β-Catenin is essential for Müllerian duct regression during male sexual differentiation

Akio Kobayashi, C. Allison Stewart, Ying Wang, Kaoru Fujioka, Nicholas C. Thomas, Soazik P. Jamin, Richard R. Behringer

Research output: Contribution to journalArticlepeer-review

74 Scopus citations

Abstract

During male sexual differentiation, the transforming growth factor-β (TGF-β) signaling molecule anti-Müllerian hormone (AMH; also known as Müllerian inhibiting substance, MIS) is secreted by the fetal testes and induces regression of the Müllerian ducts, the primordia of the female reproductive tract organs. Currently, the molecular identity of downstream events regulated by the AMH signaling pathway remains unclear. We found that male-specific Wnt4 expression in mouse Müllerian duct mesenchyme depends upon AMH signaling, implicating the WNT pathway as a downstream mediator of Müllerian duct regression. Inactivation of β-catenin, a mediator of the canonical WNT pathway, did not affect AMH signaling activation in the Müllerian duct mesenchyme, but did block Müllerian duct regression. These data suggest that β-catenin mediates AMH signaling for Müllerian duct regression during male sexual differentiation.

Original languageEnglish (US)
Pages (from-to)1967-1975
Number of pages9
JournalDevelopment
Volume138
Issue number10
DOIs
StatePublished - May 2011

Keywords

  • AMH
  • MIS
  • Mouse
  • Müllerian duct regression
  • Wnt4
  • β-Catenin

ASJC Scopus subject areas

  • Molecular Biology
  • Developmental Biology

MD Anderson CCSG core facilities

  • Advanced Technology Genomics Core

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