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A role of the Lowe syndrome protein OCRL in early steps of the endocytic pathway.

Authors
Erdmann, KS; Mao, Y; McCrea, HJ; Zoncu, R; Lee, S; Paradise, S; Modregger, J; Biemesderfer, D; Toomre, D; De Camilli, P
Citation
Developmental cell, 13(3):377-390, 2007
Journal Title
Developmental cell
ISSN
1534-58071878-1551
Abstract
Mutations in the inositol 5-phosphatase OCRL are responsible for Lowe syndrome, whose manifestations include mental retardation and renal Fanconi syndrome. OCRL has been implicated in membrane trafficking, but disease mechanisms remain unclear. We show that OCRL visits late-stage, endocytic clathrin-coated pits and binds the Rab5 effector APPL1 on peripheral early endosomes. The interaction with APPL1, which is mediated by the ASH-RhoGAP-like domains of OCRL and is abolished by disease mutations, provides a link to protein networks implicated in the reabsorptive function of the kidney and in the trafficking and signaling of growth factor receptors in the brain. Crystallographic studies reveal a role of the ASH-RhoGAP-like domains in positioning the phosphatase domain at the membrane interface and a clathrin box protruding from the RhoGAP-like domain. Our results support a role of OCRL in the early endocytic pathway, consistent with the predominant localization of its preferred substrates, PI(4,5)P(2) and PI(3,4,5)P(3), at the cell surface.
MeSH terms
Adaptor Proteins, Signal TransducingAmino Acid SequenceAnimalsCOS CellsCarrier Proteins/geneticsCarrier Proteins/metabolismCell LineCercopithecus aethiopsClathrin-Coated Vesicles/metabolismCrystallography, X-RayEndocytosis/physiology*Endosomes/enzymologyEndosomes/metabolism*Glutathione Transferase/metabolismGreen Fluorescent Proteins/metabolismHumansKidney/cytologyModels, BiologicalModels, MolecularMolecular Sequence DataMutationPhosphatidylinositol 4,5-Diphosphate/metabolismPhosphatidylinositols/metabolismPhosphoric Monoester Hydrolases/chemistryPhosphoric Monoester Hydrolases/geneticsPhosphoric Monoester Hydrolases/isolation & purificationPhosphoric Monoester Hydrolases/metabolism*PhosphorylationProtein Structure, SecondaryProtein Structure, TertiaryRecombinant Fusion Proteins/metabolismSequence Homology, Amino AcidTime Factors
DOI
10.1016/j.devcel.2007.08.004
PMID
17765681
Appears in Collections:
Journal Papers > Research Organization > Chronic Inflammatory Disease Research Center
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이, 상윤
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