ライフサイエンスコーパス: poly(A) binding protein

1 as the 47-kD protein was shown to be RB47, a poly(A) binding protein.

2 n factor I, purified poly(A) polymerase, and poly(A) binding protein.

3 oocyte masking protein FRGY2/mRNP3+4, and a poly(A) binding protein.

4 70, translation initiation factor eIF4G, and poly(A) binding protein.

5 ly long poly(A) tract in the PCL5 5' UTR and poly(A) binding protein.

6 d intact poly(A) tails and were bound by the poly(A) binding protein.

7 well as cause nuclear relocalization of the poly(A) binding protein.

8 with PBP1, which in turn recruits LSM12 and poly(A)-binding protein.

9 ith RNA, poly(A) polymerase, and the nuclear poly(A)-binding protein.

10 This process requires the presence of a poly(A)-binding protein.

11 ith eIF4A, an RNA unwinding factor, and with poly(A)-binding protein.

12 ly cytoplasmic polyadenylation, but also the poly(A)-binding protein.

13 IRES activity was enhanced moderately by the poly(A)-binding protein.

14 hich is a pattern consistent with binding of poly(A)-binding protein.

15 l, inducing nuclear accumulation of cellular poly(A)-binding protein.

16 and disrupted the association of eIF4G with poly(A)-binding protein.

17 fp36 directly interacts with the cytoplasmic poly(A)-binding protein.

18 al repression via modulating the cytoplasmic poly(A)-binding protein.

19 enylation and directly binds the cytoplasmic poly(A)-binding protein.

20 t with eIF4A, eIF4B, eIF4E isoforms, and the poly(A)-binding protein.

21 the 5' end of mRNA preactivated by eIF4F and poly(A)-binding protein.

22 e aspects of mRNA metabolism consists of the poly(A) binding proteins.

23 aracterized RNA recognition motif-containing poly(A) binding proteins.

24 ucleotides consistent with phased binding of poly(A) binding proteins.

25 did not affect its ability to interact with poly(A) binding proteins.

26 ing proteins, including ELAV/Hu, eIF-4E, and poly(A)-binding proteins.

27 immunity induction through interaction with poly(A)-binding proteins.

28 and how the poly(A) tail and the associated poly(A) binding protein 1 (Pab1p) may affect this proces

29 o which it binds, which includes cytoplasmic poly(A) binding protein 1 (PABP1).

30 eracts with HPV16 E6, as well as cytoplasmic poly(A) binding proteins 1 and 4 (PABPC1 and PABPC4).

31 Interestingly, SUP-26 associates with poly(A)-binding protein 1 (PAB-1) in vivo and may repres

32 ibonucleoprotein particles (mRNPs) via eIF4F-poly(A)-binding protein 1 (Pab1) association, suggesting

33 ments, are not co-labeled with the SG marker poly(A)-binding protein 1 (PABP-1), whereas inclusions i

34 Here we show that poly(A)-binding protein 1 (PABP1) binds preferentially t

35 ve studied the intracellular localization of poly(A)-binding protein 1 (PABP1) by indirect immunofluo

36 erived from the well-defined CARM1 substrate poly(A)-binding protein 1 (PABP1) were covalently linked

37 NAs encoding human ribosomal protein, RPS17, poly(A)-binding protein 1 (PABP1), and the elongation fa

38 the RNA-dependent interaction of G3BP1 with poly(A)-binding protein 1 (PABP1), but its RNA-independe

39 trate that regulated expression of cytosolic poly(A)-binding protein 1 (PABPC1) modulates protein syn

40 cell nuclear antigen (PCNA) and cytoplasmic poly(A)-binding protein 1 (PABPC1)-on ORF2p.

