ライフサイエンスコーパス: ribosomal DNA

1 small RNA called qiRNA that originates from ribosomal DNA.

2 g of variable regions 7-9 of prokaryotic 16S ribosomal DNA.

3 ilin modulates the association of Pol I with ribosomal DNA.

4 e profile of hybrids, enhancing formation at ribosomal DNA.

5 g transcriptional silencing at telomeres and ribosomal DNA.

6 ctors of translation, RNA polymerase III and ribosomal DNA.

7 accharide binding protein, and microbial 16s ribosomal DNA.

8 cription at telomeres, mating-type loci, and ribosomal DNA.

9 gulator complex recruitment to telomeres and ribosomal DNA.

10 g pyrosequencing of the V4 region of the 18S ribosomal DNA.

11 y elevated H3.3 occupancy, including the 45S ribosomal DNA (45S rDNA) loci, where loss of ATRX result

12 rom four nuclear gene fragments (18S and 28S ribosomal DNA, abdominal-A and RNA polymerase II) and re

13 ion of the fecal microbiota, analyzed by 16S ribosomal DNA amplicon sequencing.

14 lation forms a key element in the control of ribosomal DNA amplification as overexpression of PNC1 su

15 ble, but a number of organisms display rapid ribosomal DNA amplification at specific times or under s

16 rget of rapamycin (TOR) signaling stimulates ribosomal DNA amplification in budding yeast, linking ex

17 We show that ribosomal DNA amplification is regulated by three histon

18 overexpression of PNC1 substantially reduces ribosomal DNA amplification rate.

19 biome using molecular techniques such as 16S ribosomal DNA analysis may lead to interventions that sh

20 By 16S ribosomal DNA analysis, all six permafrost isolates were

21 nscribed spacer (ITS) regions of the nuclear ribosomal DNA and a fragment of the beta-tubulin (Tub) g

22 lus, c-Myc has been shown to be recruited to ribosomal DNA and activate RNA polymerase (pol) I-mediat

23 erminal domain binds G-quadruplex regions at ribosomal DNA and at gene promoters, including the well

24 omplex that is required for transcription of ribosomal DNA and for processing of 18 S rRNA.

25 nscribed spacer (ITS) regions of the nuclear ribosomal DNA and fragments of the translation elongatio

26 ifferentiating neutrophils also repositioned ribosomal DNA and mininucleoli to the lamina-a process t

27 t mitochondrial (matR) and nuclear loci (18S ribosomal DNA and PHYC) place Rafflesiaceae in Malpighia

28 Seminested PCR targeting Mucorales 18S ribosomal DNA and sequencing were performed on formalin-

29 sed in the linear genome, colocalize with 5S ribosomal DNA and U14 small nucleolar RNA at the nucleol

30 ing a telomeric-related repetitive sequence, ribosomal DNA, and a number of unclassified repetitive s

31 XCL10, lipopolysaccharide, soluble CD14, 16S ribosomal DNA, and interferon-alpha2 were associated wit

32 In vivo, Mot1 is associated with the ribosomal DNA, and loss of Mot1 results in decreased rRN

33 We further show that Chd1 directly binds to ribosomal DNA, and that both Chd1(-/-) epiblast cells in

34 strong clustering of centromeres, telomeres, ribosomal DNA, and virulence genes, resulting in a compl

35 In budding yeast, telomeres, the ribosomal DNA array, and HM loci are transcriptionally s

36 n fork barriers in the spacer regions of the ribosomal DNA array.

37 pindle pole body or changing the position of ribosomal DNA arrays resulted in the association of Pol

38 and Saw1 also contribute to the integrity of ribosomal DNA arrays.

39 tes with RNAPI and enforces the stability of ribosomal DNA arrays.

40 ncreased endothelial levels of bacterial 16s ribosomal DNA as well as increased subendothelial accumu

41 16S ribosomal DNA bacterial genes from DNA isolated from adv

42 Transcription of ribosomal DNA by RNA polymerase I is a central feature o

43 studies have shown that transcription of the ribosomal DNA by RNA polymerase I is a major target for

44 to simply be a function of extrachromosomal ribosomal DNA circle production.

