Wong Nathan, Wang Xiaowei
Department of Biomedical Engineering, Washington University, St. Louis, MO 63130, USA Department of Radiation Oncology, Washington University School of Medicine, St. Louis, MO 63108, USA.
Department of Radiation Oncology, Washington University School of Medicine, St. Louis, MO 63108, USA Department of Biomedical Engineering, Washington University, St. Louis, MO 63130, USA
Nucleic Acids Res. 2015 Jan;43(Database issue):D146-52. doi: 10.1093/nar/gku1104. Epub 2014 Nov 5.
MicroRNAs (miRNAs) are small non-coding RNAs that are extensively involved in many physiological and disease processes. One major challenge in miRNA studies is the identification of genes regulated by miRNAs. To this end, we have developed an online resource, miRDB (http://mirdb.org), for miRNA target prediction and functional annotations. Here, we describe recently updated features of miRDB, including 2.1 million predicted gene targets regulated by 6709 miRNAs. In addition to presenting precompiled prediction data, a new feature is the web server interface that allows submission of user-provided sequences for miRNA target prediction. In this way, users have the flexibility to study any custom miRNAs or target genes of interest. Another major update of miRDB is related to functional miRNA annotations. Although thousands of miRNAs have been identified, many of the reported miRNAs are not likely to play active functional roles or may even have been falsely identified as miRNAs from high-throughput studies. To address this issue, we have performed combined computational analyses and literature mining, and identified 568 and 452 functional miRNAs in humans and mice, respectively. These miRNAs, as well as associated functional annotations, are presented in the FuncMir Collection in miRDB.
微小RNA(miRNA)是一类小的非编码RNA,广泛参与许多生理和疾病过程。miRNA研究中的一个主要挑战是鉴定受miRNA调控的基因。为此,我们开发了一个在线资源miRDB(http://mirdb.org),用于miRNA靶标预测和功能注释。在此,我们描述了miRDB最近更新的功能,包括由6709个miRNA调控的210万个预测基因靶标。除了呈现预编译的预测数据外,一个新功能是网络服务器界面,允许提交用户提供的序列进行miRNA靶标预测。通过这种方式,用户可以灵活地研究任何感兴趣的定制miRNA或靶基因。miRDB的另一项重大更新与功能性miRNA注释有关。尽管已经鉴定出数千种miRNA,但许多报道的miRNA不太可能发挥积极的功能作用,甚至可能是在高通量研究中被错误鉴定为miRNA。为了解决这个问题,我们进行了综合计算分析和文献挖掘,分别在人类和小鼠中鉴定出568个和452个功能性miRNA。这些miRNA以及相关的功能注释在miRDB的FuncMir数据集中呈现。