ライフサイエンスコーパス: euchromatic

1 led that VZV ORFs 62, 63, 36, and 14 are all euchromatic.

2 romatic, and in D2, the transgene has become euchromatic.

3 o the more distal regions, which are largely euchromatic.

4 ce via gene regulation and reorganization of euchromatic A and heterochromatic B compartments.

5 is study describes that condensin reinforces euchromatic A compartments and promotes B-to-A transitio

6 single nucleotide polymorphisms (SNPs) from euchromatic and 1000 from heterochromatic regions.

7 e's "inaccessible" regions: sequences (often euchromatic and containing genes) that are isolated from

8 omatic and gene poor, the mouse MSY is 99.9% euchromatic and contains about 700 protein-coding genes.

9 rosophila melanogaster chromosome 4 exhibits euchromatic and heterochromatic characteristics.

10 rosophila results from new juxtapositions of euchromatic and heterochromatic chromosomal regions, and

11 Partitioning of chromosomes into euchromatic and heterochromatic domains requires mechani

12 and paired RNAs are strongly correlated with euchromatic and heterochromatic epigenetic histone modif

13 approach to identifying differences between euchromatic and heterochromatic genes.

14 n the cell-cycle-regulated interplay between euchromatic and heterochromatic histone modifications.

15 termination of lncRNA transcription in both euchromatic and heterochromatic lncRNA-based gene silenc

16 genome characterized by the presence of both euchromatic and heterochromatic marks.

17 family of Drosophila melanogaster, which has euchromatic and heterochromatic members, we find that pr

18 n was supported by its reciprocal effects on euchromatic and heterochromatic PEV; E(var)3-9 mutations

19 eveals structural properties associated with euchromatic and heterochromatic regions in the genome.

20 study changes of chromatin accessibility in euchromatic and heterochromatic regions under extended d

21 llele frequency >0.10 was 95% and 91% in the euchromatic and heterochromatic regions, respectively.

22 ays a distinct spatial segregation of active euchromatic and inactive heterochromatic regions of the

23 ions, including overrepresentation of MSI in euchromatic and intronic regions compared to heterochrom

24 lated at lysines 9 and 14, consistent with a euchromatic and nonrepressed structure.

25 ToRC subunits colocalize in euchromatic arms of polytene chromosomes.

26 equences that can be mapped to the assembled euchromatic arms, we identified sequences that are speci

27 re-proximal regions, but also throughout the euchromatic arms.

28 ng small heterochromatic regions embedded in euchromatic arms.

29 Moreover, euchromatic BACs were largely devoid of transposons or o

30 tion of heterochromatic satellite DNA in the euchromatic brown (bw) gene of Drosophila melanogaster r

31 ls, but not CD177(neg) neutrophils, showed a euchromatic CD177 promoter, unmethylated CpGs, and c-Jun

32 observations suggest that Piwi promotes the euchromatic character of 3R-TAS heterochromatin and its

33 ous component of rice CEN chromatin, and the euchromatic characteristics of rice CEN chromatin are ha

34 the terminal retrotransposon array exhibits euchromatic characteristics.

35 eukaryotes, but, interestingly, it can show euchromatic characteristics; for example, the euchromati

36 g a functional role for JIL-1 in maintaining euchromatic chromatin and counteracting heterochromatic

37 osophila phosphorylation of histone H3S10 in euchromatic chromatin regions by the JIL-1 tandem kinase

38 of PEV, suggesting a role for the protein in euchromatic chromatin structure and/or transcription.

39 tly clustered on chromosomes, even when only euchromatic chromosomal segments are considered.

40 ysis of eight "wanderer" genes (present in a euchromatic chromosome arm in one species and on the dot

41 xpectedly large fraction of sequences in the euchromatic chromosome arms exhibits a heterochromatic c

42 SMC4/condensin also acts within the mostly euchromatic chromosome arms to suppress conditionally ex

43 meters at different window sizes through the euchromatic chromosomes.

44 ferentially to the transcriptionally active, euchromatic compartment of the genome.

45 t genomes are largely confined to the active euchromatic compartment, consistent with the known funct

46 ear periphery to reside within the internal, euchromatic compartment.

47 hat signal-induced nuclear translocation and euchromatic compartmentalization constitute an additiona

48 the inactive X chromosome (Xi), it adopts a euchromatic conformation bound by CTCF.

