SDR-O:: an orphan short-chain dehydrogenase/reductase localized at mouse chromosome 10/human chromosome 12

被引:11
作者
Chen, WG [1 ]
Song, MS [1 ]
Napoli, JL [1 ]
机构
[1] Univ Calif Berkeley, Dept Nutr Sci & Toxicol, Berkeley, CA 94720 USA
关键词
short-chain dehydrogenase/reductase; retinol; retinoids; retinoic acid; sterol; steroid; hydroxysteroid dehydrogenase; orphan receptor; nuclear receptor;
D O I
10.1016/S0378-1119(02)00757-6
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report cloning a cDNA that encodes a novel short-chain dehydrogenase/reductase, SDR-O, conserved in mouse, human and rat. Human and mouse liver express SDR-O (short-chain dehydrogenase/reductase-orphan) mRNA intensely. The mouse embryo expresses SDR-O mRNA as early as day seven. Human SDR-O localizes on chromosome 12; mouse SDR-O localizes on chromosome 10 with CPAD1, CRAD2 and RDH4. SDR-O shares highest amino acid similarity with rat RoDH1 and mouse RDH1 (69-70%), but does not have the retinol and 3alpha-hydroxysteroid dehydrogenase activity of either, nor is it active as a 17beta- or 11beta-hydroxysteroid dehydrogenase. Short-chain dehydrogenase/reductases catalyse the metabolism of ligands that bind with nuclear receptors: the occurrence of 'orphan' nuclear receptors may imply existence of 'orphan' SDR, suggesting that SDR-O may catalyse the metabolism of another class of nuclear receptor ligand. Alternatively, SDR-O may not have a catalytic function, but may regulate metabolism by binding substrates/products and/or by serving as a regulatory factor. (C) 2002 Published by Elsevier Science B.V.
引用
收藏
页码:141 / 146
页数:6
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