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Proc. Natl. Acad. Sci. USA
Vol. 94,
pp. 12920-12925,
November 1997
* Department of Biochemistry, School of Dentistry, Showa University,
Hatanodai, Shinagawa-ku, Tokyo 142, Japan; § Tokyo Research
Laboratory, Kyowa Hakko Kogyo Co. Ltd., Asahimachi, Machida, Tokyo 194, Japan; ¶ Department of Internal Medicine, University of Keio,
Shinanomachi, Shinjuku-ku, Tokyo 160, Japan; and
Contributed by Hector F. DeLuca, September 16, 1997
A full-length cDNA for the rat kidney mitochondrial
cytochrome P450 mixed function oxidase, 25-hydroxyvitamin
D3-1
Biochemistry
Cloning and expression of rat 25-hydroxyvitamin
D3-1
-hydroxylase cDNA
-hydroxylase / 24-hydroxylase / P450)
, and
Department of
Biochemistry, College of Agricultural and Life Sciences, University of
Wisconsin, 420 Henry Mall, Madison, WI 53706
-hydroxylase (P4501
), was cloned from a vitamin
D-deficient rat kidney cDNA library and subcloned into the mammalian
expression vector pcDNA 3.1(+). When P4501
cDNA was transfected into
COS-7 transformed monkey kidney cells, they expressed 25-hydroxyvitamin
D3-1
-hydroxylase activity. The sequence analysis showed
that P4501
was of 2,469 bp long and contained an ORF encoding 501 amino acids. The deduced amino acid sequence showed a 53% similarity
and 44% identity to the vitamin D3-25-hydroxylase (CYP27),
whereas it has 42.6% similarity and 34% identity with the
25-hydroxyvitamin D3-24-hydroxylase (CYP24). Thus, it
composes a new subfamily of the CYP27 family. Further, it is more
closely related to the CYP27 than to the CYP24. The expression of
P4501
mRNA was greatly increased in the kidney of vitamin
D-deficient rats. In rats with the enhanced renal production of
1
,25-dihydroxyvitamin D3 (rats fed a low Ca diet),
P4501
mRNA was greatly increased in the renal proximal convoluted
tubules.
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