ライフサイエンスコーパス: heterochromatin protein 1

1 rough recruitment of histone deacetylase and heterochromatin protein 1.

2 to chromodomain-containing proteins such as Heterochromatin Protein 1.

3 ed and unexpected target loci for Drosophila heterochromatin protein 1.

4 ependent H3K9me3 and impairs localization of heterochromatin protein 1.

5 ntaining lysine-9 methylated H3 histones and heterochromatin protein 1.

6 ryonic fibroblasts, Dnmt3a co-localizes with heterochromatin protein 1 alpha (HP1 alpha) and methyl-C

7 eraction domain for the epigenetic remodeler heterochromatin protein 1 alpha (HP1alpha) and isopeptid

8 We show that DEK interacts directly with Heterochromatin Protein 1 alpha (HP1alpha) and markedly

9 was a concomitant increase in the levels of heterochromatin protein 1 alpha (Hp1alpha), suggesting t

10 ), to define the dynamic interactions of the heterochromatin protein-1 alpha (HP1alpha) and the trans

11 rimethylation on lysine 9 of histone H3, and heterochromatin protein 1-alpha in p63-null keratinocyte

12 s recognized by a protein complex containing heterochromatin protein-1 and the DIM-2 DNA methyltransf

13 her defined by H3 trimethylated at lysine 9, heterochromatin protein 1, and histone H4 trimethylated

14 chromodomain proteins Polycomb (Pc) and HP1 (heterochromatin protein 1) are highly discriminatory for

15 Heterochromatin protein 1 beta (HP1beta) is abundant in

16 H3S28 and it is necessary and sufficient for heterochromatin protein 1 binding and H3K27me3 recruitme

17 maintaining proper histone modification and heterochromatin protein 1 binding at the pericentric het

18 We observe reduced heterochromatin protein 1 binding protein 3 (HP1BP3) sta

19 the late S phase, and both are required for heterochromatin protein 1 binding to heterochromatin.

20 sequences for two Xenopus laevis isoforms of heterochromatin protein 1, corresponding to HP1alpha and

21 Fission yeast Swi6 (a Heterochromatin protein 1 counterpart) is a component of

22 inding site on chromatin for proteins of the heterochromatin protein 1 family (HP1).

23 AP1 at Ser-473 attenuated its binding to the heterochromatin protein 1 family proteins and inhibited

24 omoter to recruit DNA methyltransferases and heterochromatin protein 1 for epigenetic modifications.

25 ribonucleic acid polymerase II together with heterochromatin protein 1 gamma (HP1gamma) at NF-kappaB-

26 one H3 lysine 9 trimethylation (H3K9me3) and heterochromatin protein 1 gamma (HP1gamma), as well as r

27 ressor Daxx (a binding partner of HDAC1), or heterochromatin protein 1 gamma resulted in robust and s

28 pression of green fluorescent protein-tagged heterochromatin protein 1 (GFP-HP1) or nontagged HP1 iso

29 In fission yeast, the Heterochromatin Protein 1 homolog Swi6 recognizes H3K9me

30 In contrast, a heterochromatin protein 1 homolog, LHP1, had no effect o

31 n the early embryo and its interactions with heterochromatin protein 1 (HP-1) lead us to speculate th

32 Satellites only accumulated abundant heterochromatin protein 1 (HP1) after replicating in S p

33 ffinity tag system, which was used to purify HETEROCHROMATIN PROTEIN 1 (HP1) and associated proteins

34 We found that heterochromatin protein 1 (HP1) and G9a formed a complex

35 n from Drosophila melanogaster that binds to heterochromatin protein 1 (HP1) and has been implicated

36 Heterochromatin protein 1 (HP1) and HP1-ORC-associated p

37 he genes encoding heterochromatin components heterochromatin protein 1 (HP1) and Su(var)3-9 enhance t

38 e show that borealin interacts directly with heterochromatin protein 1 (HP1) and that this interactio

39 wn heterochromatin-forming proteins, such as heterochromatin protein 1 (HP1) and the histone H2A vari

40 histone H3K9 methyltransferase (DIM-5), and heterochromatin protein 1 (HP1) are required for DNA met

41 Loss of ATM reduces the levels of heterochromatin protein 1 (HP1) at telomeres and suppres

42 very of the heterochromatin-enriched protein heterochromatin protein 1 (HP1) by Elgin and co-workers

43 s of DNA damage, we investigated the role of heterochromatin protein 1 (HP1) during the DDR process.

