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增强子主要通过转录起始在分化过程中调控基因表达。

Enhancers predominantly regulate gene expression during differentiation via transcription initiation.

作者信息

Larke Martin S C, Schwessinger Ron, Nojima Takayuki, Telenius Jelena, Beagrie Robert A, Downes Damien J, Oudelaar A Marieke, Truch Julia, Graham Bryony, Bender M A, Proudfoot Nicholas J, Higgs Douglas R, Hughes Jim R

机构信息

MRC Molecular Haematology Unit, MRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK; MRC WIMM Centre for Computational Biology, MRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.

Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK.

出版信息

Mol Cell. 2021 Mar 4;81(5):983-997.e7. doi: 10.1016/j.molcel.2021.01.002. Epub 2021 Feb 3.

Abstract

Gene transcription occurs via a cycle of linked events, including initiation, promoter-proximal pausing, and elongation of RNA polymerase II (Pol II). A key question is how transcriptional enhancers influence these events to control gene expression. Here, we present an approach that evaluates the level and change in promoter-proximal transcription (initiation and pausing) in the context of differential gene expression, genome-wide. This combinatorial approach shows that in primary cells, control of gene expression during differentiation is achieved predominantly via changes in transcription initiation rather than via release of Pol II pausing. Using genetically engineered mouse models, deleted for functionally validated enhancers of the α- and β-globin loci, we confirm that these elements regulate Pol II recruitment and/or initiation to modulate gene expression. Together, our data show that gene expression during differentiation is regulated predominantly at the level of initiation and that enhancers are key effectors of this process.

摘要

基因转录通过一系列相关事件的循环发生,包括起始、启动子近端暂停以及RNA聚合酶II(Pol II)的延伸。一个关键问题是转录增强子如何影响这些事件以控制基因表达。在此,我们提出一种方法,该方法可在全基因组范围内,在基因表达差异的背景下评估启动子近端转录(起始和暂停)的水平及变化。这种组合方法表明,在原代细胞中,分化过程中的基因表达控制主要通过转录起始的变化来实现,而非通过Pol II暂停的释放。利用针对α - 和β - 珠蛋白基因座经功能验证的增强子进行缺失操作的基因工程小鼠模型,我们证实这些元件调节Pol II的募集和/或起始以调节基因表达。总之,我们的数据表明,分化过程中的基因表达主要在起始水平受到调控,并且增强子是这一过程的关键效应因子。

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