ライフサイエンスコーパス: transcribed spacer

1 included the 16S rRNA gene and the internal transcribed spacer.

2 region spanning the promoter and 5' external transcribed spacer.

3 to the rDNA promoter and to the 5'- external transcribed spacer.

4 sts and, in phase 2, sequencing the internal transcribed spacers.

5 kinetoplast DNA (kDNA) PCR, nested internal transcribed spacer 1 (ITS-1) PCR, and a PCR-hybridizatio

6 fic probes were directed toward the internal transcribed spacer 1 (ITS-1) region and tested in a mult

7 the hypervariable sequences of the internal transcribed spacer 1 (ITS-1) region of the rRNA gene com

8 hological measurements of males and internal transcribed spacer 1 (ITS-1) sequences of rDNA between t

9 Internal Transcribed Spacer 1 (ITS1) amplicons were sequenced by

10 Genotyping based on internal transcribed spacer 1 (ITS1) and ITS2 of the rRNA operon

11 he mouse pre-rRNA transcript in the internal transcribed spacer 1 (ITS1) are affected by depletion of

12 Processing in internal transcribed spacer 1 (ITS1) is a key step that separates

13 5-ends at processing site A2 in the internal transcribed spacer 1 (ITS1) region of the rRNA primary t

14 fication (LAMP) assay targeting the Internal Transcribed Spacer 1 (ITS1) region of these pathogens fo

15 tion and sequencing of the D1D2 and internal transcribed spacer 1 (ITS1) regions of the nuclear ribos

16 M. intracellulare were confirmed by internal transcribed spacer 1 (ITS1) sequencing and characterized

17 generated by Rat1 digestion of the internal transcribed spacer 1 (ITS1) spacer from cleavage site A(

18 servation and molecular analysis of internal transcribed spacer 1 (ITS1), 18S ribosomal RNA (18S rRNA

19 To test this hypothesis, the internal transcribed spacer 1 (ITS1), 5.8S, and ITS2 from eight h

20 equences from the 5'-ETS core, 18S, internal transcribed spacer 1 (ITS1), and 28S segments and also h

21 PCR amplification and sequencing of internal transcribed spacer 1 (ITS1), was employed.

22 as confirmed by sequencing of the internally transcribed spacer 1 (ITS1)-5.8S-ITS2 rRNA-encoding regi

23 as confirmed by sequencing of the internally transcribed spacer 1 (ITS1)-5.8S-ITS2 rRNA-encoding regi

24 ndidate genera encountered in prior internal transcribed spacer 1 (ITS1)-based surveys.

25 d to recognise FAWs on the basis of internal transcribed spacer 1 (ITS1).

26 cation showed 100% concordance with internal transcribed spacer 1 (ITS1)/ITS2 sequencing and proved t

27 Using 16S ribosomal RNA (V1-V3) and internal transcribed spacer 1 amplicon sequencing analyzed with D

28 this cross-sectional study, we use internal transcribed spacer 1 amplicon sequencing to evaluate the

29 mic DNA from dust was extracted for internal transcribed spacer 1 Illumina MiSeq sequencing to identi

30 bind overlapping regions within the internal transcribed spacer 1, and both bind directly over cleava

31 RNA processing intermediate, the 5' internal transcribed spacer 1, indicate that bud23 mutants are de

32 We used internal transcribed spacer 1-based metabarcoding to compare feca

33 subunit RNA gene (D1-D2 region) and internal transcribed spacers 1 and 2 (ITS1 and ITS2 regions), hav

34 nd Tibet, and the nuclear ribosomal internal transcribed spacer-1 sequences from each sample were obt

35 Sequences of the Internal Transcribed Spacer 2 (ITS-2) regions of the nuclear rDNA

36 rs to amplify a segment of the rRNA internal transcribed spacer 2 (ITS2) from multiple Leishmania spe

37 ribosomal DNA (rDNA) and 5.8S rDNA/internal transcribed spacer 2 (ITS2) Malassezia-specific PCR prim

38 9 polynucleotide kinase to form the internal transcribed spacer 2 (ITS2) pre-rRNA endonuclease-kinase

