ライフサイエンスコーパス: Tetrahymena thermophila

1 ifferentially modified pools of tubulin from Tetrahymena thermophila.

2 xcised from the developing somatic genome of Tetrahymena thermophila.

3 s and exconjugant development in the ciliate Tetrahymena thermophila.

4 tion-deletion polymorphisms among strains of Tetrahymena thermophila.

5 ess of conjugation in the ciliated protozoan Tetrahymena thermophila.

6 on cell pair formation during conjugation in Tetrahymena thermophila.

7 d Ca(2+) binding protein, has been cloned in Tetrahymena thermophila.

8 rocesses in zebrafish, human fibroblasts and Tetrahymena thermophila.

9 metallothionein (MTT1) gene was cloned from Tetrahymena thermophila.

10 s populations of Saccharomyces cerevisiae or Tetrahymena thermophila.

11 nd double-strand break repair in the ciliate Tetrahymena thermophila.

12 -A70 family methyltransferase-in the ciliate Tetrahymena thermophila.

13 of the somatic nucleus during development of Tetrahymena thermophila.

14 G-DNA-binding protein TGP1 from the ciliate Tetrahymena thermophila.

15 tes of phosphorylation of macronuclear H1 in Tetrahymena thermophila.

16 olecules found in ciliated protozoa, such as Tetrahymena thermophila.

17 TGP1, a G-DNA specific binding protein from Tetrahymena thermophila.

18 eloping amitotic macronucleus of the ciliate Tetrahymena thermophila.

19 matic macronucleus in the ciliated protozoan Tetrahymena thermophila.

20 d from macronuclei of the ciliated protozoan Tetrahymena thermophila.

21 hat regulate rRNA gene (rDNA) replication in Tetrahymena thermophila.

22 ly folding domain of the Group I intron from Tetrahymena thermophila.

23 uing process has been extensively studied in Tetrahymena thermophila.

24 regions, during macronuclear development in Tetrahymena thermophila.

25 hromosome breakage and telomere formation in Tetrahymena thermophila.

26 ced ciliate genomes: Oxytricha trifallax and Tetrahymena thermophila.

27 urs in the P5 helix of the group I intron of Tetrahymena thermophila.

28 he genome during macronuclear development of Tetrahymena thermophila.

29 ne H2A variant hv1 in the ciliated protozoan Tetrahymena thermophila.

30 n reactions of the self-splicing intron from Tetrahymena thermophila.

31 otic linkage data for the ciliated protozoan Tetrahymena thermophila.

32 ze 12 DRC subunits in the N-DRC structure of Tetrahymena thermophila.

33 mes using cross-linking mass spectrometry in Tetrahymena thermophila.

34 ane recruitment of Drp6, a dynamin member in Tetrahymena thermophila.

35 structure of the ciliary tip of the ciliate Tetrahymena thermophila.

36 and in vivo nucleosome maps for the ciliate Tetrahymena thermophila.

37 stered rings at the cilium base of a ciliate Tetrahymena thermophila.

38 germline micronucleus of the model organism Tetrahymena thermophila.

39 cretory granule-like vesicles in the ciliate Tetrahymena thermophila.

40 RNase T2 genes (RNT2A-RNT2H) in the ciliate Tetrahymena thermophila.

41 the first canonical PARG from the protozoan Tetrahymena thermophila.

42 re proteins, Tpt1 and Pat1, from the ciliate Tetrahymena thermophila.

43 the structural maintenance of centrioles in Tetrahymena thermophila.

44 istone H2B in the single-cell model organism Tetrahymena thermophila.

45 ogress in genome closure and reannotation of Tetrahymena thermophila.

46 al body components in the ciliated protozoan Tetrahymena thermophila.

47 ian cells, Drosophila cells, and the ciliate Tetrahymena thermophila.

48 ed to programmed DNA deletion in the ciliate Tetrahymena thermophila.

49 n boundaries by flanking inverted repeats in Tetrahymena thermophila.

