Insights on glucocorticoid receptor activity modulation through the binding of rigid steroids

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Background: The glucocorticoid receptor (GR) is a transcription factor that regulates gene expression in a ligand-dependent fashion. This modular protein is one of the major pharmacological targets due to its involvement in both cause and treatment of many human diseases. Intense efforts have been m...

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Autores principales:	Presman, D.M., Alvarez, L.D., Levi, V., Eduardo, S., Digman, M.A., Martí, M.A., Veleiro, A.S., Burton, G., Pecci, A.
Formato:	JOUR
Materias:	21 hemisuccinate 6,19 epoxyprogesterone 21 hydroxy 6,19 epoxyprogesterone dexamethasone glucocorticoid receptor glucocorticoid receptor antagonist mifepristone nuclear receptor coactivator 2 unclassified drug DNA steroid article binding affinity cell assay cell culture cell strain BHK cell strain COS7 cell strain L 929 cell type computer model conformational transition controlled study dissociation DNA drug complex drug mechanism drug receptor binding genetic transfection in vitro study in vivo study incubation time ligand binding modulation molecular dynamics oligomerization protein DNA binding protein DNA interaction protein function steroid binding structure activity relation animal cell line cell strain COS1 Cercopithecus chemical structure dimerization gel mobility shift assay immunoprecipitation metabolism protein binding Animals Cell Line Cercopithecus aethiops COS Cells Dimerization Electrophoretic Mobility Shift Assay Immunoprecipitation Models, Molecular Molecular Dynamics Simulation Protein Binding Receptors, Glucocorticoid Steroids
Acceso en línea:	http://hdl.handle.net/20.500.12110/paper_19326203_v5_n10_p_Presman
Aporte de:	Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires

