ライフサイエンスコーパス: bZIP transcription factor

1 the yeast two-hybrid system with a putative bZIP transcription factor.

2 The identities confirm sisA as an atypical bZIP transcription factor.

3 segmentation gene kreisler, which encodes a bZip transcription factor.

4 inase, which in turn phosphorylates the Atf1 bZIP transcription factor.

5 nfection response gene irg-1 using the zip-2 bZIP transcription factor.

6 floral genes through interaction with FD, a bZIP transcription factor.

7 les for AP2 and Sp1, in combination with the bZip transcription factors.

8 ng, and (v) members of the TGA/OBF family of bZIP transcription factors.

9 eral ways including direct interactions with bZIP transcription factors.

10 ncreases the transcriptional efficacy of the bZip transcription factors.

11 nd acidic amino acid-rich (PAR) subfamily of bZIP transcription factors.

12 erved among chlorophytes and present in some bZIP transcription factors.

13 g sites for basic/helix-loop-helix, MYB, and BZIP transcription factors.

14 te the activity of members of the G-group of bZIP transcription factors.

15 sly shown to induce Gcm1 expression by other bZip transcription factors.

16 hares resemblance with the Jun/Fos family of bZIP transcription factors.

17 ct to varying extents with many ABI5-related bZIP transcription factors.

18 des derived from GCN4, a yeast basic zipper (bZIP) transcription factor.

19 ces-2 encodes a basic region leucine-zipper (bZIP) transcription factor.

20 ands from human basic-region leucine zipper (bZIP) transcription factors.

21 the CREB/ATF family of basic-leucine zipper (bZIP) transcription factors.

22 to a subclass of plant basic leucine zipper (bZIP) transcription factors.

23 superfamily of basic region-leucine zipper (bZIP) transcription factors.

24 tners for human basic-region leucine zipper (bZIP) transcription factors.

25 main and CNC homolog 1 (BACH1) and NFE2 like bZIP transcription factor 1 (NFE2L1), also have roles in

26 factor 1 subunit alpha (HIF1A) and NFE2 like BZIP transcription factor 2 (NFE2L2) activation and BTB

27 The Cap'n'collar (CNC) protein NFE2 like bZIP transcription factor 2 (NFE2L2, also known as NRF2)

28 Kyn-CKA induces NFE2 like bZIP transcription factor 2- and aryl hydrocarbon recept

29 including glucose transporter 2 (Glut2), MAF BZIP transcription factor A (MafA), and uncoupling prote

30 sponse element binding basic leucine zipper (bZIP) transcription factors (ABF/AREB/ABI5 clade).

31 o a weak interaction between PpABI3A and the bZIP transcription factor ABI5, as assayed functionally

32 diated developmental checkpoint requires the bZIP transcription factor ABI5.

33 ty in Medicago truncatula, we identified the bZIP transcription factor ABSCISIC ACID INSENSITIVE5 (AB

34 l of oxidative stress, the expression of the bZip transcription factor activating transcription facto

35 OTYL 5 (HY5), a basic domain/leucine zipper (bZIP) transcription factor, acts as a master regulator o

36 onstrating an expanded repertoire of group F bZIP transcription factors, adding to the complexity of

37 Analyses of a bZIP transcription factor and receptor recognition of Fi

38 Hypoxia induced a disproportionate number of bZIP transcription factors and related targets involved

39 networks, with proteins from the families of bZIP transcription factors and the Commander complex.

40 for continued in vivo functional analysis of bZIP transcription factors and their corresponding cis e

41 a model to investigate interactions between bZIP transcription factors and their target sites.

42 study demonstrates the importance of group F bZIP transcription factors and ZIP transporters in respo

43 We studied the basic region-leucine zipper (bZIP) transcription factors and quantified bZIP dimeriza

44 domain-containing transcriptional regulator, bZIP transcription factor, and regulatory protein NPR1.

45 zip-1 encodes a putative bZIP transcription factor, and we show that zip-1 contro

46 sely related to the vertebrate PAR family of bZIP transcription factors, and a ces-2/ces-1-like pathw

47 re mediated respectively by target sites for bZIP transcription factors, and by SMAD target sites.

