Mechanisms of transcriptional activation: differences and similarities between yeast, Drosophila, and man.
about
Composite co-activator ARC mediates chromatin-directed transcriptional activationA novel TATA-binding protein-binding protein, ABT1, activates basal transcription and has a yeast homolog that is essential for growthDistinct subdomains of human TAFII130 are required for interactions with glutamine-rich transcriptional activators.An RNA polymerase II complex containing all essential initiation factors binds to the activation domain of PAR leucine zipper transcription factor thyroid embryonic factor.The coactivator dTAF(II)110/hTAF(II)135 is sufficient to recruit a polymerase complex and activate basal transcription mediated by CREBAn interplay between TATA box-binding protein and transcription factors IIE and IIA modulates DNA binding and transcriptionTranscriptional transactivation by selected short random peptides attached to lexA-GFP fusion proteinsImpaired 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.Structural and functional properties of the N transcriptional activation domain of thyroid transcription factor-1: similarities with the acidic activation domainsCluster analysis and promoter modelling as bioinformatics tools for the identification of target genes from expression array data.Cofactor requirements for transcriptional activation by Sp1.Assembly of partial TFIID complexes in mammalian cells reveals distinct activities associated with individual TATA box-binding protein-associated factors.Robust mRNA transcription in chicken DT40 cells depleted of TAF(II)31 suggests both functional degeneracy and evolutionary divergence.Mapping histone fold TAFs within yeast TFIID.The corepressor N-CoR and its variants RIP13a and RIP13Delta1 directly interact with the basal transcription factors TFIIB, TAFII32 and TAFII70.The mRNA cap-binding complex stimulates the formation of pre-initiation complex at the promoter via its interaction with Mot1p in vivo.Synthetic promoter elements obtained by nucleotide sequence variation and selection for activity.The downstream core promoter element, DPE, is conserved from Drosophila to humans and is recognized by TAFII60 of Drosophila.Chromatin, TAFs, and a novel multiprotein coactivator are required for synergistic activation by Sp1 and SREBP-1a in vitro.Activation changes the spectrum but not the diversity of genes expressed by T cells.Deciphering the combinatorial architecture of a Drosophila homeotic gene enhancerGenetic dissection of hTAF(II)130 defines a hydrophobic surface required for interaction with glutamine-rich activators.A multiplicity of mediators: alternative forms of transcription complexes communicate with transcriptional regulators.Functional analysis of Drosophila melanogaster hexokinase Hex-A locus: multiple Initiator-like elements enhance DPE containing promoter activity.Corepressor SMRT functions as a coactivator for thyroid hormone receptor T3Ralpha from a negative hormone response element.Interactions of a DNA-bound transcriptional activator with the TBP-TFIIA-TFIIB-promoter quaternary complex.Purification and enzymic properties of Mot1 ATPase, a regulator of basal transcription in the yeast Saccharomyces cerevisiae.The role of AHA motifs in the activator function of tomato heat stress transcription factors HsfA1 and HsfA2.Promoter structure and transcriptional activation with chromatin templates assembled in vitro. A single Gal4-VP16 dimer binds to chromatin or to DNA with comparable affinity.Identification of engrailed promoter elements essential for interactions with a stripe enhancer in Drosophila embryos.[Effects of tumor suppressor gene TCF21 on the proliferation, migration and apoptosis of A549 cells].Functional analysis of the Ume3p/ Srb11p-RNA polymerase II holoenzyme interaction
P2860
Q22009528-342A171C-0B15-414D-ADBC-59F2BB7EBCCFQ22011164-EFBAC177-D060-4FE4-BA54-6FD87900221EQ24522713-398F040B-4845-4C7D-BD7E-E6C1A206DD7DQ24530608-81ED1369-02BB-40FD-A590-2E5CC1A76A0BQ24555105-D0A34A88-CB0D-4399-AF33-CC672A6894A6Q24657618-E8E85489-AB32-4D78-9CB4-4F7D631232B6Q24805082-ABC0E84C-73ED-4E5D-9AFB-F9D9D4C4E3ECQ27938987-DD9A67AB-DB0D-4D8F-B495-8A7FFDF0F0C0Q28909267-8E1CF726-B3D5-46F1-9D79-9E024C49039CQ30640554-13BAACE0-9BCA-4066-BEC7-711B18D6C305Q33671375-F0225B91-C76F-4C31-A142-986FC3F29A1BQ33909730-035AE8B6-48DE-41A0-B4DD-6AD810274DC9Q33964585-54BB0FF7-1012-4C96-BC41-932BE25B4040Q34089518-8448C2B8-88F2-4E42-B2C0-EF4B90D92C81Q34669136-9275E0FA-CE99-40E7-AA33-EB6FF0462884Q34723440-8F8B22C3-BE00-43C9-A756-4029E03ACD8BQ35103817-04DFDB35-050F-4D23-8389-08C4CEDF82AFQ35196382-B2347FDF-4858-4AD2-9800-565AD28B160DQ35210134-6811119E-8F13-444D-A6DE-C3BF24B3D7A0Q36551189-3311724A-DD83-4970-A898-C02801B2CD9CQ37619852-633D6D3F-B0C7-49CC-B284-C749D710B581Q38318474-DC92FDE4-69D9-430C-8AAF-3AA3622E062EQ39722071-EDA37E4C-6906-4D91-AE78-1853546A5580Q40178453-78BFA809-5DFF-4DB9-A10F-A6E8D681BFF5Q40696155-ADFD7220-2110-4A8E-B320-E989848004DBQ41361177-8422FCAB-4E82-4C0E-BEEC-C2FA86FCEF70Q41745903-34CE5F65-737A-4B9F-AB93-F918336E76B0Q42483301-AD85A947-137F-4330-9577-E5AC1EB3EAD6Q46113275-054659C5-3E61-47F3-A9F1-AD4767D0120EQ52176984-F1DC1AF2-BDC7-41F0-A512-C92BB5EDFE9AQ55451366-BFBD01F0-74BE-46E0-99A1-4BE412A7E488Q58696257-6FC84A92-9A7B-478D-A1A2-19662ED79744
P2860
Mechanisms of transcriptional activation: differences and similarities between yeast, Drosophila, and man.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Mechanisms of transcriptional ...... en yeast, Drosophila, and man.
@en
type
label
Mechanisms of transcriptional ...... en yeast, Drosophila, and man.
@en
prefLabel
Mechanisms of transcriptional ...... en yeast, Drosophila, and man.
@en
P1476
Mechanisms of transcriptional ...... en yeast, Drosophila, and man.
@en
P304
P356
10.1016/S0959-437X(97)80126-8
P577
1997-04-01T00:00:00Z