Dipartimento di Fisica Teorica and INFN University of Torino, Torino, Italy.
PLoS Comput Biol. 2011 Mar;7(3):e1001101. doi: 10.1371/journal.pcbi.1001101. Epub 2011 Mar 10.
MicroRNAs are endogenous non-coding RNAs which negatively regulate the expression of protein-coding genes in plants and animals. They are known to play an important role in several biological processes and, together with transcription factors, form a complex and highly interconnected regulatory network. Looking at the structure of this network, it is possible to recognize a few overrepresented motifs which are expected to perform important elementary regulatory functions. Among them, a special role is played by the microRNA-mediated feedforward loop in which a master transcription factor regulates a microRNA and, together with it, a set of target genes. In this paper we show analytically and through simulations that the incoherent version of this motif can couple the fine-tuning of a target protein level with an efficient noise control, thus conferring precision and stability to the overall gene expression program, especially in the presence of fluctuations in upstream regulators. Among the other results, a nontrivial prediction of our model is that the optimal attenuation of fluctuations coincides with a modest repression of the target expression. This feature is coherent with the expected fine-tuning function and in agreement with experimental observations of the actual impact of a wide class of microRNAs on the protein output of their targets. Finally, we describe the impact on noise-buffering efficiency of the cross-talk between microRNA targets that can naturally arise if the microRNA-mediated circuit is not considered as isolated, but embedded in a larger network of regulations.
微 RNA 是内源性的非编码 RNA,在动植物中负调控蛋白质编码基因的表达。它们在多个生物过程中发挥着重要作用,与转录因子一起形成了一个复杂且高度相互关联的调控网络。从这个网络的结构来看,可以识别出几个过表达的模体,这些模体预计具有重要的基本调控功能。其中,微 RNA 介导的前馈回路起着特殊的作用,其中一个主转录因子调节一个微 RNA,并与它一起调节一组靶基因。在本文中,我们通过分析和模拟表明,该模体的非相干版本可以将靶蛋白水平的微调与有效的噪声控制结合起来,从而使整个基因表达程序具有精确性和稳定性,特别是在存在上游调控因子波动的情况下。在其他结果中,我们的模型的一个非平凡预测是,波动的最佳衰减与对靶表达的适度抑制相吻合。这一特征与预期的微调功能一致,也与广泛类别的微 RNA 对其靶蛋白输出的实际影响的实验观察结果一致。最后,我们描述了如果微 RNA 介导的回路不被视为孤立的,而是嵌入到更大的调控网络中,那么微 RNA 靶标之间的串扰对噪声缓冲效率的影响。