ライフサイエンスコーパス: repressor

1 al regulation of Ptch1, a known Hh-signaling repressor.

2 og of Escherichia coli OmpR, was a virulence repressor.

3 te the DNA-binding activities of the lactose repressor.

4 r6, a basic helix-loop-helix transcriptional repressor.

5 chromatin and functions as a transcriptional repressor.

6 epends on MNT, a MYC-related transcriptional repressor.

7 ch putatively functions as a transcriptional repressor.

8 In this study, we create 41 inducible anti-repressors.

9 CH1 and PURalpha, two androgen receptor (AR) repressors.

10 es by binding to TetR family transcriptional repressors.

11 for engineering systems of non-natural anti-repressors.

12 thy further suggests crosstalk between these repressors.

13 -protein interaction between BCL6 and its co-repressors.

14 s including association with transcriptional repressors.

15 terplay between transcription activators and repressors.

16 C transcription factors that cannot bind JAZ repressors.

17 ssion via the degradation of transcriptional repressors.

18 ers that was attributable to known and novel repressors.

19 ional activators and CRY-PER transcriptional repressors.

20 ely used naturally occurring transcriptional repressors.

21 8) or CBFA2/RUNX1 partner transcriptional co-repressor 3 (Cbfa2t3, also called Mtg16), and derived th

22 CBFA2/RUNX1 partner transcriptional co-repressor 3 (CBFA2T3, also known as MTG16 or ETO2) is a

23 whose activity is modulated by a TOPLESS co-repressor 4 (TPL4)-binding EAR repression motif.

24 studied, less is known about transcriptional repressors acting directly on IFN-I regulatory regions.

25 ve distribution of its plasmid partition and repressor activities, using a ParA with an alanine subst

26 Concordantly, rs679482-A impairs native repressor activity and increases basal and DMRT2-mediate

27 allele is compromised for partition, but its repressor activity is dramatically improved so that it b

28 Moreover, the variant displayed reduced repressor activity on BMAL1/CLOCK driven transcription,

29 1 territory, correlates with increased Gli3 repressor activity, a Hoxd negative regulator, resulting

30 nished DNA binding and concomitant decreased repressor activity.

31 G sites within the aryl-hydrocarbon receptor repressor (AHRR) associate with PTSD after adjustment fo

32 lloblastomas with high expression of the AHR repressor (AHRR) exhibited a significantly worse prognos

33 d the emergence and evolutionary dynamics of repressor alleles after P-elements invaded the Drosophil

34 nsertion in a piRNA cluster, indicating that repressor alleles are produced by de novo insertion at a

35 In many animals including Drosophila, repressor alleles are produced by transpositional insert

36 eolytic cleavage of the LexA transcriptional repressor, allowing expression of > 40 gene products inv

37 mRNAs, functioning both as the translational repressor and activator during oocyte maturation.

38 enetic evidence suggests that MerR acts as a repressor and activator of P (mer) .

39 We also discovered that H-NS is both a repressor and activator of Salmonella Pathogenicity Isla

40 ERF12 is a putative transcriptional repressor and genetically opposes the function of its re

41 of YAP nuclear function as a transcriptional repressor and highlights how loss of contact inhibition

42 of Lactococcus lactis, controlled by the CI repressor and the modulator of repression (MOR) antirepr

43 lian Gli proteins to nuclear transcriptional repressors and by activating the full-length Ci or Gli p

44 In turn, we use this collection of anti-repressors and complementary genetic architectures to co

45 from the reduced formation of Gli2 and Gli3 repressors and early depletion of adenylyl cyclase III i

46 ycomb group (PcG) of proteins are epigenetic repressors and lamin A interactors, primarily involved i

47 by the appearance of quiescent cell-specific repressors and rewiring of the interactions of protein-f

48 ocesses driving oscillations in an activator-repressor architecture and allows us to make predictions

49 urprising discovery that, in the nucleus, co-repressors are dramatically more abundant than co-activa

50 YC) activators and PERIOD-TIMELESS (PER-TIM) repressors are feedback loop components whose transcript

51 By tiling 238 proteins, we find repressors as short as ten amino acids.

52 indings describe CHD4, a classically defined repressor, as positive regulator of transcription and su

53 netic architectures represent a nascent anti-repressor based transcriptional programming structure.

