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1 uencing (a method to map heterochromatin and euchromatin).
2 quent in early S phase, in regions marked by euchromatin.
3 hat restricts transcription to gene units in euchromatin.
4 eterochromatin from transcriptionally active euchromatin.
5 (Cse4) ubiquitylation and its exclusion from euchromatin.
6 is differentially processed within hetero or euchromatin.
7 DNA damage in heterochromatin, as well as in euchromatin.
8 ome or about 78 % of the estimated 252 Mb of euchromatin.
9 ats are packaged into Xi-specific CTCF-bound euchromatin.
10 access only to lineage-specific genes in the euchromatin.
11 ing global histone acetylation and retaining euchromatin.
12 thway-specific control of gene expression in euchromatin.
13 at the junctions between heterochromatin and euchromatin.
14 tion (HR) but with striking differences from euchromatin.
15 repeat (TR) sequences in both telomeres and euchromatin.
16 ay differential roles in heterochromatin and euchromatin.
17 tionally inactive heterochromatin and active euchromatin.
18 d by its C-terminal domain to nucleosomes in euchromatin.
19 into distinct domains of heterochromatin or euchromatin.
20 y be distinct from either heterochromatin or euchromatin.
21 romatin, whereas H3K4 methylation demarcates euchromatin.
22 spreading of silent chromatin into proximal euchromatin.
23 ized with acetylated histone H3, a marker of euchromatin.
24 transition from telomeric heterochromatin to euchromatin.
25 ansion of silent chromatin into neighbouring euchromatin.
26 on, a modification typically associated with euchromatin.
27 an average spacing of <14 kb across the MSY euchromatin.
28 silent mating-type locus HMRa into flanking euchromatin.
29 ericentromeric heterochromatin, and flanking euchromatin.
30 in rearrangements and insertions uncommon in euchromatin.
31 stone acetylation patterns characteristic of euchromatin.
32 nsitional states between heterochromatin and euchromatin.
33 nd heterochromatin to restrict the spread of euchromatin.
34 1.4 times higher in heterochromatin than in euchromatin.
35 d at promoter regions of nearly all genes in euchromatin.
36 erochromatin and some repressed genes within euchromatin.
37 oximately 1500 Mbp of the maize genome is in euchromatin.
38 perating as an epigenetic mark for repressed euchromatin.
39 localize to nuclear speckles associated with euchromatin.
40 E annotations in the Drosophila melanogaster euchromatin.
41 y are located distally on the chromosomes in euchromatin.
42 parison with the same transgene construct in euchromatin.
43 16 sequence, representing over 99.9% of its euchromatin.
44 dary between pericentric heterochromatin and euchromatin.
45 methylation of H3-K9 and localizes mainly in euchromatin.
46 alized specifically to silent domains within euchromatin.
47 constitutive heterochromatin and unexpressed euchromatin.
48 nsfection but repressed promoter activity in euchromatin.
49 different parts of the putative promoter in euchromatin.
50 rays to an average of 30% of the staining in euchromatin.
51 cant amount of monomethylation within silent euchromatin.
52 rth chromosome, and to specific sites within euchromatin.
53 human genomes were found within interstitial euchromatin.
54 rform critical functions in both hetero- and euchromatin.
55 one marks at DSBs in heterochromatin but not euchromatin.
56 and by an active retention of CBP-1/p300 in euchromatin.
57 alize with H3K36me2 at non-coding regions of euchromatin.
58 tion-resistant heterochromatin (srHC) versus euchromatin.
59 educed histone modifications associated with euchromatin.
60 s its high chromatin density with respect to euchromatin.
61 e than LEDGF/p75 in directing integration to euchromatin.
62 ates with H2A.Z to evict CENP-A assembled in euchromatin.
