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Repeat RNAs associate with replication forks and post-replicative DNA
Noncoding RNA has a proven ability to direct and regulate chromatin modifications by acting as scaffolds between DNA and histone-modifying complexes. However, it is unknown if ncRNA plays any role in DNA replication and epigenome maintenance, including histone eviction and reinstallment of histone m...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7430672/ https://www.ncbi.nlm.nih.gov/pubmed/32393525 http://dx.doi.org/10.1261/rna.074757.120 |
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author | Gylling, Helene M. Gonzalez-Aguilera, Cristina Smith, Martin A. Kaczorowski, Dominik C. Groth, Anja Lund, Anders H. |
author_facet | Gylling, Helene M. Gonzalez-Aguilera, Cristina Smith, Martin A. Kaczorowski, Dominik C. Groth, Anja Lund, Anders H. |
author_sort | Gylling, Helene M. |
collection | PubMed |
description | Noncoding RNA has a proven ability to direct and regulate chromatin modifications by acting as scaffolds between DNA and histone-modifying complexes. However, it is unknown if ncRNA plays any role in DNA replication and epigenome maintenance, including histone eviction and reinstallment of histone modifications after genome duplication. Isolation of nascent chromatin has identified a large number of RNA-binding proteins in addition to unknown components of the replication and epigenetic maintenance machinery. Here, we isolated and characterized long and short RNAs associated with nascent chromatin at active replication forks and track RNA composition during chromatin maturation across the cell cycle. Shortly after fork passage, GA-rich-, alpha- and TElomeric Repeat-containing RNAs (TERRA) are associated with replicated DNA. These repeat containing RNAs arise from loci undergoing replication, suggesting an interaction in cis. Post-replication during chromatin maturation, and even after mitosis in G1, the repeats remain enriched on DNA. This suggests that specific types of repeat RNAs are transcribed shortly after DNA replication and stably associate with their loci of origin throughout the cell cycle. The presented method and data enable studies of RNA interactions with replication forks and post-replicative chromatin and provide insights into how repeat RNAs and their engagement with chromatin are regulated with respect to DNA replication and across the cell cycle. |
format | Online Article Text |
id | pubmed-7430672 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-74306722021-09-01 Repeat RNAs associate with replication forks and post-replicative DNA Gylling, Helene M. Gonzalez-Aguilera, Cristina Smith, Martin A. Kaczorowski, Dominik C. Groth, Anja Lund, Anders H. RNA Article Noncoding RNA has a proven ability to direct and regulate chromatin modifications by acting as scaffolds between DNA and histone-modifying complexes. However, it is unknown if ncRNA plays any role in DNA replication and epigenome maintenance, including histone eviction and reinstallment of histone modifications after genome duplication. Isolation of nascent chromatin has identified a large number of RNA-binding proteins in addition to unknown components of the replication and epigenetic maintenance machinery. Here, we isolated and characterized long and short RNAs associated with nascent chromatin at active replication forks and track RNA composition during chromatin maturation across the cell cycle. Shortly after fork passage, GA-rich-, alpha- and TElomeric Repeat-containing RNAs (TERRA) are associated with replicated DNA. These repeat containing RNAs arise from loci undergoing replication, suggesting an interaction in cis. Post-replication during chromatin maturation, and even after mitosis in G1, the repeats remain enriched on DNA. This suggests that specific types of repeat RNAs are transcribed shortly after DNA replication and stably associate with their loci of origin throughout the cell cycle. The presented method and data enable studies of RNA interactions with replication forks and post-replicative chromatin and provide insights into how repeat RNAs and their engagement with chromatin are regulated with respect to DNA replication and across the cell cycle. Cold Spring Harbor Laboratory Press 2020-09 /pmc/articles/PMC7430672/ /pubmed/32393525 http://dx.doi.org/10.1261/rna.074757.120 Text en © 2020 Gylling et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Article Gylling, Helene M. Gonzalez-Aguilera, Cristina Smith, Martin A. Kaczorowski, Dominik C. Groth, Anja Lund, Anders H. Repeat RNAs associate with replication forks and post-replicative DNA |
title | Repeat RNAs associate with replication forks and post-replicative DNA |
title_full | Repeat RNAs associate with replication forks and post-replicative DNA |
title_fullStr | Repeat RNAs associate with replication forks and post-replicative DNA |
title_full_unstemmed | Repeat RNAs associate with replication forks and post-replicative DNA |
title_short | Repeat RNAs associate with replication forks and post-replicative DNA |
title_sort | repeat rnas associate with replication forks and post-replicative dna |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7430672/ https://www.ncbi.nlm.nih.gov/pubmed/32393525 http://dx.doi.org/10.1261/rna.074757.120 |
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