| scholarly article | Q13442814 |
| P2093 | author name string | K Struhl | |
| M Keaveney | |||
| Z Moqtaderi | |||
| P2860 | cites work | Cloning of an intrinsic human TFIID subunit that interacts with multiple transcriptional activators | Q24309765 |
| The TAF(II)250 subunit of TFIID has histone acetyltransferase activity | Q24310327 | ||
| Human TAF(II)28 interacts with the human T cell leukemia virus type I Tax transactivator and promotes its transcriptional activity | Q24313480 | ||
| Histone-like TAFs within the PCAF histone acetylase complex | Q24317520 | ||
| General requirement for RNA polymerase II holoenzymes in vivo | Q24561963 | ||
| Structural similarity between TAFs and the heterotetrameric core of the histone octamer | Q27732598 | ||
| A multiprotein mediator of transcriptional activation and its interaction with the C-terminal repeat domain of RNA polymerase II. | Q27930548 | ||
| ADA5/SPT20 links the ADA and SPT genes, which are involved in yeast transcription | Q27932447 | ||
| Zap1p, a metalloregulatory protein involved in zinc-responsive transcriptional regulation in Saccharomyces cerevisiae | Q27933621 | ||
| The TATA-binding protein is required for transcription by all three nuclear RNA polymerases in yeast cells | Q27934537 | ||
| Yeast Gcn5 functions in two multisubunit complexes to acetylate nucleosomal histones: characterization of an Ada complex and the SAGA (Spt/Ada) complex | Q27934812 | ||
| A subset of TAF(II)s are integral components of the SAGA complex required for nucleosome acetylation and transcriptional stimulation | Q27936635 | ||
| Yeast TAF(II)145 functions as a core promoter selectivity factor, not a general coactivator | Q27937694 | ||
| An activator target in the RNA polymerase II holoenzyme | Q27938223 | ||
| Yeast TAF(II)145 required for transcription of G1/S cyclin genes and regulated by the cellular growth state | Q27938810 | ||
| ADA1, a novel component of the ADA/GCN5 complex, has broader effects than GCN5, ADA2, or ADA3. | Q27939725 | ||
| The yeast ZRT1 gene encodes the zinc transporter protein of a high-affinity uptake system induced by zinc limitation | Q27940126 | ||
| Induced alpha helix in the VP16 activation domain upon binding to a human TAF | Q28247311 | ||
| The TAFs in the HAT | Q28277194 | ||
| Biochemistry and structural biology of transcription factor IID (TFIID) | Q29620209 | ||
| An RNA polymerase II holoenzyme responsive to activators | Q29620210 | ||
| Saturation mutagenesis of a yeast his3 "TATA element": genetic evidence for a specific TATA-binding protein | Q33567358 | ||
| The downstream core promoter element, DPE, is conserved from Drosophila to humans and is recognized by TAFII60 of Drosophila | Q35196382 | ||
| Mechanism of differential utilization of the his3 TR and TC TATA elements | Q36556517 | ||
| Tc, an unusual promoter element required for constitutive transcription of the yeast HIS3 gene | Q36722871 | ||
| Constitutive and inducible Saccharomyces cerevisiae promoters: evidence for two distinct molecular mechanisms | Q36899311 | ||
| Yeast homologues of higher eukaryotic TFIID subunits | Q37047781 | ||
| Naturally occurring poly(dA-dT) sequences are upstream promoter elements for constitutive transcription in yeast | Q37539289 | ||
| Absolute mRNA levels and transcriptional initiation rates in Saccharomyces cerevisiae | Q37580107 | ||
| SPT20/ADA5 encodes a novel protein functionally related to the TATA-binding protein and important for transcription in Saccharomyces cerevisiae | Q40019111 | ||
| The ts13 mutation in the TAF(II)250 subunit (CCG1) of TFIID directly affects transcription of D-type cyclin genes in cells arrested in G1 at the nonpermissive temperature | Q40022378 | ||
| Chromatin structure and RNA polymerase II connection: implications for transcription | Q40948234 | ||
| Multiple TAFIIs directing synergistic activation of transcription | Q41259644 | ||
