Karreth Florian A
Department of Molecular Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Methods Mol Biol. 2019;1970:237-250. doi: 10.1007/978-1-4939-9207-2_13.
MicroRNAs (miRNAs) are fine-tuners of gene expression and contribute to the regulation of most, if not all, biological processes in eukaryotes by targeting both coding and noncoding RNAs. Typically, miRNAs repress numerous target transcripts and most target RNAs harbor binding sites for multiple miRNA families. It was recently proposed that transcripts sequester miRNAs and thereby regulate the abundance of other transcripts with which they have miRNA binding sites in common. Since competition for shared miRNAs is the mechanistic basis for this cross-regulation, such transcripts were termed competitive endogenous RNAs (ceRNAs). In this chapter, I discuss considerations for the computational prediction of ceRNAs based on miRNA binding site overlap. Moreover, I provide a framework for the experimental validation of miRNA-dependent reciprocal regulation of putative ceRNAs.
微小RNA(miRNA)是基因表达的微调器,通过靶向编码和非编码RNA,对真核生物中大多数(即便不是全部)生物学过程的调控发挥作用。通常,miRNA会抑制众多靶转录本,并且大多数靶RNA含有多个miRNA家族的结合位点。最近有人提出,转录本会隔离miRNA,从而调节与其具有共同miRNA结合位点的其他转录本的丰度。由于对共享miRNA的竞争是这种交叉调控的机制基础,因此这类转录本被称为竞争性内源RNA(ceRNA)。在本章中,我将讨论基于miRNA结合位点重叠对ceRNA进行计算预测时的注意事项。此外,我还提供了一个框架,用于对假定ceRNA的miRNA依赖性相互调控进行实验验证。