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Transcriptomic profiling implicates PAF1 in both active and repressive immune regulatory networks
BACKGROUND: Sitting at the interface of gene expression and host-pathogen interaction, polymerase associated factor 1 complex (PAF1C) is a rising player in the innate immune response. The complex localizes to the nucleus and associates with chromatin to modulate RNA polymerase II (RNAPII) elongation...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9713194/ https://www.ncbi.nlm.nih.gov/pubmed/36451099 http://dx.doi.org/10.1186/s12864-022-09013-6 |
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author | Kenaston, Matthew W. Pham, Oanh H. Petit, Marine J. Shah, Priya S. |
author_facet | Kenaston, Matthew W. Pham, Oanh H. Petit, Marine J. Shah, Priya S. |
author_sort | Kenaston, Matthew W. |
collection | PubMed |
description | BACKGROUND: Sitting at the interface of gene expression and host-pathogen interaction, polymerase associated factor 1 complex (PAF1C) is a rising player in the innate immune response. The complex localizes to the nucleus and associates with chromatin to modulate RNA polymerase II (RNAPII) elongation of gene transcripts. Performing this function at both proximal and distal regulatory elements, PAF1C interacts with many host factors across such sites, along with several microbial proteins during infection. Therefore, translating the ubiquity of PAF1C into specific impacts on immune gene expression remains especially relevant. RESULTS: Advancing past work, we treat PAF1 knockout cells with a slate of immune stimuli to identify key trends in PAF1-dependent gene expression with broad analytical depth. From our transcriptomic data, we confirm PAF1 is an activator of traditional immune response pathways as well as other cellular pathways correlated with pathogen defense. With this model, we employ computational approaches to refine how PAF1 may contribute to both gene activation and suppression. Specifically focusing on transcriptional motifs and regulons, we predict gene regulatory elements strongly associated with PAF1, including those implicated in an immune response. Overall, our results suggest PAF1 is involved in innate immunity at several distinct axes of regulation. CONCLUSIONS: By identifying PAF1-dependent gene expression across several pathogenic contexts, we confirm PAF1C to be a key mediator of innate immunity. Combining these transcriptomic profiles with potential regulatory networks corroborates the previously identified functions of PAF1C. With this, we foster new avenues for its study as a regulator of innate immunity, and our results will serve as a basis for targeted study of PAF1C in future validation studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-09013-6. |
format | Online Article Text |
id | pubmed-9713194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97131942022-12-01 Transcriptomic profiling implicates PAF1 in both active and repressive immune regulatory networks Kenaston, Matthew W. Pham, Oanh H. Petit, Marine J. Shah, Priya S. BMC Genomics Research BACKGROUND: Sitting at the interface of gene expression and host-pathogen interaction, polymerase associated factor 1 complex (PAF1C) is a rising player in the innate immune response. The complex localizes to the nucleus and associates with chromatin to modulate RNA polymerase II (RNAPII) elongation of gene transcripts. Performing this function at both proximal and distal regulatory elements, PAF1C interacts with many host factors across such sites, along with several microbial proteins during infection. Therefore, translating the ubiquity of PAF1C into specific impacts on immune gene expression remains especially relevant. RESULTS: Advancing past work, we treat PAF1 knockout cells with a slate of immune stimuli to identify key trends in PAF1-dependent gene expression with broad analytical depth. From our transcriptomic data, we confirm PAF1 is an activator of traditional immune response pathways as well as other cellular pathways correlated with pathogen defense. With this model, we employ computational approaches to refine how PAF1 may contribute to both gene activation and suppression. Specifically focusing on transcriptional motifs and regulons, we predict gene regulatory elements strongly associated with PAF1, including those implicated in an immune response. Overall, our results suggest PAF1 is involved in innate immunity at several distinct axes of regulation. CONCLUSIONS: By identifying PAF1-dependent gene expression across several pathogenic contexts, we confirm PAF1C to be a key mediator of innate immunity. Combining these transcriptomic profiles with potential regulatory networks corroborates the previously identified functions of PAF1C. With this, we foster new avenues for its study as a regulator of innate immunity, and our results will serve as a basis for targeted study of PAF1C in future validation studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-09013-6. BioMed Central 2022-11-30 /pmc/articles/PMC9713194/ /pubmed/36451099 http://dx.doi.org/10.1186/s12864-022-09013-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Kenaston, Matthew W. Pham, Oanh H. Petit, Marine J. Shah, Priya S. Transcriptomic profiling implicates PAF1 in both active and repressive immune regulatory networks |
title | Transcriptomic profiling implicates PAF1 in both active and repressive immune regulatory networks |
title_full | Transcriptomic profiling implicates PAF1 in both active and repressive immune regulatory networks |
title_fullStr | Transcriptomic profiling implicates PAF1 in both active and repressive immune regulatory networks |
title_full_unstemmed | Transcriptomic profiling implicates PAF1 in both active and repressive immune regulatory networks |
title_short | Transcriptomic profiling implicates PAF1 in both active and repressive immune regulatory networks |
title_sort | transcriptomic profiling implicates paf1 in both active and repressive immune regulatory networks |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9713194/ https://www.ncbi.nlm.nih.gov/pubmed/36451099 http://dx.doi.org/10.1186/s12864-022-09013-6 |
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