Glucocorticoid receptor

NR3C1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
Aliases NR3C1, GCCR, GCR, GCRST, GR, GRL, nuclear receptor subfamily 3 group C member 1, Glucocorticoid Receptor
External IDs MGI: 95824 HomoloGene: 30960 GeneCards: NR3C1
Targeted by Drug
budesonide, ciclesonide, clobetasol propionate, hydrocortisone, desoxycortone, desoximetasone, dexamethasone, difluprednate, fluocinolone acetonide, fluocinonide, fluorometholone, fluticasone, fluticasone propionate, methylprednisolone, prednisolone, prednisone, RU28362, triamcinolone, triamcinolone acetonide, betamethasone, mifepristone[1]
RNA expression pattern




More reference expression data
Orthologs
Species Human Mouse
Entrez

2908

14815

Ensembl

ENSG00000113580

ENSMUSG00000024431

UniProt

P04150
Q3MSN4

P06537

RefSeq (mRNA)

NM_008173

RefSeq (protein)

n/a

Location (UCSC) Chr 5: 143.28 – 143.44 Mb Chr 18: 39.41 – 39.49 Mb
PubMed search [2] [3]
Wikidata
View/Edit HumanView/Edit Mouse

The glucocorticoid receptor (GR, or GCR) also known as NR3C1 (nuclear receptor subfamily 3, group C, member 1) is the receptor to which cortisol and other glucocorticoids bind.

The GR is expressed in almost every cell in the body and regulates genes controlling the development, metabolism, and immune response. Because the receptor gene is expressed in several forms, it has many different (pleiotropic) effects in different parts of the body.

When the GR binds to glucocorticoids, its primary mechanism of action is the regulation of gene transcription.[4][5] The unbound receptor resides in the cytosol of the cell. After the receptor is bound to glucocorticoid, the receptor-glucorticoid complex can take either of two paths. The activated GR complex up-regulates the expression of anti-inflammatory proteins in the nucleus or represses the expression of pro-inflammatory proteins in the cytosol (by preventing the translocation of other transcription factors from the cytosol into the nucleus).

In humans, the GR protein is encoded by NR3C1 gene which is located on chromosome 5 (5q31).[6][7]

Structure

Like the other steroid receptors,[8] the glucocorticoid receptor is modular in structure[9] and contains the following domains (labeled A - F):

Ligand binding and response

In the absence of hormone, the glucocorticoid receptor (GR) resides in the cytosol complexed with a variety of proteins including heat shock protein 90 (hsp90), the heat shock protein 70 (hsp70) and the protein FKBP52 (FK506-binding protein 52).[10] The endogenous glucocorticoid hormone cortisol diffuses through the cell membrane into the cytoplasm and binds to the glucocorticoid receptor (GR) resulting in release of the heat shock proteins. The resulting activated form GR has two principal mechanisms of action, transactivation and transrepression,[11][12] described below.

Transactivation

A direct mechanism of action involves homodimerization of the receptor, translocation via active transport into the nucleus, and binding to specific DNA responsive elements activating gene transcription. This mechanism of action is referred to as transactivation. The biologic response depends on the cell type.

Transrepression

In the absence of activated GR, other transcription factors such as NF-κB or AP-1 themselves are able to transactivate target genes.[13] However activated GR can complex with these other transcription factors and prevent them from binding their target genes and hence repress the expression of genes that are normally upregulated by NF-κB or AP-1. This indirect mechanism of action is referred to as transrepression.

Clinical significance

The GR is abnormal in familial glucocorticoid resistance.[14]

In central nervous system structures, the glucocorticoid receptor is gaining interest as a novel representative of neuroendocrine integration, functioning as a major component of endocrine influence - specifically the stress response - upon the brain. The receptor is now implicated in both short and long-term adaptations seen in response to stressors and may be critical to the understanding of psychological disorders, including some or all subtypes of depression and post-traumatic stress disorder (PTSD).[15] Indeed, long-standing observations such as the mood dysregulations typical of Cushing's disease demonstrate the role of corticosteroids in regulating psychologic state; recent advances have demonstrated interactions with norepinephrine and serotonin at the neural level.[16][17]

Agonists and antagonists

Dexamethasone and other corticosteroids are agonists, and mifepristone and ketoconazole are antagonists of the GR.

