| scholarly article | Q13442814 |
| P356 | DOI | 10.1126/SCIENCE.288.5469.1242 |
| P698 | PubMed publication ID | 10817999 |
| P2093 | author name string | M R Green | |
| X Y Li | |||
| S R Bhaumik | |||
| P433 | issue | 5469 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | TATA-binding protein-associated factor TAF6 YGL112C | Q27549236 |
| Taf12p YDR145W | Q27550348 | ||
| Histone acetyltransferase YGR274C | Q27551031 | ||
| Taf10p YDR167W | Q27551449 | ||
| P304 | page(s) | 1242-4 | |
| P577 | publication date | 2000-05-19 | |
| P1433 | published in | Science | Q192864 |
| P1476 | title | Distinct classes of yeast promoters revealed by differential TAF recruitment | |
| P478 | volume | 288 |
| Q52111779 | A broad but restricted requirement for TAF-5 (human TAFII100) for embryonic transcription in Caenorhabditis elegans. |
| Q41957756 | A comprehensive genomic binding map of gene and chromatin regulatory proteins in Saccharomyces |
| Q34649355 | A conserved role for human Nup98 in altering chromatin structure and promoting epigenetic transcriptional memory |
| Q48017973 | A genome-wide housekeeping role for TFIID and a highly regulated stress-related role for SAGA in Saccharomyces cerevisiae |
| Q36856058 | Activation of a T-box-Otx2-Gsc gene network independent of TBP and TBP-related factors |
| Q24540745 | Activator-independent functions of the yeast mediator sin4 complex in preinitiation complex formation and transcription reinitiation |
| Q43975761 | Activator-specific recruitment of TFIID and regulation of ribosomal protein genes in yeast |
| Q33314905 | Adr1 and Cat8 mediate coactivator recruitment and chromatin remodeling at glucose-regulated genes |
| Q27932320 | An array of coactivators is required for optimal recruitment of TATA binding protein and RNA polymerase II by promoter-bound Gcn4p |
| Q47068840 | An extensive requirement for transcription factor IID-specific TAF-1 in Caenorhabditis elegans embryonic transcription |
| Q58422648 | Assembly of a Mediator/TFIID/TFIIA Complex Bypasses the Need for an Activator |
| Q33713593 | Association of the Mediator complex with enhancers of active genes |
| Q40736935 | Autonomous function of the amino-terminal inhibitory domain of TAF1 in transcriptional regulation |
| Q37695539 | Changes in genomewide occupancy of core transcriptional regulators during heat stress |
| Q42502032 | Chromatin is permissive to TATA-binding protein (TBP)-mediated transcription initiation |
| Q28145475 | Control of gene expression through regulation of the TATA-binding protein |
| Q27930925 | Cooperative action of NC2 and Mot1p to regulate TATA-binding protein function across the genome |
| Q40015630 | Core promoter elements and TAFs contribute to the diversity of transcriptional activation in vertebrates |
| Q36759161 | Core promoter-specific gene regulation: TATA box selectivity and Initiator-dependent bi-directionality of serum response factor-activated transcription |
| Q27639666 | Crystal structure of a subcomplex of human transcription factor TFIID formed by TATA binding protein-associated factors hTAF4 (hTAF(II)135) and hTAF12 (hTAF(II)20) |
| Q35078268 | Developmental regulation of transcription by a tissue-specific TAF homolog |
| Q34025319 | Developmental specificity of recruitment of TBP to the TATA box of the human gamma-globin gene |
| Q27935667 | Different sensitivities of bromodomain factors 1 and 2 to histone H4 acetylation |
| Q27930390 | Differential requirement of SAGA components for recruitment of TATA-box-binding protein to promoters in vivo |
| Q42839779 | Differential requirement of SAGA subunits for Mot1p and Taf1p recruitment in gene activation |
| Q37095433 | Direct TFIIA-TFIID protein contacts drive budding yeast ribosomal protein gene transcription |
| Q33832637 | Direct transactivator-transcription factor IID (TFIID) contacts drive yeast ribosomal protein gene transcription |
| Q43125554 | Dissection of coactivator requirement at RNR3 reveals unexpected contributions from TFIID and SAGA. |
| Q27936344 | Distinct mutations in yeast TAF(II)25 differentially affect the composition of TFIID and SAGA complexes as well as global gene expression patterns. |
