IDENTIFICATION OF A NUCLEAR RECEPTOR THAT IS ACTIVATED BY FARNESOL METABOLITES

被引:1099
作者
FORMAN, BM
GOODE, E
CHEN, J
ORO, AE
BRADLEY, DJ
PERLMANN, T
NOONAN, DJ
BURKA, LT
MCMORRIS, T
LAMPH, WW
EVANS, RM
WEINBERGER, C
机构
[1] SALK INST BIOL STUDIES,HOWARD HUGHES MED INST,LA JOLLA,CA 92037
[2] NIEHS,RECEPTOR BIOL GRP,RES TRIANGLE PK,NC 27709
[3] NIEHS,REPROD & DEV TOXICOL LAB,ORGAN CHEM GRP,RES TRIANGLE PK,NC 27709
[4] NIH,CELL BIOL LAB,BETHESDA,MD 20892
[5] UNIV KENTUCKY,DEPT BIOCHEM,LEXINGTON,KY 40506
[6] UNIV CALIF SAN DIEGO,DEPT CHEM,LA JOLLA,CA 92093
[7] LIGAND PHARMACEUT INC,SAN DIEGO,CA 92121
基金
美国国家卫生研究院;
关键词
D O I
10.1016/0092-8674(95)90530-8
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
Nuclear hormone receptors comprise a superfamily of ligand-modulated transcription factors that mediate the transcriptional activities of steroids, retinoids, and thyroid hormones. A growing number of related proteins have been identified that possess the structural features of hormone receptors, but that lack known ligands, Known as orphan receptors, these proteins represent targets for novel signaling molecules. We have isolated a mammalian orphan receptor that forms a heterodimeric complex with the retinoid X receptor. A screen of candidate ligands identified farnesol and related metabolites as effective activators of this complex. Farnesol metabolites are generated intracellularly and are required for the synthesis of cholesterol, bile acids, steroids, retinoids, and farnesylated proteins. Intermediary metabolites have been recognized as transcriptional regulators in bacteria and yeast. Our results now suggest that metabolite-controlled intracellular signaling systems are utilized by higher organisms.
引用
收藏
页码:687 / 693
页数:7
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