49 the locations of FM7 breakpoints to precise euchromatic coordinates and identified the flanking sequ

50 is sufficient to locally silence Arabidopsis euchromatic crossover hot spots and is associated with i

51 I10 copies is sufficient to more than double euchromatic crossovers.

52 histone methyltransferase that catalyzes the euchromatic dimethylation of histone H3 at lysine 9 (H3K

53 It represents 99.4% of the euchromatic DNA and includes one megabase of heterochrom

54 datively induced DSBs arise in HC as well as euchromatic DNA and that Artemis and ATM function in the

55 rosophila species, provide information about euchromatic DNA content, they cannot give an accurate es

56 However, euchromatic DNA methylation frequently occurs in regions

57 Euchromatic DNA spans approximately 50% of the sorghum g

58 spatially associated with early replicating, euchromatic DNA, which is predominately found in distal

59 omeric DNA is evolving very differently from euchromatic DNA.

60 mately 3-fold lower gene density compared to euchromatic DNA.

61 f gene rearrangement compared to a reference euchromatic domain.

62 Genes normally resident in euchromatic domains are silenced when packaged into hete

63 romatin structure that functions to maintain euchromatic domains while counteracting heterochromatiza

64 structure and that it functions to maintain euchromatic domains while counteracting heterochromatiza

65 ve sites were identified, some in apparently euchromatic domains, although all are close to heterochr

66 ic properties (e.g., gene density similar to euchromatic domains, replication during polytenization).

67 tionary fluidity between heterochromatic and euchromatic domains.

68 7me3 occurs in a few (roughly seven) focused euchromatic domains; (5) centromeres and CENP-C are clos

69 Collectively, these XRNs are recruited to a euchromatic DSB and are required for ssDNA production an

70 DSBs are generally repaired more slowly than euchromatic DSBs, and ATM signaling is specifically requ

71 mporal and spatial dynamics that differ from euchromatic DSBs.

72 located within transcriptionally permissive euchromatic environments, and promote deposition of hist

73 transcription factor YY1 associates with the euchromatic form of DXZ4 on the Xi.

74 s, closes 105 and extends into 72 out of 190 euchromatic gaps in the reference genome, adding 1.03 Mb

75 omatic gaps, or 10%, including two remaining euchromatic gaps on chromosome 19.

76 malian reference assembly, yet more than 160 euchromatic gaps remain and aspects of its structural va

77 equence, 363,114 bp of which close 26 of 250 euchromatic gaps, or 10%, including two remaining euchro

78 numerous processes including, surprisingly, euchromatic gene expression.

79 ith the heterochromatin boundary regions and euchromatic gene promoters.

80 3K9 dimethylation (H3K9me2) is important for euchromatic gene repression.

81 Mammalian euchromatic gene silencing results from the combined rep

82 genome and composing an estimated 70% of the euchromatic gene space.

83 -marked chromomeres, clearly demarcating the euchromatic gene space; (3) H3K9me2 is restricted to the

84 gene space; (3) H3K9me2 is restricted to the euchromatic gene space; (4) H3K27me3 occurs in a few (ro

85 ased H3K9 methylation accompanied by reduced euchromatic gene transcription and heterochromatin propa

86 transition region structure originates from euchromatic gene-containing segments of DNA that were du

87 re distinctly more dynamic than those in the euchromatic, gene-rich regions of the chromosomes.

88 ughout all heterochromatic loci and inactive euchromatic genes and is present at the 3' end of modera

89 taneously involved in both the repression of euchromatic genes brought to the vicinity of pericentric

90 topic association of silencing proteins with euchromatic genes important for cell wall integrity and

91 in complexes associate with highly expressed euchromatic genes in many different organisms.

92 moter type found in both heterochromatic and euchromatic genes of Drosophila.

93 argely conserved between heterochromatic and euchromatic genes, eliminating the hypothesis that adapt

94 elements (MITEs) are closely associated with euchromatic genes, the broader functional impact of thes

95 inary pattern of histone modifications among euchromatic genes, with active genes being hyperacetylat

96 anscriptome analysis, we identified a set of euchromatic genes-enriched in those required for the cel

97 s between dLsd1, Lid, and Notch signaling at euchromatic genes.

98 to exclusive localization and regulation of euchromatic genes.

99 s between HP1 and DNMT1 mediate silencing of euchromatic genes.

100 n international consortium is sequencing the euchromatic genespace of Medicago truncatula.

