Genome-Wide Identification of Long Noncoding RNAs in Rat Models of Cardiovascular and Renal Disease

被引:53
|
作者
Gopalakrishnan, Kathirvel [1 ]
Kumarasamy, Sivarajan [1 ]
Mell, Blair [1 ]
Joe, Bina [1 ]
机构
[1] Univ Toledo, Coll Med & Life Sci, Dept Physiol & Pharmacol, Ctr Hypertens & Personalized Med,Program Physiol, Toledo, OH 43614 USA
基金
美国国家卫生研究院;
关键词
blood pressure; rats; inbred Dahl; inbred SHR; RNA untranslated; transcriptome; MODIFICATIONS BASIC MECHANISMS; GENETIC-ANALYSIS; HYPERTENSION; REVEALS; EPIGENOMICS; LINCRNAS; LOCI; METABOLISM; PHENOTYPES; EVOLUTION;
D O I
10.1161/HYPERTENSIONAHA.114.04498
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Long noncoding RNAs (lncRNAs) are an emerging class of genomic regulatory molecules reported in various species. In the rat, which is one of the major mammalian model organisms, discovery of lncRNAs on a genome-wide scale is lagging. Renal lncRNA sequencing and lncRNA transcriptome analysis were conducted in 3 rat strains that are widely used in cardiovascular and renal research: the Dahl salt-sensitive rat, the spontaneously hypertensive rat, and the Dahl salt-resistant rat. Through the RNA sequencing approach, 3273 transcripts were identified as rat lncRNAs. A majority of lncRNAs were without predicted target genes. Differential expression of 273 and 749 lncRNAs was detected between Dahl salt-sensitive versus Dahl salt-resistant and Dahl salt-sensitive versus spontaneously hypertensive rat comparisons, respectively. To couple the observed differential expression of lncRNAs with the status of mRNAs, an mRNA transcriptome analysis was conducted. Several cis mRNA genes were coregulated with lncRNAs. Of these, the protein expression status of 4 target genes, Asb3, Chac2, Pex11b, and Sp5, were differentially expressed between the relevant strain comparisons, thereby suggesting that the differentially expressed lncRNAs associated with these genes are candidate genetic determinants of blood pressure. This study serves as a first-generation catalog of rat lncRNAs and illustrates the prioritization of lncRNAs as candidates for complex polygenic traits.
引用
收藏
页码:200 / 210
页数:11
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