SAGA is an essential in vivo target of the yeast acidic activator Gal4p
about
Chromatin dynamics at DNA replication, transcription and repairThe putative cancer stem cell marker USP22 is a subunit of the human SAGA complex required for activated transcription and cell-cycle progressionA target essential for the activity of a nonacidic yeast transcriptional activator.Distinct domains of erythroid Krüppel-like factor modulate chromatin remodeling and transactivation at the endogenous beta-globin gene promoterActivator-independent functions of the yeast mediator sin4 complex in preinitiation complex formation and transcription reinitiationAnalysis of Gal4-directed transcription activation using Tra1 mutants selectively defective for interaction with Gal4A multiplicity of coactivators is required by Gcn4p at individual promoters in vivoTranscriptional activators in yeastCellulases and beyond: the first 70 years of the enzyme producer Trichoderma reeseiNuclear roles and regulation of chromatin structure by the stress-dependent MAP kinase Sty1 of Schizosaccharomyces pombeTranscriptional regulation at the yeast nuclear envelopeA novel role for Cet1p mRNA 5'-triphosphatase in promoter proximal accumulation of RNA polymerase II in Saccharomyces cerevisiase.Use of a genetically introduced cross-linker to identify interaction sites of acidic activators within native transcription factor IID and SAGA.The 19 s proteasome subcomplex establishes a specific protein interaction network at the promoter for stimulated transcriptional initiation in vivo.Sgf29p facilitates the recruitment of TATA box binding protein but does not alter SAGA's global structural integrity in vivo.Differential requirement of SAGA components for recruitment of TATA-box-binding protein to promoters in vivo.Mutational analysis of the C-terminal FATC domain of Saccharomyces cerevisiae Tra1.Rad6 plays a role in transcriptional activation through ubiquitylation of histone H2B.Proteomics of the eukaryotic transcription machinery: identification of proteins associated with components of yeast TFIID by multidimensional mass spectrometryMutations 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)An array of coactivators is required for optimal recruitment of TATA binding protein and RNA polymerase II by promoter-bound Gcn4p.Interplay between BDF1 and BDF2 and their roles in regulating the yeast salt stress response.A SAGA-independent function of SPT3 mediates transcriptional deregulation in a mutant of the Ccr4-not complex in Saccharomyces cerevisiae.Activation of a poised RNAPII-dependent promoter requires both SAGA and mediator.Rap1p and other transcriptional regulators can function in defining distinct domains of gene expression.Transcriptional activation via sequential histone H2B ubiquitylation and deubiquitylation, mediated by SAGA-associated Ubp8.Positive and negative functions of the SAGA complex mediated through interaction of Spt8 with TBP and the N-terminal domain of TFIIA.The novel SLIK histone acetyltransferase complex functions in the yeast retrograde response pathway.SAGA-associated Sgf73p facilitates formation of the preinitiation complex assembly at the promoters either in a HAT-dependent or independent manner in vivo.Analysis of Spt7 function in the Saccharomyces cerevisiae SAGA coactivator complex.SAGA binds TBP via its Spt8 subunit in competition with DNA: implications for TBP recruitment.In vivo target of a transcriptional activator revealed by fluorescence resonance energy transferPhosphoinositide [PI(3,5)P2] lipid-dependent regulation of the general transcriptional regulator Tup1The TAF9 C-terminal conserved region domain is required for SAGA and TFIID promoter occupancy to promote transcriptional activation.Simultaneous recruitment of coactivators by Gcn4p stimulates multiple steps of transcription in vivo.SALSA, a variant of yeast SAGA, contains truncated Spt7, which correlates with activated transcriptionThe SAGA subunit Ada2 functions in transcriptional silencingThe Tup1 corepressor directs Htz1 deposition at a specific promoter nucleosome marking the GAL1 gene for rapid activation.High-affinity DNA binding by a Mot1p-TBP complex: implications for TAF-independent transcription.The Saccharomyces cerevisiae Srb8-Srb11 complex functions with the SAGA complex during Gal4-activated transcription.