54 increased expression of the transcriptional repressor Bcl6 and that Bcl6 is required for differentia

55 Deregulation of the transcriptional repressor BCL6 enables tumorigenesis of germinal center

56 mRNA extension encoding a Nab1 translational repressor binding site in a CAO knockout line it was pos

57 nal scanning of the CRISPRi KRAB maps the co-repressor binding surface and identifies substitutions t

58 The transcriptional repressor Blimp1 controls cell fate decisions in the dev

59 antly decreases the binding affinity for the repressor Broad, driving differential allele-specific nu

60 essential for it to act as a transcriptional repressor but is dispensable for partition.

61 FMBT1 was considered to be a transcriptional repressor but its role in cancer remains unclear.

62 osome thus serves not only as a general gene repressor, but also as a repressor of all transcription

63 LSD1 (KDM1A) acts as a transcriptional repressor by demethylating mono/dimethylated histone H3

64 ctivator, YAP functions as a transcriptional repressor by interacting with the multifunctional transc

65 tringent activation requirements function as repressors by blocking promoter access of SHP-bound conf

66 ntagonizing the activity of another group of repressors called PHYTOCHROME-INTERACTING FACTORs (PIFs)

67 script levels using a CRISPR-based synthetic repressor can be an effective strategy for AAV-based CRI

68 When delivered by nanoparticles, this repressor can serve as a therapeutic modality to influen

69 odestly increased expression of the ATXN1 co-repressor Capicua (Cic) in anterior cerebellar Purkinje

70 ect the ERK-dependent control of the HMG-box repressor Capicua (Cic), which plays critical roles in d

71 A decay factors, including the translational repressors CAR-1/LSM14 and CGH-1/DDX6, and the decapping

72 Small molecule inhibition of one of these repressors, CDC7, by XL413 and other inhibitors increase

73 Qtip interferes with the prophage repressor (cI(VP882)), leading to host-cell lysis.

74 on as master regulators of this multisubunit repressor complex (E2F-Rb-HDAC) to reverse its suppressi

75 hypermethylation of targets of the polycomb repressor complex 2 components.

76 on with COI1, MYC2 or MYC3, but not with the repressor complex adaptor protein NINJA.

77 expression by antagonizing this multisubunit repressor complex in EBV-positive cells.

78 s, both RBR and E2FB are abundant and form a repressor complex that is reinforced by an autoregulator

79 vators; however, they form a transcriptional repressor complex that represses MIZ1 target genes.

80 ethyltransferase activity but scaffolds a co-repressor complex, including HDAC3 and G9a.

81 ARTNER A, further elevate the amount of this repressor complex, leading to reduced leaf cell number.

82 ractions between human ZFP57 and the KAP1 co-repressor complex.

83 OF JAZ (NINJA) to assemble a transcriptional repressor complex.

84 ding activated Smad proteins and the NuRD co-repressor complex.

85 DAC3)-nuclear receptor corepressor 1 (NCoR1) repressor complex.

86 ain through its interaction with the NCoR co-repressor complex.

87 Arabidopsis polycomb-group repressor complex2 (PRC2) protein MEDEA (MEA) suppresses

88 rice FERTILIZATION-INDEPENDENT SEED-POLYCOMB REPRESSOR COMPLEX2 component, in MADS78 and 79 mutants a

89 4 proteins assemble into florigen activation/repressor complexes (FACs/FRCs), which regulate transiti

90 Mdm4 interacts with members of the Polycomb Repressor Complexes and supports the ubiquitination of H

91 mpanied by loss of recruitment of epigenetic repressor complexes containing PRMT5 and either histone

92 rs via the recruitment of co-activator or co-repressor complexes that epigenetically regulate gene ex

93 lar level, TBL1XR1 mutants co-opt SMRT/HDAC3 repressor complexes toward binding the MB cell transcrip

94 he recruitment of higher-order activator and repressor complexes, respectively.