Interactions

Glucocorticoid receptor has been shown to interact with:

See also

References

  1. ↑ "Drugs that physically interact with Glucocorticoid receptor view/edit references on wikidata".
  2. ↑ "Human PubMed Reference:".
  3. ↑ "Mouse PubMed Reference:".
  4. ↑ Lu NZ, Wardell SE, Burnstein KL, Defranco D, Fuller PJ, Giguere V, Hochberg RB, McKay L, Renoir JM, Weigel NL, Wilson EM, McDonnell DP, Cidlowski JA (2006). "International Union of Pharmacology. LXV. The pharmacology and classification of the nuclear receptor superfamily: glucocorticoid, mineralocorticoid, progesterone, and androgen receptors". Pharmacol Revl. 58 (4): 782–97. doi:10.1124/pr.58.4.9. PMID 17132855. [Free full text]
  5. ↑ Rhen T, Cidlowski JA (October 2005). "Antiinflammatory action of glucocorticoids--new mechanisms for old drugs". N. Engl. J. Med. 353 (16): 1711–23. doi:10.1056/NEJMra050541. PMID 16236742.
  6. ↑ Hollenberg SM, Weinberger C, Ong ES, Cerelli G, Oro A, Lebo R, Thompson EB, Rosenfeld MG, Evans RM (1985). "Primary structure and expression of a functional human glucocorticoid receptor cDNA". Nature. 318 (6047): 635–41. doi:10.1038/318635a0. PMID 2867473.
  7. ↑ Francke U, Foellmer BE (May 1989). "The glucocorticoid receptor gene is in 5q31-q32 [corrected]". Genomics. 4 (4): 610–2. doi:10.1016/0888-7543(89)90287-5. PMID 2744768.
  8. ↑ Kumar R, Thompson EB (1999). "The structure of the nuclear hormone receptors". Steroids. 64 (5): 310–9. doi:10.1016/S0039-128X(99)00014-8. PMID 10406480.
  9. ↑ Kumar R, Thompson EB (2005). "Gene regulation by the glucocorticoid receptor: structure:function relationship". J. Steroid Biochem. Mol. Biol. 94 (5): 383–94. doi:10.1016/j.jsbmb.2004.12.046. PMID 15876404.
  10. ↑ Pratt WB, Morishima Y, Murphy M, Harrell M (2006). "Chaperoning of glucocorticoid receptors". Handb Exp Pharmacol. 172 (172): 111–38. doi:10.1007/3-540-29717-0_5. PMID 16610357.
  11. ↑ Buckingham JC (2006). "Glucocorticoids: exemplars of multi-tasking". Br J Pharmacol. 147 (Supplement 1): S258–68. doi:10.1038/sj.bjp.0706456. PMC 1760726Freely accessible. PMID 16402112.
  12. ↑ Hayashi R, Wada H, Ito K, Adcock IM (2004). "Effects of glucocorticoids on gene transcription". Eur J Pharmacol. 500 (1-3): 51–62. doi:10.1016/j.ejphar.2004.07.011. PMID 15464020.
  13. ↑ Ray A, Prefontaine KE (January 1994). "Physical association and functional antagonism between the p65 subunit of transcription factor NF-kappa B and the glucocorticoid receptor". Proc. Natl. Acad. Sci. U.S.A. 91 (2): 752–6. doi:10.1073/pnas.91.2.752. PMC 43027Freely accessible. PMID 8290595.
  14. ↑ Mendonca B, Leite M, de Castro M, Kino T, Elias L, Bachega T, Arnhold I, Chrousos G, Latronico A (2002). "Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene". J Clin Endocrinol Metab. 87 (4): 1805–9. doi:10.1210/jc.87.4.1805. PMID 11932321.
  15. ↑ Maletic V, Robinson M, Oakes T, Iyengar S, Ball SG, Russell J (2007). "Neurobiology of depression: an integrated view of key findings". Int J Clin Pract. 61 (12): 2030–40. doi:10.1111/j.1742-1241.2007.01602.x. PMC 2228409Freely accessible. PMID 17944926. [Free full text]
  16. ↑ Savitz J, Lucki I, Drevets WC (2009). "5HT1A receptor function in Major Depressive Disorder". Prog Neurobiol. 88 (1): 17–31. doi:10.1016/j.pneurobio.2009.01.009. PMC 2736801Freely accessible. PMID 19428959. [Free full text]
