TABLE 2

RXRβ

Receptor Nomenclature NR2B2
Receptor code 4.10.1:RX:2:B2
Other names H-2RIIBP, RCoR-1,
Molecular information Hs: 533aa, P28702, chr. 6p21.31,2
Rn: 458aa, P497433
Mm: 520aa, P28704, chr. 172,47
DNA binding
   Structure Homodimer, heterodimer, RXR partner
   HRE core sequence AGGTCA (DR-1, DR-2, DR-3, DR-4, DR-5)
Partners TR2 and TR4 (physical, functional): DNA binding2,810; VDR (physical, functional): DNA binding810; RARα, RARβ, and RARγ (physical, functional): DNA binding2,814; PPARα, PPARβ, and PPARγ (physical, functional): DNA binding10,15,16; LXRα and LXRβ (physical, functional): DNA binding10,1721; FXR (physical, functional): DNA binding10,22; PXR (physical, functional): DNA binding10,2326; CAR (physical, functional): DNA binding10,27,28; NGFI-B (physical, functional): DNA binding10,29,30; NURR1 (physical, functional): DNA binding10,30
Agonists LG100268 (3–6.8 nM), LGD1069 (21 nM),* 9-cis-retinoic acid (6.2–117 nM),* [IC50]7,3139; AGN194204 (3.6 nM) [Kd]40
Antagonists LG100754 (10 nM) [IC50]36,41,42
Coactivators NCOA1, NCOA2, NCOA310,4347
Biologically important isoforms RXRβ 1 {Hs, Mm}: differs from RXRβ 2 in the A/B domain48,49; RXRβ 2 {Hs, Mm}49,50
Tissue distribution Ubiquitous {Hs, Mm, Rn} [Northern blot, in situ hybridization, Western blot]3,4,7,51
Functional assays Differentiation of 3T3-L1 cells to adipocytes measured by the accumulation of triglyceride produced within the cytoplasm of the adipocyte {Mm}34,52,53; induction of apoptosis (associated with RARα activation) in leukemia cell lines {Hs}38,54
Mutant phenotype Male sterility due to defective spermatogenesis, abnormal lipid metabolism in Sertoli cells and behavioral defects {Mm} [knockout]18,5557
  • aa, amino acid; chr, chromosome; HRE, hormone response element; NGFI-B, nerve growth factor-induced clone B

  • * Radioligand

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  • 26. Lehmann JM, McKee DD, Watson MA, Willson TM, Moore JT, and Kliewer SA (1998) The human orphan nuclear receptor PXR is activated by compounds that regulate CYP3A4 gene expression and cause drug interactions. J Clin Investig 102: 1016-1023

  • 27 Baes M, Gulick T, Choi HS, Martinoli MG, Simha D, and Moore DD (1994) A new orphan member of the nuclear hormone receptor superfamily that interacts with a subset of retinoic acid response elements. Mol Cell Biol 14: 1544-1552

  • 28. Choi HS, Chung M, Tzameli I, Simha D, Lee YK, Seol W, and Moore DD (1997) Differential transactivation by two isoforms of the orphan nuclear hormone receptor CAR. J Biol Chem 272: 23565-23571

  • 29. Forman BM, Umesono K, Chen J, and Evans RM (1995) Unique response pathways are established by allosteric interactions among nuclear hormone receptors. Cell 81: 541-550

  • 30. Perlmann T and Jansson L (1995) A novel pathway for vitamin A signaling mediated by RXR heterodimerization with NGFI-B and NURR1. Genes Dev 9: 769-782

  • 31. Allenby G, Bocquel MT, Saunders M, Kazmer S, Speck J, Rosenberger M, Lovey A, Kastner P, Grippo JF, Chambon P, et al. (1993) Retinoic acid receptors and retinoid X receptors: interactions with endogenous retinoic acids. Proc Natl Acad Sci USA 90: 30-34

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  • 42. Forman BM (2002) The antidiabetic agent LG100754 sensitizes cells to low concentrations of peroxisome proliferator-activated receptor γ ligands. J Biol Chem 277: 12503-12506

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