SRY, the mammalian Y-chromosomal sex-determining gene(1-3) encodes a protei
n characterized by a DNA-binding and -bending domain referred to as the HMG
box(4,5). Despite the pivotal role of this gene, only the HMG box region h
as been conserved through evolution(6,7), suggesting that SRY function depe
nds solely on the HMG box and therefore acts as an architectural transcript
ion factors. In mice (genus Mus) Sry also includes a large CAG trinucleotid
e repeat region encoding a carboxy-terminal glutamine-rich domain that acts
as a transcriptional trans-activator in vitro(9). The absence of this or a
ny other potential trans-activating domain in other mammals(1,9), however,
has raised doubts as to its biological relevance. To test directly whether
the glutamine-rich region is required for Sry function in vivo, we created
truncation mutations of the Mus musculus musculus Sry gene and tested their
ability to induce testis formation in XX embryos using a transgenic mouse
assay. Sry constructs that encode proteins lacking the glutamine-rich regio
n were unable to effect male sex determination, in contrast to their wild-t
ype counterparts. We conclude that the glutamine-rich repeat domain of the
mouse Sry protein has an essential role in sex determination in vivo, and t
hat Sry may act via a fundamentally different biochemical mechanism in mice
compared with other mammals.