Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice (original) (raw)
- Letter
- Published: 01 March 2001
- Francesca Vitelli1,
- Hong Su2,3,
- Masae Morishima1,
- Tuong Huynh1,
- Tiziano Pramparo1,
- Vesna Jurecic4,
- George Ogunrinu5,
- Helen F. Sutherland6,
- Peter J. Scambler6,
- Allan Bradley2,3,7,8 &
- …
- Antonio Baldini1,2,3
Nature volume 410, pages 97–101 (2001)Cite this article
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Abstract
DiGeorge syndrome is characterized by cardiovascular, thymus and parathyroid defects and craniofacial anomalies, and is usually caused by a heterozygous deletion of chromosomal region 22q11.2 (del22q11) (ref. 1). A targeted, heterozygous deletion, named Df(16)1, encompassing around 1 megabase of the homologous region in mouse causes cardiovascular abnormalities characteristic of the human disease2. Here we have used a combination of chromosome engineering and P1 artificial chromosome transgenesis to localize the haploinsufficient gene in the region, Tbx1. We show that Tbx1, a member of the T-box transcription factor family, is required for normal development of the pharyngeal arch arteries in a gene dosage-dependent manner. Deletion of one copy of Tbx1 affects the development of the fourth pharyngeal arch arteries, whereas homozygous mutation severely disrupts the pharyngeal arch artery system. Our data show that haploinsufficiency of Tbx1 is sufficient to generate at least one important component of the DiGeorge syndrome phenotype in mice, and demonstrate the suitability of the mouse for the genetic dissection of microdeletion syndromes.
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Acknowledgements
We thank R. Behringer and P. Hastings for discussions and reading of the manuscript, and Y.-C. Cheah, S. Carattini-Rivera, G. C. Schuster, S.-S. Cheah and C. Roberts for technical contributions. A.B. is an investigator with the Howard Hughes Medical Institute. This work was funded in part by grants from the National Heart, Lung and Blood Institute and (to A.B.), from the American Heart Association Texas Affiliate (to E.A.L.), and from the British Heart Foundation and Wellcome Trust (to P.J.S.). Support from the Baylor Mental Retardation Research Center is also acknowledged.
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Authors and Affiliations
- Departments of Pediatrics (Cardiology),
Elizabeth A. Lindsay, Francesca Vitelli, Masae Morishima, Tuong Huynh, Tiziano Pramparo & Antonio Baldini - Molecular & Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, 77030, Texas, USA
Hong Su, Allan Bradley & Antonio Baldini - Human Genetics, Baylor College of Medicine,
Hong Su, Allan Bradley & Antonio Baldini - University of Miami School of Medicine, 1600NW 10th Avenue, Miami, 33136, Florida, USA
Vesna Jurecic - Department of Molecular Genetics, University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, 77030, Texas, USA
George Ogunrinu - Institute of Child Health, 30 Guilford Street, London, WC1N, UK
Helen F. Sutherland & Peter J. Scambler - Sanger Centre, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1S, UK
Allan Bradley - Howard Hughest Medical Institute, One Baylor Plaza, Houston, 77030, Texas, USA
Allan Bradley
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- Elizabeth A. Lindsay
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Correspondence toAntonio Baldini.
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Lindsay, E., Vitelli, F., Su, H. et al. Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice.Nature 410, 97–101 (2001). https://doi.org/10.1038/35065105
- Received: 12 December 2000
- Accepted: 07 February 2001
- Issue Date: 01 March 2001
- DOI: https://doi.org/10.1038/35065105