J. Biol. Chem.

Podocin is a key component of the slit diaphragm in the glomerular filtration barrier, and mutations in the podocin-encoding gene are a common cause of hereditary steroid-resistant nephrotic syndrome. A mutant allele encoding podocin with a p.R138Q amino acid substitution is the most frequent pathogenic variant in European and North American children, and the corresponding mutant protein is poorly expressed and retained in the endoplasmic reticulum both and To better understand the defective trafficking and degradation of this mutant, we generated human podocyte cell lines stably expressing podocin or podocin Although it has been proposed that podocin has a hairpin topology, we present evidence for podocin-glycosylation, suggesting that most of the protein has a transmembrane topology. We find that -glycosylated podocin has a longer half-life than non-glycosylated podocin and that the latter is far more rapidly degraded than podocin Consistent with its rapid degradation, podocin is exclusively degraded by the proteasome, whereas podocin is degraded by both the proteasomal and the lysosomal proteolytic machineries. In addition, we demonstrate an enhanced interaction of podocin with calnexin as the mechanism of endoplasmic reticulum retention. Calnexin knockdown enriches the podocin non-glycosylated fraction, whereas preventing exit from the calnexin cycle increases the glycosylated fraction. Altogether, we propose a model in which hairpin podocin is rapidly degraded by the proteasome, whereas transmembrane podocin degradation is delayed due to entry into the calnexin cycle.KEYWORDSendoplasmic-reticulum-associated protein degradation (ERAD), genetic disease, glycosylation, intracellular trafficking, kidney, podocin, proteasome, steroid-resistant nephrotic syndrome© 2018 by The American Society for Biochemistry and Molecular Biology, Inc.