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Construction of the gene regulatory network identifies MYC as a transcriptional regulator of SWI/SNF complex
Precise positioning of nucleosomes at the gene regulatory elements mediated by the SWI/SNF family of remodelling complex is important for the transcriptional regulation of genes. A wide set of genes are either positively or negatively regulated by SWI/SNF. In higher eukaryotes, around thirty genes w...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6957478/ https://www.ncbi.nlm.nih.gov/pubmed/31932624 http://dx.doi.org/10.1038/s41598-019-56844-7 |
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author | Srikanth, Srimari Ramachandran, Srimathy Mohan S, Suma |
author_facet | Srikanth, Srimari Ramachandran, Srimathy Mohan S, Suma |
author_sort | Srikanth, Srimari |
collection | PubMed |
description | Precise positioning of nucleosomes at the gene regulatory elements mediated by the SWI/SNF family of remodelling complex is important for the transcriptional regulation of genes. A wide set of genes are either positively or negatively regulated by SWI/SNF. In higher eukaryotes, around thirty genes were found to code for SWI/SNF subunits. The construction of a gene regulatory network of SWI/SNF subunits identifies MYC as a common regulator for many of the SWI/SNF subunit genes. A meta-analysis study was conducted to investigate the MYC dependent regulation of SWI/SNF remodelling complex. Subunit information and the promoter sequences of the subunit genes were used to find the canonical E-box motif and its variants. Detailed analysis of mouse and human ChIP-Seq at the SWI/SNF subunit loci indicates the presence of MYC binding peaks overlapping with E-boxes. The co-expression correlation and the differential expression analysis of wt vs. MYC perturbed MEFs indicate the MYC dependent regulation of some of the SWI/SNF subunits. The extension of the analysis was done on MYC proficient and MYC deficient embryonic fibroblast cell lines, TGR1 and HO15, and in one of the MYC amplified cancer types, Medulloblastoma. A transcriptional regulatory feedback loop between MYC and SWI/SNF could be a major factor contributing to the aggressiveness of MYC dependent cancers. |
format | Online Article Text |
id | pubmed-6957478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69574782020-01-16 Construction of the gene regulatory network identifies MYC as a transcriptional regulator of SWI/SNF complex Srikanth, Srimari Ramachandran, Srimathy Mohan S, Suma Sci Rep Article Precise positioning of nucleosomes at the gene regulatory elements mediated by the SWI/SNF family of remodelling complex is important for the transcriptional regulation of genes. A wide set of genes are either positively or negatively regulated by SWI/SNF. In higher eukaryotes, around thirty genes were found to code for SWI/SNF subunits. The construction of a gene regulatory network of SWI/SNF subunits identifies MYC as a common regulator for many of the SWI/SNF subunit genes. A meta-analysis study was conducted to investigate the MYC dependent regulation of SWI/SNF remodelling complex. Subunit information and the promoter sequences of the subunit genes were used to find the canonical E-box motif and its variants. Detailed analysis of mouse and human ChIP-Seq at the SWI/SNF subunit loci indicates the presence of MYC binding peaks overlapping with E-boxes. The co-expression correlation and the differential expression analysis of wt vs. MYC perturbed MEFs indicate the MYC dependent regulation of some of the SWI/SNF subunits. The extension of the analysis was done on MYC proficient and MYC deficient embryonic fibroblast cell lines, TGR1 and HO15, and in one of the MYC amplified cancer types, Medulloblastoma. A transcriptional regulatory feedback loop between MYC and SWI/SNF could be a major factor contributing to the aggressiveness of MYC dependent cancers. Nature Publishing Group UK 2020-01-13 /pmc/articles/PMC6957478/ /pubmed/31932624 http://dx.doi.org/10.1038/s41598-019-56844-7 Text en © The Author(s) 2020 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 Srikanth, Srimari Ramachandran, Srimathy Mohan S, Suma Construction of the gene regulatory network identifies MYC as a transcriptional regulator of SWI/SNF complex |
title | Construction of the gene regulatory network identifies MYC as a transcriptional regulator of SWI/SNF complex |
title_full | Construction of the gene regulatory network identifies MYC as a transcriptional regulator of SWI/SNF complex |
title_fullStr | Construction of the gene regulatory network identifies MYC as a transcriptional regulator of SWI/SNF complex |
title_full_unstemmed | Construction of the gene regulatory network identifies MYC as a transcriptional regulator of SWI/SNF complex |
title_short | Construction of the gene regulatory network identifies MYC as a transcriptional regulator of SWI/SNF complex |
title_sort | construction of the gene regulatory network identifies myc as a transcriptional regulator of swi/snf complex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6957478/ https://www.ncbi.nlm.nih.gov/pubmed/31932624 http://dx.doi.org/10.1038/s41598-019-56844-7 |
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