Foran Gregory, Hallam Ryan Douglas, Megaly Marvel, Turgambayeva Anel, Antfolk Daniel, Li Yifeng, Luca Vincent C, Necakov Aleksandar
Department of Biological Sciences, Brock University, 1812 Sir Isaac Brock Way, St. Catharines, Ontario, Canada, L2S 3A1.
Department of Immunology, Moffitt Cancer Centre, Tampa, FL, USA.
bioRxiv. 2024 Aug 1:2023.03.17.533124. doi: 10.1101/2023.03.17.533124.
The Notch receptor is a pleiotropic signaling protein that translates intercellular ligand interactions into changes in gene expression the nuclear localization of the Notch intracellular Domain (NICD). Using a combination of immunohistochemistry, RNA , 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.
Notch受体是一种多效性信号蛋白,它将细胞间配体相互作用转化为基因表达的变化,即Notch细胞内结构域(NICD)的核定位变化。通过结合免疫组织化学、RNA、光遗传学和人类细胞中转录的超分辨率实时成像,我们发现N1ICD可以形成凝聚物,积极促进Notch靶基因的表达。我们确定N1ICD经历相分离耦合渗透(PSCP)形成转录凝聚物,这些凝聚物招募、富集并包裹广泛的核心转录蛋白。我们表明,凝聚能力归因于N1ICD固有无序的转录激活结构域。此外,这种转录凝聚物的形成有助于促进Notch介导的超级增强子环化以及MYC原癌基因表达的伴随激活。总体而言,我们引入了一种Notch1活性的新机制,其中核内N1ICD丰度的离散变化转化为转录凝聚物的组装,通过在靶基因组位点富集必需的转录机制来促进基因表达。