95 unknown pathological link between TGF-beta1 repressors, contributing to CKD.

96 vealed a major role of the carbon catabolite repressor CRE-1 in regulating the expression of major fa

97 al activators (BMAL1 and CLOCK) and negative repressors (CRYPTOCHROMEs (CRYs) and PERIODs (PERs)).

98 mice, while deletion of the transcriptional repressor (Deltargg3) increased the percentage of coloni

99 factor 9 (KLF9), a putative transcriptional repressor, demonstrate conserved responses.

100 ectly by facilitating degradation of Aux/IAA repressors, direct ETTIN-auxin interactions allow switch

101 d plants that express a fusion of TCP15 to a repressor domain (pTCP15::TCP15-EAR) had shorter stamens

102 which serves routinely as a transcriptional repressor domain in CRISPRi.

103 The SID transcriptional repressor domain is effective as a fusion to the MS2 apt

104 ourse of our studies, we discovered that the repressor domain SID (SIN3-interacting domain) derived f

105 cell lines used, SID is superior to the KRAB repressor domain, which serves routinely as a transcript

106 press prdm8, which encodes a transcriptional repressor, during motor neuron and OPC formation.

107 2F members, in particular activator E2F1 and repressors E2F7 and E2F8, form a feedback circuit at the

108 l proteolysis of both activator and atypical repressor E2Fs.

109 arget of hypoxia through the transcriptional repressor element 1-silencing transcription factor, link

110 -MYC promoter functions as a transcriptional repressor element.

111 reakpoint, which may involve inactivation of repressor elements.

112 or forced APC/C activation by targeting its repressor EMI1 are both potential therapeutic approaches

113 th certain genes showing inappropriate HDAC2 repressor enrichment.

114 -ADABA is known to induce the MocR/GabR-type repressor EnuR, which controls the expression of many ec

115 e underlying mechanism of transcriptional co-repressor ETO2 during early erythropoiesis and hemoglobi

116 oncogenic dependence on the transcriptional repressor EZH2.

117 ur study reveals that a transcription factor-repressor feedback module employs tight regulation of Tf

118 The transcriptional repressor Fezf1 is selectively expressed by postmitotic

119 variation in expression levels of the floral repressor FLOWERING LOCUS C (FLC) leads to differences i

120 epression and epigenetic silencing of floral repressor FLOWERING LOCUS C (FLC).

121 Thus, neurofibromin is a dual repressor for both Ras and ER signaling, and co-targetin

122 e with neuron-specific expression of a super-repressor form of the NF-kappaB inhibitor (IkappaBalpha-

123 Unexpectedly, a non-repressor form of Zur is found to bind chromosome tightl

124 r Zur binds to DNA tightly in its metallated repressor form to Zur box operator sites, repressing the

125 onditions, exists in its metal-deficient non-repressor forms having no significant affinity with Zur

126 re the best characterized transcriptional co-repressors from a molecular point of view.

127 We find a relationship between repressor function and evolutionary age for the KRAB dom

128 ors and cytokines, via multiple repressor-of-repressor gene circuits.

129 involving replication of the phage lambda cI repressor gene.

130 bly due to the activation of transcriptional repressor genes such as Cbfa2t3 and Jdp2 The large numbe

131 EDF1 recruits the translational repressors GIGYF2 and EIF4E2 to collided ribosomes to in

132 factors that play both activator (GliA) and repressor (GliR) roles.

