The alpha-isoform of the CCAAT/enhancer-binding protein is required for mediating cAMP responsiveness of the phosphoenolpyruvate carboxykinase promoter in hepatoma cells.
about
Luman, a new member of the CREB/ATF family, binds to herpes simplex virus VP16-associated host cellular factorDifferent transcription factor binding arrays modulate the cAMP responsivity of the phosphoenolpyruvate carboxykinase gene promoterConserved amino acids within CCAAT enhancer-binding proteins (C/EBP(alpha) and beta) regulate phosphoenolpyruvate carboxykinase (PEPCK) gene expressionIdentification of a co-repressor that inhibits the transcriptional and growth-arrest activities of CCAAT/enhancer-binding protein alphaCloning and characterization of the promoter for the liver isoform of the rat carnitine palmitoyltransferase I (L-CPT I) geneSignal-dependent control of gluconeogenic key enzyme genes through coactivator-associated arginine methyltransferase 1Functional characterisation of the regulation of CAAT enhancer binding protein alpha by GSK-3 phosphorylation of Threonines 222/226.The C/EBP family of transcription factors in the liver and other organs.Glucocorticoids are insufficient for neonatal gene induction in the liver.C/EBPbeta contributes to cAMP-activated transcription of phosphoenolpyruvate carboxykinase in LLC-PK(1)-F+ cells.A nucleoprotein complex containing CCAAT/enhancer-binding protein beta interacts with an insulin response sequence in the insulin-like growth factor-binding protein-1 gene and contributes to insulin-regulated gene expression.Characterization of elements mediating regulation of phosphoenolpyruvate carboxykinase gene transcription by protein kinase A and insulin. Identification of a distinct complex formed in cells that mediate insulin inhibition.CCAAT/enhancer-binding protein beta is an accessory factor for the glucocorticoid response from the cAMP response element in the rat phosphoenolpyruvate carboxykinase gene promoter.Glucocorticoid receptor, C/EBP, HNF3, and protein kinase A coordinately activate the glucocorticoid response unit of the carbamoylphosphate synthetase I gene.Interaction between CCAAT/enhancer binding protein and cyclic AMP response element binding protein 1 regulates human immunodeficiency virus type 1 transcription in cells of the monocyte/macrophage lineage.Differential regulation of the mitogen-activated protein and stress-activated protein kinase cascades by adrenergic agonists in quiescent and regenerating adult rat hepatocytes.CREB controls LAP/C/EBP beta transcription.C/EBP factor suppression of inhibition of type II secreted phospholipase A2 promoter in HepG2 cells: possible role of single-strand binding proteins.Gene- and activation-specific mechanisms for insulin inhibition of basal and glucocorticoid-induced insulin-like growth factor binding protein-1 and phosphoenolpyruvate carboxykinase transcription. Roles of forkhead and insulin response sequences.CREB (cAMP response element binding protein) and C/EBPalpha (CCAAT/enhancer binding protein) are required for the superstimulation of phosphoenolpyruvate carboxykinase gene transcription by adenoviral E1a and cAMP.Role of CCAAT enhancer-binding protein beta in the thyroid hormone and cAMP induction of phosphoenolpyruvate carboxykinase gene transcription.Activation of haptoglobin gene expression by cAMP involves CCAAT/enhancer-binding protein isoforms in intestinal epithelial cells.Assessment of the roles of mitogen-activated protein kinase, phosphatidylinositol 3-kinase, protein kinase B, and protein kinase C in insulin inhibition of cAMP-induced phosphoenolpyruvate carboxykinase gene transcription.A tripartite array of transcription factor binding sites mediates cAMP induction of phosphoenolpyruvate carboxykinase gene transcription and its inhibition by insulin.CCAAT-enhancer-binding protein alpha (C/EBP alpha) is required for the thyroid hormone but not the retinoic acid induction of phosphoenolpyruvate carboxykinase (PEPCK) gene transcription.Signaling pathways through which insulin regulates CCAAT/enhancer binding protein alpha (C/EBPalpha) phosphorylation and gene expression in 3T3-L1 adipocytes. Correlation with GLUT4 gene expression.Cooperative mechanism of transcriptional activation by a cyclic AMP-response element modulator alpha mutant containing a motif for constitutive binding to CREB-binding protein.Characterization of CCAAT/enhancer-binding protein alpha as a cyclic AMP-responsive nuclear regulator.
P2860
Q24336173-EBCFCEB3-0B97-4857-8B89-D8F19804B856Q28202381-E55C8320-8FB5-4BCB-BAC9-228769652D11Q28216935-EBFE48DE-789D-4CFB-B04C-3E8327FDBCB3Q28236939-3ED6A18F-1F4B-492D-A7CB-A4FED65CE3AEQ28578201-D0D3F40F-6115-4463-9607-2D9DF7C8C862Q28580398-6A440191-6F4E-44CD-A49C-7738A35F451AQ33239129-71BBC29A-A91F-47A4-9F39-1162B1B9A9C5Q33630431-D3C60895-043A-423D-BFBA-60C951BDF652Q36094015-FB7AD755-6841-4E84-92D5-A5EAB8F3B1E8Q38297050-069E41D6-75ED-47D0-8BFD-F00B3E099133Q38305808-0A2B7389-C4D5-4EC6-899F-47523CE7BE71Q38313587-868D8B6A-2E66-4053-BC49-288B26A29D4FQ38327938-16BBE301-5CF9-4932-B61E-7D07612456B1Q39576419-A038921E-5293-42EC-AAB6-2B3886155017Q39602178-906F03B3-836B-4AA7-B1AA-AA72B92F4454Q40022508-5FD91451-6039-441A-8355-A733BFF79588Q40022530-EC16F6CA-0779-4AE3-8EB3-1DAC419E7AD7Q40022822-FB385814-0652-426D-9E2B-A36583DA533FQ40793631-13F2ED92-99F8-434A-9E12-6C123691C4F7Q40841380-6BFD19AA-52B4-4861-9833-3C0D29C5875BQ40985620-77820741-6345-46D4-94A4-1258CDDFA091Q40989678-D13DBBFF-E29C-4555-93E4-538712924835Q41024614-D6B05125-3B57-4357-8D6A-B196AC7F68F5Q41024622-EA1C8E83-5985-4660-8DCC-14CD142DA75AQ41848156-D7F5E989-0A07-41E2-B74C-12E032B64A43Q42834946-79F28F65-64D5-4736-AF3A-16D2C9C293D6Q43510591-5BD1993C-877C-4BB7-977A-0F150FC9054CQ48010641-ADC12DD8-3AE8-4234-887D-0BD877362400
P2860
The alpha-isoform of the CCAAT/enhancer-binding protein is required for mediating cAMP responsiveness of the phosphoenolpyruvate carboxykinase promoter in hepatoma cells.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年学术文章
@wuu
1996年学术文章
@zh-cn
1996年学术文章
@zh-hans
1996年学术文章
@zh-my
1996年学术文章
@zh-sg
1996年學術文章
@yue
1996年學術文章
@zh
1996年學術文章
@zh-hant
name
The alpha-isoform of the CCAAT ...... se promoter in hepatoma cells.
@en
type
label
The alpha-isoform of the CCAAT ...... se promoter in hepatoma cells.
@en
prefLabel
The alpha-isoform of the CCAAT ...... se promoter in hepatoma cells.
@en
P2093
P2860
P356
P1476
The alpha-isoform of the CCAAT ...... se promoter in hepatoma cells.
@en
P2093
P2860
P304
P356
10.1074/JBC.271.14.8068
P407
P577
1996-04-01T00:00:00Z