| Q34478777 | Distinct regulatory mechanisms of eukaryotic transcriptional activation by SAGA and TFIID |
| Q39645792 | Distinct requirements for C.elegans TAF(II)s in early embryonic transcription |
| Q40337797 | Dominant role for signal transduction in the transcriptional memory of yeast GAL genes |
| Q35917477 | Eaf1p Is Required for Recruitment of NuA4 in Targeting TFIID to the Promoters of the Ribosomal Protein Genes for Transcriptional Initiation In Vivo |
| Q33335325 | Ectopic expression of TATA box-binding protein induces shoot proliferation in Arabidopsis |
| Q45983312 | Eukaryotic transcription: the core of eukaryotic gene activation. |
| Q30700508 | Evidence that TAF-TATA box-binding protein interactions are required for activated transcription in mammalian cells |
| Q27937901 | Evidence that the elongation factor TFIIS plays a role in transcription initiation at GAL1 in Saccharomyces cerevisiae |
| Q27934996 | Exchange of RNA polymerase II initiation and elongation factors during gene expression in vivo |
| Q27937030 | Fluorescence-based analyses of the effects of full-length recombinant TAF130p on the interaction of TATA box-binding protein with TATA box DNA. |
| Q35004993 | Full and partial genome-wide assembly and disassembly of the yeast transcription machinery in response to heat shock |
| Q42685039 | Functional analysis of H2B-Lys-123 ubiquitination in regulation of H3-Lys-4 methylation and recruitment of RNA polymerase II at the coding sequences of several active genes in vivo |
| Q34432893 | Gene-selective developmental roles of general transcription factors |
| Q39843802 | Genome-wide localization analysis of a complete set of Tafs reveals a specific effect of the taf1 mutation on Taf2 occupancy and provides indirect evidence for different TFIID conformations at different promoters |
| Q37732547 | Genome-wide occupancy profile of the RNA polymerase III machinery in Saccharomyces cerevisiae reveals loci with incomplete transcription complexes |
| Q43240899 | Genome-wide relationships between TAF1 and histone acetyltransferases in Saccharomyces cerevisiae |
| Q24797317 | HIV-1 Tat stimulates transcription complex assembly through recruitment of TBP in the absence of TAFs |
| Q33967804 | Heterozygous disruption of the TATA-binding protein gene in DT40 cells causes reduced cdc25B phosphatase expression and delayed mitosis. |
| Q27936250 | High-affinity DNA binding by a Mot1p-TBP complex: implications for TAF-independent transcription |
| Q41954712 | Highly redundant function of multiple AT-rich sequences as core promoter elements in the TATA-less RPS5 promoter of Saccharomyces cerevisiae |
| Q34190567 | Histone acetylases--versatile players |
| Q24291710 | Human STAGA complex is a chromatin-acetylating transcription coactivator that interacts with pre-mRNA splicing and DNA damage-binding factors in vivo |
| Q35661538 | Human mediator enhances activator-facilitated recruitment of RNA polymerase II and promoter recognition by TATA-binding protein (TBP) independently of TBP-associated factors |
| Q47987647 | Identification and distinct regulation of yeast TATA box-containing genes |
| Q44562084 | Identification of a novel TATA element-binding protein binding region at the N terminus of the Saccharomyces cerevisiae TAF1 protein |
| Q51004498 | Identification of a transcriptional activation domain in yeast repressor activator protein 1 (Rap1) using an altered DNA-binding specificity variant. |
| Q27935003 | In vivo target of a transcriptional activator revealed by fluorescence resonance energy transfer |
| Q28207045 | Independent recruitment in vivo by Gal4 of two complexes required for transcription |
| Q75231689 | Interaction of Gal4p with components of transcription machinery in vivo |
| Q27939381 | Interdependent recruitment of SAGA and Srb mediator by transcriptional activator Gcn4p |
| Q90391244 | Kin28 depletionincreases association of TFIID subunits Taf1 and Taf4 with promoters in Saccharomyces cerevisiae |
| Q33713693 | Mapping and functional characterization of the TAF11 interaction with TFIIA. |
| Q64230205 | Mechanisms of Antisense Transcription Initiation with Implications in Gene Expression, Genomic Integrity and Disease Pathogenesis |
