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Enhancer RNAs stimulate Pol II pause release by harnessing multivalent interactions to NELF
Enhancer RNAs (eRNAs) are long non-coding RNAs that originate from enhancers. Although eRNA transcription is a canonical feature of activated enhancers, the molecular features required for eRNA function and the mechanism of how eRNAs impinge on target gene transcription have not been established. Th...
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/PMC9068813/ https://www.ncbi.nlm.nih.gov/pubmed/35508485 http://dx.doi.org/10.1038/s41467-022-29934-w |
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author | Gorbovytska, Vladyslava Kim, Seung-Kyoon Kuybu, Filiz Götze, Michael Um, Dahun Kang, Keunsoo Pittroff, Andreas Brennecke, Theresia Schneider, Lisa-Marie Leitner, Alexander Kim, Tae-Kyung Kuhn, Claus-D. |
author_facet | Gorbovytska, Vladyslava Kim, Seung-Kyoon Kuybu, Filiz Götze, Michael Um, Dahun Kang, Keunsoo Pittroff, Andreas Brennecke, Theresia Schneider, Lisa-Marie Leitner, Alexander Kim, Tae-Kyung Kuhn, Claus-D. |
author_sort | Gorbovytska, Vladyslava |
collection | PubMed |
description | Enhancer RNAs (eRNAs) are long non-coding RNAs that originate from enhancers. Although eRNA transcription is a canonical feature of activated enhancers, the molecular features required for eRNA function and the mechanism of how eRNAs impinge on target gene transcription have not been established. Thus, using eRNA-dependent RNA polymerase II (Pol II) pause release as a model, we here investigate the requirement of sequence, structure and length of eRNAs for their ability to stimulate Pol II pause release by detaching NELF from paused Pol II. We find eRNAs not to exert their function through common structural or sequence motifs. Instead, eRNAs that exhibit a length >200 nucleotides and that contain unpaired guanosines make multiple, allosteric contacts with NELF subunits -A and -E to trigger efficient NELF release. By revealing the molecular determinants of eRNA function, our study establishes eRNAs as an important player in Pol II pause release, and it provides new insight into the regulation of metazoan transcription. |
format | Online Article Text |
id | pubmed-9068813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90688132022-05-05 Enhancer RNAs stimulate Pol II pause release by harnessing multivalent interactions to NELF Gorbovytska, Vladyslava Kim, Seung-Kyoon Kuybu, Filiz Götze, Michael Um, Dahun Kang, Keunsoo Pittroff, Andreas Brennecke, Theresia Schneider, Lisa-Marie Leitner, Alexander Kim, Tae-Kyung Kuhn, Claus-D. Nat Commun Article Enhancer RNAs (eRNAs) are long non-coding RNAs that originate from enhancers. Although eRNA transcription is a canonical feature of activated enhancers, the molecular features required for eRNA function and the mechanism of how eRNAs impinge on target gene transcription have not been established. Thus, using eRNA-dependent RNA polymerase II (Pol II) pause release as a model, we here investigate the requirement of sequence, structure and length of eRNAs for their ability to stimulate Pol II pause release by detaching NELF from paused Pol II. We find eRNAs not to exert their function through common structural or sequence motifs. Instead, eRNAs that exhibit a length >200 nucleotides and that contain unpaired guanosines make multiple, allosteric contacts with NELF subunits -A and -E to trigger efficient NELF release. By revealing the molecular determinants of eRNA function, our study establishes eRNAs as an important player in Pol II pause release, and it provides new insight into the regulation of metazoan transcription. Nature Publishing Group UK 2022-05-04 /pmc/articles/PMC9068813/ /pubmed/35508485 http://dx.doi.org/10.1038/s41467-022-29934-w 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 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 Gorbovytska, Vladyslava Kim, Seung-Kyoon Kuybu, Filiz Götze, Michael Um, Dahun Kang, Keunsoo Pittroff, Andreas Brennecke, Theresia Schneider, Lisa-Marie Leitner, Alexander Kim, Tae-Kyung Kuhn, Claus-D. Enhancer RNAs stimulate Pol II pause release by harnessing multivalent interactions to NELF |
title | Enhancer RNAs stimulate Pol II pause release by harnessing multivalent interactions to NELF |
title_full | Enhancer RNAs stimulate Pol II pause release by harnessing multivalent interactions to NELF |
title_fullStr | Enhancer RNAs stimulate Pol II pause release by harnessing multivalent interactions to NELF |
title_full_unstemmed | Enhancer RNAs stimulate Pol II pause release by harnessing multivalent interactions to NELF |
title_short | Enhancer RNAs stimulate Pol II pause release by harnessing multivalent interactions to NELF |
title_sort | enhancer rnas stimulate pol ii pause release by harnessing multivalent interactions to nelf |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9068813/ https://www.ncbi.nlm.nih.gov/pubmed/35508485 http://dx.doi.org/10.1038/s41467-022-29934-w |
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