50 ide-binding domain (NBD) of gamma-tubulin in Tetrahymena thermophila.

51 We have cloned the RAD51 homolog from Tetrahymena thermophila , a ciliated protozoan.

52 We show here that Tetrahymena thermophila, a bacterivorous predator, is ki

53 tified and cloned the parafusin homologue in Tetrahymena thermophila, a ciliate in which protein func

54 ved in the evolution of translation, we used Tetrahymena thermophila, a ciliate with high coding capa

55 However, its presence in Tetrahymena thermophila, a ciliated protozoan with seven

56 Here we describe, using the ciliate Tetrahymena thermophila, a previously unidentified respo

57 Tetrahymena thermophila, a widely studied model for cell

58 ndary ion mass spectrometry images of mating Tetrahymena thermophila acquired at various stages durin

59 In Tetrahymena thermophila-ag in natural isolates is the re

60 The Tetrahymena thermophila Ago/Piwi protein Twi12 is essent

61 ated reaction, intron-derived ribozymes from Tetrahymena thermophila and Candida albicans, which are

62 oding kinesin-II homologues from the ciliate Tetrahymena thermophila and constructed strains lacking

63 Protein components from the Tetrahymena thermophila and human RNase P holoenzymes fo

64 of the CP in the ciliary tip of the ciliate Tetrahymena thermophila and identify several tip protein

65 , is characterized in the ciliated protozoan Tetrahymena thermophila and is shown to be responsible f

66 w that the ectodomain of HAP2 orthologs from Tetrahymena thermophila and other species adopt a protei

67 s spectrometric analyses of H3 purified from Tetrahymena thermophila and Saccharomyces cerevisiae (ye

68 The rDNA minichromosomes of Tetrahymena thermophila and Tetrahymena pyriformis share

69 tudied ciliates include Oxytricha trifallax, Tetrahymena thermophila, and Paramecium tetraurelia, but

70 terium Trichodesmium erythraeum, the ciliate Tetrahymena thermophila, and the viruses Enterobacteria

71 Arabidopsis thaliana, Plasmodium falciparum, Tetrahymena thermophila, Archaeoglobus fulgidus, and Myc

72 regulated secretory granules in the ciliate Tetrahymena thermophila are crystal lattices composed of

73 es of the macronuclear (expressed) genome of Tetrahymena thermophila are generated by developmental f

74 e macronuclear DNA of the ciliated protozoan Tetrahymena thermophila are modified to N 6-methyladenin

75 m the developing macronucleus in the ciliate Tetrahymena thermophila are released as linear fragments

76 The genetics of the ciliate Tetrahymena thermophila are richer than for most other e

77 r linker histones of the ciliated protozoan, Tetrahymena thermophila, are extensively phosphorylated

78 quantify these NPs in the ciliated protozoan Tetrahymena thermophila as a model aquatic organism.

79 Using Tetrahymena thermophila as an example, we demonstrate on

80 and purified using the free-living ciliate, Tetrahymena thermophila as an expression system.

81 re we analyze the actions of telomerase from Tetrahymena thermophila assembled in vivo with mutated o

82 In Tetrahymena thermophila, brief exposure to secretagogue

83 s were efficiently ingested by the protozoan Tetrahymena thermophila but were neither digested nor ki

84 n-binding protein profilin was isolated from Tetrahymena thermophila by affinity chromatography, and

85 demonstrated that the group I ribozyme from Tetrahymena thermophila can perform trans-splicing react

86 Tetrahymena thermophila cells contain three forms of H2A

87 In logarithmically growing Tetrahymena thermophila cells, for example, H3 phosphory

88 e ciliate Glaucoma chattoni was expressed in Tetrahymena thermophila cells.

89 The Tetrahymena thermophila CNA1 gene encodes the centromeri

90 During Tetrahymena thermophila conjugation, new somatic macronu

91 veloping somatic genome are generated during Tetrahymena thermophila conjugation.

