ライフサイエンスコーパス: histone acetyltransferase

1 sed and was essentially mediated by the p300-histone acetyltransferase.

2 lation were associated tightly with EP300, a histone acetyltransferase.

3 romoter (-98 to -94) and recruiting the p300 histone acetyltransferase.

4 lase (HDAC) 2, and decreased expression of a histone acetyltransferase.

5 ue 3.4 x 10(-6)) in the intron of CCDC101, a histone acetyltransferase.

6 er protein of H3K36me3, and the KAT5 (TIP60) histone acetyltransferase.

7 obvious similarities between TAF1 and known histone acetyltransferases.

8 , including the transcription factor p53 and histone acetyltransferases.

9 with sequence similarity to the GCN5 family histone acetyltransferases.

10 e Il9 locus through direct interactions with histone acetyltransferases.

11 understanding the structure/function of non-histone acetyltransferases.

12 h can be used to identify substrate sites of histone acetyltransferases.

13 -B is a multisubunit complex composed of the histone acetyltransferase 1 (Hat1) catalytic subunit and

14 Histone acetyltransferase 1 (Hat1) catalyzes the acetyla

15 Histone acetyltransferase 1 (HAT1), which catalyzes H4K5

16 We also uncovered the histone acetyltransferase 1 (HAT1)-RBBP7 lysine acetylas

17 s acetylated at lysine 5 and 12 (H4K5,12) by histone acetyltransferase 1 (HAT1).

18 1.9-A resolution crystal structure of human histone acetyltransferase 1 in complex with acetyl coenz

19 Histone acetyltransferase 1 is the founding member of th

20 ther govern substrate-binding specificity of histone acetyltransferase 1.

21 ; guanylate cyclase 1, soluble, beta 3; MYST histone acetyltransferase 1; protein phosphatase 3 (form

22 tion with its reciprocally imprinted ligand, histone acetyltransferase-1 (HAT1), a gene involved in c

23 This enables recruitment of the p300 histone acetyltransferase, a domain-wide increase in his

24 Mechanistically, p300-histone acetyltransferase acetylates STAT3, which, in tu

25 One member of the complex, MOF, a histone acetyltransferase, acetylates lysine 16 of histo

26 In embryonic stem cells (ESCs), the Tip60 histone acetyltransferase activates genes required for p

27 ylase inhibitor to determine the rate due to histone acetyltransferase activity alone and in the abse

28 e histone acetyltransferase enzyme p300, and histone acetyltransferase activity and histone acetylati

29 ranscriptional corepressor with inhibitor of histone acetyltransferase activity and is a potent suppr

30 nd -b and global DNA methylation and reduced histone acetyltransferase activity and TET1, -2, and -3

31 TAF7 acts as a dissociable inhibitor of TAF1 histone acetyltransferase activity and that this event e

32 This caused a significant decrease in Gcn5 histone acetyltransferase activity in vitro and in vivo

33 In addition, inhibition of histone acetyltransferase activity of P300 significantly

34 rsor proliferation was rescued by inhibiting histone acetyltransferase activity or expressing HDAC3.

35 transcriptional coactivator associated with histone acetyltransferase activity that is stabilized by

36 hat a primary function of ATF4 is to recruit histone acetyltransferase activity to a sub-set of AAR t

37 ting RNA polymerase II, and by its intrinsic histone acetyltransferase activity.

38 REBBP) are transcriptional coactivators with histone acetyltransferase activity.

39 al control nonderepressible 5, which display histone acetyltransferase activity.

40 ng differentiation, possibly by sequestering histone acetyltransferase activity.

41 ed enhancement is dependent on its intrinsic histone acetyltransferase activity.

42 nd influences the activity of an H3-specific histone acetyltransferase activity.

43 Sp-binding sites and is independent of p300 histone acetyltransferase activity.

44 ing, phospho-Ser 2 RNA Pol II formation, and histone acetyltransferase activity.

