Endoplasmic reticulum-retained podocin mutants are massively degraded by the proteasome.

ABSTRACT: 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^R138Q</

SUBMITTER: Serrano-Perez MC 

PROVIDER: S-EPMC5858002 | biostudies-literature | 2018 Mar

REPOSITORIES: biostudies-literature