ライフサイエンスコーパス: TBP-associated factor

1 actions with itself, with Dorsal, and with a TBP-associated factor.

2 g the TATA box-binding polypeptide (TBP) and TBP-associated factors.

3 ionally and physically interact with TBP and TBP-associated factors.

4 nsferase Gcn5, Spt proteins, and a subset of TBP-associated factors.

5 TA box-binding protein (TBP), TFIIB, and the TBP-associated factor 1 (TAF1) in vitro.

6 line with a temperature-sensitive defect in TBP-associated factor 1 (TAF1), a component of the TFIID

7 st transcription factor IID (TFIID) subunit, TBP-associated factor 1 (TAF1), possesses protein kinase

8 the distinguishable FRAP behavior of TBP and TBP-associated factor 1 indicates that there are populat

9 sed to identify proteins that regulate TAF1 (TBP-associated factor 1) alternative splicing in respons

10 ociation with TATA binding protein (TBP) and TBP-associated factor 11 (TAF11).

11 sociation with TAF110 (TATA-binding protein (TBP)-associated factor 110) and the co-repressor SMRT, b

12 e cloning of human TATA box binding protein (TBP)-associated factor 20 (TAF20) and the consequent ide

13 In vitro, holo-TFIID and TBP-associated factor 250 (TAF(II)250) phosphorylated TF

14 TBP-associated factor 4 (TAF4), an essential subunit of

15 of the analyzed TSTRs, TATA-binding protein (TBP)-associated factor 7-like (TAF7L).

16 ons as a molecular switch in the exchange of TBP-associated factor 7 (TAF7) for LEC to facilitate the

17 TATA-binding protein (TBP)-associated factor 7l (Taf7l; a paralogue of Taf7) a

18 ntaining a conditional TATA binding protein (TBP)-associated factor 9 allele (TAF9).

19 Gli proteins and a transcription coactivator TBP-associated factor 9 (TAF9), and validated its functi

20 fficiency, whereas artificial recruitment of TBP-associated factors activates only chromosomal report

21 Mot1 is an essential TATA-binding protein (TBP)-associated factor and Snf2/Swi2 ATPase that both re

22 They are referred to as TAFs (TBP-associated factors), and together with TBP comprise

23 osed of TATA binding protein (TBP) and three TBP-associated factors, and the activator upstream bindi

24 Since female mice null for Taf4b, a TBP associated factor, are sterile, we sought to determi

25 scription suggest that coactivators, such as TBP-associated factors, are involved.

26 specificity via tissue-specific versions of TBP-associated factors as well as a tissue-specific TBP-

27 sed by direct recruitment of TBP and several TBP-associated factors, but not by natural activation do

28 interact with the TATA-binding protein (TBP)-TBP-associated factor complex.

29 Finally, our results suggest that TBP-associated-factor components of SAGA are differentia

30 DNA and induces a TATA box-binding protein (TBP)-associated factor-dependent footprint downstream of

31 n) gene of Drosophila encodes a homolog of a TBP-associated factor (dTAF5) protein expressed only in

32 Here we show that testis-specific TAF (TBP-associated factor) homologs required for terminal di

33 The presence of TBP-associated factors, however, helps overcome PC4 repr

34 nscription factor IIB (TFIIB), and the human TBP-associated factor hTAF(II)32 in vitro but not hTAF(I

35 s the TATA-binding protein (TBP) and several TBP-associated factors (hTAFs) that have been shown to p

36 n essential, conserved TATA-binding protein (TBP)-associated factor in Saccharomyces cerevisiae and a

37 essential, conserved, TATA-binding protein (TBP)-associated factor in Saccharomyces cerevisiae with

38 P, both of which can occur in the absence of TBP-associated factors in TFIID.

39 yeast TBP oligomerization in the presence of TBP-associated factors in the context of TFIID.

40 ing an immunopurified TFIID, indicating that TBP-associated factors may be a sufficient subset of coa

41 These high rates require the activity of the TBP-associated factor Mot1, suggesting that TBP/chromati

42 logenetically conserved, polymerase-specific TBP-associated factors or TAFIIS.

43 with recombinant TBP or TFB, indicating that TBP-associated factors or TFB-associated factors are not

44 The Taf (TBP-associated factor) subunits, shared with TFIID, occu

45 g the 130,000-Mr yeast TATA-binding protein (TBP)-associated factor TAF(II)130 (yTAF(II)130).

