The SV40 large T antigen and adenovirus E1a oncoproteins interact with distinct isoforms of the transcriptional co-activator, p300.
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HIV-1 tat transactivator recruits p300 and CREB-binding protein histone acetyltransferases to the viral promoterA novel transcriptional repression domain mediates p21(WAF1/CIP1) induction of p300 transactivationTargeting of p300/CREB binding protein coactivators by simian virus 40 is mediated through p53Scaffold/matrix attachment region elements interact with a p300-scaffold attachment factor A complex and are bound by acetylated nucleosomes.Molecular mechanisms of myogenic coactivation by p300: direct interaction with the activation domain of MyoD and with the MADS box of MEF2CThe T/t common exon of simian virus 40, JC, and BK polyomavirus T antigens can functionally replace the J-domain of the Escherichia coli DnaJ molecular chaperoneParkin-mediated monoubiquitination of the PDZ protein PICK1 regulates the activity of acid-sensing ion channelsAn intrinsically disordered region of the acetyltransferase p300 with similarity to prion-like domains plays a role in aggregationProteasome-mediated degradation of the coactivator p300 impairs cardiac transcriptionThe basic helix-loop-helix protein BETA2 interacts with p300 to coordinate differentiation of secretin-expressing enteroendocrine cellsp300 family members associate with the carboxyl terminus of simian virus 40 large tumor antigenp53 targets simian virus 40 large T antigen for acetylation by CBPAdeno-associated virus type 2 rep protein inhibits human papillomavirus type 16 E2 recruitment of the transcriptional coactivator p300.B56 regulatory subunit of protein phosphatase 2A mediates valproic acid-induced p300 degradationPhosphorylation-dependent degradation of p300 by doxorubicin-activated p38 mitogen-activated protein kinase in cardiac cells.Activation of protein kinase C triggers its ubiquitination and degradationAn exposed KID-like domain in human T-cell lymphotropic virus type 1 Tax is responsible for the recruitment of coactivators CBP/p300Human T-lymphotropic virus type 1 p30(II) regulates gene transcription by binding CREB binding protein/p300.p300 is required for MyoD-dependent cell cycle arrest and muscle-specific gene transcriptionA role for CREB binding protein and p300 transcriptional coactivators in Ets-1 transactivation functionsCell type-specific replication of simian virus 40 conferred by hormone response elements in the late promoter.Bromodomain motifs and "scaffolding"?Histone acetyltransferase (HAT) activity of p300 modulates human T lymphotropic virus type 1 p30II-mediated repression of LTR transcriptional activity.Development and characterization of a mouse floxed Bmp2 osteoblast cell line that retains osteoblast genotype and phenotype.T antigens of simian virus 40: molecular chaperones for viral replication and tumorigenesisSimian virus 40 large T antigen and two independent T-antigen segments sensitize cells to apoptosis following genotoxic damagep300 and ATF-2 are components of the DRF complex, which regulates retinoic acid- and E1A-mediated transcription of the c-jun gene in F9 cells.Antigen receptor signaling induces MAP kinase-mediated phosphorylation and degradation of the BCL-6 transcription factorRegulation of beta -catenin transformation by the p300 transcriptional coactivator.A novel simian virus 40 early-region domain mediates transactivation of the cyclin A promoter by small-t antigen and is required for transformation in small-t antigen-dependent assays.MDM2 is a target of simian virus 40 in cellular transformation and during lytic infectionCul7/p185/p193 binding to simian virus 40 large T antigen has a role in cellular transformation.Association of p300 and CBP with simian virus 40 large T antigenThe amino-terminal transforming region of simian virus 40 large T and small t antigens functions as a J domain.Adenoviral delivery of E2F-1 directs cell cycle reentry and p53-independent apoptosis in postmitotic adult myocardium in vivo.Histone deacetylase inhibitors, valproic acid and trichostatin-A induce apoptosis and affect acetylation status of p53 in ERG-positive prostate cancer cells.The N-terminal domain of p73 interacts with the CH1 domain of p300/CREB binding protein and mediates transcriptional activation and apoptosis.Loss of p19(ARF) eliminates the requirement for the pRB-binding motif in simian virus 40 large T antigen-mediated transformation.Polyomavirus large T antigen binds the transcriptional coactivator protein p300.Immortalization of T lymphocytes by human T-cell leukemia virus type 1 is independent of the tax-CBP/p300 interaction
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P2860
The SV40 large T antigen and adenovirus E1a oncoproteins interact with distinct isoforms of the transcriptional co-activator, p300.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
The SV40 large T antigen and a ...... criptional co-activator, p300.
@ast
The SV40 large T antigen and a ...... criptional co-activator, p300.
@en
type
label
The SV40 large T antigen and a ...... criptional co-activator, p300.
@ast
The SV40 large T antigen and a ...... criptional co-activator, p300.
@en
prefLabel
The SV40 large T antigen and a ...... criptional co-activator, p300.
@ast
The SV40 large T antigen and a ...... criptional co-activator, p300.
@en
P2093
P2860
P1433
P1476
The SV40 large T antigen and a ...... scriptional co-activator, p300
@en
P2093
Avantaggiati ML
Graessmann A
Nakatani Y
P2860
P304
P356
10.1002/J.1460-2075.1996.TB00577.X
P407
P577
1996-05-01T00:00:00Z