Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Genes Dev August 1, 1998; 12 (15): 2269-77.

A histone deacetylase corepressor complex regulates the Notch signal transduction pathway.

Kao HY , Ordentlich P , Koyano-Nakagawa N , Tang Z , Downes M , Kintner CR , Evans RM , Kadesch T .

The Delta-Notch signal transduction pathway has widespread roles in animal development in which it appears to control cell fate. CBF1/RBP-Jkappa, the mammalian homolog of Drosophila Suppressor of Hairless [Su(H)], switches from a transcriptional repressor to an activator upon Notch activation. The mechanism whereby Notch regulates this switch is not clear. In this report we show that prior to induction CBF1/RBP-Jkappa interacts with a corepressor complex containing SMRT (silencing mediator of retinoid and thyroid hormone receptors) and the histone deacetylase HDAC-1. This complex binds via the CBF1 repression domain, and mutants defective in repression fail to interact with the complex. Activation by Notch disrupts the formation of the repressor complex, thus establishing a molecular basis for the Notch switch. Finally, ESR-1, a Xenopus gene activated by Notch and X-Su(H), is induced in animal caps treated with TSA, an inhibitor of HDAC-1. The functional role for the SMRT/HDAC-1 complex in CBF1/RBP-Jkappa regulation reveals a novel genetic switch in which extracellular ligands control the status of critical nuclear cofactor complexes.

PubMed ID: 9694793
PMC ID: PMC317043
Article link: Genes Dev
Grant support: [+]
Genes referenced: hdac3 hes5.1 ncor2 notch1 rbpj

References [+] :
Alland, Role for N-CoR and histone deacetylase in Sin3-mediated transcriptional repression. 1997, Pubmed

Xenbase: The Xenopus Model Organism Knowledgebase.
Version: 4.14.0
Major funding for Xenbase is provided by grant P41 HD064556