<i>dEHBP1</i> controls exocytosis and recycling of Delta during asymmetric divisions

Νικόλαος Γιαγτζόγλου(Howard Hughes Medical Institute), Shinya Yamamoto(Howard Hughes Medical Institute), Diana Zitserman(Fox Chase Cancer Center), Hillary K. Graves(Howard Hughes Medical Institute), Karen L. Schulze(Howard Hughes Medical Institute), Hao Wang(Howard Hughes Medical Institute), Hayley Klein(Howard Hughes Medical Institute), Fabrice Roegiers(Fox Chase Cancer Center), Hugo J. Bellen(Howard Hughes Medical Institute)
The Journal of Cell Biology
January 2, 2012
Cited by 43Open Access
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Abstract

Notch signaling governs binary cell fate determination in asymmetrically dividing cells. Through a forward genetic screen we identified the fly homologue of Eps15 homology domain containing protein-binding protein 1 (dEHBP1) as a novel regulator of Notch signaling in asymmetrically dividing cells. dEHBP1 is enriched basally and at the actin-rich interface of pII cells of the external mechanosensory organs, where Notch signaling occurs. Loss of function of dEHBP1 leads to up-regulation of Sanpodo, a regulator of Notch signaling, and aberrant trafficking of the Notch ligand, Delta. Furthermore, Sec15 and Rab11, which have been previously shown to regulate the localization of Delta, physically interact with dEHBP1. We propose that dEHBP1 functions as an adaptor molecule for the exocytosis and recycling of Delta, thereby affecting cell fate decisions in asymmetrically dividing cells.


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