Dipartimento di Fisica, Istituto Nazionale di Fisica Nucleare, Università di Torino Torino, Italy.
Dipartimento di Oncologia, Istituto per la Ricerca sul Cancro di Candiolo-Istituto di Ricovero e Cura a Carattere Scientifico, Università di Torino Torino, Italy.
Front Genet. 2014 Oct 6;5:345. doi: 10.3389/fgene.2014.00345. eCollection 2014.
The expression of protein-coding genes is controlled by a complex network of regulatory interactions. It is becoming increasingly appreciated that post-transcriptional repression by microRNAs, a class of small non-coding RNAs, is a key layer of regulation in several biological processes. In this contribution, we discuss the interplay between microRNAs and epigenetic regulators. Among the mixed genetic circuits composed by these two different kinds of regulation, it seems that a central role is played by double-negative feedback loops in which a microRNA inhibits an epigenetic regulator and in turn is controlled at the epigenetic level by the same regulator. We discuss a few relevant properties of this class of network motifs and their potential role in cell differentiation. In particular, using mathematical modeling we show how this particular circuit can exhibit a switch-like behavior between two alternative steady states, while being robust to stochastic transitions between these two states, a feature presumably required for circuits involved in cell fate decision. Finally, we present a list of putative double-negative feedback loops from a literature survey combined with bioinformatic analysis, and discuss in detail a few examples.
蛋白质编码基因的表达受复杂的调控相互作用网络控制。越来越多的人认识到,miRNA 是一类小的非编码 RNA,其转录后抑制是几个生物学过程的关键调控层。在本研究中,我们讨论了 miRNA 和表观遗传调控因子之间的相互作用。在由这两种不同类型的调控组成的混合遗传电路中,miRNA 抑制表观遗传调节剂,而反过来又受到同一调节剂在表观遗传水平上的控制的双负反馈回路似乎起着核心作用。我们讨论了这类网络基元的一些相关特性及其在细胞分化中的潜在作用。特别是,我们使用数学建模表明,这种特定的电路如何在两种替代稳定状态之间表现出类似于开关的行为,同时对这两种状态之间的随机转换具有稳健性,这是涉及细胞命运决定的电路所需要的特征。最后,我们从文献综述和生物信息学分析中列出了一些可能的双负反馈回路,并详细讨论了几个例子。