66 nonical histone PTMs that dictate interphase euchromatin (acetylation) and heterochromatin (methylati
68 d, these elements are entirely excluded from euchromatin, although sequence fragments of HeT-A and TA
70 lysine acetylation, normally associated with euchromatin and active genes, is regulated by different
71 density 10-100 times lower than that of the euchromatin and are heavily populated by retrotransposon
72 ed in more increased chromatin compaction in euchromatin and decompaction in heterochromatin, thus fu
75 zation in Arabidopsis with distinct roles in euchromatin and heterochromatin and a dual causality on
76 s confirmed that chromosome areas containing euchromatin and heterochromatin are distinguishable base
77 lysis of repair products reveal that DSBs in euchromatin and heterochromatin are repaired with simila
78 rs exhibited inverted radial distribution of euchromatin and heterochromatin compared with that of ot
79 a plaid pattern of contact enrichment within euchromatin and heterochromatin compartments(3), and dep
81 ed a machine learning-based algorithm to map euchromatin and heterochromatin domains genome-wide and
83 s, we show that an interaction that attracts euchromatin and heterochromatin equally to the nuclear e
84 region of genes that can be embedded in both euchromatin and heterochromatin exhibits a conserved str
87 ion protein is highly mobile within both the euchromatin and heterochromatin of ex vivo resting murin
88 mine differences in the accessibility of the euchromatin and heterochromatin regions of the epigenome
89 The segregation of eukaryotic genomes into euchromatin and heterochromatin represents a fundamental
91 N(6)-mA functions at the boundaries between euchromatin and heterochromatin to restrict the spread o
92 he spatial organization of epigenetic marks, euchromatin and heterochromatin, and origins of replicat
94 hese include the differential positioning of euchromatin and heterochromatin, the territorial organiz
95 in nucleosome occupancies between Drosophila euchromatin and heterochromatin, which implies that hete
96 s targeting of loci by pathways that promote euchromatin and heterochromatin, which primes genes for
108 he segregation of the genome into accessible euchromatin and histone H3K9-methylated heterochromatin
109 nges induced by light damage include reduced euchromatin and increased heterochromatin abundance, res
110 tively specified malignant traits, including euchromatin and large organized chromatin histone H3 lys
111 a, IL-33 localized simultaneously to nuclear euchromatin and membrane-bound cytoplasmic vesicles.
112 ectural protein that binds preferentially to euchromatin and modulates the fidelity of the cellular t
113 te that evolutionary gene relocation between euchromatin and pericentric heterochromatin occurred wit
114 sights into the compositional differences of euchromatin and pericentromeric heterochromatin in this
117 ologues (MRG1 and MRG2) are localised to the euchromatin and redundantly ensure the increased transcr
119 attenuation of origin licensing within both euchromatin and telomeric heterochromatin established th
120 es accumulated within both early-replicating euchromatin and telomeric heterochromatin, and replicati
121 We find that 5hmC is mostly associated with euchromatin and that whereas 5mC is under-represented at
122 enomes are broadly divided between gene-rich euchromatin and the highly repetitive heterochromatin do
123 me segregation into transcriptionally active euchromatin and transcriptionally repressed heterochroma
124 nts correspond to cytologically discernible "euchromatin" and "heterochromatin." Gene and repetitive
125 chromosome ends, (ii) they are not found in euchromatin, and (iii) they produce both sense and antis
128 istal 1.2 Mb, the gene density is typical of euchromatin, and this region is polytene in salivary gla
129 ng DNA replication, both heterochromatin and euchromatin are disrupted ahead of the replication fork
131 These interactions of heterochromatin and euchromatin are likely to have important roles in modula
132 n, and dozens of genes previously located in euchromatin are now embedded in pericentromeric heteroch
134 hat H3K4me3Q5ser nucleosomes are enriched in euchromatin, are sensitive to cellular differentiation a
135 This uniformity made it possible to use euchromatin as a control for quantitative staining inten
136 ruitment that is embedded within a region of euchromatin-associated H3 lysine 4 (H3-K4) methylation.
