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

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

6 rosophila melanogaster chromosome 4 exhibits euchromatic and heterochromatic characteristics.

7 Partitioning of chromosomes into euchromatic and heterochromatic domains requires mechani

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

9 approach to identifying differences between euchromatic and heterochromatic genes.

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

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

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

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

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

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

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

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

18 ToRC subunits colocalize in euchromatic arms of polytene chromosomes.

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

20 ng small heterochromatic regions embedded in euchromatic arms.

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

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

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

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

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

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

27 the terminal retrotransposon array exhibits euchromatic characteristics.

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

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

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

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

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

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

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

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

36 meters at different window sizes through the euchromatic chromosomes.

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

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

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

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

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

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

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

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

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

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

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

48 However, euchromatic DNA methylation frequently occurs in regions

49 ight palindromes comprise one-quarter of the euchromatic DNA of the male-specific region of the human

50 Euchromatic DNA spans approximately 50% of the sorghum g

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

52 omeric DNA is evolving very differently from euchromatic DNA.

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

54 ons have served as preferential acceptors of euchromatic DNA.

55 mma, characteristic of silenced or senescent euchromatic DNA.

56 f gene rearrangement compared to a reference euchromatic domain.

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

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

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

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

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

62 tionary fluidity between heterochromatic and euchromatic domains.

63 7me3 occurs in a few (roughly seven) focused euchromatic domains; (5) centromeres and CENP-C are clos

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

65 mporal and spatial dynamics that differ from euchromatic DSBs.

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

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

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

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

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

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

72 numerous processes including, surprisingly, euchromatic gene expression.

73 ith the heterochromatin boundary regions and euchromatic gene promoters.

74 3K9 dimethylation (H3K9me2) is important for euchromatic gene repression.

75 Mammalian euchromatic gene silencing results from the combined rep

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

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

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

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

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

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

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

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

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

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

86 Genetic studies of rearrangements that place euchromatic genes next to blocks of heterochromatin also

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

88 sed chromatin configuration and silencing of euchromatic genes positioned near heterochromatin.

89 Euchromatic genes repositioned near heterochromatin by c

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

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

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

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

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

95 to exclusive localization and regulation of euchromatic genes.

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

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

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

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

100 behind the production of relatively complete euchromatic genome sequences.

101 3 deletions generated pushed coverage of the euchromatic genome to 98.4%.

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

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

104 ad pairs and breakpoint reads throughout the euchromatic genome.

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

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

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

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

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

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

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

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

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

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

115 0638 and UNC0642-two selective inhibitors of euchromatic histone lysine N-methyltransferase-2 (EHMT2,

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

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

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

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

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

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

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

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

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

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

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

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

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

129 Euchromatic histone PTMs are abundant during schizogony

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

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

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

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

134 In Drosophila oocytes, euchromatic homolog-homolog associations are released at

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

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

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

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

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

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

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

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

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

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

145 , suggesting that proteolysis prevents CenH3 euchromatic localization.

146 The activity of each promoter construct in euchromatic locations is also generally consistent with

147 HeT-A promoter constructs are active in all euchromatic locations tested and some display aspects of

148 ect variegation and yet most inserts were in euchromatic locations.

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

150 To characterize the physical properties of euchromatic loci bound by HP1, we developed a strategy f

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

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

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

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

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

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

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

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

159 aving the telomere and spreading to internal euchromatic loci.

160 prevent spurious siRNA-mediated silencing at euchromatic loci.

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

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

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

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

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

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

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

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

169 multitude of clustered genes, forming local euchromatic "neighborhoods."

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

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

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

173 The euchromatic organization of DXZ4 on the otherwise hetero

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

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

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

177 With the euchromatic portion of several mammalian genomes now seq

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

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

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

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

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

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

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

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

186 rosophila, recruitment of mammalian HP1 to a euchromatic promoter can establish a silenced state that

187 eterochromatic genes are very different from euchromatic promoters, but this idea has not been tested

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

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

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

191 Each UR euchromatic region contains many different deletions 10-

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

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

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

195 The euchromatic region of the chromosome comprises approxima

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

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

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

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

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

201 Htz1 is enriched in these euchromatic regions and acts synergistically with a boun

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

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

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

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

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

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

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

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

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

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

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

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

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

215 sequences correspond to approximately 1% of euchromatic regions of the human genome.

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

217 centromeric heterochromatin than in the more euchromatic regions of the nucleus.

218 ptionally inert relative to the more typical euchromatic regions that decondense during interphase.

219 3, but these modifications are also found in euchromatic regions that permit transcription.

220 ocal repatterning of hominoid chromosomes in euchromatic regions through a duplication-driven mechani

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

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

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

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

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

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

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

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

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

230 ta cells, Sir2 and Sir3 spread into flanking euchromatic regions, producing changes in histone H4 ace

231 bstitutional polymorphism relative to linked euchromatic regions.

232 Sir-dependent silent chromatin into adjacent euchromatic regions.

233 rict partitioning of the heterochromatic and euchromatic regions.

234 ith approximately 50% for previously studied euchromatic regions.

235 genes with similar integrations into TAS and euchromatic regions.

236 on B. vulgaris chromosomes predominantely in euchromatic regions.

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

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

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

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

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

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

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

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

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

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

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

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

249 million base pairs representing 99.4% of the euchromatic sequence of chromosome 7, the first metacent

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 bstitutional patterns in heterochromatic and euchromatic sequences are different, but also they provi

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

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

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

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

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

263 terochromatic sequences and three classes of euchromatic sequences: X-transposed, X-degenerate and am

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

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

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

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

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

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

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

271 -4 methylation prevents Sir3p association at euchromatic sites and therefore concentrates Sir3p at un

272 A number of euchromatic sites of localization were also reported in

273 ly assumed that these sites might constitute euchromatic sites of transcriptional repression by HP1.

274 SIR2 binds to many euchromatic sites on polytene chromosomes and colocalize

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

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

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

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

279 participates in silencing gene expression at euchromatic sites.

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

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

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

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

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

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

286 factors that acts in the setting of an open, euchromatic structure of the insulin gene.

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

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

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

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

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

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

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

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

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

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

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

298 ic analysis as a previously described 8p23.1 euchromatic variant.

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