van den Berg Aafke A, Depken Martin
Department of Bionanoscience, Kavli Institute of Nanoscience, Faculty of Applied Sciences, Delft University of Technology, Van der Maasweg 9, 2629 HZ Delft, The Netherlands.
Nucleic Acids Res. 2017 Jul 27;45(13):7623-7632. doi: 10.1093/nar/gkx513.
During eukaryotic transcription, RNA polymerase (RNAP) translocates along DNA molecules covered with nucleosomes and other DNA binding proteins. Though the interactions between a single nucleosome and RNAP are by now fairly well understood, this understanding has not been synthesized into a description of transcription on crowded genes, where multiple RNAP transcribe through nucleosomes while preserving the nucleosome coverage. We here take a deductive modeling approach to establish the consequences of RNAP-nucleosome interactions for transcription in crowded environments. We show that under physiologically crowded conditions, the interactions of RNAP with nucleosomes induce a strong kinetic attraction between RNAP molecules, causing them to self-organize into stable and moving pelotons. The peloton formation quantitatively explains the observed nucleosome and RNAP depletion close to the initiation site on heavily transcribed genes. Pelotons further translate into short-timescale transcriptional bursts at termination, resulting in burst characteristics consistent with instances of bursty transcription observed in vivo. To facilitate experimental testing of our proposed mechanism, we present several analytic relations that make testable quantitative predictions.
在真核生物转录过程中,RNA聚合酶(RNAP)沿着覆盖有核小体和其他DNA结合蛋白的DNA分子移动。尽管目前对单个核小体与RNAP之间的相互作用已经有了相当深入的了解,但这种理解尚未整合到对密集基因转录的描述中,在密集基因中,多个RNAP穿过核小体,同时保持核小体的覆盖。我们在这里采用演绎建模方法来确定RNAP - 核小体相互作用对拥挤环境中转录的影响。我们表明,在生理拥挤条件下,RNAP与核小体的相互作用会在RNAP分子之间诱导强烈的动力学吸引力,导致它们自组织成稳定且移动的聚合体。聚合体的形成定量地解释了在高度转录基因起始位点附近观察到的核小体和RNAP缺失现象。聚合体在终止时进一步转化为短时间尺度的转录爆发,产生与体内观察到的爆发性转录实例一致的爆发特征。为了便于对我们提出的机制进行实验测试,我们提出了几个可进行实验验证的定量预测分析关系。