45 Rtg2p also suppresses ribosomal DNA circle production.

46 Accumulation of extrachromosomal ribosomal DNA circles (ERCs) appears to be an important

47 in the cellular content of extrachromosomal ribosomal DNA circles (ERCs), which can cause the demise

48 leads to the production of extrachromosomal ribosomal DNA circles, which cause yeast demise.

49 at these factors rapidly exchange on and off ribosomal DNA clusters and that the kinetics of exchange

50 in which the dynamic association of UBF with ribosomal DNA clusters recruits the pol I transcription

51 ication of the ITS2 subregion of the nuclear ribosomal DNA, commonly used for genotyping within this

52 act in concert to mediate rapid, directional ribosomal DNA copy number change.

53 ibosome synthesis capacity of cells with low ribosomal DNA copy number, and we find that these cells

54 t, linking external nutrient availability to ribosomal DNA copy number.

55 Ribosomal DNA data, sequence information from nematode-p

56 cts, many of which necessarily encompass the ribosomal DNA, detailed information on the prevalence an

57 elease prevents heterochromatin formation at ribosomal DNA during quiescence maintenance.

58 ves of silencing loss in the heterochromatic ribosomal DNA during the early phases of aging, followed

59 om across North and South America and used a ribosomal DNA-fingerprinting method to compare bacterial

60 Ribosomal DNA frameworks with sequence data from more th

61 the internal transcribed spacer 2 region of ribosomal DNA from Aspergillus flavus, Aspergillus fumig

62 we have extracted, amplified, and sequenced ribosomal DNA from S. cerevisiae.

63 of essentially full-length PCR-amplified 16S ribosomal DNA from the bronchial aspirates of intubated

64 nt results were resolved by D2 large-subunit ribosomal DNA fungal sequencing.

65 ons and the D1-D2 variable domain of the 28S ribosomal DNA gene (28S), the case isolate and four othe

66 t natural replication-impeding loci like the ribosomal DNA gene cluster.

67 The use of other loci (16S and 18S ribosomal DNA gene regions) also added the detection of

68 Here, we show that treacle is involved in ribosomal DNA gene transcription by interacting with ups

69 reported a function for mammalian treacle in ribosomal DNA gene transcription by its interaction with

70 anscribed spacer and D1/D2 region of the 28S ribosomal DNA gene.

71 actor (UBF) and affects transcription of the ribosomal DNA gene.

72 , the E2 protein interacts with the repeated ribosomal DNA genes found in this location and colocaliz

73 Ribosomal DNA genes in many eukaryotes contain insertion

74 pe 8 (HPV8) E2 protein binds to the repeated ribosomal DNA genes that are found on the short arm of h

75 es, which are present at a high frequency in ribosomal DNA genes, and potently and rapidly represses

76 disruption of the SIN domain lead to loss of ribosomal DNA heterochromatic gene silencing (Lrs(-) phe

77 o examine the V3-V5 regions of bacterial 16S ribosomal DNA in 40 samples of lung from 5 patients with

78 RTG2 did not affect silencing of ribosomal DNA in either grandes or petites, which were s

79 of these organisms, together with feline 28S ribosomal DNA, in a single tube.

80 mutants exhibit similar phenotypes involving ribosomal DNA, including (i) loss of transcriptional sil

81 Silencing of ribosomal DNA increased with replicative age in either t

82 lated from seawater, followed by analysis of ribosomal DNA, indicated that the cells represented thre

83 -length polymorphism analysis of the 16S-23S ribosomal DNA intergenic spacer, clinical isolates of Bo

84 Using DNA sequence analysis of the ribosomal DNA intergenic transcribed spacer (ITS) region

85 pture probes designed in the D1/D2 region of ribosomal DNA, internal transcribed spacer regions, and

86 the factors that influence transcription of ribosomal DNA is lacking.

87 cassettes, and synXII, specifically when the ribosomal DNA is moved to another chromosome.

88 nscribed spacer (ITS) as one part of nuclear ribosomal DNA is one of the most extensively sequenced m

89 Nuclear ribosomal DNA is particularly complex with respect to th

90 ernal transcribed spacer (ITS) region of the ribosomal DNA is the conventional marker region for fung

91 nal transcribed spacer (ITS2) of the nuclear ribosomal DNA] is highly suitable for all.

