Wnt-dependent regulation of inner ear morphogenesis is balanced by the opposing and supporting roles of Shh

  1. Martin M. Riccomagno1,2,
  2. Shinji Takada3, and
  3. Douglas J. Epstein1,4
  1. 1Department of Genetics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA; 2Institute of Cell Biology and Neuroscience, University of Buenos Aires School of Medicine, 1121 Buenos Aires, Argentina; 3Okazaki Institute for Integrative Biosciences, National Institutes of Natural Sciences Okazaki 444 8787, Japan

Abstract

The inner ear is partitioned along its dorsal/ventral axis into vestibular and auditory organs, respectively. Gene expression studies suggest that this subdivision occurs within the otic vesicle, the tissue from which all inner ear structures are derived. While the specification of ventral otic fates is dependent on Shh secreted from the notochord, the nature of the signal responsible for dorsal otic development has not been described. In this study, we demonstrate that Wnt signaling is active in dorsal regions of the otic vesicle, where it functions to regulate the expression of genes (Dlx5/6 and Gbx2) necessary for vestibular morphogenesis. We further show that the source of Wnt impacting on dorsal otic development emanates from the dorsal hindbrain, and identify Wnt1 and Wnt3a as the specific ligands required for this function. The restriction of Wnt target genes to the dorsal otocyst is also influenced by Shh. Thus, a balance between Wnt and Shh signaling activities is key in distinguishing between vestibular and auditory cell types.

Keywords

Footnotes

  • Article published online ahead of print. Article and publication date are at http://www.genesdev.org/cgi/doi/10.1101/gad.1303905.

  • 4 Corresponding author.

    4 E-MAIL epsteind{at}mail.med.upenn.edu; FAX (215) 573-5892.

    • Accepted May 13, 2005.
    • Received February 9, 2005.
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