101 Notably, we found that virtually the entire euchromatic genome (including intergenics) is transcribe

102 enes) that are isolated from the rest of the euchromatic genome by heterochromatin and other repeat-r

103 3 deletions generated pushed coverage of the euchromatic genome to 98.4%.

104 third chromosome ( approximately 36% of the euchromatic genome) for suppressor mutations of piwi2 an

105 a rich resource for completion of the human euchromatic genome.

106 ad pairs and breakpoint reads throughout the euchromatic genome.

107 at a time largely separable from that of the euchromatic genome.

108 ate that the fraction of the human and mouse euchromatic genomes encoding lincRNAs is more than twofo

109 one H3 (H3K4), owing to its association with euchromatic genomic regions.

110 accessibility to DNase I and an induction of euchromatic H3 and H4 histone acetylations upon nicotina

111 Here, we report that a euchromatic H3K9 methyltransferase, EHMT1, functions as

112 This analysis revealed the pervasive loss of euchromatic H3K9me2 as a conserved feature of pathologic

113 mics and spatial features of the majority of euchromatic H3K9me3 domains over the genome.

114 Following the "finished," euchromatic, haploid human reference genome sequence, th

115 DM4A (dKDM4A), previously characterized as a euchromatic histone H3 K36 demethylase and transcription

116 G9a methyltransferase is a euchromatic histone H3 lysine 9 methyltransferase.

117 0638 and UNC0642-two selective inhibitors of euchromatic histone lysine N-methyltransferase-2 (EHMT2,

118 s of histone acetylation, whereas removal of euchromatic histone methylation occurs gradually through

119 y factor 1 (NRF1) regulates transcription of euchromatic histone methyltransferase 1 (EHMT1) to ensur

120 hylation of H3-K9 by the recently identified euchromatic histone methyltransferase SETDB1/ESET may be

121 ant disorder caused by haploinsufficiency of euchromatic histone methyltransferase-1 (EHMT1).

122 e H3 dimethylation at lysine 9 (H3K9me2) and euchromatic histone methyltransferases EHMT1 and EHMT2 w

123 eveals that LSD2 forms active complexes with euchromatic histone methyltransferases G9a and NSD3 as w

124 of LMP1 and LMP2A correlated with a loss of euchromatic histone modification H3K9ac and a correspond

125 As shown by chromatin immunoprecipitation, euchromatic histone modification H3K9ac is added at prom

126 uchromatic characteristics; for example, the euchromatic histone modification mark dimethylated H3 Ly

127 ipitation-chip to study the patterns of four euchromatic histone modification marks: H3K4me2, trimeth

128 We also show that Piwi promotes euchromatic histone modifications and piRNA transcriptio

129 e 3R-TAS1 piRNA coding sequence restores the euchromatic histone modifications of 3R-TAS and the expr

130 on in the absence of HDA6 activity; instead, euchromatic histone modifications typical of active gene

131 In piwi mutants, 3R-TAS loses euchromatic histone modifications yet accumulates hetero

132 cal interactions between genes with specific euchromatic histone modifications.

133 gh the recruitment of a factor that protects euchromatic histone modifications.

134 Euchromatic histone PTMs are abundant during schizogony

135 Here we show that euchromatic histone-lysine N-methyltransferase 1 (EHMT1)

136 ased H3K9me2/3 in CIITA via up-regulation of euchromatic histone-lysine N-methyltransferase 2 (G9a).

137 Euchromatic histone-lysine N-methyltransferase 2, also k

138 Nerve injury increased activity of euchromatic histone-lysine N-methyltransferase-2 (G9a),

139 ned with the requirement of transcription of euchromatic homologous sequences, suggests a role of dou

140 e3 influences expression of both hetero- and euchromatic host genes.

141 al analysis is undertaken to verify that the euchromatic human genome is sufficiently complete--conta

142 Tens of millions of base pairs of euchromatic human genome sequence, including many protei

143 mosome, which represents just over 5% of the euchromatic human genome.

144 M1 and the DNA methyltransferase MET1 of the euchromatic, imprinted gene FWA, as its promoter is prov

145 me scale, with pericentromeric decreases and euchromatic increases in recombination.

146 nase in Drosophila localizes specifically to euchromatic interband regions of polytene chromosomes an

147 Early S nuclei exhibited widely distributed euchromatic labeling preferentially localized to regions

148 e S nuclei also exhibited widely distributed euchromatic labeling, but the label was preferentially l

149 te that P-Ser 83-HP1gamma has an exclusively euchromatic localization, interacts with Ku70 (a regulat

150 n is toxic to psh1Delta cells and results in euchromatic localization.

