A missense variant in the titin gene in Doberman pinscher dogs with familial dilated cardiomyopathy and sudden cardiac death

The dog provides a large animal model of familial dilated cardiomyopathy for the study of important aspects of this common familial cardiovascular disease. We have previously demonstrated a form of canine dilated cardiomyopathy in the Doberman pinscher breed that is inherited as an autosomal dominan...

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Veröffentlicht in:Human genetics 2019-05, Vol.138 (5), p.515-524
Hauptverfasser: Meurs, Kathryn M., Friedenberg, Steven G., Kolb, Justin, Saripalli, Chandra, Tonino, Paola, Woodruff, Kathleen, Olby, Natasha J., Keene, Bruce W., Adin, Darcy B., Yost, Oriana L., DeFrancesco, Teresa C., Lahmers, Sunshine, Tou, Sandra, Shelton, G. Diane, Granzier, Henk
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Sprache:eng
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Zusammenfassung:The dog provides a large animal model of familial dilated cardiomyopathy for the study of important aspects of this common familial cardiovascular disease. We have previously demonstrated a form of canine dilated cardiomyopathy in the Doberman pinscher breed that is inherited as an autosomal dominant trait and is associated with a splice site variant in the pyruvate dehydrogenase kinase 4 ( PDK4 ) gene, however, genetic heterogeneity exists in this species as well and not all affected dogs have the PDK4 variant. Whole genome sequencing of a family of Doberman pinchers with dilated cardiomyopathy and sudden cardiac death without the PDK4 variant was performed. A pathologic missense variant in the titin gene located in an immunoglobulin-like domain in the I-band spanning region of the molecule was identified and was highly associated with the disease ( p  
ISSN:0340-6717
1432-1203
DOI:10.1007/s00439-019-01973-2