Graduate Program in Biophysical Sciences, The University of Chicago, Chicago, IL 60637, USA; Institute for Biophysical Dynamics, The University of Chicago, Chicago, IL 60637, USA.
Department of Biochemistry and Molecular Biology, The University of Chicago, Chicago, IL 60637, USA.
Cell Rep. 2021 Sep 28;36(13):109764. doi: 10.1016/j.celrep.2021.109764.
Small RNAs (sRNAs) are important gene regulators in bacteria. Many sRNAs act post-transcriptionally by affecting translation and degradation of the target mRNAs upon base-pairing interactions. Here we present a general approach combining imaging and mathematical modeling to determine kinetic parameters at different levels of sRNA-mediated gene regulation that contribute to overall regulation efficacy. Our data reveal that certain sRNAs previously characterized as post-transcriptional regulators can regulate some targets co-transcriptionally, leading to a revised model that sRNA-mediated regulation can occur early in an mRNA's lifetime, as soon as the sRNA binding site is transcribed. This co-transcriptional regulation is likely mediated by Rho-dependent termination when transcription-coupled translation is reduced upon sRNA binding. Our data also reveal several important kinetic steps that contribute to the differential regulation of mRNA targets by an sRNA. Particularly, binding of sRNA to the target mRNA may dictate the regulation hierarchy observed within an sRNA regulon.
小 RNA(sRNA)是细菌中重要的基因调控因子。许多 sRNA 通过碱基配对相互作用影响靶 mRNA 的翻译和降解来发挥转录后作用。在这里,我们提出了一种结合成像和数学建模的通用方法,以确定不同水平的 sRNA 介导的基因调控的动力学参数,这些参数有助于整体调控效果。我们的数据表明,以前被表征为转录后调控因子的某些 sRNA 可以在转录水平上调控某些靶标,从而提出了一个修正的模型,即 sRNA 介导的调控可以在 mRNA 的生命周期早期发生,只要 sRNA 结合位点被转录。这种共转录调控可能是由 Rho 依赖性终止介导的,当 sRNA 结合时,转录偶联翻译减少。我们的数据还揭示了几个有助于 sRNA 对 mRNA 靶标进行差异调控的重要动力学步骤。特别是,sRNA 与靶 mRNA 的结合可能决定了在 sRNA 调控子中观察到的调控层次。