The Journal of Cell Biology · 2007 · 172 citations · 54 references
Life SciencesCell BiologyMolecular BiologyEndocytosisIntracellular TransportMembrane TraffickingCargo SortingEndomembrane SystemIron TransportLate EndosomesProtein SortingProtein TargetingEndocytic Pathway RegulationEndocytic Recycling PathwaysEndocytic RegulationEndosome-golgi TransportRab Gtpase FunctionRetromer ComplexRetromer-mediated RecyclingRetromer-mediated Sorting
Amajor function of the endocytic system is the sorting of cargo to various organelles. Endocytic sorting of the yeast reductive iron transporter, which is composed of the Fet3 and Ftr1 proteins, is regulated by available iron. When iron is provided to iron-starved cells, Fet3p-Ftr1p is targeted to the lysosome-like vacuole and degraded. In contrast, when iron is not available, Fet3p-Ftr1p is maintained on the plasma membrane via an endocytic recycling pathway requiring the sorting nexin Grd19/Snx3p, the pentameric retromer complex, and the Ypt6p Golgi Rab GTPase module. A recycling signal in Ftr1p was identified and found to bind directly to Grd19/Snx3p. Retromer and Grd19/Snx3p partially colocalize to tubular endosomes, where they are physically associated. After export from the endosome, Fet3p-Ftr1p transits through the Golgi apparatus for resecretion. Thus, Grd19/Snx3p, functions as a cargo-specific adapter for the retromer complex, establishing a precedent for a mechanism by which sorting nexins expand the repertoire of retromer-dependent cargos.
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A Permease-Oxidase Complex Involved in High-Affinity Iron Uptake in Yeast
Robert S. Stearman, Daniel Yuan, Yuko Yamaguchi‐Iwai et al. · Science · 1996 · 681 citations
The FET3 gene of S. cerevisiae encodes a multicopper oxidase required for ferrous iron uptake
Candice C. Askwith, David Eide, Anthony Van Ho et al. · Cell · 1994 · 673 citations