92 Anopheles species assignments based on ribosomal DNA ITS2 and mitochondrial DNA COI were compar

93 Independent of age, CD4(+) T-cell count, 16S ribosomal DNA load, and regulatory T-cell count, positiv

94 ite present in the nontranscribed spacers of ribosomal DNA, located in chromosome III.

95 Several epigenetic phenomena occur at ribosomal DNA loci in eukaryotic cells, including the si

96 s of host mitotic chromosomes, including the ribosomal DNA loci.

97 ited, along with upstream-binding factor, to ribosomal DNA loci.

98 anscription and genetic recombination at the ribosomal DNA locus (rDNA) have provided insight into th

99 of COMPASS are required for silencing at the ribosomal DNA locus (rDNA), a telomere, and the silent m

100 that occurs preferentially in the repetitive ribosomal DNA locus (rDNA).

101 ect on transcriptional silencing both at the ribosomal DNA locus and at telomeres, suggesting that po

102 The ribosomal DNA locus and the nucleolus seem to be particu

103 stalled at replication fork barriers of the ribosomal DNA locus compared with wild-type cells.

104 Subdomains of the multicopy ribosomal DNA locus containing transcription units of RN

105 calizes with Topo IIalpha on UFBs and at the ribosomal DNA locus, and the timely resolution of both s

106 DNA repeats, found at the ribosomal DNA locus, telomeres and subtelomeric regions,

107 Now we use the ribosomal DNA locus, which is a good model for all stage

108 rporation and increased transcription at the ribosomal DNA locus.

109 A polymerase I-directed transcription of the ribosomal DNA locus.

110 at the 5' end, and originate mostly from the ribosomal DNA locus.

111 silencing of Pol II-transcribed genes in the ribosomal DNA locus.

112 telomere and mating type loci but not at the ribosomal DNA locus.

113 rids (R-loops) that prime replication in the ribosomal DNA locus.

114 plasmic chloroplast (cp) genomes and nuclear ribosomal DNA (nR) are the primary sequences used to und

115 Unusual polymorphism of ribosomal DNA observed in individual spores of AM fungi

116 oup I intron at position S943 of the nuclear ribosomal DNA of the lichen-forming fungus Pleopsidium.

117 The ribosomal DNA origin binding protein Tif1p regulates the

118 to LINE; retrotransposon insertion sites in ribosomal DNA (p<0.01).

119 gradient gel electrophoresis (DGGE) of a 16S ribosomal DNA PCR product was used to differentiate 32 m

120 8S rRNA was accomplished with a (3)H-labeled ribosomal DNA probe specific to the external transcribed

121 t of the nucleolar remodeling complex to the ribosomal DNA promoter.

122 ne tested, but not at the RNAP I-transcribed ribosomal DNA promoter.

123 rotein that recruits RNA polymerase I to the ribosomal DNA promoter.

124 silent VSG ES and immediately downstream of ribosomal DNA promoters and is abundant in the nucleolus

125 n3 activates Pol I, fostering recruitment to ribosomal DNA promoters.

126 bacteria and fungi, measured by 16S and 18S ribosomal DNA quantity.

127 y, using a metagenomic approach based on 16S ribosomal DNA (rDNA) amplification, we demonstrated that

128 soriasis were analyzed using broad-range 18S ribosomal DNA (rDNA) and 5.8S rDNA/internal transcribed

129 akazakii strains were investigated using 16S ribosomal DNA (rDNA) and hsp60 sequencing.

130 Spt6 is essential for Pol I occupancy of the ribosomal DNA (rDNA) and rRNA synthesis.

131 components displayed disorganized nucleoli, ribosomal DNA (rDNA) and satellite DNAs.

132 show that in budding yeast separation of the ribosomal DNA (rDNA) and telomeres also requires Cdc14,

133 nces genomic regions that include telomeres, ribosomal DNA (rDNA) and the cryptic mating-type loci.

