Title |
KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron
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Published in |
Nature Genetics, March 2012
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DOI | 10.1038/ng.2218 |
Pubmed ID | |
Authors |
Hélène Louis-Dit-Picard, Julien Barc, Daniel Trujillano, Stéphanie Miserey-Lenkei, Nabila Bouatia-Naji, Olena Pylypenko, Geneviève Beaurain, Amélie Bonnefond, Olivier Sand, Christophe Simian, Emmanuelle Vidal-Petiot, Christelle Soukaseum, Chantal Mandet, Françoise Broux, Olivier Chabre, Michel Delahousse, Vincent Esnault, Béatrice Fiquet, Pascal Houillier, Corinne Isnard Bagnis, Jens Koenig, Martin Konrad, Paul Landais, Chebel Mourani, Patrick Niaudet, Vincent Probst, Christel Thauvin, Robert J Unwin, Steven D Soroka, Georg Ehret, Stephan Ossowski, Mark Caulfield, Patrick Bruneval, Xavier Estivill, Philippe Froguel, Juliette Hadchouel, Jean-Jacques Schott, Xavier Jeunemaitre |
Abstract |
Familial hyperkalemic hypertension (FHHt) is a Mendelian form of arterial hypertension that is partially explained by mutations in WNK1 and WNK4 that lead to increased activity of the Na(+)-Cl(-) cotransporter (NCC) in the distal nephron. Using combined linkage analysis and whole-exome sequencing in two families, we identified KLHL3 as a third gene responsible for FHHt. Direct sequencing of 43 other affected individuals revealed 11 additional missense mutations that were associated with heterogeneous phenotypes and diverse modes of inheritance. Polymorphisms at KLHL3 were not associated with blood pressure. The KLHL3 protein belongs to the BTB-BACK-kelch family of actin-binding proteins that recruit substrates for Cullin3-based ubiquitin ligase complexes. KLHL3 is coexpressed with NCC and downregulates NCC expression at the cell surface. Our study establishes a role for KLHL3 as a new member of the complex signaling pathway regulating ion homeostasis in the distal nephron and indirectly blood pressure. |
X Demographics
Geographical breakdown
Country | Count | As % |
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Spain | 1 | 25% |
India | 1 | 25% |
Unknown | 2 | 50% |
Demographic breakdown
Type | Count | As % |
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Members of the public | 4 | 100% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
---|---|---|
United Kingdom | 2 | 1% |
Japan | 1 | <1% |
France | 1 | <1% |
Argentina | 1 | <1% |
Unknown | 151 | 97% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Researcher | 34 | 22% |
Student > Ph. D. Student | 33 | 21% |
Student > Master | 15 | 10% |
Student > Bachelor | 14 | 9% |
Professor > Associate Professor | 10 | 6% |
Other | 32 | 21% |
Unknown | 18 | 12% |
Readers by discipline | Count | As % |
---|---|---|
Agricultural and Biological Sciences | 43 | 28% |
Medicine and Dentistry | 41 | 26% |
Biochemistry, Genetics and Molecular Biology | 34 | 22% |
Pharmacology, Toxicology and Pharmaceutical Science | 4 | 3% |
Engineering | 4 | 3% |
Other | 12 | 8% |
Unknown | 18 | 12% |