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DEVELOPMENT AND DISEASE |
1 Department of Pediatrics (Cardiology), Baylor College of Medicine, Houston TX 77030, USA
2 Department of Pediatrics and Cell Biology, Duke University Medical Center, Durham NC 27710, USA
3 Department of Molecular and Human Genetics, Baylor College of Medicine, Houston TX 77030, USA
*Author for correspondence (e-mail: baldini{at}bcm.tmc.edu)
Accepted 1 July 2002
Tbx1 haploinsufficiency causes aortic arch abnormalities in mice because of early growth and remodeling defects of the fourth pharyngeal arch arteries. The function of Tbx1 in the development of these arteries is probably cell non-autonomous, as the gene is not expressed in structural components of the artery but in the surrounding pharyngeal endoderm. We hypothesized that Tbx1 may trigger signals from the pharyngeal endoderm directed to the underlying mesenchyme. We show that the expression patterns of Fgf8 and Fgf10, which partially overlap with Tbx1 expression pattern, are altered in Tbx1/ mutants. In particular, Fgf8 expression is abolished in the pharyngeal endoderm. To understand the significance of this finding for the pathogenesis of the mutant Tbx1 phenotype, we crossed Tbx1 and Fgf8 mutants. Double heterozygous Tbx1+/;Fgf8+/ mutants present with a significantly higher penetrance of aortic arch artery defects than do Tbx1+/;Fgf8+/+ mutants, while Tbx1+/+;Fgf8+/ animals are normal. We found that Fgf8 mutation increases the severity of the primary defect caused by Tbx1 haploinsufficiency, i.e. early hypoplasia of the fourth pharyngeal arch arteries, consistent with the time and location of the shared expression domain of the two genes. Hence, Tbx1 and Fgf8 interact genetically in the development of the aortic arch. Our data provide the first evidence of a genetic link between Tbx1 and FGF signaling, and the first example of a modifier of the Tbx1 haploinsufficiency phenotype. We speculate that the FGF8 locus might affect the penetrance of cardiovascular defects in individuals with chromosome 22q11 deletions involving TBX1.
Key words: Pharyngeal endoderm, Pharyngeal arch arteries, Phenotypic modifiers
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