Department of Computational Biology, Cornell University, Ithaca, NY 14853, USA.
Weill Institute for Cell and Molecular Biology, Cornell University, Ithaca, NY 14853, USA.
Hum Mol Genet. 2022 Oct 20;31(R1):R97-R104. doi: 10.1093/hmg/ddac204.
Enhancers are pivotal for regulating gene transcription that occurs at promoters. Identification of the interacting enhancer-promoter pairs and understanding the mechanisms behind how they interact and how enhancers modulate transcription can provide fundamental insight into gene regulatory networks. Recently, advances in high-throughput methods in three major areas-chromosome conformation capture assay, such as Hi-C to study basic chromatin architecture, ectopic reporter experiments such as self-transcribing active regulatory region sequencing (STARR-seq) to quantify promoter and enhancer activity, and endogenous perturbations such as clustered regularly interspaced short palindromic repeat interference (CRISPRi) to identify enhancer-promoter compatibility-have further our knowledge about transcription. In this review, we will discuss the major method developments and key findings from these assays.
增强子对于调节启动子处的基因转录至关重要。鉴定相互作用的增强子-启动子对,并了解它们相互作用的机制以及增强子如何调节转录,可以深入了解基因调控网络。最近,在三个主要领域的高通量方法方面取得了进展,包括用于研究基本染色质结构的染色体构象捕获测定法,如 Hi-C;用于定量启动子和增强子活性的异位报告实验,如自我转录活性调控区测序(STARR-seq);以及用于鉴定增强子-启动子兼容性的内源性扰动,如成簇规律间隔短回文重复干扰(CRISPRi)。这些方法进一步加深了我们对转录的了解。在这篇综述中,我们将讨论这些测定法的主要方法进展和关键发现。