44 The heterochromatin protein 1 (HP1) family of proteins is in

45 Prohibitin could bind to heterochromatin protein 1 (HP1) family proteins and colo

46 Heterochromatin protein 1 (HP1) family proteins are cons

47 The heterochromatin protein 1 (HP1) family proteins HPL-1 an

48 Although phosphorylation of Heterochromatin Protein 1 (HP1) family proteins regulate

49 essor, which in turn recruits members of the heterochromatin protein 1 (HP1) family.

50 lpha-bound regulatory depots are tethered to heterochromatin protein 1 (HP1) for coordinated chromati

51 w that a young and rapidly evolving X-linked heterochromatin protein 1 (HP1) gene, HP1D2, plays a key

52 Heterochromatin protein 1 (HP1) has been proposed to pro

53 The heterochromatin protein 1 (HP1) homolog Rhino binds to t

54 ell as Su(var)205; the latter gene codes for heterochromatin protein 1 (HP1) in Drosophila.

55 lysine 9 of histone 3 (H3K9) and binding of heterochromatin protein 1 (HP1) in the promoter regions

56 Tethered heterochromatin protein 1 (HP1) induced H3K9me3, DNA met

57 finger, a PHD domain and a newly identified Heterochromatin Protein 1 (HP1) interaction motif that m

58 Heterochromatin protein 1 (HP1) is a central factor in e

59 Heterochromatin protein 1 (HP1) is a conserved chromosom

60 Heterochromatin protein 1 (HP1) is a conserved component

61 Heterochromatin protein 1 (HP1) is a conserved factor cr

62 Heterochromatin protein 1 (HP1) is a conserved non-histo

63 Heterochromatin protein 1 (HP1) is a key component of co

64 Heterochromatin protein 1 (HP1) is a major component of

65 Heterochromatin protein 1 (HP1) is a nonhistone chromoso

66 Heterochromatin Protein 1 (HP1) is a structural componen

67 Here, we show that heterochromatin protein 1 (HP1) is an essential CPC comp

68 Heterochromatin protein 1 (HP1) is localized at heteroch

69 Heterochromatin protein 1 (HP1) is well known as a silen

70 an increase in repressive H3K9me3 marks and heterochromatin protein 1 (HP1) on the reporter locus.

71 analyzed the genome-wide distribution of the heterochromatin protein 1 (HP1) ortholog HPL-2 and compa

72 be, the H3-K9 methyltransferase Clr4 and the heterochromatin protein 1 (HP1) ortholog Swi6 are critic

73 The identification of heterochromatin protein 1 (HP1) paved the way for a mole

74 Heterochromatin protein 1 (HP1) plays an important role

75 Heterochromatin protein 1 (HP1) proteins are "gatekeeper

76 occur in part as a result of the ability of heterochromatin protein 1 (HP1) proteins to spread acros

77 ith E2F transcription factors and recruiting heterochromatin protein 1 (HP1) proteins.

78 In Drosophila, heterochromatin protein 1 (HP1) suppresses the expressio

79 A heterochromatin protein 1 (HP1) tethering system was dev

80 tone H3 lysine 9 is important for recruiting heterochromatin protein 1 (HP1) to discrete regions of t

81 ne 9 (H3 Lys 9), and the specific binding of heterochromatin protein 1 (HP1) to methylated H3 Lys 9.

82 anscription (STAT) physically interacts with heterochromatin protein 1 (HP1) to promote heterochromat

83 Binding of heterochromatin protein 1 (HP1) to the histone H3 lysine

84 heterochromatin, because the chromodomain of heterochromatin protein 1 (HP1) typically recognizes his

85 ervation, Cuff physically interacts with the Heterochromatin Protein 1 (HP1) variant Rhino (Rhi).

86 The chromoshadow domain (CSD) of heterochromatin protein 1 (HP1) was recently shown to co

87 rtant role in stabilizing the interaction of heterochromatin protein 1 (HP1) with chromatin.

88 ified an interaction between hTAF(II)130 and heterochromatin protein 1 (HP1), a chromatin-associated

89 ral blood monocytes the MIEP associates with heterochromatin protein 1 (HP1), a chromosomal protein i

90 Heterochromatin protein 1 (HP1), a highly conserved non-

91 t that MITR, HDAC4, and HDAC5 associate with heterochromatin protein 1 (HP1), an adaptor protein that

92 ylation of histone H3 lysine 9 (H3K9me), and heterochromatin protein 1 (HP1), and is a model to inves

93 vo interaction with the epigenetic regulator heterochromatin protein 1 (HP1), and this methyl-depende

