<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Matlik K</submitter><funding>NINDS NIH HHS</funding><pubmed_abstract>Developing neurons undergo a progression of morphological and gene expression changes as they transition from neuronal progenitors to mature, multipolar neurons. Here we use RNA-seq and H3K4me3 and H3K27me3 ChIP-seq to analyze how chromatin modifications control gene expression in a specific type of CNS neuron, the mouse cerebellar granule cell (GC). We find that in proliferating GC progenitors (GCPs), H3K4me3/H3K27me3 bivalency is common at neuronal genes and undergoes dynamic changes that correlate with gene expression during migration and circuit formation. Expressing a fluorescent sensor for bivalent H3K4me3 and H3K27me3 domains revealed subnuclear bivalent foci in proliferating GCPs. Inhibiting H3K27 methyltransferases EZH1 and EZH2 &lt;i>in vitro&lt;/i> and in organotypic cerebellar slices</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2023.02.02.526881</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9915618</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Histone bivalency regulates the timing of cerebellar granule cell development.</pubmed_title><pmcid>PMC9915618</pmcid><funding_grant_id>R21 NS114545</funding_grant_id><pubmed_authors>Allis CD</pubmed_authors><pubmed_authors>Matlik K</pubmed_authors><pubmed_authors>Paul MR</pubmed_authors><pubmed_authors>Hatten ME</pubmed_authors><pubmed_authors>Govek EE</pubmed_authors></additional><is_claimable>false</is_claimable><name>Histone bivalency regulates the timing of cerebellar granule cell development.</name><description>Developing neurons undergo a progression of morphological and gene expression changes as they transition from neuronal progenitors to mature, multipolar neurons. Here we use RNA-seq and H3K4me3 and H3K27me3 ChIP-seq to analyze how chromatin modifications control gene expression in a specific type of CNS neuron, the mouse cerebellar granule cell (GC). We find that in proliferating GC progenitors (GCPs), H3K4me3/H3K27me3 bivalency is common at neuronal genes and undergoes dynamic changes that correlate with gene expression during migration and circuit formation. Expressing a fluorescent sensor for bivalent H3K4me3 and H3K27me3 domains revealed subnuclear bivalent foci in proliferating GCPs. Inhibiting H3K27 methyltransferases EZH1 and EZH2 &lt;i>in vitro&lt;/i> and in organotypic cerebellar slices</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2026-04-08T14:22:17.152Z</modification><creation>2025-02-19T02:23:33.255Z</creation></dates><accession>S-EPMC9915618</accession><cross_references><pubmed>36778390</pubmed><doi>10.1101/2023.02.02.526881</doi></cross_references></HashMap>