41 The nuclear poly(A)-binding protein 1 (PABPN1) is a ubiquitously exp

42 within the N-terminal domain of the nuclear poly(A)-binding protein 1 (PABPN1) to maximally 17 alani

43 RSK2 colocalizes in granules with TIA-1 and poly(A)-binding protein 1, and the sequestration of RSK2

44 ulin and at least two mRNA-binding proteins, polyA-binding protein 1 and a 130 kDa polyA-mRNA binding

45 ine triplet repeat expansion in the gene for poly(A) binding protein 2 (PABP2) and is found in isolat

46 odes for a ubiquitous nuclear protein called poly(A) binding protein 2 (PABP2).

47 nucleotide repeat expansion in exon 1 of the poly(A) binding protein 2 gene (PABP2), in which (GCG)(6

48 In this work, we identified the poly(A)-binding protein 4 (PABPC4) as a new NCoR1 intera

49 In each species, poly(A)-binding protein-a core marker of stress granules

50 Poly(A) binding protein, along with PCBP 1 and 2, also c

51 onal ortholog, CNBP also associates with the poly(A) binding protein and accumulates in stress granul

52 forms cytoplasmic granules that contain the poly(A) binding protein and possibly represent storage s

53 o proteins involved in mRNA recognition, the poly(A) binding protein and the translation initiation f

54 Poly(A)-binding protein and eIF4B mainly affect the eIF4

55 ing protein eIF4E, eIF4E kinase Mnk1, eIF4A, poly(A)-binding protein and eIF4G.

56 of factors eIF4E, eIF4A, eIF4E kinase Mnk1, poly(A)-binding protein, and adaptor protein eIF4G.

57 th poly(A) tails, inhibit the association of poly(A)-binding protein, and confer increased stability

58 teractions of eIF4G with eIF4E, eIF4A, eIF3, poly(A)-binding protein, and Mnk1/2 have been mapped to

59 port receptor (transportin), the cytoplasmic poly(A)-binding protein, and mRNA.

60 tion, i.e., eukaryotic initiation factor 4G, poly(A)-binding protein, and poly(A) tail.

61 2, forms a complex with PAB-1, a cytoplasmic polyA-binding protein, and that ATX-2 is required for de

62 in of the large ribosomal subunit), pab-1 [a poly(A)-binding protein], and glp-3/eft-3 (an elongation

63 Poly(A) binding proteins are a family of eukaryotic, cyt

64 e canonical RNA recognition motif-containing poly(A) binding proteins as the sole family of poly(A)-s

65 an unexpected molecular function for ancient poly(A)-binding proteins as regulators of biomolecular c

66 We identify poly(A)-binding proteins as unconventional RNA-dependent

67 of Psk1, which phosphorylates and activates poly(A)- binding protein binding protein 1 (Pbp1), which

68 Yeast ataxin-2, also known as Pbp1 (polyA binding protein-binding protein 1), is an intrinsi

69 cloverleaf RNA structure interacts with the poly(A) binding protein bound to the 3' poly(A) tail, th

70 ate that was dependent on a poly(A) tail and poly(A)-binding protein, but was independent of eIF4F fu

71 d formation between RNA binding domains in a poly(A)-binding protein can be used to regulate the abil

72 role of poly(A) tails is much more complex: poly(A)-binding protein can stimulate poly(A) tail remov

73 promotes deadenylation, whereas the putative poly(A) binding protein CG4612 promotes oligomeric Orb2-

74 ich may be a consequence of the poly(A) tail-poly(A)-binding protein complex functioning as a steric

75 d to regulate translation in organisms whose poly(A)-binding proteins contain these critical cysteine

76 dation protein, DEAD box helicase 5, and the poly(A) binding protein cytoplasmic 1.

77 Poly(A) Binding Protein Cytoplasmic 4 (PABPC4), Serine/C

78 Here, we identify Poly(A)-Binding Protein Cytoplasmic 1 (PABPC1), a core S

79 D-translation and termination codon-proximal poly(A) binding protein-depend on the ATPase activity of

80 il represses decapping of RNAs in vitro in a poly(A)-binding protein-dependent fashion.

81 The phosphorylation of eIF-2beta (p38) or poly(A)-binding protein did not change either during ger

82 ribosome entry site interaction with eIF4F, poly(A)-binding protein did not increase eIF4F binding.

