ライフサイエンスコーパス: facultative heterochromatin

1 sal of this process results in reassembly of facultative heterochromatin.

2 ociated with silenced developmental genes at facultative heterochromatin.

3 ethyltransferase complexes to form localized facultative heterochromatin.

4 r in mediating a switch from constitutive to facultative heterochromatin.

5 iptional repression through the spreading of facultative heterochromatin.

6 X chromosomes packaged into euchromatin and facultative heterochromatin.

7 HP1 is important for normal localization of facultative heterochromatin.

8 nt functions in maintaining the stability of facultative heterochromatin.

9 rate histone H2A variant that is enriched on facultative heterochromatin.

10 ve X chromosome (Xi) to mediate formation of facultative heterochromatin.

11 ructures, in the regulation and formation of facultative heterochromatin.

12 modifications that have been associated with facultative heterochromatin.

13 s 20 methylation, a mark of constitutive and facultative heterochromatin.

14 ted at Lys9 is also a distinguishing mark of facultative heterochromatin.

15 de' involved in establishing and maintaining facultative heterochromatin.

16 n linked to the formation and maintenance of facultative heterochromatin, although the underlying mec

17 We explore the connection between facultative heterochromatin and replication control and

18 Cbx7 associates with facultative heterochromatin and, more specifically, is e

19 d X chromosome inactivation in female cells (facultative heterochromatin), and the stable shutdown of

20 e underlying the resolution and formation of facultative heterochromatin, and they demonstrate that B

21 Cellular long, noncoding RNAs induce facultative heterochromatin, and this study shows that t

22 proteins, but the chromatin modifications of facultative heterochromatin are less clear.

23 ltransferase G9a directly interact to induce facultative heterochromatin assembly and regulate epigen

24 on (H3K9me2), a modification associated with facultative heterochromatin assembly and the resulting t

25 ese analyses reveal the role of Shelterin in facultative heterochromatin assembly at late origins, wh

26 lex (EMC), to promote meiotic mRNA decay and facultative heterochromatin assembly.

27 l1-Red1 core and the exosome are involved in facultative heterochromatin assembly; however, the exact

28 Formation of facultative heterochromatin at specific genomic loci is

29 ing the appearance of specialized domains of facultative heterochromatin called senescence-associated

30 escence is often characterized by domains of facultative heterochromatin, called senescence-associate

31 escence is often characterized by domains of facultative heterochromatin, called senescence-associate

32 cent cells accumulate specialized domains of facultative heterochromatin, called Senescence-Associate

33 Specialized domains of facultative heterochromatin, called senescence-associate

34 3 lysine 9 trimethylation (H3K9Me3), whereas facultative heterochromatin displays DNA hypomethylation

35 Reversibly silenced facultative heterochromatin domains are often enriched f

36 matin block and by the presence of prominent facultative heterochromatin domains that are localized a

37 by preventing transcriptional activation of facultative heterochromatin during differentiation.

38 tions, with H3K27me3, which is indicative of facultative heterochromatin, exhibiting the highest enri

39 rd "facultas" literally means "opportunity." Facultative heterochromatin (fHC) then designates genomi

40 ovo cytosine methylation events required for facultative heterochromatin formation and higher-order h

41 nation, to promote premature termination and facultative heterochromatin formation at meiotic genes.

42 gene expression and found that RelB induces facultative heterochromatin formation by directly intera

43 ers, that serve to demarcate the boundary of facultative heterochromatin formation.

44 le for chromatin modulations associated with facultative heterochromatin formation.

45 stemic inflammatory (SSI), the generation of facultative heterochromatin from euchromatin reversibly

46 Hence, CTCF is required to insulate facultative heterochromatin from impinging euchromatin t

47 erochromatin and stably active, euchromatin, facultative heterochromatin has the capacity to alternat

48 omosome (Xi), the most extensive instance of facultative heterochromatin in mammals, replicates later

49 n is developmentally up-regulated to promote facultative heterochromatin in mature rod photoreceptors

50 3, modifications that are characteristic of facultative heterochromatin in plants, increase at FLC c

51 barley whereby intergenic H3K27me3 specifies facultative heterochromatin in the telomere-proximal reg

52 e there are different mechanisms for forming facultative heterochromatin in vertebrates.

53 27 on histone H3 (H3K27me) marks repressed "facultative heterochromatin," including developmentally

54 The arrangement of facultative heterochromatin into spatially and temporall

55 Facultative heterochromatin is a cytological manifestati

56 Therefore, the formation of facultative heterochromatin is dependent on factors that

57 ression via dicer-independent siRNA-mediated facultative heterochromatin is largely independent of, a

58 Facultative heterochromatin is of particular interest, b

59 The most extensive example of facultative heterochromatin is the mammalian inactive X

60 thylated on lysine 27 (H3K27me3), a mark for facultative heterochromatin, is lost on the inactive X c

61 Here, we describe facultative heterochromatin islands in fission yeast and

62 Previously, we identified facultative heterochromatin islands in the fission yeast

63 s in the distribution of H3K27me; regions of facultative heterochromatin lost H3K27me3, while regions

64 and a site associated with the formation of facultative heterochromatin, lysine 27 (H3K27).

65 clusters in F. fujikuroi are located within facultative heterochromatin marked by trimethylated lysi

66 the LAT region showed reduced levels of the facultative heterochromatin marker (H3K27me3) along with

67 xamined histone modifications and HP1 in the facultative heterochromatin of nucleated erythrocytes an

68 Here we report that, as observed in the facultative heterochromatin of the inactive X chromosome

69 modifications that normally characterize the facultative heterochromatin of the inactive X-chromosome

70 the other one localized to the more plastic facultative heterochromatin, or next to it.

71 often near centromeres and telomeres, where facultative heterochromatin plays a role in transcriptio

72 scriptional interference and the blocking of facultative heterochromatin propagation by transcription

73 Facultative heterochromatin regulates gene expression, b

74 utive heterochromatin segment and a 16.17-kb facultative heterochromatin segment that form part of th

75 We reported that gene-selective formation of facultative heterochromatin silences transcription of ac

76 Facultative heterochromatin silencing at frq functions i

77 ker histone plays a role in establishing the facultative heterochromatin territory and architecture i

78 Facultative heterochromatin that changes during cellular

79 g in the formation of extraordinarily stable facultative heterochromatin that is faithfully propagate

80 ion of a viral noncoding RNA can also induce facultative heterochromatin to promote lytic gene silenc