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J. Biol. Chem., Vol. 263, Issue 34, 17995-18002, 12, 1988
T Matsunaga, K Nagata, EJ Holsztynska, DP Lapenson, A Smith, R Kato, HV Gelboin, DJ Waxman and FJ Gonzalez
Previous studies on regulation of the rat hepatic P-450 IIA1 cDNA have
provided evidence for a second gene closely related to but regulated in a
manner quite distinct from P-450 IIA1. Experiments were carried out to
isolate the cDNA for this second P-450 gene, designated IIA2, in order to
study more directly its regulation and relationship to IIA1. A full length
cDNA to IIA2 was isolated from an adult male rat liver lambda gt11 library
and sequenced completely. The IIA2 cDNA shared 93% nucleotide and 88%
deduced amino acid similarities with the previously characterized IIA1 cDNA
(Nagata, K., Matsunaga, T., Gillette, J., Gelboin, H. V., and Gonzalez, F.
J. (1987) J. Biol. Chem. 262, 2787- 2793). The protein, deduced from the
cDNA, contained 492 amino acids and a calculated Mr of 56,352. Comparison
of the IIA1 and IIA2 cDNAs revealed areas of low nucleotide similarity
interspersed with areas of absolute identity, suggesting that gene
conversions have played a role in the evolution of the IIA subfamily.
Expression of IIA1 and IIA2 mRNAs in rat liver during development was
studied with use of specific oligonucleotide probes. IIA1 mRNA was
increased within 1 week after birth in both male and female rats; however,
its postpubertal expression was decreased in males yet remained elevated in
females. In contrast, IIA2 mRNA was markedly induced in male rat liver at
puberty but was not detectable in females at any age examined. Furthermore,
only IIA1 mRNA was induced by treatment of rats with 3- methylcholanthrene.
Although IIA1 and IIA2 mRNAs were actively expressed in hepatic tissue, no
evidence for their expression was found in lung, kidney, or intestine,
suggesting that the IIA genes have tissue-specific promoters. Reconstituted
enzyme assays on the purified protein products P-450 IIA1 and P-450 IIA2
showed that, although both enzymes share considerable sequence similarity,
their positional specificities toward the prototype substrate testosterone
are strikingly different.
Gene conversion and differential regulation in the rat P-450 IIA gene subfamily. Purification, catalytic activity, cDNA and deduced amino acid sequence, and regulation of an adult male-specific hepatic testosterone 15 alpha-hydroxylase
Laboratory of Molecular Carcinogenesis, National Cancer Institute, Bethesda, Maryland 20892.
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