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record_format	dspace
institution	Universidad de Buenos Aires
institution_str	I-28
repository_str	R-134
collection	Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic	21 hemisuccinate 6,19 epoxyprogesterone 21 hydroxy 6,19 epoxyprogesterone dexamethasone glucocorticoid receptor glucocorticoid receptor antagonist mifepristone nuclear receptor coactivator 2 unclassified drug DNA glucocorticoid receptor steroid article binding affinity cell assay cell culture cell strain BHK cell strain COS7 cell strain L 929 cell type computer model conformational transition controlled study dissociation DNA drug complex drug mechanism drug receptor binding genetic transfection in vitro study in vivo study incubation time ligand binding modulation molecular dynamics oligomerization protein DNA binding protein DNA interaction protein function steroid binding structure activity relation animal cell line cell strain COS1 Cercopithecus chemical structure dimerization gel mobility shift assay immunoprecipitation metabolism protein binding Animals Cell Line Cercopithecus aethiops COS Cells Dimerization DNA Electrophoretic Mobility Shift Assay Immunoprecipitation Models, Molecular Molecular Dynamics Simulation Protein Binding Receptors, Glucocorticoid Steroids
spellingShingle	21 hemisuccinate 6,19 epoxyprogesterone 21 hydroxy 6,19 epoxyprogesterone dexamethasone glucocorticoid receptor glucocorticoid receptor antagonist mifepristone nuclear receptor coactivator 2 unclassified drug DNA glucocorticoid receptor steroid article binding affinity cell assay cell culture cell strain BHK cell strain COS7 cell strain L 929 cell type computer model conformational transition controlled study dissociation DNA drug complex drug mechanism drug receptor binding genetic transfection in vitro study in vivo study incubation time ligand binding modulation molecular dynamics oligomerization protein DNA binding protein DNA interaction protein function steroid binding structure activity relation animal cell line cell strain COS1 Cercopithecus chemical structure dimerization gel mobility shift assay immunoprecipitation metabolism protein binding Animals Cell Line Cercopithecus aethiops COS Cells Dimerization DNA Electrophoretic Mobility Shift Assay Immunoprecipitation Models, Molecular Molecular Dynamics Simulation Protein Binding Receptors, Glucocorticoid Steroids Presman, D.M. Alvarez, L.D. Levi, V. Eduardo, S. Digman, M.A. Martí, M.A. Veleiro, A.S. Burton, G. Pecci, A. Insights on glucocorticoid receptor activity modulation through the binding of rigid steroids
topic_facet	21 hemisuccinate 6,19 epoxyprogesterone 21 hydroxy 6,19 epoxyprogesterone dexamethasone glucocorticoid receptor glucocorticoid receptor antagonist mifepristone nuclear receptor coactivator 2 unclassified drug DNA glucocorticoid receptor steroid article binding affinity cell assay cell culture cell strain BHK cell strain COS7 cell strain L 929 cell type computer model conformational transition controlled study dissociation DNA drug complex drug mechanism drug receptor binding genetic transfection in vitro study in vivo study incubation time ligand binding modulation molecular dynamics oligomerization protein DNA binding protein DNA interaction protein function steroid binding structure activity relation animal cell line cell strain COS1 Cercopithecus chemical structure dimerization gel mobility shift assay immunoprecipitation metabolism protein binding Animals Cell Line Cercopithecus aethiops COS Cells Dimerization DNA Electrophoretic Mobility Shift Assay Immunoprecipitation Models, Molecular Molecular Dynamics Simulation Protein Binding Receptors, Glucocorticoid Steroids
description	Background: The glucocorticoid receptor (GR) is a transcription factor that regulates gene expression in a ligand-dependent fashion. This modular protein is one of the major pharmacological targets due to its involvement in both cause and treatment of many human diseases. Intense efforts have been made to get information about the molecular basis of GR activity. Methodology/Principal Findings: Here, the behavior of four GR-ligand complexes with different glucocorticoid and antiglucocorticoid properties were evaluated. The ability of GR-ligand complexes to oligomerize in vivo was analyzed by performing the novel Number and Brightness assay. Results showed that most of GR molecules form homodimers inside the nucleus upon ligand binding. Additionally, in vitro GR-DNA binding analyses suggest that ligand structure modulates GRDNA interaction dynamics rather than the receptor's ability to bind DNA. On the other hand, by coimmunoprecipitation studies we evaluated the in vivo interaction between the transcriptional intermediary factor 2 (TIF2) coactivator and different GR-ligand complexes. No correlation was found between GR intranuclear distribution, cofactor recruitment and the homodimerization process. Finally, Molecular determinants that support the observed experimental GR LBD-ligand/TIF2 interaction were found by Molecular Dynamics simulation. Conclusions/Significance: The data presented here sustain the idea that in vivo GR homodimerization inside the nucleus can be achieved in a DNA-independent fashion, without ruling out a dependent pathway as well. Moreover, since at least one GR-ligand complex is able to induce homodimer formation while preventing TIF2 coactivator interaction, results suggest that these two events might be independent from each other. Finally, 21-hydroxy-6,19-epoxyprogesterone arises as a selective glucocorticoid with potential pharmacological interest. Taking into account that GR homodimerization and cofactor recruitment are considered essential steps in the receptor activation pathway, results presented here contribute to understand how specific ligands influence GR behavior. © 2010 Presman et al.