83 ific target of Hsp27, as eIF4E, eIF4A, Mnk1, poly(A)-binding protein, eIF4B, and eIF3 were not bound

84 An isoform containing the binding site for poly(A)-binding protein, eIF4G-1e(DM), was more active i

85 The addition of eIF4B and poly(A)-binding protein enhanced the association rate of

86 We recently identified an embryonic poly(A)-binding protein (ePAB) in Xenopus.

87 or Azoospermia-like (DAZL) and the embryonic poly(A)-binding protein (ePAB).

88 sashi1 needs to associate with the embryonic poly(A)-binding protein (ePABP) or the canonical somatic

89 ian and Xenopus PABP1 and is the predominant poly(A)-binding protein expressed in the stage VI oocyte

90 drial targeting of a member of the cytosolic poly(A) binding protein family, PABPC5, and of the RNA/D

91 d identified this protein as a member of the poly(A) binding protein family.

92 nt roles for the interaction of Musashi with poly(A)-binding protein family members in response to ex

93 RB47 is a member of the poly(A)-binding protein family, and binds with high affi

94 ration of eIF4F or eIFiso4F and required the poly(A)-binding protein for optimal function.

95 The poly(A)-binding protein from Saccharomyces cerevisiae la

96 en reported that the expression of the yeast poly(A) binding protein gene (PAB1) in plants leads to a

97 Because association of Musashi1 with poly(A)-binding proteins has previously been implicated

98 E-binding protein called ePAB (for embryonic poly(A)-binding protein) has been purified from this ext

99 in this category, overexpression of Acinus1, Poly(a) binding protein, HNRPA2B1, Bop1, and Gemin5 was

100 mains to be elucidated, the highly conserved poly(A) binding protein I (PABP) mediates poly(A)-depend

101 protein) via its effector domain targets the poly(A)-binding protein II (PABII) of the cellular 3'-en

102 eIF-4B, eIF-4F, eIF-iso4F, and eIF-2 and the poly(A)-binding protein in the seed, during germination,

103 RP with stress granules and colocalizes with polyA binding protein in a variant-dependent manner.

104 ; PABP, a poly(A) binding protein; PAIP-1, a poly(A) binding protein interacting protein; hnRNP D, an

105 inhibitors is mediated, at least in part, by poly(A)-binding protein-interacting protein 2 (PAIP2), w

106 Additionally, two other proteins, poly(A)-binding protein-interacting proteins 1 and 2 (PA

107 ues in RNA binding domains 2 and 3, and this poly(A)-binding protein lacks the ability to be regulate

108 he gene encoding the Leishmania homologue of poly(A)-binding protein (Lm PAB1), as an approach to the

109 These data also suggest that poly(A) binding proteins may play a wider role in transl

110 ain with eukaryotic initiation factor 4A and poly(A) binding protein mediate repression, indicating t

111 ) specific 3' exoribonuclease, mtPARN, and a poly(A)binding protein, mtPABP1.

112 s the cap-binding complex [CBC]) at the cap, poly(A)-binding protein N1 (PABPN1) and PABPC1 at the po

113 -expansion mutation in the gene encoding for poly(A) binding protein nuclear 1 (expPABPN1).

114 The wild-type Poly(A) binding protein nuclear 1 (PABPN1) forms benign

115 sease caused by polyalanine expansion in the poly(A) binding protein nuclear 1 (PABPN1).

116 tide-expansion mutation in the gene encoding poly(A) binding protein nuclear 1 (PABPN1).

117 Here, we report poly(A)-binding protein nuclear 1 (PABPN1) as a novel TD

118 Alanine expansion mutations in poly(A)-binding protein nuclear 1 (PABPN1) cause muscle

119 -13) expansions within the first exon of the poly(A)-binding protein nuclear 1 gene (PABPN1), leading

120 Protein levels of the APA regulator, poly(A)-binding protein nuclear-1 were substantially dow

121 olyalanine tract within the coding region of polyA binding protein nuclear 1 (PABPN1).