139 ed) DNA probes detects surprisingly abundant euchromatin-associated RNA comprised predominantly of re
141 isiae, histone variant H2A.Z is deposited in euchromatin at the flanks of silent heterochromatin to p
142 to the epigenetic balance of heterochromatin/euchromatin at three distinct loci showing position-effe
144 ribe the draft sequence of the M. truncatula euchromatin based on a recently completed BAC assembly s
145 X chromosome, inactivation is organized into euchromatin bound by the insulator protein CCCTC-binding
146 the epigenetic regulation of heterochromatin/euchromatin boundaries by Lid and dLsd1 and showing thei
148 mutants dramatically shift a heterochromatin-euchromatin boundary in Chr1, suggesting a novel role in
150 e unique classes: (I) those that localize to euchromatin but do not alter kinetochore function, (II)
151 me and the reduction of RNA polymerase II in euchromatin but its increase in pericentric regions in p
154 TC exposure not only blocked HDAC binding to euchromatin but was also associated with hypomethylation
155 oaches have been applied successfully to the euchromatin, but analysis of the heterochromatin has lag
156 e highly undercondensed, particularly in the euchromatin, but nevertheless contain phosphorylated his
161 mes, EST density is about fourfold higher in euchromatin compared with heterochromatin, while DNA den
165 n and topo II colocalize along both rDNA and euchromatin, consistent with coordination of their activ
166 oss of repeat-rich, stable nuclear RNAs from euchromatin corresponds to aberrant chromatin distributi
167 opic pericentric heterochromatin embedded in euchromatin display additional cohesin-dependent constri
170 from constitutive heterochromatin (cHC) and euchromatin (EC) and discusses various concepts regardin
171 me into subnuclear compartments, with active euchromatin enriched centrally and silent heterochromati
173 g that controlled by H2AX, in the context of euchromatin, excluding the implication of such an HR fun
175 stitutive heterochromatin and stably active, euchromatin, facultative heterochromatin has the capacit
176 ns through histone modifications and altered euchromatin formation, leading to the persistence and pa
178 chizosaccharomyces pombe heterochromatin and euchromatin fragments and analyze their composition by u
180 emodeling complex (Ino80C) directly prevents euchromatin from invading transcriptionally silent chrom
182 ing domain and a Gal4-reporter integrated in euchromatin, Gal4-SirT1 expression resulted in the deace
184 g reveal distinct roles of H1 on hetero- and euchromatin: H1 is necessary to form heterochromatic dom
186 ed is representative, we estimate that human euchromatin has expanded 30 Mb and 550 Mb compared to th
188 f1p functions to restrict silencing at yeast euchromatin-heterochromatin boundaries; therefore we del
191 s response to small extensions (<3 mum), and euchromatin/heterochromatin levels modulate the stiffnes
193 rozygous mutations or deletions of the human Euchromatin Histone Methyltransferase 1 (EHMT1) gene are
195 rlapping marks in the genome related to both euchromatin (histone H3 dimethyl lysine-4 [H3K4Me2]) and
196 nactive X chromosome usually associated with euchromatin: histone H4 acetylation and histone H3 lysin
197 alpha locus migrates from heterochromatin to euchromatin in a progressive fashion, reaching euchromat
202 tes to a balance between heterochromatin and euchromatin in the nucleus, and alterations in rDNA--ind
206 nces of genes located at the heterochromatin:euchromatin interface, with a very strong correlation be
207 cture, but the kinetics and pathway by which euchromatin is converted to the stable heterochromatin s
208 cription factors (TFs) to repressed genes in euchromatin is essential to activate new transcriptional
210 n conventional nuclei, microscopy shows that euchromatin is localized in the nuclear interior and het
214 We suggest that Lid2 enzymatic activity in euchromatin is regulated through a dynamic interplay wit
215 DNA can be packaged in two distinct forms: euchromatin is relatively accessible to DNA binding prot
217 nuclear RNAi, MET-1-mediated encroachment of euchromatin leads to detrimental decondensation of germl
218 stinct regions of the genome are packaged as euchromatin (less condensed, more active) or heterochrom
221 hese data suggest an active role for Bdf1 in euchromatin maintenance and antisilencing through a hist
222 esses, including transcriptional activation, euchromatin maintenance, and heterochromatin formation.