45 Such a function is mediated via its targeted histone acetyltransferase activity.

46 o, alphasyn reduced p300 levels and its HAT (histone acetyltransferase) activity, thereby contributin

47 t that CSRP2BP, a coactivator for CRP2, is a histone acetyltransferase and a driver of smooth muscle

48 SAGA contains a histone acetyltransferase and a ubiquitin protease.

49 These acetylations require the Gcn5 histone acetyltransferase and are reversed by the sirtui

50 firm that nucleosomal H3K4me3 stimulates the histone acetyltransferase and H2Av exchange activities o

51 ensitivity to depletion and/or inhibition of histone acetyltransferases and CDK9 and less sensitivity

52 tion of histones and non-histone proteins by histone acetyltransferases and deacetylases (HDACs) play

53 factor Sp1, with commensurate recruitment of histone acetyltransferases and deacetylases, increased h

54 on residue T34 upregulates the activities of histone acetyltransferases and deacetylases, which then

55 on residue T34 upregulates the activities of histone acetyltransferases and deacetylases.

56 27ac), which correlated with the presence of histone acetyltransferases and deacetylases.

57 y, we ectopically overexpressed 21 different histone acetyltransferases and found that KAT6A, KAT6B a

58 tion status is modulated antagonistically by histone acetyltransferases and histone deacetylases (HDA

59 Histone acetyltransferases and histone deacetylases (HDA

60 ion, is controlled by the opposing action of histone acetyltransferases and histone deacetylases (HDA

61 d because of the limited specificity of most histone acetyltransferases and histone deacetylases.

62 ction of Elk-1 with co-activators, including histone acetyltransferases and the Mediator complex.

63 in the absence of the normally required Gcn5 histone acetyltransferase, and HO expression even in the

64 ow that suppressor of Ty (Spt)10, a putative histone acetyltransferase, and its binding partner Spt21

65 The three histone acetyltransferases are MOZ, MORF, and HBO1, whic

66 Taybi syndrome (caused by mutations in other histone acetyltransferases) are discussed.

67 BRPF1 encodes a protein modifier of two histone acetyltransferases associated with ID: KAT6A (al

68 s well as peaks of acetylated H4K16 and KAT8 histone acetyltransferase at the transcription start sit

69 Levels of some histone acetyltransferases at this gene (PCAF and MOF) w

70 ons by disrupting the histone deacetylase-to-histone acetyltransferase balance in the nucleus.

71 on assays demonstrated SP-1, p300, and PCA/F histone acetyltransferase binding and histone H4 hyperac

72 Histone acetyltransferase binding to origin recognition

73 dicating that another as of yet unidentified histone acetyltransferase binds to SMAD3 at PLOD2.

74 lation leads to a specific activation of the histone acetyltransferase Brd2, which results in histone

75 TAT1 has an overall fold similar to the Gcn5 histone acetyltransferase but contains a relatively wide

76 hanced on nucleosomes acetylated by the NuA4 histone acetyltransferase, but recognition of nucleosome

77 GNATs are known for their role as histone acetyltransferases, but non-histone bacterial pr

78 l activity stimulates binding of IPMK to the histone acetyltransferase CBP and enhances its recruitme

79 was observed when cells were depleted of the histone acetyltransferase CBP.

80 e acetylation associated with recruitment of histone acetyltransferase CBP.

81 (MLL) histone methylases (MLL2 and MLL3) and histone acetyltransferase CBP/P300 bind to the EZH2 prom

82 The histone acetyltransferases CBP/p300 are involved in recu

83 nt a small-molecule (TTK21) activator of the histone acetyltransferases CBP/p300, which, when conjuga

84 BMAL1, a partner and regulator of circadian histone acetyltransferase CLOCK, that both proteins loca

85 L2 suppressed this process by inhibiting the histone acetyltransferase coactivator p300, preventing t

86 nents of the nuclear Hat1p-containing type B histone acetyltransferase complex (NuB4) and have found

87 The evolutionarily conserved histone acetyltransferase complex Elongator was identifi

88 this study, we show that the conserved Mst2 histone acetyltransferase complex in fission yeast regul

89 Deletion of components of the yeast NuA4 histone acetyltransferase complex in ncr1Delta strains c

90 ic interactions with mutations affecting the histone acetyltransferase complex NuA4, vps15Delta and v

91 hat Ing4 is a subunit of the HB01-JADE-hEAF6 histone acetyltransferase complex responsible for most n

92 plant homeodomain, thus recruiting the HBO1 histone acetyltransferase complex to target promoters.

