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解析正超螺旋积累导致转录锁的体内动力学。

Dissecting the in vivo dynamics of transcription locking due to positive supercoiling buildup.

机构信息

Laboratory of Biosystem Dynamics, BioMediTech, Faculty of Medicine and Health Technology, Tampere University, 33101 Tampere, Finland.

Laboratory of Biosystem Dynamics, BioMediTech, Faculty of Medicine and Health Technology, Tampere University, 33101 Tampere, Finland.

出版信息

Biochim Biophys Acta Gene Regul Mech. 2020 May;1863(5):194515. doi: 10.1016/j.bbagrm.2020.194515. Epub 2020 Feb 27.

Abstract

Positive supercoiling buildup (PSB) is a pervasive phenomenon in the transcriptional programs of Escherichia coli. After finding a range of Gyrase concentrations where the inverse of the transcription rate of a chromosome-integrated gene changes linearly with the inverse of Gyrase concentration, we apply a LineWeaver-Burk plot to dissect the expected in vivo transcription rate in absence of PSB. We validate the estimation by time-lapse microscopy of single-RNA production kinetics of the same gene when single-copy plasmid-borne, shown to be impervious to Gyrase inhibition. Next, we estimate the fraction of time in locked states and number of transcription events prior to locking, which we validate by measurements under Gyrase inhibition. Replacing the gene of interest by one with slower transcription rate decreases the fraction of time in locked states due to PSB. Finally, we combine data from both constructs to infer a range of possible transcription initiation locking kinetics in a chromosomal location, obtainable by tuning the transcription rate. We validate with measurements of transcription activity at different induction levels. This strategy for dissecting transcription initiation locking kinetics due to PSB can contribute to resolve the transcriptional programs of E. coli and in the engineering of synthetic genetic circuits.

摘要

正超螺旋积累(PSB)是大肠杆菌转录程序中普遍存在的现象。在发现一系列拓扑异构酶浓度范围内,染色体整合基因的转录速率的倒数与拓扑异构酶浓度的倒数呈线性关系后,我们应用LineWeaver-Burk 图来剖析无 PSB 时预期的体内转录速率。我们通过对同一基因的单 RNA 产生动力学进行延时显微镜验证来验证估计值,该基因在单拷贝质粒携带时不受拓扑异构酶抑制的影响。接下来,我们估计在锁定状态下的时间分数和在锁定之前的转录事件数量,我们通过在拓扑异构酶抑制下的测量来验证这一点。用转录速率较慢的基因取代感兴趣的基因,由于 PSB,锁定状态的时间分数会减少。最后,我们结合来自两种构建体的数据来推断在染色体位置上可能的转录起始锁定动力学范围,通过调整转录速率来获得。我们通过在不同诱导水平下测量转录活性来验证。这种由于 PSB 而剖析转录起始锁定动力学的策略有助于解析大肠杆菌的转录程序和合成遗传电路的工程设计。

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