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XB-ART-14888
Genes Dev. May 1, 1998; 12 (9): 1269-77.

BXR, an embryonic orphan nuclear receptor activated by a novel class of endogenous benzoate metabolites.

Blumberg B , Kang H , Bolado J , Chen H , Craig AG , Moreno TA , Umesono K , Perlmann T , De Robertis EM , Evans RM .


Abstract
Nuclear receptors are ligand-modulated transcription factors that respond to steroids, retinoids, and thyroid hormones to control development and body physiology. Orphan nuclear receptors, which lack identified ligands, provide a unique, and largely untapped, resource to discover new principles of physiologic homeostasis. We describe the isolation and characterization of the vertebrate orphan receptor, BXR, which heterodimerizes with RXR and binds high-affinity DNA sites composed of a variant thyroid hormone response element. A bioactivity-guided screen of embryonic extracts revealed that BXR is activatable by low-molecular-weight molecules with spectral patterns distinct from known nuclear receptor ligands. Mass spectrometry and 1H NMR analysis identified alkyl esters of amino and hydroxy benzoic acids as potent, stereoselective activators. In vitro cofactor association studies, along with competable binding of radiolabeled compounds, establish these molecules as bona fide ligands. Benzoates comprise a new molecular class of nuclear receptor ligand and their activity suggests that BXR may control a previously unsuspected vertebrate signaling pathway.

PubMed ID: 9573044
PMC ID: PMC316771
Article link: Genes Dev.
Grant support: R37 HD021502-13 NICHD NIH HHS , R37 HD021502 NICHD NIH HHS , R37 HD021502 NICHD NIH HHS , R37 HD021502-13 NICHD NIH HHS

Genes referenced: nr1i2


References:
Altschul, 1990, Pubmed[+]


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