Glucocorticoid receptor mutants that are constitutive activators of transcriptional enhancement - PubMed (original) (raw)
. 1987 Jan;325(6102):365-8.
doi: 10.1038/325365a0.
- PMID: 3808033
- DOI: 10.1038/325365a0
Glucocorticoid receptor mutants that are constitutive activators of transcriptional enhancement
P J Godowski et al. Nature. 1987 Jan.
Erratum in
- Nature 1987 Mar 5-11;326(6108):105
Abstract
Glucocorticoids, a class of steroid hormones, associate specifically with intracellular receptors, facilitating a conformational change that converts the receptor in vitro to a DNA-binding protein and in vivo to a nuclear species that activates a class of transcriptional enhancers termed glucocorticoid response elements (GREs). The DNA sequences recognized specifically by the hormone-receptor complex correspond directly to those required for GRE enhancement. The structural transition that accompanies steroid binding, 'receptor transformation', has been monitored by changes in receptor chromatographic properties, accessibility to monoclonal antibodies, association with other receptor subunits or with heterologous proteins, and aqueous two-phase partition coefficient. However, the significance of the structural change for the biological activity of the receptor is not understood. We have used cloned rat glucocorticoid-receptor coding sequences to produce and characterize a novel class of receptor mutants that elicit GRE enhancer function in transfected cells even in the absence of hormone. The constitutive activity of those receptor derivatives, together with mapping studies that distinguish between the DNA- and hormone-binding domains of the receptor, imply that the conformational change corresponding to receptor transformation may simply unmask pre-existing functional domains for DNA binding, enhancer activation, or both.
Similar articles
- Glucocorticoid activation of chromogranin A gene expression. Identification and characterization of a novel glucocorticoid response element.
Rozansky DJ, Wu H, Tang K, Parmer RJ, O'Connor DT. Rozansky DJ, et al. J Clin Invest. 1994 Dec;94(6):2357-68. doi: 10.1172/JCI117601. J Clin Invest. 1994. PMID: 7989592 Free PMC article. - Requirement of hormone for thermal conversion of the glucocorticoid receptor to a DNA-binding state.
Denis M, Poellinger L, Wikstöm AC, Gustafsson JA. Denis M, et al. Nature. 1988 Jun 16;333(6174):686-8. doi: 10.1038/333686a0. Nature. 1988. PMID: 3374615 - Mutational analysis of the mouse glucocorticoid receptor.
Danielsen M, Hinck L, Ringold GM. Danielsen M, et al. Cancer Res. 1989 Apr 15;49(8 Suppl):2286s-2291s. Cancer Res. 1989. PMID: 2702668 - Molecular genetics of corticosteroid action.
Miesfeld RL. Miesfeld RL. Am Rev Respir Dis. 1990 Feb;141(2 Pt 2):S11-7. Am Rev Respir Dis. 1990. PMID: 2178510 Review. - Structure-function aspects of the glucocorticoid receptor.
Gustafsson JA, Dahlman-Wright K, Strömstedt PE, Wright T, Carlstedt-Duke J. Gustafsson JA, et al. Princess Takamatsu Symp. 1990;21:137-55. Princess Takamatsu Symp. 1990. PMID: 2134673 Review.
Cited by
- The activity of the androgen receptor variant AR-V7 is regulated by FOXO1 in a PTEN-PI3K-AKT-dependent way.
Mediwala SN, Sun H, Szafran AT, Hartig SM, Sonpavde G, Hayes TG, Thiagarajan P, Mancini MA, Marcelli M. Mediwala SN, et al. Prostate. 2013 Feb 15;73(3):267-77. doi: 10.1002/pros.22566. Epub 2012 Jul 20. Prostate. 2013. PMID: 22821817 Free PMC article. - The transcriptional activation function located in the hormone-binding domain of the human oestrogen receptor is not encoded in a single exon.
Webster NJ, Green S, Tasset D, Ponglikitmongkol M, Chambon P. Webster NJ, et al. EMBO J. 1989 May;8(5):1441-6. doi: 10.1002/j.1460-2075.1989.tb03526.x. EMBO J. 1989. PMID: 2767048 Free PMC article. - Characterization of the hormone-binding domain of the chicken c-erbA/thyroid hormone receptor protein.
Muñoz A, Zenke M, Gehring U, Sap J, Beug H, Vennström B. Muñoz A, et al. EMBO J. 1988 Jan;7(1):155-9. doi: 10.1002/j.1460-2075.1988.tb02795.x. EMBO J. 1988. PMID: 3359993 Free PMC article. - Effects of different osmolytes on the induced folding of the N-terminal activation domain (AF1) of the glucocorticoid receptor.
Kumar R, Serrette JM, Khan SH, Miller AL, Thompson EB. Kumar R, et al. Arch Biochem Biophys. 2007 Sep 15;465(2):452-60. doi: 10.1016/j.abb.2007.06.019. Epub 2007 Jun 29. Arch Biochem Biophys. 2007. PMID: 17655821 Free PMC article. - A cellular factor stimulates ligand-dependent release of hsp90 from the basic helix-loop-helix dioxin receptor.
McGuire J, Whitelaw ML, Pongratz I, Gustafsson JA, Poellinger L. McGuire J, et al. Mol Cell Biol. 1994 Apr;14(4):2438-46. doi: 10.1128/mcb.14.4.2438-2446.1994. Mol Cell Biol. 1994. PMID: 8139547 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources