Referenced in: none

Automatically associated channels: ClC4 , ClC5

Title: Heterogeneity in the processing of CLCN5 mutants related to Dent disease.

Authors: Teddy Grand, Sébastien L'Hoste, David Mordasini, Nadia Defontaine, Mathilde Keck, Thomas Pennaforte, Mathieu Genete, Kamel Laghmani, Jacques Teulon, Stéphane Lourdel

Journal, date & volume: Hum. Mutat., 2011 Apr , 32, 476-83

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/21305656

Abstract
Mutations in the electrogenic Cl(-)/H(+) exchanger ClC-5 gene CLCN5 are frequently associated with Dent disease, an X-linked recessive disorder affecting the proximal tubules. Here, we investigate the consequences in Xenopus laevis oocytes and in HEK293 cells of nine previously reported, pathogenic, missense mutations of ClC-5, most of them which are located in regions forming the subunit interface. Two mutants trafficked normally to the cell surface and to early endosomes, and displayed complex glycosylation at the cell surface like wild-type ClC-5, but exhibited reduced currents. Three mutants displayed improper N-glycosylation, and were nonfunctional due to being retained and degraded at the endoplasmic reticulum. Functional characterization of four mutants allowed us to identify a novel mechanism leading to ClC-5 dysfunction in Dent disease. We report that these mutant proteins were delayed in their processing, and that the stability of their complex glycosylated form was reduced, causing lower cell surface expression. The early endosome distribution of these mutants was normal. Half of these mutants displayed reduced currents, whereas the other half showed abolished currents. Our study revealed distinct cellular mechanisms accounting for ClC-5 loss of function in Dent disease.