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The nuclear receptor NOR-1 regulates the small muscle protein, X-linked (SMPX) and myotube differentiation
Recent works have highlighted the role of NOR-1 in both smooth and skeletal muscle, and have proposed this nuclear receptor as a nexus that coordinates muscle performance and metabolic capacity. However, no muscle specific genes regulated by NOR-1 have been identified so far. To identify NOR-1 targe...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867575/ https://www.ncbi.nlm.nih.gov/pubmed/27181368 http://dx.doi.org/10.1038/srep25944 |
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author | Ferrán, Beatriz Martí-Pàmies, Ingrid Alonso, Judith Rodríguez-Calvo, Ricardo Aguiló, Silvia Vidal, Francisco Rodríguez, Cristina Martínez-González, José |
author_facet | Ferrán, Beatriz Martí-Pàmies, Ingrid Alonso, Judith Rodríguez-Calvo, Ricardo Aguiló, Silvia Vidal, Francisco Rodríguez, Cristina Martínez-González, José |
author_sort | Ferrán, Beatriz |
collection | PubMed |
description | Recent works have highlighted the role of NOR-1 in both smooth and skeletal muscle, and have proposed this nuclear receptor as a nexus that coordinates muscle performance and metabolic capacity. However, no muscle specific genes regulated by NOR-1 have been identified so far. To identify NOR-1 target genes, we over-expressed NOR-1 in human vascular smooth muscle cells (VSMC). These cells subjected to sustained over-expression of supraphysiological levels of NOR-1 experienced marked phenotypic changes and up-regulated the skeletal muscle protein X-linked (SMPX), a protein typically expressed in striated muscle and associated to cell shape. By transcriptional studies and DNA-protein binding assays, we identified a non-consensus NBRE site in human SMPX promoter, critical for NOR-1 responsiveness. The expression of SMPX was higher in human skeletal muscle myoblasts (HSMM) than in human VSMC, and further increased in HSMM differentiated to myotubes. NOR-1 silencing prevented SMPX expression in HSMM, as well as their differentiation to myotubes, but the up-regulation of SMPX was dispensable for HSMM differentiation. Our results indicate that NOR-1 regulate SMPX in human muscle cells and acts as a muscle regulatory factor, but further studies are required to unravel its role in muscle differentiation and hypertrophy. |
format | Online Article Text |
id | pubmed-4867575 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48675752016-05-31 The nuclear receptor NOR-1 regulates the small muscle protein, X-linked (SMPX) and myotube differentiation Ferrán, Beatriz Martí-Pàmies, Ingrid Alonso, Judith Rodríguez-Calvo, Ricardo Aguiló, Silvia Vidal, Francisco Rodríguez, Cristina Martínez-González, José Sci Rep Article Recent works have highlighted the role of NOR-1 in both smooth and skeletal muscle, and have proposed this nuclear receptor as a nexus that coordinates muscle performance and metabolic capacity. However, no muscle specific genes regulated by NOR-1 have been identified so far. To identify NOR-1 target genes, we over-expressed NOR-1 in human vascular smooth muscle cells (VSMC). These cells subjected to sustained over-expression of supraphysiological levels of NOR-1 experienced marked phenotypic changes and up-regulated the skeletal muscle protein X-linked (SMPX), a protein typically expressed in striated muscle and associated to cell shape. By transcriptional studies and DNA-protein binding assays, we identified a non-consensus NBRE site in human SMPX promoter, critical for NOR-1 responsiveness. The expression of SMPX was higher in human skeletal muscle myoblasts (HSMM) than in human VSMC, and further increased in HSMM differentiated to myotubes. NOR-1 silencing prevented SMPX expression in HSMM, as well as their differentiation to myotubes, but the up-regulation of SMPX was dispensable for HSMM differentiation. Our results indicate that NOR-1 regulate SMPX in human muscle cells and acts as a muscle regulatory factor, but further studies are required to unravel its role in muscle differentiation and hypertrophy. Nature Publishing Group 2016-05-16 /pmc/articles/PMC4867575/ /pubmed/27181368 http://dx.doi.org/10.1038/srep25944 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Ferrán, Beatriz Martí-Pàmies, Ingrid Alonso, Judith Rodríguez-Calvo, Ricardo Aguiló, Silvia Vidal, Francisco Rodríguez, Cristina Martínez-González, José The nuclear receptor NOR-1 regulates the small muscle protein, X-linked (SMPX) and myotube differentiation |
title | The nuclear receptor NOR-1 regulates the small muscle protein, X-linked (SMPX) and myotube differentiation |
title_full | The nuclear receptor NOR-1 regulates the small muscle protein, X-linked (SMPX) and myotube differentiation |
title_fullStr | The nuclear receptor NOR-1 regulates the small muscle protein, X-linked (SMPX) and myotube differentiation |
title_full_unstemmed | The nuclear receptor NOR-1 regulates the small muscle protein, X-linked (SMPX) and myotube differentiation |
title_short | The nuclear receptor NOR-1 regulates the small muscle protein, X-linked (SMPX) and myotube differentiation |
title_sort | nuclear receptor nor-1 regulates the small muscle protein, x-linked (smpx) and myotube differentiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867575/ https://www.ncbi.nlm.nih.gov/pubmed/27181368 http://dx.doi.org/10.1038/srep25944 |
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