Nicolas Damien, Phillips Nick E, Naef Felix
The Institute of Bioengineering, School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
Mol Biosyst. 2017 Jun 27;13(7):1280-1290. doi: 10.1039/c7mb00154a.
Isogenic cells in a common environment present a large degree of heterogeneity in gene expression. Part of this variability is attributed to transcriptional bursting: the stochastic activation and inactivation of promoters that leads to the discontinuous production of mRNA. The diversity in bursting patterns displayed by different genes suggests the existence of a connection between bursting and gene regulation. Experimental strategies such as single-molecule RNA FISH, MS2-GFP or short-lived protein reporters allow the quantification of transcriptional bursting and the comparison of bursting kinetics between conditions, allowing therefore the identification of molecular mechanisms modulating transcriptional bursting. In this review we recapitulate the impact on transcriptional bursting of different molecular aspects of transcription such as the chromatin environment, nucleosome occupancy, histone modifications, the number and affinity of regulatory elements, DNA looping and transcription factor availability. More specifically, we examine their role in tuning the burst size or the burst frequency. While some molecular mechanisms involved in transcription such as histone marks can affect every aspect of bursting, others predominantly influence the burst size (e.g. the number and affinity of cis-regulatory elements) or frequency (e.g. transcription factor availability).
处于共同环境中的同基因细胞在基因表达上呈现出很大程度的异质性。这种变异性部分归因于转录爆发:启动子的随机激活和失活导致mRNA的不连续产生。不同基因所表现出的爆发模式的多样性表明爆发与基因调控之间存在联系。诸如单分子RNA荧光原位杂交、MS2-绿色荧光蛋白或短寿命蛋白质报告基因等实验策略能够对转录爆发进行定量,并比较不同条件下的爆发动力学,从而有助于识别调节转录爆发的分子机制。在这篇综述中,我们概括了转录的不同分子层面(如染色质环境、核小体占有率、组蛋白修饰、调控元件的数量和亲和力、DNA环化以及转录因子的可利用性)对转录爆发的影响。更具体地说,我们研究它们在调节爆发大小或爆发频率方面的作用。虽然一些参与转录的分子机制(如组蛋白标记)可以影响爆发的各个方面,但其他机制主要影响爆发大小(如顺式调控元件的数量和亲和力)或频率(如转录因子的可利用性)。