Use of RNA-seq to identify cardiac genes and gene pathways differentially expressed between dogs with and without dilated cardiomyopathy

被引:7
|
作者
Friedenberg, Steven G. [1 ,4 ]
Chdid, Lhoucine [1 ]
Keene, Bruce [1 ,4 ]
Sherry, Barbara [2 ,4 ]
Motsinger-Reif, Alison [3 ,4 ]
Meurs, Kathryn M. [1 ,4 ]
机构
[1] N Carolina State Univ, Coll Vet Med, Dept Clin Sci, Raleigh, NC 27607 USA
[2] N Carolina State Univ, Coll Vet Med, Dept Mol Biomed Sci, Raleigh, NC 27607 USA
[3] N Carolina State Univ, Dept Stat, Raleigh, NC 27607 USA
[4] N Carolina State Univ, Ctr Comparat Med & Translat Res, Raleigh, NC 27607 USA
关键词
MUTATIONS; COACTIVATOR; ASSOCIATION; WEBGESTALT;
D O I
10.2460/ajvr.77.7.693
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
OBJECTIVE To identify cardiac tissue genes and gene pathways differentially expressed between dogs with and without dilated cardiomyopathy (DCM). ANIMALS 8 dogs with and 5 dogs without DCM. PROCEDURES Following euthanasia, samples of left ventricular myocardium were collected from each dog. Total RNA was extracted from tissue samples, and RNA sequencing was performed on each sample. Samples from dogs with and without DCM were grouped to identify genes that were differentially regulated between the 2 populations. Overrepresentation analysis was performed on upregulated and downregulated gene sets to identify altered molecular pathways in dogs with DCM. RESULTS Genes involved in cellular energy metabolism, especially metabolism of carbohydrates and fats, were significantly downregulated in dogs with DCM. Expression of cardiac structural proteins was also altered in affected dogs. CONCLUSIONS AND CLINICAL RELEVANCE Results suggested that RNA sequencing may provide important insights into the pathogenesis of DCM in dogs and highlight pathways that should be explored to identify causative mutations and develop novel therapeutic interventions.
引用
收藏
页码:693 / 699
页数:7
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