scholarly article | Q13442814 |
P2093 | author name string | Sharon Y R Dent | |
Evangelia Koutelou | |||
Calley L Hirsch | |||
P2860 | cites work | E2F transcriptional activation requires TRRAP and GCN5 cofactors | Q24291353 |
Human STAGA complex is a chromatin-acetylating transcription coactivator that interacts with pre-mRNA splicing and DNA damage-binding factors in vivo | Q24291710 | ||
A TFTC/STAGA module mediates histone H2A and H2B deubiquitination, coactivates nuclear receptors, and counteracts heterochromatin silencing | Q24307408 | ||
The putative cancer stem cell marker USP22 is a subunit of the human SAGA complex required for activated transcription and cell-cycle progression | Q24307439 | ||
Chk1 is a histone H3 threonine 11 kinase that regulates DNA damage-induced transcriptional repression | Q24309909 | ||
The double-histone-acetyltransferase complex ATAC is essential for mammalian development | Q24310357 | ||
Human ATAC Is a GCN5/PCAF-containing acetylase complex with a novel NC2-like histone fold module that interacts with the TATA-binding protein | Q24320022 | ||
Mammalian GCN5 and P/CAF acetyltransferases have homologous amino-terminal domains important for recognition of nucleosomal substrates | Q24522706 | ||
Microarray analysis identifies a death-from-cancer signature predicting therapy failure in patients with multiple types of cancer | Q24528253 | ||
Host cell factor and an uncharacterized SANT domain protein are stable components of ATAC, a novel dAda2A/dGcn5-containing histone acetyltransferase complex in Drosophila | Q24537631 | ||
Cloning of Drosophila GCN5: conserved features among metazoan GCN5 family members | Q24548063 | ||
The essential cofactor TRRAP recruits the histone acetyltransferase hGCN5 to c-Myc | Q24554343 | ||
The structural basis for the recognition of acetylated histone H4 by the bromodomain of histone acetyltransferase gcn5p | Q24596953 | ||
Multivalent binding of p53 to the STAGA complex mediates coactivator recruitment after UV damage | Q24655422 | ||
Glutamine-expanded ataxin-7 alters TFTC/STAGA recruitment and chromatin structure leading to photoreceptor dysfunction. | Q25256616 | ||
ADA3, a putative transcriptional adaptor, consists of two separable domains and interacts with ADA2 and GCN5 in a trimeric complex | Q27930121 | ||
Functional organization of the yeast SAGA complex: distinct components involved in structural integrity, nucleosome acetylation, and TATA-binding protein interaction. | Q27930736 | ||
Polyglutamine-expanded spinocerebellar ataxia-7 protein disrupts normal SAGA and SLIK histone acetyltransferase activity | Q27931763 | ||
The deubiquitylation activity of Ubp8 is dependent upon Sgf11 and its association with the SAGA complex | Q27932453 | ||
Recruitment of HAT complexes by direct activator interactions with the ATM-related Tra1 subunit | Q27933602 | ||
Transcriptional activation via sequential histone H2B ubiquitylation and deubiquitylation, mediated by SAGA-associated Ubp8. | Q27933975 | ||
SAGA-associated Sgf73p facilitates formation of the preinitiation complex assembly at the promoters either in a HAT-dependent or independent manner in vivo | Q27934681 | ||
Yeast Gcn5 functions in two multisubunit complexes to acetylate nucleosomal histones: characterization of an Ada complex and the SAGA (Spt/Ada) complex | Q27934812 | ||
In vivo target of a transcriptional activator revealed by fluorescence resonance energy transfer | Q27935003 | ||
A subset of TAF(II)s are integral components of the SAGA complex required for nucleosome acetylation and transcriptional stimulation | Q27936635 | ||
Yeast Ataxin-7 links histone deubiquitination with gene gating and mRNA export | Q27936733 | ||
The STAGA subunit ADA2b is an important regulator of human GCN5 catalysis | Q39927575 | ||
In-depth profiling of post-translational modifications on the related transcription factor complexes TFIID and SAGA. | Q39949372 | ||
SAGA and a novel Drosophila export complex anchor efficient transcription and mRNA export to NPC. | Q40045995 | ||
Functional similarity and physical association between GCN5 and ADA2: putative transcriptional adaptors. | Q40793485 | ||
Global position and recruitment of HATs and HDACs in the yeast genome. | Q41233273 | ||
SAGA-mediated H2B deubiquitination controls the development of neuronal connectivity in the Drosophila visual system | Q41953553 | ||
HAT-HDAC interplay modulates global histone H3K14 acetylation in gene-coding regions during stress | Q42563421 | ||
Molecular architecture of the S. cerevisiae SAGA complex. | Q42631699 | ||
The Gcn5 bromodomain of the SAGA complex facilitates cooperative and cross-tail acetylation of nucleosomes | Q43148421 | ||
Genome-wide relationships between TAF1 and histone acetyltransferases in Saccharomyces cerevisiae | Q43240899 | ||
Site-specific cross-linking of TBP in vivo and in vitro reveals a direct functional interaction with the SAGA subunit Spt3. | Q43247301 | ||
High-resolution genome-wide mapping of histone modifications | Q47244312 | ||
