A molecular approach to sex determination in mammals

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Abstract
Mammalian sex determination occurs in the gonad of the developing embryo. This process is dependent on the Y‐chromosome‐encoded Sry gene that acts in the somatic cells of the genital ridge. The transient nature of Sry gene expression suggests that it acts as a switch from one cell fate to another. One of the roles of Sry is to initiate the differentiation of Sertoli cells, which are the first cell type of the testis to be formed. Two genes are thought to be important in Sertoli cell differentiation and function, Sox9, an Sry‐related gene, and SF‐1, a nuclear hormone receptor. Sox9 is expressed in Sertoli cells throughout development of the mouse embryo, and inactivating mutations in this gene in humans give rise to XY females. SF‐1 is also expressed in Sertoli cells and is thought to activate the AMH gene – an early marker of these cells. DAX‐1, an X‐linked member of the nuclear hormone superfamily, is a candidate for a human condition in which duplication of regions of the X chromosome results in XY females. Expression of this gene during mouse development is associated with ovary development and is down‐regulated in the differentiating testis. Mutations in DAX‐1 in humans have shown that this gene is not necessary for testis development. The properties of the DAX‐1 gene suggest that it is important in ovary determination and might therefore be antagonistic to the action of the Sry gene. □ Sex determination, Sry gene, Sox9 gene, SF‐1 gene, AMH gene, DAX‐1 gene, ovary, testis