Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Gene Regulation Observatory, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Nat Rev Mol Cell Biol. 2024 Jul;25(7):574-591. doi: 10.1038/s41580-024-00710-6. Epub 2024 Feb 27.
The primary regulators of metazoan gene expression are enhancers, originally functionally defined as DNA sequences that can activate transcription at promoters in an orientation-independent and distance-independent manner. Despite being crucial for gene regulation in animals, what mechanisms underlie enhancer selectivity for promoters, and more fundamentally, how enhancers interact with promoters and activate transcription, remain poorly understood. In this Review, we first discuss current models of enhancer-promoter interactions in space and time and how enhancers affect transcription activation. Next, we discuss different mechanisms that mediate enhancer selectivity, including repression, biochemical compatibility and regulation of 3D genome structure. Through 3D polymer simulations, we illustrate how the ability of 3D genome folding mechanisms to mediate enhancer selectivity strongly varies for different enhancer-promoter interaction mechanisms. Finally, we discuss how recent technical advances may provide new insights into mechanisms of enhancer-promoter interactions and how technical biases in methods such as Hi-C and Micro-C and imaging techniques may affect their interpretation.
真核生物基因表达的主要调控元件是增强子,最初在功能上被定义为能够以非定向和非距离依赖的方式激活启动子转录的 DNA 序列。尽管增强子对动物的基因调控至关重要,但增强子对启动子的选择性的机制基础,以及更根本的是,增强子如何与启动子相互作用并激活转录,仍知之甚少。在这篇综述中,我们首先讨论了增强子-启动子相互作用在时空上的现有模型,以及增强子如何影响转录激活。接下来,我们讨论了介导增强子选择性的不同机制,包括抑制、生化兼容性和调节 3D 基因组结构。通过 3D 聚合物模拟,我们说明了 3D 基因组折叠机制介导增强子选择性的能力因不同的增强子-启动子相互作用机制而有很大差异。最后,我们讨论了最近的技术进步如何可能为增强子-启动子相互作用的机制提供新的见解,以及 Hi-C 和 Micro-C 等方法以及成像技术中的技术偏差如何影响它们的解释。