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RITA, a novel modulator of Notch signalling, acts via nuclear export of RBP-J

Authors: 
Wacker SA, Alvarado C, von Wichert G, Knippschild U, Wiedenmann J, Clauß K, Nienhaus GU, Hameister H, Baumann B, Borggrefe T, Knöchel W, Oswald F
Citation: 
EMBO J. 2010 Nov 23. [Epub ahead of print]
Abstract: 
The evolutionarily conserved Notch signal transduction pathway regulates fundamental cellular processes during embryonic development and in the adult. Ligand binding induces presenilin-dependent cleavage of the receptor and a subsequent nuclear translocation of the Notch intracellular domain (NICD). In the nucleus, NICD binds to the recombination signal sequence-binding protein J (RBP-J)/CBF-1 transcription factor to induce expression of Notch target genes. Here, we report the identification and functional characterization of RBP-J interacting and tubulin associated (RITA) (C12ORF52) as a novel RBP-J/CBF-1-interacting protein. RITA is a highly conserved 36 kDa protein that, most interestingly, binds to tubulin in the cytoplasm and shuttles rapidly between cytoplasm and nucleus. This shuttling RITA exports RBP-J/CBF-1 from the nucleus. Functionally, we show that RITA can reverse a Notch-induced loss of primary neurogenesis in Xenopus laevis. Furthermore, RITA is able to downregulate Notch-mediated transcription. Thus, we propose that RITA acts as a negative modulator of the Notch signalling pathway, controlling the level of nuclear RBP-J/CBF-1, where its amounts are limiting.
Organism or Cell Type: 
Xenopus
Delivery Method: 
Microinjection