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Sci. STKE, 18 November 2003 EDITORS' CHOICEMOLECULAR INTERACTIONS Cytosolic Regulation of JNK by Glucocorticoid Receptors
Although the glucocorticoid receptor (GR) is a member of the nuclear receptor family of ligand-activated transcription factors, some effects of glucocorticoids occur in the absence of DNA binding and without requiring glucocorticoid-stimulated gene expression. Bruna et al. show that the glucocorticoids stimulate a direct interaction (coimmunoprecipitation and glutathione S-transferase pull-down assays) between the GR and c-Jun N-terminal kinase (JNK), which decreased the interaction between JNK and its activating kinase MKK7. A mitogen-activated protein kinase docking motif in the ligand-binding domain of GR, a sequence that is uniquely present in the GR out of all of the other members of the nuclear receptor family, was responsible for the ligand-stimulated disruption of interaction of GR and JNK. Mutants of the GR that could not interact with JNK did not mediate glucocorticoid inhibition of JNK protein kinase activity stimulated by tumor necrosis factor- A. Bruna, M. Nicolās, A. Muņoz, J. M. Kyriakis, C. Caelles, Glucocorticoid receptor-JNK interaction mediates inhibition of the JNK pathway by glucocorticoids. EMBO J. 22, 6035-6044 (2003). [Abstract] [Full Text]
Citation: Cytosolic Regulation of JNK by Glucocorticoid Receptors. Sci. STKE 2003, tw445 (2003). The editors suggest the following Related Resources on Science sites:
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Science Signaling. ISSN 1937-9145 (pre-2008: Science's STKE. ISSN 1525-8882)