| Literature DB >> 26792178 |
Markus M Rinschen1, Puneet Bharill2, Xiongwu Wu3, Priyanka Kohli4, Matthäus J Reinert5, Oliver Kretz6, Isabel Saez7, Bernhard Schermer8, Martin Höhne8, Malte P Bartram5, Sriram Aravamudhan9, Bernard R Brooks3, David Vilchez7, Tobias B Huber10, Roman-Ulrich Müller8, Marcus Krüger11, Thomas Benzing1.
Abstract
The PHB-domain protein podocin maintains the renal filtration barrier and its mutation is an important cause of hereditary nephrotic syndrome. Podocin and its Caenorhabditis elegans orthologue MEC-2 have emerged as key components of mechanosensitive membrane protein signalling complexes. Whereas podocin resides at a specialized cell junction at the podocyte slit diaphragm, MEC-2 is found in neurons required for touch sensitivity. Here, we show that the ubiquitin ligase Ubr4 is a key component of the podocin interactome purified both from cultured podocytes and native glomeruli. It colocalizes with podocin and regulates its stability. In C. elegans, this process is conserved. Here, Ubr4 is responsible for the degradation of mislocalized MEC-2 multimers. Ubiquitylomic analysis of mouse glomeruli revealed that podocin is ubiquitylated at two lysine residues. These sites were Ubr4-dependent and were conserved across species. Molecular dynamics simulations revealed that ubiquitylation of one site, K301, do not only target podocin/MEC-2 for proteasomal degradation, but may also affect stability and disassembly of the multimeric complex. We suggest that Ubr4 is a key regulator of podocyte foot process proteostasis.Entities:
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Year: 2016 PMID: 26792178 PMCID: PMC4787903 DOI: 10.1093/hmg/ddw016
Source DB: PubMed Journal: Hum Mol Genet ISSN: 0964-6906 Impact factor: 6.150