Lu Jike, Chen Chen, Hao Limin, Zheng Zhiqiang, Zhang Naixun, Wang Zhenyu
School of Life Sciences, Zhengzhou University, Zhengzhou, Henan, 450001, China.
Department of People's Liberation Army, The Quartermaster Equipment Institute of General Logistics, Beijing, 100010, China.
Cell Biol Int. 2016 Aug;40(8):873-86. doi: 10.1002/cbin.10627. Epub 2016 Jun 6.
In order to investigate the potential regulatory roles of microRNAs (miRNAs) in mouse response to ionizing radiation (IR), the small RNA libraries from liver tissues of mice with or without ionizing radiation (IR) were sequenced by high-throughput deep sequencing technology. A total of 270 miRNAs including 212 known and 58 potentially novel miRNAs were identified. Within these miRNAs, there were 48 miRNAs that were differentially expressed, including 27 known and 21 novel miRNAs. The results of quantitative RT-polymerase chain reaction (qRT-PCR) were in consistent with the sequencing analysis. Target gene prediction, function annotation, and pathway of the identified miRNAs were analyzed using RNAhybrid, miRanda software and Swiss-Prot, Gene Ontology (GO), Clusters of Orthologous Groups (COG), Kyoto Encyclopedia of Genes, and Genomes (KEGG) and non-redundant (NR) databases. These results should be useful to investigate the biological function of miRNAs under IR-induced liver injury.
为了研究微小RNA(miRNA)在小鼠对电离辐射(IR)反应中的潜在调控作用,利用高通量深度测序技术对有或无电离辐射(IR)的小鼠肝脏组织的小RNA文库进行了测序。共鉴定出270个miRNA,包括212个已知的和58个潜在的新miRNA。在这些miRNA中,有48个miRNA差异表达,包括27个已知的和21个新的miRNA。定量逆转录聚合酶链反应(qRT-PCR)结果与测序分析一致。使用RNAhybrid、miRanda软件以及瑞士蛋白质数据库、基因本体论(GO)、直系同源簇(COG)、京都基因与基因组百科全书(KEGG)和非冗余(NR)数据库对鉴定出的miRNA的靶基因预测、功能注释和途径进行了分析。这些结果对于研究IR诱导的肝损伤下miRNA的生物学功能应该是有用的。