Abstract

Transcription of the gene encoding the catalytic subunit of glucose-6-phosphatase (G6Pase) is stimulated by glucocorticoids and strongly repressed by insulin. We have explored the signaling pathways by which insulin mediates the repression of G6Pase transcription in H4IIE cells. Wortmannin, a phosphatidylinositide 3-kinase (PtdIns 3-kinase) inhibitor blocked the repression of G6Pase mRNA expression by insulin. However, both rapamycin, which inhibits p70S6 kinase activation, and PD98059, an inhibitor of mitogen-activated protein kinase activation, were without effect. Insulin inhibited dexamethasone-induced luciferase expression from a transiently transfected plasmid that places the luciferase gene under the control of the G6Pase promoter. This effect of insulin was mimicked by the overexpression of a constitutively active PtdIns 3-kinase but not by a constitutively active protein kinase B. Taken together, these data demonstrate that PtdIns 3-kinase activation is both necessary and at least partly sufficient for the repression of G6Pase expression by insulin, but neither mitogen-activated protein kinase nor p70S6 kinase are involved. In addition, activation of protein kinase B alone is not sufficient for repression of the G6Pase gene. These results imply the existence of a novel signaling pathway downstream of PtdIns 3 kinase that is involved in the regulation of G6Pase expression by insulin.

Highlights

  • The hydrolysis of glucose-6-phosphate to glucose by glucose6-phosphatase (G6Pase)1 represents the final step of both gluconeogenesis and glycogen breakdown in the liver

  • The insulin response sequence (IRS) identified in the phosphoenolpyruvate carboxykinase, tyrosine aminotransferase, and apolipoprotein CIII promoters all contain this same motif, whereas the IRS in the insulin-like growth factor-binding protein-1 promoter has two copies of this motif arranged as an inverted palindrome (6 –11)

  • To determine whether PtdIns 3-kinase activation is required for insulin to suppress G6Pase gene expression, H4IIE cells were incubated in the absence or presence of various combinations of 100 nM wortmannin and 200 nM insulin

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Summary

Introduction

The hydrolysis of glucose-6-phosphate to glucose by glucose6-phosphatase (G6Pase)1 represents the final step of both gluconeogenesis and glycogen breakdown in the liver. To determine whether PtdIns 3-kinase activation is required for insulin to suppress G6Pase gene expression, H4IIE cells were incubated in the absence or presence of various combinations of 100 nM wortmannin and 200 nM insulin.

Results
Conclusion
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