92 The genome of Tetrahymena thermophila contains 39 loci encoding NIMA-r

93 The macronucleus of the ciliate Tetrahymena thermophila contains a fragmented somatic ge

94 The ciliate Tetrahymena thermophila contains at least four centrin g

95 The macronucleus of the binucleate ciliate Tetrahymena thermophila contains fragmented and amplifie

96 The ciliate protozoan Tetrahymena thermophila contains two types of structural

97 In telomeric DNA mutants of Tetrahymena thermophila, created by expression of a telo

98 he H2A.F/Z variant of the ciliated protozoan Tetrahymena thermophila, cross-react with proteins from

99 Although the ciliate Tetrahymena thermophila desaturates sterols at the C-22

100 ation of a novel G4-DNA binding protein from Tetrahymena thermophila, designated TGP2.

101 In Tetrahymena thermophila, developmentally regulated DNA e

102 eus (MAC) and germline micronucleus (MIC) of Tetrahymena thermophila differ in chromosome numbers, si

103 In binuclear ciliates, including Tetrahymena thermophila, DNA elimination occurs during t

104 The ciliate Tetrahymena thermophila encodes numerous PPD proteins ex

105 In the ciliated protozoan Tetrahymena thermophila, extensive DNA elimination is as

106 icient than the amber suppressor tRNA THG73 (Tetrahymena thermophila G73), which has been used extens

107 The gene (GTU1) encoding Tetrahymena thermophila gamma-tubulin was cloned and ana

108 e now report the cloning and sequencing of a Tetrahymena thermophila gene whose encoded protein has t

109 We cloned a Tetrahymena thermophila gene, IFT52, encoding a homolog

110 entified the centromeric histone gene in the Tetrahymena thermophila genome (CNA1).

111 The haploid Tetrahymena thermophila genome contains a single alpha-t

112 We have found that the Tetrahymena thermophila genome contains two POT1 gene ho

113 Here, we show that, in the protozoan Tetrahymena thermophila, germline-specific internally el

114 e P5b stem loop from the P4-P6 domain of the Tetrahymena thermophila group I intron and a 58-nt fragm

115 independently folding P4-P6 domain from the Tetrahymena thermophila group I intron by single molecul

116 An RNA comprising the two domains of the Tetrahymena thermophila group I intron catalytic core re

117 bdomain (tP5abc, a 56-nucleotide RNA) of the Tetrahymena thermophila group I intron ribozyme changes

118 of the P5abc subdomain (a 56-nt RNA) of the Tetrahymena thermophila group I intron ribozyme has been

119 zyme constructs consist of the self-splicing Tetrahymena thermophila group I intron ribozyme that is

120 to define the folding landscape of the L-21 Tetrahymena thermophila group I intron structurally and

121 for Mg(2+) and Na(+)-mediated folding of the Tetrahymena thermophila group I intron using this combin

122 or exemplary RNA sequences (hairpins and the Tetrahymena thermophila group I intron), we compute the

123 isfolded state in the folding pathway of the Tetrahymena thermophila group I intron, a paradigmatic R

124 In particular, the P456 domain of the Tetrahymena thermophila group I intron, and a 58 nt 23s

125 ent of the 5 S rRNA and the P5c helix of the Tetrahymena thermophila group I intron.

126 The Mg2+-induced folding of Tetrahymena thermophila group I ribozyme shows the capab

127 independently folding tertiary domain of the Tetrahymena thermophila group I ribozyme, is known to fo

128 The Tetrahymena thermophila group I self-splicing intron was

129 lete sequence of the mitochondrial genome of Tetrahymena thermophila has been determined and compared

130 The unicellular eukaryote Tetrahymena thermophila has seven mating types.

131 In Tetrahymena thermophila, highly phosphorylated histone H

132 A truncated cDNA clone encoding Tetrahymena thermophila histone H2A2 was isolated using

133 H2A.Y is an essential, divergent Tetrahymena thermophila histone variant.

134 experimental range expansions of the protist Tetrahymena thermophila in landscapes with a uniform env

135 for semiconservative transmission of 6mA in Tetrahymena thermophila In wild-type (WT) cells, 6mA occ

136 ure of one of these, the P4-P6 domain of the Tetrahymena thermophila intron, is described.

