Core promoter specificities of the Sp1 and VP16 transcriptional activation domains
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Novel cofactors and TFIIA mediate functional core promoter selectivity by the human TAFII150-containing TFIID complex.CIF150, a human cofactor for transcription factor IID-dependent initiator functionDifferent core promoters possess distinct regulatory activities in the Drosophila embryoMolecular cloning and analysis of two subunits of the human TFIID complex: hTAFII130 and hTAFII100Specific TATAA and bZIP requirements suggest that HTLV-I Tax has transcriptional activity subsequent to the assembly of an initiation complexGts1p activates SNF1-dependent derepression of HSP104 and TPS1 in the stationary phase of yeast growth.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.Synthetic reversal of epigenetic silencingTranscriptional activity of the paired-like homeodomain proteins CHX10 and VSX1Functional analysis of the rat N-methyl-D-aspartate receptor 2A promoter: multiple transcription starts points, positive regulation by Sp factors, and translational regulationVitamin D-binding protein gene transcription is regulated by the relative abundance of hepatocyte nuclear factors 1alpha and 1betaNegative transcriptional modulation and silencing of the bi-exonic Rnf35 gene in the preimplantation embryo. Binding of the CCAAT-displacement protein/Cux to the untranslated exon 1 sequenceTranscriptional modulation of the pre-implantation embryo-specific Rnf35 gene by the Y-box protein NF-Y/CBFStimulation of DNA replication in Saccharomyces cerevisiae by a glutamine- and proline-rich transcriptional activation domain.The downstream promoter element DPE appears to be as widely used as the TATA box in Drosophila core promoters.Context-dependent transcriptional regulation.The two Saccharomyces cerevisiae SUA7 (TFIIB) transcripts differ at the 3'-end and respond differently to stress.Two Sp1/Sp3 binding sites in the major immediate-early proximal enhancer of human cytomegalovirus have a significant role in viral replication.ATG deserts define a novel core promoter subclass.Analysis of core promoter sequences located downstream from the TATA element in the hsp70 promoter from Drosophila melanogaster.Different modes of regulation of transcription and pre-mRNA processing of the structurally juxtaposed homologs, Rnf33 and Rnf35, in eggs and in pre-implantation embryos.Rational design of a super core promoter that enhances gene expression.The ETS family member ERM contains an alpha-helical acidic activation domain that contacts TAFII60.Sp1 and Egr1 regulate transcription of the Dmrt1 gene in Sertoli cellsDistinct transcriptional pathways regulate basal and activated major histocompatibility complex class I expression.Enhancer-promoter specificity mediated by DPE or TATA core promoter motifs.Engineered Promoters for Potent Transient Overexpression.Synergistic and promoter-selective activation of transcription by recruitment of transcription factors TFIID and TFIIB.HIV-1 tat binds TAFII250 and represses TAFII250-dependent transcription of major histocompatibility class I genes.Regulation of the human p21/WAF1/Cip1 promoter in hepatic cells by functional interactions between Sp1 and Smad family members.Position-dependent transcriptional regulation of the murine dihydrofolate reductase promoter by the E2F transactivation domain.Transactivation domains facilitate promoter occupancy for the dioxin-inducible CYP1A1 gene in vivo.A general strategy to enhance the potency of chimeric transcriptional activators.Core promoter-specific gene regulation: TATA box selectivity and Initiator-dependent bi-directionality of serum response factor-activated transcriptionRole of the cytomegalovirus major immediate early enhancer in acute infection and reactivation from latency.Artemisinin blocks prostate cancer growth and cell cycle progression by disrupting Sp1 interactions with the cyclin-dependent kinase-4 (CDK4) promoter and inhibiting CDK4 gene expression.The CREB site in the proximal enhancer is critical for cooperative interaction with the other transcription factor binding sites to enhance transcription of the major intermediate-early genes in human cytomegalovirus-infected cells.Bipartite functions of the CREB co-activators selectively direct alternative splicing or transcriptional activationTranscription of the lymphocyte-specific terminal deoxynucleotidyltransferase gene requires a specific core promoter structureDifferential regulation of p53-dependent and -independent proliferating cell nuclear antigen gene transcription by 12 S E1A oncoprotein requires CBP.