  17. ↑ Schechter DS, Moser DA, Paoloni-Giacobino A, Stenz A, Gex-Fabry M, Aue T, Adouan W, Cordero MI, Suardi F, Manini A, Sancho Rossignol A, Merminod G, Ansermet F, Dayer AG, Rusconi Serpa S (epub May 29, 2015). Methylation of NR3C1 is related to maternal PTSD, parenting stress and maternal medial prefrontal cortical activity in response to child separation among mothers with histories of violence exposure. Frontiers in Psychology. To view the online publication, please click here: http://www.frontiersin.org/Journal/Abstract.aspx?s=944&name=psychology_for_clinical_settings&ART_DOI=10.3389/fpsyg.2015.00690&utm_source=Email_to_authors_&utm_medium=Email&utm_content=T1_11.5e1_author&utm_campaign=Email_publication&field=&journalName=Frontiers_in_Psychology&id=139466
  18. ↑ Kullmann M, Schneikert J, Moll J, Heck S, Zeiner M, Gehring U, Cato AC (June 1998). "RAP46 is a negative regulator of glucocorticoid receptor action and hormone-induced apoptosis". J. Biol. Chem. 273 (23): 14620–5. doi:10.1074/jbc.273.23.14620. PMID 9603979.
  19. ↑ Schneikert J, Hübner S, Langer G, Petri T, Jäättelä M, Reed J, Cato AC (December 2000). "Hsp70-RAP46 interaction in downregulation of DNA binding by glucocorticoid receptor". EMBO J. 19 (23): 6508–16. doi:10.1093/emboj/19.23.6508. PMC 305849Freely accessible. PMID 11101523.
  20. ↑ Boruk M, Savory JG, Haché RJ (November 1998). "AF-2-dependent potentiation of CCAAT enhancer binding protein beta-mediated transcriptional activation by glucocorticoid receptor". Mol. Endocrinol. 12 (11): 1749–63. doi:10.1210/mend.12.11.0191. PMID 9817600.
  21. ↑ Almlöf T, Wallberg AE, Gustafsson JA, Wright AP (June 1998). "Role of important hydrophobic amino acids in the interaction between the glucocorticoid receptor tau 1-core activation domain and target factors". Biochemistry. 37 (26): 9586–94. doi:10.1021/bi973029x. PMID 9649342.
  22. 1 2 Hulkko SM, Wakui H, Zilliacus J (August 2000). "The pro-apoptotic protein death-associated protein 3 (DAP3) interacts with the glucocorticoid receptor and affects the receptor function". Biochem. J. 349. Pt 3: 885–93. doi:10.1042/bj3490885. PMC 1221218Freely accessible. PMID 10903152.
  23. ↑ Lin DY, Lai MZ, Ann DK, Shih HM (May 2003). "Promyelocytic leukemia protein (PML) functions as a glucocorticoid receptor co-activator by sequestering Daxx to the PML oncogenic domains (PODs) to enhance its transactivation potential". J. Biol. Chem. 278 (18): 15958–65. doi:10.1074/jbc.M300387200. PMID 12595526.
  24. ↑ Jibard N, Meng X, Leclerc P, Rajkowski K, Fortin D, Schweizer-Groyer G, Catelli MG, Baulieu EE, Cadepond F (March 1999). "Delimitation of two regions in the 90-kDa heat shock protein (Hsp90) able to interact with the glucocorticosteroid receptor (GR)". Exp. Cell Res. 247 (2): 461–74. doi:10.1006/excr.1998.4375. PMID 10066374.
  25. ↑ Kanelakis KC, Shewach DS, Pratt WB (September 2002). "Nucleotide binding states of hsp70 and hsp90 during sequential steps in the process of glucocorticoid receptor.hsp90 heterocomplex assembly". J. Biol. Chem. 277 (37): 33698–703. doi:10.1074/jbc.M204164200. PMID 12093808.
  26. ↑ Hecht K, Carlstedt-Duke J, Stierna P, Gustafsson J, Brönnegârd M, Wikström AC (October 1997). "Evidence that the beta-isoform of the human glucocorticoid receptor does not act as a physiologically significant repressor". J. Biol. Chem. 272 (42): 26659–64. doi:10.1074/jbc.272.42.26659. PMID 9334248.
