Citation

  • Authors: Mosesson, Y., Chetrit, D., Schley, L., Berghoff, J., Ziv, T., Carvalho, S., Milanezi, F., Admon, A., Schmitt, F., Ehrlich, M., Yarden, Y.
  • Year: 2009
  • Journal: Dev Cell 16 687-98
  • Applications: in vitro / DNA / jetPEI
  • Cell type: HeLa
    Description: Human cervix epitheloid carcinoma cells

Abstract

Genetic screens performed in worms identified major regulators of the epidermal growth factor receptor (EGFR) pathway, including the ubiquitin ligase Cbl/SLI-1. Here we focus on the less-characterized Lst2 protein and confirm suppression of MAPK signals. Unexpectedly, human Lst2, a monoubiquitinylated phosphoprotein, does not localize to endosomes, despite an intrinsic phosphoinositol-binding FYVE domain. By constructing an ubiquitinylation-defective mutant and an ubiquitin fusion, we conclude that endosomal localization of Lst2, along with an ability to divert incoming EGFR molecules to degradation in lysosomes, is regulated by ubiquitinylation/deubiquitinylation cycles. Consistent with bifurcating roles, Lst2 physically binds Trim3/BERP, which interacts with Hrs and a complex that biases cargo recycling. These results establish an ubiquitin-based endosomal switch of receptor sorting, functionally equivalent to the mechanism inactivating Hrs via monoubiquitinylation.

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