Gregory Foran, Ryan Douglas Hallam, Marvel Megaly, Anel Turgambayeva, Daniel Antfolk, Yifeng Li, Vincent C Luca, Aleksandar Necakov
{"title":"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。","authors":"Gregory Foran, Ryan Douglas Hallam, Marvel Megaly, Anel Turgambayeva, Daniel Antfolk, Yifeng Li, Vincent C Luca, Aleksandar Necakov","doi":"10.1101/2023.03.17.533124","DOIUrl":null,"url":null,"abstract":"<p><p>The Notch receptor is a pleiotropic signaling protein that translates intercellular ligand interactions into changes in gene expression <i>via</i> the nuclear localization of the Notch intracellular Domain (NICD). Using a combination of immunohistochemistry, RNA <i>in situ</i>, 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.</p>","PeriodicalId":51078,"journal":{"name":"Journal of Coastal Research","volume":"107 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11312450/pdf/","citationCount":"0","resultStr":"{\"title\":\"Notch1 Phase Separation Coupled Percolation facilitates target gene expression and enhancer looping.\",\"authors\":\"Gregory Foran, Ryan Douglas Hallam, Marvel Megaly, Anel Turgambayeva, Daniel Antfolk, Yifeng Li, Vincent C Luca, Aleksandar Necakov\",\"doi\":\"10.1101/2023.03.17.533124\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The Notch receptor is a pleiotropic signaling protein that translates intercellular ligand interactions into changes in gene expression <i>via</i> the nuclear localization of the Notch intracellular Domain (NICD). Using a combination of immunohistochemistry, RNA <i>in situ</i>, 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.</p>\",\"PeriodicalId\":51078,\"journal\":{\"name\":\"Journal of Coastal Research\",\"volume\":\"107 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11312450/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Coastal Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1101/2023.03.17.533124\",\"RegionNum\":4,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Earth and Planetary Sciences\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Coastal Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2023.03.17.533124","RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Earth and Planetary Sciences","Score":null,"Total":0}
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.
期刊介绍:
The Journal of Coastal Research (JCR) is one of the leading international journals for coastal studies and processes, and is published bi-monthly by the Coastal Education & Research Foundation [CERF]. By covering the entire field of coastal research, the JCR encompasses all subjects relevant to natural and engineered environments (freshwater, brackish, or marine) and the protection/management of their resources in the vicinity of coastlines of the world. Even though the journal broadly focuses on immediate shoreline zones, the JCR also embraces those coastal environments that either reach some indefinite distance inland or that extend seaward beyond the outer margins of the sublittoral (neritic) zone. The JCR disseminates accurate information to both the public and research specialists around the world on all aspects of coastal issues in an effort to maintain or improve the quality of our planet''s shoreline resources.