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The CFTR (cystic fibrosis transmembrane conductance regulator) gene shows a complex pattern of expression with tissue-specific and temporal regulation. However, the genetic elements and transcription factors that control CFTR expression are largely unidentified. The CFTR promoter does not confer tissue specificity on gene expression, suggesting that there are regulatory elements outside the upstream region. Analysis of potential regulatory elements defined as DNase 1-hypersensitive sites within introns of the gene revealed multiple predicted binding sites for the HNF1alpha (hepatocyte nuclear factor 1alpha) transcription factor. HNF1alpha, which is expressed in many of the same epithelial cell types as CFTR and shows similar differentiation-dependent changes in gene expression, bound to these sites in vitro. Overexpression of heterologous HNF1alpha augmented CFTR transcription in vivo. In contrast, antisense inhibition of HNF1 alpha transcription decreased the CFTR mRNA levels. Hnf1 alpha knockout mice showed lower levels of CFTR mRNA in their small intestine in comparison with wild-type mice. This is the first report of a transcription factor, which confers tissue specificity on the expression of this important disease-associated gene.

Original publication

DOI

10.1042/BJ20031157

Type

Journal article

Journal

Biochem J

Publication Date

15/03/2004

Volume

378

Pages

909 - 918

Keywords

Animals, Base Sequence, Binding Sites, Cell Line, Tumor, Cystic Fibrosis Transmembrane Conductance Regulator, DNA-Binding Proteins, Deoxyribonuclease I, Gene Expression Regulation, Hepatocyte Nuclear Factor 1, Hepatocyte Nuclear Factor 1-alpha, Humans, Intestine, Small, Introns, Mice, Mice, Knockout, Molecular Sequence Data, Nuclear Proteins, Oligoribonucleotides, Antisense, Organ Specificity, RNA, Messenger, Transcription Factors