P2860
Q22003968-94182B03-9967-4960-B531-761F794CD039Q24317302-4276F237-850E-46B7-9EEC-B9F0DDC9CA33Q24607337-0B229D3B-F1EF-46FB-AE90-44C7FC786683Q24682969-91EB044B-7623-4C33-961C-7A4258B59318Q24798610-28D9435F-DA97-4FAA-87D2-940AA54D0446Q27934424-6C9E95ED-056D-4EC7-BC0F-E473F32665BDQ27938987-D2D72D1A-9648-4FF1-BE33-E2507DF52EB7Q28240581-80025838-9F9D-4D9D-B879-4E0760D17C53Q28302177-A27DCA3F-F452-433B-8202-6CFA675DA9F8Q28566552-12810E71-283A-4F8D-AD8F-7C2FDA77782AQ28569662-094D8145-397C-4277-8748-177856C92141Q28585985-101BB56E-D4D7-4296-8DFA-EC5BB3D09CC6Q28592501-BBD1E349-F1BF-486A-9D3C-469F64590D51Q30304323-F32F7C68-543D-45D1-BFF6-2CD297166809Q30877990-A9F1A798-0441-40C9-961C-0644A7EA29D9Q33748147-A834BA30-EF00-42BC-BF98-6E497BFB7A4EQ33834234-A758B9A9-6EBC-4234-AE81-BF5F5C0A4A30Q33908697-9F5DE922-5CA0-4A33-96FC-D09D51EACA24Q33942566-D82DE31F-5D76-4F4C-A66D-17DF585A0140Q33967210-3D05DA45-C92B-423F-820F-E860ED30C2E9Q34369259-94CED8D7-B06F-4531-BA89-FC5FC036DF14Q34584346-397A7864-2D30-4A0F-AF77-909CB1F5648DQ34645357-F1CE2CFB-340E-460A-B73F-DA3A845DF8C3Q34751788-CDBD02A4-02B7-43B3-803D-C1C92C98BDE8Q34980792-D77761DF-6703-4926-8B78-C01AEB2C925FQ35081772-370EDF30-8372-4B6C-9335-26C321D12111Q35922412-65F8B825-17A9-4787-8779-CDFFF70772DBQ36300660-3A052DF7-BA35-493A-BFDC-00B04DA621D1Q36314833-E4C64A7A-1822-43BC-9D38-8F547EE21FD3Q36486862-4F8307E4-35E3-4014-AA9D-E91B99487DC3Q36567545-A45B87A1-EE4D-4EC3-99CD-1420067C257CQ36568936-928A8C47-D2C8-464D-98DC-27DCE4956CB0Q36703333-95D5FA6D-6E10-4729-8D7A-057A8AF13A38Q36759161-265EE1A4-D12A-4D25-84EA-BA077C7B8097Q37039648-897CEA56-8891-4255-A32D-461C08D14862Q37068031-2465A822-5F61-473A-AF14-E8D8905B4292Q37333784-42669833-EAB5-4D9E-A983-C14024E18171Q37360004-5E560F6D-50B6-49AF-A6A3-4B41F4C97F7AQ37636436-054FF2FC-34A0-47CF-9EA3-A703599F9A54Q38335891-9F1067C4-FDFE-46D2-9CB7-DC62106B4DEE
P2860
Core promoter specificities of the Sp1 and VP16 transcriptional activation domains
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年学术文章
@wuu
1995年学术文章
@zh-cn
1995年学术文章
@zh-hans
1995年学术文章
@zh-my
1995年学术文章
@zh-sg
1995年學術文章
@yue
1995年學術文章
@zh
1995年學術文章
@zh-hant
name
Core promoter specificities of the Sp1 and VP16 transcriptional activation domains
@en
type
label
Core promoter specificities of the Sp1 and VP16 transcriptional activation domains
@en
prefLabel
Core promoter specificities of the Sp1 and VP16 transcriptional activation domains
@en
P2093
P2860
P356
P1476
Core promoter specificities of the Sp1 and VP16 transcriptional activation domains
@en
P2093
P2860
P304
P356
10.1128/MCB.15.11.5906
P407
P577
1995-11-01T00:00:00Z