| Binding of TAFs to core elements directs promoter selectivity by RNA polymerase II | Q41333550 | ||
| Promoter-selective transcriptional defect in cell cycle mutant ts13 rescued by hTAFII250. | Q41487995 | ||
| The SAGA unfolds: convergence of transcription regulators in chromatin-modifying complexes. | Q42459431 | ||
| Assembly of recombinant TFIID reveals differential coactivator requirements for distinct transcriptional activators | Q42491732 | ||
| Drosophila TAFII40 interacts with both a VP16 activation domain and the basal transcription factor TFIIB. | Q42502083 | ||
| TBP-associated factors are not generally required for transcriptional activation in yeast | Q42522148 | ||
| TAF(II)s mediate activation of transcription in the Drosophila embryo | Q42528499 | ||
| A general mechanism for transcriptional synergy by eukaryotic activators | Q46144332 | ||
| Transcription activation via enhanced preinitiation complex assembly in a human cell-free system lacking TAFIIs | Q47858026 | ||
| Transcriptional activation independent of TFIIH kinase and the RNA polymerase II mediator in vivo | Q47991678 | ||
| Transcription activation in cells lacking TAFIIS. | Q48060189 | ||
| Eukaryotic activators function during multiple steps of preinitiation complex assembly | Q59058665 | ||
| Variants of the TATA-binding protein can distinguish subsets of RNA polymerase I, II, and III promoters | Q68126686 | ||
| Yeast TAF(II)90 is required for cell-cycle progression through G2/M but not for general transcription activation | Q71574610 | ||
| Conserved and nonconserved functions of the yeast and human TATA-binding proteins | Q72718769 | ||
| A mechanism for TAFs in transcriptional activation: activation domain enhancement of TFIID-TFIIA--promoter DNA complex formation | Q72718834 | ||
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | TATA-binding protein-associated factor TAF6 YGL112C | Q27549236 |
| Chromatin modification protein YMR236W | Q27549905 | ||
| Histone acetyltransferase YGR274C | Q27551031 | ||
| P304 | page(s) | 675-82 | |
| P577 | publication date | 1998-11-01 | |
| P1433 | published in | Molecular Cell | Q3319468 |
| P1476 | title | The histone H3-like TAF is broadly required for transcription in yeast | |
| P478 | volume | 2 |
| Q33651485 | A TATA-binding protein mutant defective for TFIID complex formation in vivo |
| Q30976876 | A cell system with targeted disruption of the SMN gene: functional conservation of the SMN protein and dependence of Gemin2 on SMN. |
| Q34092100 | A composite nuclear export signal in the TBP-associated factor TAFII105. |
| Q27935262 | A functional module of yeast mediator that governs the dynamic range of heat-shock gene expression |
| Q27938450 | A yeast taf17 mutant requires the Swi6 transcriptional activator for viability and shows defects in cell cycle-regulated transcription |
| Q43975761 | Activator-specific recruitment of TFIID and regulation of ribosomal protein genes in yeast |
| Q47068840 | An extensive requirement for transcription factor IID-specific TAF-1 in Caenorhabditis elegans embryonic transcription |
| Q37258622 | An initiation element in the yeast CUP1 promoter is recognized by RNA polymerase II in the absence of TATA box-binding protein if the DNA is negatively supercoiled |
| Q27939741 | Analysis of TAF90 mutants displaying allele-specific and broad defects in transcription |
| Q33909730 | Assembly of partial TFIID complexes in mammalian cells reveals distinct activities associated with individual TATA box-binding protein-associated factors |
| Q35128380 | Bicoid functions without its TATA-binding protein-associated factor interaction domains |
| Q27931210 | Bromodomain factor 1 corresponds to a missing piece of yeast TFIID. |
| Q24797549 | Coordinate regulation of RARgamma2, TBP, and TAFII135 by targeted proteolysis during retinoic acid-induced differentiation of F9 embryonal carcinoma cells |
