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An NMR study on the intrinsically disordered core transactivation domain of human glucocorticoid receptor
A large number of transcriptional activation domains (TADs) are intrinsically unstructured, meaning they are devoid of a three-dimensional structure. The fact that these TADs are transcriptionally active without forming a 3-D structure raises the question of what features in these domains enable the...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society for Biochemistry and Molecular Biology
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5683822/ https://www.ncbi.nlm.nih.gov/pubmed/28946939 http://dx.doi.org/10.5483/BMBRep.2017.50.10.152 |
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author | Kim, Do-Hyoung Wright, Anthony Han, Kyou-Hoon |
author_facet | Kim, Do-Hyoung Wright, Anthony Han, Kyou-Hoon |
author_sort | Kim, Do-Hyoung |
collection | PubMed |
description | A large number of transcriptional activation domains (TADs) are intrinsically unstructured, meaning they are devoid of a three-dimensional structure. The fact that these TADs are transcriptionally active without forming a 3-D structure raises the question of what features in these domains enable them to function. One of two TADs in human glucocorticoid receptor (hGR) is located at its N-terminus and is responsible for ~70% of the transcriptional activity of hGR. This 58-residue intrinsically-disordered TAD, named tau1c in an earlier study, was shown to form three helices under trifluoroethanol, which might be important for its activity. We carried out heteronuclear multi-dimensional NMR experiments on hGR tau1c in a more physiological aqueous buffer solution and found that it forms three helices that are ~30% pre-populated. Since pre-populated helices in several TADs were shown to be key elements for transcriptional activity, the three pre-formed helices in hGR tau1c delineated in this study should be critical determinants of the transcriptional activity of hGR. The presence of pre-structured helices in hGR tau1c strongly suggests that the existence of pre-structured motifs in target-unbound TADs is a very broad phenomenon. |
format | Online Article Text |
id | pubmed-5683822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Korean Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-56838222017-11-21 An NMR study on the intrinsically disordered core transactivation domain of human glucocorticoid receptor Kim, Do-Hyoung Wright, Anthony Han, Kyou-Hoon BMB Rep Articles A large number of transcriptional activation domains (TADs) are intrinsically unstructured, meaning they are devoid of a three-dimensional structure. The fact that these TADs are transcriptionally active without forming a 3-D structure raises the question of what features in these domains enable them to function. One of two TADs in human glucocorticoid receptor (hGR) is located at its N-terminus and is responsible for ~70% of the transcriptional activity of hGR. This 58-residue intrinsically-disordered TAD, named tau1c in an earlier study, was shown to form three helices under trifluoroethanol, which might be important for its activity. We carried out heteronuclear multi-dimensional NMR experiments on hGR tau1c in a more physiological aqueous buffer solution and found that it forms three helices that are ~30% pre-populated. Since pre-populated helices in several TADs were shown to be key elements for transcriptional activity, the three pre-formed helices in hGR tau1c delineated in this study should be critical determinants of the transcriptional activity of hGR. The presence of pre-structured helices in hGR tau1c strongly suggests that the existence of pre-structured motifs in target-unbound TADs is a very broad phenomenon. Korean Society for Biochemistry and Molecular Biology 2017-10 2017-10-31 /pmc/articles/PMC5683822/ /pubmed/28946939 http://dx.doi.org/10.5483/BMBRep.2017.50.10.152 Text en Copyright © 2017 by the The Korean Society for Biochemistry and Molecular Biology http://creativecommons.org/licenses/by-nc/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Kim, Do-Hyoung Wright, Anthony Han, Kyou-Hoon An NMR study on the intrinsically disordered core transactivation domain of human glucocorticoid receptor |
title | An NMR study on the intrinsically disordered core transactivation domain of human glucocorticoid receptor |
title_full | An NMR study on the intrinsically disordered core transactivation domain of human glucocorticoid receptor |
title_fullStr | An NMR study on the intrinsically disordered core transactivation domain of human glucocorticoid receptor |
title_full_unstemmed | An NMR study on the intrinsically disordered core transactivation domain of human glucocorticoid receptor |
title_short | An NMR study on the intrinsically disordered core transactivation domain of human glucocorticoid receptor |
title_sort | nmr study on the intrinsically disordered core transactivation domain of human glucocorticoid receptor |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5683822/ https://www.ncbi.nlm.nih.gov/pubmed/28946939 http://dx.doi.org/10.5483/BMBRep.2017.50.10.152 |
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