48 cascades, phosphorylation of c-Jun and ATF-2 bZIP transcription factors, and finally to selective ind

49 ed Nrl, a member of the Maf-Nrl subfamily of bZIP transcription factors, and the Nrl response element

50 T 1 (RFT1), OsFD-like basic leucine zipper (bZIP) transcription factors, and Gf14 proteins assemble

51 The eukaryotic bZIP transcription factors are critical players in organ

52 Because bZIP transcription factors are obligate dimers, and beca

53 We considered four bZIP transcription factors as candidates for this putati

54 he mRNA for the basic domain leucine zipper (bZip) transcription factor ATB2/AtbZip11, translation of

55 The Arabidopsis basic leucine zipper (bZIP) transcription factor AtbZIP10 shuttles between the

56 Homologs of the bZIP transcription factor Atf1 are required for virulenc

57 inding and genome-wide redistribution of the bZIP transcription factor ATF3, which in turn repressed

58 Here we examine pX interactions with bZip transcription factors ATF3, gadd153/Chop10, ICER II

59 egulated in stressed cells, primarily by the bZIP transcription factor ATF4 through its recruitment t

60 We found expression of the bZip transcription factor ATF5 in all 29 human glioblast

61 We report that the bZIP transcription factor ATF5 plays a major regulatory

62 The bZIP transcription factor ATF6a is a master regulator of

63 The basic leucine zipper (bZIP) transcription factor AtfB, a member of the bZIP/CR

64 ical producing E. coli mutant, including the bZip transcription factor atfs-1 (activating transcripti

65 in Caenorhabditis elegans, we find that the bZIP transcription factor ATFS-1/Atf5 (refs.

66 Numerous reports have identified MAF BZIP Transcription Factor B (MAFB) to be present in huma

67 erties in common with the more studied human bZIP transcription factors, but also includes novel stru

68 nergistically with the basic leucine zipper (bZIP) transcription factor bZIP10 to induce dsCYC2 trans

69 nction of three basic region/leucine zipper (bZIP) transcription factors: bZIP16, bZIP68, and GBF1.

70 rane-associated basic domain/leucine zipper (bZIP) transcription factor, bZIP28.

71 The bZIP transcription factor c-Jun, which is part of the AP

72 bserve AT2s retain fate plasticity until the bZIP transcription factor C/EBPalpha suppresses Notch si

73 The bZIP transcription factor C/EBPbeta is a target of Ras s

74 ng to examine the expression patterns of two bZip transcription factors, c-Fos and FosB, in the stria

75 The level of bZIP transcription factor CCAAT enhancer-binding protein

76 ystem that acts directly downstream of C/EBP bZip transcription factor CEBP-1, we find unexpected pos

77 TYL5 (HY5) is a basic domain/leucine zipper (bZIP) transcription factor, central for the regulation o

78 This is the first demonstration of a potato bZIP transcription factor complementing genetic defects

79 ER TRUSS (SFT) and two mutations affecting a bZIP transcription factor component of the 'florigen act

80 the X box in a manner consistent with other bZIP transcription factor contact patterns.

81 LCR-F1 is a mammalian bZIP transcription factor containing a basic amino acid

82 The basic/leucine zipper (bZip) transcription factor, CREB, binds to the CRE eleme

83 ic amino acid-rich basic leucine zipper (PAR bZIP) transcription factor DBP expression/activity.

84 is a homologue of a Saccharomyces cerevisiae bZip transcription factor designated Yap1p that is both

85 Previously, we have described a bZIP transcription factor, DimA, which is required for c

86 We have purified a novel bZIP transcription factor, DimB, by affinity chromatogra

87 escribe the identification of a DimA-related bZIP transcription factor, DimB.