93 he NuA4, nucleosome acetyltransferase of H4, histone acetyltransferase complex, (ii) the switching de

94 We identified components of the SAGA histone acetyltransferase complex, in particular Gcn5, a

95 lation, likely through interactions with the histone acetyltransferase complex.

96 FD1 interactors were components of the TIP60 histone acetyltransferase complex.

97 mplexes, including the Mediator and multiple histone acetyltransferase complexes, among which are the

98 folding protein required for the assembly of histone acetyltransferase complexes, where the gene of M

99 al tail lysine residues by the NuA4 and SAGA histone acetyltransferase complexes.

100 yeast Spt-Ada-Gcn5-acetyltransferase (SAGA) histone acetyltransferase complexes.

101 actor 4-like 1 (MORF4L1) is a relatively new histone acetyltransferase component that exists as a hom

102 nd K148Q, abolished its self-assembly of the histone acetyltransferase component.

103 g protein (p38IP) is a component of the GCN5 histone acetyltransferase-containing coactivator complex

104 The histone acetyltransferase CREB-binding protein (CBP) med

105 ent binding (CREB) interaction domain of the histone acetyltransferase CREB-binding protein (CBP).

106 encodes the transcriptional coactivator and histone acetyltransferase CREB-binding protein (CREBBP,

107 overexpression of HDAC8 or knocking down the histone acetyltransferase CREB-binding protein/p300, kno

108 riched for the activating marker H3K27ac and histone acetyltransferase CREBBP after MED25 overexpress

109 Plants treated with an inhibitor of histone acetyltransferases, curcumin, previous to the UV

110 comb histone methyltransferase complex and a histone acetyltransferase-dependent "on state." Regulati

111 3 is involved in histone acetylation via its histone acetyltransferase domain (HAT) and, as a result,

112 38IP N terminus (1-381 amino acids) and GCN5 histone acetyltransferase domain and bromodomain.

113 Rescue experiments with a MOF histone acetyltransferase domain mutant illustrated the

114 and pRb into a ternary complex, bringing the histone acetyltransferase domain of CBP/p300 into proxim

115 histone UAS elements and contains a putative histone acetyltransferase domain.

116 s substitutions in conserved residues of the histone acetyltransferase domain.

117 Current inhibitors of the p300 and CBP histone acetyltransferase domains, including natural pro

118 Here, we show that co-expression of histone acetyltransferase E1A binding protein p300 drama

119 Once in the nucleus, sSDC1 binds to the histone acetyltransferase enzyme p300, and histone acety

120 mechanistically, far less is known about non-histone acetyltransferase enzymes.

121 , chronic stress increased expression of the histone acetyltransferase EP300 and increased histone ac

122 In turn, Hdac3 recruited histone acetyltransferase Ep300 to form an enhanceosome

123 acetylases and concurrent recruitment of the histone acetyltransferase EP300 to MEF2 target gene regu

124 somal rearrangements of the ZNF384 gene with histone acetyltransferases EP300 and CREBBP ZNF384-rearr

125 through its interaction with the MYST family histone acetyltransferase Esa1.

