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Systematic identification of NF90 target RNAs by iCLIP analysis
RNA-binding proteins (RBPs) interact with and determine the fate of many cellular RNAs directing numerous essential roles in cellular physiology. Nuclear Factor 90 (NF90) is an RBP encoded by the interleukin enhancer-binding factor 3 (ILF3) gene that has been found to influence RNA metabolism at sev...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748789/ https://www.ncbi.nlm.nih.gov/pubmed/35013429 http://dx.doi.org/10.1038/s41598-021-04101-1 |
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author | Lodde, Valeria Floris, Matteo Munk, Rachel Martindale, Jennifer L. Piredda, Davide Napodano, Catello Mario Panu Cucca, Francesco Uzzau, Sergio Abdelmohsen, Kotb Gorospe, Myriam Noh, Ji Heon Idda, M. Laura |
author_facet | Lodde, Valeria Floris, Matteo Munk, Rachel Martindale, Jennifer L. Piredda, Davide Napodano, Catello Mario Panu Cucca, Francesco Uzzau, Sergio Abdelmohsen, Kotb Gorospe, Myriam Noh, Ji Heon Idda, M. Laura |
author_sort | Lodde, Valeria |
collection | PubMed |
description | RNA-binding proteins (RBPs) interact with and determine the fate of many cellular RNAs directing numerous essential roles in cellular physiology. Nuclear Factor 90 (NF90) is an RBP encoded by the interleukin enhancer-binding factor 3 (ILF3) gene that has been found to influence RNA metabolism at several levels, including pre-RNA splicing, mRNA turnover, and translation. To systematically identify the RNAs that interact with NF90, we carried out iCLIP (individual-nucleotide resolution UV crosslinking and immunoprecipitation) analysis in the human embryonic fibroblast cell line HEK-293. Interestingly, many of the identified RNAs encoded proteins involved in the response to viral infection and RNA metabolism. We validated a subset of targets and investigated the impact of NF90 on their expression levels. Two of the top targets, IRF3 and IRF9 mRNAs, encode the proteins IRF3 and IRF9, crucial regulators of the interferon pathway involved in the SARS-CoV-2 immune response. Our results support a role for NF90 in modulating key genes implicated in the immune response and offer insight into the immunological response to the SARS-CoV-2 infection. |
format | Online Article Text |
id | pubmed-8748789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87487892022-01-11 Systematic identification of NF90 target RNAs by iCLIP analysis Lodde, Valeria Floris, Matteo Munk, Rachel Martindale, Jennifer L. Piredda, Davide Napodano, Catello Mario Panu Cucca, Francesco Uzzau, Sergio Abdelmohsen, Kotb Gorospe, Myriam Noh, Ji Heon Idda, M. Laura Sci Rep Article RNA-binding proteins (RBPs) interact with and determine the fate of many cellular RNAs directing numerous essential roles in cellular physiology. Nuclear Factor 90 (NF90) is an RBP encoded by the interleukin enhancer-binding factor 3 (ILF3) gene that has been found to influence RNA metabolism at several levels, including pre-RNA splicing, mRNA turnover, and translation. To systematically identify the RNAs that interact with NF90, we carried out iCLIP (individual-nucleotide resolution UV crosslinking and immunoprecipitation) analysis in the human embryonic fibroblast cell line HEK-293. Interestingly, many of the identified RNAs encoded proteins involved in the response to viral infection and RNA metabolism. We validated a subset of targets and investigated the impact of NF90 on their expression levels. Two of the top targets, IRF3 and IRF9 mRNAs, encode the proteins IRF3 and IRF9, crucial regulators of the interferon pathway involved in the SARS-CoV-2 immune response. Our results support a role for NF90 in modulating key genes implicated in the immune response and offer insight into the immunological response to the SARS-CoV-2 infection. Nature Publishing Group UK 2022-01-10 /pmc/articles/PMC8748789/ /pubmed/35013429 http://dx.doi.org/10.1038/s41598-021-04101-1 Text en © The Author(s) 2022 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 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/) . |
spellingShingle | Article Lodde, Valeria Floris, Matteo Munk, Rachel Martindale, Jennifer L. Piredda, Davide Napodano, Catello Mario Panu Cucca, Francesco Uzzau, Sergio Abdelmohsen, Kotb Gorospe, Myriam Noh, Ji Heon Idda, M. Laura Systematic identification of NF90 target RNAs by iCLIP analysis |
title | Systematic identification of NF90 target RNAs by iCLIP analysis |
title_full | Systematic identification of NF90 target RNAs by iCLIP analysis |
title_fullStr | Systematic identification of NF90 target RNAs by iCLIP analysis |
title_full_unstemmed | Systematic identification of NF90 target RNAs by iCLIP analysis |
title_short | Systematic identification of NF90 target RNAs by iCLIP analysis |
title_sort | systematic identification of nf90 target rnas by iclip analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748789/ https://www.ncbi.nlm.nih.gov/pubmed/35013429 http://dx.doi.org/10.1038/s41598-021-04101-1 |
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