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Notch induces transcription by stimulating release of paused RNA polymerase II

  • Julia M. Rogers
  • , Claudia A. Mimoso
  • , Benjamin J.E. Martin
  • , Alexandre P. Martin
  • , Jon C. Aster
  • , Karen Adelman
  • , Stephen C. Blacklow
  • Harvard University
  • Brigham and Women’s Hospital
  • Broad Institute
  • Dana-Farber Cancer Institute

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Notch proteins undergo ligand-induced proteolysis to release a nuclear effector that influences a wide range of cellular processes by regulating transcription. Despite years of study, however, how Notch induces the transcription of its target genes remains unclear. Here, we comprehensively examine the response to human Notch1 across a time course of activation using high-resolution genomic assays of chromatin accessibility and nascent RNA production. Our data reveal that Notch induces target gene transcription primarily by releasing paused RNA polymerase II (RNAPII). Moreover, in contrast to prevailing models suggesting that Notch acts by promoting chromatin accessibility, we found that open chromatin was established at Notch-responsive regulatory elements prior to Notch signal induction through SWI/SNF-mediated remodeling. Together, these studies show that the nuclear response to Notch signaling is dictated by the pre-existing chromatin state and RNAPII distribution at the time of signal activation.

Original languageEnglish
Pages (from-to)965-978
Number of pages14
JournalGenes and Development
Volume38
Issue number21-24
DOIs
StatePublished - Nov 2024

Keywords

  • ATAC-seq
  • NOTCH1
  • Notch signaling
  • PRO-seq
  • SWI/SNF
  • TT-seq

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