Distal-less homeobox genes Dlx5/6 regulate Mullerian duct regression

Dlx5 and Dlx6 encode distal-less homeodomain transcription factors that are present in the genome as a linked pair at a single locus. Dlx5 and Dlx6 have redundant roles in craniofacial, skeletal, and uterine development. Previously, we performed a transcriptome comparison for anti-Mullerian hormone (AMH)-induced genes expressed in the Mullerian duct mesenchyme of male and female mouse embryos. In that study, we found that Dlx5 transcripts were nearly seven-fold higher in males compared to females and Dlx6 transcripts were found only in males, suggesting they may be AMH-induced genes. Therefore, we investigated the role of Dlx5 and Dlx6 during AMH-induced Mullerian duct regression. We found that Dlx5 was detected in the male Mullerian duct mesenchyme from E14.5 to E16.5. In contrast, in female embryos Dlx5 was detected in the Mullerian duct epithelium. Dlx6 expression in Mullerian duct mesenchyme was restricted to males. Dlx6 expression was not detected in female Mullerian duct mesenchyme or epithelium. Genetic experiments showed that AMH signaling is necessary for Dlx5 and Dlx6 expression. Mullerian duct regression was variable in Dlx5 homozygous mutant males at E16.5, ranging from regression like controls to a block in Mullerian duct regression. In E16.5 Dlx6 homozygous mutants, Mullerian duct tissue persisted primarily in the region adjacent to the testes. In Dlx5-6 double homozygous mutant males Mullerian duct regression was also found to be incomplete but more severe than either single mutant. These studies suggest that Dlx5 and Dlx6 act redundantly to mediate AMH-induced Mullerian duct regression during male differentiation.

Automated summary

Dlx5 and Dlx6 are linked transcription factors that play redundant roles in craniofacial, skeletal, and uterine development. They are potentially AMH-induced genes and are involved in mediating AMH-induced regression of the Mullerian duct. Their expression is regulated by AMH signaling, and their absence or mutations can lead to incomplete or severe Mullerian duct regression.