ライフサイエンスコーパス: minichromosome

1 irectly to that of the bulk, non-transcribed minichromosome.

2 protein required for replication of the SV40 minichromosome.

3 a y+ rescue element on a freely segregating minichromosome.

4 centromere present in the Drosophila Dp1187 minichromosome.

5 of DDX5 enhanced transcription from the HBV minichromosome.

6 ion, but not from the additional copy of the minichromosome.

7 ciate with cellular histone proteins to form minichromosomes.

8 endogenous origins and at origins located on minichromosomes.

9 stones associated with the transcribing SV40 minichromosomes.

10 aplotypes of the two polymorphic loci on the minichromosomes.

11 DNA ends to generate functional macronuclear minichromosomes.

12 epresentation of IS elements, similar to the minichromosomes.

13 undant telomeres due to the presence of many minichromosomes.

14 the mitotic stability of centromere-bearing minichromosomes.

15 s, translocations, and formation of acentric minichromosomes.

16 rase delta (POLD1), DNA primase (PRIM1), and minichromosome 6 (MCM6).

17 an be suppressed by the presence of a second minichromosome, a phenomenon termed "trans-suppression."

18 In this study, by using minichromosome affinity purification (MAP) and mass spec

19 omes are tethered to host histones to form a minichromosome also known as an "episome." Histones, whi

20 osomes, but not the cenRNA from the circular minichromosome, an increase in minichromosome loss was s

21 cription of the Tetrahymena thermophila rDNA minichromosome and are required for cell cycle-controlle

22 ments, rearranged into a 'palindromic' 21 kb minichromosome and extensively amplified.

23 cleus of the infected hepatocyte as a stable minichromosome and functions as the viral transcriptiona

24 ent in the chromatin from 48-h-postinfection minichromosomes and disrupted virions.

25 and their histone tail modifications in SV40 minichromosomes and in the SV40 chromatin found in virio

26 se cellular proteins are recruited to cccDNA minichromosomes and induce the posttranslational modific

27 T1, SMCHD1, and PML were recruited to cccDNA minichromosomes and phenocopied the IFN-alpha-induced po

28 ption in the inactive VSG Basic Copy arrays, minichromosomes and procyclin loci.

29 in required for the efficient replication of minichromosomes and the transcriptional regulation of ea

30 in the late direction from what was found in minichromosomes, and the level of modified histones was

31 oresis reveal that sisters of 26 kb circular minichromosomes are held together by catenation as well

32 s easily produced in bacteria, and it formed minichromosomes as HBV cccDNA episome DNA does when it w

33 HPV origin-containing plasmids partition as minichromosomes, attributable to an association of the v

34 HBV covalently closed circular DNA (cccDNA) minichromosome, both in cultured cells in which HBV is r

35 Engineered minichromosomes can be easily constructed by a telomere-

36 For example, minichromosomes can be used as a platform for efficient

37 We employ a biotin-streptavidin minichromosome capture assay to show that yRad51 or hRad

38 red de novo methylation by using replicating minichromosomes carrying various ICs as targets.

39 , and its suppression, using a non-essential minichromosome, Ch(16), in fission yeast.

40 ue DSB could be generated in a non-essential minichromosome, Ch(16), using the Saccharomyces cerevisi

41 The results show that the two types of minichromosome contain the same number of nucleosomes as

42 In contrast, minichromosomes containing 7 kb of chromosomal DNA inclu

43 iotic centromeric cohesion is compromised in minichromosomes depending on their size and cannot be ma

44 two de novo centromeres on Zea mays (maize) minichromosomes derived from euchromatic sites with high

45 A collection of minichromosomes derived from the chromosome type breakag

46 The other eight minichromosomes did not pair with themselves, and the si

47 cohesin rings concatenate individual sister minichromosome DNA molecules.

48 Terminal deletions of a Drosophila minichromosome (Dp(1;f)1187) dramatically increase the p

49 egulation of cenRNAs; an increased loss of a minichromosome; elevated aneuploidy; a down-regulation o

50 Fourteen minichromosomes from this set could pair with each other

51 s at both telomeres and several cross-linked minichromosomes had t-loops at both ends.

