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Transcriptional and post-transcriptional control of adipocyte differentiation by Jumonji domain-containing protein 6
Jumonji domain-containing protein 6 (JMJD6) is a nuclear protein involved in histone modification, transcription and RNA processing. Although JMJD6 is crucial for tissue development, the link between its molecular functions and its roles in any given differentiation process is unknown. We report tha...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4652747/ https://www.ncbi.nlm.nih.gov/pubmed/26117538 http://dx.doi.org/10.1093/nar/gkv645 |
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author | Hu, Yu-Jie Belaghzal, Houda Hsiao, Wen-Yu Qi, Jun Bradner, James E. Guertin, David A. Sif, Saïd Imbalzano, Anthony N. |
author_facet | Hu, Yu-Jie Belaghzal, Houda Hsiao, Wen-Yu Qi, Jun Bradner, James E. Guertin, David A. Sif, Saïd Imbalzano, Anthony N. |
author_sort | Hu, Yu-Jie |
collection | PubMed |
description | Jumonji domain-containing protein 6 (JMJD6) is a nuclear protein involved in histone modification, transcription and RNA processing. Although JMJD6 is crucial for tissue development, the link between its molecular functions and its roles in any given differentiation process is unknown. We report that JMJD6 is required for adipogenic gene expression and differentiation in a manner independent of Jumonji C domain catalytic activity. JMJD6 knockdown led to a reduction of C/EBPβ and C/EBPδ protein expression without affecting mRNA levels in the early phase of differentiation. However, ectopic expression of C/EBPβ and C/EBPδ did not rescue differentiation. Further analysis demonstrated that JMJD6 was associated with the Pparγ2 and Cebpα loci and putative enhancers. JMJD6 was previously found associated with bromodomain and extra-terminal domain (BET) proteins, which can be targeted by the bromodomain inhibitor JQ1. JQ1 treatment prevented chromatin binding of JMJD6, Pparγ2 and Cebpα expression, and adipogenic differentiation, yet had no effect on C/EBPβ and C/EBPδ expression or chromatin binding. These results indicate dual roles for JMJD6 in promoting adipogenic gene expression program by post-transcriptional regulation of C/EBPβ and C/EBPδ and direct transcriptional activation of Pparγ2 and Cebpα during adipocyte differentiation. |
format | Online Article Text |
id | pubmed-4652747 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-46527472015-11-25 Transcriptional and post-transcriptional control of adipocyte differentiation by Jumonji domain-containing protein 6 Hu, Yu-Jie Belaghzal, Houda Hsiao, Wen-Yu Qi, Jun Bradner, James E. Guertin, David A. Sif, Saïd Imbalzano, Anthony N. Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Jumonji domain-containing protein 6 (JMJD6) is a nuclear protein involved in histone modification, transcription and RNA processing. Although JMJD6 is crucial for tissue development, the link between its molecular functions and its roles in any given differentiation process is unknown. We report that JMJD6 is required for adipogenic gene expression and differentiation in a manner independent of Jumonji C domain catalytic activity. JMJD6 knockdown led to a reduction of C/EBPβ and C/EBPδ protein expression without affecting mRNA levels in the early phase of differentiation. However, ectopic expression of C/EBPβ and C/EBPδ did not rescue differentiation. Further analysis demonstrated that JMJD6 was associated with the Pparγ2 and Cebpα loci and putative enhancers. JMJD6 was previously found associated with bromodomain and extra-terminal domain (BET) proteins, which can be targeted by the bromodomain inhibitor JQ1. JQ1 treatment prevented chromatin binding of JMJD6, Pparγ2 and Cebpα expression, and adipogenic differentiation, yet had no effect on C/EBPβ and C/EBPδ expression or chromatin binding. These results indicate dual roles for JMJD6 in promoting adipogenic gene expression program by post-transcriptional regulation of C/EBPβ and C/EBPδ and direct transcriptional activation of Pparγ2 and Cebpα during adipocyte differentiation. Oxford University Press 2015-09-18 2015-06-27 /pmc/articles/PMC4652747/ /pubmed/26117538 http://dx.doi.org/10.1093/nar/gkv645 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Gene regulation, Chromatin and Epigenetics Hu, Yu-Jie Belaghzal, Houda Hsiao, Wen-Yu Qi, Jun Bradner, James E. Guertin, David A. Sif, Saïd Imbalzano, Anthony N. Transcriptional and post-transcriptional control of adipocyte differentiation by Jumonji domain-containing protein 6 |
title | Transcriptional and post-transcriptional control of adipocyte differentiation by Jumonji domain-containing protein 6 |
title_full | Transcriptional and post-transcriptional control of adipocyte differentiation by Jumonji domain-containing protein 6 |
title_fullStr | Transcriptional and post-transcriptional control of adipocyte differentiation by Jumonji domain-containing protein 6 |
title_full_unstemmed | Transcriptional and post-transcriptional control of adipocyte differentiation by Jumonji domain-containing protein 6 |
title_short | Transcriptional and post-transcriptional control of adipocyte differentiation by Jumonji domain-containing protein 6 |
title_sort | transcriptional and post-transcriptional control of adipocyte differentiation by jumonji domain-containing protein 6 |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4652747/ https://www.ncbi.nlm.nih.gov/pubmed/26117538 http://dx.doi.org/10.1093/nar/gkv645 |
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