| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S1097-2765(00)80164-1 |
| P698 | PubMed publication ID | 9844638 |
| P2093 | author name string | S Buratowski | |
| B Michel | |||
| P Komarnitsky | |||
| P2860 | cites work | Crystal structure of the nucleosome core particle at 2.8 A resolution | Q22122355 |
| Histone-like TAFs within the PCAF histone acetylase complex | Q24317520 | ||
| Human TAF(II)28 and TAF(II)18 interact through a histone fold encoded by atypical evolutionary conserved motifs also found in the SPT3 family | Q24321892 | ||
| General requirement for RNA polymerase II holoenzymes in vivo | Q24561963 | ||
| Structural similarity between TAFs and the heterotetrameric core of the histone octamer | Q27732598 | ||
| Site-directed mutagenesis by overlap extension using the polymerase chain reaction | Q27860503 | ||
| The histone H3-like TAF is broadly required for transcription in yeast | Q27930236 | ||
| A multiprotein mediator of transcriptional activation and its interaction with the C-terminal repeat domain of RNA polymerase II. | Q27930548 | ||
| Genetic analysis of the large subunit of yeast transcription factor IIE reveals two regions with distinct functions | Q27933410 | ||
| The TATA-binding protein is required for transcription by all three nuclear RNA polymerases in yeast cells | Q27934537 | ||
| 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 | ||
| Yeast TAF(II)145 required for transcription of G1/S cyclin genes and regulated by the cellular growth state | Q27938810 | ||
| Improved method for high efficiency transformation of intact yeast cells | Q28131608 | ||
| A rapid method for localized mutagenesis of yeast genes | Q28131692 | ||
| A histone octamer-like structure within TFIID | Q28275895 | ||
| Characterization of the yeast transcriptome | Q28302110 | ||
| TBP, a universal eukaryotic transcription factor? | Q28626484 | ||
| Regulation of gene expression by TBP-associated proteins | Q28679170 | ||
| Biochemistry and structural biology of transcription factor IID (TFIID) | Q29620209 | ||
| An RNA polymerase II holoenzyme responsive to activators | Q29620210 | ||
| The histone fold: a ubiquitous architectural motif utilized in DNA compaction and protein dimerization | Q33761918 | ||
| Identification and characterization of a TFIID-like multiprotein complex from Saccharomyces cerevisiae | Q33958879 | ||
| The downstream core promoter element, DPE, is conserved from Drosophila to humans and is recognized by TAFII60 of Drosophila | Q35196382 | ||
| A new class of histone H2A mutations in Saccharomyces cerevisiae causes specific transcriptional defects in vivo | Q36550361 | ||
| Factors involved in specific transcription by mammalian RNA polymerase II: purification, genetic specificity, and TATA box-promoter interactions of TFIID. | Q36846156 | ||
| Yeast homologues of higher eukaryotic TFIID subunits | Q37047781 | ||
| 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 | ||
| TBP-associated factors are not generally required for transcriptional activation in yeast | Q42522148 | ||
| Drosophila TAFII150: similarity to yeast gene TSM-1 and specific binding to core promoter DNA. | Q45931803 | ||
| Transcription activation in cells lacking TAFIIS. | Q48060189 | ||
| Yeast TAFIIS in a multisubunit complex required for activated transcription. | Q52541518 | ||
| The Histone Folds in Transcription Factor TFIID | Q58484446 | ||
| Yeast TAF(II)90 is required for cell-cycle progression through G2/M but not for general transcription activation | Q71574610 | ||
| P433 | issue | 5 | |
| P304 | page(s) | 663-673 | |
| P577 | publication date | 1998-11-01 | |
| P1433 | published in | Molecular Cell | Q3319468 |
| P1476 | title | Histone-like TAFs are essential for transcription in vivo | |
| 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. |
| Q27938450 | A yeast taf17 mutant requires the Swi6 transcriptional activator for viability and shows defects in cell cycle-regulated transcription |
| Q33905777 | Alternative splicing of TAF6: downstream transcriptome impacts and upstream RNA splice control elements |
| Q47068840 | An extensive requirement for transcription factor IID-specific TAF-1 in Caenorhabditis elegans embryonic transcription |
| 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 |
| 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 |