39 nventional PCR amplification of the internal transcribed spacer 2 (ITS2) region (ITS2-PCR) followed b

40 DNA sequence analysis of the internal transcribed spacer 2 (ITS2) region of rRNA genes from re

41 The internal transcribed spacer 2 (ITS2) region of the fungal ribosom

42 on of sequence polymorphisms in the internal transcribed spacer 2 (ITS2) region of the rRNA genes as

43 ific polymorphisms in the noncoding internal transcribed spacer 2 (ITS2) region of the rRNA operon pr

44 found that sequence analysis of the internal transcribed spacer 2 (ITS2) region provided further iden

45 This assay targeted the internal transcribed spacer 2 (ITS2) ribosomal gene by obtaining

46 exit, and the domain including the internal transcribed spacer 2 (ITS2) that separates 5.8S and 25S

47 tochrome c oxidase subunit 1 (COI), internal transcribed spacer 2 (ITS2), and tyrosine hydroxylase (T

48 y of these proteins bind at or near internal transcribed spacer 2 (ITS2), but in their absence, ITS1

49 PCR amplicons from the internal transcribed spacer 2 and the D2 region of 28S ribosomal

50 e genotyping analysis targeting the Internal transcribed spacer 2 of rDNA, we report for the first ti

51 encing analysis of a portion of the internal transcribed spacer 2 region (ITS2) for identification of

52 probes were designed to target the internal transcribed spacer 2 region of Coccidioides.

53 onucleotide probes, directed to the internal transcribed spacer 2 region of ribosomal DNA from Asperg

54 fects in processing of the pre-rRNA internal transcribed spacer 2 region.

55 Next-generation metagenomics and internal transcribed spacer 2 sequencing delineated fecal bacteri

56 for the endonucleolytic cleavage in internal transcribed spacer 2 that separates the 5.8S rRNA from t

57 ear genetic loci such as 5.8S rRNA, Internal Transcribed Spacer 2, and 28S rRNA regions, which are co

58 g amplicon sequencing of the fungal internal transcribed spacer 2, we studied the root and rhizospher

59 Independently, the ribosomal DNA internal transcribed spacer-2 (ITS-2) regions from these species

60 The panfungal PCR using internal transcribed spacer 3 (ITS3) and ITS4 primers yielded a p

61 The T.thermophila 5' non-transcribed spacer (5' NTS) is sufficient for replicatio

62 nts that include cleavage of the 5' external transcribed spacer (5'ETS) and 18S rRNA maturation.

63 The 5' external transcribed spacer (5'ETS) is removed from pre-small sub

64 olic controls using fungal-specific internal transcribed spacer amplicon sequencing of fecal samples.

65 on was confirmed using 26S-rDNA and internal transcribed spacer amplifications.

66 ive sequence analyses by use of the internal transcribed spacer and beta-tubulin regions.

67 ed by DNA sequencing using both the internal transcribed spacer and D1/D2 region of the 28S ribosomal

68 uences and the boundary between the external transcribed spacer and the 18S coding sequence in a clon

69 owed that a large segment of the 5' external transcribed spacer and the entire first internal transcr

70 biogenesis complexes assist the 5' external transcribed spacer and U3 small nucleolar RNA in providi

71 terminator sequences are present in rDNA non-transcribed spacers and a region immediately preceding t

72 , and also sequence analysis of the internal-transcribed-spacer and D1/D2 rDNA regions, the yeast was

73 C-01 nucleotide sequences (gltA and internal transcribed spacer) and protein band banding pattern wer

74 nteractions, designated the U3-ETS (external transcribed spacer) and U3-18S duplexes, are essential t

75 ication initiates from origins in the 5' non-transcribed spacer, and forks moving toward the center o

76 , the major SIR-Responsive Region in the non-transcribed spacer, and SRR2, in the 18S rRNA coding reg

77 Nevertheless, embedded in the internal transcribed spacers are several short sequence elements

78 e identified by sequencing the 5.8S internal transcribed spacer as Pichia fermentans, Wickerhamomyces

79 y subjects followed by 16S gene and internal transcribed spacer-based microbiota sequencing.

