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Am J Respir Cell Mol Biol. 2010 Sep;43(3):334-41. doi: 10.1165/rcmb.2009-0149OC. Epub 2009 Oct 23.

Multiple mechanisms influence regulation of the cystic fibrosis transmembrane conductance regulator gene promoter.

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1
Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL 60614, USA.

Abstract

The cystic fibrosis transmembrane conductance regulator (CFTR) gene is driven by a promoter that cannot alone account for the temporal and tissue-specific regulation of the gene. This has led to the search for additional regulatory elements that cooperate with the basal promoter to achieve coordinated expression. We previously identified two alternative upstream exons of the gene that were mutually exclusive of the first exon, and one of which showed temporal regulation in the human and sheep lung. We now demonstrate that this alternative splice product generates a stable protein, which initiates translation at an ATG in exon 4, and thus lacks the N terminus of CFTR. The other splice variant inhibits translation of the protein. In a search for the promoter used by the upstream exons, we identified a novel element that contributes to the activity of the basal CFTR promoter in airway epithelial cells, but does not function independently. Finally, we demonstrate that, in primary airway cells, skin fibroblasts, and both airway and intestinal cell lines, the CFTR promoter is unmethylated, irrespective of CFTR expression status. Thus, methylation is not the main cause of inactivation of CFTR transcription.

PMID:
19855085
PMCID:
PMC2933549
DOI:
10.1165/rcmb.2009-0149OC
[Indexed for MEDLINE]
Free PMC Article
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