225 onded to a two- to threefold increase in the euchromatin marker histone H3 dimethyl-Lys4 at their res
226 hird, a poor correlation is observed between euchromatin marks (H3-K9/K14Ac, H3-K4Me2, H3-K36Me2, and
227 f heterochromatin marks and the reduction of euchromatin marks on viral chromatin at both early and l
230 Further, Snail interacted with G9a, a major euchromatin methyltransferase responsible for H3K9me2, a
233 h histone deacetylase inhibitors to increase euchromatin or histone methyltransferase inhibitors to d
234 oding preproinsulin, requires an appropriate euchromatin (or "open") DNA template characterized by hy
235 er to active (or inactive) compartments like euchromatin (or heterochromatin), and this is usually as
236 ct of huntingtin function in heterochromatin/euchromatin organization is evolutionarily conserved acr
237 ustrate the dynamic chromatin changes during euchromatin-originated de novo centromere formation, whi
238 We conclude that patterns of heterochromatin/euchromatin packaging show greater complexity and plasti
239 matin patterns reveals distinct profiles for euchromatin, pericentric heterochromatin, and the 4th ch
240 ally distinct domains of heterochromatin and euchromatin play important roles in the maintenance of c
244 ne H2A with the histone variant H2A.Z within euchromatin prevents silent chromatin proteins from migr
245 Here, we investigated heterochromatin and euchromatin profiles of the entire fission yeast genome
248 centromeric repeat arrays interspersing the euchromatin provides a previously unidentified type of c
249 cleus, PGC-1alpha was associated mainly with euchromatin rather than heterochromatin, consistent with
250 hanges that enhance meiotic recombination in euchromatin regions but are not sufficient to induce the
252 nding of Sir3p, and Sir4p at telomere-distal euchromatin regions, correlating with decreased gene exp
253 patterns in the human genome, especially in euchromatin regions, have not been systematically charac
255 olysis prevents CENP-A from mislocalizing to euchromatin, regulatory factors have not been identified
258 neration of facultative heterochromatin from euchromatin reversibly silences transcription of a set o
259 cluding the recruitment of promoter regions, euchromatin-rich domains, and differentially expressed g
261 ight coverage capturing approximately 65% of euchromatin sequence from the cat genome, these comparat
263 leosome density distribution and mobility in euchromatin, spatial arrangement of nanodomains, histone
266 function, likely through the maintenance of euchromatin structure at genes necessary for glucose-sti
267 res present on the latent provirus to active euchromatin structures containing acetylated histones.
270 istone modification patterns consistent with euchromatin, suggesting that rice centromeric chromatin
272 potent ability to regulate large domains of euchromatin than to influence the transcription of indiv
274 hances the separation of heterochromatin and euchromatin through its condensate partitioning properti
275 olutionary transition of a gene cluster from euchromatin to heterochromatin, which occurred <20 milli
278 e facultative heterochromatin from impinging euchromatin to produce discrete positional identities.
279 SCL2, indicating that JHDM3A may function in euchromatin to remove histone methylation marks that are
280 experience selective pressures distinct from euchromatin, tolerating rapid, dynamic changes in struct
282 tion to its previously characterized role in euchromatin, utilizes both enzymatic and structural mech
287 Histone H3 methylated at Lys4, which defines euchromatin, was not only distributed across most of the
290 whether they occurred in heterochromatin or euchromatin, were strongly associated with DNase hyperse
291 matin can be found interspersed in gene-rich euchromatin, where it regulates gene expression pertinen
292 inding directs HIV-1 to actively transcribed euchromatin, where the integrase-LEDGF/p75 interaction d
293 pression of CENP-A causes mislocalization to euchromatin, which could lead to deleterious consequence
294 n a coarse scale, the genome is divided into euchromatin, which harbors the majority of genes and is
295 same nucleoplasmic liquid as the surrounding euchromatin, which has implications for our understandin
296 karyotic cells, chromatin is classified into euchromatin, which is active in transcription, and heter
297 ed crossover increases occur in subtelomeric euchromatin, which is reminiscent of sex differences in
298 amplified DTC transposons (CACTA family) in euchromatin, which may silence euchromatic transposons t
299 is packaged as transcriptionally permissive euchromatin with few loci embedded in silenced heterochr
300 eterochromatin segment in juxtaposition with euchromatin without affecting the epigenetic landscape.