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
  • [21] Activation of the nuclear receptor LXR by oxysterols defines a new hormone response pathway
    Lehmann, JM
    Kliewer, SA
    Moore, LB
    SmithOliver, TA
    Oliver, BB
    Su, JL
    Sundseth, SS
    Winegar, DA
    Blanchard, DE
    Spencer, TA
    Willson, TM
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (06) : 3137 - 3140
  • [22] THE RXR HETERODIMERS AND ORPHAN RECEPTORS
    MANGELSDORF, DJ
    EVANS, RM
    [J]. CELL, 1995, 83 (06) : 841 - 850
  • [23] THE NUCLEAR RECEPTOR SUPERFAMILY - THE 2ND DECADE
    MANGELSDORF, DJ
    THUMMEL, C
    BEATO, M
    HERRLICH, P
    SCHUTZ, G
    UMESONO, K
    BLUMBERG, B
    KASTNER, P
    MARK, M
    CHAMBON, P
    EVANS, RM
    [J]. CELL, 1995, 83 (06) : 835 - 839
  • [24] MOORES SL, 1991, J BIOL CHEM, V266, P14603
  • [25] MORISAKI M, 1977, CHEM PHARM BULL, V25, P2576
  • [26] RARS AND RXRS - EVIDENCE FOR 2 AUTONOMOUS TRANSACTIVATION FUNCTIONS (AF-1 AND AF-2) AND HETERODIMERIZATION INVIVO
    NAGPAL, S
    FRIANT, S
    NAKSHATRI, H
    CHAMBON, P
    [J]. EMBO JOURNAL, 1993, 12 (06) : 2349 - 2360
  • [27] PROTEIN PRENYLATION IN EUKARYOTIC MICROORGANISMS - GENETICS, BIOLOGY AND BIOCHEMISTRY
    OMER, CA
    GIBBS, JB
    [J]. MOLECULAR MICROBIOLOGY, 1994, 11 (02) : 219 - 225
  • [28] INHIBITION OF PURIFIED P21RAS FARNESYL - PROTEIN TRANSFERASE BY CYS-AAX TETRAPEPTIDES
    REISS, Y
    GOLDSTEIN, JL
    SEABRA, MC
    CASEY, PJ
    BROWN, MS
    [J]. CELL, 1990, 62 (01) : 81 - 88
  • [29] Silver ion high pressure liquid chromatography provides unprecedented separation of sterols: Application to the enzymatic formation of cholesta-5,8-dien-3 beta-ol
    Ruan, BF
    Shey, J
    Gerst, N
    Wilson, WK
    Schroepfer, GJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (21) : 11603 - 11608
  • [30] APPLICATION OF WITTIG REACTION TO SYNTHESIS OF STEROIDAL SIDE-CHAINS - POSSIBILITY OF 3 BETA-PHENOXY FORMATION AS A SECONDARY REACTION
    SCHMIT, JP
    PIRAUX, M
    PILETTE, JF
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 1975, 40 (11) : 1586 - 1588