122 hort abnormal (GCN) triplet expansion in the polyA-binding protein nuclear 1 (PABPN1) gene leads to P

123 an N-terminal expanded polyalanine tract in polyA-binding protein nuclear 1 (PABPN1).

124 e to a trinucleotide repeat expansion in the polyA-binding protein nuclear-1 gene.

125 Poly(A)-binding protein (PAB) binds to the poly(A) tail

126 Poly(A)-binding protein (PAB) is an evolutionarily conse

127 he translation apparatus, and also binds the poly(A) binding protein Pab1.

128 ith the canonical MademoiseLLE domain of the poly(A)-binding protein Pab1 disclosed unique characteri

129 the proline-rich region and RRM1 domains of poly(A) binding protein (PAB1) as necessary for CCR4 dea

130 s internal initiation via recruitment of the poly(A) binding protein (Pab1) to the 5' untranslated re

131 Poly(A)-binding protein (Pab1 in yeast) is involved in m

132 We show that poly(A)-binding protein (Pab1 in yeast), a defining mark

133 lly identified as a suppressor mutation of a poly(A)-binding protein (PAB1) gene deletion, stabilizes

134 shown, in turn, to necessitate a functional poly(A)-binding protein (PAB1) in which removal of the R

135 duced biomolecular condensates of endogenous poly(A)-binding protein (Pab1) orders of magnitude more

136 Poly(A)-binding protein (Pab1), a canonical stress granu

137 in Saccharomyces cerevisiae stress granules, poly(A)-binding protein (Pab1).

138 In this study, we identify the poly(A)-binding protein, Pab1, and the poly(A) nuclease,

139 ted by the cap-binding complex eIF4F and the poly(A)-binding protein, Pab1.

140 found to coimmunoprecipitate with the yeast poly(A) binding protein Pab1p.

141 We demonstrate that the poly(A)-binding protein Pab1p is required for PUF-mediat

142 h both the cap-binding protein eIF4E and the poly(A)-binding protein Pab1p.

143 ase is inhibited in vitro by addition of the poly(A) binding protein (Pab1p), suggesting that dissoci

144 x, and the translation/mRNA stability factor poly(A) binding protein (Pab1p).

145 tail interacts with a conserved polypeptide, poly(A) binding protein (Pab1p).

146 that the yeast protein Pbp1p associates with poly(A)-binding protein (Pab1p) and controls the extent

147 otic mRNA 3' poly(A) tail and its associated poly(A)-binding protein (Pab1p) are important regulators

148 The yeast poly(A)-binding protein (Pab1p) contains four RNA recogn

149 associated with this 3'-end structure is the poly(A)-binding protein (Pab1p) encoded by the PAB1 gene

150 Tethered poly(A)-binding protein (Pab1p), used as a mimic of a no

151 d Pan3p subunits, as well as the presence of poly(A)-binding protein (Pab1p).

152 accharomyces cerevisiae is stimulated by the poly(A)-binding protein (Pab1p).

153 d two protein components other than Scp160p: poly(A) binding protein, Pab1p, and Bfr1p.

154 suggested to be due to an interaction of the poly(A) binding protein, Pab1p, with eukaryotic translat

155 tic backgrounds, these granules also contain poly(A)-binding protein, Pab1p, and additional mRNA expo

156 be recapitulated in vitro by the cytoplasmic poly(A)-binding protein PABP through a direct and specif

157 regulates the synthesis of Dscam through the poly(A)-binding protein PABP-C.

158 Recently, the poly(A) binding protein (PABP) and cap-binding protein,

159 ich region is removed, we decided to examine poly(A) binding protein (PABP) as a candidate member of

160 Participation of a poly(A) binding protein (PABP) in coupling of editing an

161 The ubiquitous and abundant cytoplasmic poly(A) binding protein (PABP) is a highly conserved mul

162 Poly(A) binding protein (PABP) is an essential, well-con

163 and cattle, utilize a functional homolog of poly(A) binding protein (PABP) known as nonstructural pr

164 d cells stimulates synthesis of the cellular poly(A) binding protein (PABP), significantly increasing

165 ewly elongated poly(A) tail becomes bound by poly(A) binding protein (PABP), which in turn binds eIF4

166 tails of eukaryotic mRNAs are complexed with poly(A) binding protein (PABP).

