An element in intron 1 of the CFTR gene augments intestinal expression in vivo

Hum Mol Genet. 2001 Jul 1;10(14):1455-64. doi: 10.1093/hmg/10.14.1455.

Abstract

The elements controlling the complex developmental and tissue-specific expression of the cystic fibrosis transmembrane conductance regulator (CFTR) gene lie outside the basal promoter region and have not been characterized. We previously identified a tissue-specific DNase I hypersensitive site (DHS) in intron 1 (185 + 10 kb) of the CFTR gene. Here we show that removal of the core element abolishes the activity of this DHS in transient transfection assays of reporter/enhancer gene constructs. We then compared expression from a 310 kb yeast artificial chromosome (YAC) that contains the entire CFTR gene with expression from the same YAC from which the DHS element had been deleted. Stable transfection of a human colon carcinoma cell line showed that transcription from the deleted YAC was reduced by approximately 60%. In transgenic mice, deletion of the intron 1 DHS had no effect on expression in the lung, but reduced expression in the intestine by approximately 60%. Thus, the regulatory element associated with the intron 1 DHS is tissue-specific and is required for normal CFTR expression levels in the intestinal epithelium in vivo.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Caco-2 Cells
  • Cell Line
  • Chromosomes, Artificial, Yeast
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
  • DNA-Binding Proteins / metabolism
  • Deoxyribonuclease I / metabolism
  • Gene Expression Regulation*
  • Humans
  • Intestinal Mucosa / metabolism*
  • Introns*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Polymerase Chain Reaction
  • Regulatory Sequences, Nucleic Acid*
  • Tissue Distribution
  • Transcription, Genetic
  • Transfection

Substances

  • CFTR protein, human
  • DNA-Binding Proteins
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • Deoxyribonuclease I