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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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.
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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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