Department of Molecular Cell Biology, Weizmann Institute of Science, Herzl Street 234, 76100 Rehovot, Israel.
Biozentrum, University of Basel and Swiss Institute of Bioinformatics, Klingelbergstrasse 50-70, 4156 Basel, Switzerland.
Nat Rev Genet. 2014 Sep;15(9):599-612. doi: 10.1038/nrg3765. Epub 2014 Jul 15.
Comparative genomics analyses and high-throughput experimental studies indicate that a microRNA (miRNA) binds to hundreds of sites across the transcriptome. Although the knockout of components of the miRNA biogenesis pathway has profound phenotypic consequences, most predicted miRNA targets undergo small changes at the mRNA and protein levels when the expression of the miRNA is perturbed. Alternatively, miRNAs can establish thresholds in and increase the coherence of the expression of their target genes, as well as reduce the cell-to-cell variability in target gene expression. Here, we review the recent progress in identifying miRNA targets and the emerging paradigms of how miRNAs shape the dynamics of target gene expression.
比较基因组学分析和高通量实验研究表明,一个 microRNA(miRNA)可以结合转录组中的数百个位点。尽管 miRNA 生物发生途径的组成部分的敲除会产生深远的表型后果,但当 miRNA 的表达受到干扰时,大多数预测的 miRNA 靶标在 mRNA 和蛋白质水平上只发生微小变化。相反,miRNAs 可以在其靶基因的表达中建立阈值并增加其表达的协调性,并降低靶基因表达的细胞间变异性。在这里,我们回顾了最近在鉴定 miRNA 靶标方面的进展,以及 miRNA 如何塑造靶基因表达动态的新兴范例。