167 IF4G, eIF4A) and the eIF4F-associated factor poly(A) binding protein (PABP).

168 that can bind poly(A) RNA and interact with poly(A) binding protein (PABP).

169 unit to an mRNA and for interacting with the poly(A) binding protein (PABP).

170 e replication complexes, as well as cellular poly(A) binding protein (PABP).

171 multiple initiation factors, mRNA, rRNA, and poly(A) binding protein (PABP).

172 Viral 3C protease (3Cpro) cleaves poly(A)-binding protein (PABP) and removes the C-termina

173 complex, whose binding domains for eIF4E and poly(A)-binding protein (PABP) are thought to enhance fo

174 IF-4F and eIF-iso4F) and eIF-4B, bind to the poly(A)-binding protein (PABP) both in the presence and

175 of the poly(A) tail was mediated through the poly(A)-binding protein (PABP) bound to the poly(A) tail

176 Cleavage of poly(A)-binding protein (PABP) by 3C(pro) has been shown

177 Further equilibrium studies showed that poly(A)-binding protein (PABP) enhanced the cap binding

178 their binding to the transcript excludes the poly(A)-binding protein (PABP) from the complex.

179 The cocrystal structure of human poly(A)-binding protein (PABP) has been determined at 2.

180 cleavage of eIF4GI, cleavage of eIF4GII and poly(A)-binding protein (PABP) has been recently propose

181 ion of the seemingly contradictory roles for poly(A)-binding protein (PABP) in facilitating both prot

182 from norovirus and FCV were found to cleave poly(A)-binding protein (PABP) in the absence of other v

183 Recent studies demonstrated that wheat germ poly(A)-binding protein (PABP) interacted with translati

184 The poly(A)-binding protein (PABP) interacts with the cap-as

185 The poly(A)-binding protein (PABP) interacts with the eukary

186 Poly(A)-binding protein (PABP) is a major component of t

187 Eukaryotic poly(A)-binding protein (PABP) is a ubiquitous, essentia

188 A FLAG-tagged poly(A)-binding protein (PABP) is expressed in a specifi

189 des, which is consistent with the binding of poly(A)-binding protein (PABP) monomers.

190 Co-injection of poly(A)-binding protein (PABP) mRNA increased the functi

191 utants due to nucleolar sequestration of the poly(A)-binding protein (PABP) Nab2.

192 that the highly conserved 70-kDa cytoplasmic poly(A)-binding protein (PABP) participates directly in

193 The poly(A)-binding protein (PABP) recognizes the 3' mRNA po

194 ocarditis virus (EMCV) infection on the host poly(A)-binding protein (PABP) remains unknown.

195 genes, fabM, which is predicted to encode a poly(A)-binding protein (PABP) that is constitutively ex

196 nteractions between the poly(A) tail and the poly(A)-binding protein (PABP) to achieve maximal IRES-m

197 LARP4 interacts with poly(A)-binding protein (PABP) to protect messenger RNAs

198 mini are brought together by interactions of poly(A)-binding protein (PABP) with both the poly(A) tai

199 The poly(A)-binding protein (PABP), a key component of diffe

200 molog, ATX2, assemble with polyribosomes and poly(A)-binding protein (PABP), a key regulator of mRNA

201 The poly(A)-binding protein (PABP), a protein that contains

202 ts interactions with eIF4A, eIF4G, eIF3, the poly(A)-binding protein (PABP), and RNA.

203 s a complex with initiation factor eIF4G and poly(A)-binding protein (PABP), and strongly and selecti

204 YF associates with a 5'-cap-binding complex, poly(A)-binding protein (PABP), as well as per and tim t

205 ter correction for mRNA load: genes encoding poly(A)-binding protein (PABP), heat-shock proteins hsp7

206 nally, PDCD4 has been shown to interact with poly(A)-binding protein (PABP), which affects translatio

207 NA stability through an association with the poly(A)-binding protein (PABP).

208 tified the 73-kDa protein as the cytoplasmic poly(A)-binding protein (PABP).

