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Molecular and Cellular Biology, November 2004, p. 9736-9743, Vol. 24, No. 22
0270-7306/04/$08.00+0 DOI: 10.1128/MCB.24.22.9736-9743.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
Neonatal Lethality of LGR5 Null Mice Is Associated with Ankyloglossia and Gastrointestinal Distension
Hiroki Morita,1
Sabine Mazerbourg,1
Donna M. Bouley,2
Ching-Wei Luo,1
Kazuhiro Kawamura,1
Yoshimitsu Kuwabara,1
Helene Baribault,3
Hui Tian,3 and
Aaron J. W. Hsueh1*
Division of Reproductive Biology, Department of Obstetrics and Gynecology,1
Department of Comparative Medicine, Stanford University School of Medicine, Stanford,2
Tularik, Inc., South San Francisco, California3
Received 11 May 2004/
Returned for modification 23 June 2004/
Accepted 15 August 2004
The physiological role of an orphan G protein-coupled receptor, LGR5, was investigated by targeted deletion of this seven-transmembrane protein containing a large N-terminal extracellular domain with leucine-rich repeats. LGR5 null mice exhibited 100% neonatal lethality characterized by gastrointestinal tract dilation with air and an absence of milk in the stomach. Gross and histological examination revealed fusion of the tongue to the floor of oral cavity in the mutant newborns and immunostaining of LGR5 expression in the epithelium of the tongue and in the mandible of the wild-type embryos. The observed ankyloglossia phenotype provides a model for understanding the genetic basis of this craniofacial defect in humans and an opportunity to elucidate the physiological role of the LGR5 signaling system during embryonic development.
* Corresponding author. Mailing address: Division of Reproductive Biology, Stanford University School of Medicine, Stanford, CA 94305-5317. Phone: (650) 725-6802. Fax: (650) 725-7102. E-mail:
aaron.hsueh{at}stanford.edu.
Molecular and Cellular Biology, November 2004, p. 9736-9743, Vol. 24, No. 22
0022-538X/04/$08.00+0 DOI: 10.1128/MCB.24.22.9736-9743.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
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