| Q34989940 | Copper metalloregulation of gene expression |
| Q40015630 | Core promoter elements and TAFs contribute to the diversity of transcriptional activation in vertebrates |
| Q43754467 | Death signals changes in TFIID. |
| Q34730910 | Derepression of DNA damage-regulated genes requires yeast TAF(II)s |
| Q28776386 | Different upstream transcriptional activators have distinct coactivator requirements |
| Q35131734 | Displacement of histones at promoters of Saccharomyces cerevisiae heat shock genes is differentially associated with histone H3 acetylation |
| Q39645792 | Distinct requirements for C.elegans TAF(II)s in early embryonic transcription |
| Q22254120 | Divergent hTAFII31-binding motifs hidden in activation domains |
| Q34097281 | Domain-wide displacement of histones by activated heat shock factor occurs independently of Swi/Snf and is not correlated with RNA polymerase II density |
| Q38359357 | Dynamic chromatin alterations triggered by natural and synthetic activation domains |
| Q77665569 | Enhanced apoptosis of B and T lymphocytes in TAFII105 dominant-negative transgenic mice is linked to nuclear factor-kappa B |
| Q30700508 | Evidence that TAF-TATA box-binding protein interactions are required for activated transcription in mammalian cells |
| Q50721140 | Expression of TAFII70 RNA and protein during oogenesis and development of the amphibian Pleurodeles waltl. |
| Q28202398 | Functional analysis of the TFIID-specific yeast TAF4 (yTAF(II)48) reveals an unexpected organization of its histone-fold domain |
| Q33719389 | Functional interplay between chromatin remodeling complexes RSC, SWI/SNF and ISWI in regulation of yeast heat shock genes |
| Q27939082 | Genetic analysis of TAF68/61 reveals links to cell cycle regulators |
| Q41954712 | Highly redundant function of multiple AT-rich sequences as core promoter elements in the TATA-less RPS5 promoter of Saccharomyces cerevisiae |
| Q39458102 | Histone folds mediate selective heterodimerization of yeast TAF(II)25 with TFIID components yTAF(II)47 and yTAF(II)65 and with SAGA component ySPT7. |
| Q77652527 | Histone-like TAFs are essential for transcription in vivo |
| Q22010401 | Human transcription factor hTAF(II)150 (CIF150) is involved in transcriptional regulation of cell cycle progression |
| Q27936204 | Identification of a yeast transcription factor IID subunit, TSG2/TAF48. |
| Q34093393 | Identification of hTAF(II)80 delta links apoptotic signaling pathways to transcription factor TFIID function |
| Q27931284 | Identification of two novel TAF subunits of the yeast Saccharomyces cerevisiae TFIID complex |
| Q27938987 | Impaired core promoter recognition caused by novel yeast TAF145 mutations can be restored by creating a canonical TATA element within the promoter region of the TUB2 gene |
| Q22011058 | Isolation and characterization of human orthologs of yeast CCR4-NOT complex subunits |
| Q28586142 | Isolation of mouse TFIID and functional characterization of TBP and TFIID in mediating estrogen receptor and chromatin transcription |
| Q27940055 | Molecular and genetic characterization of a Taf1p domain essential for yeast TFIID assembly. |
| Q39528206 | Molecular genetic dissection of TAF25, an essential yeast gene encoding a subunit shared by TFIID and SAGA multiprotein transcription factors |
| Q34286865 | Mot1 associates with transcriptionally active promoters and inhibits association of NC2 in Saccharomyces cerevisiae |
| Q57971028 | NF-Y Recruitment of TFIID, Multiple Interactions with Histone Fold TAFIIs |
| Q37800070 | Novel aspects of heat shock factors: DNA recognition, chromatin modulation and gene expression |
| Q37657760 | Promoter architecture and the evolvability of gene expression |
| Q27930749 | Protein-protein interaction map for yeast TFIID. |
| Q38679087 | Quick or quality? How mRNA escapes nuclear quality control during stress |
| Q34324685 | Redundant role of tissue-selective TAF(II)105 in B lymphocytes |