134 Effort was focussed on 35S and 5S nuclear ribosomal DNA (rDNA) and the HRS60 satellite family of t

135 target of rapamycin, causes condensation of ribosomal DNA (rDNA) array and nucleolar contraction in

136 n budding yeast, the unique structure of the ribosomal DNA (rDNA) array is thought to cause late SCI

137 In the repetitive ribosomal DNA (rDNA) array of the budding yeast Saccharo

138 The repetitive ribosomal DNA (rDNA) array, however, undergoes little or

139 Tandemly repeated ribosomal DNA (rDNA) arrays are among the most evolution

140 When two ribosomal DNA (rDNA) arrays are present, one native and

141 n the number and the chromosomal location of ribosomal DNA (rDNA) arrays within populations of the al

142 Expansion segments in ribosomal DNA (rDNA) can show length variation at the le

143 liana, 45S rRNA genes are found in two large ribosomal DNA (rDNA) clusters and little is known about

144 This study was undertaken to determine if ribosomal DNA (rDNA) copy number was constant or variabl

145 proliferative gills was used to amplify 16S ribosomal DNA (rDNA) for molecular phylogenetic analyses

146 d support a specific function for H3K56ac in ribosomal DNA (rDNA) gene transcription and nascent rRNA

147 Ribosomal RNA (rRNA) is transcribed from the ribosomal DNA (rDNA) genes by RNA polymerase I (Pol I).

148 Ribosomal DNA (rDNA) genes in eukaryotes are organized i

149 h quiescence, residual replication stress on ribosomal DNA (rDNA) genes leads to the formation of nuc

150 arriers within nontranscribed regions of the ribosomal DNA (rDNA) genes of many eukaryotes to coordin

151 y we used broad-specificity amplification of ribosomal DNA (rDNA) genes to survey organisms present i

152 ork barriers or Ter sites located within the ribosomal DNA (rDNA) intergenic spacer regions during un

153 etrotransposons, and noncoding RNAs from the ribosomal DNA (rDNA) intergenic spacers, consistent with

154 We analyzed plastid and nuclear ribosomal DNA (rDNA) internal transcribed spacer (ITS) s

155 Mitotic disjunction of the repetitive ribosomal DNA (rDNA) involves specialized segregation me

156 The ribosomal DNA (rDNA) is a specialized genomic region not

157 Cohesin binding to the ribosomal DNA (rDNA) is evolutionarily conserved from ba

158 Despite its importance, ribosomal DNA (rDNA) is not included in current genome a

159 Eukaryotic nuclear ribosomal DNA (rDNA) is typically arranged as a series o

160 vegetative cell nuclei, genetically unlinked ribosomal DNA (rDNA) loci are uniquely clustered togethe

161 ese genes, R2 elements have persisted in the ribosomal DNA (rDNA) loci of insects for hundreds of mil

162 lated nucleolar protein that associates with ribosomal DNA (rDNA) loci, where it interacts with the R

163 o promote silencing of genes at telomeric or ribosomal DNA (rDNA) loci.

164 d that 10 chromosomes (two per genome) carry ribosomal DNA (rDNA) loci.

165 ntain transcriptional output from eukaryotic ribosomal DNA (rDNA) loci.

166 d heterochromatin protein 1alpha at multiple ribosomal DNA (rDNA) loci.

167 polymerase II-dependent transcription in the ribosomal DNA (rDNA) locus (rDNA silencing).

168 ound that increased DNA damage occurs at the ribosomal DNA (rDNA) locus in PHF6-deficient cells.

169 evisiae occurs at the HM loci, telomeres and ribosomal DNA (rDNA) locus.

170 the replication of the tandem repeats of the ribosomal DNA (rDNA) locus.

171 zes sequences in the Tetrahymena thermophila ribosomal DNA (rDNA) minichromosome that are required fo

172 Resequencing Project (SGRP) within which the ribosomal DNA (rDNA) of 36 strains of S.cerevisiae were

173 In the ribosomal DNA (rDNA) of Saccharomyces cerevisiae, RNA po

174 ranscribed genes at telomeres and within the ribosomal DNA (rDNA) of the nucleolus.