52 fragment taken from the VP1 gene in the SV40 minichromosome has been measured in polyacrylamide gels

53 We conclude that in transcribing SV40 minichromosomes histone hyperacetylation and deacetylati

54 traps sister DNAs of circular but not linear minichromosomes implies that cohesin functions using a t

55 Here, using a non-essential minichromosome in fission yeast, we identify roles for t

56 DNA) of hepadnaviruses exists as an episomal minichromosome in the nucleus of an infected hepatocyte

57 ed with multiple human tumors, persists as a minichromosome in the nucleus of B lymphocytes and induc

58 lity as seen by the high-frequency loss of a minichromosome in yeast.

59 The 17alpha HAC vectors generated artificial minichromosomes in 32-79% of the HT1080 clones screened,

60 intain their genomes as extrachromosomal DNA minichromosomes in actively dividing cells.

61 The final construct generates minichromosomes in HT1080 cells and the HPRT gene is exp

62 Minichromosomes in the nuclear genome of Trypanosoma bru

63 Segregation of T. brucei minichromosomes in these stalled cells is impaired, impl

64 histone H3, a correlate of cohesion, in the minichromosomes in which sister chromatids separated dur

65 s by using patch-methylated stable episomes (minichromosomes) in human cells.

66 Despite this, replication of the rDNA minichromosome initiates precociously.

67 ation during the encapsidation of late-stage minichromosomes into virions, we mapped the locations of

68 e found in the regulatory region of the SV40 minichromosome is directed to slide during the formation

69 ive to a normal B chromosome, the progenitor minichromosome is estimated to be at least several megab

70 some-free, while that of the non-transcribed minichromosome is nucleosome covered.

71 t minichromosomes or on host chromosomes and minichromosomes, is confirmed using chromosome conformat

72 e acetylation and methylation throughout the minichromosome LCR/hGH-N domain.

73 rapamycin complex 1 (TORC1) by the increased minichromosome loss 1/ GTPase-activating proteins toward

74 CenRNA knockdown partially alleviates minichromosome loss in cbf1Delta, htz1Delta, and cbf1Del

75 nase domain and rad53 null mutants display a minichromosome loss phenotype, Rad53 is important in the

76 lting in an F391I change) showed a classical minichromosome loss phenotype.

77 Surprisingly, DSB-induced minichromosome loss was significantly reduced in ku70Del

78 the circular minichromosome, an increase in minichromosome loss was still observed, suggesting that

79 elta strains exhibited a modest elevation in minichromosome loss, similar to cbh1Delta or abp1Delta s

80 The minichromosome maintenance (MCM) 2-7 helicase complex fu

81 In the presence of the T. kodakaraensis minichromosome maintenance (MCM) 3' --> 5' DNA helicase,

82 Our studies identified members of the minichromosome maintenance (MCM) complex as potential LA

83 emporally discrete steps: a double hexameric minichromosome maintenance (MCM) complex is first loaded

84 The heterohexameric minichromosome maintenance (MCM) complex is the core com

85 The minichromosome maintenance (MCM) complex is the replicat

86 The minichromosome maintenance (MCM) complex is thought to f

87 one mutation corresponds to a subunit of the minichromosome maintenance (MCM) complex of proteins, MC

88 eukaryotic DNA replication by recruiting the minichromosome maintenance (MCM) complex onto DNA.

89 The origin recognition complex, Cdc6 and the minichromosome maintenance (MCM) complex play essential

90 The minichromosome maintenance (MCM) complex plays essential

91 The DNA translocation activity of the minichromosome maintenance (MCM) complex powers DNA stra

92 port the identification of the heterohexamic minichromosome maintenance (MCM) complex that interacts

93 requires the recruitment of the six-subunit minichromosome maintenance (Mcm) complex to chromatin th

94 he remaining factor that is necessary as the minichromosome maintenance (MCM) complex, a cellular hel

95 The minichromosome maintenance (MCM) complex, a replicative

96 hase, inhibition of chromatin loading of the minichromosome maintenance (Mcm) complex, and a reduced

97 In archaea, the replicative helicase is the minichromosome maintenance (MCM) complex.

98 be a functional homologue of the eukaryotic minichromosome maintenance (MCM) complex.

99 sphorylation of target proteins, such as the minichromosome maintenance (Mcm) complex.

100 for the eukaryotic replicative helicase, the minichromosome maintenance (MCM) complex.

101 n complex containing the ATPase Cdc6 and the minichromosome maintenance (Mcm) complex.

102 rated for recombinant archaeal homohexameric minichromosome maintenance (MCM) complexes and their yea

103 Members of the minichromosome maintenance (MCM) family have pivotal rol

104 The eukaryotic minichromosome maintenance (MCM) family of proteins (MCM

105 The minichromosome maintenance (MCM) family of proteins is c

106 The minichromosome maintenance (MCM) gene family is essentia

107 cyclin, E2F1, cell division cycle (CDC), and minichromosome maintenance (MCM) genes.

