Molecular cloning of cDNA and genomic DNA for human 25-hydroxyvitamin D-3 1 alpha-hydroxylase

被引:108
作者
Monkawa, T
Yoshida, T
Wakino, S
Shinki, T
Anazawa, H
DeLuca, HF
Suda, T
Hayashi, M
Saruta, T
机构
[1] KEIO UNIV, SCH MED, DEPT INTERNAL MED, SHINJUKU KU, TOKYO 160, JAPAN
[2] SHOWA UNIV, SCH DENT, DEPT BIOCHEM, TOKYO, JAPAN
[3] KYOWA HAKKO KOGYO CO LTD, TOKYO RES LABS, TOKYO 194, JAPAN
[4] UNIV WISCONSIN, COLL AGR & LIFE SCI, DEPT BIOCHEM, MADISON, WI 53706 USA
基金
日本学术振兴会;
关键词
D O I
10.1006/bbrc.1997.7508
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The 25-hydroxyvitamin D-3 1 alpha-hydroxylase (1 alpha-hydroxylase) is a cytochrome P450 enzyme that catalyzes the conversion of 25-hydroxyvitamin D-2 to 1 alpha,25-dihydroxyvitamin D-3. This enzyme plays an important role in calcium homeostasis. Here we report the molecular cloning of cDNA and gene for human 1 alpha-hydroxylase. The cDNA clone was obtained from a human kidney cDNA library by cross-hybridization with a previously cloned rat cDNA probe. The cDNA consists of 2469 bp and encodes a protein of 508 amino acids that shows 82.5% sequence identity with the rat enzyme. A computer-aided homology search revealed that 1 alpha-hydroxylase shares a relatively high homology with vitamin D-3 25-hydroxylase (about 40% amino acid identity). Northern blot analysis showed that the 2.5-kb mRNA is most abundant in kidney, The gene for human 1 alpha-hydroxylase spans approximately 6 kb, is composed of nine exons, and is present as a single copy. This molecular cloning makes it possible to investigate the genetic mechanism of diseases related to calcium metabolism, including vitamin D-dependency rickets type I. (C) 1997 Academic Press.
引用
收藏
页码:527 / 533
页数:7
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