175 , which confers specificity to the amplified ribosomal DNA (rDNA) origin by base pairing with an esse

176 both traditional methods and broad-range 18S ribosomal DNA (rDNA) polymerase chain reaction, we exami

177 array composed of 10,462 small subunit (SSU) ribosomal DNA (rDNA) probes (7167 unique sequences) sele

178 how further that Tor1 is associated with 35S ribosomal DNA (rDNA) promoter chromatin in a rapamycin-

179 R) by IGF-I increases transcription from the ribosomal DNA (rDNA) promoter in both myeloid cells and

180 -catenin, but only IRS-1 is recruited to the ribosomal DNA (rDNA) promoter.

181 enhance nucleolar occupancy of FGFR2 at the ribosomal DNA (rDNA) promoter.

182 DNA was analyzed both quantitatively by 16S ribosomal DNA (rDNA) quantitative polymerase chain react

183 We discovered a link to ribosomal DNA (rDNA) recombination when we found an inte

184 occurs between the intergenic spacer of the ribosomal DNA (rDNA) repeats and the intergenic sequence

185 lex maintains the integrity and silencing of ribosomal DNA (rDNA) repeats in the nucleolus.

186 The presence of ribosomal DNA (rDNA) repeats on the right arm of chromos

187 Silencing within the yeast ribosomal DNA (rDNA) repeats protects the integrity of t

188 matic over tandem repeat families, including ribosomal DNA (rDNA) repeats, but rDNA methylation was s

189 The Tetrahymena thermophila ribosomal DNA (rDNA) replicon contains dispersed cis-act

190 al of approximately 12 million diatom V9-18S ribosomal DNA (rDNA) ribotypes, derived from 293 size-fr

191 micromorphology, growth at 42 degrees C, and ribosomal DNA (rDNA) sequence analysis, and also sequenc

192 RF) length polymorphisms (T-RFLP) due to 16S ribosomal DNA (rDNA) sequence diversity to rapidly ident

193 iae, that stability of the highly repetitive ribosomal DNA (rDNA) sequences requires a Sir2-containin

194 are usually classified on the basis of their ribosomal DNA (rDNA) sequences.

195 without cultivation by characterizing their ribosomal DNA (rDNA) sequences.

196 ecies identification obtained by partial 16S ribosomal DNA (rDNA) sequencing by the MicroSeq 500 syst

197 ience with a MicroSeq D2 large-subunit (LSU) ribosomal DNA (rDNA) sequencing kit for identification o

198 16S ribosomal DNA (rDNA) sequencing results revealed three n

199 Using small subunit (SSU) ribosomal DNA (rDNA) sequencing, we developed a targeted

200 ulture and internal transcribed spacer (ITS) ribosomal DNA (rDNA) sequencing.

201 -dependent histone deacetylase Sir2 controls ribosomal DNA (rDNA) silencing by inhibiting recombinati

202 lar mechanisms for SUMO-dependent control of ribosomal DNA (rDNA) silencing through the opposing acti

203 The ribosomal DNA (rDNA) tandem array in Saccharomyces cerev

204 Chromosome XII carries the ribosomal DNA (rDNA) that defines the nucleolus, a major

205 ignaling by starvation or rapamycin inhibits ribosomal DNA (rDNA) transcription and causes condensin-

206 plify nucleolar targeting of FGFR2, activate ribosomal DNA (rDNA) transcription and delay differentia

207 nd TCOF1, a nucleolar protein that regulates ribosomal DNA (rDNA) transcription and is mutated in Tre

208 he nucleolus is important for the control of ribosomal DNA (rDNA) transcription and ribosome biogenes

209 complex that functions in the activation of ribosomal DNA (rDNA) transcription by RNA polymerase I (

210 rithms predict that diseases with defects in ribosomal DNA (rDNA) transcription have mitochondrial dy

211 d transcription factor that is essential for ribosomal DNA (rDNA) transcription.

212 ast Rrn3, a 72-kDa protein, is essential for ribosomal DNA (rDNA) transcription.

213 (Pol I) from the nucleolus and inhibition of ribosomal DNA (rDNA) transcription.

