TY - JOUR
T1 - Canine candidate genes for Dilated cardiomyopathy: Annotation of and polymorphic markers for 14 genes
AU - Wiersma, Anje C.
AU - Leegwater, Peter AJ
AU - Van Oost, Bernard A.
AU - Ollier, William E.
AU - Dukes-McEwan, Joanna
N1 - DA - 20071022IS - 1746-6148 (Electronic)LA - ENGPT - JOURNAL ARTICLE
PY - 2007
Y1 - 2007
N2 - Background: Dilated cardiomyopathy is a myocardial disease occurring in humans and domestic animals and is characterized by dilatation of the left ventricle, reduced systolic function and increased sphericity of the left ventricle. Dilated cardiomyopathy has been observed in several, mostly large and giant, dog breeds, such as the Dobermann and the Great Dane. A number of genes have been identified, which are associated with dilated cardiomyopathy in the human, mouse and hamster. These genes mainly encode structural proteins of the cardiac myocyte. Results: We present the annotation of, and marker development for, 14 of these genes of the dog genome, i.e. α-cardiac actin, caveolin 1, cysteine-rich protein 3, desmin, lamin A/C, LIM-domain binding factor 3, myosin heavy polypeptide 7, phospholamban, sarcoglycan δ;, titin cap, α-tropomyosin, troponin I, troponin T and vinculin. A total of 33 Single Nucleotide Polymorphisms were identified for these canine genes and 11 polymorphic microsatellite repeats were developed. Conclusion: The presented polymorphisms provide a tool to investigate the role of the corresponding genes in canine Dilated Cardiomyopathy by linkage analysis or association studies. © 2007 Wiersma et al; licensee BioMed Central Ltd.
AB - Background: Dilated cardiomyopathy is a myocardial disease occurring in humans and domestic animals and is characterized by dilatation of the left ventricle, reduced systolic function and increased sphericity of the left ventricle. Dilated cardiomyopathy has been observed in several, mostly large and giant, dog breeds, such as the Dobermann and the Great Dane. A number of genes have been identified, which are associated with dilated cardiomyopathy in the human, mouse and hamster. These genes mainly encode structural proteins of the cardiac myocyte. Results: We present the annotation of, and marker development for, 14 of these genes of the dog genome, i.e. α-cardiac actin, caveolin 1, cysteine-rich protein 3, desmin, lamin A/C, LIM-domain binding factor 3, myosin heavy polypeptide 7, phospholamban, sarcoglycan δ;, titin cap, α-tropomyosin, troponin I, troponin T and vinculin. A total of 33 Single Nucleotide Polymorphisms were identified for these canine genes and 11 polymorphic microsatellite repeats were developed. Conclusion: The presented polymorphisms provide a tool to investigate the role of the corresponding genes in canine Dilated Cardiomyopathy by linkage analysis or association studies. © 2007 Wiersma et al; licensee BioMed Central Ltd.
KW - ACADEMIC JOURNAL PAPERS
KW - ORIGINAL ARTICLES
U2 - 10.1186/1746-6148-3-28
DO - 10.1186/1746-6148-3-28
M3 - Article
VL - 3
JO - BMC Veterinary Research
JF - BMC Veterinary Research
SN - 1746-6148
M1 - 28
ER -