Baker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Department of Genetics and Biochemistry, Clemson University, Clemson, SC, USA.
Nat Genet. 2023 Aug;55(8):1370-1380. doi: 10.1038/s41588-023-01442-7. Epub 2023 Jul 10.
How enhancers control target gene expression over long genomic distances remains an important unsolved problem. Here we investigated enhancer-promoter communication by integrating data from nucleosome-resolution genomic contact maps, nascent transcription and perturbations affecting either RNA polymerase II (Pol II) dynamics or the activity of thousands of candidate enhancers. Integration of new Micro-C experiments with published CRISPRi data demonstrated that enhancers spend more time in close proximity to their target promoters in functional enhancer-promoter pairs compared to nonfunctional pairs, which can be attributed in part to factors unrelated to genomic position. Manipulation of the transcription cycle demonstrated a key role for Pol II in enhancer-promoter interactions. Notably, promoter-proximal paused Pol II itself partially stabilized interactions. We propose an updated model in which elements of transcriptional dynamics shape the duration or frequency of interactions to facilitate enhancer-promoter communication.
增强子如何在长距离的基因组上控制靶基因的表达仍然是一个重要的未解决的问题。在这里,我们通过整合来自核小体分辨率基因组接触图谱、新生转录和影响 RNA 聚合酶 II(Pol II)动力学或数千个候选增强子活性的扰动的数据,研究了增强子-启动子之间的通讯。新的 Micro-C 实验与已发表的 CRISPRi 数据的整合表明,与非功能增强子-启动子对相比,功能增强子-启动子对中的增强子在更接近其靶启动子的位置花费更多时间,这部分归因于与基因组位置无关的因素。转录周期的操作表明 Pol II 在增强子-启动子相互作用中起着关键作用。值得注意的是,启动子近端暂停的 Pol II 本身部分稳定了相互作用。我们提出了一个更新的模型,其中转录动力学的元素形成了相互作用的持续时间或频率,以促进增强子-启动子通讯。
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