Glucose-mediated transactivation of carbohydrate response element-binding protein requires cooperative actions from Mondo conserved regions and essential trans-acting factor 14-3-3
about
Glucose activates ChREBP by increasing its rate of nuclear entry and relieving repression of its transcriptional activityTranscriptional regulation of hepatic lipogenesisThe Krüppel-like zinc finger protein Glis3 directly and indirectly activates insulin gene transcriptionTranscriptional control of hepatic lipid metabolism by SREBP and ChREBP.Glucose controls nuclear accumulation, promoter binding, and transcriptional activity of the MondoA-Mlx heterodimer.Activation and repression of glucose-stimulated ChREBP requires the concerted action of multiple domains within the MondoA conserved regionA novel N-terminal domain may dictate the glucose response of Mondo proteins.ChREBP mediates glucose repression of peroxisome proliferator-activated receptor alpha expression in pancreatic beta-cells.Importin-alpha protein binding to a nuclear localization signal of carbohydrate response element-binding protein (ChREBP).Genome-Wide Analysis of ChREBP Binding Sites on Male Mouse Liver and White Adipose Chromatin.ChREBP Regulates Itself and Metabolic Genes Implicated in Lipid Accumulation in β-Cell LineFABP4-Cre Mediated Expression of Constitutively Active ChREBP Protects Against Obesity, Fatty Liver, and Insulin ResistanceInduction of the ChREBPβ Isoform Is Essential for Glucose-Stimulated β-Cell ProliferationStructural characterization of a unique interface between carbohydrate response element-binding protein (ChREBP) and 14-3-3β protein.ChREBP regulates fructose-induced glucose production independently of insulin signaling.Proteomic analysis of bovine sperm YWHA binding partners identify proteins involved in signaling and metabolism.Drug discovery based on genetic and metabolic findings in schizophrenia.O-GlcNAcylation Links ChREBP and FXR to Glucose-SensingIntegration of ChREBP-Mediated Glucose Sensing into Whole Body Metabolism.The regulation and role of carbohydrate response element binding protein in metabolic homeostasis and disease.Glucose induces protein targeting to glycogen in hepatocytes by fructose 2,6-bisphosphate-mediated recruitment of MondoA to the promoter.Glucose-6-phosphate mediates activation of the carbohydrate responsive binding protein (ChREBP).Glucose induces expression of rat pyruvate carboxylase through a carbohydrate response element in the distal gene promoter.Dietary carbohydrate and control of hepatic gene expression: mechanistic links from ATP and phosphate ester homeostasis to the carbohydrate-response element-binding protein.
P2860
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P2860
Glucose-mediated transactivation of carbohydrate response element-binding protein requires cooperative actions from Mondo conserved regions and essential trans-acting factor 14-3-3
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Glucose-mediated transactivati ...... ial trans-acting factor 14-3-3
@ast
Glucose-mediated transactivati ...... ial trans-acting factor 14-3-3
@en
type
label
Glucose-mediated transactivati ...... ial trans-acting factor 14-3-3
@ast
Glucose-mediated transactivati ...... ial trans-acting factor 14-3-3
@en
prefLabel
Glucose-mediated transactivati ...... ial trans-acting factor 14-3-3
@ast
Glucose-mediated transactivati ...... ial trans-acting factor 14-3-3
@en
P2093
P2860
P356
P1476
Glucose-mediated transactivati ...... ial trans-acting factor 14-3-3
@en
P2093
Lawrence Chan
Minako Imamura
Naravat Poungvarin
P2860
P304
P356
10.1210/ME.2007-0560
P50
P577
2008-04-24T00:00:00Z