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Transcription factor NFYA directs male meiotic entry by facilitating accessible chromatin at the promoters of genes expressed during meiosis [ATAC-seq]

GSE295941 Mus musculus Genome binding/occupancy profiling by high throughput sequencing 9 samples Submitted 2025/05/10 Platform GPL21626
Summary
Meiotic prophase I characterized by homologous recombination and synapsis is an intricate step for spermatogenesis. This process entails extensive changes to chromatin and transcription. Recent studies have revealed that prior to prophase I, accessible chromatin bound by paused Pol II at meiotic gene promoters is essential for their timely activation during later stages of prophase I. However, the factor responsible for promoting accessible chromatin at meiotic gene promoters before entry into prophase I is unknown. Here, we discovered that NFYA expressed in pre-meiotic germ cells promotes accessible chromatin at meiotic gene promoters. Concordantly, conditional germline deletion of Nfya in male mice blocks meiotic entry. Functionally, our spatial and single-cell ATAC-seq data revealed that loss of NFYA in pre-meiotic cells disrupts accessible chromatin at meiotic gene promoters. Our study identifies a pioneer role for NFYA in facilitating permissive chromatin at meiotic gene promoters before meiosis, thereby controlling the timely activation of meiotic genetic program during later meiosis.
Published in
Transcription factor NFYA directs male meiotic entry by regulating accessible chromatin at meiotic promoters in mice
Säflund M, Askari M, Eghbali A et al. · The EMBO journal 2026 · PMID 41857150 · doi:10.1038/s44318-026-00756-6
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Also filed as BioProject PRJNA1256837 and SRA study SRP582155. Searching any of these in the dataset finder brings you back here.

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