| Q37122772 | Mechanisms of antisense transcription initiation from the 3' end of the GAL10 coding sequence in vivo |
| Q47644109 | Mechanistic Differences in Transcription Initiation at TATA-Less and TATA-Containing Promoters |
| Q27934831 | Molecular characterization of Saccharomyces cerevisiae TFIID. |
| Q34286865 | Mot1 associates with transcriptionally active promoters and inhibits association of NC2 in Saccharomyces cerevisiae |
| Q27939600 | Mot1-mediated control of transcription complex assembly and activity |
| Q38362422 | Mot1p is essential for TBP recruitment to selected promoters during in vivo gene activation |
| Q22122454 | Multi-protein complexes in eukaryotic gene transcription |
| Q47673298 | Multiple Taf subunits of TFIID interact with Ino2 activation domains and contribute to expression of genes required for yeast phospholipid biosynthesis. |
| Q42494682 | Mutations in the TATA-binding protein, affecting transcriptional activation, show synthetic lethality with the TAF145 gene lacking the TAF N-terminal domain in Saccharomyces cerevisiae |
| 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) |
| Q42796601 | Mutations on the DNA binding surface of TBP discriminate between yeast TATA and TATA-less gene transcription. |
| Q36374700 | Non-canonical TAF complexes regulate active promoters in human embryonic stem cells |
| Q45007503 | On the mechanism of constitutive Pdr1 activator-mediated PDR5 transcription in Saccharomyces cerevisiae: evidence for enhanced recruitment of coactivators and altered nucleosome structures |
| Q36332929 | Preferential repair of DNA double-strand break at the active gene in vivo |
| Q27930749 | Protein-protein interaction map for yeast TFIID. |
| Q27931371 | Proteomics of the eukaryotic transcription machinery: identification of proteins associated with components of yeast TFIID by multidimensional mass spectrometry |
| Q40406028 | Quantitative sequential chromatin immunoprecipitation, a method for analyzing co-occupancy of proteins at genomic regions in vivo |
| Q34011585 | Region of yeast TAF 130 required for TFIID to associate with promoters |
| Q36736199 | Regulation of Antisense Transcription by NuA4 Histone Acetyltransferase and Other Chromatin Regulatory Factors |
| Q61809022 | Requirements for RNA polymerase II preinitiation complex formation in vivo |
| Q78482031 | Responses of four yeast genes to changes in the transcriptional machinery are determined by their promoters |
| Q35558697 | Roles for BTAF1 and Mot1p in dynamics of TATA-binding protein and regulation of RNA polymerase II transcription |
| Q28345347 | SAGA is an essential in vivo target of the yeast acidic activator Gal4p |
| Q27934681 | SAGA-associated Sgf73p facilitates formation of the preinitiation complex assembly at the promoters either in a HAT-dependent or independent manner in vivo |
| Q42861193 | SWI/SNF is required for transcriptional memory at the yeast GAL gene cluster |
| Q74604712 | Selective recruitment of TAFs by yeast upstream activating sequences. Implications for eukaryotic promoter structure |
| Q41999510 | Sequential Recruitment of SAGA and TFIID in a Genomic Response to DNA Damage in Saccharomyces cerevisiae |
| Q27935555 | Simultaneous recruitment of coactivators by Gcn4p stimulates multiple steps of transcription in vivo |
| Q43247301 | Site-specific cross-linking of TBP in vivo and in vitro reveals a direct functional interaction with the SAGA subunit Spt3. |
| Q39745923 | Structural and functional analysis of mutations along the crystallographic dimer interface of the yeast TATA binding protein |
| Q35669885 | Structure and function of the TFIID complex |
| Q35758805 | Structure and mechanism of the RNA polymerase II transcription machinery |
| Q27939428 | Systematic analysis of essential yeast TAFs in genome-wide transcription and preinitiation complex assembly |
| Q52162403 | TAC, a TBP-sans-TAFs complex containing the unprocessed TFIIAalphabeta precursor and the TFIIAgamma subunit |
| Q40791931 | TATA-binding protein-associated factors enhance the recruitment of RNA polymerase II by transcriptional activators |
| 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 |
