Department of Physics and Center for the Physics of Living Cells, University of Illinois at Urbana-Champaign, Loomis Laboratory of Physics, 1110 West Green Street, Urbana, Illinois 61801, USA and Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, 1206 West Gregory Drive, Urbana, Illinois 61801, USA.
Phys Rev Lett. 2021 Nov 19;127(21):218101. doi: 10.1103/PhysRevLett.127.218101.
Transcription of genes can be affected by both biochemical and mechanical factors. Recent experiments suggested that the mechanical stress associated with transcription-induced DNA supercoiling is responsible for the transition from cooperative to antagonistic group dynamics of RNA polymerases (RNAPs) upon promoter repression. To underpin the mechanism behind this drastic transition, we developed a continuum deterministic model for transcription under torsion. In our model, the speed of an RNAP is affected by the local DNA supercoiling, as well as two global factors: (i) the number of RNAPs on the gene affecting the torsional stress experienced by individual RNAPs and (ii) transcription factors blocking the diffusion of DNA supercoils. Our minimal model can successfully reproduce the experimental findings and helps elucidate the interplay of mechanical and biological factors in the collective dynamics of molecular machines involved in gene expression.
基因转录可以受到生化和机械因素的影响。最近的实验表明,与转录诱导的 DNA 超螺旋相关的机械应力是导致 RNA 聚合酶(RNAP)在启动子抑制时从协同到拮抗的群体动力学转变的原因。为了支持这种剧烈转变背后的机制,我们开发了一种用于扭转下转录的连续体确定性模型。在我们的模型中,RNAP 的速度受到局部 DNA 超螺旋的影响,以及两个全局因素:(i)影响单个 RNAP 所经历的扭转应力的基因上的 RNAP 数量,以及(ii)阻止 DNA 超螺旋扩散的转录因子。我们的最小模型可以成功地再现实验结果,并有助于阐明机械和生物因素在参与基因表达的分子机器的集体动力学中的相互作用。