209 controlled by the 3' poly(A) tail (PAT) and poly(A)-binding protein (PABP).

210 ed 3' end translational stimulatory protein, poly(A)-binding protein (PABP).

211 ovides evidence that this is mediated by the poly(A)-binding protein (PABP).

212 in 4 (LARP4) directly binds both poly(A) and poly(A)-binding protein (PABP).

213 genetically with, the translation regulator poly(A)-binding protein (PABP).

214 eIF4GI, poly(A)-binding protein (PABP)1, eIF3, eIF4AI, and eIF2a

215 icoid, and with genes encoding eIF4E, Larp1, polyA binding protein (PABP), and Ago2.

216 We show that Cup and polyA-binding protein (PABP) interact physically with Sq

217 cts with a central stress granule component, polyA-binding protein (PABP).

218 ARP4A, oligoA RNA and the MLLE domain of the PolyA-binding protein (PABP).

219 creen of RBPs and identified the cytoplasmic poly(A)-binding protein, pAbp, as an RBP that mediates W

220 our different trypanosome proteins as baits: poly(A)-binding proteins PABP1 and PABP2, mRNA export re

221 e methylation of two known CARM1 substrates, poly(A)-binding protein (PABP1) and the transcriptional

222 However, the cytoplasmic somatic cell poly(A)-binding protein (PABP1) is not expressed until l

223 tes poly(A)RNA transport via deacetylating a poly(A)-binding protein, PABP1.

224 ncoding the testis-specific isoform of mouse poly(A) binding protein (Pabp2) has been isolated and se

225 The mammalian nuclear poly(A) binding protein, PABP2, controls the length of t

226 plexes specifically recruited one of the two poly(A)-binding proteins, PABP2, and one of the six cap-

227 demonstrate that accumulation of cytoplasmic poly(A) binding protein (PABPC) in the nucleus, which ca

228 Recent studies have found the cytoplasmic poly(A) binding protein (PABPC) to have opposing effects

229 It is bound by the cytoplasmic poly(A) binding protein (PABPC), an evolutionarily conse

230 Overexpressing cytoplasmic poly(A)-binding protein (PABPC) in Xenopus oocytes speci

231 n over an ~100 kb distance by recruiting the poly(A) binding protein PABPC1 and the transcription fac

232 proteins hrp36 and hrp38 and the cytoplasmic poly(A)-binding protein PABPC1 as novel functional compo

233 rotein (ePABP) or the canonical somatic cell poly(A)-binding protein PABPC1 for activation of Musashi

234 role in deadenylation, while the cytoplasmic poly(A)-binding protein PABPC1 typically protects mRNAs

235 eadenylation of poly(A) bound by cytoplasmic poly(A)-binding protein PABPC1.

236 ndently binds to poly(A) RNA, RACK1, and the poly(A)-binding protein (PABPC1).

237 nscripts are sequestered in the nucleus with polyA binding protein (PABPC1), and dsRNA is degraded to

238 ntiviral functions for the yeast homologs of polyA-binding protein (PABPC1) and the La-domain contain

239 clease complex CCR4-CAF1 and the cytoplasmic poly(A)-binding protein, PABPC1.

240 s of NFX1-123, including several cytoplasmic poly(A) binding proteins (PABPCs) that interacted with N

241 RT expression through binding to cytoplasmic poly(A) binding proteins (PABPCs).

242 We demonstrate that the nuclear poly(A)-binding protein PABPN1 interacts specifically wi

243 BR-5 physical interactor, namely the nuclear poly(A)-binding protein PABPN1 ortholog PABP-2, worked a

244 We identified the RRMs of poly(A)-binding protein (PABPN1) and nucleolin (NCL) as

245 e cases, splicing is promoted by the nuclear poly(A) binding protein, PABPN1, and poly(A) polymerase

246 ression of the PAB5 gene encoding one of the poly(A) binding proteins (PABPs) in Arabidopsis is restr

247 Poly(A) binding proteins (PABPs) specifically bind the p

248 These roles are largely mediated by Poly(A) Binding Proteins (PABPs) that coat poly(A)-tails

249 avage and polyadenylation complex (CPAC) and poly(A) binding proteins (PABPs).