80 scribed spacer and the entire first internal transcribed spacer, both of which flank 18S rRNA, are no

81 work analysis based on 16S rDNA and internal transcribed spacer deep sequencing.

82 The transcribed spacers differ very extensively from those o

83 ns and deletions have played a major role in transcribed spacer divergence in Xenopus.

84 h mitochondrial (cox1) and nuclear (internal transcribed spacer) DNA data from the Schistosoma eggs o

85 is in turn implies that large regions of the transcribed spacers do not play a sequence-specific role

86 osomal and transfer RNA maturation, external transcribed spacer (ETS) and internal transcribed spacer

87 nd the subsequent removal of the 3' external transcribed spacer (ETS) at the dense fibrillar componen

88 n in rRNA or snRNA processing, 5' externally transcribed spacer (ETS) degradation, or viability.

89 did not contain the short-lived 5'-external transcribed spacer (ETS) leader segment upstream from th

90 of by-products derived from the 5'-external transcribed spacer (ETS) of 45S pre-rRNA, as MTR4 does.

91 e interaction with region E1 of the external transcribed spacer (ETS) of pre-rRNA.

92 u hybridization with a probe to the external transcribed spacer (ETS) region of the pre-rRNA shows th

93 ternal transcribed spacer (ITS) and external transcribed spacer (ETS) sequences.

94 ge and complementary regions in the external transcribed spacer (ETS); these interactions are phyloge

95 better target than the 16S-23S rRNA internal transcribed spacer for DNA sequence-based species identi

96 We used 16S, 18S, plastid and internal transcribed spacer (for Synechococcus strains) sequencin

97 necessary for the removal of the 3' external transcribed spacer from 28S rRNA and productive downstre

98 is required for cleavage of the 3' external transcribed spacer from unprocessed pre-rRNA and for pro

99 biota composition was determined by internal transcribed spacer gene sequencing in HDs (n = 23) and p

100 d of PAM based on sequencing of the internal transcribed spacers, including the 5.8S rRNA genes.

101 biome studies rely on sequencing of internal transcribed spacer (ITS) amplicons.

102 soils were pyrosequenced for fungal internal transcribed spacer (ITS) amplicons.

103 olds were sequence identified using internal transcribed spacer (ITS) and 28S (yeasts) or ITS, transl

104 made using two genetic markers, the internal transcribed spacer (ITS) and a fragment of the beta-tubu

105 ofile, and Sanger sequencing of the internal transcribed spacer (ITS) and D1/D2 regions of the riboso

106 creened by sequence analysis of the internal transcribed spacer (ITS) and D1/D2 ribosomal DNA regions

107 ing tool with great accuracy, while internal transcribed spacer (ITS) and D1/D2 sequencing were succe

108 ic range of the tribe, with nuclear internal transcribed spacer (ITS) and external transcribed spacer

109 ndent set of genotypes for both the internal transcribed spacer (ITS) and large subunit (LSU) ribosom

110 t amplicon sequencing of the fungal internal transcribed spacer (ITS) and prokaryotic 16S DNA regions

111 is, and Debaryomyces fabryi using intergenic transcribed spacer (ITS) and/or intergenic spacer (IGS)

112 encing methods with confirmation by internal transcribed spacer (ITS) and/or partial 16S rRNA gene se

113 The internal transcribed spacer (ITS) as one part of nuclear ribosoma

114 us sequence analysis using rpoB and internal transcribed spacer (ITS) as targets was performed.

115 n based on pyrosequencing of fungal internal transcribed spacer (ITS) barcode markers.

116 Taxa in internal transcribed spacer (ITS) Clade 6 are especially numerous

117 Fungi were isolated, and a fungal internal transcribed spacer (ITS) clone library survey was perfor

118 bacterial 16S rRNA gene and fungal internal transcribed spacer (ITS) copy numbers and extracellular

119 ermatrix data set was combined with internal transcribed spacer (ITS) data sets for Astraeus, Calosto

120 f ECM fungi was determined using an internal transcribed spacer (ITS) database terminal restriction f

121 sequence analysis of the ribosomal internal transcribed spacer (ITS) from specimens obtained from hu

122 nt using Illumina sequencing of the internal transcribed spacer (ITS) gene.

