Binding specificity and modulation of the human ApoCIII promoter activity by heterodimers of ligand-dependent nuclear receptors

Human apolipoprotein CIII (apoCIII) is a major determinant of plasma trigly ceride metabolism. The regulatory elements that control both hepatic and in testinal transcription of the human apoCIII gene are localized between nucl eotides -792 and -25 of the apoCIII promoter. Elements important for apoCII I promoter activity are three hormone response elements (HREs) and three SP 1-binding sites. Orphan members of the nuclear hormone receptor superfamily can bind the HREs and strongly enhance or repress apoCIII promoter activit y. In the present study we have investigated the ability of ligand-dependen t nuclear hormone receptors to bind and modulate the human apoCIII promoter activity. Experiments using DNA binding and competition assays showed that the proximal element B (-87/-72) binds strongly, in addition to HNF-4, ARP -1, EAR-2, and EAR-3, heterodimers of RXR alpha with RAR alpha, and less ef ficiently, homodimers of RAR alpha and heterodimers of RXR alpha with T3R b eta or PPAR alpha. Element G (-669/-648), which was shown previously to bin d ARP-1 and EAR-3 but not HNF-4, binds strongly heterodimers of RXR alpha w ith either RAR alpha or T3Rbeta. Finally element I-4 (-732/-712), which was shown to bind HNF-4, also binds strongly ARP-1 and EAR-3, as well as RXR a lpha/RAR alpha heterodimers and less efficiently, RXR alpha/T3R beta hetero dimers. Methylation interference experiments have identified the protein-DN A interactions between different nuclear receptors and the respective HREs on the apoCIII promoter. RXR alpha/RAR alpha heterodimers and HNF-4 homodim ers bind to DR-1 motifs on elements B and I-4, respectively. RXR alpha/T3R beta heterodimers and ARP-1 bind to DR-5 and DR-0 motifs respectively on el ement G. Cotransfection experiments in HepG2 cells showed that RXR alpha or a combination of RXR alpha and RAR alpha increased the apoCIII promoter ac tivity approximately 2-fold in the presence of the ligands 9-cis or all-tra ns RA. In contrast, a combination of RXR alpha and T3R beta transactivated the apoCIII promoter 1.5-fold in the presence of 9-cis RA but it repressed the apoCIII promoter activity in the presence of T-3. Mutations in the HREs of elements B, G, or I-4 or in the SP1-binding site of element H, which ab olished the binding of nuclear hormone receptors or SP1 to their cognate si te, reduced the promoter strength and exhibited different responses to the ligand-dependent nuclear receptors. The findings suggest that modulation of the apoCIII promoter activity by orphan and ligand-dependent nuclear recep tors involves complex interactions among nuclear receptors, SP1 and possibl y other factors bound to the enhancer and the proximal promoter region.