Mammalian TAF(II)30 is required for cell cycle progression and specific cellular differentiation programmes
about
The TFIID components human TAF(II)140 and Drosophila BIP2 (TAF(II)155) are novel metazoan homologues of yeast TAF(II)47 containing a histone fold and a PHD fingerTAF7 (TAFII55) plays a role in the transcription activation by c-JunThe nuclear import of TAF10 is regulated by one of its three histone fold domain-containing interaction partnersNovel complex integrating mitochondria and the microtubular cytoskeleton with chromosome remodeling and tumor suppressor RASSF1 deduced by in silico homology analysis, interaction cloning in yeast, and colocalization in cultured cellsTAF9b (formerly TAF9L) is a bona fide TAF that has unique and overlapping roles with TAF9Coordinate regulation of RARgamma2, TBP, and TAFII135 by targeted proteolysis during retinoic acid-induced differentiation of F9 embryonal carcinoma cellsTargeting TBP-Associated Factors in Ovarian CancerdTAF10- and dTAF10b-Containing Complexes Are Required for Ecdysone-Driven Larval-Pupal Morphogenesis in Drosophila melanogasterDistinct mutations in yeast TAF(II)25 differentially affect the composition of TFIID and SAGA complexes as well as global gene expression patterns.Genetic analysis of TAF68/61 reveals links to cell cycle regulators.Systematic analysis of essential yeast TAFs in genome-wide transcription and preinitiation complex assemblyFunctional analysis of the TFIID-specific yeast TAF4 (yTAF(II)48) reveals an unexpected organization of its histone-fold domainThe retinoic acid-metabolizing enzyme, CYP26A1, is essential for normal hindbrain patterning, vertebral identity, and development of posterior structures.Switching of the core transcription machinery during myogenesisAlternative splicing targeting the hTAF4-TAFH domain of TAF4 represses proliferation and accelerates chondrogenic differentiation of human mesenchymal stem cellsCloning and expression of a novel nuclear matrix-associated protein that is regulated during the retinoic acid-induced neuronal differentiation.Temporary expression of the TAF10 gene and its requirement for normal development of Arabidopsis thaliana.Identification of mammalian TOM22 as a subunit of the preprotein translocase of the mitochondrial outer membrane.TAF4 inactivation in embryonic fibroblasts activates TGF beta signalling and autocrine growth.Two novel Drosophila TAF(II)s have homology with human TAF(II)30 and are differentially regulated during development.Robust mRNA transcription in chicken DT40 cells depleted of TAF(II)31 suggests both functional degeneracy and evolutionary divergence.Prodos is a conserved transcriptional regulator that interacts with dTAF(II)16 in Drosophila melanogaster.Heterozygous disruption of the TATA-binding protein gene in DT40 cells causes reduced cdc25B phosphatase expression and delayed mitosis.A composite nuclear export signal in the TBP-associated factor TAFII105.Molecular processes during fat cell development revealed by gene expression profiling and functional annotation.Derepression of DNA damage-regulated genes requires yeast TAF(II)s.TAF10 (TAF(II)30) is necessary for TFIID stability and early embryogenesis in mice.Cytoplasmic TAF2-TAF8-TAF10 complex provides evidence for nuclear holo-TFIID assembly from preformed submodules.Human mediator enhances activator-facilitated recruitment of RNA polymerase II and promoter recognition by TATA-binding protein (TBP) independently of TBP-associated factors.Holo-TFIID controls the magnitude of a transcription burst and fine-tuning of transcription.Differentially expressed genes in sporadic amyotrophic lateral sclerosis spinal cords--screening by molecular indexing and subsequent cDNA microarray analysis.Distinct requirements for C.elegans TAF(II)s in early embryonic transcription.TATA-binding protein-like protein (TLP/TRF2/TLF) negatively regulates cell cycle progression and is required for the stress-mediated G(2) checkpoint.TATA-binding protein-associated factors enhance the recruitment of RNA polymerase II by transcriptional activators.TATA-binding protein-associated factor 7 regulates polyamine transport activity and polyamine analog-induced apoptosis.Quantitative mass spectrometry of TATA binding protein-containing complexes and subunit phosphorylations during the cell cycle.The TAF10-containing TFIID and SAGA transcriptional complexes are dispensable for early somitogenesis in the mouse embryo.Abundant expression in vascular tissue of plant TAF10, an orthologous gene for TATA box-binding protein-associated factor 10, in Flaveria trinervia and abnormal morphology of Arabidopsis thaliana transformants on its overexpression.The Arabidopsis mutant stg1 identifies a function for TBP-associated factor 10 in plant osmotic stress adaptation.Reversible male sterility in eggplant (Solanum melongena L.) by artificial microRNA-mediated silencing of general transcription factor genes
P2860
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P2860
Mammalian TAF(II)30 is required for cell cycle progression and specific cellular differentiation programmes
description
1999 nî lūn-bûn
@nan
1999 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Mammalian TAF(II)30 is require ...... lar differentiation programmes
@ast
Mammalian TAF(II)30 is require ...... lar differentiation programmes
@en
Mammalian TAF(II)30 is require ...... lar differentiation programmes
@en-gb
Mammalian TAF(II)30 is require ...... lar differentiation programmes
@nl
type
label
Mammalian TAF(II)30 is require ...... lar differentiation programmes
@ast
Mammalian TAF(II)30 is require ...... lar differentiation programmes
@en
Mammalian TAF(II)30 is require ...... lar differentiation programmes
@en-gb
Mammalian TAF(II)30 is require ...... lar differentiation programmes
@nl
prefLabel
Mammalian TAF(II)30 is require ...... lar differentiation programmes
@ast
Mammalian TAF(II)30 is require ...... lar differentiation programmes
@en
Mammalian TAF(II)30 is require ...... lar differentiation programmes
@en-gb
Mammalian TAF(II)30 is require ...... lar differentiation programmes
@nl
P356
P1433
P1476
Mammalian TAF(II)30 is require ...... lar differentiation programmes
@en
P2093
P304
P356
10.1093/EMBOJ/18.17.4823
P407
P577
1999-09-01T00:00:00Z