214 cation pausing at tRNA genes, telomeres, and ribosomal DNA (rDNA) was not as great as in rrm3Delta ce

215 SWI/SNF physically associated with ribosomal DNA (rDNA) within the coding region, with an a

216 for quantification of EBV types 1 and 2; 16S ribosomal DNA (rDNA), a marker of microbial translocatio

217 r eukaryotic genomic elements, including the ribosomal DNA (rDNA), are composed of repeated sequences

218 nt of the large subunit (LSU) of the nuclear ribosomal DNA (rDNA), as well as fragments of the transl

219 During replication of nuclear ribosomal DNA (rDNA), clashes with the transcription app

220 replication defects at multiple sites within ribosomal DNA (rDNA), including at the replication fork

221 etitive sequences, including centromere, 45S ribosomal DNA (rDNA), knob, and telomere repeats.

222 The transcription of ribosomal DNA (rDNA), the processing of nascent rRNA mol

223 n of loci connected with the function of the ribosomal DNA (rDNA), which itself has high QFP.

224 process their substrates in both 601- and 5S ribosomal DNA (rDNA)-based nucleosomes.

225 By the use of 16S ribosomal DNA (rDNA)-based sequencing, we identified a l

226 mutants also display increased silencing in ribosomal DNA (rDNA).

227 the efficient segregation of the repetitive ribosomal DNA (rDNA).

228 en growth restriction and DNA methylation at ribosomal DNA (rDNA).

229 ed and organized around actively transcribed ribosomal DNA (rDNA).

230 Here, nonnative rRNA gene [ribosomal DNA (rDNA)] copies were identified in a set of

231 ntrolled replication and gene amplification (ribosomal DNA [rDNA] type I elements).

232 ng from imperfect concerted evolution of the ribosomal DNA region follows a U-shaped allele frequency

233 internal transcribed spacer (ITS) and D1/D2 ribosomal DNA regions in an effort to obtain a species i

234 telomere position effect (TPE), silencing of ribosomal DNA, regulation of genes involved in nutrient

235 t replacing a boundary element (IR-R) with a ribosomal DNA repeat (rDNA-R).

236 red for replication fork progression through ribosomal DNA repeats and subtelomeric and telomeric DNA

237 ustering into foci at the nuclear periphery, ribosomal DNA repeats localizing within a single nucleol

238 Spontaneous Brc1 foci colocalize with ribosomal DNA repeats, a region prone to fork pausing an

239 luding a major preference for integration in ribosomal DNA repeats, and 13 other hotspots that contai

240 are required to prevent fork collapse in the ribosomal DNA repeats, and they also prevent irreversibl

241 ENT complex, which mediates silencing at the ribosomal DNA repeats.

242 directly that DNA replication pausing at the ribosomal DNA replication fork barrier (RFB) is accompan

243 ic endonuclease Slx1 to ensure completion of ribosomal DNA replication.

244 ric and silent mating-type loci, but not the ribosomal DNA, requires the Sir proteins.

245 is of whole-cell proteins, and amplified 16S ribosomal DNA restriction analysis indicated the strains

246 Streptococcus bovis strains had the same 16S ribosomal DNA restriction fragment length polymorphism a

247 We examined partial 18S ribosomal DNA (Rns) sequences of Acanthamoeba isolates c

248 simulate multitemplate amplification of 16S ribosomal DNA sample and subsequent detection of these a

249 range of clinical sources were evaluated by ribosomal DNA sequence analysis, multilocus sequence ana

250 Ribosomal DNA sequence data abounds from numerous studie

251 rk of Theaceae based on plastome and nuclear ribosomal DNA sequence data, the temporal history of the

252 The 1,493-bp 16S ribosomal DNA sequence had only 96% homology with L. san

253 Phylogenetic analysis of the 16S ribosomal DNA sequence indicated that this isolate was a

254 ent with these physiological traits, the 16S ribosomal DNA sequence showed that it was phylogenetical

255 quencing Project, we identify a rich seam of ribosomal DNA sequence variation, characterising 1,068 a

256 We analyzed 18S ribosomal DNA sequences across the intermediate plankton

257 Molecular phylogenetic analysis based on 18S ribosomal DNA sequences consistently has placed this spe

258 16S ribosomal DNA sequences in 20 "H. heilmannii"-infected c

259 2062 polymerase chain reaction-amplified 16S ribosomal DNA sequences obtained from the fecal DNAs of