| Q38311191 | Redundant roles for the TFIID and SAGA complexes in global transcription |
| Q34011585 | Region of yeast TAF 130 required for TFIID to associate with promoters |
| Q33966940 | Remodeling of yeast CUP1 chromatin involves activator-dependent repositioning of nucleosomes over the entire gene and flanking sequences |
| Q33964585 | Robust mRNA transcription in chicken DT40 cells depleted of TAF(II)31 suggests both functional degeneracy and evolutionary divergence |
| Q35558697 | Roles for BTAF1 and Mot1p in dynamics of TATA-binding protein and regulation of RNA polymerase II transcription |
| Q37432193 | SAGA and Rpd3 chromatin modification complexes dynamically regulate heat shock gene structure and expression |
| Q47141163 | SAGA mediates transcription from the TATA-like element independently of Taf1p/TFIID but dependent on core promoter structures in Saccharomyces cerevisiae. |
| Q74604712 | Selective recruitment of TAFs by yeast upstream activating sequences. Implications for eukaryotic promoter structure |
| Q33903270 | Specific interaction of TAFII105 with OCA-B is involved in activation of octamer-dependent transcription |
| Q35669885 | Structure and function of the TFIID complex |
| Q39446445 | Synergistic transcriptional activation by TATA-binding protein and hTAFII28 requires specific amino acids of the hTAFII28 histone fold |
| Q42604308 | TAF25p, a non-histone-like subunit of TFIID and SAGA complexes, is essential for total mRNA gene transcription in vivo |
| Q24302399 | TAF9b (formerly TAF9L) is a bona fide TAF that has unique and overlapping roles with TAF9 |
| Q30587319 | TAFs revisited: more data reveal new twists and confirm old ideas |
| Q33962132 | TATA-binding protein mutants that increase transcription from enhancerless and repressed promoters in vivo |
| Q33832058 | TBP-associated factors (TAFIIs): multiple, selective transcriptional mediators in common complexes |
| Q38313033 | TFIIA has activator-dependent and core promoter functions in vivo |
| Q33967253 | TFIIA interacts with TFIID via association with TATA-binding protein and TAF40 |
| Q24545962 | TFIID and Spt-Ada-Gcn5-acetyltransferase functions probed by genome-wide synthetic genetic array analysis using a Saccharomyces cerevisiae taf9-ts allele |
| Q35207267 | TFIID-specific yeast TAF40 is essential for the majority of RNA polymerase II-mediated transcription in vivo |
| Q34286148 | The Ccr4-not complex and yTAF1 (yTaf(II)130p/yTaf(II)145p) show physical and functional interactions |
| Q27935406 | The TAF9 C-terminal conserved region domain is required for SAGA and TFIID promoter occupancy to promote transcriptional activation. |
| Q77772079 | The TATA-binding protein and its associated factors are differentially expressed in adult mouse tissues |
| Q24657679 | The alpha-helical FXXPhiPhi motif in p53: TAF interaction and discrimination by MDM2 |
| Q24554357 | The human TFIID components TAF(II)135 and TAF(II)20 and the yeast SAGA components ADA1 and TAF(II)68 heterodimerize to form histone-like pairs |
| Q22253412 | The human transcription factor IID subunit human TATA-binding protein-associated factor 28 interacts in a ligand-reversible manner with the vitamin D(3) and thyroid hormone receptors |
| Q77654626 | The role of TAFs in RNA polymerase II transcription |
| Q36579354 | The role of chromatin structure in regulating stress-induced transcription in Saccharomyces cerevisiae |
| Q34608335 | Transcriptional activation in yeast cells lacking transcription factor IIA. |
| Q48372990 | Two WD repeat-containing TATA-binding protein-associated factors in fission yeast that suppress defects in the anaphase-promoting complex |
| Q27929763 | Use of a genetically introduced cross-linker to identify interaction sites of acidic activators within native transcription factor IID and SAGA. |
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