  27. ↑ de Castro M, Elliot S, Kino T, Bamberger C, Karl M, Webster E, Chrousos GP (September 1996). "The non-ligand binding beta-isoform of the human glucocorticoid receptor (hGR beta): tissue levels, mechanism of action, and potential physiologic role". Mol. Med. 2 (5): 597–607. PMC 2230188Freely accessible. PMID 8898375.
  28. ↑ van den Berg JD, Smets LA, van Rooij H (February 1996). "Agonist-free transformation of the glucocorticoid receptor in human B-lymphoma cells". J. Steroid Biochem. Mol. Biol. 57 (3-4): 239–49. doi:10.1016/0960-0760(95)00271-5. PMID 8645634.
  29. ↑ Stancato LF, Silverstein AM, Gitler C, Groner B, Pratt WB (April 1996). "Use of the thiol-specific derivatizing agent N-iodoacetyl-3-[125I]iodotyrosine to demonstrate conformational differences between the unbound and hsp90-bound glucocorticoid receptor hormone binding domain". J. Biol. Chem. 271 (15): 8831–6. doi:10.1074/jbc.271.15.8831. PMID 8621522.
  30. ↑ Eggert M, Michel J, Schneider S, Bornfleth H, Baniahmad A, Fackelmayer FO, Schmidt S, Renkawitz R (November 1997). "The glucocorticoid receptor is associated with the RNA-binding nuclear matrix protein hnRNP U". J. Biol. Chem. 272 (45): 28471–8. doi:10.1074/jbc.272.45.28471. PMID 9353307.
  31. 1 2 3 4 5 Zilliacus J, Holter E, Wakui H, Tazawa H, Treuter E, Gustafsson JA (April 2001). "Regulation of glucocorticoid receptor activity by 14--3-3-dependent intracellular relocalization of the corepressor RIP140". Mol. Endocrinol. 15 (4): 501–11. doi:10.1210/mend.15.4.0624. PMID 11266503.
  32. 1 2 Hittelman AB, Burakov D, Iñiguez-Lluhí JA, Freedman LP, Garabedian MJ (October 1999). "Differential regulation of glucocorticoid receptor transcriptional activation via AF-1-associated proteins". EMBO J. 18 (19): 5380–8. doi:10.1093/emboj/18.19.5380. PMC 1171607Freely accessible. PMID 10508170.
  33. ↑ Savory JG, Préfontaine GG, Lamprecht C, Liao M, Walther RF, Lefebvre YA, Haché RJ (February 2001). "Glucocorticoid receptor homodimers and glucocorticoid-mineralocorticoid receptor heterodimers form in the cytoplasm through alternative dimerization interfaces". Mol. Cell. Biol. 21 (3): 781–93. doi:10.1128/MCB.21.3.781-793.2001. PMC 86670Freely accessible. PMID 11154266.
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  35. ↑ Subramaniam N, Treuter E, Okret S (June 1999). "Receptor interacting protein RIP140 inhibits both positive and negative gene regulation by glucocorticoids". J. Biol. Chem. 274 (25): 18121–7. doi:10.1074/jbc.274.25.18121. PMID 10364267.
  36. ↑ Stevens A, Garside H, Berry A, Waters C, White A, Ray D (May 2003). "Dissociation of steroid receptor coactivator 1 and nuclear receptor corepressor recruitment to the human glucocorticoid receptor by modification of the ligand-receptor interface: the role of tyrosine 735". Mol. Endocrinol. 17 (5): 845–59. doi:10.1210/me.2002-0320. PMID 12569182.
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  40. 1 2 3 Hsiao PW, Fryer CJ, Trotter KW, Wang W, Archer TK (September 2003). "BAF60a mediates critical interactions between nuclear receptors and the BRG1 chromatin-remodeling complex for transactivation". Mol. Cell. Biol. 23 (17): 6210–20. doi:10.1128/MCB.23.17.6210-6220.2003. PMC 180928Freely accessible. PMID 12917342.
  41. 1 2 Préfontaine, G G; Walther R; Giffin W; Lemieux M E; Pope L; Haché R J (Sep 1999). "Selective binding of steroid hormone receptors to octamer transcription factors determines transcriptional synergism at the mouse mammary tumor virus promoter". J. Biol. Chem. UNITED STATES. 274 (38): 26713–9. doi:10.1074/jbc.274.38.26713. ISSN 0021-9258. PMID 10480874.
