Department of Systems Biology, University of Massachusetts Chan Medical School, Worcester, MA, USA.
Howard Hughes Medical Institute, Chevy Chase, MD, USA.
Nat Struct Mol Biol. 2022 Dec;29(12):1239-1251. doi: 10.1038/s41594-022-00890-9. Epub 2022 Dec 8.
Cohesin-mediated loop extrusion has been shown to be blocked at specific cis-elements, including CTCF sites, producing patterns of loops and domain boundaries along chromosomes. Here we explore such cis-elements, and their role in gene regulation. We find that transcription termination sites of active genes form cohesin- and RNA polymerase II-dependent domain boundaries that do not accumulate cohesin. At these sites, cohesin is first stalled and then rapidly unloaded. Start sites of transcriptionally active genes form cohesin-bound boundaries, as shown before, but are cohesin-independent. Together with cohesin loading, possibly at enhancers, these sites create a pattern of cohesin traffic that guides enhancer-promoter interactions. Disrupting this traffic pattern, by removing CTCF, renders cells sensitive to knockout of genes involved in transcription initiation, such as the SAGA complexes, and RNA processing such DEAD/H-Box RNA helicases. Without CTCF, these factors are less efficiently recruited to active promoters.
黏合蛋白介导的环挤出已被证明在特定的顺式元件(包括 CTCF 位点)处被阻断,从而在染色体上产生环和结构域边界的模式。在这里,我们探索了这些顺式元件及其在基因调控中的作用。我们发现,活跃基因的转录终止位点形成依赖于黏合蛋白和 RNA 聚合酶 II 的结构域边界,这些边界不会积累黏合蛋白。在这些位点上,黏合蛋白首先停滞,然后迅速卸载。正如之前所显示的,转录活跃基因的起始位点形成黏合蛋白结合的边界,但与黏合蛋白无关。与黏合蛋白的加载一起(可能在增强子处),这些位点创建了一个黏合蛋白流的模式,指导增强子-启动子相互作用。通过去除 CTCF 破坏这种流模式,会使细胞对参与转录起始(如 SAGA 复合物)和 RNA 加工(如 DEAD/H-Box RNA 解旋酶)的基因的敲除变得敏感。没有 CTCF,这些因子更难以有效地招募到活跃的启动子。