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As the liver and gastrointestinal tract are both important sites of glucuronidation and express significant levels of one or both HNF1 proteins, it is thought that these homeoproteins may play a role in transcriptional regulation of UGTs. This chapter explores the current evidence that HNF1 transcription factors are explicitly involved in the transcription of mammalian UGT genes. Most data supporting this hypothesis come from in vitro reporter assays, site‐directed mutagenesis, and electrophoretic mobility‐shift assays, for which methods are detailed.
J. Biol. Chem. 267, 3257–3261. Ritter, J. , Crawford, J. , and Owens, I. S. (1991). Cloning of two human liver bilirubin UDP‐glucuronosyltransferase cDNAs with expression in COS‐1 cells. J. Biol. Chem. 266, 1043–1047. Ritter, J. , Yeatman, M. , and Owens, I. S. (1992b). Identification of a genetic alteration in the code for bilirubin UDP‐glucuronosyltransferase in the UGT1 gene complex of a Crigler‐Najjar type I patient. J. Clin. Invest. 90, 150–155. , and Sawada, J. (2003). Three novel single nucleotide polymorphisms in UGT1A9.
Biol. Chem. 267, 3257–3261. Ritter, J. , Crawford, J. , and Owens, I. S. (1991). Cloning of two human liver bilirubin UDP‐glucuronosyltransferase cDNAs with expression in COS‐1 cells. J. Biol. Chem. 266, 1043–1047. Ritter, J. , Yeatman, M. , and Owens, I. S. (1992b). Identification of a genetic alteration in the code for bilirubin UDP‐glucuronosyltransferase in the UGT1 gene complex of a Crigler‐Najjar type I patient. J. Clin. Invest. 90, 150–155. , and Sawada, J. (2003). Three novel single nucleotide polymorphisms in UGT1A9.