FB2026_02 , released June 18, 2026
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Citation
Kuang, Y., Pyo, A., Eafergan, N., Cain, B., Gutzwiller, L.M., Axelrod, O., Gagliani, E.K., Weirauch, M.T., Kopan, R., Kovall, R.A., Sprinzak, D., Gebelein, B. (2021). Enhancers with cooperative Notch binding sites are more resistant to regulation by the Hairless co-repressor.  PLoS Genet. 17(9): e1009039.
FlyBase ID
FBrf0251537
Publication Type
Research paper
Abstract
Notch signaling controls many developmental processes by regulating gene expression. Notch-dependent enhancers recruit activation complexes consisting of the Notch intracellular domain, the Cbf/Su(H)/Lag1 (CSL) transcription factor (TF), and the Mastermind co-factor via two types of DNA sites: monomeric CSL sites and cooperative dimer sites called Su(H) paired sites (SPS). Intriguingly, the CSL TF can also bind co-repressors to negatively regulate transcription via these same sites. Here, we tested how synthetic enhancers with monomeric CSL sites versus dimeric SPSs bind Drosophila Su(H) complexes in vitro and mediate transcriptional outcomes in vivo. Our findings reveal that while the Su(H)/Hairless co-repressor complex similarly binds SPS and CSL sites in an additive manner, the Notch activation complex binds SPSs, but not CSL sites, in a cooperative manner. Moreover, transgenic reporters with SPSs mediate stronger, more consistent transcription and are more resistant to increased Hairless co-repressor expression compared to reporters with the same number of CSL sites. These findings support a model in which SPS containing enhancers preferentially recruit cooperative Notch activation complexes over Hairless repression complexes to ensure consistent target gene activation.
PubMed ID
PubMed Central ID
PMC8494340 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    PLoS Genet.
    Title
    PLoS Genetics
    Publication Year
    2005-
    ISBN/ISSN
    1553-7404 1553-7390
    Data From Reference
    Alleles (20)
    Genes (8)
    Physical Interactions (2)
    Natural transposons (2)
    Insertions (20)
    Experimental Tools (4)
    Transgenic Constructs (19)