Requirement of Bmpr1a for Müllerian duct regression during male sexual development

Nat Genet. 2002 Nov;32(3):408-10. doi: 10.1038/ng1003. Epub 2002 Oct 7.


Elimination of the developing female reproductive tract in male fetuses is an essential step in mammalian sexual differentiation. In males, the fetal testis produces the transforming growth factor beta (TGF-beta) family member anti-Müllerian hormone (Amh, also known as Müllerian-inhibiting substance (Mis)), which causes regression of the Müllerian ducts, the primordia of the oviducts, uterus and upper vagina. Amh induces regression by binding to a specific type II receptor (Amhr2) expressed in the mesenchyme surrounding the ductal epithelium. Mutations in AMH or AMHR2 in humans and mice disrupt signaling, producing male pseudohermaphrodites that possess oviducts and uteri. The type I receptor and Smad proteins that are required in vivo for Müllerian duct regression have not yet been identified. Here we show that targeted disruption of the widely expressed type I bone morphogenetic protein (BMP) receptor Bmpr1a (also known as Alk3) in the mesenchymal cells of the Müllerian ducts leads to retention of oviducts and uteri in males. These results identify Bmpr1a as a type I receptor for Amh-induced regression of Müllerian ducts. Because Bmpr1a is evolutionarily conserved, these findings indicate that a component of the BMP signaling pathway has been co-opted during evolution for male sexual development in amniotes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Activin Receptors, Type I / genetics*
  • Activin Receptors, Type I / physiology*
  • Alleles
  • Animals
  • Bone Morphogenetic Protein Receptors, Type I
  • Exons
  • In Situ Hybridization
  • Ligands
  • Male
  • Mice
  • Mice, Transgenic
  • Models, Genetic
  • Mullerian Ducts / pathology*
  • Mullerian Ducts / physiology
  • Mutation*
  • Protein-Serine-Threonine Kinases*
  • Receptors, Growth Factor*
  • Recombination, Genetic
  • Sex Differentiation*
  • Testis / embryology*
  • Time Factors


  • Ligands
  • Receptors, Growth Factor
  • Protein-Serine-Threonine Kinases
  • Activin Receptors, Type I
  • Bmpr1a protein, mouse
  • Bone Morphogenetic Protein Receptors, Type I