2. Academic Validation
  3. Sac2/INPP5F is an inositol 4-phosphatase that functions in the endocytic pathway

Sac2/INPP5F is an inositol 4-phosphatase that functions in the endocytic pathway

  • J Cell Biol. 2015 Apr 13;209(1):85-95. doi: 10.1083/jcb.201409064.
Fubito Nakatsu 1,  Mirko Messa 1,  Ramiro Nández 1,  Heather Czapla 1,  Yixiao Zou 2,  Stephen M Strittmatter 2,  Pietro De Camilli 3
Affiliations

Affiliations

  • 1 Department of Cell Biology, Howard Hughes Medical Institute, Department of Neurology, and Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale University School of Medicine, New Haven, CT 06510 Department of Cell Biology, Howard Hughes Medical Institute, Department of Neurology, and Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale University School of Medicine, New Haven, CT 06510 Department of Cell Biology, Howard Hughes Medical Institute, Department of Neurology, and Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale University School of Medicine, New Haven, CT 06510.
  • 2 Department of Cell Biology, Howard Hughes Medical Institute, Department of Neurology, and Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale University School of Medicine, New Haven, CT 06510 Department of Cell Biology, Howard Hughes Medical Institute, Department of Neurology, and Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale University School of Medicine, New Haven, CT 06510.
  • 3 Department of Cell Biology, Howard Hughes Medical Institute, Department of Neurology, and Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale University School of Medicine, New Haven, CT 06510 Department of Cell Biology, Howard Hughes Medical Institute, Department of Neurology, and Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale University School of Medicine, New Haven, CT 06510 Department of Cell Biology, Howard Hughes Medical Institute, Department of Neurology, and Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale University School of Medicine, New Haven, CT 06510 [email protected].
PMID: 25869668 DOI: 10.1083/jcb.201409064
Abstract

The recruitment of inositol phosphatases to endocytic membranes mediates dephosphorylation of PI(4,5)P2, a phosphoinositide concentrated in the plasma membrane, and prevents its accumulation on endosomes. The importance of the conversion of PI(4,5)P2 to PtdIns during endocytosis is demonstrated by the presence of both a 5-phosphatase and a 4-phosphatase (Sac domain) module in the synaptojanins, endocytic PI(4,5)P2 phosphatases conserved from yeast to humans and the only PI(4,5)P2 phosphatases in yeast. OCRL, another 5-phosphatase that couples endocytosis to PI(4,5)P2 dephosphorylation, lacks a Sac domain. Here we show that Sac2/INPP5F is a PI4P Phosphatase that colocalizes with OCRL on endocytic membranes, including vesicles formed by clathrin-mediated endocytosis, macropinosomes, and Rab5 endosomes. An OCRL-Sac2/INPP5F interaction could be demonstrated by coimmunoprecipitation and was potentiated by Rab5, whose activity is required to recruit Sac2/INPP5F to endosomes. Sac2/INPP5F and OCRL may cooperate in the sequential dephosphorylation of PI(4,5)P2 at the 5 and 4 position of inositol in a partnership that mimics that of the two Phosphatase modules of synaptojanin.

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