Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2176886 | Developmental Cell | 2013 | 15 Pages |
•Loss of Six1/Six4 leads to impaired Sry expression and gonadal size reduction•Sry transgene rescued male differentiation but not initial precursor cell growth•Six1/Six4 regulate Fog2, which is a direct regulator of Sry expression•Six1/Six4 regulate Nr5a1, which controls gonad size in an independent pathway
SummaryThe Y-linked gene Sry regulates mammalian sex determination in bipotential embryonic gonads. Here, we report that the transcription factors Six1 and Six4 are required for male gonadal differentiation. Loss of Six1 and Six4 together, but neither alone, resulted in a male-to-female sex-reversal phenotype in XY mutant gonads accompanied by a failure in Sry activation. Decreased gonadal precursor cell formation at the onset of Sry expression and a gonadal size reduction in both sexes were also found in mutant embryos. Forced Sry transgene expression in XY mutant gonads rescued testicular development but not the initial disruption to precursor growth. Furthermore, we identified two downstream targets of Six1/Six4 in gonadal development, Fog2 (Zfpm2) and Nr5a1 (Ad4BP/Sf1). These two distinct Six1/Six4-regulated pathways are considered to be crucial for gonadal development. The regulation of Fog2 induces Sry expression in male sex determination, and the regulation of Nr5a1 in gonadal precursor formation determines gonadal size.
Graphical AbstractFigure optionsDownload full-size imageDownload high-quality image (143 K)Download as PowerPoint slide