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利用功能基因组分析方法来注释全基因组范围内的增强子-启动子相互作用。

Functional genomic assays to annotate enhancer-promoter interactions genome wide.

机构信息

Department of Computational Biology, Cornell University, Ithaca, NY 14853, USA.

Weill Institute for Cell and Molecular Biology, Cornell University, Ithaca, NY 14853, USA.

出版信息

Hum Mol Genet. 2022 Oct 20;31(R1):R97-R104. doi: 10.1093/hmg/ddac204.

Abstract

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.

摘要

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。

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