108 element (DUE)-binding protein DUE-B and the minichromosome maintenance (MCM) helicase activator Cdc4

109 replication stress presented by a defective minichromosome maintenance (MCM) helicase allele in yeas

110 to replication origins coordinately with the minichromosome maintenance (MCM) helicase and the helica

111 The minichromosome maintenance (MCM) helicase complex is ess

112 st human genome duplication requires loading minichromosome maintenance (MCM) helicase complexes at m

113 aromyces pombe Mcm4,6,7 complex and archaeal minichromosome maintenance (MCM) helicase from Methanoth

114 auses subunit-specific changes of sumoylated minichromosome maintenance (MCM) helicase in addition to

115 The minichromosome maintenance (MCM) helicase is the replica

116 Using minichromosome maintenance (MCM) helicase mutant protein

117 Specifically, minichromosome maintenance (MCM) helicase proteins are l

118 y of a replication origin and recruitment of minichromosome maintenance (MCM) helicase to that origin

119 re-replication complex (pre-RC), such as the minichromosome maintenance (MCM) helicase.

120 Minichromosome maintenance (MCM) helicases are the presu

121 gins requires the loading of two ring-shaped minichromosome maintenance (MCM) helicases around DNA in

122 The solved atomic structure of an archaeal minichromosome maintenance (MCM) homolog provides insigh

123 In many archaea, there is a single minichromosome maintenance (MCM) homologue, presumed to

124 rrent models indicate that direct binding to minichromosome maintenance (MCM) plays a role, but the d

125 analysis, we identified components from the minichromosome maintenance (MCM) protein and chromatin-r

126 The hexameric Minichromosome Maintenance (MCM) protein complex forms a

127 The minichromosome maintenance (Mcm) proteins 2-7 are requir

128 The minichromosome maintenance (MCM) proteins are essential

129 Minichromosome maintenance (MCM) proteins are essential

130 Minichromosome maintenance (MCM) proteins are key elemen

131 Minichromosome maintenance (MCM) proteins are loaded ont

132 The minichromosome maintenance (MCM) proteins are thought to

133 Loading of the six related Minichromosome Maintenance (MCM) proteins as head-to-hea

134 Minichromosome maintenance (MCM) proteins facilitate rep

135 Origin Recognition Complex (ORC) and minichromosome maintenance (MCM) proteins form prereplic

136 Eukaryotes have six minichromosome maintenance (MCM) proteins that are essen

137 This group included all of the minichromosome maintenance (MCM) proteins that are requi

138 and Glossina, but we identified a complex of minichromosome maintenance (MCM) proteins that functiona

139 ication are licensed in G1 by recruiting the minichromosome maintenance (MCM) proteins to form a prer

140 th the PBD of Plk1, we identified two of the minichromosome maintenance (MCM) proteins, Mcm2 and Mcm7

141 aracterize the interactions between LANA and minichromosome maintenance (MCM) proteins, members of th

142 The minichromosome maintenance (MCM) proteins, together with

143 s have suggested a two-step binding mode for minichromosome maintenance (MCM) proteins, with transien

144 Excess dormant origins bound by the minichromosome maintenance (MCM) replicative helicase co

145 The Minichromosome Maintenance (MCM) replicative helicase is

146 Tissue was fixed, immunostained for minichromosome maintenance (MCM)-2, a marker of replicat

147 P(4) reciprocally regulate the expression of minichromosome maintenance (MCM)-2, a protein that is an

148 the origin recognition complex (ORC) and the minichromosome maintenance (MCM)2-7 complex, the replica

149 leads to the assembly of double hexamers of minichromosome maintenance (Mcm2-7) at origin sites.

150 The heterohexameric minichromosome maintenance (MCM2-7) complex is an ATPase

151 well as decreased levels of chromatin-bound minichromosome maintenance (MCM2-7) complex.

152 ation is the assembly of the heterohexameric minichromosome maintenance (MCM2-7) helicase complex at

153 We focus on the minichromosome maintenance (MCM2-7) proteins, which form

154 xample, the archaeal Sulfolobus solfataricus minichromosome maintenance (SsoMCM) helicase has been sh

155 soDnaG) with the replicative S. solfataricus minichromosome maintenance (SsoMCM) helicase on DNA.