250 Poly(A)-binding proteins (PABPs) are multifunctional pro

251 Cytoplasmic poly(A)-binding proteins (PABPs) link mRNA 3' termini to

252 Poly(A)-binding proteins (PABPs) play crucial roles in m

253 The family of Poly(A)-binding proteins (PABPs) regulates the stability

254 R-motif-dependent translation is executed by poly(A)-binding proteins (PABPs) through preferential as

255 We show that DAZL proteins interact with poly(A)-binding proteins (PABPs), which are critical for

256 cally associated with A3G and A3F, including poly(A)-binding proteins (PABPs), YB-1, Ro-La, RNA helic

257 interdependent and coordinately regulated by poly(A)-binding proteins (PABPs), yet how PABPs are them

258 pacted by its 3' poly(A) tail and associated poly(A)-binding proteins (PABPs).

259 tely related to the functions of the cognate poly(A)-binding proteins (PABPs).

260 It is widely believed that the poly(A)-binding proteins (PABs) uniformly bind to poly(A

261 the poly(A) tail of mRNA transcripts, called poly(A)-binding proteins (Pabs), play critical roles in

262 , a purine-rich RNA binding protein; PABP, a poly(A) binding protein; PAIP-1, a poly(A) binding prote

263 amydomonas reinhardtii chloroplast-localized poly(A)-binding protein RB47 is predicted to contain a n

264 Binding of the chloroplast poly(A)-binding protein, RB47, to the psbA mRNA is regul

265 Here, we identify Nab2p as a nuclear poly(A)-binding protein required for both poly(A) tail l

266 ith ICP27 most likely when bound to cap- and poly(A)-binding proteins, respectively.

267 These data argue that ePAB is the poly(A)-binding protein responsible for stabilization of

268 serine residue inhibits its interaction with poly(A)-binding protein, resulting in reduced translatio

269 tibodies against mrnp 41 and the cytoplasmic poly(A) binding protein showed colocalization to the cyt

270 -function mutations in SIS1 as well as PAB1 (poly(A)-binding protein), suggesting a functional intera

271 ndependently of the nuclear speckle resident poly(A)-binding protein SUT-2/MSUT2.

272 mouse Pabp2 retroposon encodes an isoform of poly(A) binding protein that is expressed in meiotic and

273 component of the 30 S ribosomal subunit, are poly(A)-binding proteins that interact functionally and

274 Poly(A)-binding protein, the most abundant eukaryotic mR

275 AL4 When applied to the general mRNA-binder, poly(A)-binding protein, the RNA profile obtained by thi

276 in physically interacted with polyadenylate [poly(A)]-binding protein through it RGG motifs.

277 Poly(A)-binding protein thus acts as a physiological str

278 Here, we show that ePAB, embryonic poly(A)-binding protein, transiently associates with the

279 We identified that both poly(A) binding proteins were associated with the L1 rib

280 Two binding sites for the poly(A)-binding protein were mapped to a region within e

281 Indeed, FMRP and ribosomal proteins, but not poly(A)-binding protein, were enriched in isolated nucle

282 element of the cap-binding complex, and the poly(A)-binding protein, which binds to the complex.

283 enylation and the consequent dissociation of poly(A) binding protein will result in PTC-like terminat

284 y(A) tail is mediated through interaction of poly(A)-binding protein with eukaryotic initiation facto

285 fense responses by accumulation of the yeast poly(A) binding protein would turn off the expression of

286 BP2-TRP) of Xenopus laevis embryonic type II poly(A)-binding protein (XlePABP2).