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ATAC-seq of DP thymocytes from Suv39h1 and Suv39h2 double knockout chimeric mice

GSE256244 Mus musculus Genome binding/occupancy profiling by high throughput sequencing 4 samples Submitted 2024/03/27 Platform GPL30172
Summary
H3K9me3-dependent heterochromatin is critical for the silencing of repeat-rich pericentromeric regions and also has key roles in repressing lineage-inappropriate protein-coding genes for healthy cellular function. Within all eukaryotic nuclei, heterochromatin and euchromatin are spatially segregated, with euchromatin typically located in the nuclear interior and heterochromatin at the nuclear periphery. Here we investigate the changes in DNA accessibilty in the absence of H3K9me3-dependent heterochromatin by performing ATAC-seq in primary immune cells deficient in both Suv39h1 and Suv39h2 (Suv39DKO), the major mammalian histone methyltransferase enzymes which catalyse heterochromatic H3K9me3 deposition.
Published in
Suv39h-catalyzed H3K9me3 is critical for euchromatic genome organization and the maintenance of gene transcription
Keenan CR, Coughlan HD, Iannarella N et al. · Genome research 2024 · PMID 38719473 · doi:10.1101/gr.279119.124
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Also filed as BioProject PRJNA1078779 and SRA study SRP490717. Searching any of these in the dataset finder brings you back here.

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