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An RNA-immunoprecipitation via CRISPR/dCas13 reveals an interaction between the SARS-CoV-2 5'UTR RNA and the process of human lipid metabolism
We herein elucidate the function of SARS-CoV-2derived 5'UTR in the human cells. 5'UTR bound host cellular RNAs were immunoprecipitated by gRNA-dCas13 (targeting luciferase RNA fused to SARS-CoV-2 5'UTR) in HEK293T and A549 cells. The 5'UTR bound RNA extractions were predominantly...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10300121/ https://www.ncbi.nlm.nih.gov/pubmed/37369697 http://dx.doi.org/10.1038/s41598-023-36680-6 |
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author | Shimizu, Yurika Bandaru, Srinivas Hara, Mari Young, Sonny Sano, Toshikazu Usami, Kaya Kurano, Yuta Lee, Suni Kumagai-Takei, Naoko Takashiba, Shogo Sano, Shunji Ito, Tatsuo |
author_facet | Shimizu, Yurika Bandaru, Srinivas Hara, Mari Young, Sonny Sano, Toshikazu Usami, Kaya Kurano, Yuta Lee, Suni Kumagai-Takei, Naoko Takashiba, Shogo Sano, Shunji Ito, Tatsuo |
author_sort | Shimizu, Yurika |
collection | PubMed |
description | We herein elucidate the function of SARS-CoV-2derived 5'UTR in the human cells. 5'UTR bound host cellular RNAs were immunoprecipitated by gRNA-dCas13 (targeting luciferase RNA fused to SARS-CoV-2 5'UTR) in HEK293T and A549 cells. The 5'UTR bound RNA extractions were predominantly enriched for regulating lipid metabolism. Overexpression of SARS-CoV-2 5'UTR RNA altered the expression of factors involved in the process of the human Mevalonate pathway. In addition, we found that HMG-CoA reductase inhibitors were shown to suppress SARS-CoV-2 5'UTR-mediated translation activities. In conclusion, we deduce the array of host RNAs interacting with SARS-CoV-2 5'UTR that drives SARS-CoV-2 translation and influences host metabolic pathways. |
format | Online Article Text |
id | pubmed-10300121 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103001212023-06-29 An RNA-immunoprecipitation via CRISPR/dCas13 reveals an interaction between the SARS-CoV-2 5'UTR RNA and the process of human lipid metabolism Shimizu, Yurika Bandaru, Srinivas Hara, Mari Young, Sonny Sano, Toshikazu Usami, Kaya Kurano, Yuta Lee, Suni Kumagai-Takei, Naoko Takashiba, Shogo Sano, Shunji Ito, Tatsuo Sci Rep Article We herein elucidate the function of SARS-CoV-2derived 5'UTR in the human cells. 5'UTR bound host cellular RNAs were immunoprecipitated by gRNA-dCas13 (targeting luciferase RNA fused to SARS-CoV-2 5'UTR) in HEK293T and A549 cells. The 5'UTR bound RNA extractions were predominantly enriched for regulating lipid metabolism. Overexpression of SARS-CoV-2 5'UTR RNA altered the expression of factors involved in the process of the human Mevalonate pathway. In addition, we found that HMG-CoA reductase inhibitors were shown to suppress SARS-CoV-2 5'UTR-mediated translation activities. In conclusion, we deduce the array of host RNAs interacting with SARS-CoV-2 5'UTR that drives SARS-CoV-2 translation and influences host metabolic pathways. Nature Publishing Group UK 2023-06-27 /pmc/articles/PMC10300121/ /pubmed/37369697 http://dx.doi.org/10.1038/s41598-023-36680-6 Text en © The Author(s) 2023 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 Shimizu, Yurika Bandaru, Srinivas Hara, Mari Young, Sonny Sano, Toshikazu Usami, Kaya Kurano, Yuta Lee, Suni Kumagai-Takei, Naoko Takashiba, Shogo Sano, Shunji Ito, Tatsuo An RNA-immunoprecipitation via CRISPR/dCas13 reveals an interaction between the SARS-CoV-2 5'UTR RNA and the process of human lipid metabolism |
title | An RNA-immunoprecipitation via CRISPR/dCas13 reveals an interaction between the SARS-CoV-2 5'UTR RNA and the process of human lipid metabolism |
title_full | An RNA-immunoprecipitation via CRISPR/dCas13 reveals an interaction between the SARS-CoV-2 5'UTR RNA and the process of human lipid metabolism |
title_fullStr | An RNA-immunoprecipitation via CRISPR/dCas13 reveals an interaction between the SARS-CoV-2 5'UTR RNA and the process of human lipid metabolism |
title_full_unstemmed | An RNA-immunoprecipitation via CRISPR/dCas13 reveals an interaction between the SARS-CoV-2 5'UTR RNA and the process of human lipid metabolism |
title_short | An RNA-immunoprecipitation via CRISPR/dCas13 reveals an interaction between the SARS-CoV-2 5'UTR RNA and the process of human lipid metabolism |
title_sort | rna-immunoprecipitation via crispr/dcas13 reveals an interaction between the sars-cov-2 5'utr rna and the process of human lipid metabolism |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10300121/ https://www.ncbi.nlm.nih.gov/pubmed/37369697 http://dx.doi.org/10.1038/s41598-023-36680-6 |
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