Priest David G, Kumar Sandip, Yan Yan, Dunlap David D, Dodd Ian B, Shearwin Keith E
School of Molecular and Biomedical Science (Biochemistry), University of Adelaide, Adelaide, SA 5005, Australia; and.
Departments of Cell Biology.
Proc Natl Acad Sci U S A. 2014 Oct 21;111(42):E4449-57. doi: 10.1073/pnas.1410764111. Epub 2014 Oct 6.
Eukaryotic gene regulation involves complex patterns of long-range DNA-looping interactions between enhancers and promoters, but how these specific interactions are achieved is poorly understood. Models that posit other DNA loops--that aid or inhibit enhancer-promoter contact--are difficult to test or quantitate rigorously in eukaryotic cells. Here, we use the well-characterized DNA-looping proteins Lac repressor and phage λ CI to measure interactions between pairs of long DNA loops in E. coli cells in the three possible topological arrangements. We find that side-by-side loops do not affect each other. Nested loops assist each other's formation consistent with their distance-shortening effect. In contrast, alternating loops, where one looping element is placed within the other DNA loop, inhibit each other's formation, thus providing clear support for the loop domain model for insulation. Modeling shows that combining loop assistance and loop interference can provide strong specificity in long-range interactions.
真核基因调控涉及增强子与启动子之间复杂的远程DNA环化相互作用模式,但这些特定相互作用是如何实现的,目前还知之甚少。提出其他DNA环(即协助或抑制增强子-启动子接触的环)的模型,很难在真核细胞中进行严格测试或定量分析。在这里,我们使用特征明确的DNA环化蛋白Lac阻遏物和噬菌体λ CI,来测量大肠杆菌细胞中三对长DNA环在三种可能拓扑排列下的相互作用。我们发现,并排的环彼此不影响。嵌套环相互协助形成,这与其缩短距离的效应一致。相比之下,交替环(即一个环化元件置于另一个DNA环内)则会抑制彼此的形成,从而为绝缘的环结构域模型提供了明确支持。建模显示,结合环协助和环干扰可以在远程相互作用中提供强大的特异性。