Abstract
Supravalvular aortic stenosis (SVAS) is a congenital narrowing of the ascending aorta, which can occur sporadically as an autosomal dominant condition or as one component of the Williams–Beuren syndrome, a complex developmental genomic disorder associated with cardiovascular, neurobehavioral, craniofacial, and metabolic abnormalities, caused by a microdeletion at 7q11.23. We report the identification of seven novel mutations within the elastin gene in 31 familial and sporadic cases of nonsyndromic SVAS. Five are frameshift mutations within the coding region of the ELN gene that result in premature stop codons (PTCs); the other two mutations abolish the donor splice site of introns 3 and 28, respectively, and are predicted to alter splicing efficiency resulting in the generation of a PTC within the same introns of the gene. In vitro analysis using minigenes and cycloheximide showed that some selected frameshift mutant alleles are substrates of nonsense-mediated mRNA decay (NMD), confirming that the functional haploinsufficiency of the ELN gene is the main pathomechanism underlying SVAS. Interestingly, molecular analysis on patient fibroblasts showed that the c.2044+5G>C mutant allele encodes for an aberrant shorter form of the elastin polypeptide that may hamper the normal assembly of elastin fibers in a dominant-negative manner.
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Acknowledgements
We are very grateful to the SVAS families, whose cooperation made this study possible. We thank Youngho Kim for ELN primer sequences. This study was conducted with the support of the Italian Ministry of Health (Ricerca Corrente 2006-2009), the Fondazione Banca del Monte di Foggia ‘Domenico Siniscalco Ceci’ and the Jérôme Lejeune Foundation to GM, and the VI Framework Program of the European Commission (LSHG-CT-2006-037627) to LAPJ.
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Micale, L., Turturo, M., Fusco, C. et al. Identification and characterization of seven novel mutations of elastin gene in a cohort of patients affected by supravalvular aortic stenosis. Eur J Hum Genet 18, 317–323 (2010). https://doi.org/10.1038/ejhg.2009.181
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DOI: https://doi.org/10.1038/ejhg.2009.181
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