137 crystal structure of the P4-P6 domain of the Tetrahymena thermophila intron.

138 Conjugation in the freshwater ciliate Tetrahymena thermophila involves a developmental program

139 yme derived from the self-splicing intron of Tetrahymena thermophila involves at least two steps.

140 The ciliate Tetrahymena thermophila is a useful model organism that

141 The ciliate Tetrahymena thermophila is a well-established unicellula

142 As a unicellular model organism, Tetrahymena thermophila is among the first eukaryotes re

143 The SerH locus of Tetrahymena thermophila is one of several paralogous loc

144 Tetrahymena thermophila is the best studied of the cilia

145 Tetrahymena thermophila is the only ciliate in which a s

146 the H2A.Z variant of the ciliated protozoan TETRAHYMENA: thermophila is able to rescue the phenotype

147 hv2, an H3 variant in the ciliated protozoan Tetrahymena thermophila, is synthesized and deposited in

148 f various guanosine, or G, substrates to the Tetrahymena thermophila L-21 ScaI ribozyme have been inv

149 The Tetrahymena thermophila L-21 ScaI ribozyme utilizes Mg2+

150 into a site within a variable region in the Tetrahymena thermophila large subunit rRNA gene.

151 secondary and/or tertiary structures in the Tetrahymena thermophila large subunit rRNA-DeltaP5abc gr

152 ersally conserved site in this region of the Tetrahymena thermophila LSU rRNA confers anisomycin resi

153 ed by the recently completed sequence of the Tetrahymena thermophila macronuclear genome.

154 Tetrahymena thermophila macronuclear histone H1 is phosp

155 T).d(AACCCC) repeat tracts (G4T2 repeats) in Tetrahymena thermophila macronuclei were shown previousl

156 oper S-phase progression and division of the Tetrahymena thermophila macronucleus.

157 In conjugating Tetrahymena thermophila, massive DNA elimination occurs

158 The eight DRPs in the ciliate Tetrahymena thermophila might contribute to aspects of c

159 Here, we report the structures of Tetrahymena thermophila MTA1 (TthMTA1), Paramecium tetra

160 ingle-particle cryo-EM-based analyses of the Tetrahymena thermophila native doublet microtubule and i

161 We show that the ciliate Tetrahymena thermophila not only possesses a homodimeric

162 equences (such as TTGGGG in the G-strand for Tetrahymena thermophila) of double-stranded DNA with a s

163 The ciliate Tetrahymena thermophila offers a simple system in which

164 The ciliated protozoan, Tetrahymena thermophila, offers an attractive medium for

165 ins that contained eRF1 domain 1 from either Tetrahymena thermophila or Euplotes octocarinatus fused

166 The Tetrahymena thermophila origin recognition complex (ORC)

167 Two telomerase proteins from Tetrahymena thermophila, p80 and p95, were identified on

168 unction, we determined crystal structures of Tetrahymena thermophila Pah2 (Tt Pah2) that directly fus

169 reported the first PAP enzyme structures of Tetrahymena thermophila Pah2 at 3.0 angstrom resolution.

170 esolution (1.95-2.40 angstrom) structures of Tetrahymena thermophila Pah2 that represent active state

171 In Tetrahymena thermophila, peptides secreted via dense-cor

172 The L-21 ScaI ribozyme derived from the Tetrahymena thermophila pre-rRNA group I intron catalyze

173 The targeted disruption of somatic genes in Tetrahymena thermophila presents the opportunity to dete

174 base pairing within the telomerase RNA from Tetrahymena thermophila prevent the stable assembly in v

175 resulted in cystic kidneys, and knockdown in Tetrahymena thermophila produced shortened or absent cil

176 an be transferred to and biomagnified in the Tetrahymena thermophila protozoa that prey on the bacter

177 enantiomer-specific toxicity in the case of Tetrahymena thermophila, protozoa that are utilized duri

178 Tetrahymena thermophila RAD51 encodes a 36.3 kDa protein

179 The Tetrahymena thermophila RAD51 gene was recently cloned,

180 The Tetrahymena thermophila rDNA exists as a 21 kb palindrom

181 Self-splicing of the group I IVS from Tetrahymena thermophila rDNA is limited by the time requ

182 tion fork movement, and transcription of the Tetrahymena thermophila rDNA minichromosome and are requ

183 f replication forks and transcription of the Tetrahymena thermophila rDNA minichromosome.