123 g to isolate and characterize nrDNA internal transcribed spacer (ITS) homeologues from multiple acces

124 The sequences of the internal transcribed spacer (ITS) of Pneumocystis carinii f. sp.

125 Variation in the internal transcribed spacer (ITS) of the rRNA (rrn) operon is inc

126 DNA barcoding of nuclear ribosomal internal transcribed spacer (ITS) of the rRNA gene with fungal sp

127 n the number of GTTT repeats in the internal transcribed spacer (ITS) of the rRNA have been described

128 We found that the internal transcribed spacer (ITS) of the X-linked rDNA has two di

129 subunit (SSU) rRNA genes and fungal Internal Transcribed Spacer (ITS) rDNA sequences, samples contain

130 conserved portion of the T. foetus internal transcribed spacer (ITS) region (ITS1 and ITS2) and the

131 0% in agreement with the contiguous internal transcribed spacer (ITS) region (ITS1-5.8S-ITS2) sequenc

132 Sequencing of the internal transcribed spacer (ITS) region (ITS1-5.8S-ITS2) was per

133 g 16S ribosomal RNA (rRNA) gene and internal transcribed spacer (ITS) region amplicon sequencing, we

134 ochrome b as well as in the nuclear internal transcribed spacer (ITS) region and 28 S rRNA.

135 h included sequence analysis of the internal transcribed spacer (ITS) region and a fragment of the la

136 It targets the nuclear ribosomal internal transcribed spacer (ITS) region and offers nearly 10 mil

137 Using internal transcribed spacer (ITS) region as the phylogenetic mark

138 f PCR products generated from the intergenic transcribed spacer (ITS) region did not differentiate am

139 R targeting the 16S-23S rRNA gene intergenic transcribed spacer (ITS) region has been proposed as a r

140 gions of the ribosomal cistron, the internal transcribed spacer (ITS) region has the highest probabil

141 The ribosomal DNA internal transcribed spacer (ITS) region of a recently cultured h

142 Primers for the internal transcribed spacer (ITS) region of nuclear rRNA genes an

143 mparing their DNA sequences for the internal transcribed spacer (ITS) region of the 18S-26S ribosomal

144 The internal transcribed spacer (ITS) region of the ribosomal DNA is

145 , a nested PCR method targeting the internal transcribed spacer (ITS) region of the rRNA operon was v

146 control PCR, and PCR targeting the internal transcribed spacer (ITS) region were shown.

147 PCR assay targeting the 16S-to-23S internal transcribed spacer (ITS) region with use of MGB Eclipse

148 The genetic markers used were the internal transcribed spacer (ITS) region, and fragments of the be

149 The contiguous internal transcribed spacer (ITS) region, ITS 1-5.8S-ITS 2, from

150 Based on the sequences of the internal transcribed spacer (ITS) region, the fungi were identifi

151 ungal barcode-the nuclear ribosomal internal transcribed spacer (ITS) region-and offers all ~1 000 00

152 d on the variable 16S-23S rRNA gene internal transcribed spacer (ITS) region.

153 by 454 pyrosequencing of the fungal internal transcribed spacer (ITS) region.

154 n of the 28S ribosomal gene and the internal transcribed spacer (ITS) regions 1 and 2 of the rRNA ope

155 nce analysis of the ribosomal DNA intergenic transcribed spacer (ITS) regions and the D1-D2 variable

156 The intervening transcribed spacer (ITS) regions between the small- and

157 First, two internal transcribed spacer (ITS) regions flanking the 5.8S subun

158 ty of sequences of the nuclear rDNA internal transcribed spacer (ITS) regions for phylogenetic analys

159 The secondary structure of the internal transcribed spacer (ITS) regions of nuclear rRNA transcr

160 uence analysis of the hypervariable internal transcribed spacer (ITS) regions of ribosomal DNA (rDNA)

