Ferro Elsi, Szischik Candela L, Ventura Alejandra C, Bosia Carla
Department of Applied Science and Technology, Politecnico di Torino, Corso Duca degli Abruzzi 24, 10129 Torino, Italy.
IIGM Foundation-Italian Institute for Genomic Medicine, c/o IRCCS, SP 142 km 3,95, Candiolo, 10060 Torino, Italy.
Nucleic Acids Res. 2025 Sep 5;53(17). doi: 10.1093/nar/gkaf867.
Cells may exploit oscillatory gene expression to encode biological information. Temporal features of oscillations, such as pulse frequency and amplitude, are determinant for the outcome of signalling pathways. However, little effort has been devoted to unveiling the role of pulsatility in the context of post-transcriptional gene regulation, where microRNAs act by binding to RNAs and regulate their expression. Here, we study the effects of periodic against constant microRNA synthesis within minimal microRNA-target networks. We find that there is a repressive advantage of pulsatile over constant microRNA synthesis, and that the extent of repression depends on the frequency of pulses, thus uncovering frequency preference behaviours. We show that the preference for specific input frequencies is determined by relative microRNA and target kinetic rates and can lead to exclusive frequency-dependent repression on distinct RNA species, thereby highlighting a potential mechanism of selective dynamical target regulation. Moreover, we show that frequencies observed in periodically expressed microRNAs, such as those involved in circadian rhythms and development, can be selectively favored. Our findings might have implications for experimental studies aimed at understanding how periodic patterns drive biological responses through microRNA-mediated signalling and provide suggestions for validation in synthetic networks.
细胞可能利用振荡基因表达来编码生物信息。振荡的时间特征,如脉冲频率和幅度,对于信号通路的结果起着决定性作用。然而,在转录后基因调控的背景下,人们很少致力于揭示脉动性的作用,在转录后基因调控中,微小RNA通过与RNA结合并调节其表达来发挥作用。在这里,我们研究了在最小的微小RNA-靶标网络中,周期性微小RNA合成与恒定微小RNA合成的效果。我们发现,脉动性微小RNA合成相对于恒定微小RNA合成具有抑制优势,并且抑制程度取决于脉冲频率,从而揭示了频率偏好行为。我们表明,对特定输入频率的偏好由相对微小RNA和靶标的动力学速率决定,并且可以导致对不同RNA种类的排他性频率依赖性抑制,从而突出了选择性动态靶标调控的潜在机制。此外,我们表明,在周期性表达的微小RNA中观察到的频率,如那些参与昼夜节律和发育的频率,可以被选择性地偏好。我们的发现可能对旨在理解周期性模式如何通过微小RNA介导的信号传导驱动生物反应的实验研究具有启示意义,并为合成网络中的验证提供建议。