133 hough changes in the state of activators and repressors has been characterized, how their status is t

134 However, transcriptional anti-repressors have largely been absent with regard to the r

135 Recently, non-natural transcription factors (repressors) have been engineered and employed in synthet

136 ggered overexpression of the transcriptional repressor Hes-related family BHLH transcription factor w

137 n this repressor system, two transcriptional repressors-heterochromatin protein 1 (HP1a) and Kruppel-

138 of canonical splicing activators (SRSF) and repressors (HNRNP).

139 B3 domain-containing transcriptional repressors HSI2/VAL1 and HSL1/VAL2 silence seed dormancy

140 obacter and regulated by the transcriptional repressor HutC.

141 cular analysis of constitutive activator and repressor HY5 fusion proteins.

142 IAA33 competes with the canonical AUX/IAA repressor IAA5 for binding to ARF10/16 to protect them f

143 anscription factor E2-2 and inhibited by its repressor Id2.

144 o induce E2-2, LIF paradoxically induced its repressor Id2.

145 ith rates that depended on both receptor and repressor identities.

146 acterize an R2R3-MYB activator and an R3-MYB repressor in monkeyflowers (Mimulus).

147 ion over time required Gli3, the predominant repressor in neural patterning.

148 ins MvaT and MvaU act coordinately as global repressors in Pseudomonas aeruginosa by binding to AT-ri

149 ally improved so that it behaves as a "super-repressor." In vitro, ParA(R351A) binds and hydrolyzes A

150 gnals on short photoperiods induce circadian repressors including DEC1, suppressing BMAL2 and the EYA

151 ent in limb buds devoid of GLI activator and repressor, indicating that their activity is primarily r

152 n of the heterochromatin-inducing epigenetic repressor KAP1/TRIM28 in a subpopulation of cells.

153 , and Botts-Morales formalisms), and genetic repressor kinetics, thereby allowing a large class of mo

154 on of the well-characterized transcriptional repressor Kruppel-like factor 3 (KLF3), which, in turn,

155 liary structure coinciding with reduced Gli3 repressor levels.

156 rigen gene FTa1 and repression of the floral repressor LF Our results establish the conserved importa

157 neuron-specific expression of IkappaB super-repressor mitigated behavioral and pathologic changes in

158 The MAX network transcriptional repressor (MNT) is an MXD family transcription factor of

159 The transcription co-repressors MTG8 and MTG16 were highly expressed by +4/5

160 Here, we identify a Cro/CI-like repressor, named ErfA, which together with Vfr, a CRP-li

161 miR-US5-2 downregulates the transcriptional repressor NGFI-A binding protein (NAB1) to induce myelos

162 ssion (EAR) domain-dependent transcriptional repressors: NO abolished this activity for SRG3 but not

163 her these results identify TFII-I as a novel repressor of a subset of TGFbeta-responsive genes throug

164 Thus, MAF1 functions as a chronic repressor of active pol III loci and can modulate transc

165 y as a general gene repressor, but also as a repressor of all transcription (genic, intragenic, and i

166 We identified miR-298 as a repressor of APP, BACE1, and the two primary forms of Ab

167 nd a previously unknown and highly conserved repressor of ATGL-1 called HLH-11/AP4.

168 gs identify FOXF1 as a novel transcriptional repressor of ATX and demonstrate that loss of FOXF1 prom

169 MSCs via its role as a novel transcriptional repressor of autocrine motility-stimulating factor Autot

170 We first identified H-NS as a repressor of bioluminescence gene expression, for which

171 and an unexpected role of XBP1u as a potent repressor of both XBP1s and ATF6-mediated activation.

