CCAAT/enhancer-binding protein beta (C/EEP beta) and C/EBP delta contribute to growth hormone-regulated transcription of c-fos

Using the c-fos enhancer as a model to analyze growth hormone (GH)-promoted gene expression, the roles of CCAAT/enhancer-binding proteins (C/EBPs) in GH-regulated transcription were investigated. In 3T3-F442A fibroblasts stab ly expressing the c-fos promoter mutated at the C/EBP binding site upstream of luciferase, c-fos promoter activity is stimulated by GH 6-7-fold; wild type c-fos promoter shows only a 2-fold induction by GH, This suggests that C/EBP restrains GH-stimulated expression of c-fos. Electrophoretic mobilit y shift assays with nuclear extracts from 3T3-F442A cells indicate that GH rapidly (2-5 min) increases binding of C/EBP beta and C/EBP delta, to the c -fos C/EBP binding site. Both liver activating protein (LAP) and liver inhi bitory protein (LIP), forms of C/EBP delta, are detected in 3T3-F442A cells by immunoblotting, GH increases the binding of LAP/LAP and LAP/LIP dimers, Overexpression elf LIP interferes with GH-promoted reporter expression in CHO cells expressing GH receptors, consistent with the possibility that LIP restrains GH-stimulated c-fos expression. Overexpression of LAP elevates b asal luciferase activity but does not influence promoter activation by GH, while overexpressed C/EBP delta elevates basal promoter activity and enhanc es the stimulation by GH. GH stimulates the expression of mRNA for C/EBP be ta and -delta and increases levels of C/EBP delta. Although C/EBP beta is n ot detectably altered, GH induces a shift to more rapidly migrating forms o f LIP and LAP upon immunoblotting. Treatment of extracts from GH-treated ce lls with alkaline phosphatase causes a shift of the slower migrating form t o the rapidly migrating form, consistent with GH promoting dephosphorylatio n of LIP and LAP. These studies implicate C/EBP beta and -delta in GH-regul ated gene expression. They also indicate that GH stimulates the blinding of C/EBP beta and -delta to the c-fos promoter and promotes the dephosphoryla tion of LIP and LAP. These events may contribute to the ability of C/EBP be ta and -delta to regulate GH-stimulated expression of c-fos.