161 The nucleotide sequences of internal transcribed spacer (ITS) regions of rRNA genes of 24 iso

162 ysis of the large subunit (LSU) and internal transcribed spacer (ITS) regions of the nuclear ribosoma

163 sequence analysis that included the internal transcribed spacer (ITS) regions of the nuclear ribosoma

164 n was achieved by sequencing of the internal transcribed spacer (ITS) regions of the rRNA gene and by

165 tube nested PCR which amplifies the internal transcribed spacer (ITS) regions of the rRNA genes of hu

166 nce variations in the ITS1 and ITS2 internal transcribed spacer (ITS) regions of the rRNA genes were

167 n of the secondary structure of the internal transcribed spacer (ITS) regions separating nuclear ribo

168 ific primers were designed from the internal transcribed spacer (ITS) regions, ITS1 and ITS2, of the

169 as identified by fungal culture and internal transcribed spacer (ITS) ribosomal DNA (rDNA) sequencing

170 ence analysis of the 283-bp 16S-23S internal transcribed spacer (ITS) sequence showed only 95% identi

171 heir origin was traceable via their internal transcribed spacer (ITS) sequence to five distinct Panic

172 id and nuclear ribosomal DNA (rDNA) internal transcribed spacer (ITS) sequence variation within the C

173 ternal transcribed spacer (ETS) and internal transcribed spacer (ITS) sequences are excised and, as n

174 ylogenetic analysis of nuclear rDNA internal transcribed spacer (ITS) sequences from a worldwide samp

175 cum, Winteraceae, and Zea ribosomal internal transcribed spacer (ITS) sequences.

176 ping was performed using 3'hsp65and internal transcribed spacer (ITS) sequencing.

177 t sequencing for the 16S-23S rRNA internally transcribed spacer (ITS) to examine ecotype and fine-sca

178 The identification of P. jirovecii internal transcribed spacer (ITS) types was performed on P. jirov

179 sed variation in nuclear sequences (internal transcribed spacer (ITS)) and two types of chloroplast D

180 arkers used for sequencing were the internal transcribed spacer (ITS), a portion of the nuclear large

181 ress this question using the fungal internal transcribed spacer (ITS), which is central in many phylo

182 locations in China were examined by internal transcribed spacer (ITS)-based PCR.

183 The internal transcribed spacers (ITS) exhibit concerted evolution by

184 Portions of two transcribed spacers (ITS-1 and 5' ETS) and the non-trans

185 ompared with genomic DNA sequences (internal transcribed spacer, ITS).

186 ucted using sequences from nuclear (internal transcribed spacer, ITS; and alcohol dehydrogenase 1A, A

187 it of ribosomal RNA (rRNA), and the internal transcribed spacer ITS1 of rRNA established an order for

188 r distinct sites located within the internal transcribed spacers ITS1 and ITS2 and the 3' external sp

189 tial sequences of nuclear ribosomal internal transcribed spacers (ITS1 and ITS2) and intergenic space

190 The two internal transcribed spacers (ITS1 and ITS2) of nuclear ribosomal

191 zed as a single transcript with two internal transcribed spacers (ITS1 and ITS2), which are removed b

192 e preferentially cleaved the second internal transcribed spacer (ITS2) approximately 250 nt downstrea

193 One [second internal transcribed spacer (ITS2) of the nuclear ribosomal DNA]

194 lear small-subunit rDNA, and second internal transcribed spacer, mitochondrial large-subunit rDNA, an

195 loroplast DNA and nuclear ribosomal internal transcribed spacer (nrITS) phylogenies.

196 ribed spacers (ITS-1 and 5' ETS) and the non-transcribed spacer (NTS) or intergenic spacer (IGS) form

197 Sequence analysis of the ribosomal internal transcribed spacer of 56 Mycobacterium avium complex iso

198 U3 subsequently base pairing to the external transcribed spacer of pre-rRNA, thus positioning U3 snoR

199 S ribosomal RNA, D2-D3 of 28S rRNA, internal transcribed spacer of rRNA, mitochondrial cytochrome oxi

200 gion and complementary bases in the external transcribed spacer of the pre-rRNA.

