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Human Molecular Genetics, 2001, Vol. 10, No. 22 2549-2556
© 2001 Oxford University Press

Mice overexpressing genes from the 22q11 region deleted in velo-cardio-facial syndrome/DiGeorge syndrome have middle and inner ear defects

Birgit Funke, Jonathan A. Epstein1, Lazaros K. Kochilas1, Min Min Lu1, Raj K. Pandita, Jun Liao, Ralf Bauerndistel2, Tanja Schüler2, Hubert Schorle2, M. Christian Brown3, Joe Adams3 and Bernice E. Morrow+

Department of Molecular Genetics, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA, 1Cardiovascular Division, University of Pennsylvania, 954 BRB II, 421 Curie Boulevard, Philadelphia, PA 19104, USA, 2Forschungszentrum Karlsruhe, Institut fuer Toxikologie und Genetik, Postfach 3640, 76133 Karlsruhe, Germany and 3Eaton-Peabody Laboratory, Department of Otology and Laryngology, Harvard Medical School, Massachusetts Eye and Ear Infirmary, 243 Charles Street, Boston, MA 02114, USA

Velo-cardio-facial syndrome/DiGeorge syndrome (VCFS/DGS) is a congenital anomaly disorder associated with hemizygous 22q11 deletions. We previously showed that bacterial artificial chromosome (BAC) transgenic mice overexpressing four transgenes, PNUTL1, (CDCrel-1), GP1Bß, TBX1 and WDR14, had reduced viability, cardiovascular malformations and thymus gland hypoplasia. Since these are hallmark features of VCFS/DGS, we analyzed the mice for additional anomalies. We found that the mice have important defects in the middle and inner ear that are directly relevant to the disorder. The most striking defect was the presence of chronic otitis media, a common finding in VCFS/DGS patients. In addition, the mice had a hyperactive circling behavior and sensorineural hearing loss. This was associated with middle and inner ear malformations, analogous to Mondini dysplasia in humans reported to occur in VCFS/DGS patients. We propose that overexpression of one or more of the transgenes is responsible for the etiology of the ear defects in the mice. Based upon its pattern of expression in the ear and functional studies of the gene, TbX1 likely plays a central role. Haploinsufficiency of TBX1 may be responsible for ear disorders in VCFS/DGS patients.

+ To whom correspondence should be addressed. Tel: +1 718 430 4274; Fax: +1 718 430 8778; Email: morrow@aecom.yu.edu


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