Department of Genetics, Stanford University, Stanford, California 94305-5324, USA.
Genome Res. 2012 Dec;22(12):2418-26. doi: 10.1101/gr.136515.111. Epub 2012 Aug 1.
miRNAs are post-transcriptional regulators of gene activity that reduce protein accumulation from target mRNAs. Elucidating precise molecular effects that animal miRNAs have on target transcripts has proven complex, with varied evidence indicating that miRNA regulation may produce different molecular outcomes in different species, systems, and/or physiological conditions. Here we use high-throughput ribosome profiling to analyze detailed translational parameters for five well-studied targets of miRNAs that regulate C. elegans developmental timing. For two targets of the miRNA lin-4 (lin-14 and lin-28), functional down-regulation was associated with decreases in both overall mRNA abundance and ribosome loading; however, these changes were of substantially smaller magnitude than corresponding changes observed in protein abundance. For three functional targets of the let-7 miRNA family for which down-regulation is critical in temporal progression of the animal (daf-12, hbl-1, and lin-41), we observed only modest changes in mRNA abundance and ribosome loading. lin-41 provides a striking example in that populations of ribosome-protected fragments from this gene remained essentially unchanged during the L3-L4 time interval when lin-41 activity is substantially down-regulated by let-7. Spectra of ribosomal positions were also examined for the five lin-4 and let-7 target mRNAs as a function of developmental time, with no indication of miRNA-induced ribosomal drop-off or significant pauses in translation. These data are consistent with models in which physiological regulation by this set of C. elegans miRNAs derives from combinatorial effects including suppressed recruitment/activation of translational machinery, compromised stability of target messages, and post- or peri-translational effects on lifetimes of polypeptide products.
miRNAs 是基因活性的转录后调控因子,可减少靶 mRNA 翻译产生的蛋白质积累。阐明动物 miRNAs 对靶转录本的确切分子影响非常复杂,因为有不同的证据表明 miRNA 调控可能在不同的物种、系统和/或生理条件下产生不同的分子结果。在这里,我们使用高通量核糖体分析来分析调节线虫发育时间的五个经过充分研究的 miRNA 靶标的详细翻译参数。对于 miRNA lin-4(lin-14 和 lin-28)的两个靶标,功能下调与总 mRNA 丰度和核糖体加载的降低有关;然而,这些变化的幅度远小于在蛋白质丰度中观察到的变化。对于 let-7 miRNA 家族的三个功能靶标,下调在动物时间进程中是关键的(daf-12、hbl-1 和 lin-41),我们只观察到 mRNA 丰度和核糖体加载的适度变化。lin-41 提供了一个引人注目的例子,即在 lin-41 活性被 let-7 显著下调的 L3-L4 时间间隔期间,该基因的核糖体保护片段的群体基本上保持不变。还检查了这五个 lin-4 和 let-7 靶 mRNA 的核糖体位置谱作为发育时间的函数,没有迹象表明 miRNA 诱导的核糖体脱落或翻译中显著停顿。这些数据与模型一致,即这组线虫 miRNAs 的生理调控源自组合效应,包括抑制翻译机制的募集/激活、靶消息稳定性受损以及对多肽产物寿命的翻译后或翻译前效应。