New clues to the puzzle of mammalian sex determination
© BioMed Central Ltd 2001
Published: 29 August 2001
WT1 and SOX9 are transcription factors with critical roles in mammalian sex determination and gonadal development. Recent studies in vivo clarify the roles of two alternative splice isoforms of WT1, and demonstrate that SOX9 can induce male sex determination.
Activation, repression, and interaction - the evidence so far
Previous studies have shed some light on the complex interrelationships among the sex determination and sexual differentiation genes in mammals (Figure 1). During male development, SRY activity leads to the expression of SOX9, which in turn activates transcription of Amh and genes required for testis development (reviewed in ). WT1 and SF1 form heterodimers and, together with SOX9, synergistically activate the expression of Amh [6,7]. WT1-KTS isoforms appear to play a role in the initial activation of SRY expression [8,9]. In female development, DAX1 antagonizes the activation of both Amh [6,10] and Sox9 (see ), probably through a direct association with SF1 [12,13]. Dax1 itself may be activated by WT1-KTS and SF1 [14,15].
The many roles of WT1
At least 24 different isoforms of WT1 have been described. The best-studied variants are known as WT1+KTS and WT1-KTS; they differ by the presence or absence, respectively, of a lysine-threonine-serine motif between the third and fourth zinc fingers. WT1+KTS associates with the spliceosome and binds to RNA, suggesting a role in RNA processing, whereas WT1-KTS exhibits diffuse nuclear staining and appears to act as a classical transcription factor [6,9,15,16,17]. Clinical and experimental data indicate that WT1 plays important roles in kidney and gonadal development. Wt1-null knockout mice die in utero with a complete absence of kidneys and gonads . Gonadal development is initiated but is then arrested at a very early stage, indicating a role for WT1 in early establishment of the genital ridges, in addition to roles in regulating sex-specific gene expression. WT1 mutations are associated with Wilms' tumor and several human conditions that involve developmental abnormalities of the kidneys and gonads . In Frasier syndrome, mutations that prevent the production of WT1+KTS act dominantly to cause male-to-female sex reversal, male pseudohermaphroditism and gonadal dysgenesis. In Denys-Drash Syndrome (DDS), mutations are found in the zinc-finger region of the protein, and act dominantly to cause urogenital abnormalities and small, degenerated ('streak') gonads.
KTS isoform-specific deletions of WT1 in mice
In order to clarify the etiology of Frasier and Denys-Drash syndromes, and to understand the distinct functions of WT1+KTS and WT1-KTS, Schedl and co-workers made isoform-specific deletions in mice by gene targeting . The authors refer to mice lacking WT1+KTS as Frasier mice, and to those lacking WT1-KTS as KTS mice.
Although heterozygous Frasier mice showed similar kidney pathology to human Frasier syndrome patients, two features of the mice generated in this study compromised their usefulness as models of human disease and tools for molecular analysis of the sex-determining pathway. First, neither mutant mouse showed gonadal abnormalities in the heterozygous state, unlike human Frasier and DDS patients. This observation is in accord with growing evidence that there are species differences with respect to critical gene threshold levels during sex determination [5,13]. Secondly, overall levels of Wt1 expression were not altered in either Frasier or KTS mice. This situation complicates analysis of the mice, because deletion of one WT1KTS isoform simultaneously causes overexpression of the other.
Phenotypes of WT1-isoform-specific knockout mice
Sry (11.5 dpc)
Sox9 (12.5 dpc)
Dax1 (11.5 dpc)
Amh (12.5 dpc)
Frasier mice (no WT1+KTS)
Similar or slight increase
relative to wild type*
KTS mice (no WT1-KTS)
- (+ in rare cells)
- (+ in rare cells)
Homozygous KTS mice (no WT1-KTS, increased WT1+KTS) died within 24 hours of birth. Both XX and XY KTS mice had small, poorly differentiated gonads and abnormal genital ducts at birth, a phenotype not unlike that of DDS patients. The reduction in gonadal size was less pronounced at 12.5 days post coitum (dpc), and was probably due to apoptosis, which the authors showed to be more prevalent than in the wild-type at 11.5 dpc. This observation suggests that WT1-KTS is required for differentiation and survival of gonadal cells in both sexes. Sry expression levels were not determined, but expression levels of Dax1, Sox9 and Amh were low, perhaps directly resulting from a lack of activation of Sry, Dax1 and Amh by WT1-KTS (Figure 1, Table 1). The authors suggest that these low expression levels indicate that the sex-determination pathway is compromised but not completely blocked in KTS mice. Intriguingly, neither Frasier nor KTS mice showed the complete blockage of genital-ridge development shown by Wt1-null mice. This observation suggests that some form of WT1, irrespective of the presence or absence of KTS, is essential for early genital-ridge development.
Sox9 induces testis development in XX mice
Sox9 is expressed specifically in the developing male gonad in a number of species; mutations in SOX9 are associated with male-to-female sex reversal in humans, and derepression of Sox9 in 'Odsex' XX mice and duplication of the SOX9 gene in a human can induce female-to-male sex reversal (reviewed in ). These and other lines of evidence have indicated that SOX9 is necessary and sufficient to induce male sex determination in mammals.
A new study, also from Schedl's group, shows that ectopic expression of Sox9, driven by the regulatory sequences of Wt1 in a yeast artificial chromosome (YAC), is sufficient to induce female-to-male sex reversal in XX mice . The phenotype of these mice is not detectably different from that of sex-reversed XX mice produced by overexpression of Sry using its own regulatory sequences . It remains formally possible that SOX9 achieves this effect by acting as a molecular mimic of SRY, by virtue of the similar HMG domains of the two proteins; it will be of interest to determine whether other SOX proteins, when similarly mis-expressed, can elicit the same phenotype. This seems unlikely, however, given the differences in biochemical properties, interacting factors and target genes of the various SOX proteins, all of which share a similar HMG domain.
In combination with previous observations, it seems more likely that this study underlines the essential role Sox9 plays in mammalian sex determination, and implies that all downstream effects of Sry expression must feed through Sox9. In this scenario, Sry is merely a Y-chromosomal switch whose role is to activate Sox9, which is then responsible for initiating differentiation of bipotential supporting cells of the gonad into Sertoli cells, marking the beginning of male sexual differentiation in mammals. Further investigation is required, however, to determine just how similar the Wt1-Sox9 transgenic mice are to Sry transgenic mice, or indeed to normal XY mice, at the molecular and cellular levels.
The molecular genetics of sex determination in mammals is often described as a puzzle with many missing pieces. Although no new pieces have been identified in these studies, they do provide new information regarding the range of function of two known proteins, WT1 and SOX9.
Our work is supported by the National Health and Medical Research Council of Australia and by the Australian Research Council. P.K. is an Australian Senior Research Fellow of the Australian Research Council.
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