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Single cell ATAC-seq analysis of H3.3K4M WT and Hom brain samples (10X Genomics Multiome)

GSE293655 Mus musculus Genome binding/occupancy profiling by high throughput sequencing 16 samples 2025/07/14 GPL24247
Summary
Methylation of lysine4 on Histone H3 (H3K4) is require for promoter and enhancer activation at gene loci and presents distinct methylation patterns over developmental gene clusters. Disrupting in the writer, eraser and reader of H3K4 methylation is associated with developmental syndromes. However, less studies focus on the role of H3K4 methylation in development of interneuron and hypothalamus. Here, we explore the role of H3K4 methylation in the medial ganglionic eminence (MGE) derive interneuron and hypothalamus by directly mutating the lysine 4 on H3.3 to the methionine in mice.
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