Literature DB >> 1321524

The dioxin and peroxisome proliferator-activated receptors: nuclear receptors in search of endogenous ligands.

L Poellinger1, M Göttlicher, J A Gustafsson.   

Abstract

Dioxins and peroxisome proliferators represent two diverse classes of xenobiotic compounds that induce transcription of specific genes encoding cytochrome P-450 drug-metabolizing enzymes. Signal transduction by these chemicals is mediated by two distinct nuclear receptors, one of which has recently been demonstrated to be a member of the steroid hormone receptor superfamily of ligand-activated transcription factors. However, no endogenous ligand has so far been identified for either of these nuclear receptors. Lorenz Poellinger, Martin Göttlicher and Jan-Ake Gustafsson review properties of both these xenobiotic receptor systems and discuss how the molecular details in the receptor activation pathways compare with those of nuclear hormone receptors.

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Year:  1992        PMID: 1321524     DOI: 10.1016/0165-6147(92)90076-i

Source DB:  PubMed          Journal:  Trends Pharmacol Sci        ISSN: 0165-6147            Impact factor:   14.819


  16 in total

1.  Transactivation domains facilitate promoter occupancy for the dioxin-inducible CYP1A1 gene in vivo.

Authors:  H P Ko; S T Okino; Q Ma; J P Whitlock
Journal:  Mol Cell Biol       Date:  1997-07       Impact factor: 4.272

2.  p27(Kip1) induction and inhibition of proliferation by the intracellular Ah receptor in developing thymus and hepatoma cells.

Authors:  S K Kolluri; C Weiss; A Koff; M Göttlicher
Journal:  Genes Dev       Date:  1999-07-01       Impact factor: 11.361

3.  Ligand-dependent recruitment of the Arnt coregulator determines DNA recognition by the dioxin receptor.

Authors:  M Whitelaw; I Pongratz; A Wilhelmsson; J A Gustafsson; L Poellinger
Journal:  Mol Cell Biol       Date:  1993-04       Impact factor: 4.272

4.  Cross-coupling of signal transduction pathways: the dioxin receptor mediates induction of cytochrome P-450IA1 expression via a protein kinase C-dependent mechanism.

Authors:  A Berghard; K Gradin; I Pongratz; M Whitelaw; L Poellinger
Journal:  Mol Cell Biol       Date:  1993-01       Impact factor: 4.272

5.  Distinct roles of the molecular chaperone hsp90 in modulating dioxin receptor function via the basic helix-loop-helix and PAS domains.

Authors:  C Antonsson; M L Whitelaw; J McGuire; J A Gustafsson; L Poellinger
Journal:  Mol Cell Biol       Date:  1995-02       Impact factor: 4.272

6.  A cellular factor stimulates ligand-dependent release of hsp90 from the basic helix-loop-helix dioxin receptor.

Authors:  J McGuire; M L Whitelaw; I Pongratz; J A Gustafsson; L Poellinger
Journal:  Mol Cell Biol       Date:  1994-04       Impact factor: 4.272

7.  A functional glucocorticoid-responsive unit composed of two overlapping inactive receptor-binding sites: evidence for formation of a receptor tetramer.

Authors:  M Garlatti; M Daheshia; E Slater; J Bouguet; J Hanoune; M Beato; R Barouki
Journal:  Mol Cell Biol       Date:  1994-12       Impact factor: 4.272

8.  Functional interference between hypoxia and dioxin signal transduction pathways: competition for recruitment of the Arnt transcription factor.

Authors:  K Gradin; J McGuire; R H Wenger; I Kvietikova; M L fhitelaw; R Toftgård; L Tora; M Gassmann; L Poellinger
Journal:  Mol Cell Biol       Date:  1996-10       Impact factor: 4.272

Review 9.  Peroxisome proliferator-activated receptors and Alzheimer's disease: hitting the blood-brain barrier.

Authors:  Juan M Zolezzi; Nibaldo C Inestrosa
Journal:  Mol Neurobiol       Date:  2013-03-14       Impact factor: 5.590

10.  Heat shock protein hsp90 regulates dioxin receptor function in vivo.

Authors:  M L Whitelaw; J McGuire; D Picard; J A Gustafsson; L Poellinger
Journal:  Proc Natl Acad Sci U S A       Date:  1995-05-09       Impact factor: 11.205

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