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Volume 271,
Number 17,
Issue of April 26, 1996 pp. 9947-9954
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
A
Regulatory Element in Intron 1 of the Cystic Fibrosis Transmembrane
Conductance Regulator Gene
(Received for publication, November 29, 1995; and in revised form, February 9, 1996)
Annabel N.
Smith ,
Maria Luiza
Barth ,
Tarra L.
McDowell,
Danielle
S.
Moulin ,
Hugh N.
Nuthall ,
Michael A.
Hollingsworth
,
Ann
Harris
The cystic fibrosis transmembrane conductance regulator (CFTR)
gene exhibits a tightly regulated pattern of expression in human
epithelial cells. The mechanism of this regulation is complex and is
likely to involve a number of genetic elements that effect temporal and
spatial expression. To date none of the elements that have been
identified in the CFTR promoter regulate tissue-specific expression. We
have identified a putative regulatory element within the first intron
of the CFTR gene at 181+10kb. The region containing this element
was first identified as a DNase I hypersensitive site that was present
in cells that express the CFTR gene but absent from cells not
transcribing CFTR. In vitro analysis of binding of proteins to
this region of DNA sequence by gel mobility shift assays and DNase I
footprinting revealed that some proteins that are only present in
CFTR-expressing cells bound to specific elements, and other proteins
that bound to adjacent elements were present in all epithelial cells
irrespective of their CFTR expression status. When assayed in transient
expression systems in a cell line expressing CFTR endogenously, this
DNA sequence augmented reporter gene expression through activation of
the CFTR promoter but had no effect in nonexpressing cells.

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Copyright © 1996 by the American Society for Biochemistry and Molecular Biology.
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