Feinberg School of Medicine, Division Hematology/Oncology, Northwestern University, Chicago, Illinois, United States of America.
PLoS One. 2011;6(10):e26521. doi: 10.1371/journal.pone.0026521. Epub 2011 Oct 26.
micro(mi)RNAs are small non-coding RNAs that negatively regulate expression of most mRNAs. They are powerful regulators of various differentiation stages, and the expression of genes that either negatively or positively correlate with expressed miRNAs is expected to hold information on the biological state of the cell and, hence, of the function of the expressed miRNAs. We have compared the large amount of available gene array data on the steady state system of the NCI60 cell lines to two different data sets containing information on the expression of 583 individual miRNAs. In addition, we have generated custom data sets containing expression information of 54 miRNA families sharing the same seed match. We have developed a novel strategy for correlating miRNAs with individual genes based on a summed Pearson Correlation Coefficient (sPCC) that mimics an in silico titration experiment. By focusing on the genes that correlate with the expression of miRNAs without necessarily being direct targets of miRNAs, we have clustered miRNAs into different functional groups. This has resulted in the identification of three novel miRNAs that are linked to the epithelial-to-mesenchymal transition (EMT) in addition to the known EMT regulators of the miR-200 miRNA family. In addition, an analysis of gene signatures associated with EMT, c-MYC activity, and ribosomal protein gene expression allowed us to assign different activities to each of the functional clusters of miRNAs. All correlation data are available via a web interface that allows investigators to identify genes whose expression correlates with the expression of single miRNAs or entire miRNA families. miRConnect.org will aid in identifying pathways regulated by miRNAs without requiring specific knowledge of miRNA targets.
miRNAs 是一种小的非编码 RNA,可负向调节大多数 mRNAs 的表达。它们是各种分化阶段的强大调节剂,与表达的 miRNAs 呈负相关或正相关的基因的表达有望提供关于细胞的生物学状态的信息,因此,提供了表达的 miRNAs 的功能的信息。我们将已有的大量 NCI60 细胞系稳态系统的基因芯片数据与包含 583 个单个 miRNAs 表达信息的两个不同数据集进行了比较。此外,我们生成了包含 54 个 miRNA 家族表达信息的定制数据集,这些家族具有相同的种子匹配。我们开发了一种基于模拟虚拟滴定实验的总和 Pearson 相关系数(sPCC)的新策略,用于将 miRNAs 与单个基因相关联。通过关注与 miRNAs 表达相关但不一定是 miRNAs 直接靶标的基因,我们将 miRNAs 聚类为不同的功能组。这导致鉴定出三个新的 miRNAs,除了已知的 miR-200 miRNA 家族的 EMT 调节剂之外,还与上皮-间充质转化(EMT)有关。此外,与 EMT、c-MYC 活性和核糖体蛋白基因表达相关的基因特征分析使我们能够将每个 miRNA 功能簇的不同活性分配给每个 miRNA 功能簇。所有的相关数据都可以通过一个网络界面获得,该界面允许研究人员识别表达与单个 miRNAs 或整个 miRNA 家族表达相关的基因。miRConnect.org 将有助于在不需要特定 miRNA 靶标知识的情况下识别受 miRNAs 调节的途径。