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Histone bivalency regulates the timing of cerebellar granule cell development
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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9915618/ https://www.ncbi.nlm.nih.gov/pubmed/36778390 http://dx.doi.org/10.1101/2023.02.02.526881 |
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author | Mätlik, Kärt Govek, Eve-Ellen Paul, Matthew R. Allis, C. David Hatten, Mary E. |
author_facet | Mätlik, Kärt Govek, Eve-Ellen Paul, Matthew R. Allis, C. David Hatten, Mary E. |
author_sort | Mätlik, Kärt |
collection | PubMed |
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 in vitro and in organotypic cerebellar slices dramatically altered the expression of bivalent genes and induced the downregulation of migration-related genes and upregulation of synaptic genes, inhibited glial-guided migration, and accelerated terminal differentiation. Thus, histone bivalency is required to regulate the timing of the progression from progenitor cells to mature neurons. |
format | Online Article Text |
id | pubmed-9915618 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-99156182023-02-11 Histone bivalency regulates the timing of cerebellar granule cell development Mätlik, Kärt Govek, Eve-Ellen Paul, Matthew R. Allis, C. David Hatten, Mary E. bioRxiv Article 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 in vitro and in organotypic cerebellar slices dramatically altered the expression of bivalent genes and induced the downregulation of migration-related genes and upregulation of synaptic genes, inhibited glial-guided migration, and accelerated terminal differentiation. Thus, histone bivalency is required to regulate the timing of the progression from progenitor cells to mature neurons. Cold Spring Harbor Laboratory 2023-02-03 /pmc/articles/PMC9915618/ /pubmed/36778390 http://dx.doi.org/10.1101/2023.02.02.526881 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Mätlik, Kärt Govek, Eve-Ellen Paul, Matthew R. Allis, C. David Hatten, Mary E. Histone bivalency regulates the timing of cerebellar granule cell development |
title | Histone bivalency regulates the timing of cerebellar granule cell development |
title_full | Histone bivalency regulates the timing of cerebellar granule cell development |
title_fullStr | Histone bivalency regulates the timing of cerebellar granule cell development |
title_full_unstemmed | Histone bivalency regulates the timing of cerebellar granule cell development |
title_short | Histone bivalency regulates the timing of cerebellar granule cell development |
title_sort | histone bivalency regulates the timing of cerebellar granule cell development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9915618/ https://www.ncbi.nlm.nih.gov/pubmed/36778390 http://dx.doi.org/10.1101/2023.02.02.526881 |
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