Notch1 相分离耦合渗透促进了目标基因的表达和增强子的循环。

Gregory Foran, Ryan Douglas Hallam, Marvel Megaly, Anel Turgambayeva, Daniel Antfolk, Yifeng Li, Vincent C Luca, Aleksandar Necakov
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引用次数: 0

摘要

Notch受体是一种多效应信号蛋白,它通过Notch胞内域(NICD)的核定位将细胞间配体的相互作用转化为基因表达的变化。我们结合使用免疫组织化学、原位核糖核酸、光遗传学和人体细胞转录超分辨率实时成像技术,证明了 N1ICD 可以形成凝聚体,积极促进 Notch 靶基因的表达。我们确定,N1ICD 经过相分离耦合渗流(PSCP)形成转录凝聚体,这些凝聚体招募、富集并封装了一系列核心转录蛋白。我们的研究表明,N1ICD的转录激活结构域本质上是无序的,因此具有凝聚能力。此外,这种转录凝聚体的形成还能促进 Notch 介导的超级增强子循环,并同时激活 MYC 原癌基因的表达。总之,我们介绍了一种新的 Notch1 活动机制,在这种机制中,核 N1ICD 丰度的离散变化转化为转录凝聚体的组装,这种凝聚体通过在目标基因组位点富集重要的转录机制来促进基因表达。
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Notch1 Phase Separation Coupled Percolation facilitates target gene expression and enhancer looping.

The Notch receptor is a pleiotropic signaling protein that translates intercellular ligand interactions into changes in gene expression via the nuclear localization of the Notch intracellular Domain (NICD). Using a combination of immunohistochemistry, RNA in situ, Optogenetics and super-resolution live imaging of transcription in human cells, we show that the N1ICD can form condensates that positively facilitate Notch target gene expression. We determined that N1ICD undergoes Phase Separation Coupled Percolation (PSCP) into transcriptional condensates, which recruit, enrich, and encapsulate a broad set of core transcriptional proteins. We show that the capacity for condensation is due to the intrinsically disordered transcriptional activation domain of the N1ICD. In addition, the formation of such transcriptional condensates acts to promote Notch-mediated super enhancer-looping and concomitant activation of the MYC protooncogene expression. Overall, we introduce a novel mechanism of Notch1 activity in which discrete changes in nuclear N1ICD abundance are translated into the assembly of transcriptional condensates that facilitate gene expression by enriching essential transcriptional machineries at target genomic loci.

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