172 BRASSINOSTEROID-INSENSITIVE 2 (BIN2), a key repressor of brassinosteroid signaling, to repress hypoc

173 active protein synthesis and that 4E-BP1, a repressor of cap-dependent protein translation, specific

174 TED (RBR), a sugar-dependent transcriptional repressor of cell proliferation, depletes meristematic a

175 We report here that a Transcriptional Repressor of EIN3-dependent Ethylene-response 1 (TREE1)

176 LHP1 is a transcriptional repressor of flowering-related genes, such as FLOWERING

177 nscription factor that functions as a global repressor of fungal secondary metabolism in Aspergillus

178 BCL11A is a repressor of gamma-globin expression and HbF production

179 rectly stimulates transcription of BCL11A, a repressor of gamma-globin transcription, by binding to i

180 specific tRF-5' tRF-Gly-GCC, or tRF-GG-as a repressor of genes associated with the endogenous retroe

181 Here, we identified TFII-I as a novel repressor of GLI2 expression.

182 ZBED2 is a sequence-specific transcriptional repressor of IFN-stimulated genes, which occurs through

183 The transcription factor ZBED6 acts as a repressor of Igf2 and affects directly or indirectly the

184 nding transcription activator3 (CAMTA3) is a repressor of immunity-related genes but an activator of

185 insights into YAP as a broad transcriptional repressor of key regulators of the cell cycle, in turn i

186 hat Leish4E-IP2 could serve as a broad-range repressor of Leishmania protein synthesis.

187 These findings establish OTUD3 as a repressor of MAVS and uncover a previously unknown regul

188 BTB Domain Containing 7C, a transcriptional repressor of membrane metalloproteases (MMP).

189 n, likely due to activation of E2F1, a known repressor of miR-223 transcription.

190 endent upon the presence of MntR, which is a repressor of mntABC transcription.

191 RR3b(H6) appears to act as a transcriptional repressor of multiple predicted circadian clock genes, i

192 ge genes, including Sox1 and Foxd4, and as a repressor of Nodal signalling.

193 n PHC1, which functions as a transcriptional repressor of Notch genes.

194 Blimp-1, a known repressor of PD-1, recruited LSD1 to the Pdcd1 gene duri

195 he nuclear import of MYB4, a transcriptional repressor of phenylpropanoid metabolism.

196 The apocarotenoid acted in parallel to the repressor of photomorphogenesis, DEETIOLATED1 (DET1), to

197 OsRAV9/OsTEM1 has a conserved function as a repressor of photoperiodic flowering upstream of the flo

198 Here we identify TGF-beta1 as a principle repressor of PPM1A, as conditional renal tubular-specifi

199 her neuronal overexpression of 4E-BP1, a key repressor of protein translation, can protect against mi

200 ing peptide, Phr*pLS20, inactivates the anti-repressor of RcopLS20, named RappLS20, which belongs to

201 screen, we identified FBXO44 as an essential repressor of REs in cancer cells.

202 ncoded by CBFB-MYH11, is a dominant negative repressor of RUNX1.

203 The 5-methylcytosine DNA glycosylase/lyase REPRESSOR OF SILENCING 1 (ROS1)-mediated active DNA deme

204 eurin-dependent dephosphorylation of Orm2, a repressor of SL biosynthesis.

205 the Skp-Cullin-F-box (SCF) complex and/or a repressor of SL signaling, PhD53A.

206 Here, we identify Ankmy2 as a repressor of the Hedgehog pathway via adenylyl cyclase t

207 h by functioning as a direct transcriptional repressor of the master regulator of growth, Myc.

208 MexR functions as a transcriptional repressor of the mexAB-oprM operon.

209 e AcrIIA1(NTD) is a critical transcriptional repressor of the strong anti-CRISPR promoter.

210 we show that RUNX1 functions as a bona fide repressor of transcription activated by AML1-ETO.

211 is a nucleoid structuring protein and global repressor of virulence and horizontally-acquired genes i

212 in the biochemical network of activators and repressors of cytoskeleton dynamics have been invoked to

213 old-induced, vernalization-related genes and repressors of endodormancy release was found.

214 dly degrading target proteins, including the repressors of hormone signaling.