88 The basic-region leucine zipper (BR-LZ or bZIP) transcription factors dimerize via their LZ domain

89 Meq, a bZIP transcription factor discovered in the 1990s, is cr

90 insight into the mechanism by which dimeric bZIP transcription factors discriminate between closely

91 Here we show that the basic leucine zipper (bZIP) transcription factor E4BP4 (also called NFIL3) is

92 The bZIP transcription factor ELONGATED HYPOCOTYL5 (HY5) act

93 The bZIP transcription factor ELONGATED HYPOCOTYL5 (HY5) rep

94 Here, we identified that two bZIP transcription factors, ELONGATED HYPOCOTYLE 5 (HY5)

95 of transcriptional activators, including the bZIP transcription factor encoded by the kreisler gene c

96 no (val), a zebrafish homologue of the mouse bzip transcription factor-encoding gene, kreisler, is re

97 rotein beta (C/EBP beta), from two different bZIP transcription factor families, has been determined

98 DRINK ME (DKM; bZIP30) is a member of the bZIP transcription factor family, and is expressed in me

99 bitors of DeltaFOSB and other members of the bZIP transcription factor family.

100 Atf2, the gene for the basic leucine zipper (bZIP) transcription factor family member ATF-2.

101 members of the basic region leucine zipper (bZIP) transcription factor family.

102 atial information is mediated in part by the bZIP transcription factor FD, which is already expressed

103 FL1 is recruited to thousands of loci by the bZIP transcription factor FD.

104 pment and identifying it as a homolog of the bZIP transcription factor FD.

105 omain of MAF, a basic region leucine zipper (bZIP) transcription factor, first identified as an oncog

106 Upstream regulators including the bZIP transcription factor FlbB activate the expression o

107 ATF-2 is a bZip transcription factor for activation of cAMP respons

108 TGACG-motif binding (TGA) basic Leu zipper (bZIP) transcription factors for recruitment to DNA.

109 we find that the CrebA/Creb3-like family of bZip transcription factors functions to up-regulate expr

110 Arabidopsis bZIP transcription factor, GBF1, acts as a differential

111 nd that one candidate regulator, the G-class bZIP transcription factor GBF2, can modulate vascular ge

112 The yeast bZIP transcription factor GCN4 does not induce DNA bendi

113 derived from the yeast basic leucine zipper (bZIP) transcription factor GCN4 bound to AP-1 sites in d

114 ent of the DNA basic region (br) of the GCN4 bZIP transcription factor has been modified to include t

115 the CCAAT enhancer binding protein family of bZIP transcription factors has been linked to both growt

116 ed factor 2 (Nrf2), an oxidant-activated CNC bZip transcription factor, has been implicated in defens

117 tified to date, HY5, a basic leucine zipper (bZIP) transcription factor, has been investigated extens

118 ollar family of basic region-leucine zipper (bZIP) transcription factors, has been implicated as an e

119 ecific class of basic-region leucine zipper (bZIP) transcription factors, have been isolated in a num

120 homologous to the PAR subfamily of mammalian bZIP transcription factors HLF, DBP and VBP/TEF.

121 We have found that Pap1, a bZIP transcription factor homologous to human c-Jun, can

122 tiated by the maternally supplied SKN-1/Nrf2 bZIP transcription factor; however, the requirement for

123 The barley bZIP transcription factor HvABI5 mediates abscisic acid

124 A barley basic domain/Leu zipper (bZIP) transcription factor, HvABI5, is able to recognize

125 light receptor phytochrome A (phyA) and the bZIP transcription factor HY5 HOMOLOG (HYH) are both req

126 n the dark, COP1 directly interacts with the bZIP transcription factor HY5, a positive regulator of p

127 and interaction between the light regulatory bZip transcription factors HY5 and HYH.

128 reconstructing ancestral interactions among bZIP transcription factors, imputing missing present-day

129 reaction was used to identify three TGA-type bZIP transcription factors in an AZ cDNA library.

130 e-varying alterations in the inducibility of bZIP transcription factors in individual striatal neuron

131 4 forms at least five distinct heterodimeric bZIP transcription factors in skeletal muscle fibers.

132 uced changes in expression and activation of bZIP transcription factors in the postsynaptic motor neu

133 The relationship between PvALF and ABI5, a bZIP transcription factor, in mediating phas expression

134 hat regulates steady-state levels of Nrf2, a bZIP transcription factor, in response to oxidative stre

135 Two FT monomers and two DNA-binding bZIP transcription factors interact with a dimeric 14-3-

136 s identifies a novel mechanism through which bZip transcription factors interact.