184 ation fork movement and transcription of the Tetrahymena thermophila rDNA minichromosome.

185 The model ciliate Tetrahymena thermophila removes 34% of its germline micr

186 into the genome of a somatic macronucleus in Tetrahymena thermophila requires several DNA rearrangeme

187 -nucleotide bulge of the group I intron from Tetrahymena thermophila results in an electrophoreticall

188 C protein, TIF1, recognizes sequences in the Tetrahymena thermophila ribosomal DNA (rDNA) minichromos

189 horesis was used to study replication of the Tetrahymena thermophila ribosomal DNA (rDNA) minichromos

190 The Tetrahymena thermophila ribosomal DNA (rDNA) replicon co

191 During macronuclear development the Tetrahymena thermophila ribosomal RNA gene is excised fr

192 lent cation-induced folding of the L-21 Sca1 Tetrahymena thermophila ribozyme and a selected mutant w

193 inding in the folding of the P4-P6 domain of Tetrahymena thermophila ribozyme by examining the Mg2+-i

194 e Mg(2+)-dependent folding of the L-21 Sca 1 Tetrahymena thermophila ribozyme has been followed using

195 The Mg2 +-mediated folding of the Tetrahymena thermophila ribozyme is characterized by rap

196 d the catalysis by and folding of individual Tetrahymena thermophila ribozyme molecules.

197 compaction upon Mg2+-mediated folding of the Tetrahymena thermophila ribozyme.

198 -helix junction, and the P5abc domain of the Tetrahymena thermophila ribozyme.

199 ctivities of different split variants of the Tetrahymena thermophila ribozyme.

200 and fold during Mg2+-mediated folding of the Tetrahymena thermophila ribozyme.

201 ibosome entry sequence of hepatitis C virus, Tetrahymena thermophila rRNA intron, 100 tRNAs and 14 RN

202 The Tetrahymena thermophila self-splicing RNA is trapped in

203 In the self-splicing group I intron from Tetrahymena thermophila, several divalent metals can ser

204 During differentiation of the Tetrahymena thermophila somatic nucleus, its germline-de

205 The NMR structure of Tetrahymena thermophila stem-loop IV shows a highly stru

206 The Tetrahymena thermophila strain SB281 fails to synthesize

207 dicted structural similarities for human and Tetrahymena thermophila telomerase as well as the specie

208 An active Tetrahymena thermophila telomerase complex can be recons

209 Tetrahymena thermophila telomerase contains two essentia

210 Here we describe the architecture of Tetrahymena thermophila telomerase holoenzyme determined

211 nce of telomere binding by each of the seven Tetrahymena thermophila telomerase holoenzyme proteins T

212 entification of three additional subunits of Tetrahymena thermophila telomerase holoenzyme.

213 lass of atypical RRM first identified in the Tetrahymena thermophila telomerase LARP7 protein p65.

214 the sequences and structures of recombinant Tetrahymena thermophila telomerase RNA necessary for phy

215 Here, using circularly permuted variants of Tetrahymena thermophila telomerase RNA, we identify the

216 structure of the TBE element (helix II) from Tetrahymena thermophila telomerase RNA.

217 In Tetrahymena thermophila telomerase, LARP7 protein p65 to

218 tic activity and protein-RNA interaction for Tetrahymena thermophila telomerase.

