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Peer-reviewed veterinary case report

Gene mutation linked to dilated heart disease in Doberman pinschers

By Meurs, Kathryn M et al.·Published in Human genetics·2012·North Carolina State University College of Veterinary Medicine, United States·View original on PubMed

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Original publication title: A splice site mutation in a gene encoding for PDK4, a mitochondrial protein, is associated with the development of dilated cardiomyopathy in the Doberman pinscher.

Species:
dog

Plain-English summary

A group of Doberman pinschers with familial dilated cardiomyopathy (a heart condition that can lead to heart failure) was studied to find a genetic cause. Researchers discovered a specific mutation in a gene called PDK4 that seems to be linked to this heart disease. The affected dogs showed signs of heart muscle damage when examined under a microscope. Understanding this genetic mutation could help in diagnosing and managing heart problems in Doberman pinschers.

People also search for: Doberman pinscher heart disease symptoms · dilated cardiomyopathy in dogs · PDK4 gene mutation in dogs

Abstract

Familial dilated cardiomyopathy is a primary myocardial disease that can result in the development of congestive heart failure and sudden cardiac death. Spontaneous animal models of familial dilated cardiomyopathy exist and the Doberman pinscher dog is one of the most commonly reported canine breeds. The objective of this study was to evaluate familial dilated cardiomyopathy in the Doberman pinscher dog using a genome-wide association study for a genetic alteration(s) associated with the development of this disease in this canine model. Genome-wide association analysis identified an area of statistical significance on canine chromosome 14 (p(raw) = 9.999e-05 corrected for genome-wide significance), fine-mapping of additional SNPs flanking this region localized a signal to 23,774,190-23,781,919 (p = 0.001) and DNA sequencing identified a 16-base pair deletion in the 5' donor splice site of intron 10 of the pyruvate dehydrogenase kinase 4 gene in affected dogs (p < 0.0001). Electron microscopy of myocardium from affected dogs demonstrated disorganization of the Z line, mild to moderate T tubule and sarcoplasmic reticulum dilation, marked pleomorphic mitochondrial alterations with megamitochondria, scattered mitochondria with whorling and vacuolization and mild aggregates of lipofuscin granules. In conclusion, we report the identification of a splice site deletion in the PDK4 gene that is associated with the development of familial dilated cardiomyopathy in the Doberman pinscher dog.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/22447147/