126 resulted in identification of the essential histone acetyltransferase EsaA, able to complement an es

127 eases Acetyl-CREB-binding protein (CBP/p300) histone acetyltransferase expression in a time and dose-

128 On the other hand, PAF increased p300 histone acetyltransferase expression, and the acetylatio

129 RTT109 is a histone acetyltransferase for histone H3 lysine 56 (H3K5

130 ous studies have shown perturbations in SAGA histone acetyltransferase function and transcriptional a

131 Li et al. now show that Mof, a MYST family histone acetyltransferase, functions as a coactivator of

132 ere significantly inhibited by inhibitors of histone acetyltransferase (garcinol and antisense agains

133 The histone acetyltransferase GCN5 (general control non-repr

134 /36/37 residues, which specifically recruits histone acetyltransferase GCN5 for subsequent H3 acetyla

135 We previously demonstrated that the histone acetyltransferase Gcn5 is required for U2 snRNP

136 tz1 inherently enhances the occupancy of the histone acetyltransferase Gcn5 on chromatin to promote h

137 Using the yeast histone acetyltransferase Gcn5p as a case study, we demo

138 truncating mutations in the highly conserved histone acetyltransferase gene KAT6B (MYST4/MORF)) in th

139 lators, including histone chaperones and the histone-acetyltransferase general control nonderepressib

140 As one of the most important histone acetyltransferases, general control non-derepres

141 and positively with DOG1 expression, as were histone acetyltransferase genes, with histone deacetylas

142 The monocytic leukemic zinc finger (MOZ) histone acetyltransferase (HAT) acetylates free histones

143 actor 1 (TAF1), possesses protein kinase and histone acetyltransferase (HAT) activities.

144 iptional coactivator p300/CBP possesses both histone acetyltransferase (HAT) activity and scaffolding

145 Loss of the histone acetyltransferase (HAT) activity blocks oogenesi

146 pplementation; this microRNA alters HDAC and histone acetyltransferase (HAT) activity, which suggests

147 e exhibited increased renal HDAC and reduced histone acetyltransferase (HAT) activity; on the contrar

148 contains two enzymatic modules, which house histone acetyltransferase (HAT) and deubiquitinase (DUB)

149 Chromatin remodeling through histone acetyltransferase (HAT) and histone deactylase (

150 Using steady-state histone acetyltransferase (HAT) assays, we show that an

151 We find that the histone acetyltransferase (HAT) Chameau (Chm) binds to a

152 Previous studies have established that the histone acetyltransferase (HAT) complex Hat1p/Hat2p medi

153 Brd1 is a subunit of the Hbo1 histone acetyltransferase (HAT) complex responsible for

154 nstrate that the ATAC (Ada two A containing) histone acetyltransferase (HAT) complex serves as a tran

155 Piccolo NuA4 is an essential yeast histone acetyltransferase (HAT) complex that targets his

156 udor domain of PHF20, which recruits the MOF histone acetyltransferase (HAT) complex to ERalpha targe

157 n PHD finger 1) is a core subunit of the MOZ histone acetyltransferase (HAT) complex, critical for no

158 mine tract in ATXN7, a component of the SAGA histone acetyltransferase (HAT) complex.

159 The lysine acetyltransferase 6 (KAT6) histone acetyltransferase (HAT) complexes are highly con

160 ed factor] and MOZ are catalytic subunits of histone acetyltransferase (HAT) complexes essential in h

161 SEs of the multisubunit Mediator and several histone acetyltransferase (HAT) complexes, including Spt

162 tations in several subunits of SAGA and NuA4 histone acetyltransferase (HAT) complexes.

163 (ADA3) is an essential component of specific histone acetyltransferase (HAT) complexes.

164 of several transcriptional co-activator and histone acetyltransferase (HAT) complexes.

165 specific DNA binding protein with a putative histone acetyltransferase (HAT) domain.

166 Tip60 is a histone acetyltransferase (HAT) enzyme that epigenetical

167 te has been shown to inhibit the activity of histone acetyltransferase (HAT) enzymes in vitro, we hyp

168 tein microarray analysis that identified the histone acetyltransferase (HAT) Hbo1 as a novel cyclin E

169 en Phytophthora sojae acts as a modulator of histone acetyltransferase (HAT) in plants.