137 Although Yap1p and Yap2p are both bZIP transcription factors involved in multiple stress r

138 , a well-characterized basic leucine zipper (bZIP) transcription factor involved in the unfolded prot

139 dimerization of basic region-leucine zipper (bZIP) transcription factors is required for their transc

140 MAF, one of a family of large Maf bZIP transcription factors, is mutated in human developm

141 at JunD, an AP1 family basic-leucine zipper (bZip) transcription factor, is one of the ferritin H ARE

142 ember of the AP-1 subfamily of basic zipper (bZIP) transcription factors, is necessary and sufficient

143 domain arrangement is like that seen in the bZIP transcription factors it has been termed the bZIP-l

144 n cellular target of the beta-propeller is a bZIP transcription factor known as LZIP or Luman.

145 These results establish Hac1 as the first bZIP transcription factor known to adopt more than one b

146 s lacking this regulation, we identified the bZIP transcription factor LONG HYPOCOTYL 5 (HY5) as a ne

147 s shown to be allelic with a knockout of the bZIP transcription factor, Maf.

148 indicates that although other typical plant bZIP transcription factors may bind ABRCs in vitro, HvAB

149 The basic motif-leucine zipper (bZIP) transcription factor neural retina leucine zipper

150 LCR-F1 and the related bZIP transcription factors NF-E2 p45 and NRF2 must compe

151 The bZIP transcription factor Nfil3 (also known as E4BP4) is

152 e identified a novel interaction between two bZIP transcription factors, Nrf1 and the CCAAT enhancer-

153 The bZIP transcription factor Nrf2 controls a genetic progra

154 ion of Keap1-dependent ubiquitination of the bZIP transcription factor Nrf2 enables Nrf2 to activate

155 The bZIP transcription factor Nrf2 has emerged as a key regu

156 sion is mediated through accumulation of the bZIP transcription factor, Nrf2, in the nucleus, and tha

157 The bZIP transcription factor NRL (neural retina leucine zip

158 ell as lower synergistic activation with the bZIP transcription factor NRL.

159 The basic motif-leucine zipper (bZIP) transcription factor NRL controls the expression o

160 ion requires the basic motif-leucine zipper (bZIP) transcription factor NRL, because loss of Nrl in m

161 We recently demonstrated that the bZip transcription factor nuclear factor erythroid-deriv

162 uggest that cross-coupling between EREBP and bZIP transcription factors occurs and may therefore be i

163 NRL, a bZIP transcription factor of the Maf subfamily, interact

164 lso found in LZIP and Zhangfei, two cellular bZIP transcription factors of unknown function.

165 We identified FEA4 as a bZIP transcription factor, orthologous to Arabidopsis th

166 transcriptional activation complex with the bZIP transcription factor OsFD1 to start panicle develop

167 tion system-dependent manner, one encoding a bZIP transcription factor (OsTFX1) and the other the sma

168 Specific bZIP transcription factors partially mediate primary KIN

169 precipitation assays to demonstrate that the bZIP transcription factor PERIANTHIA (PAN) plays a role

170 ear factor E2 p45-related factor 2 (Nrf2), a bZIP transcription factor, plays a central role in the r

171 rization of the basic-region leucine-zipper (bZIP) transcription factors presents a vivid example of

172 Basic leucine zipper (bZip) transcription factors regulate cellular gene expre

173 Basic region leucine zipper (bZIP) transcription factors regulate gene expression cri

174 Hepatic leukemia factor (HLF) is a bZIP transcription factor related to the CES-2 protein,

175 Of the 32 bZIP transcription factors represented on the GeneChip,

176 g atf1(+) mRNA, which encodes a subunit of a bZIP transcription factor required for gene expression d

177 e nitrogen source requires the heterodimeric bZip transcription factors Rtg1 and Rtg3 and correlates

178 ins (C/EBP) are basic region/leucine zipper (bZIP) transcription factors selectively expressed during

179 Sage and Fkh drive expression of the bZip transcription factor Senseless (Sens), which boosts

180 ith chromatin opening in regions occupied by bZIP transcription factors, specifically BATF, known to