219 first complete replacement of the nine base TETRAHYMENA: thermophila telomerase templating region in

220 e about the structure of the DNA terminus at Tetrahymena thermophila telomeres, we have devised a lig

221 In Tetrahymena thermophila, telomeres become long at 30 deg

222 We previously purified epitope-tagged Tetrahymena thermophila TERT and characterized two of th

223 such as Saccharomyces cerevisiae (yeast) and Tetrahymena thermophila (Tet), for example, contain more

224 e interaction of telomeric DNA fragment from Tetrahymena thermophila (TET25, 5'-G(TTGGGG)(4-)3') with

225 We have identified a family of genes in Tetrahymena thermophila that encode proteins homologous

226 We identified a gene, TWI1, in Tetrahymena thermophila that is homologous to piwi and i

227 We report a pioneering approach using Tetrahymena thermophila that permits rapid identificatio

228 ciliate species--Paramecium tetraurelia and Tetrahymena thermophila--that reassign the stop codons T

229 In the ciliated protozoan Tetrahymena thermophila the ribosomal DNA (rDNA) minichr

230 In Tetrahymena thermophila, the cdaA alleles prevent the fo

231 In Tetrahymena thermophila, the development of a transcript

232 Here, we characterize, in the protist Tetrahymena thermophila, the EZL1 (E(z)-like 1) complex,

233 ker histone H1 knockout strain (delta H1) of Tetrahymena thermophila, the number of mature RNAs produ

234 In the genome of Tetrahymena thermophila, the only ORF sharing similariti

235 In the ciliate Tetrahymena thermophila, the polypeptides stored in secr

236 In ciliates such as Tetrahymena thermophila, the resulting crystals function

237 In the ciliate Tetrahymena thermophila, the telomerase holoenzyme consi

238 In the ciliate Tetrahymena thermophila, thousands of DNA segments of va

239 ere we describe a unique ORC-like complex in Tetrahymena thermophila, TIF4, which bound in an ATP-dep

240 lectron microscopy studies were performed in Tetrahymena thermophila to determine how proteins assemb

241 We used the ciliate protist Tetrahymena thermophila to gain a better understanding o

242 chers have manipulated the unique biology of Tetrahymena thermophila to generate a premier experiment

243 RNase P activity from the ciliate protozoan Tetrahymena thermophila to learn more about the biochemi

244 ted proteins from the macronuclear genome of Tetrahymena thermophila to query prokaryotic and eukaryo

245 xamined the respiratory chain of the ciliate Tetrahymena thermophila (Tt).

246 he doublet microtubule (DMT) in the cilia of Tetrahymena thermophila using a combination of cryo-elec

247 lyzed the role of tubulin polyglycylation in Tetrahymena thermophila using in vivo mutagenesis and im

248 essed MWCNT bioaccumulation in the protozoan Tetrahymena thermophila via trophic transfer from bacter

249 acronuclear genome of the ciliated protozoan Tetrahymena thermophila was analyzed by indirect end lab

250 tagenesis and homologous gene replacement in Tetrahymena thermophila, we analyzed mutations, deletion

251 ccumulation experiments in the model ciliate Tetrahymena thermophila, we estimate that its base-subst

252 hnique and exploiting the unique genetics of Tetrahymena thermophila, we have identified and characte

253 In the ciliate Tetrahymena thermophila, we identified TXR1, encoding a

254 ronuclear genomes of Oxytricha trifallax and Tetrahymena thermophila, we prove that ADFinder is effec

255 For the first time in Tetrahymena thermophila, we use comparative whole-genome

256 Mating Tetrahymena thermophila were bombarded with ribosomal DN

257 breakage has been most rigorously defined in Tetrahymena thermophila, where it consists of a 15-bp DN

258 To address this question we used Tetrahymena thermophila, which expresses two SAS-6 homol

259 truct is a modification of tRNAGln(CUA) from Tetrahymena thermophila, which naturally recognizes the

260 estigate nine variants of telomeric DNA from Tetrahymena thermophila with the repeat (TTGGGG)n.

261 modification and microtubule-based movement, Tetrahymena thermophila xylan catabolism and meiosis, Di