156 Dbf4-dependent kinase (DDK) phosphorylates minichromosome maintenance 2 (Mcm2) during S phase in ye

157 The MiniChromosome Maintenance 2-7 (MCM2-7) complex provides

158 The MINICHROMOSOME MAINTENANCE 2-7 (MCM2-7) complex, a ring-

159 3 recruits cell division cycle 45 (Cdc45) to minichromosome maintenance 2-7 (Mcm2-7).

160 ontaining the cell division cycle 45 (Cdc45)/minichromosome maintenance 2-7 (Mcm2-7)/Go, Ichi, Nii, a

161 egulation of RBR3-type genes, as well as the MINICHROMOSOME MAINTENANCE 2-7 gene family and PROLIFERA

162 roliferating cell nuclear antigen (PCNA) and minichromosome maintenance 4 (MCM4) proteins without cha

163 ion of PGC-1beta decreased the expression of minichromosome maintenance 4 (MCM4), which leads to a de

164 oblasts (MEFs), we show here that NCOA4 is a minichromosome maintenance 7 (MCM7)-interacting protein

165 the presence of a pathogenic variant of the minichromosome maintenance 8 gene (MCM8, c.446C>G; p.P14

166 onents (origin recognition complex [ORC] and minichromosome maintenance [MCM] complex).

167 ies a subunit of the replicative CMG (Cdc45, minichromosome maintenance [MCM] subunits 2-7, and the G

168 A1, origin recognition complex 2 (ORC2), and minichromosome maintenance complex (MCM) association wit

169 An essential G1 process is minichromosome maintenance complex (MCM) loading at DNA

170 nsing mechanisms that prevent loading of the minichromosome maintenance complex (MCM2-7) onto replica

171 ion complex (ORC), Cdc6/Cdc18, Cdt1, and the minichromosome maintenance complex (Mcm2-Mcm7, or Mcm2-7

172 association of the key replication proteins minichromosome maintenance complex component (MCM7) and

173 S-phase kinase-associated protein 2 (SKP2), minichromosome maintenance complex component 4 (MCM4), a

174 iency as mutation in the MCM4 gene, encoding minichromosome maintenance complex component 4.

175 between a lactase persistence (LP) SNP, the minichromosome maintenance complex component 6 (MCM6)-rs

176 of HPNE and PDAC cells, and correlated with minichromosome maintenance complex components (MCMs) and

177 bited, there is an unexpected loading of the minichromosome maintenance complex onto chromatin.

178 Dpb11 stimulates DDK phosphorylation of the minichromosome maintenance complex protein Mcm4 alone an

179 Cell cycle analysis indicated that the minichromosome maintenance complex protein, MCM3, bound

180 Because minichromosome maintenance complex proteins are thought

181 eregulated cells, consistent with a role for minichromosome maintenance complex proteins in initiatio

182 Y600 to increase its association with other minichromosome maintenance complex proteins, thereby pro

183 A replication and compromised loading of the minichromosome maintenance complex, resulting in replica

184 report that mutations in the heterohexameric minichromosome maintenance complex-the DNA replicative h

185 , Ki-67, proliferating cell nuclear antigen, minichromosome maintenance deficient 3, and phosphorylat

186 of 734 residues of this protein also called minichromosome maintenance deficient 5 (MCM5) or cell di

187 ed with G1/S cell-cycle transition including minichromosome maintenance deficient proteins, as well a

188 quence analysis of beta-tubulin, calmodulin, minichromosome maintenance factor, DNA-dependent RNA pol

189 The minichromosome maintenance genes (MCM2-7) are transcribe

190 The proliferation marker Ki67, minichromosome maintenance genes 2-5, antiapoptotic gene

191 hese reports suggest a critical role for the minichromosome maintenance helicase complex in NK cells

192 The minichromosome maintenance helicase from the archaeon Me

193 f the Methanothermobacter thermautotrophicus minichromosome maintenance helicase is described.

194 ulator of DNA replication through effects on minichromosome maintenance helicase loading and activati

195 In contrast, the minichromosome maintenance helicase was unable to unwind

196 complex and Cdc45 to activate the eukaryotic minichromosome maintenance helicase.

197 Minichromosome maintenance helicases are ring-shaped com

198 Here, we show that Tax associates with the minichromosome maintenance MCM2-7 helicase complex and l

199 In Saccharomyces cerevisiae, minichromosome maintenance protein (Mcm) 10 interacts wi

200 Minichromosome maintenance protein (Mcm) 10 regulates th

201 The minichromosome maintenance protein (MCM) complex is an e

202 Minichromosome maintenance protein 1 (Mcm1) is required

203 ar polyadenylated RNA-binding protein 3, and minichromosome maintenance protein 1.