201 types identified by analysis of the internal transcribed spacer of the rRNA gene.

202 confirmed to be Sporothrix genus by internal transcribed spacer or beta-tubulin PCR sequencing were i

203 ts containing sequences from the 5' external transcribed spacer or the first internal transcribed spa

204 th polymorphisms of PCR products (intergenic transcribed spacer PCR [ITS-PCR] ribotyping) could disti

205 evidence for recombination in their internal transcribed spacer profiles indicates that they are of r

206 S rRNA gene and fungal nuclear rRNA internal transcribed spacer profiling.

207 The internal transcribed spacer region (ITS) of the nuclear rDNA cist

208 s performed by amplification of the internal transcribed spacer region (ITS) that contained the targe

209 ation and genomic sequencing of the internal transcribed spacer region (ITS), partial beta-tubulin (B

210 cleotide sequence variations in the internal transcribed spacer region 1 (ITS1) and region 2 (ITS2) o

211 After bronchoscopy, ribosomal internal transcribed spacer region 1 DNA was amplified and sequen

212 PCR amplification and sequencing of internal transcribed spacer region 1.

213 lar screening and DNA sequencing of internal transcribed spacer region 1.

214 g (~80-90%) and members of the same internal transcribed spacer region 2 (ITS2) type were phylogeneti

215 base-pair fragments of DNA from the internal transcribed spacer region 2 from 28 historic herbarium s

216 We amplified the internal transcribed spacer region 2 of the nuclear ribosomal ope

217 ncing analysis of 20 nucleotides of internal transcribed spacer region 2 rapidly and robustly disting

218 16S ribosomal RNA gene) and fungal (internal transcribed spacer region 2) biomarker sequencing.

219 6S amplicon sequencing) and fungal (internal transcribed spacer region amplicon sequencing) communiti

220 Amplification of the internal transcribed spacer region and 5.8S rRNA, beta-tubulin, a

221 s of the following three genes: the internal transcribed spacer region and domains D1 plus D2 of the

222 Phylogenetic analysis of the internal transcribed spacer region and portions of the beta-tubul

223 targets including the 16S-23S rDNA internal transcribed spacer region and the rpoB gene (partial seq

224 clade, large-subunit ribosomal and internal transcribed spacer region DNA sequences were determined

225 utility of sequence analysis of the internal transcribed spacer region is highlighted; however, furth

226 ribosomal DNA probe specific to the external transcribed spacer region located at the 5' end of the r

227 at the two tandem termini present in the non-transcribed spacer region located between the sequences

228 alysis based on the sequence of the internal transcribed spacer region of fungal ribosomal RNA encodi

229 phylogeny based on sequences of the internal-transcribed spacer region of nuclear ribosomal DNA to tr

230 irected at the amplification of the internal transcribed spacer region of the Mycobacterium genome wi

231 Internal transcribed spacer region of the nuclear rDNA (ITS) sequ

232 agment length polymorphism of the internally transcribed spacer region of the rRNA operon (ITS PCR-RF

233 ribosomal DNA probe specific to the external transcribed spacer region or to the 28S region of the ri

234 um using 16S ribosomal RNA gene and internal transcribed spacer region sequencing to profile bacteria

235 fied polymorphic DNA analysis and internally transcribed spacer region sequencing, by testing species

236 he 16S rRNA gene, 18S rRNA gene and internal transcribed spacer region sequencing, we analysed multip

237 ods were identified on the basis of internal transcribed spacer region sequencing.

238 con sequencing of the ribosomal RNA internal transcribed spacer region to examine the microdiversity

239 P. gingivalis-specific amplification was the transcribed spacer region within the ribosomal operon.

240 f the rRNAs (5S, 16S and 23S), an internally transcribed spacer region, and the number of tRNA genes.

241 the bacterial 16S rRNA and fungal internally transcribed spacer region, as well as bacterial genus-sp

242 g, respectively, atpE genes and the internal transcribed spacer region.

243 ndent upon sequence analysis of the internal transcribed spacer region.

244 ently it has mostly been reported in the non-transcribed spacer region.

