SNX27 mediates PDZ-directed sorting from endosomes to the plasma membrane

Author:

Lauffer Benjamin E.L.1,Melero Cristina1,Temkin Paul11,Lei Cai2,Hong Wanjin2,Kortemme Tanja1,von Zastrow Mark111

Affiliation:

1. Program in Pharmaceutical Sciences and Pharmacogenomics, Department of Bioengineering and Therapeutic Sciences, Program in Cell Biology, Department of Biochemistry and Biophysics, Department of Psychiatry, and Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94158

2. Membrane and Biology Laboratory, Institute of Molecular and Cell Biology, Singapore 138673

Abstract

Postsynaptic density 95/discs large/zonus occludens-1 (PDZ) domain–interacting motifs, in addition to their well-established roles in protein scaffolding at the cell surface, are proposed to act as cis-acting determinants directing the molecular sorting of transmembrane cargo from endosomes to the plasma membrane. This hypothesis requires the existence of a specific trans-acting PDZ protein that mediates the proposed sorting operation in the endosome membrane. Here, we show that sorting nexin 27 (SNX27) is required for efficient PDZ-directed recycling of the β2-adrenoreceptor (β2AR) from early endosomes. SNX27 mediates this sorting function when expressed at endogenous levels, and its recycling activity requires both PDZ domain–dependent recognition of the β2AR cytoplasmic tail and Phox homology (PX) domain–dependent association with the endosome membrane. These results identify a discrete role of SNX27 in PDZ-directed recycling of a physiologically important signaling receptor, and extend the concept of cargo-specific molecular sorting in the recycling pathway.

Publisher

Rockefeller University Press

Subject

Cell Biology

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