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(Received for publication, April 15, 1996, and in revised form, June 12, 1996)
From the Department of Environmental Toxicology, University of
California, Davis, California 95616-8588
Polycyclic aromatic hydrocarbons such as
3-methylcholanthrene are toxic to rat epidermal cells in low passages
(3 to 6), but cultures of high passage (
Volume 271, Number 37,
Issue of September 13, 1996
pp. 22746-22753
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
15) are resistant. Since such
compounds can be metabolically activated by cytochrome P4501A1, we have
examined the regulation of this gene in low and high passage cells.
Consistent with this difference, little or no
2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-inducible
P4501A1 mRNA or enzyme activity was observed in high passage
as compared to low passage cultures. Similarly, transfection of a
luciferase reporter construct containing
1317 to +256 base pairs of
the 5
-flanking region of the murine CYP1A1 gene was TCDD-inducible in
low but not high passage cells. Ligand binding and transfection
experiments demonstrated the presence of functional Ah receptor
complexes in both high and low passage cells. Deletion analysis
identified a 26-base pair negative regulatory DNA (NeRD) element
contained within the upstream regulatory region of the CYP1A1 gene
responsible for this effect. Nuclear extracts from both low and high
passage cells contain a protein which specifically binds to
NeRD-containing DNA. Thus, the loss of polycyclic aromatic
hydrocarbon sensitivity in high passage rat epidermal cells appears to
be due to decreased expression of CYP1A1, and this effect may be
mediated by an altered NeRD binding factor(s) present in these
cells.
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