THE LUNG-SPECIFIC SURFACTANT PROTEIN-B GENE PROMOTER IS A TARGET FOR THYROID TRANSCRIPTION FACTOR-1 AND HEPATOCYTE NUCLEAR FACTOR-3, INDICATING COMMON FACTORS FOR ORGAN-SPECIFIC GENE-EXPRESSION ALONG THE FOREGUT AXIS

We used the lung epithelial cell-specific surfactant protein B (SPB) g ene promoter as a model,vith which to investigate mechanisms involved in transcriptional control of lung-specific genes. In a previous study , we showed that the SPB promoter specifically activated expression of a linked reporter gene in the continuous H411 lung cell line and that H441 nuclear proteins specifically protected a region of this promote r from bp -111 to -73. In this study, we further show that this region is a complex binding site for thyroid transcription factor 1 (TTF-1) and hepatocyte nuclear factor 3 (HNF-3). Whereas TTF-1 bound two highl y degenerate and closely spaced sites, HNF-3 proteins bound a TGT3 mot if (TCTTTGT) that is also found in several liver-specific gene regulat ory regions, where it appears to be a weak affinity site for HNF-3. Po int mutations of these binding sites eliminated factor binding and res ulted in significant decreases in transfected SPB promoter activity. I n addition, we developed a cotransfection assay and showed that a fami ly of lung-specific gene promoters that included the SPB, SPC, SPA, an d Clara cell secretory protein (CCSP) gene promoters were specifically activated by cotransfected TTF-1. We conclude that TTF-1 and HNF-3 ar e major activators of lung-specific genes and propose that these facto rs are involved in a general mechanism of lung-specific gene transcrip tion. Importantly, these data also show that common factors are involv ed in organ-specific gene expression along the mammalian foregut axis.