Shih Yu-Huan, Zhang Yuji, Ding Yonghe, Ross Christian A, Li Hu, Olson Timothy M, Xu Xiaolei
From the Department of Biochemistry and Molecular Biology (Y.-H.S., Y.D., X.X.), Information Technology (C.A.R.), Department of Molecular Pharmacology and Experimental Therapeutics (H.L.), Department of Pediatric and Adolescent Medicine (T.M.O.), and Division of Cardiovascular Diseases (T.M.O., X.X.), Mayo Clinic, Rochester, MN; Division of Biostatistics and Bioinformatics, University of Maryland Greenebaum Cancer Center, Baltimore (Y.Z.); and Department of Epidemiology and Public Health, University of Maryland School of Medicine, Baltimore (Y.Z.).
Circ Cardiovasc Genet. 2015 Apr;8(2):261-9. doi: 10.1161/CIRCGENETICS.114.000702. Epub 2015 Jan 11.
Genetic studies of cardiomyopathy and heart failure have limited throughput in mammalian models. Adult zebrafish have been recently pursued as a vertebrate model with higher throughput, but genetic conservation must be tested.
We conducted transcriptome analysis of zebrafish heart and searched for fish homologues of 51 known human dilated cardiomyopathy-associated genes. We also identified genes with high cardiac expression and genes with differential expression between embryonic and adult stages. Among tested genes, 30 had a single zebrafish orthologue, 14 had 2 homologues, and 5 had ≥3 homologues. By analyzing the expression data on the basis of cardiac abundance and enrichment hypotheses, we identified a single zebrafish gene for 14 of 19 multiple-homologue genes and 2 zebrafish homologues of high priority for ACTC1. Of note, our data suggested vmhc and vmhcl as functional zebrafish orthologues for human genes MYH6 and MYH7, respectively, which are established molecular markers for cardiac remodeling.
Most known genes for human dilated cardiomyopathy have a corresponding zebrafish orthologue, which supports the use of zebrafish as a conserved vertebrate model. Definition of the cardiac transcriptome and fetal gene program will facilitate systems biology studies of dilated cardiomyopathy in zebrafish.
心肌病和心力衰竭的基因研究在哺乳动物模型中的通量有限。成年斑马鱼最近被用作具有更高通量的脊椎动物模型,但必须测试其基因保守性。
我们对斑马鱼心脏进行了转录组分析,并寻找51个已知的人类扩张型心肌病相关基因的鱼类同源物。我们还鉴定了心脏高表达基因以及胚胎期和成年期差异表达的基因。在测试的基因中,30个有单个斑马鱼直系同源物,14个有2个同源物,5个有≥3个同源物。通过基于心脏丰度和富集假设分析表达数据,我们为19个多同源基因中的14个鉴定了单个斑马鱼基因,以及ACTC1的2个高优先级斑马鱼同源物。值得注意的是,我们的数据表明vmhc和vmhcl分别是人类基因MYH6和MYH7的功能性斑马鱼直系同源物,这两个基因是心脏重塑的既定分子标记。
大多数已知的人类扩张型心肌病基因都有相应的斑马鱼直系同源物,这支持将斑马鱼用作保守的脊椎动物模型。心脏转录组和胎儿基因程序的定义将有助于斑马鱼扩张型心肌病的系统生物学研究。