260 More than 90% of the 16S ribosomal DNA sequences recovered from hydrothermal wate

261 obial sensitivities and identical in its 16S ribosomal DNA sequences to the Balamuthia isolate from t

262 this study, we evaluated the utility of 16S ribosomal DNA sequencing as a means of identifying clini

263 obacteria identified by conventional and 16S ribosomal DNA sequencing by using the MicroSeq 500 micro

264 roperties, ultrastructural features, and 16S ribosomal DNA sequencing classified this organism as a n

265 sceptible to all antibiotics tested, and 16S ribosomal DNA sequencing of available isolates to confir

266 munity production, with high-throughput 18 S ribosomal DNA sequencing to elucidate the relationship b

267 Culture, 16S ribosomal DNA sequencing, and histochemistry were used t

268 d microbiota composition was analyzed by 16S ribosomal DNA sequencing.

269 ot be differentiated from one another by 16S ribosomal DNA sequencing; however, the method provides f

270 locations on the nucleosome: (1) the loss of ribosomal DNA silencing (LRS) surface in the nucleosome

271 to clinical isolates representing 2 distinct ribosomal DNA spacer restriction fragment-length polymor

272 Using short-subunit ribosomal DNA (SSU rDNA) sequences as key evidence, with

273 ynthesis, ribonucleotide levels, and affects ribosomal DNA stability, leading to the formation of a n

274 ssion of meiotic recombination, and maintain ribosomal DNA stability.

275 ogenetic analyses of protein markers and 18S ribosomal DNA support the reclassification of E. oleoabu

276 cruzi kinetoplast DNA (TckDNA), T. cruzi 18S ribosomal DNA (Tc18SrDNA), and murine mitochondrial DNA

277 mes, and key functional elements such as the ribosomal DNA tend to be formed of high copy repeated se

278 required for efficient fork movement in the ribosomal DNA, the mating type locus, tRNA, 5S ribosomal

279 ortion of the nuclear large subunit (LSU) of ribosomal DNA, the RNA polymerase II second-largest subu

280 og that promotes the stability of repetitive ribosomal DNA, the same mechanism by which Sir2 extends

281 components differ in their requirements for ribosomal DNA; the two actively assembling components fa

282 KDM4A and consequently its association with ribosomal DNA through the SGK1 downstream kinase.

283 eferentially binds the transcribed region of ribosomal DNA to repress the transcription of ribosomal

284 ies also provide an in vivo model simulating ribosomal DNA transactivation outside the nucleolus, all

285 tochondrial dysfunction caused by defects in ribosomal DNA transcription and activation of the DNA da

286 ort interfering RNA results in inhibition of ribosomal DNA transcription and cell growth.

287 bolism, potentially linking and coordinating ribosomal DNA transcription and pre-rRNA processing to a

288 l of cytidine deaminase-deficient cells, and ribosomal DNA transcription and stability.

289 Increased ribosomal DNA transcription has been proposed to limit m

290 sion, this work supports a role for impaired ribosomal DNA transcription in Cockayne syndrome and sug

291 Indeed, inhibition of ribosomal DNA transcription leads to mitochondrial dysfu

292 ication is exclusively enriched over the 35S ribosomal DNA transcriptional unit.

293 Luciferase and ribosomal DNA trees both indicate that the Lingulodinium

294 the assembly of eNoSC and protecting active ribosomal DNA units from heterochromatin formation.

295 The variable V6-V8 region of bacterial 16S ribosomal DNA was amplified, and PCR amplicons separated

296 Pg ribosomal DNA was found in the aortas, livers, and heart

297 primers and probe targeted to bacterial 16S ribosomal DNA was used to measure the levels of bacteria

298 , Epstein-Barr virus (EBV) and bacterial 16S ribosomal DNA were detected.

299 omponents fail to assemble in the absence of ribosomal DNA, whereas the thermodynamically driven comp

300 Sequencing of the D1-D2 region of the 28S ribosomal DNA yielded Apophysomyces trapeziformis in all