P2860
Q22065678-2D32F0D9-7801-4791-B6D4-241F707DC035Q24307439-0686DAFB-AE42-4BF4-8C12-C428821A82E6Q24530656-0C1363AF-4BE3-4DF9-BB8C-3E6B8BF6874CQ24538309-B8981D3C-6AB9-420E-ACF9-3A720DE1348CQ24540745-BB62A11D-B62E-4CEA-AEAF-57FD6E296392Q24633259-C7867DCC-A711-4D20-9647-FAC6CCB7F559Q24684851-F549A3D5-01B5-4C27-8933-CC379DF6D3C8Q25257450-A265902D-1130-4E4B-BB34-5FE60F8A2544Q26747109-550ADD20-F356-4CAC-AE93-47447F262815Q26853128-0925B595-950A-4196-9CC4-65A4030B8FCCQ26863161-A6D4E904-D1CE-4EB5-80A9-F20420233ACEQ27929496-DFC9976F-95E3-4F7B-9341-14C87621AFC2Q27929763-601D47CE-4660-4AB9-A356-1EDB2624313DQ27929848-1A5D8D54-655E-4583-A6BF-AB7C3593A2C4Q27930044-5904B03E-7982-4A3E-A69D-748F4CD33657Q27930390-6315C953-3F80-47C1-8AE5-F497E6421015Q27930623-4F8C31C5-4C8B-4E4E-9EBA-ACAF721C28D1Q27930655-E610F7DC-DF3F-450E-86A3-B921DBDFAA96Q27931371-1CF8F67B-5E39-4A2E-AB76-24A10E899E45Q27932095-A0D914FB-1B93-4484-A101-D028DC605B7CQ27932320-647FE29B-C72A-45DA-B5CA-746676F295B9Q27932525-35C5586C-4FE6-42FE-9634-220A705E0189Q27932596-C5CF56F4-5F73-402C-A30E-9A4C6B04995CQ27933190-FA3EECF9-F6E6-4B5C-A1AF-2A9B7CFBC6F6Q27933245-CCCD41F6-99D6-49BE-AA4D-473F8A7221FAQ27933975-49882259-84C7-4B8C-912A-5B9E87DBCB05Q27933987-50C79A94-47DE-4C63-8416-72008222B1A4Q27934606-5200BFAB-16D6-4228-8971-454FE0CDFB08Q27934681-7B8AD977-F44F-43EA-9A63-6C64D9D03010Q27934769-61337E6B-7D7E-49F6-876F-0A661F9AD75FQ27934876-2E2DF56F-4340-41B5-B709-A2BB0B12C45EQ27935003-F383080F-E9C4-4390-AF0C-52F05CA2D757Q27935240-CD1AE8D4-8949-4ABF-87DC-674475E999EAQ27935406-9D1A6BA0-405E-494C-BED4-6B990D7EDC3AQ27935555-69DDD120-C934-470C-93FC-C09B22938C12Q27936016-07F238B5-2F1A-4A52-85C1-6809AFF03D81Q27936163-A2E2F137-A5E4-4A44-B1C5-1E8DDB4770B5Q27936207-F72783FC-C880-411A-85A7-4D9AAD455B31Q27936250-19FE6B76-A4FD-40BD-B10E-150C40BEAABAQ27937037-EDCD1143-8E6D-4997-8186-08DEAD21FF14
P2860
SAGA is an essential in vivo target of the yeast acidic activator Gal4p
description
2001 nî lūn-bûn
@nan
2001 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
SAGA is an essential in vivo target of the yeast acidic activator Gal4p
@ast
SAGA is an essential in vivo target of the yeast acidic activator Gal4p
@en
SAGA is an essential in vivo target of the yeast acidic activator Gal4p
@nl
type
label
SAGA is an essential in vivo target of the yeast acidic activator Gal4p
@ast
SAGA is an essential in vivo target of the yeast acidic activator Gal4p
@en
SAGA is an essential in vivo target of the yeast acidic activator Gal4p
@nl
prefLabel
SAGA is an essential in vivo target of the yeast acidic activator Gal4p
@ast
SAGA is an essential in vivo target of the yeast acidic activator Gal4p
@en
SAGA is an essential in vivo target of the yeast acidic activator Gal4p
@nl
P2860
P3181
P356
P1433
P1476
SAGA is an essential in vivo target of the yeast acidic activator Gal4p
@en
P2093
S R Bhaumik
P2860
P304
P3181
P356
10.1101/GAD.911401
P407
P577
2001-08-01T00:00:00Z