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A lncRNA-SWI/SNF complex crosstalk controls transcriptional activation at specific promoter regions
LncRNAs have been shown to be direct players in chromatin regulation, but little is known about their role at active genomic loci. We investigate the role of lncRNAs in gene activation by profiling the RNA interactome of SMARCB1-containing SWI/SNF complexes in proliferating and senescent conditions....
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/PMC7028943/ https://www.ncbi.nlm.nih.gov/pubmed/32071317 http://dx.doi.org/10.1038/s41467-020-14623-3 |
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author | Grossi, Elena Raimondi, Ivan Goñi, Enrique González, Jovanna Marchese, Francesco P. Chapaprieta, Vicente Martín-Subero, José I. Guo, Shuling Huarte, Maite |
author_facet | Grossi, Elena Raimondi, Ivan Goñi, Enrique González, Jovanna Marchese, Francesco P. Chapaprieta, Vicente Martín-Subero, José I. Guo, Shuling Huarte, Maite |
author_sort | Grossi, Elena |
collection | PubMed |
description | LncRNAs have been shown to be direct players in chromatin regulation, but little is known about their role at active genomic loci. We investigate the role of lncRNAs in gene activation by profiling the RNA interactome of SMARCB1-containing SWI/SNF complexes in proliferating and senescent conditions. The isolation of SMARCB1-associated transcripts, together with chromatin profiling, shows prevalent association to active regions where SMARCB1 differentially binds locally transcribed RNAs. We identify SWINGN, a lncRNA interacting with SMARCB1 exclusively in proliferating conditions, exerting a pro-oncogenic role in some tumor types. SWINGN is transcribed from an enhancer and modulates the activation of GAS6 oncogene as part of a topologically organized region, as well as a larger network of pro-oncogenic genes by favoring SMARCB1 binding. Our results indicate that SWINGN influences the ability of the SWI/SNF complexes to drive epigenetic activation of specific promoters, suggesting a SWI/SNF-RNA cooperation to achieve optimal transcriptional activation. |
format | Online Article Text |
id | pubmed-7028943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70289432020-02-25 A lncRNA-SWI/SNF complex crosstalk controls transcriptional activation at specific promoter regions Grossi, Elena Raimondi, Ivan Goñi, Enrique González, Jovanna Marchese, Francesco P. Chapaprieta, Vicente Martín-Subero, José I. Guo, Shuling Huarte, Maite Nat Commun Article LncRNAs have been shown to be direct players in chromatin regulation, but little is known about their role at active genomic loci. We investigate the role of lncRNAs in gene activation by profiling the RNA interactome of SMARCB1-containing SWI/SNF complexes in proliferating and senescent conditions. The isolation of SMARCB1-associated transcripts, together with chromatin profiling, shows prevalent association to active regions where SMARCB1 differentially binds locally transcribed RNAs. We identify SWINGN, a lncRNA interacting with SMARCB1 exclusively in proliferating conditions, exerting a pro-oncogenic role in some tumor types. SWINGN is transcribed from an enhancer and modulates the activation of GAS6 oncogene as part of a topologically organized region, as well as a larger network of pro-oncogenic genes by favoring SMARCB1 binding. Our results indicate that SWINGN influences the ability of the SWI/SNF complexes to drive epigenetic activation of specific promoters, suggesting a SWI/SNF-RNA cooperation to achieve optimal transcriptional activation. Nature Publishing Group UK 2020-02-18 /pmc/articles/PMC7028943/ /pubmed/32071317 http://dx.doi.org/10.1038/s41467-020-14623-3 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 Grossi, Elena Raimondi, Ivan Goñi, Enrique González, Jovanna Marchese, Francesco P. Chapaprieta, Vicente Martín-Subero, José I. Guo, Shuling Huarte, Maite A lncRNA-SWI/SNF complex crosstalk controls transcriptional activation at specific promoter regions |
title | A lncRNA-SWI/SNF complex crosstalk controls transcriptional activation at specific promoter regions |
title_full | A lncRNA-SWI/SNF complex crosstalk controls transcriptional activation at specific promoter regions |
title_fullStr | A lncRNA-SWI/SNF complex crosstalk controls transcriptional activation at specific promoter regions |
title_full_unstemmed | A lncRNA-SWI/SNF complex crosstalk controls transcriptional activation at specific promoter regions |
title_short | A lncRNA-SWI/SNF complex crosstalk controls transcriptional activation at specific promoter regions |
title_sort | lncrna-swi/snf complex crosstalk controls transcriptional activation at specific promoter regions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7028943/ https://www.ncbi.nlm.nih.gov/pubmed/32071317 http://dx.doi.org/10.1038/s41467-020-14623-3 |
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