Developmental potential of Gcn5(-/-) embryonic stem cells in vivo and in vitro. | Q51988778 | ||
Gcn5 promotes acetylation, eviction, and methylation of nucleosomes in transcribed coding regions. | Q53577981 | ||
H2B Ubiquitylation Acts as a Barrier to Ctk1 Nucleosomal Recruitment Prior to Removal by Ubp8 within a SAGA-Related Complex | Q54998786 | ||
Transcription-linked acetylation by Gcn5p of histones H3 and H4 at specific lysines | Q59051030 | ||
Expanded lysine acetylation specificity of Gcn5 in native complexes | Q74456705 | ||
The ATM-related cofactor Tra1 is a component of the purified SAGA complex | Q27937594 | ||
Tetrahymena histone acetyltransferase A: a homolog to yeast Gcn5p linking histone acetylation to gene activation | Q27937778 | ||
Sus1, a functional component of the SAGA histone acetylase complex and the nuclear pore-associated mRNA export machinery | Q27937843 | ||
Role of the Ada2 and Ada3 transcriptional coactivators in histone acetylation | Q27939467 | ||
H2B ubiquitin protease Ubp8 and Sgf11 constitute a discrete functional module within the Saccharomyces cerevisiae SAGA complex. | Q27939759 | ||
The mRNA export factor Sus1 is involved in Spt/Ada/Gcn5 acetyltransferase-mediated H2B deubiquitinylation through its interaction with Ubp8 and Sgf11. | Q27940177 | ||
c-Myc transformation domain recruits the human STAGA complex and requires TRRAP and GCN5 acetylase activity for transcription activation | Q28186628 | ||
Intrinsic ubiquitination activity of PCAF controls the stability of the oncoprotein Hdm2 | Q28287716 | ||
The c-MYC oncoprotein is a substrate of the acetyltransferases hGCN5/PCAF and TIP60 | Q28295870 | ||
Deregulated expression of a novel component of TFTC/STAGA histone acetyltransferase complexes, rat SGF29, in hepatocellular carcinoma: possible implication for the oncogenic potential of c-Myc | Q28575519 | ||
Loss of Gcn5 acetyltransferase activity leads to neural tube closure defects and exencephaly in mouse embryos | Q28593423 | ||
The histone H3 acetylase dGcn5 is a key player in Drosophila melanogaster metamorphosis | Q28769333 | ||
Genome-wide map of nucleosome acetylation and methylation in yeast | Q29614525 | ||
Histone ubiquitination: triggering gene activity | Q29617523 | ||
The SAGA continues: expanding the cellular role of a transcriptional co-activator complex | Q30438554 | ||
Loss of Gcn5l2 leads to increased apoptosis and mesodermal defects during mouse development | Q30936148 | ||
Glial cells mediate target layer selection of retinal axons in the developing visual system of Drosophila. | Q31965148 | ||
Deubiquitination of histone H2B by a yeast acetyltransferase complex regulates transcription. | Q33195734 | ||
Gcn5 and SAGA regulate shelterin protein turnover and telomere maintenance. | Q33493740 | ||
Acetylation by the transcriptional coactivator Gcn5 plays a novel role in co-transcriptional spliceosome assembly | Q33510906 | ||
Polyglutamine-expanded ataxin-7 inhibits STAGA histone acetyltransferase activity to produce retinal degeneration | Q33854083 | ||
Distinct but overlapping roles of histone acetylase PCAF and of the closely related PCAF-B/GCN5 in mouse embryogenesis | Q35275796 | ||
STAGA recruits Mediator to the MYC oncoprotein to stimulate transcription and cell proliferation | Q36421035 | ||
Transcriptional adaptor ADA3 of Drosophila melanogaster is required for histone modification, position effect variegation, and transcription | Q36421102 | ||
Distinct GCN5/PCAF-containing complexes function as co-activators and are involved in transcription factor and global histone acetylation. | Q36908396 | ||
Sus1 is recruited to coding regions and functions during transcription elongation in association with SAGA and TREX2. | Q36942429 | ||
The S. pombe SAGA complex controls the switch from proliferation to sexual differentiation through the opposing roles of its subunits Gcn5 and Spt8. | Q36995417 | ||
Histone h3 lysine 56 acetylation is linked to the core transcriptional network in human embryonic stem cells. | Q37164089 | ||
Drosophila Ada2b is required for viability and normal histone H3 acetylation | Q37493058 | ||
Insights into SAGA function during gene expression | Q37553936 | ||
Redundant roles for the TFIID and SAGA complexes in global transcription | Q38311191 | ||
The essential gene wda encodes a WD40 repeat subunit of Drosophila SAGA required for histone H3 acetylation | Q38411598 | ||
The Sas3p and Gcn5p histone acetyltransferases are recruited to similar genes. | Q38606253 | ||
Screen for DNA-damage-responsive histone modifications identifies H3K9Ac and H3K56Ac in human cells | Q39858162 | ||
Mdm2 and PCAF increase Chk2 ubiquitination and degradation independently of their intrinsic E3 ligase activities | Q39889832 | ||
P433 | issue | 3 | |
P304 | page(s) | 374-382 | |
P577 | publication date | 2010-04-02 | |
P1433 | published in | Current Opinion in Cell Biology | Q13505682 |
P1476 | title | Multiple faces of the SAGA complex | |
P478 | volume | 22 |
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