245 specific sequence, belonging to the Internal Transcribed Spacers region, was used to design the real-

246 isms (RFLPs) of the PCR-amplified intergenic transcribed spacer regions (including the 5.8S ribosomal

247 A unique primer set amplified internal transcribed spacer regions (ITS) 1 and 2 of the rRNA ope

248 of the nuclear ribosomal RNA (rRNA) internal transcribed spacer regions (ITS1 and -2) to detect and d

249 nomic assertions based on ribosomal internal transcribed spacer regions (ITS1/2) and expanded protein

250 sm (TRFLP) and sequencing of cloned internal transcribed spacer regions and 16S rRNA genes, respectiv

251 Here we use analyses of the nuclear internal transcribed spacer regions and other genetic traits to r

252 eaction primer set that targets the internal transcribed spacer regions between conserved bacterial g

253 porulating molds (NSM).We sequenced internal transcribed spacer regions from 50 cultures of NSM and f

254 cleotide sequence variations in the internal transcribed spacer regions I and II (ITS1 and ITS2, resp

255 The sequences of ITS1 of the internal transcribed spacer regions of nuclear ribosomal DNA from

256 sing sequences of both ndhF and the internal transcribed spacer regions of nuclear ribosomal DNA reve

257 y PCR with primers specific for the internal transcribed spacer regions of rRNA.

258 Target sequences in the noncoding internal transcribed spacer regions of the rRNA operon were simul

259 tive nucleotide bases in repetitive internal transcribed spacer regions of the rRNA-encoding DNA (rDN

260 rmatitidis; for 5, we sequenced the internal transcribed spacer regions, and for 4 others the whole g

261 rmatitidis; for 5, we sequenced the internal transcribed spacer regions, and for the other 4 we seque

262 the D1/D2 region of ribosomal DNA, internal transcribed spacer regions, and intergenic spacer region

263 e of 18S and 28S ribosomal genes, internally transcribed spacer regions, and mitochondrial genes.

264 riations were identified within the internal transcribed spacer regions.

265 Sequence analysis of the internal transcribed spacer revealed the isolate to be closely re

266 lar pre-ribosomal assembly - the 5' external transcribed spacer ribonucleoprotein - provides a mechan

267 ome requires the presence of the 5' external transcribed spacer RNA and all ribosomal RNA domains.

268 ents adjacent to the telomere, followed by a transcribed Spacer sequence, a G-rich microsatellite and

269 Cloned internal transcribed spacer sequences (ITS-1 and ITS-2, flanking

270 od phylogenetic methods to identify internal transcribed spacer sequences from the UNITE database for

271 (A0) in the 3' region of vertebrate external transcribed spacer sequences.

272 nomic units, representing worldwide internal transcribed spacer sequences.

273 We performed 18S and internal transcribed spacer sequencing and used the neutral model

274 Bacterial 16S rDNA and fungal internal transcribed spacer sequencing was used to profile organi

275 nd the oral fungal microbiome using internal transcribed spacer sequencing.

276 riome (16S rRNA) and mycobiome (18S Internal Transcribed Spacer) sequencing (total, 228 microbiomes).

277 production is sustained upon introduction of transcribed spacers that reposition SNV RU5 35 to 200 nu

278 nal transcribed spacer or the first internal transcribed spacer, the enzyme preferentially cleaved th

279 the nucleotide sequences of the two internal transcribed spacers, the adjacent ribosomal coding seque

280 fication, zinc finger protein, rRNA external transcribed spacer, thymosin beta-4, cyclin B1 and sever

281 le regions (e.g. 16S rRNA or fungal Internal Transcribed Spacer) to assess diversity or compare popul

282 e of this study was to evaluate the Internal Transcribed Spacer units 1 and 2 (ITS) of the rDNA opero

283 regions of chloroplast DNA and rDNA internal transcribed spacer were incongruent in most New World sp

284 tion of pre-ribosomal RNA at the 5' external transcribed spacer, which directs the early association

285 In contrast the non-transcribed spacer, which makes up the majority of the 4

286 tes by DNA sequence analysis of the internal transcribed spacer with or without D1/D2 ribosomal RNA r