format	JOUR
author	Presman, D.M. Alvarez, L.D. Levi, V. Eduardo, S. Digman, M.A. Martí, M.A. Veleiro, A.S. Burton, G. Pecci, A.
author_facet	Presman, D.M. Alvarez, L.D. Levi, V. Eduardo, S. Digman, M.A. Martí, M.A. Veleiro, A.S. Burton, G. Pecci, A.
author_sort	Presman, D.M.
title	Insights on glucocorticoid receptor activity modulation through the binding of rigid steroids
title_short	Insights on glucocorticoid receptor activity modulation through the binding of rigid steroids
title_full	Insights on glucocorticoid receptor activity modulation through the binding of rigid steroids
title_fullStr	Insights on glucocorticoid receptor activity modulation through the binding of rigid steroids
title_full_unstemmed	Insights on glucocorticoid receptor activity modulation through the binding of rigid steroids
title_sort	insights on glucocorticoid receptor activity modulation through the binding of rigid steroids
url	http://hdl.handle.net/20.500.12110/paper_19326203_v5_n10_p_Presman
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_version_	1782030350998831104
spelling	todo:paper_19326203_v5_n10_p_Presman2023-10-03T16:35:03Z Insights on glucocorticoid receptor activity modulation through the binding of rigid steroids Presman, D.M. Alvarez, L.D. Levi, V. Eduardo, S. Digman, M.A. Martí, M.A. Veleiro, A.S. Burton, G. Pecci, A. 21 hemisuccinate 6,19 epoxyprogesterone 21 hydroxy 6,19 epoxyprogesterone dexamethasone glucocorticoid receptor glucocorticoid receptor antagonist mifepristone nuclear receptor coactivator 2 unclassified drug DNA glucocorticoid receptor steroid article binding affinity cell assay cell culture cell strain BHK cell strain COS7 cell strain L 929 cell type computer model conformational transition controlled study dissociation DNA drug complex drug mechanism drug receptor binding genetic transfection in vitro study in vivo study incubation time ligand binding modulation molecular dynamics oligomerization protein DNA binding protein DNA interaction protein function steroid binding structure activity relation animal cell line cell strain COS1 Cercopithecus chemical structure dimerization gel mobility shift assay immunoprecipitation metabolism protein binding Animals Cell Line Cercopithecus aethiops COS Cells Dimerization DNA Electrophoretic Mobility Shift Assay Immunoprecipitation Models, Molecular Molecular Dynamics Simulation Protein Binding Receptors, Glucocorticoid Steroids Background: The glucocorticoid receptor (GR) is a transcription factor that regulates gene expression in a ligand-dependent fashion. This modular protein is one of the major pharmacological targets due to its involvement in both cause and treatment of many human diseases. Intense efforts have been made to get information about the molecular basis of GR activity. Methodology/Principal Findings: Here, the behavior of four GR-ligand complexes with different glucocorticoid and antiglucocorticoid properties were evaluated. The ability of GR-ligand complexes to oligomerize in vivo was analyzed by performing the novel Number and Brightness assay. Results showed that most of GR molecules form homodimers inside the nucleus upon ligand binding. Additionally, in vitro GR-DNA binding analyses suggest that ligand structure modulates GRDNA interaction dynamics rather than the receptor's ability to bind DNA. On the other hand, by coimmunoprecipitation studies we evaluated the in vivo interaction between the transcriptional intermediary factor 2 (TIF2) coactivator and different GR-ligand complexes. No correlation was found between GR intranuclear distribution, cofactor recruitment and the homodimerization process. Finally, Molecular determinants that support the observed experimental GR LBD-ligand/TIF2 interaction were found by Molecular Dynamics simulation. Conclusions/Significance: The data presented here sustain the idea that in vivo GR homodimerization inside the nucleus can be achieved in a DNA-independent fashion, without ruling out a dependent pathway as well. Moreover, since at least one GR-ligand complex is able to induce homodimer formation while preventing TIF2 coactivator interaction, results suggest that these two events might be independent from each other. Finally, 21-hydroxy-6,19-epoxyprogesterone arises as a selective glucocorticoid with potential pharmacological interest. Taking into account that GR homodimerization and cofactor recruitment are considered essential steps in the receptor activation pathway, results presented here contribute to understand how specific ligands influence GR behavior. © 2010 Presman et al. Fil:Presman, D.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Alvarez, L.D. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Levi, V. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Martí, M.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Veleiro, A.S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Burton, G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Pecci, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_19326203_v5_n10_p_Presman

Insights on glucocorticoid receptor activity modulation through the binding of rigid steroids

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