| Q34012433 | Developmental and transcriptional consequences of mutations in Drosophila TAF(II)60 |
| Q30846886 | Different functional domains of TAFII250 modulate expression of distinct subsets of mammalian genes |
| Q27935667 | Different sensitivities of bromodomain factors 1 and 2 to histone H4 acetylation |
| Q28776386 | Different upstream transcriptional activators have distinct coactivator requirements |
| Q27930390 | Differential requirement of SAGA components for recruitment of TATA-box-binding protein to promoters in vivo |
| Q27936344 | Distinct mutations in yeast TAF(II)25 differentially affect the composition of TFIID and SAGA complexes as well as global gene expression patterns. |
| Q39645792 | Distinct requirements for C.elegans TAF(II)s in early embryonic transcription |
| Q22254120 | Divergent hTAFII31-binding motifs hidden in 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. |
| Q53645204 | Functional analysis of TFIID components using conditional mutants. |
| Q28202398 | Functional analysis of the TFIID-specific yeast TAF4 (yTAF(II)48) reveals an unexpected organization of its histone-fold domain |
| Q27939082 | Genetic analysis of TAF68/61 reveals links to cell cycle regulators |
| Q33967804 | Heterozygous disruption of the TATA-binding protein gene in DT40 cells causes reduced cdc25B phosphatase expression and delayed mitosis. |
| 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. |
| 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 |
| Q33713693 | Mapping and functional characterization of the TAF11 interaction with TFIIA. |
| Q34089518 | Mapping histone fold TAFs within yeast TFIID. |
| 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 |
| Q27932095 | Mutations in the histone fold domain of the TAF12 gene show synthetic lethality with the TAF1 gene lacking the TAF N-terminal domain (TAND) by different mechanisms from those in the SPT15 gene encoding the TATA box-binding protein (TBP) |
| Q57971028 | NF-Y Recruitment of TFIID, Multiple Interactions with Histone Fold TAFIIs |
| Q28299795 | Nine-amino-acid transactivation domain: establishment and prediction utilities |
| Q27930749 | Protein-protein interaction map for yeast TFIID. |
| Q38311191 | Redundant roles for the TFIID and SAGA complexes in global transcription |
| Q33964585 | Robust mRNA transcription in chicken DT40 cells depleted of TAF(II)31 suggests both functional degeneracy and evolutionary divergence |
| Q74604712 | Selective recruitment of TAFs by yeast upstream activating sequences. Implications for eukaryotic promoter structure |
| 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 |
| Q27939428 | Systematic analysis of essential yeast TAFs in genome-wide transcription and preinitiation complex assembly |
| Q33351996 | TAF6delta controls apoptosis and gene expression in the absence of p53. |
| Q33526062 | TAF6delta orchestrates an apoptotic transcriptome profile and interacts functionally with p53. |
| Q30587319 | TAFs revisited: more data reveal new twists and confirm old ideas |
| Q33832058 | TBP-associated factors (TAFIIs): multiple, selective transcriptional mediators in common complexes |
| Q33967253 | TFIIA interacts with TFIID via association with TATA-binding protein and TAF40 |
| Q39752283 | TFIIB-facilitated recruitment of preinitiation complexes by a TAF-independent mechanism |
| 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 |
| Q52043544 | The Arabidopsis TFIID factor AtTAF6 controls pollen tube growth. |
| Q27938455 | The Gal4 activation domain binds Sug2 protein, a proteasome component, in vivo and in vitro |
| Q28513184 | The PCAF acetylase complex as a potential tumor suppressor |
| 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 |
| Q34214329 | The histone fold is a key structural motif of transcription factor TFIID. |
| 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 |
| Q36053034 | Transcriptional activities of retinoic acid receptors |
| Q48372990 | Two WD repeat-containing TATA-binding protein-associated factors in fission yeast that suppress defects in the anaphase-promoting complex |
| Q27938360 | Yeast TFIID serves as a coactivator for Rap1p by direct protein-protein interaction |
| Q47804934 | Yeast two-hybrid map of Arabidopsis TFIID. |
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