204 Minichromosome maintenance protein 10 (Mcm10) is an esse

205 The minichromosome maintenance protein 10 (Mcm10) is an evol

206 The Minichromosome maintenance protein 10 (Mcm10), an import

207 n identify colorectal cancer by detection of minichromosome maintenance protein 2 (MCM2) expression i

208 Minichromosome maintenance protein 2 (MCM2) is a compone

209 on of hypoxia-inducible factor-1 (HIF-1) and minichromosome maintenance protein 2 (mcm2).

210 lation sites in the carboxyl terminus of the minichromosome maintenance protein 3 (MCM3), a component

211 e retinoblastoma protein phosphorylation and minichromosome maintenance protein 6 expression.

212 the retinoblastoma protein, and induction of minichromosome maintenance protein 6.

213 hibited the expression of S phase-regulatory minichromosome maintenance protein 6.

214 From this study, we identify minichromosome maintenance protein 7 (MCM7) and p16 as p

215 damage marker gammaH2AX is upregulated under minichromosome maintenance protein 7 (MCM7) knockdown in

216 We then used our mouse model to identify minichromosome maintenance protein 7 (MCM7), an E2F-indu

217 asmid DNA template by DNA polymerases (pol), minichromosome maintenance protein complex (Mcm), topois

218 The heterohexameric minichromosome maintenance protein complex (Mcm2-7) func

219 regulate DNA replication; are members of the minichromosome maintenance protein complex family; or en

220 be essential to recruit and load MCM2-7, the minichromosome maintenance protein complex, around DNA a

221 etylation and RNR levels, maintains helicase minichromosome maintenance protein complexes (Mcm2-7) on

222 The minichromosome maintenance protein homologs MCM8 and MCM

223 The archaeal minichromosome maintenance protein MCM forms a homohexam

224 nd largest subunit of RNA polymerase II, and minichromosome maintenance protein).

225 genome requires the evolutionarily conserved minichromosome maintenance protein, Mcm10.

226 Minichromosome maintenance proteins (Mcm's) are componen

227 Minichromosome maintenance proteins (Mcm) are essential

228 ession of E2F-5, centromere protein A and E, minichromosome maintenance proteins (MCM)-2, -3, -5, -6

229 ognition complex, and the elongation factors minichromosome maintenance proteins (MCM)2-7 and prolife

230 ication, involves the loading of six related minichromosome maintenance proteins (Mcm2-7) into prerep

231 Interestingly, the genes coding for the minichromosome maintenance proteins (MCMs), which consti

232 egulated loading of the replicative helicase minichromosome maintenance proteins 2-7 (MCM2-7) onto re

233 r subsequent use by loading complexes of the minichromosome maintenance proteins 2-7 (Mcm2-7).

234 ereplication complex that contains a Mcm2-7 (minichromosome maintenance proteins 2-7) double hexamer.

235 bers, whereas Double-parked protein/Cdt1 and minichromosome maintenance proteins are apparently essen

236 monstrate that uncontrolled DNA unwinding by minichromosome maintenance proteins upon Cdt1 overexpres

237 (origin recognition complex [ORC], Cdc6, and minichromosome maintenance proteins) causes a cell cycle

238 virions did not reveal the presence of ORCs, minichromosome maintenance proteins, or LANA.

239 clear antigen, ribonucleotide reductase, and minichromosome maintenance) and of the retinoblastoma-re

240 The Mcm2-7 (minichromosome maintenance) complex is a toroidal AAA(+)

241 ryotic DNA replicative helicase, the Mcm2-7 (minichromosome maintenance) complex, is loaded at each o

242 litator of chromatin transcription) and MCM (minichromosome maintenance) complexes.

243 INS (go ichi ni san) complex allows the MCM (minichromosome maintenance) helicase to interact with ke

244 the atomic structure of an archaeal MCM (for minichromosome maintenance) homologue.

245 The MCM2-7 (minichromosome maintenance) proteins are a family of evo

246 fi1, Dnt1 is required for rDNA silencing and minichromosome maintenance, and both Dnt1 and Net1/Cfi1

247 e-3-phosphate dehydrogenase, proteoglycan 4, minichromosome maintenance, complex component 9, high mo

248 The antibody against minichromosome maintenance-2 (MCM2) protein was tested f

249 atients identified a variant (c.71-1insG) in minichromosome maintenance-deficient 4 (MCM4) that was p

250 Mcm4 (minichromosome maintenance-deficient 4 homolog) encodes

251 oth Set1 and Bre1 are required for efficient minichromosome maintenance.