215 circSamd4 associated with PURA and PURB, two repressors of myogenesis that inhibit transcription of t

216 SUPPRESSOR OF PHYA (SPA), one of the central repressors of photomorphogenesis, is critical for mainta

217 Collectively, FBXO44/SUV39H1 are crucial repressors of RE transcription, and their inhibition sel

218 CHMP2BIntron5 expression, we have uncovered repressors of retrovirus (RV) activity as modifiers of C

219 RF6, ERF016 and ORA59 appear to act as trans-repressors of RPW8.1, with OAR59 being able to directly

220 repressor, REST, function as transcriptional-repressors of SPINK1, and AR-antagonists alleviate this

221 DELLA proteins are repressors of the gibberellin (GA) hormone signaling pat

222 bitory receptors and cytokines, via multiple repressor-of-repressor gene circuits.

223 both proteins interacting with their partner repressors, only Qtip drives polar localization.

224 es controlled as a unit, usually by the same repressor or activator gene, is known as a regulon.

225 H) mutations, editing of transcriptional HbF repressors or their binding sites and/or regulating epig

226 the super-enhancer for the circadian rhythm repressor Per2.

227 e with aging through inhibition of the clock repressor PER2.

228 Furthermore, the super-repressor phenotype is explained by an increased pool of

229 GAs induce DELLA repressor protein degradation and thereby control a numb

230 Here we show that Spen, an Xist-binding repressor protein essential for XCI , binds to ancient r

231 untranslated region with dCas9 fused to the repressor protein Kruppel-associated box (KRAB).

232 Mutations in the methyl-DNA-binding repressor protein MeCP2 cause the devastating neurodevel

233 ctor) protein, a neuronal gene transcription repressor protein, is responsible for NE gene expression

234 ss of O-GlcNAc from multiple transcriptional repressor proteins associated with TRIM28.

235 binds auxin, leading to dissociation from co-repressor proteins of the TOPLESS/TOPLESS-RELATED family

236 All 16 maize auxin/indole-3-acetic acid repressor proteins were degraded in response to auxin wi

237 as a temperature-responsive transcriptional repressor, providing rhythmicity and temperature respons

238 on plants suggests a role as transcriptional repressor, putatively targeting pathways involved in cel

239 Recently, the ribose operon repressor, RbsR, was also defined as a pleiotropic regul

240 Genetically restoring Gli3 repressor rescues the decreased indirect neurogenesis in

241 This study identifies a transcription repressor responsible for awn inhibition at the B1 locus

242 identify a critical role for the epigenetic repressor REST corepressor 1 (CoREST) in promoting Treg

243 Here, we reveal that the transcriptional repressor role of SerRS is inactivated under hypoxia thr

244 nitiation via the downstream transcriptional repressor Schnurri.

245 hology, when supplemented by constitutive Ci repressor, showing that Hh can signal normally in the ab

246 lated by the activity of the transcriptional repressor, SinR, and its inactivation by its primary ant

247 Here we report epigenetic repressor Smchd1 as a novel maternal effect gene that re

248 y and stabilizes the nephrin transcriptional repressor SNAIL.

249 en identified, including the transcriptional repressor SPEN(1-3), the loss of which has been associat

250 that direct repression of WOX9 by WUS clade repressor STF/LAM1 is required for correct blade archite

251 the KRAB domains, discover that Homeodomain repressor strength is collinear with Hox genetic organiz

252 In this repressor system, two transcriptional repressors-heteroc

253 TALED repression system with the natural lac repressor system.

254 l activator, Tbx5, and T-box transcriptional repressor, Tbx3, determined the molecular and functional

255 c plaques, inclusions of the transcriptional repressor TDP-43, angiopathy, neuron loss and gliosis.