46 The TATA-binding protein (TBP)-associated factor TAF(II)250 is the largest compone

47 part, through a direct interaction with the TBP-associated factor TAF(II)250.

48 nd SAGA contain common TATA-binding protein (TBP)-associated factor (TAF(II)) subunits and each compl

49 y c-Jun depends on the TATA-binding protein (TBP)-associated factor (TAF) subunits of transcription f

50 iptional initiation of TATA-binding protein (TBP)-associated factor (TAF)-dependent ribosomal protein

51 s position, performs a TATA-binding protein (TBP)-associated factor (TAF)-like function.

52 wi2-related ATPase and TATA-binding protein (TBP)-associated factor (TAF).

53 tions of this TATA box-binding protein (TBP)/TBP-associated factor (TAF) complex.

54 d sufficient for in vitro transcription, the TBP-associated factor (TAF) subunits recognize downstrea

55 Of the 14 TBP-associated factor (TAF) subunits that compose TFIID,

56 host kinases and association with different TBP-associated factor (TAF) subunits.

57 scription factor TFIID for promoter DNA in a TBP-associated factor (TAF)-dependent manner.

58 emical characterization of an abundant human TBP-associated factor (TAF-172) which is homologous to t

59 However, the role of tissue-specific TBP-associated factors (TAF(II)s) and other tissue-speci

60 The TATA box-binding protein (TBP) and TBP-associated factors (TAF(II)s) compose the general tr

61 ption under some circumstances, the roles of TBP-associated factors (TAF(II)s) in TFIID-mediated acti

62 d of TATA box-binding protein (TBP) and many TBP-associated factors (TAF(II)s).

63 e TATA box binding protein (TBP) and several TBP-associated factors (TAF(II)s).

64 s the TATA-binding protein (TBP) and several TBP-associated factors (TAF(II)s).

65 prises the TATA-binding protein (TBP) and 13 TBP-associated factors (TAF1-13), which specifically int

66 Here, we report that the orphan TBP-associated factor TAF9B is selectively up-regulated

67 directly and is the likely homolog of human TBP-associated factor TAFII18, we propose that RSP5/hRPF

68 A TBP mutant defective in interaction with TBP-associated factor TAFII250 also failed to mediate tr

69 of these mutations on binding of TBP to the TBP-associated factor TAFII250 in vitro.

70 nsists of the TATA-binding protein (TBP) and TBP associated factors (TAFIIs).

71 TATA-box-binding protein (TBP) and a set of TBP-associated factors (TAFIIs).

72 e TATA-binding protein (TBP) and an array of TBP-associated factors (TAFIIs).

73 one receptors requires TATA-binding protein (TBP)-associated factors (TAFs) as well as the multi-subu

74 , is dependent both on TATA binding protein (TBP)-associated factors (TAFs) in TFIID and on TFIIH.

75 The majority of the TATA-binding protein (TBP)-associated factors (TAFs) that constitute transcrip

76 Mediator requires the TATA-binding protein (TBP)-associated factors (TAFs) within the TFIID complex

77 TATA box-binding protein (TBP)-associated factors (TAFs), evolutionarily conserved

78 mposed of the TATA-binding protein (TBP) and TBP-associated factors (TAFs) and is the only component

79 How TATA box-binding protein (TBP) and the TBP-associated factors (TAFs) are assembled into a funct

80 defective for interaction with certain yeast TBP-associated factors (TAFs) at the restrictive tempera

81 lymerase II, TATA-binding protein (TBP), and TBP-associated factors (TAFs) bind to initiate transcrip

82 the TATA-box-binding protein (TBP) and three TBP-associated factors (TAFs) called TAF(I)48, TAF(I)63

83 contains the TATA-binding protein (TBP) and TBP-associated factors (TAFs) implicated in the function

84 found in large complexes with either TBP, as TBP-associated factors (TAFs) in the general factor TFII

85 uestions remain concerning the role of TFIID TBP-associated factors (TAFs) in transcription, includin

86 ptional activation in vivo and in binding to TBP-associated factors (TAFs) in vitro, although still c

87 In yeast, the TBP-associated factors (TAFs) Taf17, Taf60, and Taf61(68

88 binding protein (TBP) and with several human TBP-associated factors (TAFs) that include TAFII250.