170 e ability of garcinol, a naturally-occurring histone acetyltransferase (HAT) inhibitor derived from t

171 The histone acetyltransferase (HAT) inhibitor garcinol or ve

172 Several histone acetyltransferase (HAT) inhibitors with these li

173 contains a separable subcomplex known as the histone acetyltransferase (HAT) module that contains the

174 The histone acetyltransferase (HAT) Mof is essential for mou

175 In this manner, we discovered the H4K16 histone acetyltransferase (HAT) MOF to be important for

176 Rtt109 is a yeast histone acetyltransferase (HAT) that associates with his

177 The histone acetyltransferase (HAT) Tip60 epigenetically reg

178 Besides the primary histone acetyltransferase (HAT)-mediated chromatin remod

179 Here, we identify a trypanosome histone acetyltransferase (HAT3) and a deacetylase (SIR2

180 acetylation state of histones, controlled by histone acetyltransferases (HATs) and deacetylases (HDAC

181 n of histones by chromatin-modifying enzymes histone acetyltransferases (HATs) and histone deacetylas

182 ected histone lysine residues is governed by histone acetyltransferases (HATs) and histone deacetylas

183 lts from the balance between the activity of histone acetyltransferases (HATs) and histone deacetylas

184 rsible acetylation of proteins, catalysed by histone acetyltransferases (HATs) and histone deacetylas

185 Histone acetyltransferases (HATs) and histone deacetylas

186 KAT6 histone acetyltransferases (HATs) are highly conserved i

187 KAT6 histone acetyltransferases (HATs) are highly conserved i

188 ether other histone deacetylases (HDACs) and histone acetyltransferases (HATs) are involved in MSH2 d

189 transformation requires interaction with the histone acetyltransferases (HATs) CBP/p300 and now repor

190 Most histone acetyltransferases (HATs) function as multisubun

191 Histone acetyltransferases (HATs) have a central role in

192 Although histone acetyltransferases (HATs) have been well charact

193 sequencing to screen the levels of all known histone acetyltransferases (HATs) in the hippocampal CA1

194 olvement of histone deacetylases (HDACs) and histone acetyltransferases (HATs) in the regulation of a

195 The MYST family of histone acetyltransferases (HATs) plays critical roles i

196 y, EP300, two highly related histone and non-histone acetyltransferases (HATs) that act as transcript

197 ted 300 kDa protein) are two closely related histone acetyltransferases (HATs) that play a key role i

198 We assess the ability of seven histone acetyltransferases (HATs) to catalyze acylations

199 Histone acetylation is regulated by histone acetyltransferases (HATs), which acetylate histo

200 nstrated using pharmacological inhibitors of histone acetyltransferases (HATs).

201 Whereas histone acetyltransferases have been extensively studied

202 erones, nucleosome remodeling complexes, and histone acetyltransferases have been implicated in nucle

203 MYST histone acetyltransferases have crucial functions in tra

204 Histone acetyltransferase HBO1 might acetylate this resi

205 total HDAC activity but increased the total histone acetyltransferase/HDAC activity ratio in mouse l

206 l HDAC activity, and it diminished the total histone acetyltransferase/HDAC activity ratio in mouse l

207 The MYST family histone acetyltransferase hMOF (human MOF) is responsibl

208 other anti-silencing factors, including the histone acetyltransferase IDM1 and the alpha-crystallin

209 histone acetylation marks and for different histone acetyltransferases in long-range gene regulation

210 repeat and Jumonji domain-containing 2C, and histone acetyltransferases including CBP and p300 are re

211 CRE-binding protein-binding protein (CBP), a histone acetyltransferase, induced base-line and IL-13-i

212 anscriptional co-repressor with inhibitor of histone acetyltransferase (INHAT) activity and has previ

213 ly, prevention of histone acetylation by the histone acetyltransferase inhibitor curcumin diminished

214 tion, as reducing JunD acetylation using the histone acetyltransferase inhibitor curcumin reverses th

