4.7 Article

dEHBP1 controls exocytosis and recycling of Delta during asymmetric divisions

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JOURNAL OF CELL BIOLOGY
卷 196, 期 1, 页码 65-83

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ROCKEFELLER UNIV PRESS
DOI: 10.1083/jcb.201106088

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资金

  1. National Institutes of Health [P30HD024064, RO1 NS059971]
  2. European Molecular Biology Organization
  3. Howard Hughes Medical Institute
  4. Nakajima Foundation
  5. Pennsylvania Tobacco Settlement fund

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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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