Cargando…
Global mapping of RNA-chromatin contacts reveals a proximity-dominated connectivity model for ncRNA-gene interactions
Non-coding RNAs (ncRNAs) are transcribed throughout the genome and provide regulatory inputs to gene expression through their interaction with chromatin. Yet, the genomic targets and functions of most ncRNAs are unknown. Here we use chromatin-associated RNA sequencing (ChAR-seq) to map the global ne...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10539311/ https://www.ncbi.nlm.nih.gov/pubmed/37770513 http://dx.doi.org/10.1038/s41467-023-41848-9 |
_version_ | 1785113470299013120 |
---|---|
author | Limouse, Charles Smith, Owen K. Jukam, David Fryer, Kelsey A. Greenleaf, William J. Straight, Aaron F. |
author_facet | Limouse, Charles Smith, Owen K. Jukam, David Fryer, Kelsey A. Greenleaf, William J. Straight, Aaron F. |
author_sort | Limouse, Charles |
collection | PubMed |
description | Non-coding RNAs (ncRNAs) are transcribed throughout the genome and provide regulatory inputs to gene expression through their interaction with chromatin. Yet, the genomic targets and functions of most ncRNAs are unknown. Here we use chromatin-associated RNA sequencing (ChAR-seq) to map the global network of ncRNA interactions with chromatin in human embryonic stem cells and the dynamic changes in interactions during differentiation into definitive endoderm. We uncover general principles governing the organization of the RNA-chromatin interactome, demonstrating that nearly all ncRNAs exclusively interact with genes in close three-dimensional proximity to their locus and provide a model predicting the interactome. We uncover RNAs that interact with many loci across the genome and unveil thousands of unannotated RNAs that dynamically interact with chromatin. By relating the dynamics of the interactome to changes in gene expression, we demonstrate that activation or repression of individual genes is unlikely to be controlled by a single ncRNA. |
format | Online Article Text |
id | pubmed-10539311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105393112023-09-30 Global mapping of RNA-chromatin contacts reveals a proximity-dominated connectivity model for ncRNA-gene interactions Limouse, Charles Smith, Owen K. Jukam, David Fryer, Kelsey A. Greenleaf, William J. Straight, Aaron F. Nat Commun Article Non-coding RNAs (ncRNAs) are transcribed throughout the genome and provide regulatory inputs to gene expression through their interaction with chromatin. Yet, the genomic targets and functions of most ncRNAs are unknown. Here we use chromatin-associated RNA sequencing (ChAR-seq) to map the global network of ncRNA interactions with chromatin in human embryonic stem cells and the dynamic changes in interactions during differentiation into definitive endoderm. We uncover general principles governing the organization of the RNA-chromatin interactome, demonstrating that nearly all ncRNAs exclusively interact with genes in close three-dimensional proximity to their locus and provide a model predicting the interactome. We uncover RNAs that interact with many loci across the genome and unveil thousands of unannotated RNAs that dynamically interact with chromatin. By relating the dynamics of the interactome to changes in gene expression, we demonstrate that activation or repression of individual genes is unlikely to be controlled by a single ncRNA. Nature Publishing Group UK 2023-09-28 /pmc/articles/PMC10539311/ /pubmed/37770513 http://dx.doi.org/10.1038/s41467-023-41848-9 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 Limouse, Charles Smith, Owen K. Jukam, David Fryer, Kelsey A. Greenleaf, William J. Straight, Aaron F. Global mapping of RNA-chromatin contacts reveals a proximity-dominated connectivity model for ncRNA-gene interactions |
title | Global mapping of RNA-chromatin contacts reveals a proximity-dominated connectivity model for ncRNA-gene interactions |
title_full | Global mapping of RNA-chromatin contacts reveals a proximity-dominated connectivity model for ncRNA-gene interactions |
title_fullStr | Global mapping of RNA-chromatin contacts reveals a proximity-dominated connectivity model for ncRNA-gene interactions |
title_full_unstemmed | Global mapping of RNA-chromatin contacts reveals a proximity-dominated connectivity model for ncRNA-gene interactions |
title_short | Global mapping of RNA-chromatin contacts reveals a proximity-dominated connectivity model for ncRNA-gene interactions |
title_sort | global mapping of rna-chromatin contacts reveals a proximity-dominated connectivity model for ncrna-gene interactions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10539311/ https://www.ncbi.nlm.nih.gov/pubmed/37770513 http://dx.doi.org/10.1038/s41467-023-41848-9 |
work_keys_str_mv | AT limousecharles globalmappingofrnachromatincontactsrevealsaproximitydominatedconnectivitymodelforncrnageneinteractions AT smithowenk globalmappingofrnachromatincontactsrevealsaproximitydominatedconnectivitymodelforncrnageneinteractions AT jukamdavid globalmappingofrnachromatincontactsrevealsaproximitydominatedconnectivitymodelforncrnageneinteractions AT fryerkelseya globalmappingofrnachromatincontactsrevealsaproximitydominatedconnectivitymodelforncrnageneinteractions AT greenleafwilliamj globalmappingofrnachromatincontactsrevealsaproximitydominatedconnectivitymodelforncrnageneinteractions AT straightaaronf globalmappingofrnachromatincontactsrevealsaproximitydominatedconnectivitymodelforncrnageneinteractions |