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CARM1 and BAF155: an example of how chromatin remodeling factors can be relocalized and contribute to cancer
In a recent article, Wang and colleagues reported the discovery of a mechanism by which CARM1 regulates the genomic localization of BAF155 (a SWI/SNF subunit involved in chromatin remodeling) through post-translational methylation at R1064 arginine residues. This modification leads to the relocaliza...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053224/ https://www.ncbi.nlm.nih.gov/pubmed/25927994 http://dx.doi.org/10.1186/bcr3657 |
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author | Stefansson, Olafur A Esteller, Manel |
author_facet | Stefansson, Olafur A Esteller, Manel |
author_sort | Stefansson, Olafur A |
collection | PubMed |
description | In a recent article, Wang and colleagues reported the discovery of a mechanism by which CARM1 regulates the genomic localization of BAF155 (a SWI/SNF subunit involved in chromatin remodeling) through post-translational methylation at R1064 arginine residues. This modification leads to the relocalization of BAF155-containing SWI/SNF complexes to regions containing genes involved in the Myc oncogenic pathway. The results presented are evidence that these interactions constitute a mechanism by which the BAF155 chromatin remodeling factor contributes to cancer. |
format | Online Article Text |
id | pubmed-4053224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40532242014-11-19 CARM1 and BAF155: an example of how chromatin remodeling factors can be relocalized and contribute to cancer Stefansson, Olafur A Esteller, Manel Breast Cancer Res Viewpoint In a recent article, Wang and colleagues reported the discovery of a mechanism by which CARM1 regulates the genomic localization of BAF155 (a SWI/SNF subunit involved in chromatin remodeling) through post-translational methylation at R1064 arginine residues. This modification leads to the relocalization of BAF155-containing SWI/SNF complexes to regions containing genes involved in the Myc oncogenic pathway. The results presented are evidence that these interactions constitute a mechanism by which the BAF155 chromatin remodeling factor contributes to cancer. BioMed Central 2014 2014-05-19 /pmc/articles/PMC4053224/ /pubmed/25927994 http://dx.doi.org/10.1186/bcr3657 Text en Copyright © 2014 Esteller and Stefansson; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 The licensee has exclusive rights to distribute this article, in any medium, for 12 months following its publication. After this time, the article is available under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Viewpoint Stefansson, Olafur A Esteller, Manel CARM1 and BAF155: an example of how chromatin remodeling factors can be relocalized and contribute to cancer |
title | CARM1 and BAF155: an example of how chromatin remodeling factors can be relocalized and contribute to cancer |
title_full | CARM1 and BAF155: an example of how chromatin remodeling factors can be relocalized and contribute to cancer |
title_fullStr | CARM1 and BAF155: an example of how chromatin remodeling factors can be relocalized and contribute to cancer |
title_full_unstemmed | CARM1 and BAF155: an example of how chromatin remodeling factors can be relocalized and contribute to cancer |
title_short | CARM1 and BAF155: an example of how chromatin remodeling factors can be relocalized and contribute to cancer |
title_sort | carm1 and baf155: an example of how chromatin remodeling factors can be relocalized and contribute to cancer |
topic | Viewpoint |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053224/ https://www.ncbi.nlm.nih.gov/pubmed/25927994 http://dx.doi.org/10.1186/bcr3657 |
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