2 NUCLEAR SIGNALING PATHWAYS FOR VITAMIN-D

被引:533
作者
CARLBERG, C
BENDIK, I
WYSS, A
MEIER, E
STURZENBECKER, LJ
GRIPPO, JF
HUNZIKER, W
机构
[1] F HOFFMANN LA ROCHE & CO LTD, DEPT PHARMA RES NEW TECHNOL, CH-4002 BASEL, SWITZERLAND
[2] HOFFMANN LA ROCHE INC, DEPT TOXICOL & PATHOL, NUTLEY, NJ 07110 USA
关键词
D O I
10.1038/361657a0
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
THE dihydroxylated form of vitamin D3(1,25-dihydroxy-D3) mediates a biological response by binding to intracellular receptors1-4 which belong to the steroid receptor superfamily5. These receptors act as ligand-dependent transcription factors that bind to specific DNA sequences (reviewed in refs 6-9). We have identified two classes of vitamin D response elements that are activated either by the vitamin D receptor (VDR) alone or by heterodimers of VDR and the retinoid-X receptor-alpha (RXR-alpha)10. The motif GGGTGA arranged as a direct repeat with a spacing of six nucleotides or as a palindrome without spacing, or as an inverted palindrome with a 12-nucleotide spacing, confers vitamin D inducibility mediated by VDR alone. A second class of response elements, composed of directly repeated pairs of motifs (GGTCCA, AGGTCA, or GGGTGA) spaced by three nucleotides, is synergistically activated by RXR and VDR, but only in the presence of both ligands. Thus, the RXR ligand and the nature of the response element determine whether a nuclear receptor is co-regulated by RXR.
引用
收藏
页码:657 / 660
页数:4
相关论文
共 32 条
  • [1] LIGAND AND DNA-DEPENDENT PHOSPHORYLATION OF HUMAN PROGESTERONE-RECEPTOR INVITRO
    BAGCHI, MK
    TSAI, SY
    TSAI, MJ
    OMALLEY, BW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (07) : 2664 - 2668
  • [2] CLONING AND EXPRESSION OF FULL-LENGTH CDNA-ENCODING HUMAN VITAMIN-D RECEPTOR
    BAKER, AR
    MCDONNELL, DP
    HUGHES, M
    CRISP, TM
    MANGELSDORF, DJ
    HAUSSLER, MR
    PIKE, JW
    SHINE, J
    OMALLEY, BW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (10) : 3294 - 3298
  • [3] GENE-REGULATION BY STEROID-HORMONES
    BEATO, M
    [J]. CELL, 1989, 56 (03) : 335 - 344
  • [4] RXR-ALPHA, A PROMISCUOUS PARTNER OF RETINOIC ACID AND THYROID-HORMONE RECEPTORS
    BUGGE, TH
    POHL, J
    LONNOY, O
    STUNNENBERG, HG
    [J]. EMBO JOURNAL, 1992, 11 (04) : 1409 - 1418
  • [5] DELUCA HF, 1990, KIDNEY INT, V38, pS2
  • [6] THE STEROID AND THYROID-HORMONE RECEPTOR SUPERFAMILY
    EVANS, RM
    [J]. SCIENCE, 1988, 240 (4854) : 889 - 895
  • [7] RECOMBINANT GENOMES WHICH EXPRESS CHLORAMPHENICOL ACETYLTRANSFERASE IN MAMMALIAN-CELLS
    GORMAN, CM
    MOFFAT, LF
    HOWARD, BH
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1982, 2 (09) : 1044 - 1051
  • [8] NUCLEAR RECEPTORS ENHANCE OUR UNDERSTANDING OF TRANSCRIPTION REGULATION
    GREEN, S
    CHAMBON, P
    [J]. TRENDS IN GENETICS, 1988, 4 (11) : 309 - 314
  • [9] HAUSSLER MR, 1988, RECENT PROG HORM RES, V44, P263
  • [10] 9-CIS RETINOIC ACID IS A HIGH-AFFINITY LIGAND FOR THE RETINOID-X RECEPTOR
    HEYMAN, RA
    MANGELSDORF, DJ
    DYCK, JA
    STEIN, RB
    EICHELE, G
    EVANS, RM
    THALLER, C
    [J]. CELL, 1992, 68 (02) : 397 - 406