Publication:
Repeat RNAs associate with replication forks and post-replicative DNA.

dc.contributor.authorGylling, Helene M
dc.contributor.authorGonzalez-Aguilera, Cristina
dc.contributor.authorSmith, Martin A
dc.contributor.authorKaczorowski, Dominik C
dc.contributor.authorGroth, Anja
dc.contributor.authorLund, Anders H
dc.date.accessioned2023-02-08T14:49:59Z
dc.date.available2023-02-08T14:49:59Z
dc.date.issued2020-05-11
dc.description.abstractNoncoding 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.
dc.identifier.doi10.1261/rna.074757.120
dc.identifier.essn1469-9001
dc.identifier.pmcPMC7430672
dc.identifier.pmid32393525
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7430672/pdf
dc.identifier.unpaywallURLhttp://rnajournal.cshlp.org/content/26/9/1104.full.pdf
dc.identifier.urihttp://hdl.handle.net/10668/15545
dc.issue.number9
dc.journal.titleRNA (New York, N.Y.)
dc.journal.titleabbreviationRNA
dc.language.isoen
dc.organizationCentro Andaluz de Biología Molecular y Medicina Regenerativa-CABIMER
dc.page.number1104-1117
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rights.accessRightsopen access
dc.subjectDNA replication
dc.subjectRNA
dc.subjectchromatin
dc.subjectrepeats
dc.subject.meshCell Cycle
dc.subject.meshCell Line, Tumor
dc.subject.meshChromatin
dc.subject.meshDNA
dc.subject.meshDNA Replication
dc.subject.meshHeLa Cells
dc.subject.meshHistones
dc.subject.meshHumans
dc.subject.meshProtein Processing, Post-Translational
dc.subject.meshRNA
dc.titleRepeat RNAs associate with replication forks and post-replicative DNA.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number26
dspace.entity.typePublication

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