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 Previously, mice lacking TBP-associated factor 4b (Taf4b) were shown to exhibit a

16 Arabidopsis to a premature stop codon within TBP-ASSOCIATED FACTOR 4b (TAF4b), which encodes a subuni

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

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

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

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

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

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

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

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

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

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

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

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

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

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

31 epigenetic complexes, including the elusive TBP-associated-factor complex as well as two distinct GC

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

57 TBP-associated factor (TAF) family proteins, including T

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

84 ccupancies of TATA-binding protein (TBP) and TBP-associated factors (Tafs) at mammalian promoters are

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

117 sed of the TATA-binding protein (TBP) and 13 TBP-associated factors (TAFs).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

136 crucial event stimulated by testis-specific TBP-associated factors (tTAFs) to drive spermatocyte dif

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

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

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

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

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