with TATA-binding protein (TBP), TFIIA, and TFIIB.

243 -globin gene promoter impairs recruitment of TATA-binding protein (TBP), TFIIB, and RNA polymerase II

244 16 activation domain directly interacts with TATA-binding protein (TBP), TFIIB, and the SAGA histone

245 tion factor IIIB (TFIIIB), consisting of the TATA-binding protein (TBP), TFIIB-related factor (Brf1)

246 TFIIIB-DNA complexes in yeast comprise the TATA-binding protein (TBP), the TFIIB-related factor TFI

247 n remodelers and the Mot1p-NC2 regulators of TATA-binding protein (TBP), we detected synthetic geneti

248 the central transcription initiation factor, TATA-binding protein (TBP), were examined.

249 n is recognition of the promoter TATA by the TATA-binding protein (TBP), which then allows TFIIA and

250 riptional activation by c-Jun depends on the TATA-binding protein (TBP)-associated factor (TAF) subun

251 (KAT) promotes transcriptional initiation of TATA-binding protein (TBP)-associated factor (TAF)-depen

252 is an essential Snf2/Swi2-related ATPase and TATA-binding protein (TBP)-associated factor (TAF).

253 between BORIS and one of the analyzed TSTRs, TATA-binding protein (TBP)-associated factor 7-like (TAF

254 TATA-binding protein (TBP)-associated factor 7l (Taf7l;

255 Mot1 is an essential TATA-binding protein (TBP)-associated factor and Snf2/Sw

256 Mot1 is an essential, conserved, TATA-binding protein (TBP)-associated factor in Saccharo

257 Mot1 is an essential, conserved TATA-binding protein (TBP)-associated factor in Saccharo

258 diated by nuclear hormone receptors requires TATA-binding protein (TBP)-associated factors (TAFs) as

259 The majority of the TATA-binding protein (TBP)-associated factors (TAFs) tha

260 ctivation by HMGA1 and Mediator requires the TATA-binding protein (TBP)-associated factors (TAFs) wit

261 ed through interaction of p53 with TFIIIB, a TATA-binding protein (TBP)-containing factor.

262 The lack of direct targets for TATA-binding protein (TBP)-like factors (TLFs) confounds

263 ed libraries for proteins that interact with TATA-binding protein (TBP).

264 A boxes, which are potential targets for the TATA-binding protein (TBP).

265 a gain-of-function V71E substitution in the TATA-binding protein (TBP).

266 ts role in modifying histones and recruiting TATA-binding protein (TBP).

267 f a PT-ACRAMTU-modified TATA box sequence by TATA-binding protein (TBP).

268 e a Trypanosoma brucei factor related to the TATA-binding protein (TBP).

269 e transcription through direct contacts with TATA-binding protein (TBP).

270 the genomic distribution and activity of the TATA-binding protein (TBP).

271 molecules: U7 small nuclear RNA, coilin, and TATA-binding protein (TBP).

272 phosphorylation and subsequent activation of TATA-binding protein (TBP).

273 between "TATA" bearing promoter DNA and the TATA-binding protein (TBP).

274 gh mobility group box (HMGB) domains and the TATA-binding protein (TBP).

275 tionally conserved dynamics in ubiquitin and TATA-binding protein (TBP).

276 d and bent by the basal transcription factor TATA-binding protein (TBP).

277 sion of the TFIIIB components, Brf1, and the TATA-binding protein (TBP).

278 e caused by a polyglutamine expansion in the TATA-binding protein (TBP).

279 n with the pan-specific transcription factor TATA-binding protein (TBP).

280 pon the function of the transcription factor TATA-binding protein (TBP).

281 to discrete functional surfaces of the yeast TATA-binding protein (TBP).

282 particular genes by controlling the level of TATA-binding protein (TBP/Spt15) associated with the TAT

283 lity of Maf1 to repress transcription of the TATA binding protein, TBP.

284 that Bdbd significantly inhibited binding of TATA-binding protein, TBP to both Cyclin B1 and Aurora A

285 The 180-amino acid core of the TATA-binding protein (TBPcore) is conserved from Archae

286 s C range, in conjunction with their cognate TATA-binding proteins (TBPs) and with heterologous TBPs.

287 Ultimately we found that Pol II, TATA-binding protein, TFIIB and TFIIF can form a quatern

288 criptional activity is highly dependent upon TATA-binding protein, TFIIB and TFIIF.

289 nuclear factor that can form complexes with TATA-binding protein, TFIIB, TFIIF, RNA polymerase II, a

290 Both proteins stabilize/increase binding of TATA binding protein/TFIID to promoter elements.

291 HSP70, the global transcriptional regulator Tata-binding protein/TFIID, cytoskeleton proteins actin

292 d/or genetically interacts with RNAPII, TBP (TATA-binding protein), TFIIS (transcription factor IIS),

293 Why should a polyglutamine stretch in the TATA-binding protein (that is important in all cells) pa

294 f MEF2 changes--MEF2 now associates with the TATA binding protein to bind a distinct TATA box sequenc

295 This region of hsTAF1 binds TATA-binding protein to repress TFIID DNA binding and tr

296 a regulatory process can shift weakly bound TATA-binding protein to stable promoter interactions, th

297 ion and the binding of RNA polymerase II and TATA-binding protein to the core promoter.

298 in part, by Ptr2-mediated recruitment of the TATA-binding protein to the promoter.

299 nuclear transcription factors YY1, SP1, and TATA binding protein were found to colocalize with virus

300 In the current study, recombinant wild type TATA-binding protein, wild type and mutant Brf1, and Bdp