181 Here, we show that clade I bZIP transcription factors TGA1 and TGA4, previously ass

182 HY5 is a bZIP transcription factor that binds directly to the pro

183 interaction between OsTBP2 and RF2a, a rice bZIP transcription factor that bound to the box II cis e

184 the molecular switch protein, ZEBRA, a viral bZIP transcription factor that initiates transcription f

185 sh ortholog of mafB/Kreisler (Kr), encodes a bZip transcription factor that is required cell autonomo

186 This screen identified zip-2, a bZIP transcription factor that is required for inducing

187 Keap1 is a negative regulator of Nrf2, a bZIP transcription factor that mediates adaptation to ox

188 hancer-binding protein beta (C/EBPbeta) is a bZip transcription factor that plays crucial roles in im

189 ction with and negative regulation of HY5, a bZIP transcription factor that positively regulates phot

190 Arabidopsis HY5 is a bZIP transcription factor that promotes photomorphogenes

191 RF2a is a bZIP transcription factor that regulates expression of t

192 at Arabidopsis ELONGATED HYPOCOTYL5 (HY5), a bZIP transcription factor that regulates growth in respo

193 Atf1 and Atf21 are bZIP transcription factors that are most closely related

194 f1 and Nrf2 are members of the CNC family of bZIP transcription factors that exhibit structural simil

195 erences of coiled-coil peptides derived from bZIP transcription factors that performs very well when

196 2 is a cellular basic region-leucine zipper (bZIP) transcription factor that can mediate diverse tran

197 ransactivator Zta is a basic leucine zipper (bZIP) transcription factor that causes G0/G1 cell cycle

198 PDP1 is a basic leucine zipper (bZip) transcription factor that is expressed at high lev

199 is a cap-n-collar basic leucine zipper (CNC-bZIP) transcription factor that is well established as a

200 E4BP4 is a basic leucine zipper (bZIP) transcription factor that represses or activates t

201 ode a family of basic domain-leucine zipper (bZIP) transcription factors that are conserved in higher

202 psis thaliana group S1 basic leucine zipper (bZIP) transcription factors that orchestrate the starvat

203 ns (C/EBPs) are basic region leucine zipper (bZIP) transcription factors that regulate cell different

204 and little is known about the role of other bZIP transcription factors, the combinatorial complexity

205 mbers from a family of conserved Arabidopsis bZIP transcription factors, the TGA proteins, are regula

206 an enhancer of the DNA binding potential of bZip transcription factors, thereby increasing the trans

207 coli mutant may directly activate the ATFS-1/bZIP transcription factor to induce mitochondrial stress

208 is the first member of the PAR subfamily of bZIP transcription factors to be identified in Drosophil

209 r-responsive S(1)-basic-leucine-zipper (S(1)-bZIP) transcription factors, we disclosed their largely

210 in the IVDT response of P. patens, ELIPs and bZIP transcription factors, were functionally investigat

211 sease virus, encodes a basic leucine zipper (bZIP) transcription factor which contains a large prolin

212 and mediated by NapA, a homolog of AP-1-like bZIP transcription factor, which is essential for the re

213 ibility of chromatin regions with motifs for bZIP transcription factors, which impacts the transcript

214 zipper) is a key basic motif-leucine zipper (bZIP) transcription factor, which orchestrates rod photo

215 /enhancer-binding protein (C/EBP) alpha is a bZIP transcription factor whose expression is restricted

216 pe CREB3L2 was expressed in the thyroid as a bZIP transcription factor with a transmembrane domain th

217 gene of Schizosaccharomyces pombe encodes a bZIP transcription factor with strong homology to the ma

218 n Arabidopsis thaliana basic leucine zipper (bZIP) transcription factor with a transmembrane domain,

219 Here, we report that the bZIP transcription factor Xrp1 is required for ATF4-inde

220 on element (ARE) of the major-groove binding bZIP transcription factor yAP-1, the yeast analogue of m

221 SRA-1 and SAGO-2, which are activated by the bZIP transcription factor ZIP-1.

222 The Caenorhabditis elegans bZIP transcription factor ZIP-2 is activated by toxins o

223 We asked whether a viral bZIP transcription factor, Zta (BZLF1, ZEBRA, EB1), driv