Department of Developmental and Cell Biology, School of the Biological Sciences, University of California, Irvine, CA, USA.
Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
Nat Genet. 2024 Apr;56(4):675-685. doi: 10.1038/s41588-024-01681-2. Epub 2024 Mar 20.
Remote enhancers are thought to interact with their target promoters via physical proximity, yet the importance of this proximity for enhancer function remains unclear. Here we investigate the three-dimensional (3D) conformation of enhancers during mammalian development by generating high-resolution tissue-resolved contact maps for nearly a thousand enhancers with characterized in vivo activities in ten murine embryonic tissues. Sixty-one percent of developmental enhancers bypass their neighboring genes, which are often marked by promoter CpG methylation. The majority of enhancers display tissue-specific 3D conformations, and both enhancer-promoter and enhancer-enhancer interactions are moderately but consistently increased upon enhancer activation in vivo. Less than 14% of enhancer-promoter interactions form stably across tissues; however, these invariant interactions form in the absence of the enhancer and are likely mediated by adjacent CTCF binding. Our results highlight the general importance of enhancer-promoter physical proximity for developmental gene activation in mammals.
远程增强子被认为通过物理接近与其靶启动子相互作用,但这种接近对增强子功能的重要性仍不清楚。在这里,我们通过在十个鼠胚胎组织中生成近千个具有特征性体内活性的增强子的高分辨率组织分辨接触图谱,研究了哺乳动物发育过程中增强子的三维(3D)构象。61%的发育增强子绕过其邻近的基因,这些基因通常被启动子 CpG 甲基化标记。大多数增强子表现出组织特异性的 3D 构象,并且增强子-启动子和增强子-增强子相互作用在体内增强子激活时适度但一致地增加。不到 14%的增强子-启动子相互作用在组织间稳定形成;然而,这些不变的相互作用在没有增强子的情况下形成,并且可能由相邻的 CTCF 结合介导。我们的结果强调了增强子-启动子物理接近对于哺乳动物发育基因激活的普遍重要性。