256 E2F8 is a transcriptional repressor that antagonizes E2F1 at the crossroads of the

257 We show that ARID1A is a repressor that binds chromatin at ER cis-regulatory elem

258 mRNA turnover that binds DCP2, but also as a repressor that binds MARF1 to prevent the decay of MARF1

259 CRY1 is a repressor that binds to the transcription factor CLOCK:B

260 expected role for Blimp-1, a transcriptional repressor that constrains autoimmunity, as an upstream p

261 (CIC) is a highly conserved transcriptional repressor that is differentially regulated through mitog

262 ompeting with H-NS, a global transcriptional repressor that oligomerizes on DNA to form filaments and

263 Gfi1 is a zinc-finger transcriptional repressor that plays an important role in hematopoiesis.

264 Further, we identify a transcriptional repressor that preferentially binds an unmethylated prom

265 oncoding regulatory activities, as a cis-DNA repressor that regulates neighboring genes and as a lncR

266 asic helix-loop-helix-orange transcriptional repressor that regulates neurogenesis in several develop

267 e encodes a C2H2 zinc-finger transcriptional repressor that regulates the floral organ number in the

268 TrpR is a tryptophan-dependent repressor that regulates the major promoter (P(trpR)), w

269 uence (FRS) 7 and FRS12, two transcriptional repressors that accumulate in short-day conditions, as r

270 roteins comprise a family of transcriptional repressors that modulate jasmonate (JA) responses.

271 omplemented by 14 additional engineered anti-repressors that respond to the ligand isopropyl beta-d-1

272 ic exclusion conferred by the phage immunity repressor, the phenotype observed in B3-like lysogens su

273 rogen receptor-alpha (ER) transcriptional co-repressor through leucine/isoleucine-rich motifs that ar

274 inactivated FOXA1 binding to its interacting repressors TLE3, HDAC7, and NFIC, thereby blocking FOXA1

275 rk for active genes, but requires the CoREST repressor to act on nucleosome substrates.

276 ormation transformed Orb2 from a translation repressor to an activator and "seed" for further transla

277 he functional conversion of EZH2 from a gene repressor to an activator is unclear.

278 Fs) that mediate association of Tup1-Cyc8 co-repressor to its promoter.

279 uce an enhanced CRISPR-based transcriptional repressor to reprogram immune homeostasis in vivo.

280 e super-enhancers by tethering transcription repressors to enhancers significantly reduces target gen

281 ue to the intrinsic challenges of connecting repressors to gene upregulation in complex cell types wi

282 romatin enables a network of transcriptional repressors to regulate expression levels of class A ARF

283 aling molecule c-di-GMP binds BldD, a master repressor, to control initiation of development.

284 , including C2H2 zinc finger transcriptional repressor TraesCS5A02G542800 upregulated in developing s

285 blishes a mechanism by which transcriptional repressor TREE1 interacts with EIN3 to inhibit shoot gro

286 teins of E. coli such as the transcriptional repressor ulaR, and the ankyrins repeat proteins.

287 een the transcription factor TEAD and its co-repressor VGL4, both playing a central role in the Hippo

288 With the enhanced repressor, we demonstrate transcriptional repression of

289 vators and Rgg3 proteins are transcriptional repressors, we propose that both are capable of transcri

290 f-activating activator that also activates a repressor, which inhibits the activator and diffuses to

291 ng with the induction of the CcMADS19 floral repressor, which prevents the activation of the floral p

292 ERF4 acts as a transcriptional repressor whose activity is modulated by a TOPLESS co-re

293 degrades Rim4, an amyloid-like translational repressor whose timed clearance regulates protein produc

294 PULSE combines a blue-light-regulated repressor with a red-light-inducible switch.

295 a dichotomous transcriptional activator and repressor, with a non-canonical deacetylase-independent

296 gether with the modern clade transcriptional repressor WOX genes in embryogenesis and meristems maint

297 nisms by direct interaction of activator and repressor WOX genes may be required for cell proliferati

298 an operator sequence for the iron-dependent repressor YtgR to regulate trpBA expression.

299 Furthermore, repurposing the iron-dependent repressor YtgR underscores the fundamental importance of

300 eport that the BTB-ZF family transcriptional repressor Zbtb20 negatively regulates CD8 T cell metabol