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Temporal-iCLIP captures co-transcriptional RNA-protein interactions
Dynamic RNA-protein interactions govern the co-transcriptional packaging of RNA polymerase II (RNAPII)-derived transcripts. Yet, our current understanding of this process in vivo primarily stems from steady state analysis. To remedy this, we here conduct temporal-iCLIP (tiCLIP), combining RNAPII tra...
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/PMC9908952/ https://www.ncbi.nlm.nih.gov/pubmed/36755023 http://dx.doi.org/10.1038/s41467-023-36345-y |
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author | Cordiner, Ross A. Dou, Yuhui Thomsen, Rune Bugai, Andrii Granneman, Sander Heick Jensen, Torben |
author_facet | Cordiner, Ross A. Dou, Yuhui Thomsen, Rune Bugai, Andrii Granneman, Sander Heick Jensen, Torben |
author_sort | Cordiner, Ross A. |
collection | PubMed |
description | Dynamic RNA-protein interactions govern the co-transcriptional packaging of RNA polymerase II (RNAPII)-derived transcripts. Yet, our current understanding of this process in vivo primarily stems from steady state analysis. To remedy this, we here conduct temporal-iCLIP (tiCLIP), combining RNAPII transcriptional synchronisation with UV cross-linking of RNA-protein complexes at serial timepoints. We apply tiCLIP to the RNA export adaptor, ALYREF; a component of the Nuclear Exosome Targeting (NEXT) complex, RBM7; and the nuclear cap binding complex (CBC). Regardless of function, all tested factors interact with nascent RNA as it exits RNAPII. Moreover, we demonstrate that the two transesterification steps of pre-mRNA splicing temporally separate ALYREF and RBM7 binding to splicing intermediates, and that exon-exon junction density drives RNA 5′end binding of ALYREF. Finally, we identify underappreciated steps in snoRNA 3′end processing performed by RBM7. Altogether, our data provide a temporal view of RNA-protein interactions during the early phases of transcription. |
format | Online Article Text |
id | pubmed-9908952 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99089522023-02-10 Temporal-iCLIP captures co-transcriptional RNA-protein interactions Cordiner, Ross A. Dou, Yuhui Thomsen, Rune Bugai, Andrii Granneman, Sander Heick Jensen, Torben Nat Commun Article Dynamic RNA-protein interactions govern the co-transcriptional packaging of RNA polymerase II (RNAPII)-derived transcripts. Yet, our current understanding of this process in vivo primarily stems from steady state analysis. To remedy this, we here conduct temporal-iCLIP (tiCLIP), combining RNAPII transcriptional synchronisation with UV cross-linking of RNA-protein complexes at serial timepoints. We apply tiCLIP to the RNA export adaptor, ALYREF; a component of the Nuclear Exosome Targeting (NEXT) complex, RBM7; and the nuclear cap binding complex (CBC). Regardless of function, all tested factors interact with nascent RNA as it exits RNAPII. Moreover, we demonstrate that the two transesterification steps of pre-mRNA splicing temporally separate ALYREF and RBM7 binding to splicing intermediates, and that exon-exon junction density drives RNA 5′end binding of ALYREF. Finally, we identify underappreciated steps in snoRNA 3′end processing performed by RBM7. Altogether, our data provide a temporal view of RNA-protein interactions during the early phases of transcription. Nature Publishing Group UK 2023-02-08 /pmc/articles/PMC9908952/ /pubmed/36755023 http://dx.doi.org/10.1038/s41467-023-36345-y 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 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 Cordiner, Ross A. Dou, Yuhui Thomsen, Rune Bugai, Andrii Granneman, Sander Heick Jensen, Torben Temporal-iCLIP captures co-transcriptional RNA-protein interactions |
title | Temporal-iCLIP captures co-transcriptional RNA-protein interactions |
title_full | Temporal-iCLIP captures co-transcriptional RNA-protein interactions |
title_fullStr | Temporal-iCLIP captures co-transcriptional RNA-protein interactions |
title_full_unstemmed | Temporal-iCLIP captures co-transcriptional RNA-protein interactions |
title_short | Temporal-iCLIP captures co-transcriptional RNA-protein interactions |
title_sort | temporal-iclip captures co-transcriptional rna-protein interactions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9908952/ https://www.ncbi.nlm.nih.gov/pubmed/36755023 http://dx.doi.org/10.1038/s41467-023-36345-y |
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