EC:3.4.25.1 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:3.4.25.1 (proteasome)
28,817 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Podocin is a key component of the slit diaphragm in the glomerular filtration barrier, and mutations in the podocin-encoding gene NPHS2 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 in vitro and in vivo To better understand the defective trafficking and degradation of this mutant, we generated human podocyte cell lines stably expressing podocin^wt or podocin^R138Q Although it has been proposed that podocin has a hairpin topology, we present evidence for podocin^R138QN-glycosylation, suggesting that most of the protein has a transmembrane topology. We find that N-glycosylated podocin^R138Q has a longer half-life than non-glycosylated podocin^R138Q and that the latter is far more rapidly degraded than podocin^wt Consistent with its rapid degradation, podocin^R138Q is exclusively degraded by the proteasome, whereas podocin^wt is degraded by both the proteasomal and the lysosomal proteolytic machineries. In addition, we demonstrate an enhanced interaction of podocin^R138Q with calnexin as the mechanism of endoplasmic reticulum retention. Calnexin knockdown enriches the podocin^R138Q non-glycosylated fraction, whereas preventing exit from the calnexin cycle increases the glycosylated fraction. Altogether, we propose a model in which hairpin podocin^R138Q is rapidly degraded by the proteasome, whereas transmembrane podocin^R138Q degradation is delayed due to entry into the calnexin cycle.
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PMID:Endoplasmic reticulum-retained podocin mutants are massively degraded by the proteasome. 2938 18