Positive regulation of connexin32 transcription by hepatocyte nuclear factor-1α

Abstract Connexin32 ( Cx32 ) encodes the predominant gap junction protein expressed by hepatocytes. We investigated the transcriptional control of Cx32 in expressing and nonexpressing rat liver cell lines and hypothesized that a putative hepatocyte nuclear factor-1 (HNF-1) binding site (centered at mp −187) in the liver-active, P1 promoter is essential for transcription of Cx32 . HNF-1α was expressed by Cx32 -expressing rat liver cell lines and bound the promoter at the −187 site, but was not expressed by non- Cx32 -expressing hepatic lines. Stable transfection of non- Cx32 -expressing WB-F344 rat liver epithelial cells with HNF-1α stimulated a transfected Cx32 promoter element (mp −244 to −33), binding of HNF-1α to the −187 site, and expression of endogenous Cx32 . Site-directed mutagenesis of this HNF-1 binding site abolished HNF-1α binding and proximal promoter activity. Hepatic Cx32 expression was also significantly decreased in HNF -1α −/− mice. These data indicate that HNF-1α is a positive regulator of Cx32 expression in hepatic cells.