151 , suggesting that proteolysis prevents CenH3 euchromatic localization.

152 ibution of SIRT1 to epigenetic regulation at euchromatic loci and whether it acts in concert with oth

153 that its targets are the expressed genes or euchromatic loci in Arabidopsis genome.

154 orcing epigenetic marks for the silencing of euchromatic loci in Chlamydomonas.

155 ngle DSB system for both heterochromatic and euchromatic loci in Drosophila melanogaster Live imaging

156 that tethering Clr4 via DNA-binding sites at euchromatic loci induces heterochromatin assembly, with

157 ncing proteins and discovered 238 unexpected euchromatic loci that exhibited enrichment of all three.

158 lso precludes nucleosome turnover at several euchromatic loci to prevent R-loop formation, ensuring p

159 ilencing complex that is also distributed at euchromatic loci, and with RNA interference component Ar

160 so mediates degradation of antisense RNAs at euchromatic loci, but the underlying mechanism has remai

161 aving the telomere and spreading to internal euchromatic loci.

162 prevent spurious siRNA-mediated silencing at euchromatic loci.

163 is only 25% lower than in early-replicating euchromatic loci.

164 e3 and DNA methylation at a normally active, euchromatic locus but did not bypass the requirement of

165 Moreover, tethering Stc1 to a euchromatic locus is sufficient to induce silencing and

166 on the Y maintains a surprisingly gene-rich, euchromatic mammalian male chromosome.

167 Strikingly, 90% to 95% of the total genomic euchromatic marks histone H3 acetylated at lysine 9 and

168 er per physical length over the distal first euchromatic megabase pairs of the X chromosome, our data

169 Here we report that euchromatic methylation of H3 Lys-4 is necessary to main

170 r the recruitment of G9a, the main mammalian euchromatic methyltransferase, and defines nonembryonic

171 d into smaller chromatin loops than flanking euchromatic mouse chromatin.

172 localize to a largely non-overlapping set of euchromatic nuclear speckles, suggesting that Set1A and

173 Cerebellar Purkinje neurons have large and euchromatic nuclei, whereas granule cell nuclei are smal

174 ighboring genes, occurs independent of their euchromatic or heterochromatic location.

175 The euchromatic organization of DXZ4 on the otherwise hetero

176 ultiple individuals, we targeted gaps in the euchromatic part of the human genome.

177 ns at these loci from a heterochromatic to a euchromatic pattern.

178 n RNAi-dependent H3K9 methylation of several euchromatic pockets, prior to which Argonaute1-associate

179 With the euchromatic portion of several mammalian genomes now seq

180 oding DNA comprises approximately 80% of the euchromatic portion of the Drosophila melanogaster genom

181 ed improvement of the 117-Mb sequence in the euchromatic portion of the genome and 21 Mb in the heter

182 ial and approximately equal fractions of the euchromatic portion of the genome are inferred to contri

183 Furthermore, a smaller fraction of the euchromatic portion of the genome is in a repressive chr

184 nflates the variation in coverage across the euchromatic portion of the genome.

185 anscriptional, and chromatin features of the euchromatic portion of the maize genome provide evidence

186 SOL project is the sequencing of the entire euchromatic portion of the tomato genome.

187 locus is similar to that described in other euchromatic portions of the tomato genome despite the re

188 sociated with the liver lineage by acting at euchromatic promoter regions.

189 s with H3K27me3-postive and H3K4me3-positive euchromatic promoters were prematurely induced in hepato

190 e.g., dense packaging, late replication) and euchromatic properties (e.g., gene density similar to eu

191 Despite these euchromatic properties, the inactive X chromosome was re

192 chromatin structure, and the high levels of euchromatic rDNA induced by the BBDS mutations direct nu

193 Each UR euchromatic region contains many different deletions 10-

194 es indicated that in juvenile-stage rice the euchromatic region is more actively transcribed than is

195 a 200 copy transgene array integrated into a euchromatic region of chromosome 1 in human U2OS cells.

196 calization of Rf1 to a approximately 0.4-Mbp euchromatic region of LG-08.

197 The euchromatic region of the chromosome comprises approxima

198 The map spans almost the entire euchromatic region of the chromosome, of which 20-25% (a

199 itical in obtaining complete sequence of the euchromatic region of the horse Y chromosome, with an ai

200 A chromosome inversion was observed in the euchromatic region of the short arms.

201 molecular markers and a linkage map for the euchromatic region of the Syrian hamster X chromosome th

202 nd cells, we define 112 underreplicated (UR) euchromatic regions 60-480 kb in size.

