scholarly article | Q13442814 |
P356 | DOI | 10.1101/GAD.8.9.995 |
P698 | PubMed publication ID | 7926793 |
P2093 | author name string | P M Lieberman | |
A J Berk | |||
P2860 | cites work | Cloning and expression of human TAFII250: a TBP-associated factor implicated in cell-cycle regulation | Q24308057 |
P433 | issue | 9 | |
P304 | page(s) | 995-1006 | |
P577 | publication date | 1994-05-01 | |
P1433 | published in | Genes & Development | Q1524533 |
P1476 | title | A mechanism for TAFs in transcriptional activation: activation domain enhancement of TFIID-TFIIA--promoter DNA complex formation | |
P478 | volume | 8 |
Q42280074 | A TAF4 coactivator function for E proteins that involves enhanced TFIID binding |
Q34443389 | A TATA binding protein mutant with increased affinity for DNA directs transcription from a reversed TATA sequence in vivo |
Q38303044 | A TATA binding protein regulatory network that governs transcription complex assembly. |
Q36556030 | A class of activation domains interacts directly with TFIIA and stimulates TFIIA-TFIID-promoter complex assembly |
Q34776433 | A compilation of composite regulatory elements affecting gene transcription in vertebrates |
Q36550652 | A direct interaction between a glutamine-rich activator and the N terminus of TFIIB can mediate transcriptional activation in vivo |
Q35154603 | A downstream element in the human beta-globin promoter: evidence of extended sequence-specific transcription factor IID contacts |
Q46144332 | A general mechanism for transcriptional synergy by eukaryotic activators |
Q42514084 | A heterochromatin-dependent transcription machinery drives piRNA expression. |
Q28275895 | A histone octamer-like structure within TFIID |
Q36561614 | A new class of activation-defective TATA-binding protein mutants: evidence for two steps of transcriptional activation in vivo |
Q35873179 | A replication function associated with the activation domain of the Epstein-Barr virus Zta transactivator |
Q33867066 | A role for TBP dimerization in preventing unregulated gene expression |
Q36565816 | A severely defective TATA-binding protein-TFIIB interaction does not preclude transcriptional activation in vivo |
Q30829987 | A testis-specific transcription factor IIA (TFIIAtau) stimulates TATA-binding protein-DNA binding and transcription activation |
Q33786910 | Acetyl coenzyme A stimulates RNA polymerase II transcription and promoter binding by transcription factor IID in the absence of histones |
Q36347875 | Activation domain–mediator interactions promote transcription preinitiation complex assembly on promoter DNA |
Q24311404 | Adenovirus E1A functions as a cofactor for retinoic acid receptor beta (RAR beta) through direct interaction with RAR beta |
Q35881137 | Alteration of a single serine in the basic domain of the Epstein-Barr virus ZEBRA protein separates its functions of transcriptional activation and disruption of latency |
Q27937697 | Analysis of TFIIA function In vivo: evidence for a role in TATA-binding protein recruitment and gene-specific activation |
Q27931415 | Analysis of the yeast transcription factor TFIIA: distinct functional regions and a polymerase II-specific role in basal and activated transcription |
Q39583813 | Association of transcription factor IIA with TATA binding protein is required for transcriptional activation of a subset of promoters and cell cycle progression in Saccharomyces cerevisiae |
Q40736935 | Autonomous function of the amino-terminal inhibitory domain of TAF1 in transcriptional regulation |
Q38363144 | Biochemical mechanism of transcriptional activation by GAL4-VP16. |
Q24317302 | CIF150, a human cofactor for transcription factor IID-dependent initiator function |
Q41368117 | Characterization of a HeLa cell factor which negatively regulates transcriptional activation in vitro by transcriptional enhancer factor-1 (TEF-1). |
Q24315758 | Cloning and characterization of hTAFII18, hTAFII20 and hTAFII28: three subunits of the human transcription factor TFIID |
Q60078040 | Connecting a promoter-bound protein to TBP bypasses the need for a transcriptional activation domain |
Q36035094 | Considerations of transcriptional control mechanisms: do TFIID-core promoter complexes recapitulate nucleosome-like functions? |
Q40970406 | Contacts in context: promoter specificity and macromolecular interactions in transcription |
Q35624739 | Core promoter-selective function of HMGA1 and Mediator in Initiator-dependent transcription |
Q33729443 | Core promoter-specific function of a mutant transcription factor TFIID defective in TATA-box binding |
