Proceedings of the National Academy of Sciences · 1990 · 226 citations · 39 references
Life SciencesBiochemistryMolecular BiologyGene ExpressionSignal TransductionTranscriptional RegulationPromoter RegulationProtein Kinase CascadesTranscription FactorsTranscription In EukaryotesTranscriptional ControlTranscriptional Regulation In EukaryotesAdenylate Cyclase RegulationAdenylate Cyclase SignalingCamp-responsive Gene ExpressionPhosphorylation-dependent RegulationPositive RegulationProtein Kinase A SignalingProtein Phosphorylation In Gene RegulationTranscriptional Repression Mechanisms
We have shown that the transcriptional activity of the protooncogene jun (c-jun) promoter is repressed by a transcription factor, the cAMP response element-binding protein (CREB). This repression can be alleviated when CREB is phosphorylated by the catalytic subunit of protein kinase A. Repression cannot be alleviated by a mutant CREB deficient in the protein kinase A phosphorylation site (M1 CREB Ser-133----Ala), suggesting that phosphorylation of CREB at this site is essential for the relief of repression. Repression by CREB requires its binding to the c-jun promoter. In NIH 3T3 cells stably expressing CREB, c-jun is no longer induced by serum, but this repression can be relieved by treatment of the cells with forskolin, an agonist of the adenylate cyclase pathway. Thus, CREB has a dual function, that of a repressor in the absence of phosphorylation and an activator when phosphorylated by protein kinase A.
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Douglas A. Melton, Paul A. Krieg, Michael R. Rebagliati et al. · Nucleic Acids Research · 1984 · 6.4K citations · Full text