MondoA, a novel basic helix-loop-helix-leucine zipper transcriptional activator that constitutes a positive branch of a max-like network
about
MondoA-Mlx heterodimers are candidate sensors of cellular energy status: mitochondrial localization and direct regulation of glycolysisThe subcellular localization of the ChoRE-binding protein, encoded by the Williams-Beuren syndrome critical region gene 14, is regulated by 14-3-3Glucose activates ChREBP by increasing its rate of nuclear entry and relieving repression of its transcriptional activityA novel heterodimerization domain, CRM1, and 14-3-3 control subcellular localization of the MondoA-Mlx heterocomplex.Coordination of nutrient availability and utilization by MAX- and MLX-centered transcription networksFunctional interactions among members of the MAX and MLX transcriptional network during oncogenesisThe Caenorhabditis elegans Myc-Mondo/Mad complexes integrate diverse longevity signalsMondo/ChREBP-Mlx-regulated transcriptional network is essential for dietary sugar tolerance in DrosophilaMondoA-Mlx transcriptional activity is limited by mTOR-MondoA interactionMondoA coordinately regulates skeletal myocyte lipid homeostasis and insulin signalingGlucose 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.Myc, mondo, and metabolismNew perspectives in the regulation of hepatic glycolytic and lipogenic genes by insulin and glucose: a role for the transcription factor sterol regulatory element binding protein-1c.Drosophila Myc: A master regulator of cellular performance.Transcriptional and Translational Downregulation of Thioredoxin Interacting Protein Is Required for Metabolic Reprogramming during G(1).Williams-Beuren syndrome: a challenge for genotype-phenotype correlations.Evolution of the Max and Mlx networks in animals.MondoA senses non-glucose sugars: regulation of thioredoxin-interacting protein (TXNIP) and the hexose transport curb.MondoA deficiency enhances sprint performance in mice.Metabolic reprogramming in triple-negative breast cancer through Myc suppression of TXNIPA critical role for the loop region of the basic helix-loop-helix/leucine zipper protein Mlx in DNA binding and glucose-regulated transcription.Assembly of b/HLH/z proteins c-Myc, Max, and Mad1 with cognate DNA: importance of protein-protein and protein-DNA interactions.MondoA senses adenine nucleotides: transcriptional induction of thioredoxin-interacting proteinAdaptive metabolic response to 4 weeks of sugar-sweetened beverage consumption in healthy, lightly active individuals and chronic high glucose availability in primary human myotubes.The Regulation of Muscle Structure and Metabolism by Mio/dChREBP in Drosophila.Carbon source metabolism and its regulation in cancer cells.A C. elegans Myc-like network cooperates with semaphorin and Wnt signaling pathways to control cell migration.The glucose-sensing transcription factor MLX promotes myogenesis via myokine signalingGlucose sensing by MondoA:Mlx complexes: a role for hexokinases and direct regulation of thioredoxin-interacting protein expression.Glucose-mediated transactivation of carbohydrate response element-binding protein requires cooperative actions from Mondo conserved regions and essential trans-acting factor 14-3-3The role of the glucose-sensing transcription factor carbohydrate-responsive element-binding protein pathway in termite queen fertilitydMyc expression in the fat body affects DILP2 release and increases the expression of the fat desaturase Desat1 resulting in organismal growth.An overview of MYC and its interactome.Hepatic glucose sensing and integrative pathways in the liver.Acquisition of essential somatic cell cycle regulatory protein expression and implied activity occurs at the second to third cell division in mouse preimplantation embryos.Specific SR protein-dependent splicing substrates identified through genomic SELEX.MNT and Emerging Concepts of MNT-MYC AntagonismThe regulation and role of carbohydrate response element binding protein in metabolic homeostasis and disease.
P2860
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P2860
MondoA, a novel basic helix-loop-helix-leucine zipper transcriptional activator that constitutes a positive branch of a max-like network
description
2000 nî lūn-bûn
@nan
2000 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի դեկտեմբերին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
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name
MondoA, a novel basic helix-lo ...... e branch of a max-like network
@ast
MondoA, a novel basic helix-lo ...... e branch of a max-like network
@en
MondoA, a novel basic helix-lo ...... e branch of a max-like network
@nl
type
label
MondoA, a novel basic helix-lo ...... e branch of a max-like network
@ast
MondoA, a novel basic helix-lo ...... e branch of a max-like network
@en
MondoA, a novel basic helix-lo ...... e branch of a max-like network
@nl
prefLabel
MondoA, a novel basic helix-lo ...... e branch of a max-like network
@ast
MondoA, a novel basic helix-lo ...... e branch of a max-like network
@en
MondoA, a novel basic helix-lo ...... e branch of a max-like network
@nl
P2093
P2860
P921
P3181
P1476
MondoA, a novel basic helix-lo ...... e branch of a max-like network
@en
P2093
A L Eilers
K L Coulter
P2860
P304
P3181
P356
10.1128/MCB.20.23.8845-8854.2000
P407
P577
2000-12-01T00:00:00Z