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  43. 1 2 Rao, Mira A; Cheng Helen; Quayle Alandra N; Nishitani Hideo; Nelson Colleen C; Rennie Paul S (Dec 2002). "RanBPM, a nuclear protein that interacts with and regulates transcriptional activity of androgen receptor and glucocorticoid receptor". J. Biol. Chem. United States. 277 (50): 48020–7. doi:10.1074/jbc.M209741200. ISSN 0021-9258. PMID 12361945.
  44. ↑ Nissen RM, Yamamoto KR (September 2000). "The glucocorticoid receptor inhibits NFkappaB by interfering with serine-2 phosphorylation of the RNA polymerase II carboxy-terminal domain". Genes Dev. 14 (18): 2314–29. doi:10.1101/gad.827900. PMC 316928Freely accessible. PMID 10995388.
  45. ↑ Caldenhoven E, Liden J, Wissink S, Van de Stolpe A, Raaijmakers J, Koenderman L, Okret S, Gustafsson JA, Van der Saag PT (April 1995). "Negative cross-talk between RelA and the glucocorticoid receptor: a possible mechanism for the antiinflammatory action of glucocorticoids". Mol. Endocrinol. 9 (4): 401–12. doi:10.1210/me.9.4.401. PMID 7659084.
  46. ↑ Li G, Wang S, Gelehrter TD (October 2003). "Identification of glucocorticoid receptor domains involved in transrepression of transforming growth factor-beta action". J. Biol. Chem. 278 (43): 41779–88. doi:10.1074/jbc.M305350200. PMID 12902338.
  47. ↑ Song CZ, Tian X, Gelehrter TD (October 1999). "Glucocorticoid receptor inhibits transforming growth factor-beta signaling by directly targeting the transcriptional activation function of Smad3". Proc. Natl. Acad. Sci. U.S.A. 96 (21): 11776–81. doi:10.1073/pnas.96.21.11776. PMC 18362Freely accessible. PMID 10518526.
  48. ↑ Wallberg AE, Neely KE, Hassan AH, Gustafsson JA, Workman JL, Wright AP (March 2000). "Recruitment of the SWI-SNF chromatin remodeling complex as a mechanism of gene activation by the glucocorticoid receptor tau1 activation domain". Mol. Cell. Biol. 20 (6): 2004–13. doi:10.1128/MCB.20.6.2004-2013.2000. PMC 110817Freely accessible. PMID 10688647.
  49. ↑ Lerner L, Henriksen MA, Zhang X, Darnell JE (October 2003). "STAT3-dependent enhanceosome assembly and disassembly: synergy with GR for full transcriptional increase of the alpha 2-macroglobulin gene". Genes Dev. 17 (20): 2564–77. doi:10.1101/gad.1135003. PMC 218150Freely accessible. PMID 14522952.
  50. ↑ Zhang Z, Jones S, Hagood JS, Fuentes NL, Fuller GM (December 1997). "STAT3 acts as a co-activator of glucocorticoid receptor signaling". J. Biol. Chem. 272 (49): 30607–10. doi:10.1074/jbc.272.49.30607. PMID 9388192.
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  52. ↑ Makino Y, Yoshikawa N, Okamoto K, Hirota K, Yodoi J, Makino I, Tanaka H (January 1999). "Direct association with thioredoxin allows redox regulation of glucocorticoid receptor function". J. Biol. Chem. 274 (5): 3182–8. doi:10.1074/jbc.274.5.3182. PMID 9915858.
  53. ↑ Chang CJ, Chen YL, Lee SC (October 1998). "Coactivator TIF1beta interacts with transcription factor C/EBPbeta and glucocorticoid receptor to induce alpha1-acid glycoprotein gene expression". Mol. Cell. Biol. 18 (10): 5880–7. doi:10.1128/mcb.18.10.5880. PMC 109174Freely accessible. PMID 9742105.
  54. ↑ Wakui H, Wright AP, Gustafsson J, Zilliacus J (March 1997). "Interaction of the ligand-activated glucocorticoid receptor with the 14-3-3 eta protein". J. Biol. Chem. 272 (13): 8153–6. doi:10.1074/jbc.272.13.8153. PMID 9079630.

Further reading

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