215 We conclude that the CSRP2BP histone acetyltransferase is a coactivator for CRP2 that

216 The results suggest that the CLOCK histone acetyltransferase is a component of the viral tr

217 The MYST family of histone acetyltransferases is autoacetylated at an activ

218 by complexes containing opposing lysine and histone acetyltransferase (KAT and HAT) and deacetylase

219 ORC to the origin, suggesting that multiple histone acetyltransferases may be recruited during origi

220 ssesses an activation domain that couples to histone acetyltransferase-mediated pathways, as well as

221 Histone acetyltransferase mortality factor 4-like 1 (MOR

222 The histone acetyltransferase MOZ (MYST3, KAT6A) is the targ

223 ng proteins important for the recruitment of histone acetyltransferases of the MYST family to chromat

224 ng proteins important for the recruitment of histone acetyltransferases of the MYST family to chromat

225 Mechanistically, Wnt3a does not alter histone acetyltransferase or deacetylase activities but,

226 tion is accomplished by a dominant action of histone acetyltransferases over repressive histone-modif

227 l roles in protein activation, including the histone acetyltransferase p300 acetylated in its activat

228 )/CD28 stimulation by forming a complex with histone acetyltransferase p300 and NF-kappaB transcripti

229 ough certain chromatin features, such as the histone acetyltransferase P300 and the histone modificat

230 f different epigenetic modifiers showed that histone acetyltransferase p300 could enhance both TALE-V

231 own of GATA6 or transcriptional co-activator/histone acetyltransferase p300 decreased AQP5 expression

232 The histone acetyltransferase p300 has been implicated in th

233 Overexpression of the histone acetyltransferase p300 is implicated in the prol

234 Once HDAC1 is tethered, histone acetyltransferase p300 is no longer recruited to

235 The histone acetyltransferase p300 is normally associated wi

236 Consistent with this idea, the histone acetyltransferase p300 is recruited to organizer

237 al activators Sp1 and HIF-1 colocalized with histone acetyltransferase p300 on ncx1-Br with a consequ

238 ain interactions, whereas sites bound by the histone acetyltransferase p300 or the transcription fact

239 ated beta-HPV E6 protein suggesting that the histone acetyltransferase p300 plays a role in promoting

240 Furthermore, we found that histone acetyltransferase p300 supported the recruitment

241 d-chromatin association, and associates with histone acetyltransferase p300 to enhance Smad transcrip

242 to the VMP1 promoter and complexes with the histone acetyltransferase p300 to regulate promoter acti

243 hosphatase 6, the sumoylation machinery, the histone acetyltransferase p300, and downstream transcrip

244 tylation upon HDAC inhibition, partly by the histone acetyltransferase p300, and that both NF-kappaB

245 ders Il9 locus accessible via recruitment of histone acetyltransferase p300, and together with inhibi

246 Furthermore, the histone acetyltransferase P300, recruited via bone morph

247 ding histone H3K4 methyltransferase SET1 and histone acetyltransferase p300, whose levels are also el

248 g of IL10 through their interaction with the histone acetyltransferase p300.

249 chromatin environment via recruitment of the histone acetyltransferase p300.

250 described E3 ligase function of BRMS1 on the histone acetyltransferase p300.

251 F-kappaB through direct interaction with the histone acetyltransferase p300.

252 LL4 (H3K4 methyltransferase) complex and the histone acetyltransferase p300.

253 rough systematic epigenetic studies that the histone acetyltransferase p300/CBP-associated factor (PC

254 Here, we identify a novel activity of the histone acetyltransferase p300/CREB-binding protein (CBP

255 ZBP-89 physically associates with the histone acetyltransferases p300 and Gcn5/Trrap, and occu

256 Furthermore, histone acetyltransferases p300 and P300/CBP-associated

257 eraction between the DUX4 C-terminus and the histone acetyltransferases p300/CBP.

