Sex determination involves synergistic action of SRY and SF1 on a specific Sox9 enhancer.
The mammalian Y chromosome acts as a dominant male determinant as a result of the action of a single gene, Sry, whose role in sex determination is to initiate testis rather than ovary development from early bipotential gonads. It does so by triggering the differentiation of Sertoli cells from supporting cell precursors, which would otherwise give follicle cells. The related autosomal gene Sox9 is also known from loss-of-function mutations in mice and humans to be essential for Sertoli cell differentiation; moreover, its abnormal expression in an XX gonad can lead to male development in the absence of Sry. These genetic data, together with the finding that Sox9 is upregulated in Sertoli cell precursors just after SRY expression begins, has led to the proposal that Sox9 could be directly regulated by SRY. However, the mechanism by which SRY action might affect Sox9 expression was not understood. Here we show that SRY binds to multiple elements within a Sox9 gonad-specific enhancer in mice, and that it does so along with steroidogenic factor 1 (SF1, encoded by the gene Nr5a1 (Sf1)), an orphan nuclear receptor. Mutation, co-transfection and sex-reversal studies all point to a feedforward, self-reinforcing pathway in which SF1 and SRY cooperatively upregulate Sox9 and then, together with SF1, SOX9 also binds to the enhancer to help maintain its own expression after that of SRY has ceased. Our results open up the field, permitting further characterization of the molecular mechanisms regulating sex determination and how they have evolved, as well as how they fail in cases of sex reversal.
Pubmed ID: 18454134
June 12, 2008
- Agency: Medical Research Council, Id: MC_U117562207
- Agency: Medical Research Council, Id:
- Chromatin Immunoprecipitation
- Enhancer Elements, Genetic
- Gene Expression Regulation, Developmental
- Gene Library
- High Mobility Group Proteins
- SOX9 Transcription Factor
- Sex Determination Processes
- Sex-Determining Region Y Protein
- Steroidogenic Factor 1
- Transcription Factors
- Campomelic dysplasia with autosomal sex reversal is related to genes SOX9, CMD1, SRA1 which are autosomal dominant according to the OMIM database.
- 46XY sex reversal 3 is related to genes NR5A1, FTZF1, FTZ1, SF1, AD4BP, POF7, SRXY3, SPGF8.
- Premature ovarian failure 7 is related to genes NR5A1, FTZF1, FTZ1, SF1, AD4BP, POF7, SRXY3, SPGF8.
- 46XX sex reversal 1 is related to genes SRY, TDF, TDY, SRXX1, SRXY1.
- Campomelic dysplasia is related to genes SOX9, CMD1, SRA1 which are autosomal dominant according to the OMIM database.
- Spermatogenic failure 8 is related to genes NR5A1, FTZF1, FTZ1, SF1, AD4BP, POF7, SRXY3, SPGF8 which are autosomal recessive according to the OMIM database.
- Acampomelic campomelic dysplasia is related to genes SOX9, CMD1, SRA1 which are autosomal dominant according to the OMIM database.
- 46XY sex reversal 1 is related to genes SRY, TDF, TDY, SRXX1, SRXY1.