89 tified a primary TATA binding subunit (TBP), TBP-associated factors (TAFs) that interact with and med

90 ng protein (TBP) associated with a series of TBP-associated factors (TAFs) that together participate

91 each case, TBP interacts with class-specific TBP-associated factors (TAFs) to form class-specific tra

92 TBP) associates with other proteins known as TBP-associated factors (TAFs) to form multisubunit trans

93 vivo, TBP is complexed with approximately 14 TBP-associated factors (TAFs) to form the general transc

94 ay perform a function similar to that of the TBP-associated factors (TAFs) which make up TFIID.

95 omprising the TATA-binding protein (TBP) and TBP-associated factors (TAFs), associates specifically w

96 of TATA element-binding protein (TBP) and 14 TBP-associated factors (TAFs), can directly recognize co

97 prised of the TATA-binding protein (TBP) and TBP-associated factors (TAFs), is a general transcriptio

98 the TATA box-binding protein (TBP) and many TBP-associated factors (TAFs), plays a central role in b

99 In addition, endogenous TBP and TBP-associated factors (TAFs), specific for RNA polymera

100 in transcriptional activation and binding to TBP-associated factors (TAFs), was similarly defective i

101 rikingly, some polypeptides are identical to TBP-associated factors (TAFs), which are subunits of TFI

102 he TATA box binding protein, and 14 distinct TBP-associated factors (TAFs), which range in size from

103 f the TATA-binding protein (TBP) and several TBP-associated factors (TAFs), whose primary sequences a

104 sed of the TATA-binding protein (TBP) and 13 TBP-associated factors (TAFs)-assembles into a functiona

105 -a complex of TATA-binding protein (TBP) and TBP-associated factors (TAFs)-is a central component of

106 comprising TATA-binding protein (TBP) and 13 TBP-associated factors (TAFs).

107 s, being associated with polymerase-specific TBP-associated factors (TAFs).

108 s the TATA-binding protein (TBP) and several TBP-associated factors (TAFs).

109 f activation is similar to that proposed for TBP-associated factors (TAFs).

110 TATA box-binding protein (TBP) and multiple TBP-associated factors (TAFs).

111 -binding protein (TBP) and approximately ten TBP-associated factors (TAFs).

112 ng protein (TBP) and polymerase III-specific TBP-associated factors (TAFs).

113 x-binding protein (TBP) and approximately 14 TBP-associated factors (TAFs).

114 e TATA-binding protein (TBP) and a series of TBP-associated factors (TAFs).

115 of the TATA binding protein (TBP) and 12-15 TBP-associated factors (TAFs).

116 sed of the TATA-binding protein (TBP) and 14 TBP-associated factors (TAFs).

117 binding protein (TBP) and a set of conserved TBP-associated factors (TAFs).

118 ding protein (TBP) and approximately a dozen TBP-associated factors (TAFs).

119 e TATA binding protein (TBP) and 14 distinct TBP-associated factors (TAFs).

120 f TATA-binding protein (TBP) and 14 distinct TBP-associated factors (TAFs).

121 TATA box binding protein (TBP) and multiple TBP-associated factors (TAFs).

122 sed of TATA box-binding protein (TBP) and 13 TBP-associated factors (Tafs).

123 TFIIA, and TFIIB, but not with occupancy by TBP-associated factors (TAFs).

124 TATA box binding protein (TBP) and multiple TBP-associated factors (TAFs).

125 nsists of the TATA-binding protein (TBP) and TBP-associated factors (TAFs).

126 ng protein (TBP) and class III gene-specific TBP-associated factors (TAFs).

127 al initiation of TFIID (a complex of TBP and TBP-associated factors [TAFs])-dependent ribosomal prote

128 contains TATA-binding protein (TBP) and four TBP-associated factors that are specific for polymerase

129 ranscription program regulated by the testis TBP-associated factor (tTAF) or meiosis arrest complex (

130 time that a discrete fragment of a mammalian TBP-associated factor which targets a specific activator

131 encoding TAF25p, that this non-histone-like TBP-associated factor, which is shared between the TFIID

132 rtain eukaryotic TAFs (TATA binding protein (TBP) associated factors) whose binding to TBP results in

133 In addition, NuA3 contains the TBP- associated factor, yTAF(II)30, which is also a comp

134 nsertion mutation in the gene encoding yeast TBP-associated factor yTAFII61/68 that impairs Gcn4p-ind