Q39575245 | DA-complex assembly activity required for VP16C transcriptional activation |
Q33652156 | DNA bending and wrapping around RNA polymerase: a "revolutionary" model describing transcriptional mechanisms. |
Q40551612 | Differential cellular requirements for activation of herpes simplex virus type 1 early (tk) and late (gC) promoters by ICP4. |
Q73023861 | Differentiation of neuroblastoma cells by phorbol esters and insulin-like growth factor 1 is associated with induction of retinoic acid receptor beta gene expression |
Q37095433 | Direct TFIIA-TFIID protein contacts drive budding yeast ribosomal protein gene transcription |
Q35273904 | Distinct cAMP response element-binding protein (CREB) domains stimulate different steps in a concerted mechanism of transcription activation |
Q35900078 | Drosophila TAF(II)230 and the transcriptional activator VP16 bind competitively to the TATA box-binding domain of the TATA box-binding protein |
Q42085734 | Dual targets of a transcriptional activator that tracks on DNA |
Q34685230 | Efficient induction of nuclear aggresomes by specific single missense mutations in the DNA-binding domain of a viral AP-1 homolog |
Q38597247 | Epstein-Barr Virus Lytic Cycle Reactivation |
Q35476446 | Epstein-Barr virus transcription factor Zta acts through distal regulatory elements to directly control cellular gene expression |
Q45983312 | Eukaryotic transcription: the core of eukaryotic gene activation. |
Q40020721 | Evidence that Spt3 functionally interacts with Mot1, TFIIA, and TATA-binding protein to confer promoter-specific transcriptional control in Saccharomyces cerevisiae |
Q30700508 | Evidence that TAF-TATA box-binding protein interactions are required for activated transcription in mammalian cells |
Q24337254 | Evolutionary conservation of human TATA-binding-polypeptide-associated factors TAFII31 and TAFII80 and interactions of TAFII80 with other TAFs and with general transcription factors |
Q24649809 | Fos-Jun dimerization promotes interaction of the basic region with TFIIE-34 and TFIIF |
Q24647472 | Functional dissection of a human Dr1-DRAP1 repressor complex |
Q34640455 | Functional significance of the TATA element major groove in transcription initiation by RNA polymerase II |
Q45766038 | G0/G1 growth arrest mediated by a region encompassing the basic leucine zipper (bZIP) domain of the Epstein-Barr virus transactivator Zta. |
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 |
Q39574625 | Hepatitis B virus pX targets TFIIB in transcription coactivation |
Q41954712 | Highly redundant function of multiple AT-rich sequences as core promoter elements in the TATA-less RPS5 promoter of Saccharomyces cerevisiae |
Q24644626 | Human TATA-binding protein-related factor-2 (hTRF2) stably associates with hTFIIA in HeLa cells |
Q36554764 | Human TFIID binds to core promoter DNA in a reorganized structural state |
Q33558899 | Human Taf(II)130 is a coactivator for NFATp |
Q24315678 | Human general transcription factor TFIIA: characterization of a cDNA encoding the small subunit and requirement for basal and activated transcription |
Q36570063 | Identification of RTF1, a novel gene important for TATA site selection by TATA box-binding protein in Saccharomyces cerevisiae |
Q22009968 | Identification of a general transcription factor TFIIAalpha/beta homolog selectively expressed in testis |
Q39604695 | Identification of acidic and aromatic residues in the Zta activation domain essential for Epstein-Barr virus reactivation |
Q35841284 | Identification of cellular target genes of the Epstein-Barr virus transactivator Zta: activation of transforming growth factor beta igh3 (TGF-beta igh3) and TGF-beta 1 |
Q38301752 | Identification of functional targets of the Zta transcriptional activator by formation of stable preinitiation complex intermediates |
Q52566722 | Identification of highly conserved amino-terminal segments of dTAFII230 and yTAFII145 that are functionally interchangeable for inhibiting TBP-DNA interactions in vitro and in promoting yeast cell growth in vivo. |
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 |
Q44991848 | Interaction between acidic transcriptional activation domains of herpes simplex virus activator protein VP16 and transcriptional initiation factor IID. |
Q36561858 | Interaction of the human T-cell lymphotropic virus type 1 tax transactivator with transcription factor IIA |
Q39607106 | Interaction with the Epstein-Barr virus helicase targets Zta to DNA replication compartments |