252 In the present study, we employ a novel minichromosome model of the hGH-N regulatory domain and

253 he transgenes would reside on an independent minichromosome, not linked to any endogenous genes; thus

254 In minichromosomes obtained late in infection, nucleosomes

255 telomeres that cap the linear chromosome and minichromosomes of Borrelia burgdorferi.

256 n approach is feasible for the generation of minichromosomes of normal A chromosomes by selection of

257 Twenty-two minichromosomes of related origin but varying in size ar

258 we follow the catenation status of circular minichromosomes of three sizes during the Saccharomyeces

259 Minichromosomes of wild-type polyomavirus were previousl

260 ranscription units, whether on two different minichromosomes or on host chromosomes and minichromosom

261 lar chromosome and two large megaplasmids or minichromosomes, pNRC100 and pNRC200.

262 g emulsion PCR (LE-PCR) enables formation of minichromosomes preserving phase information of two poly

263 In anaphase II, the minichromosomes progressed to one pole or the other.

264 bstitutes for outer repeats on plasmid-based minichromosomes, promoting de novo CENP-A(Cnp1) and kine

265 d whether incorporation of Sir proteins into minichromosomes regulates early steps of recombinational

266 h the initiation and the elongation steps of minichromosome replication in vitro.

267 d-type (WT) chromosomes and de novo circular minichromosomes revealed that meiosis-specific HORMA-dom

268 iz- cells shows that SUMO E3 is required for minichromosome segregation and thus has a positive role

269 SIZ1 and SIZ2 genes we demonstrate that the minichromosome segregation defect and dicentric minichro

270 In addition, our analysis of the plasmid minichromosome shows that T(3)-bound TR disrupts the nor

271 ichromosome segregation defect and dicentric minichromosome stabilization, both characteristic for Sm

272 We used a "sensitized" minichromosome substrate (J21A) to screen approximately

273 l centromeres in vivo, using a budding yeast minichromosome system and temperature-sensitive mutation

274 The engineered minichromosome technology can also be used in combinatio

275 With the advent of engineered minichromosome technology in plants, an understanding of

276 Minichromosome technology provides one solution to the s

277 Tetrahymena thermophila ribosomal DNA (rDNA) minichromosome that are required for origin activation.

278 nal regulatory region of the simian virus 40 minichromosome that is being transcribed in the cell is

279 the nucleus of the infected hepatocyte as a minichromosome that serves as the transcription template

280 n-Barr virus (EBV) persists as chromatinized minichromosomes that are replicated by the host replicat

281 meiosis I, is still present at anaphase I on minichromosomes that divide equationally.

282 ell lines and in larval tissues that contain minichromosomes that have structurally defined centromer

283 ts into cells, where they are assembled into minichromosomes that the cellular machinery replicates a

284 ence of the HBV genome, which forms a stable minichromosome, the covalently closed circular DNA (cccD

285 vely with origin sequences in the 21 kb rDNA minichromosome, the interaction between ORC and the non-

286 In plants containing one minichromosome, the sister chromatids also separated at

287 The first artificial minichromosome was constructed by cloning the centromere

288 In cells containing thousands of minichromosomes, we found (using fluorescence in situ hy

289 Engineered minichromosomes were constructed in maize by modifying n

290 nd H3 in transcribing simian virus 40 (SV40) minichromosomes were determined.

291 st to the hypoacetylated state of NG59, NG59 minichromosomes were hypermethylated at specific lysines

292 Many minichromosomes were lost after long-term culture in the

293 Maize meiotic mutants and minichromosomes were used to study the role of H2AThr133

294 can be recapitulated on intracellular human minichromosomes where immunoglobulin 12- and 23-signals

295 plicate through dsDNA intermediates and form minichromosomes which carry the same epigenetic marks as

296 the left side of the enhancer in late-stage minichromosomes while also allowing late transcription.

297 ression of early transcription found in late minichromosomes while likely also repressing late transc

298 Coating of non-cross-linked minichromosomes with Escherichia coli single-strand bind

299 nto extrachromosomal arrays resembling extra minichromosomes with repetitive structures.

300 Minichromosomes with structurally intact centromeres wer