203 ed heterozygous deletions tiling ~70% of the euchromatic regions and examined their influence on this

204 r Complex), punctate nuclear localisation in euchromatic regions and overlap with Polycomb Group tran

205 e of methylation on meiotic recombination in euchromatic regions and suggests that additional factors

206 hila endocycle, heterochromatin and specific euchromatic regions are underreplicated and reduced in c

207 ng high levels of homolog pairing at all six euchromatic regions assayed and variably lower levels in

208 JIL-1 kinase activity functions to maintain euchromatic regions by antagonizing Su(var)3-9-mediated

209 erochromatin from spreading into neighboring euchromatic regions by recruiting transcription factor T

210 enabled localization of heterochromatic and euchromatic regions for each chromosome of both species.

211 ricentromeres and transformed large formerly euchromatic regions into repeat-rich pericentromeric reg

212 repeat sequences, yet with 30% more compact euchromatic regions it is the smallest known grass genom

213 ses correct in reconstructing megabase-scale euchromatic regions of an eutherian ancestral genome fro

214 - and trimethylation of histone 3 (H3) K9 in euchromatic regions of chromosomes, inhibiting gene tran

215 ions and target genes in heterochromatin and euchromatic regions of reduced recombination, as well as

216 The distal euchromatic regions of sorghum chromosomes 3-7 and 10 ar

217 es "ectopic heterochromatin" at sites within euchromatic regions of the Drosophila melanogaster genom

218 ARP-1-dependent Sox2-binding sites reside in euchromatic regions of the genome with relatively high n

219 mediated effects occurring throughout active euchromatic regions of the genome, with very little know

220 ative labeling was widely distributed across euchromatic regions of the nucleoplasm.

221 3, but these modifications are also found in euchromatic regions that permit transcription.

222 However, some elements are located in euchromatic regions throughout the genome and have been

223 Surprisingly, the adjacent euchromatic regions underwent crossing over at twice the

224 we show that MLL5 is recruited to gene-rich euchromatic regions via the interaction of its plant hom

225 tic recombination between markers located in euchromatic regions was significantly higher in both het

226 ciated significantly more often than average euchromatic regions with heterochromatic chromocenters (

227 hese proteins were also enriched in the same euchromatic regions with the high Sir protein levels.

228 Rather than being moved to adjacent euchromatic regions, as in animals, heterochromatin unde

229 including those typically found in gene-rich euchromatic regions, lose DNA methylation in a mutant la

230 n ectopic spreading of H3K9me2 into adjacent euchromatic regions, mimicking the phenotype observed in

231 as methylated in low-turnover nucleosomes in euchromatic regions, notably in the coding regions of lo

232 on B. vulgaris chromosomes predominantely in euchromatic regions.

233 bstitutional polymorphism relative to linked euchromatic regions.

234 Sir-dependent silent chromatin into adjacent euchromatic regions.

235 rict partitioning of the heterochromatic and euchromatic regions.

236 ith approximately 50% for previously studied euchromatic regions.

237 genes with similar integrations into TAS and euchromatic regions.

238 repeat (180-bp knob sequence) or an abundant euchromatic retroelement (Opie) are undetectable within

239 k1, a core subunit of the CLRC complex, to a euchromatic RNA mediates RNAi-dependent silencing that p

240 gamma-H2AX, by comparing HR occurring at the euchromatic ROSA26 locus between mouse embryonic stem ce

241 s homolog interactions and the initiation of euchromatic SC assembly independent of DSBs.

242 em persist long after the disassembly of the euchromatic SC at the end of pachytene.

243 Furthermore, the early euchromatic SC initiation events at mid-zygotene may be

244 The centromeric and first euchromatic SC initiation sites depend on the cohesion p

245 es; these findings are in marked contrast to euchromatic segments in these species that exhibit only

246 In both heterochromatic and euchromatic segments of the genome, H3K27me2 enrichment

247 ger than 5 kb, totaling around 550-750 kb of euchromatic sequence across their genomes.

