Abstract
Mutations in the gene encoding smooth muscle cell alpha actin (ACTA2) have recently been shown to cause familial thoracic aortic aneurysms leading to type A dissections (TAAD) and predispose to premature stroke and coronary artery disease. In order to further explore the role of ACTA2 variations in the pathogenesis of TAAD, we sequenced the coding regions of this gene in 40 unrelated German patients with TAAD (with (n=21) or without (n=19) clinical features suggestive of Marfan syndrome). All patients had previously tested negative for mutations in the FBN1 and TGFBR2 genes. We identified three novel ACTA2 mutations and mapped them on a three-dimensional model of actin. Two mutations affect residues within (M49V) or adjacent to (R39C), the DNAse-I-binding loop within subdomain 2 of alpha actin. They were observed in families with recurrent aortic aneurysm (R39C) or aortic dissection (M49V). The third mutation causes an exchange in the vicinity of the ATP-binding site (G304R) in a patient thought to have isolated TAAD. None of the affected individuals had clinical features typical for Marfan syndrome, and no case of premature stroke or coronary artery disease was reported from the affected families. In conclusion, we underscore the role of ACTA2 mutations in nonsyndromic TAAD and suggest that ACTA2 should be included in the genes routinely investigated for syndromic and nonsyndromic TAAD. Detailed clinical investigations of additional families are warranted to further explore the full range of phenotypic signs associated with the three novel mutations described here.
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Acknowledgements
We would like to thank Joanne Davies, Janine Haremza, Melanie Müller and Kirsten Rackebrandt for technical assistance and the patients for participating in this study.
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URLs for data presented herein are as follows:
GenBank, http://www.ncbi.nih.gov/Genbank/index.html
RCSB Protein Data Bank, http://www.rcsb.org/pdb/Welcome.do
OMIM, http://www.ncbi.nlm.nih.gov/Omim/
HGVS, http://www.hgvs.org/
PANTHER, http://www.pantherdb.org/tools/csnpScoreForm.jsp
PolyPhen, http://genetics.bwh.harvard.edu/pph/
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Hoffjan, S., Waldmüller, S., Blankenfeldt, W. et al. Three novel mutations in the ACTA2 gene in German patients with thoracic aortic aneurysms and dissections. Eur J Hum Genet 19, 520–524 (2011). https://doi.org/10.1038/ejhg.2010.239
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DOI: https://doi.org/10.1038/ejhg.2010.239
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