| Literature DB >> 25466283 |
Estelle Colin1, Evelyne Huynh Cong2, Géraldine Mollet2, Agnès Guichet3, Olivier Gribouval2, Christelle Arrondel2, Olivia Boyer4, Laurent Daniel5, Marie-Claire Gubler4, Zelal Ekinci6, Michel Tsimaratos7, Brigitte Chabrol8, Nathalie Boddaert9, Alain Verloes10, Arnaud Chevrollier1, Naig Gueguen1, Valérie Desquiret-Dumas1, Marc Ferré1, Vincent Procaccio1, Laurence Richard11, Benoit Funalot11, Anne Moncla12, Dominique Bonneau1, Corinne Antignac13.
Abstract
Galloway-Mowat syndrome is a rare autosomal-recessive condition characterized by nephrotic syndrome associated with microcephaly and neurological impairment. Through a combination of autozygosity mapping and whole-exome sequencing, we identified WDR73 as a gene in which mutations cause Galloway-Mowat syndrome in two unrelated families. WDR73 encodes a WD40-repeat-containing protein of unknown function. Here, we show that WDR73 was present in the brain and kidney and was located diffusely in the cytoplasm during interphase but relocalized to spindle poles and astral microtubules during mitosis. Fibroblasts from one affected child and WDR73-depleted podocytes displayed abnormal nuclear morphology, low cell viability, and alterations of the microtubule network. These data suggest that WDR73 plays a crucial role in the maintenance of cell architecture and cell survival. Altogether, WDR73 mutations cause Galloway-Mowat syndrome in a particular subset of individuals presenting with late-onset nephrotic syndrome, postnatal microcephaly, severe intellectual disability, and homogenous brain MRI features. WDR73 is another example of a gene involved in a disease affecting both the kidney glomerulus and the CNS.Entities:
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Year: 2014 PMID: 25466283 PMCID: PMC4259970 DOI: 10.1016/j.ajhg.2014.10.011
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025