248 e nucleotide polymorphism in the most distal euchromatic sequence are approximately one order of magn

249 ed telomeric deficiencies cause deletions of euchromatic sequence followed by subsequent "healing" by

250 The finished euchromatic sequence of chromosome 9 comprises 109,044,3

251 We have determined 99.3% of the euchromatic sequence of the X chromosome.

252 Euchromatic sequence that flanks sites of LCR16a integra

253 we report 2,488,842 bp of previously unknown euchromatic sequence, 363,114 bp of which close 26 of 25

254 aster genome, with the most recent update of euchromatic sequence, gives the first genome-wide view o

255 on base pairs of the human genome's unplaced euchromatic sequence, including more than a dozen protei

256 entire published 34.9-Mb human chromosome 22 euchromatic sequence.

257 The binding of D1 to euchromatic sequences is less studied and the functional

258 rmed by this localization of genes and other euchromatic sequences that are embedded within highly re

259 evels of trimethyl H3K9 or the repression of euchromatic sequences were not affected by SET3 downregu

260 -A elements just distal to unique, canonical euchromatic sequences.

261 ome 4, representing more than 99.6% of their euchromatic sequences.

262 ect largely completed the detailing of human euchromatic sequences; however, the most highly repetiti

263 anscription is substantial (typically 19% of euchromatic signal).

264 describe a mechanism for spatial encoding of euchromatic signals that repel heterochromatin invasion.

265 ng that this histone variant is required for euchromatic silencing and heterochromatin formation.

266 ut angiosperms in gene body DNA methylation, euchromatic silencing of transposons and repeats, as wel

267 ein 1a (HP1a) accumulation at this otherwise euchromatic site.

268 nhistone/DNA complexes located at a specific euchromatic site.

269 observed broadly distributed throughout all euchromatic sites analyzed, with selective depletion in

270 -4 methylation prevents Sir3p association at euchromatic sites and therefore concentrates Sir3p at un

271 coding of heterochromatin containment within euchromatic sites remain opaque.

272 ea mays (maize) minichromosomes derived from euchromatic sites with high-density gene distributions b

273 Sir3 also bound to a surprising number of euchromatic sites, largely at genes expressed at high le

274 ing with Taz1 and the RNAi machinery, and to euchromatic sites, via mechanism(s) distinct from its he

275 d-zygotene" oocytes, SC initiates at several euchromatic sites.

276 ne protein H3K9(Ac) and thus maintained in a euchromatic state during latency.

277 through XCI establishment and "reverts" to a euchromatic state during XCI maintenance.

278 noprecipitation (ChIP) assays to analyze the euchromatic state of ORFs 62 and 63 compared to the cent

279 ed heterochromatin-like state to a more open euchromatic state.

280 ene is unmethylated and fully expressed in a euchromatic state.

281 We resolve the complete sequence of 26,079 euchromatic structural variants at the base-pair level,

282 d as a doorstep, maintaining the established euchromatic structure in adult tissue.

283 Here we identified more than 20,000 euchromatic SVs from 14 Drosophila melanogaster genome a

284 one H3K9me2) to nearby DNA occurs at >50% of euchromatic TEs, and can extend up to 20 kb.

285 demonstrates that the epigenetic effects of euchromatic TEs, and host genetic factors modulating suc

286 Greater microcolinearity in recombinogenic (euchromatic) than nonrecombinogenic (heterochromatic) re

287 in these regions and promoting a switch from euchromatic to heterochromatic states.

288 ls or genomic regions that switched from the euchromatic to the heterochromatic compartment during ne

289 n regulating heterochromatin propagation and euchromatic transcription and also suggest that misregul

290 ctive, contain modifications associated with euchromatic transcription, and couple RNAi-mediated tran

291 hromatin cofactors rather than components of euchromatic transcriptionally active condensates.

292 ino-2-phenylindole-negative zones containing euchromatic (transcriptionally active) DNA.

293 gets small, AT-rich, and nucleosome-depleted euchromatic transposable elements.

294 Still mysterious though is how Piwi targets euchromatic transposons for silencing, but not the speci

295 piRNA loci interact with potentially active, euchromatic transposons to form an adaptive system for t

296 hich support roles for H3K27me2 in silencing euchromatic transposons to maintain genome stability and

297 TA family) in euchromatin, which may silence euchromatic transposons to maintain genome stability dur

298 We identify sites of euchromatic underreplication that are common to all thre

299 aldehyde-3-phosphate dehydrogenase promoter (euchromatic), we show that the promoters of ORFs 62 and

300 ction of pachytene chromosome length that is euchromatic, we estimate that approximately 1500 Mbp of