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High-sensitive nascent transcript sequencing reveals BRD4-specific control of widespread enhancer and target gene transcription

Gene transcription by RNA polymerase II (Pol II) is under control of promoters and distal regulatory elements known as enhancers. Enhancers are themselves transcribed by Pol II correlating with their activity. How enhancer transcription is regulated and coordinated with transcription at target genes...

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Autores principales: Bressin, Annkatrin, Jasnovidova, Olga, Arnold, Mirjam, Altendorfer, Elisabeth, Trajkovski, Filip, Kratz, Thomas A., Handzlik, Joanna E., Hnisz, Denes, Mayer, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10435483/
https://www.ncbi.nlm.nih.gov/pubmed/37591883
http://dx.doi.org/10.1038/s41467-023-40633-y
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author Bressin, Annkatrin
Jasnovidova, Olga
Arnold, Mirjam
Altendorfer, Elisabeth
Trajkovski, Filip
Kratz, Thomas A.
Handzlik, Joanna E.
Hnisz, Denes
Mayer, Andreas
author_facet Bressin, Annkatrin
Jasnovidova, Olga
Arnold, Mirjam
Altendorfer, Elisabeth
Trajkovski, Filip
Kratz, Thomas A.
Handzlik, Joanna E.
Hnisz, Denes
Mayer, Andreas
author_sort Bressin, Annkatrin
collection PubMed
description Gene transcription by RNA polymerase II (Pol II) is under control of promoters and distal regulatory elements known as enhancers. Enhancers are themselves transcribed by Pol II correlating with their activity. How enhancer transcription is regulated and coordinated with transcription at target genes has remained unclear. Here, we developed a high-sensitive native elongating transcript sequencing approach, called HiS-NET-seq, to provide an extended high-resolution view on transcription, especially at lowly transcribed regions such as enhancers. HiS-NET-seq uncovers new transcribed enhancers in human cells. A multi-omics analysis shows that genome-wide enhancer transcription depends on the BET family protein BRD4. Specifically, BRD4 co-localizes to enhancer and promoter-proximal gene regions, and is required for elongation activation at enhancers and their genes. BRD4 keeps a set of enhancers and genes in proximity through long-range contacts. From these studies BRD4 emerges as a general regulator of enhancer transcription that may link transcription at enhancers and genes.
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spelling pubmed-104354832023-08-19 High-sensitive nascent transcript sequencing reveals BRD4-specific control of widespread enhancer and target gene transcription Bressin, Annkatrin Jasnovidova, Olga Arnold, Mirjam Altendorfer, Elisabeth Trajkovski, Filip Kratz, Thomas A. Handzlik, Joanna E. Hnisz, Denes Mayer, Andreas Nat Commun Article Gene transcription by RNA polymerase II (Pol II) is under control of promoters and distal regulatory elements known as enhancers. Enhancers are themselves transcribed by Pol II correlating with their activity. How enhancer transcription is regulated and coordinated with transcription at target genes has remained unclear. Here, we developed a high-sensitive native elongating transcript sequencing approach, called HiS-NET-seq, to provide an extended high-resolution view on transcription, especially at lowly transcribed regions such as enhancers. HiS-NET-seq uncovers new transcribed enhancers in human cells. A multi-omics analysis shows that genome-wide enhancer transcription depends on the BET family protein BRD4. Specifically, BRD4 co-localizes to enhancer and promoter-proximal gene regions, and is required for elongation activation at enhancers and their genes. BRD4 keeps a set of enhancers and genes in proximity through long-range contacts. From these studies BRD4 emerges as a general regulator of enhancer transcription that may link transcription at enhancers and genes. Nature Publishing Group UK 2023-08-17 /pmc/articles/PMC10435483/ /pubmed/37591883 http://dx.doi.org/10.1038/s41467-023-40633-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
Bressin, Annkatrin
Jasnovidova, Olga
Arnold, Mirjam
Altendorfer, Elisabeth
Trajkovski, Filip
Kratz, Thomas A.
Handzlik, Joanna E.
Hnisz, Denes
Mayer, Andreas
High-sensitive nascent transcript sequencing reveals BRD4-specific control of widespread enhancer and target gene transcription
title High-sensitive nascent transcript sequencing reveals BRD4-specific control of widespread enhancer and target gene transcription
title_full High-sensitive nascent transcript sequencing reveals BRD4-specific control of widespread enhancer and target gene transcription
title_fullStr High-sensitive nascent transcript sequencing reveals BRD4-specific control of widespread enhancer and target gene transcription
title_full_unstemmed High-sensitive nascent transcript sequencing reveals BRD4-specific control of widespread enhancer and target gene transcription
title_short High-sensitive nascent transcript sequencing reveals BRD4-specific control of widespread enhancer and target gene transcription
title_sort high-sensitive nascent transcript sequencing reveals brd4-specific control of widespread enhancer and target gene transcription
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10435483/
https://www.ncbi.nlm.nih.gov/pubmed/37591883
http://dx.doi.org/10.1038/s41467-023-40633-y
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