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Ikaros mediates the DNA methylation-independent silencing of MCJ/DNAJC15 gene expression in macrophages
MCJ (DNAJC15) is a mitochondrial protein that regulates the mitochondrial metabolic status of macrophages and their response to inflammatory stimuli. CpG island methylation in cancer cells constitutes the only mechanism identified for the regulation of MCJ gene expression. However, whether DNA methy...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588509/ https://www.ncbi.nlm.nih.gov/pubmed/26419808 http://dx.doi.org/10.1038/srep14692 |
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author | Navasa, Nicolás Martin-Ruiz, Itziar Atondo, Estíbaliz Sutherland, James D. Angel Pascual-Itoiz, Miguel Carreras-González, Ana Izadi, Hooman Tomás-Cortázar, Julen Ayaz, Furkan Martin-Martin, Natalia Torres, Iviana M Barrio, Rosa Carracedo, Arkaitz Olivera, Elias R. Rincón, Mercedes Anguita, Juan |
author_facet | Navasa, Nicolás Martin-Ruiz, Itziar Atondo, Estíbaliz Sutherland, James D. Angel Pascual-Itoiz, Miguel Carreras-González, Ana Izadi, Hooman Tomás-Cortázar, Julen Ayaz, Furkan Martin-Martin, Natalia Torres, Iviana M Barrio, Rosa Carracedo, Arkaitz Olivera, Elias R. Rincón, Mercedes Anguita, Juan |
author_sort | Navasa, Nicolás |
collection | PubMed |
description | MCJ (DNAJC15) is a mitochondrial protein that regulates the mitochondrial metabolic status of macrophages and their response to inflammatory stimuli. CpG island methylation in cancer cells constitutes the only mechanism identified for the regulation of MCJ gene expression. However, whether DNA methylation or transcriptional regulation mechanisms are involved in the physiological control of this gene expression in non-tumor cells remains unknown. We now demonstrate a mechanism of regulation of MCJ expression that is independent of DNA methylation. IFNγ, a protective cytokine against cardiac inflammation during Lyme borreliosis, represses MCJ transcription in macrophages. The transcriptional regulator, Ikaros, binds to the MCJ promoter in a Casein kinase II-dependent manner, and mediates the repression of MCJ expression. These results identify the MCJ gene as a transcriptional target of IFNγ and provide evidence of the dynamic adaptation of normal tissues to changes in the environment as a way to adapt metabolically to new conditions. |
format | Online Article Text |
id | pubmed-4588509 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45885092015-10-13 Ikaros mediates the DNA methylation-independent silencing of MCJ/DNAJC15 gene expression in macrophages Navasa, Nicolás Martin-Ruiz, Itziar Atondo, Estíbaliz Sutherland, James D. Angel Pascual-Itoiz, Miguel Carreras-González, Ana Izadi, Hooman Tomás-Cortázar, Julen Ayaz, Furkan Martin-Martin, Natalia Torres, Iviana M Barrio, Rosa Carracedo, Arkaitz Olivera, Elias R. Rincón, Mercedes Anguita, Juan Sci Rep Article MCJ (DNAJC15) is a mitochondrial protein that regulates the mitochondrial metabolic status of macrophages and their response to inflammatory stimuli. CpG island methylation in cancer cells constitutes the only mechanism identified for the regulation of MCJ gene expression. However, whether DNA methylation or transcriptional regulation mechanisms are involved in the physiological control of this gene expression in non-tumor cells remains unknown. We now demonstrate a mechanism of regulation of MCJ expression that is independent of DNA methylation. IFNγ, a protective cytokine against cardiac inflammation during Lyme borreliosis, represses MCJ transcription in macrophages. The transcriptional regulator, Ikaros, binds to the MCJ promoter in a Casein kinase II-dependent manner, and mediates the repression of MCJ expression. These results identify the MCJ gene as a transcriptional target of IFNγ and provide evidence of the dynamic adaptation of normal tissues to changes in the environment as a way to adapt metabolically to new conditions. Nature Publishing Group 2015-09-30 /pmc/articles/PMC4588509/ /pubmed/26419808 http://dx.doi.org/10.1038/srep14692 Text en Copyright © 2015, 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 Navasa, Nicolás Martin-Ruiz, Itziar Atondo, Estíbaliz Sutherland, James D. Angel Pascual-Itoiz, Miguel Carreras-González, Ana Izadi, Hooman Tomás-Cortázar, Julen Ayaz, Furkan Martin-Martin, Natalia Torres, Iviana M Barrio, Rosa Carracedo, Arkaitz Olivera, Elias R. Rincón, Mercedes Anguita, Juan Ikaros mediates the DNA methylation-independent silencing of MCJ/DNAJC15 gene expression in macrophages |
title | Ikaros mediates the DNA methylation-independent silencing of MCJ/DNAJC15 gene expression in macrophages |
title_full | Ikaros mediates the DNA methylation-independent silencing of MCJ/DNAJC15 gene expression in macrophages |
title_fullStr | Ikaros mediates the DNA methylation-independent silencing of MCJ/DNAJC15 gene expression in macrophages |
title_full_unstemmed | Ikaros mediates the DNA methylation-independent silencing of MCJ/DNAJC15 gene expression in macrophages |
title_short | Ikaros mediates the DNA methylation-independent silencing of MCJ/DNAJC15 gene expression in macrophages |
title_sort | ikaros mediates the dna methylation-independent silencing of mcj/dnajc15 gene expression in macrophages |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588509/ https://www.ncbi.nlm.nih.gov/pubmed/26419808 http://dx.doi.org/10.1038/srep14692 |
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