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Epromoters function as a hub to recruit key transcription factors required for the inflammatory response

Gene expression is controlled by the involvement of gene-proximal (promoters) and distal (enhancers) regulatory elements. Our previous results demonstrated that a subset of gene promoters, termed Epromoters, work as bona fide enhancers and regulate distal gene expression. Here, we hypothesized that...

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Autores principales: Santiago-Algarra, David, Souaid, Charbel, Singh, Himanshu, Dao, Lan T. M., Hussain, Saadat, Medina-Rivera, Alejandra, Ramirez-Navarro, Lucia, Castro-Mondragon, Jaime A., Sadouni, Nori, Charbonnier, Guillaume, Spicuglia, Salvatore
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8602369/
https://www.ncbi.nlm.nih.gov/pubmed/34795220
http://dx.doi.org/10.1038/s41467-021-26861-0
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author Santiago-Algarra, David
Souaid, Charbel
Singh, Himanshu
Dao, Lan T. M.
Hussain, Saadat
Medina-Rivera, Alejandra
Ramirez-Navarro, Lucia
Castro-Mondragon, Jaime A.
Sadouni, Nori
Charbonnier, Guillaume
Spicuglia, Salvatore
author_facet Santiago-Algarra, David
Souaid, Charbel
Singh, Himanshu
Dao, Lan T. M.
Hussain, Saadat
Medina-Rivera, Alejandra
Ramirez-Navarro, Lucia
Castro-Mondragon, Jaime A.
Sadouni, Nori
Charbonnier, Guillaume
Spicuglia, Salvatore
author_sort Santiago-Algarra, David
collection PubMed
description Gene expression is controlled by the involvement of gene-proximal (promoters) and distal (enhancers) regulatory elements. Our previous results demonstrated that a subset of gene promoters, termed Epromoters, work as bona fide enhancers and regulate distal gene expression. Here, we hypothesized that Epromoters play a key role in the coordination of rapid gene induction during the inflammatory response. Using a high-throughput reporter assay we explored the function of Epromoters in response to type I interferon. We find that clusters of IFNa-induced genes are frequently associated with Epromoters and that these regulatory elements preferentially recruit the STAT1/2 and IRF transcription factors and distally regulate the activation of interferon-response genes. Consistently, we identified and validated the involvement of Epromoter-containing clusters in the regulation of LPS-stimulated macrophages. Our findings suggest that Epromoters function as a local hub recruiting the key TFs required for coordinated regulation of gene clusters during the inflammatory response.
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spelling pubmed-86023692021-12-03 Epromoters function as a hub to recruit key transcription factors required for the inflammatory response Santiago-Algarra, David Souaid, Charbel Singh, Himanshu Dao, Lan T. M. Hussain, Saadat Medina-Rivera, Alejandra Ramirez-Navarro, Lucia Castro-Mondragon, Jaime A. Sadouni, Nori Charbonnier, Guillaume Spicuglia, Salvatore Nat Commun Article Gene expression is controlled by the involvement of gene-proximal (promoters) and distal (enhancers) regulatory elements. Our previous results demonstrated that a subset of gene promoters, termed Epromoters, work as bona fide enhancers and regulate distal gene expression. Here, we hypothesized that Epromoters play a key role in the coordination of rapid gene induction during the inflammatory response. Using a high-throughput reporter assay we explored the function of Epromoters in response to type I interferon. We find that clusters of IFNa-induced genes are frequently associated with Epromoters and that these regulatory elements preferentially recruit the STAT1/2 and IRF transcription factors and distally regulate the activation of interferon-response genes. Consistently, we identified and validated the involvement of Epromoter-containing clusters in the regulation of LPS-stimulated macrophages. Our findings suggest that Epromoters function as a local hub recruiting the key TFs required for coordinated regulation of gene clusters during the inflammatory response. Nature Publishing Group UK 2021-11-18 /pmc/articles/PMC8602369/ /pubmed/34795220 http://dx.doi.org/10.1038/s41467-021-26861-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Santiago-Algarra, David
Souaid, Charbel
Singh, Himanshu
Dao, Lan T. M.
Hussain, Saadat
Medina-Rivera, Alejandra
Ramirez-Navarro, Lucia
Castro-Mondragon, Jaime A.
Sadouni, Nori
Charbonnier, Guillaume
Spicuglia, Salvatore
Epromoters function as a hub to recruit key transcription factors required for the inflammatory response
title Epromoters function as a hub to recruit key transcription factors required for the inflammatory response
title_full Epromoters function as a hub to recruit key transcription factors required for the inflammatory response
title_fullStr Epromoters function as a hub to recruit key transcription factors required for the inflammatory response
title_full_unstemmed Epromoters function as a hub to recruit key transcription factors required for the inflammatory response
title_short Epromoters function as a hub to recruit key transcription factors required for the inflammatory response
title_sort epromoters function as a hub to recruit key transcription factors required for the inflammatory response
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8602369/
https://www.ncbi.nlm.nih.gov/pubmed/34795220
http://dx.doi.org/10.1038/s41467-021-26861-0
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