The orphan nuclear receptor LXR alpha is positively and negatively regulated by distinct products of mevalonate metabolism

被引:236
作者
Forman, BM
Ruan, BF
Chen, J
Schroepfer, GJ
Evans, RM
机构
[1] SALK INST BIOL STUDIES,LA JOLLA,CA 92037
[2] HOWARD HUGHES MED INST,GENE EXPRESS LAB,LA JOLLA,CA 92037
[3] RICE UNIV,DEPT BIOCHEM & CELL BIOL,HOUSTON,TX 77005
[4] RICE UNIV,DEPT CHEM,HOUSTON,TX 77005
关键词
D O I
10.1073/pnas.94.20.10588
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
LXR alpha is an orphan member of the nuclear hormone receptor superfamily that displays constitutive transcriptional activity, We reasoned that this activity may result from the production of an endogenous activator that is a component of intermediary metabolism. The use of metabolic inhibitors revealed that mevalonic acid biosynthesis is required for LXR alpha activity, Mevalonic acid is a common metabolite used by virtually all eukaryotic cells. It serves as a precursor to a large number of important molecules including farnesyl pyrophosphate, geranylgeranyl pyrophosphate, cholesterol, and oxysterols. Inhibition of LXR alpha could be reversed by addition of mevalonic acid and certain oxysterols but not by other products of mevalonic acid metabolism. Surprisingly, the constitutive activity of LXR alpha was inhibited bg geranylgeraniol, a metabolite of mevalonic acid, These findings suggest that LXR alpha may represent a central component of a signaling pathway that is both positively and negatively regulated by multiple products of mevalonate metabolism.
引用
收藏
页码:10588 / 10593
页数:6
相关论文
共 43 条
[1]   A NOVEL ORPHAN RECEPTOR-SPECIFIC FOR A SUBSET OF THYROID HORMONE-RESPONSIVE ELEMENTS AND ITS INTERACTION WITH THE RETINOID/THYROID HORMONE-RECEPTOR SUBFAMILY [J].
APFEL, R ;
BENBROOK, D ;
LERNHARDT, E ;
ORTIZ, MA ;
SALBERT, G ;
PFAHL, M .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (10) :7025-7035
[2]  
BANNAI K, 1976, CHEM SOC PERKIN, V1, P2116
[3]   STEREOSPECIFIC SYNTHESIS OF 4 20,22-EPOXYCHOLESTEROLS AND OF (Z)-20(22)-DEHYDROCHOLESTEROL [J].
BYON, CY ;
GUT, M .
JOURNAL OF ORGANIC CHEMISTRY, 1976, 41 (23) :3716-3722
[4]   SYNTHESIS AND STEREOCHEMISTRY OF (22R)-20ALPHA,22-DIHYDROXYCHOLESTEROL (22S)-20ALPHA,22-DIHYDROXYCHOLESTEROL [J].
CHAUDHURI, NK ;
NICKOLSON, R ;
KIMBALL, H ;
GUT, M .
STEROIDS, 1970, 15 (04) :525-+
[5]   UTILIZATION OF GERANYLGERANIOL FOR PROTEIN ISOPRENYLATION IN C6 GLIAL-CELLS [J].
CRICK, DC ;
WAECHTER, CJ ;
ANDRES, DA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 205 (01) :955-961
[6]   FARNESOL IS UTILIZED FOR PROTEIN ISOPRENYLATION AND THE BIOSYNTHESIS OF CHOLESTEROL IN MAMMALIAN-CELLS [J].
CRICK, DC ;
ANDRES, DA ;
WAECHTER, CJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 211 (02) :590-599
[7]  
CUTHBERT JA, 1995, CANCER RES, V55, P1732
[8]   ISOLATION OF CRYSTALLINE 22R-HYDROXYCHOLESTEROL AND 20ALPHA,22R-DIHYDROXYCHOLESTEROL FROM BOVINE ADRENALS [J].
DIXON, R ;
FURUTACHI, T ;
LIEBERMAN, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1970, 40 (01) :161-+
[9]   UNIQUE RESPONSE PATHWAYS ARE ESTABLISHED BY ALLOSTERIC INTERACTIONS AMONG NUCLEAR HORMONE RECEPTORS [J].
FORMAN, BM ;
UMESONO, K ;
CHEN, J ;
EVANS, RM .
CELL, 1995, 81 (04) :541-550
[10]   Hypolipidemic drugs, polyunsaturated fatty acids, and eicosanoids are ligands for peroxisome proliferator-activated receptors alpha and delta [J].
Forman, BM ;
Chen, J ;
Evans, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (09) :4312-4317