Institute of Microbiology ASCR vvi, Prague, Czech Republic.
Nucleic Acids Res. 2010 Aug;38(14):4579-85. doi: 10.1093/nar/gkq220. Epub 2010 Apr 5.
Post-transcriptional control of mRNA by micro-RNAs (miRNAs) represents an important mechanism of gene regulation. miRNAs act by binding to the 3' untranslated region (3'UTR) of an mRNA, affecting the stability and translation of the target mRNA. Here, we present a numerical model of miRNA-mediated mRNA downregulation and its application to analysis of temporal microarray data of HepG2 cells transfected with miRNA-124a. Using the model our analysis revealed a novel mechanism of mRNA accumulation control by miRNA, predicting that specific mRNAs are controlled in a digital, switch-like manner. Specifically, the contribution of miRNAs to mRNA degradation is switched from maximum to zero in a very short period of time. Such behaviour suggests a model of control in which mRNA is at a certain moment protected from binding of miRNA and further accumulates with a basal rate. Genes associated with this process were identified and parameters of the model for all miRNA-124a affected mRNAs were computed.
miRNAs 对 mRNA 的转录后调控是基因调控的重要机制。miRNAs 通过与 mRNA 的 3'非翻译区(3'UTR)结合,影响靶 mRNA 的稳定性和翻译。在这里,我们提出了一个 miRNA 介导的 mRNA 下调的数值模型,并将其应用于转染 miRNA-124a 的 HepG2 细胞的时间性微阵列数据分析。通过该模型的分析,我们揭示了 miRNA 对 mRNA 积累控制的一种新机制,预测特定的 mRNA 以数字、开关式的方式受到控制。具体来说,miRNA 对 mRNA 降解的贡献在很短的时间内从最大值切换到零。这种行为表明,mRNA 在某个时刻受到 miRNA 结合的保护,并以基础速率进一步积累的控制模型。确定了与该过程相关的基因,并计算了所有受 miRNA-124a 影响的 mRNA 的模型参数。