AI Article Synopsis

  • Gonadal sex determination is influenced by Sertoli cells in testes and granulosa cells in ovaries, but the role of epigenetics in suppressing female differentiation in testes is not well understood.
  • * In this study, researchers demonstrated that Polycomb repressive complex 1 (PRC1) is crucial for preventing a female gene regulatory network in Sertoli cells, as its disruption leads to cell proliferation issues and eventual degeneration of adult testes.
  • * The findings reveal that PRC1 suppresses genes necessary for female cell type development through specific chromatin modifications, thus maintaining Sertoli cell identity and preventing ovarian differentiation.

Article Abstract

Gonadal sex determination and differentiation are controlled by somatic support cells of testes (Sertoli cells) and ovaries (granulosa cells). In testes, the epigenetic mechanism that maintains chromatin states responsible for suppressing female sexual differentiation remains unclear. Here, we show that Polycomb repressive complex 1 (PRC1) suppresses a female gene regulatory network in postnatal Sertoli cells. We genetically disrupted PRC1 function in embryonic Sertoli cells after sex determination, and we found that PRC1-depleted postnatal Sertoli cells exhibited defective proliferation and cell death, leading to the degeneration of adult testes. In adult Sertoli cells, PRC1 suppressed specific genes required for granulosa cells, thereby inactivating the female gene regulatory network. Chromatin regions associated with female-specific genes were marked by Polycomb-mediated repressive modifications: PRC1-mediated H2AK119ub and PRC2-mediated H3K27me3. Taken together, this study identifies a critical Polycomb-based mechanism that suppresses ovarian differentiation and maintains Sertoli cell fate in adult testes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10403552PMC
http://dx.doi.org/10.1038/s41419-023-05996-6DOI Listing

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