scholarly journals CREB Binding Protein Coordinates the Function of Multiple Transcription Factors Including Nuclear Factor I to Regulate Phosphoenolpyruvate Carboxykinase (GTP) Gene Transcription

1999 ◽  
Vol 274 (13) ◽  
pp. 8813-8822 ◽  
Author(s):  
Patrick Leahy ◽  
Deborah R. Crawford ◽  
Gregory Grossman ◽  
Richard M. Gronostajski ◽  
Richard W. Hanson
Author(s):  
Laura A. Pérez-Casellas ◽  
Xiaoying Wang ◽  
Kristy D. Howard ◽  
Mark W. Rehage ◽  
Donna D. Strong ◽  
...  

2017 ◽  
Vol 410 ◽  
pp. 124-138 ◽  
Author(s):  
Kok-Siong Chen ◽  
Jonathan W.C. Lim ◽  
Linda J. Richards ◽  
Jens Bunt

1995 ◽  
Vol 15 (3) ◽  
pp. 1747-1758 ◽  
Author(s):  
R M O'Brien ◽  
E L Noisin ◽  
A Suwanichkul ◽  
T Yamasaki ◽  
P C Lucas ◽  
...  

The rate of transcription of the hepatic phosphoenolpyruvate carboxykinase (PEPCK) and insulin-like growth factor-binding protein 1 (IGFBP-1) genes is stimulated by glucocorticoids and inhibited by insulin. In both cases, the effect of insulin is dominant, since it suppresses both basal and glucocorticoid-stimulated PEPCK or IGFBP-1 gene transcription. Analyses of both promoters by transfection of PEPCK or IGFBP-1-chloramphenicol acetyltransferase fusion genes into rat hepatoma cells has led to the identification of insulin response sequences (IRSs) in both genes. The core IRS, T(G/A)TTTTG, is the same in both genes, but the PEPCK promoter has a single copy of this element whereas the IGFBP-1 promoter has two copies arranged as an inverted palindrome. The IGFBP-1 IRS and PEPCK IRS both bind the alpha and beta forms of hepatic nuclear factor 3 (HNF-3), although the latter does so with a sixfold-lower relative affinity. Both the PEPCK and the IGFBP-1 IRSs also function as accessory factor binding sites required for the full induction of gene transcription by glucocorticoids. A combination of transient transfection and DNA binding studies suggests that HNF-3 is the accessory factor that supports glucocorticoid-induced gene transcription. In both genes, the HNF-3 binding site overlaps the IRS core motif(s). A model in which insulin is postulated to mediate its negative effect on glucocorticoid-induced PEPCK and IGFBP-1 gene transcription indirectly by inhibiting HNF-3 action is proposed.


1998 ◽  
Vol 273 (22) ◽  
pp. 13387-13390 ◽  
Author(s):  
Deborah R. Crawford ◽  
Patrick Leahy ◽  
Ching Y. Hu ◽  
Ali Chaudhry ◽  
Richard Gronostajski ◽  
...  

2006 ◽  
Vol 84 (7) ◽  
pp. 713-724 ◽  
Author(s):  
Catherine Mounier ◽  
Barry I. Posner

Insulin, after binding to its receptor, regulates many cellular processes and the expression of several genes. For a subset of genes, insulin exerts a negative effect on transcription; for others, the effect is positive. Insulin controls gene transcription by modifying the binding of transcription factors on insulin-response elements or by regulating their transcriptional activities. Different insulin-signaling cascades have been characterized as mediating the insulin effect on gene transcription. In this review, we analyze recent data on the molecular mechanisms, mostly in the liver, through which insulin exerts its effect. We first focus on the key transcription factors (viz. Foxo, sterol-response-element-binding protein family (SREBP), and Sp1) involved in the regulation of gene transcription by insulin. We then present current information on the way insulin downregulates and upregulates gene transcription, using as examples of downregulation phosphoenolpyruvate carboxykinase (PEPCK) and insulin-like growth factor binding protein 1 (IGFBP-1) genes and of upregulation the fatty acid synthase and malic enzyme genes. The last part of the paper focuses on the signaling cascades activated by insulin in the liver, leading to the modulation of gene transcription.


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