Shen W H, Moore C C, Ikeda Y, Parker K L, Ingraham H A
Department of Obstetrics, Gynocology, and Reproductive Sciences, University of California, San Francisco 94143-0556.
Cell. 1994 Jun 3;77(5):651-61. doi: 10.1016/0092-8674(94)90050-7.
Normal male sex differentiation requires that Sertoli cells in the embryonic testes produce müllerian inhibiting substance (MIS), a TGF beta-like hormone that causes müllerian duct regression. In primary Sertoli cells, the orphan nuclear receptor, steroidogenic factor 1 (SF-1), regulates the MIS gene by binding to a conserved upstream regulatory element. In heterologous (HeLa) cells, MIS gene activation by SF-1 requires removal of the SF-1 ligand-binding domain, implicating a Sertoli cell-specific ligand or cofactor. Finally, the sexually dimorphic expression of SF-1 during development coincides with MIS expression and müllerian duct regression. We propose that SF-1 regulates MIS in vivo and participates directly in the process of mammalian sex determination.
正常的男性性别分化要求胚胎睾丸中的支持细胞产生苗勒管抑制物质(MIS),这是一种TGF-β样激素,可导致苗勒管退化。在原代支持细胞中,孤儿核受体类固醇生成因子1(SF-1)通过与保守的上游调控元件结合来调节MIS基因。在异源(HeLa)细胞中,SF-1激活MIS基因需要去除SF-1配体结合域,这暗示存在一种支持细胞特异性配体或辅因子。最后,发育过程中SF-1的性别二态性表达与MIS表达和苗勒管退化同时出现。我们提出,SF-1在体内调节MIS,并直接参与哺乳动物性别决定过程。