Institute for Integrative Biology of the Cell (I2BC), CEA, CNRS, University of Paris-Sud, University of Paris-Saclay, Gif-sur-Yvette, France.
Microbiol Spectr. 2018 Jul;6(4). doi: 10.1128/microbiolspec.RWR-0021-2018.
Most noncoding small RNAs (sRNAs) that regulate gene expression do so by base-pairing with mRNAs, affecting their translation and/or stability. Regulators as evolutionarily distant as the -encoded sRNAs of bacteria and the microRNAs (miRNAs) of higher eukaryotes share the property of targeting short sequence segments that occur in multiple copies in bacterial and eukaryotic transcriptomes. This target promiscuity has major implications for sRNA function. On the one hand, it allows the sRNA to coordinately control several different targets and thus be at the center of regulatory networks. On the other hand, it allows the existence of target mimics or decoys that divert the sRNA/miRNA away from bona fide targets and thus serve as mechanisms to regulate the regulator. In addition, by competing for pairing with the same sRNA, bona fide targets establish a cross talk that can impact on each other's expression levels. Here we review evidence that target mimicry and competition are important components of the regulatory architecture of bacterial sRNA networks.
大多数调节基因表达的非编码小 RNA(sRNA)通过与 mRNA 碱基配对来实现这一点,从而影响其翻译和/或稳定性。在进化上相距甚远的调控因子,如细菌编码的 sRNA 和高等真核生物的 microRNAs(miRNAs),具有靶向短序列片段的特性,这些短序列片段在细菌和真核生物转录组中多次出现。这种靶向的混杂性对 sRNA 的功能具有重要意义。一方面,它允许 sRNA 协调控制几个不同的靶标,从而成为调控网络的中心。另一方面,它允许存在靶标模拟物或诱饵,将 sRNA/miRNA 从真正的靶标转移开,从而成为调控调控因子的机制。此外,通过竞争与相同 sRNA 的配对,真正的靶标建立了一种相互交流的关系,从而可能影响彼此的表达水平。在这里,我们回顾了证据表明,靶标模拟和竞争是细菌 sRNA 网络调控结构的重要组成部分。