The mitotic STAG3–cohesin complex shapes male germline nucleome [ChIP-seq]

Germ cells are unique in that they tailor chromatin toward generating totipotency. Accordingly, mammalian spermatogonia, including spermatogonial stem cells (SSCs) which constitute the source for male gametes, acquire distinctive chromatin organization with weak insulation, but the underlying mechanism remains unknown. Here, we show that STAG3, this far known to exclusively form meiotic cohesins, generates a mitotic cohesin for male germline nucleome programming in mice. Due to its shorter chromatin residence, STAG3–cohesin attenuates topologically associating domains (TADs), rewires enhancer–promoter and Polycomb-mediated repressive interactions, and facilitates finer and more strengthened compartments, establishing a distinctive spermatogonial nucleome. Moreover, in the absence of STAG3–cohesin, SSCs show an impaired differentiation priming for spermatogenesis. Mitotic STAG3–cohesin is also expressed in human B cells and their malignant variations, promoting their propagation. Our findings on mitotic STAG3–cohesin elucidate a principle of male germline nucleome programming, demonstrate an unexpected mitotic role for STAG3 and might potentially improve understanding of human malignancies. Overall design: ChIP-seq against RAD21, STAG1, STAG2, STAG3, CTCF, GFP, H3K27ac, H3K27me3, H3K9me3 for STAG3-cohesin characterization in Stag3 KO, Stag1-only, Stag2-only, Stag3-only, and WT GSCs, Stag3-only and WT ESCs, WT EpiLCs, d2 PGCLCs and d4c7 PGCLCs.