MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.
Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
Nat Struct Mol Biol. 2022 Sep;29(9):891-897. doi: 10.1038/s41594-022-00821-8. Epub 2022 Sep 12.
The regulatory landscapes of developmental genes in mammals can be complex, with enhancers spread over many hundreds of kilobases. It has been suggested that three-dimensional genome organization, particularly topologically associating domains formed by cohesin-mediated loop extrusion, is important for enhancers to act over such large genomic distances. By coupling acute protein degradation with synthetic activation by targeted transcription factor recruitment, here we show that cohesin, but not CTCF, is required for activation of the target gene Shh by distant enhancers in mouse embryonic stem cells. Cohesin is not required for activation directly at the promoter or by an enhancer located closer to the Shh gene. Our findings support the hypothesis that chromatin compaction via cohesin-mediated loop extrusion allows for genes to be activated by enhancers that are located many hundreds of kilobases away in the linear genome and suggests that cohesin is dispensable for enhancers located more proximally.
哺乳动物发育基因的调控景观可能很复杂,增强子分布在数百千碱基对以上。有人提出,三维基因组组织,特别是由黏连蛋白介导的环挤出形成的拓扑关联域,对于增强子在如此大的基因组距离上发挥作用很重要。通过将急性蛋白质降解与靶向转录因子募集的合成激活相结合,我们在这里表明,黏连蛋白,但不是 CTCF,对于远处增强子在小鼠胚胎干细胞中激活靶基因 Shh 是必需的。黏连蛋白不需要直接在启动子或更靠近 Shh 基因的增强子处被激活。我们的发现支持了这样一种假设,即通过黏连蛋白介导的环挤出实现的染色质紧缩允许通过位于线性基因组中数百千碱基对之外的增强子激活基因,并表明黏连蛋白对于位于更接近的增强子是可有可无的。