Yoon Young Soo, Jeong Sangkyun, Rong Qi, Park Kye-Yoon, Chung Jae Hoon, Pfeifer Karl
Laboratory of Mammalian Genes and Development, NICHD, NIH, Bethesda, MD 20892, USA.
Mol Cell Biol. 2007 May;27(9):3499-510. doi: 10.1128/MCB.02170-06. Epub 2007 Mar 5.
Transcriptional insulators are specialized cis-acting elements that protect promoters from inappropriate activation by distal enhancers. The H19 imprinting control region (ICR) functions as a CTCF-dependent, methylation-sensitive transcriptional insulator. We analyzed several insertional mutations and demonstrate that the ICR can function as a methylation-regulated maternal chromosome-specific insulator in novel chromosomal contexts. We used chromosome conformation capture and chromatin immunoprecipitation assays to investigate the configuration of cis-acting elements at these several insertion sites. By comparing maternal and paternal organizations on wild-type and mutant chromosomes, we hoped to identify mechanisms for ICR insulator function. We found that promoter and enhancer elements invariably associate to form DNA loop domains at transcriptionally active loci. Conversely, active insulators always prevent these promoter-enhancer interactions. Instead, the ICR insulator forms novel loop domains by associating with the blocked promoters and enhancers. We propose that these associations are fundamental to insulator function.
转录绝缘子是一种特殊的顺式作用元件,可保护启动子免受远端增强子的不适当激活。H19印记控制区(ICR)作为一种依赖CTCF、对甲基化敏感的转录绝缘子发挥作用。我们分析了几个插入突变,并证明ICR在新的染色体环境中可作为甲基化调节的母源染色体特异性绝缘子发挥作用。我们使用染色体构象捕获和染色质免疫沉淀分析来研究这几个插入位点处顺式作用元件的构型。通过比较野生型和突变染色体上的母源和父源组织,我们希望确定ICR绝缘子功能的机制。我们发现,启动子和增强子元件在转录活跃位点总是相互关联形成DNA环结构域。相反,活性绝缘子总是阻止这些启动子-增强子相互作用。取而代之的是,ICR绝缘子通过与被阻断的启动子和增强子结合形成新的环结构域。我们认为这些关联对于绝缘子功能至关重要。