Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.
Howard Hughes Medical Institute.
Mol Cell. 2014 Mar 20;53(6):1031-1043. doi: 10.1016/j.molcel.2014.02.013. Epub 2014 Mar 13.
MicroRNA (miRNA) regulation clearly impacts animal development, but the extent to which development-with its resulting diversity of cellular contexts-impacts miRNA regulation is unclear. Here, we compared cohorts of genes repressed by the same miRNAs in different cell lines and tissues and found that target repertoires were largely unaffected, with secondary effects explaining most of the differential responses detected. Outliers resulting from differential direct targeting were often attributable to alternative 3' UTR isoform usage that modulated the presence of miRNA sites. More inclusive examination of alternative 3' UTR isoforms revealed that they influence ∼10% of predicted targets when comparing any two cell types. Indeed, considering alternative 3' UTR isoform usage improved prediction of targeting efficacy significantly beyond the improvements observed when considering constitutive isoform usage. Thus, although miRNA targeting is remarkably consistent in different cell types, considering the 3' UTR landscape helps predict targeting efficacy and explain differential regulation that is observed.
微小 RNA (miRNA) 调控显然会影响动物的发育,但发育过程中细胞环境的多样性对 miRNA 调控的影响程度尚不清楚。在这里,我们比较了在不同细胞系和组织中受相同 miRNA 抑制的基因群体,发现靶基因谱在很大程度上不受影响,大多数差异反应可以用次要效应来解释。由差异直接靶向产生的离群值通常归因于调节 miRNA 结合位点存在的替代性 3'UTR 异构体的使用。对替代性 3'UTR 异构体更全面的考察表明,当比较两种细胞类型时,它们会影响约 10%的预测靶基因。事实上,与考虑组成型异构体使用时观察到的改进相比,考虑替代性 3'UTR 异构体的使用显著提高了靶向效率的预测。因此,尽管 miRNA 靶向在不同的细胞类型中非常一致,但考虑 3'UTR 景观有助于预测靶向效率并解释观察到的差异调控。