{"title":"A MicroRNA Catalog of Swine Umbilical Vein Endothelial Cells Identified by Deep Sequencing","authors":"Chen DAI, Yan-ming ZHANG, Qian ZHANG, Zong-song WU, Wen DENG, Xu ZHANG, Kang-kang GUO, Qing-hai TANG, Bo HOU","doi":"10.1016/S1671-2927(11)60140-5","DOIUrl":null,"url":null,"abstract":"<div><p>MicroRNAs (miRNAs) are endogenous ∼22 nt RNAs that play important regulatory roles in targeting mRNAs for cleavage or translational repression. Despite the discovery of increasing numbers of human and mouse miRNAs, little is known about miRNAs from pig. In this study, we sought to extend the repertoire of porcine small regulatory RNAs using Solexa sequencing. We sequenced a library of small RNAs prepared from immortalized swine umbilical vein endothelial cells (SUVECs). We produced over 13.6 million short sequence reads, of which 8547658 perfectly mapped to the pig genome. A bioinformatics pipeline was used to identify authentic mature miRNA sequences. We identified 154 porcine miRNA genes, among which 146 were conserved across species, and 8 were pig-specific miRNA genes. The 146 miRNA genes encoded 116 conserved mature miRNAs and 66 miRNA*. The 8 pig-specific miRNA genes encoded 4 mature miRNAs. Four potential novel miRNAs were identified. The secondary structures of the 154 miRNA genes were predicted; 13 miRNAs have 2 structures, and miR-9 and miR-199 have 4 and 3 structures, respectively. 36 miRNAs were organized into 19 compact clusters. miR-206, miR-21 and miR-378 were the relatively highly expressed miRNAs. In conclusion, Solexa sequencing allowed the successful discovery of known and novel porcine miRNAs with high accuracy and efficiency. Furthermore, our results supply new data to the somewhat insufficient pig miRBase, and are useful for investigating features of the blood-brain barrier, vascular diseases and inflammation.</p></div>","PeriodicalId":7475,"journal":{"name":"Agricultural Sciences in China","volume":"10 9","pages":"Pages 1467-1474"},"PeriodicalIF":0.0000,"publicationDate":"2011-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S1671-2927(11)60140-5","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Agricultural Sciences in China","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1671292711601405","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
MicroRNAs (miRNAs) are endogenous ∼22 nt RNAs that play important regulatory roles in targeting mRNAs for cleavage or translational repression. Despite the discovery of increasing numbers of human and mouse miRNAs, little is known about miRNAs from pig. In this study, we sought to extend the repertoire of porcine small regulatory RNAs using Solexa sequencing. We sequenced a library of small RNAs prepared from immortalized swine umbilical vein endothelial cells (SUVECs). We produced over 13.6 million short sequence reads, of which 8547658 perfectly mapped to the pig genome. A bioinformatics pipeline was used to identify authentic mature miRNA sequences. We identified 154 porcine miRNA genes, among which 146 were conserved across species, and 8 were pig-specific miRNA genes. The 146 miRNA genes encoded 116 conserved mature miRNAs and 66 miRNA*. The 8 pig-specific miRNA genes encoded 4 mature miRNAs. Four potential novel miRNAs were identified. The secondary structures of the 154 miRNA genes were predicted; 13 miRNAs have 2 structures, and miR-9 and miR-199 have 4 and 3 structures, respectively. 36 miRNAs were organized into 19 compact clusters. miR-206, miR-21 and miR-378 were the relatively highly expressed miRNAs. In conclusion, Solexa sequencing allowed the successful discovery of known and novel porcine miRNAs with high accuracy and efficiency. Furthermore, our results supply new data to the somewhat insufficient pig miRBase, and are useful for investigating features of the blood-brain barrier, vascular diseases and inflammation.
MicroRNAs (miRNAs)是内源性的~ 22 nt rna,在靶向mrna进行切割或翻译抑制中发挥重要的调节作用。尽管发现了越来越多的人类和小鼠的mirna,但对猪的mirna知之甚少。在这项研究中,我们试图使用Solexa测序来扩展猪小调控rna的库。我们对永生化猪脐静脉内皮细胞(SUVECs)制备的小rna文库进行了测序。我们产生了超过1360万个短序列,其中8547658个与猪基因组完美匹配。使用生物信息学管道来鉴定真实的成熟miRNA序列。共鉴定出154个猪miRNA基因,其中跨种保守的有146个,8个为猪特异性miRNA基因。146个miRNA基因编码116个保守的成熟miRNA和66个miRNA*。8个猪特异性miRNA基因编码4个成熟miRNA。鉴定出四种潜在的新型mirna。预测154个miRNA基因的二级结构;13种mirna有2种结构,miR-9和miR-199分别有4种和3种结构。36个mirna被组织成19个紧凑的簇。miR-206、miR-21和miR-378是相对高表达的mirna。总之,Solexa测序能够以高精度和高效率成功发现已知和新的猪mirna。此外,我们的研究结果为猪miRBase的不足提供了新的数据,并有助于研究血脑屏障、血管疾病和炎症的特征。