Dynamics of RNA m5C modification during brain development

dc.contributor.authorJohnson, Zacharyen
dc.contributor.authorXu, Xiguangen
dc.contributor.authorLin, Yuen
dc.contributor.authorXie, Hehuangen
dc.date.accessioned2025-05-12T12:55:52Zen
dc.date.available2025-05-12T12:55:52Zen
dc.date.issued2023-05en
dc.description.abstractPost-transcriptional RNA modifications have been recognized as key regulators of neuronal differentiation and synapse development in the mammalian brain. While distinct sets of 5-methylcytosine (m5C) modified mRNAs have been detected in neuronal cells and brain tissues, no study has been performed to characterize methylated mRNA profiles in the developing brain. Here, together with regular RNA-seq, we performed transcriptome-wide bisulfite sequencing to compare RNA cytosine methylation patterns in neural stem cells (NSCs), cortical neuronal cultures, and brain tissues at three postnatal stages. Among 501 m5C sites identified, approximately 6% are consistently methylated across all five conditions. Compared to m5C sites identified in NSCs, 96% of them were hypermethylated in neurons and enriched for genes involved in positive transcriptional regulation and axon extension. In addition, brains at the early postnatal stage demonstrated substantial changes in both RNA cytosine methylation and gene expression of RNA cytosine methylation readers, writers, and erasers. Furthermore, differentially methylated transcripts were significantly enriched for genes regulating synaptic plasticity. Altogether, this study provides a brain epitranscriptomic dataset as a new resource and lays the foundation for further investigations into the role of RNA cytosine methylation during brain development.en
dc.description.versionPublished versionen
dc.format.extent11 page(s)en
dc.format.mimetypeapplication/pdfen
dc.identifierARTN 110604 (Article number)en
dc.identifier.doihttps://doi.org/10.1016/j.ygeno.2023.110604en
dc.identifier.eissn1089-8646en
dc.identifier.issn0888-7543en
dc.identifier.issue3en
dc.identifier.orcidXie, Hehuang [0000-0001-5739-1653]en
dc.identifier.orcidXu, Xiguang [0000-0001-6862-7545]en
dc.identifier.otherS0888-7543(23)00048-4 (PII)en
dc.identifier.pmid36889368en
dc.identifier.urihttps://hdl.handle.net/10919/131424en
dc.identifier.volume115en
dc.language.isoenen
dc.publisherElsevieren
dc.relation.urihttps://www.ncbi.nlm.nih.gov/pubmed/36889368en
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en
dc.subjectBrain developmenten
dc.subjectNeuronen
dc.subjectNeural stem cellen
dc.subjectRNA cytosine methylationen
dc.subjectRNA bisulfite sequencingen
dc.subjectRNA-seqen
dc.subject.meshBrainen
dc.subject.meshAnimalsen
dc.subject.meshMammalsen
dc.subject.meshCytosineen
dc.subject.meshRNAen
dc.subject.meshRNA, Messengeren
dc.subject.meshDNA Methylationen
dc.subject.meshTranscriptomeen
dc.titleDynamics of RNA m<sup>5</sup>C modification during brain developmenten
dc.title.serialGenomicsen
dc.typeArticle - Refereeden
dc.type.dcmitypeTexten
dc.type.otherArticleen
dc.type.otherJournalen
dcterms.dateAccepted2023-03-03en
pubs.organisational-groupVirginia Techen
pubs.organisational-groupVirginia Tech/Veterinary Medicineen
pubs.organisational-groupVirginia Tech/Veterinary Medicine/Biomedical Sciences and Pathobiologyen
pubs.organisational-groupVirginia Tech/Faculty of Health Sciencesen
pubs.organisational-groupVirginia Tech/All T&R Facultyen
pubs.organisational-groupVirginia Tech/Veterinary Medicine/CVM T&R Facultyen
pubs.organisational-groupVirginia Tech/Post-docsen
pubs.organisational-groupVirginia Tech/Veterinary Medicine/Biomedical Sciences and Pathobiology/Otheren

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