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(Received for publication, August 8, 1996)
From the Transcriptional regulation by the aryl
hydrocarbon receptor, for which the environmental toxin
2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) is the most
potent ligand, leads in mammalian liver to the induction of genes for
two distinct cytochrome P450 (CYP)1A enzymes, CYP1A1 and -1A2. Fish
seem to have only one CYP1A enzyme. CYP1A enzymes have been regarded as
injurious largely because of their ability to activate chemical
carcinogens. We report here the cloning and sequencing of cDNAs for
two catalytically distinct TCDD-induced CYP enzymes in chick embryo
liver. One mediates classic CYP1A1 activities. The other has some
-1A2-like activities and is also responsible for TCDD-induced
arachidonic acid epoxygenation, a much more conspicuous effect in liver
of chicks than of mammalian species. Amino acid sequence analysis shows
that although each chick enzyme can be classified in the CYP1A family,
both are more like CYP1A1 than -1A2, and neither can be said to be
directly orthologous to CYP1A1 or -1A2. Phylogenetic analysis shows
that the two chick enzymes form a separate branch in the CYP1A family tree distinct from mammalian CYP1A1 and -1A2 and from fish CYP1A enzymes. The findings suggest that CYP1A progenitors split into two CYP
enzymes with some parallel functions independently in two evolutionary
lines, evidence for convergent evolution in the CYP1A family. Northern
analysis shows that the chick enzymes have a different tissue
distribution from CYP1A1 and -1A2. Polymerase chain reaction and
in situ hybridization data show that both chick enzymes are
expressed in response to TCDD even before organ morphogenesis. The
findings further suggest that beyond their role in activating carcinogens, CYP1A enzymes have conferred evolutionary and
developmental advantages, perhaps as defenses in maintaining
homeostatic responses to toxic chemicals.
Volume 271, Number 51,
Issue of December 20, 1996
pp. 33054-33059
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
,
,
**
Department of Pharmacology,
¶ Department of Cell Biology, and ** Department of Medicine,
Cornell University Medical College, New York, New York 10021
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