Item Type: | Article |
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Title: | Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy |
Creators Name: | Heuser, A., Plovie, E.R., Ellinor, P.T., Grossmann, K.S., Shin, J.T., Wichter, T., Basson, C.T., Lerman, B.B., Sasse-Klaassen, S., Thierfelder, L., MacRae, C.A. and Gerull, B. |
Abstract: | Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a genetically heterogeneous heart-muscle disorder characterized by progressive fibrofatty replacement of right ventricular myocardium and an increased risk of sudden cardiac death. Mutations in desmosomal proteins that cause ARVC have been previously described; therefore, we investigated 88 unrelated patients with the disorder for mutations in human desmosomal cadherin desmocollin-2 (DSC2). We identified a heterozygous splice-acceptorsite mutation in intron 5 (c.631-2A->G) of the DSC2 gene, which led to the use of a cryptic splice-acceptor site and the creation of a downstream premature termination codon. Quantitative analysis of cardiac DSC2 expression in patient specimens revealed a marked reduction in the abundance of the mutant transcript. Morpholino knockdown in zebrafish embryos revealed a requirement for dsc2 in the establishment of the normal myocardial structure and function, with reduced desmosomal plaque area, loss of the desmosome extracellular electron-dense midlines, and associated myocardial contractility defects. These data identify DSC2 mutations as a cause of ARVC in humans and demonstrate that physiologic levels of DSC2 are crucial for normal cardiac desmosome formation, early cardiac morphogenesis, and cardiac function. |
Keywords: | Amino Acid Sequence, Arrhythmogenic Right Ventricular Dysplasia, Base Sequence, Desmocollins, Nonmammalian Embryo, Molecular Sequence Data, Mutation, Myocardial Contraction, Animals, Zebrafish |
Source: | American Journal of Human Genetics |
ISSN: | 0002-9297 |
Publisher: | University of Chicago Press |
Volume: | 79 |
Number: | 6 |
Page Range: | 1081-1088 |
Date: | December 2006 |
Official Publication: | https://doi.org/10.1086/509044 |
PubMed: | View item in PubMed |
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