258 On the molecular level, hG9a interacted with histone acetyltransferase, p300/CBP, resulting in increa

259 t H3K9 acetylation by the NeuroD1-associated histone acetyltransferase, P300/CBP-associated factor (P

260 II histone deacetylase (HDAC), HDAC4, and a histone acetyltransferase, p300/CREB-binding protein-ass

261 The histone acetyltransferase paralogues p300 and CREB-bindi

262 The histone acetyltransferase PCAF-mediated acetylation and

263 Here, we show that the histone acetyltransferase PCAF/KAT2B is an important fac

264 h an E1A mutant that can no longer bind to a histone acetyltransferase (PCAF) is as capable as wild-t

265 II histone deacetylase (HDAC), HDAC4, and a histone acetyltransferase, PCAF, associate with cardiac

266 acterization demonstrated that SMAD2 and the histone acetyltransferase, PCAF, participate in this reg

267 Histone acetyltransferases play important roles in the r

268 Interestingly, CBP, a histone acetyltransferase previously implicated in repre

269 Such an enhanced targeting of NuA4 HAT (histone acetyltransferase) promotes the recruitment of t

270 ponent of the MOF (male absent on the first) histone acetyltransferase protein complex, suggesting it

271 Novel inhibitor of histone acetyltransferase repressor (NIR) is a transcrip

272 y Naa50p complex with the peptide-bound Gcn5 histone acetyltransferase revealed that the two enzymes

273 Loss of the histone acetyltransferase Rtt109 also suppressed ctk1-de

274 from two repairable DSBs also depends on the histone acetyltransferase Rtt109 and the cullin subunit

275 g high-throughput screen (HTS) targeting the histone acetyltransferase Rtt109 were such compounds.

276 genome-wide screen and demonstrated that the histone acetyltransferase SAGA and the activity of histo

277 , namely the chromatin remodeler Swi/Snf and histone acetyltransferases SAGA and NuA4, suggesting tha

278 fferent epigenetic marks and activates three histone acetyltransferases, so it is both a reader and a

279 ltransferase 1 is the founding member of the histone acetyltransferase superfamily and catalyzes lysi

280 nteraction between Arabidopsis MRE11 and the histone acetyltransferase TAF1, a TATA-binding protein A

281 Together, this study identifies the first histone acetyltransferase that activates ERalpha express

282 e ERalpha, suggesting MYST3 functioning as a histone acetyltransferase that activates ERalpha promote

283 Tat-interactive protein 60 (Tip60) is a MYST histone acetyltransferase that catalyses acetylation of

284 is a MOZ, Ybf2/Sas3, Sas2, Tip60 (MYST)-type histone acetyltransferase that functions as a coactivato

285 regulates the availability of acetyl-CoA for histone acetyltransferases, thus representing a link bet

286 The histone acetyltransferase TIP60 is a coregulator of tran

287 normal compaction pathway is defective, the histone acetyltransferase Tip60 is recruited to pericent

288 Foxp3(gfp) was unable to interact with the histone acetyltransferase Tip60, the histone deacetylase

289 cell master regulator Foxp3 mediated by the histone acetyltransferase Tip60, which targeted Foxp3 fo

290 zymes including histone demethylase LSD1 and histone acetyltransferase Tip60.

291 stly, we show that ETS2 cooperates with p300 histone acetyltransferase to remodel chromatin and promo

292 BRD4-NUT recruits histone acetyltransferases to induce histone hyperacetyl

293 ction in Th9 cells by binding and recruiting histone acetyltransferases to the Il9 locus at sites dis

294 tion of these 2 CpGs impaired binding of the histone acetyltransferase/transcriptional coactivator p3

295 Many histone acetyltransferases undergo autoacetylation, eith

296 Activity of HDAC and histone acetyltransferase was measured in peripheral blo

297 ocytic leukemia zinc finger protein (MOZ), a histone acetyltransferase, we demonstrate that mutation

298 selectively target the catalytic activity of histone acetyltransferases, which may provide effective

299 ne expression and identify KAT8 as the first histone acetyltransferase with an essential function in

300 Sustained association of NFAT and p300 histone acetyltransferase with the IP-10 gene required p