Q36563655 | Interferon regulatory factors and TFIIB cooperatively regulate interferon-responsive promoter activity in vivo and in vitro |
Q27940351 | Intermediates in formation and activity of the RNA polymerase II preinitiation complex: holoenzyme recruitment and a postrecruitment role for the TATA box and TFIIB. |
Q48097366 | Investigation of single and synergic effects of NLRC5 and PD-L1 variants on the risk of colorectal cancer |
Q24522478 | Involvement of TFIID and USA components in transcriptional activation of the human immunodeficiency virus promoter by NF-kappaB and Sp1. |
Q34180268 | K-bZIP of Kaposi's sarcoma-associated herpesvirus/human herpesvirus 8 (KSHV/HHV-8) binds KSHV/HHV-8 Rta and represses Rta-mediated transactivation |
Q73078912 | Kinetic analysis of Sp1-mediated transcriptional activation of the human DNA polymerase beta promoter |
Q33583978 | Magnesium is required for specific DNA binding of the CREB B-ZIP domain |
Q33713693 | Mapping and functional characterization of the TAF11 interaction with TFIIA. |
Q74567405 | Maximal activity of an erythroid-specific enhancer requires the presence of specific protein binding sites in linked promoters |
Q54248129 | Mechanism of activation of the BNLF2a immune evasion gene of Epstein-Barr virus by Zta. |
Q40443665 | Mechanism of synergy between TATA and initiator: synergistic binding of TFIID following a putative TFIIA-induced isomerization |
Q54102655 | Mechanism of transcriptional repression of E2F by the retinoblastoma tumor suppressor protein. |
Q27934831 | Molecular characterization of Saccharomyces cerevisiae TFIID. |
Q29620260 | Molecular genetics of the RNA polymerase II general transcriptional machinery |
Q22122454 | Multi-protein complexes in eukaryotic gene transcription |
Q33957679 | Multiple layers of cooperativity regulate enhanceosome-responsive RNA polymerase II transcription complex assembly |
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) |
Q36555209 | Mutations on the DNA-binding surface of TATA-binding protein can specifically impair the response to acidic activators in vivo |
Q57971028 | NF-Y Recruitment of TFIID, Multiple Interactions with Histone Fold TAFIIs |
Q33836726 | Origin-independent assembly of Kaposi's sarcoma-associated herpesvirus DNA replication compartments in transient cotransfection assays and association with the ORF-K8 protein and cellular PML. |
Q35122852 | Phosphorylation of Epstein-Barr virus ZEBRA protein at its casein kinase 2 sites mediates its ability to repress activation of a viral lytic cycle late gene by Rta. |
Q39445227 | Phosphorylation of TFIIA stimulates TATA binding protein-TATA interaction and contributes to maximal transcription and viability in yeast |
Q27933987 | Positive and negative functions of the SAGA complex mediated through interaction of Spt8 with TBP and the N-terminal domain of TFIIA. |
Q60073354 | Pre-bending of a promoter sequence enhances affinity for the TATA-binding factor |
Q47829612 | Preinitation complex assembly: potentially a bumpy path. |
Q41100064 | Promoters and basal transcription machinery in eubacteria and eukaryotes: concepts, definitions, and analogies |
Q45970861 | Protease footprinting analysis of ternary complex formation by human TFIIA. |
Q58701536 | RNA polymerase II transcription complex assembly in nuclear extracts |
Q38296033 | Replication of Epstein-Barr virus oriLyt: lack of a dedicated virally encoded origin-binding protein and dependence on Zta in cotransfection assays. |
Q40876736 | Repression of CIITA by the Epstein-Barr virus transcription factor Zta is independent of its dimerization and DNA binding |
Q40023879 | Requirement for transcription factor IIA (TFIIA)-TFIID recruitment by an activator depends on promoter structure and template competition |
Q36567515 | Retinoid X receptor:vitamin D3 receptor heterodimers promote stable preinitiation complex formation and direct 1,25-dihydroxyvitamin D3-dependent cell-free transcription |
Q37531957 | Separation of the transcriptional coactivator and antirepression functions of transcription factor IIA |
Q33774811 | Simian virus 40 large T antigen stabilizes the TATA-binding protein-TFIIA complex on the TATA element |
Q36652659 | Slow dimer dissociation of the TATA binding protein dictates the kinetics of DNA binding |
Q39457338 | Stimulation of CREB binding protein nucleosomal histone acetyltransferase activity by a class of transcriptional activators |
Q27732598 | Structural similarity between TAFs and the heterotetrameric core of the histone octamer |
