Functional Identification of Regulatory Elements within the\ud Promoter Region of Platelet-Derived Growth Factor 2

Human platelet-derived growth factor (PDGF) is composed of two polypeptide chains, PDGF-1 and PDGF-2,the human homolog of the v-sis oncogene. Deregulation of PDGF-2 expression can confer a growth advantage to cells possessing the cognate receptor and, thus, may contribute to the malignant phenotype. We investigated the regulation of PDGF-2 mRNA expression during megakaryocytic differentiation of K562 cells. Induction by 12-O-tetradecanoylphorbol-13-acetate (TPA) led to a greater than 200-fold increase in PDGF-2 transcript levels in these cells. Induction was dependent on protein synthesis and was not enhanced by cycloheximide exposure.In our initial investigation of the PDGF-2 promoter, a minimal promoter region, which included sequences extending only 42 base pairs upstream of the TATA signal, was found to be as efficient as 4 kilobase pairs\ud upstream of the TATA signal in driving expression of a reporter gene in uninduced K562 cells. We also\ud functionally identified different regulatory sequence elements of the PDGF-2 promoter in TPA-induced K562\ud cells. One region acted as a transcriptional silencer, while another region was necessary for maximal activity\ud of the promoter in megakaryoblasts. This region was shown to bind nuclear factors and was the target for\ud trans-activation in normal and tumor cells. In one tumor cell line, which expressed high PDGF-2 mRNA levels,\ud the presence of the positive regulatory region resulted in a 30-fold increase in promoter activity. However, the\ud ability of the minimal PDGF-2 promoter to drive reporter gene expression in uninduced K562 cells and normal\ud fibroblasts, which contained no detectable PDGF-2 transcripts, implies the existence of other negative control\ud mechanisms beyond the regulation of promoter activity