| Literature DB >> 36103831 |
José Miguel Fernández-Justel1, Cristina Santa-María1, Sara Martín-Vírgala1, Shreya Ramesh1, Alberto Ferrera-Lagoa1, Mónica Salinas-Pena2, Javier Isoler-Alcaraz1, Magdalena M Maslon3, Albert Jordan2, Javier F Cáceres3, María Gómez4.
Abstract
Linker histones are highly abundant chromatin-associated proteins with well-established structural roles in chromatin and as general transcriptional repressors. In addition, it has been long proposed that histone H1 exerts context-specific effects on gene expression. Here, we identify a function of histone H1 in chromatin structure and transcription using a range of genomic approaches. In the absence of histone H1, there is an increase in the transcription of non-coding RNAs, together with reduced levels of m6A modification leading to their accumulation on chromatin and causing replication-transcription conflicts. This strongly suggests that histone H1 prevents non-coding RNA transcription and regulates non-coding transcript turnover on chromatin. Accordingly, altering the m6A RNA methylation pathway rescues the replicative phenotype of H1 loss. This work unveils unexpected regulatory roles of histone H1 on non-coding RNA turnover and m6A deposition, highlighting the intimate relationship between chromatin conformation, RNA metabolism, and DNA replication to maintain genome performance.Entities:
Keywords: CP: Molecular biology; R-loops; chromatin RNAs; chromatin conformation; histone H1; lncRNAs; m6A; mESCs; replication-transcription conflicts; replicative stress
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Year: 2022 PMID: 36103831 PMCID: PMC7613722 DOI: 10.1016/j.celrep.2022.111329
Source DB: PubMed Journal: Cell Rep Impact factor: 9.995