Somatic cell‐derived BMPs induce premature meiosis in male germ cells during the embryonic stage by upregulating Dazl expression

Abstract

Although germ cell fate is believed to be determined by signaling factors from differentiated somatic cells, the molecular mechanism behind this process remains obscure. In this study, premature meiosis in male germ cells was observed during the embryonic stage by conditional activation of β‐catenin in Sertoli cells. Somatic and germ cell transcriptome results indicated that the BMP signaling pathway was enriched after β‐catenin activation. In addition, we observed a decreased DNA methylation within a reduction of DNMT3A in germ cells of β‐catenin activated testes and reversed increase after inhibiting BMP signaling pathway with LDN‐193189. We also found that Dazl expression was increased in β‐catenin activated testes and decreased after LDN treatment. Taken together, this study demonstrates that male germ cells entered meiosis prematurely during the embryonic stage after β‐catenin activated in Sertoli cells. BMP signaling pathway involved in germ cell meiosis initiation by mediating DNA methylation to induce meiotic genes expression.

The Regulation of Gonadal Somatic Cell Differentiation in Humans

“…Notably, different gonadal somatic cells exhibit different responses to BMP inhibition. BMP and RA signaling pathways play critical roles in regulating the meiosis of germ cells [6] , [20] , [21] , [22] . These results would provide important information for better understanding the regulation of meiosis initiation in germ cells.…”