| Q24674080 | TFIID and human mediator coactivator complexes assemble cooperatively on promoter DNA |
| Q64978684 | TOR Facilitates the Targeting of the 19S Proteasome Subcomplex To Enhance Transcription Complex Assembly at the Promoters of the Ribosomal Protein Genes. |
| Q27938515 | Targeted histone acetylation at the yeast CUP1 promoter requires the transcriptional activator, the TATA boxes, and the putative histone acetylase encoded by SPT10. |
| Q29555842 | Targeted recruitment of Set1 histone methylase by elongating Pol II provides a localized mark and memory of recent transcriptional activity |
| Q27929848 | The 19 s proteasome subcomplex establishes a specific protein interaction network at the promoter for stimulated transcriptional initiation in vivo |
| Q35823742 | The 19S proteasome subcomplex promotes the targeting of NuA4 HAT to the promoters of ribosomal protein genes to facilitate the recruitment of TFIID for transcriptional initiation in vivo |
| Q42380607 | The C Terminus of the RNA Polymerase II Transcription Factor IID (TFIID) Subunit Taf2 Mediates Stable Association of Subunit Taf14 into the Yeast TFIID Complex |
| Q37057264 | The FACT complex travels with elongating RNA polymerase II and is important for the fidelity of transcriptional initiation in vivo |
| Q35805519 | The NC2 alpha and beta subunits play different roles in vivo |
| Q27940298 | The S. cerevisiae SAGA complex functions in vivo as a coactivator for transcriptional activation by Gal4. |
| Q27937037 | The Saccharomyces cerevisiae Srb8-Srb11 complex functions with the SAGA complex during Gal4-activated transcription |
| Q27935406 | The TAF9 C-terminal conserved region domain is required for SAGA and TFIID promoter occupancy to promote transcriptional activation. |
| Q91658425 | The TAFs of TFIID Bind and Rearrange the Topology of the TATA-Less RPS5 Promoter |
| Q38288193 | The TBP-inhibitory domain of TAF145 limits the effects of nonclassical transcriptional activators |
| Q34723440 | The mRNA cap-binding complex stimulates the formation of pre-initiation complex at the promoter via its interaction with Mot1p in vivo |
| Q24681624 | The new core promoter element XCPE1 (X Core Promoter Element 1) directs activator-, mediator-, and TATA-binding protein-dependent but TFIID-independent RNA polymerase II transcription from TATA-less promoters |
| Q59591382 | The study of macromolecular complexes by quantitative proteomics |
| Q27939855 | The transcriptional repressor activator protein Rap1p is a direct regulator of TATA-binding protein |
| Q34952743 | Transcription activation: unveiling the essential nature of TFIID. |
| Q34183825 | Transcription and chromatin converge: lessons from yeast genetics. |
| Q47790162 | Transcription of Nearly All Yeast RNA Polymerase II-Transcribed Genes Is Dependent on Transcription Factor TFIID. |
| Q28199910 | Transcriptional coactivator, CIITA, is an acetyltransferase that bypasses a promoter requirement for TAF(II)250 |
| Q35542072 | Transcriptional regulation in Saccharomyces cerevisiae: transcription factor regulation and function, mechanisms of initiation, and roles of activators and coactivators. |
| Q49988874 | Two Distinct Regulatory Mechanisms of Transcriptional Initiation in Response to Nutrient Signaling |
| Q33425417 | Two modes of transcriptional activation at native promoters by NF-kappaB p65 |
| Q92490294 | Two roles for the yeast transcription coactivator SAGA and a set of genes redundantly regulated by TFIID and SAGA |
| Q42222766 | Ubp8p, a histone deubiquitinase whose association with SAGA is mediated by Sgf11p, differentially regulates lysine 4 methylation of histone H3 in vivo |
| Q27929763 | Use of a genetically introduced cross-linker to identify interaction sites of acidic activators within native transcription factor IID and SAGA. |
| Q33967909 | Yeast NC2 associates with the RNA polymerase II preinitiation complex and selectively affects transcription in vivo |
| Q27938360 | Yeast TFIID serves as a coactivator for Rap1p by direct protein-protein interaction |
| Q39918361 | p300 is involved in formation of the TBP-TFIIA-containing basal transcription complex, TAC. |
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