Q27620828 | TATA element recognition by the TATA box-binding protein has been conserved throughout evolution |
Q49165220 | TATA-binding protein residues implicated in a functional interplay between negative cofactor NC2 (Dr1) and general factors TFIIA and TFIIB. |
Q40791931 | TATA-binding protein-associated factors enhance the recruitment of RNA polymerase II by transcriptional activators |
Q27933367 | TFIIA and the transactivator Rap1 cooperate to commit TFIID for transcription initiation |
Q33967253 | TFIIA interacts with TFIID via association with TATA-binding protein and TAF40 |
Q34718574 | TFIIA plays a role in the response to oxidative stress |
Q52576836 | TFIIA-TAF regulatory interplay: NMR evidence for overlapping binding sites on TBP. |
Q39752283 | TFIIB-facilitated recruitment of preinitiation complexes by a TAF-independent mechanism |
Q39723706 | TFIID (TBP) stabilizes the binding of MyoD to its DNA site at the promoter and MyoD facilitates the association of TFIIB with the preinitiation complex |
Q24674080 | TFIID and human mediator coactivator complexes assemble cooperatively on promoter DNA |
Q36088808 | Taspase1 processing alters TFIIA cofactor properties in the regulation of TFIID. |
Q33785198 | The Epstein-Barr virus lytic transactivator Zta interacts with the helicase-primase replication proteins. |
Q35876325 | The ICP22 protein of equine herpesvirus 1 cooperates with the IE protein to regulate viral gene expression. |
Q28623816 | The Oct-1 POU domain activates snRNA gene transcription by contacting a region in the SNAPc largest subunit that bears sequence similarities to the Oct-1 coactivator OBF-1 |
Q51222168 | The OsHAPL1-DTH8-Hd1 complex functions as the transcription regulator to repress heading date in rice. |
Q27939451 | The TBP-TFIIA Interaction in the Response to Acidic Activators in Vivo |
Q33794695 | The activation domain of GAL4 protein mediates cooperative promoter binding with general transcription factors in vivo |
Q39444671 | The amino-terminal C/H1 domain of CREB binding protein mediates zta transcriptional activation of latent Epstein-Barr virus |
Q38299741 | The bovine papillomavirus 1 E2 protein contains two activation domains: one that interacts with TBP and another that functions after TBP binding. |
Q24598984 | The coactivator p15 (PC4) initiates transcriptional activation during TFIIA-TFIID-promoter complex formation |
Q43483356 | The evolutionarily conserved TOUGH protein is required for proper development of Arabidopsis thaliana. |
Q27930236 | The histone H3-like TAF is broadly required for transcription in yeast |
Q40018147 | The major histocompatibility complex class II Ea promoter requires TFIID binding to an initiator sequence |
Q35201509 | The mammalian transcriptional repressor RBP (CBF1) targets TFIID and TFIIA to prevent activated transcription |
Q97557186 | The role of genetic polymorphism within PD-L1 gene in cancer. Review |
Q74009630 | The stability of the TFIIA-TBP-DNA complex is dependent on the sequence of the TATAAA element |
Q41079103 | The transcriptional corepressor DSP1 inhibits activated transcription by disrupting TFIIA-TBP complex formation |
Q40022378 | 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 |
Q33771547 | The yeast TAF145 inhibitory domain and TFIIA competitively bind to TATA-binding protein |
Q60083846 | Topology and reorganization of a human TFIID–promoter complex |
Q39716921 | Transcription activation by GC-boxes: evaluation of kinetic and equilibrium contributions |
Q28272088 | Transcription factor IIA derepresses TATA-binding protein (TBP)-associated factor inhibition of TBP-DNA binding |
Q24310214 | Transcription factor IIA mutations show activator-specific defects and reveal a IIA function distinct from stimulation of TBP-DNA binding |
Q41044026 | Transcription: basal factors and activation. |
Q34608335 | Transcriptional activation in yeast cells lacking transcription factor IIA. |
Q58049054 | Transcriptional activity of the TFIIA four-helix bundle in vivo |
Q73019085 | Transcriptional enhancement by acidic activators |
Q38307266 | Virtually unidirectional binding of TBP to the AdMLP TATA box within the quaternary complex with TFIIA and TFIIB. |
Q24810390 | cAMP-responsive element in TATA-less core promoter is essential for haploid-specific gene expression in mouse testis |
Q38833599 | p53 Dynamically Directs TFIID Assembly on Target Gene Promoters |
Q24550965 | p53 Stimulates TFIID-TFIIA-promoter complex assembly, and p53-T antigen complex inhibits TATA binding protein-TATA interaction |
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