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Hsp70 and Hsp40 inhibit an inter-domain interaction necessary for transcriptional activity in the androgen receptor

Molecular chaperones such as Hsp40 and Hsp70 hold the androgen receptor (AR) in an inactive conformation. They are released in the presence of androgens, enabling transactivation and causing the receptor to become aggregation-prone. Here we show that these molecular chaperones recognize a region of...

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Autores principales: Eftekharzadeh, Bahareh, Banduseela, Varuna C., Chiesa, Giulio, Martínez-Cristóbal, Paula, Rauch, Jennifer N., Nath, Samir R., Schwarz, Daniel M. C., Shao, Hao, Marin-Argany, Marta, Di Sanza, Claudio, Giorgetti, Elisa, Yu, Zhigang, Pierattelli, Roberta, Felli, Isabella C., Brun-Heath, Isabelle, García, Jesús, Nebreda, Ángel R., Gestwicki, Jason E., Lieberman, Andrew P., Salvatella, Xavier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687723/
https://www.ncbi.nlm.nih.gov/pubmed/31395886
http://dx.doi.org/10.1038/s41467-019-11594-y
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author Eftekharzadeh, Bahareh
Banduseela, Varuna C.
Chiesa, Giulio
Martínez-Cristóbal, Paula
Rauch, Jennifer N.
Nath, Samir R.
Schwarz, Daniel M. C.
Shao, Hao
Marin-Argany, Marta
Di Sanza, Claudio
Giorgetti, Elisa
Yu, Zhigang
Pierattelli, Roberta
Felli, Isabella C.
Brun-Heath, Isabelle
García, Jesús
Nebreda, Ángel R.
Gestwicki, Jason E.
Lieberman, Andrew P.
Salvatella, Xavier
author_facet Eftekharzadeh, Bahareh
Banduseela, Varuna C.
Chiesa, Giulio
Martínez-Cristóbal, Paula
Rauch, Jennifer N.
Nath, Samir R.
Schwarz, Daniel M. C.
Shao, Hao
Marin-Argany, Marta
Di Sanza, Claudio
Giorgetti, Elisa
Yu, Zhigang
Pierattelli, Roberta
Felli, Isabella C.
Brun-Heath, Isabelle
García, Jesús
Nebreda, Ángel R.
Gestwicki, Jason E.
Lieberman, Andrew P.
Salvatella, Xavier
author_sort Eftekharzadeh, Bahareh
collection PubMed
description Molecular chaperones such as Hsp40 and Hsp70 hold the androgen receptor (AR) in an inactive conformation. They are released in the presence of androgens, enabling transactivation and causing the receptor to become aggregation-prone. Here we show that these molecular chaperones recognize a region of the AR N-terminal domain (NTD), including a FQNLF motif, that interacts with the AR ligand-binding domain (LBD) upon activation. This suggests that competition between molecular chaperones and the LBD for the FQNLF motif regulates AR activation. We also show that, while the free NTD oligomerizes, binding to Hsp70 increases its solubility. Stabilizing the NTD-Hsp70 interaction with small molecules reduces AR aggregation and promotes its degradation in cellular and mouse models of the neuromuscular disorder spinal bulbar muscular atrophy. These results help resolve the mechanisms by which molecular chaperones regulate the balance between AR aggregation, activation and quality control.
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spelling pubmed-66877232019-08-12 Hsp70 and Hsp40 inhibit an inter-domain interaction necessary for transcriptional activity in the androgen receptor Eftekharzadeh, Bahareh Banduseela, Varuna C. Chiesa, Giulio Martínez-Cristóbal, Paula Rauch, Jennifer N. Nath, Samir R. Schwarz, Daniel M. C. Shao, Hao Marin-Argany, Marta Di Sanza, Claudio Giorgetti, Elisa Yu, Zhigang Pierattelli, Roberta Felli, Isabella C. Brun-Heath, Isabelle García, Jesús Nebreda, Ángel R. Gestwicki, Jason E. Lieberman, Andrew P. Salvatella, Xavier Nat Commun Article Molecular chaperones such as Hsp40 and Hsp70 hold the androgen receptor (AR) in an inactive conformation. They are released in the presence of androgens, enabling transactivation and causing the receptor to become aggregation-prone. Here we show that these molecular chaperones recognize a region of the AR N-terminal domain (NTD), including a FQNLF motif, that interacts with the AR ligand-binding domain (LBD) upon activation. This suggests that competition between molecular chaperones and the LBD for the FQNLF motif regulates AR activation. We also show that, while the free NTD oligomerizes, binding to Hsp70 increases its solubility. Stabilizing the NTD-Hsp70 interaction with small molecules reduces AR aggregation and promotes its degradation in cellular and mouse models of the neuromuscular disorder spinal bulbar muscular atrophy. These results help resolve the mechanisms by which molecular chaperones regulate the balance between AR aggregation, activation and quality control. Nature Publishing Group UK 2019-08-08 /pmc/articles/PMC6687723/ /pubmed/31395886 http://dx.doi.org/10.1038/s41467-019-11594-y Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Eftekharzadeh, Bahareh
Banduseela, Varuna C.
Chiesa, Giulio
Martínez-Cristóbal, Paula
Rauch, Jennifer N.
Nath, Samir R.
Schwarz, Daniel M. C.
Shao, Hao
Marin-Argany, Marta
Di Sanza, Claudio
Giorgetti, Elisa
Yu, Zhigang
Pierattelli, Roberta
Felli, Isabella C.
Brun-Heath, Isabelle
García, Jesús
Nebreda, Ángel R.
Gestwicki, Jason E.
Lieberman, Andrew P.
Salvatella, Xavier
Hsp70 and Hsp40 inhibit an inter-domain interaction necessary for transcriptional activity in the androgen receptor
title Hsp70 and Hsp40 inhibit an inter-domain interaction necessary for transcriptional activity in the androgen receptor
title_full Hsp70 and Hsp40 inhibit an inter-domain interaction necessary for transcriptional activity in the androgen receptor
title_fullStr Hsp70 and Hsp40 inhibit an inter-domain interaction necessary for transcriptional activity in the androgen receptor
title_full_unstemmed Hsp70 and Hsp40 inhibit an inter-domain interaction necessary for transcriptional activity in the androgen receptor
title_short Hsp70 and Hsp40 inhibit an inter-domain interaction necessary for transcriptional activity in the androgen receptor
title_sort hsp70 and hsp40 inhibit an inter-domain interaction necessary for transcriptional activity in the androgen receptor
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687723/
https://www.ncbi.nlm.nih.gov/pubmed/31395886
http://dx.doi.org/10.1038/s41467-019-11594-y
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