94 matin protein like-2 (HPL-2), the homolog of heterochromatin protein 1 (HP1), down-regulates the UPR

95 Heterochromatin protein 1 (HP1), first discovered in Dro

96 its of the origin recognition complex (ORC), heterochromatin protein 1 (HP1), histone H3 trimethyl K9

97 y a chromodomain-containing protein, such as heterochromatin protein 1 (HP1), leading to transcriptio

98 ases (Dnmts) and respective binding proteins heterochromatin protein 1 (HP1), polycomb protein comple

99 ional activation is partially antagonized by heterochromatin protein 1 (HP1), the code reader for his

100 n of lysine 9 in histone H3 is recognized by heterochromatin protein 1 (HP1), which directs the bindi

101 Heterochromatin protein 1 (HP1), which interacts with Rb

102 Central to heterochromatin spread is heterochromatin protein 1 (HP1), which recognizes H3K9-m

103 een these two methyl marks is facilitated by heterochromatin protein 1 (HP1), which serves as an adap

104 histone H3 lysine 9 methyltransferase DIM-5, Heterochromatin Protein 1 (HP1), which specifically bind

105 DNA breaks swiftly mobilize heterochromatin protein 1 (HP1)-beta (also called CBX1),

106 rochromatin formation by recruiting multiple heterochromatin protein 1 (HP1)-containing complexes tha

107 histone H3 at lysine 9 (H3K9), which allows heterochromatin protein 1 (HP1)-related chromodomain pro

108 9 of histone H3 (H3K9me), a binding site for heterochromatin protein 1 (HP1).

109 d was enhanced by the classical PEV modifier heterochromatin protein 1 (HP1).

110 acts as a recognition signal for binding of heterochromatin protein 1 (HP1).

111 ks of middle repetitious DNA associated with heterochromatin protein 1 (HP1).

112 that controls its reversible association to heterochromatin protein 1 (HP1).

113 uctural and functional homologue of metazoan heterochromatin protein 1 (HP1).

114 terochromatin protein 2 (HP2) interacts with heterochromatin protein 1 (HP1).

115 ine 9 and recruitment of its binding partner heterochromatin protein 1 (HP1).

116 H3 lysine 9 (DiMetH3K9) and the presence of heterochromatin protein 1 (HP1).

117 ion and serve as a specific binding site for heterochromatin protein 1 (HP1).

118 n homologue (M31) of Drosophila melanogaster heterochromatin protein 1 (HP1; refs 7,8) in transgenic

119 The role of Heterochromatin Protein-1 (HP1) during mitosis has been

120 at, similar to the histone variant macroH2A, heterochromatin protein-1 (HP1), histone H1 and the high

121 our analyses of Rhino, a novel member of the Heterochromatin Protein 1(HP1) subfamily of chromo box p

122 Heterochromatin protein 1 (HP1a in Drosophila) is a cons

123 Heterochromatin protein 1 (HP1a) has conserved roles in

124 ins--origin recognition complex 2 (Orc2) and heterochromatin protein 1 (HP1alpha)--in Xi silencing.

125 Heterochromatin protein 1 (HP1beta), a key component of

126 Heterochromatin protein 1 Hsalpha (HP1(Hsalpha)) is one

127 Heterochromatin protein 1(Hsalpha) (HP1(Hsalpha)), one o

128 Here, we show that heterochromatin protein 1 in fission yeast (Swi6) is los

129 Heterochromatin protein 1 is an epigenetic modifier of g

130 LIKE HETEROCHROMATIN PROTEIN 1 (LHP1) binds Polycomb-deposite

131 Here, we report that A. thaliana LIKE HETEROCHROMATIN PROTEIN 1 (LHP1) is necessary to maintai

132 ard genetic screen for enhancers of the like heterochromatin protein 1 (lhp1) mutant, which shows rel

133 ng proteins were identified, among them LIKE HETEROCHROMATIN PROTEIN 1 (LHP1).

134 such as proliferating cell nuclear antigen, heterochromatin protein 1, methyl-CpG binding protein 2,

135 f histone H3 at lysine 9, and association of heterochromatin protein 1 on the heterochromatic regions

136 We find heterochromatin protein 1/origin recognition complex-ass

137 Overexpression of heterochromatin protein 1 significantly inhibited E2F1-K

138 sion of JHDM3A abrogates recruitment of HP1 (heterochromatin protein 1) to heterochromatin, indicatin

139 Expression of the heterochromatin protein 1 was increased, and expression

140 nt of the FLC silenced state but not on LIKE HETEROCHROMATIN PROTEIN 1, which functions to maintain s