COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.

Published

Journal Article

Steroid-resistant nephrotic syndrome (SRNS) is a frequent cause of end-stage renal failure. Identification of single-gene causes of SRNS has generated some insights into its pathogenesis; however, additional genes and disease mechanisms remain obscure, and SRNS continues to be treatment refractory. Here we have identified 6 different mutations in coenzyme Q10 biosynthesis monooxygenase 6 (COQ6) in 13 individuals from 7 families by homozygosity mapping. Each mutation was linked to early-onset SRNS with sensorineural deafness. The deleterious effects of these human COQ6 mutations were validated by their lack of complementation in coq6-deficient yeast. Furthermore, knockdown of Coq6 in podocyte cell lines and coq6 in zebrafish embryos caused apoptosis that was partially reversed by coenzyme Q10 treatment. In rats, COQ6 was located within cell processes and the Golgi apparatus of renal glomerular podocytes and in stria vascularis cells of the inner ear, consistent with an oto-renal disease phenotype. These data suggest that coenzyme Q10-related forms of SRNS and hearing loss can be molecularly identified and potentially treated.

Full Text

Duke Authors

Cited Authors

  • Heeringa, SF; Chernin, G; Chaki, M; Zhou, W; Sloan, AJ; Ji, Z; Xie, LX; Salviati, L; Hurd, TW; Vega-Warner, V; Killen, PD; Raphael, Y; Ashraf, S; Ovunc, B; Schoeb, DS; McLaughlin, HM; Airik, R; Vlangos, CN; Gbadegesin, R; Hinkes, B; Saisawat, P; Trevisson, E; Doimo, M; Casarin, A; Pertegato, V; Giorgi, G; Prokisch, H; Rötig, A; Nürnberg, G; Becker, C; Wang, S; Ozaltin, F; Topaloglu, R; Bakkaloglu, A; Bakkaloglu, SA; Müller, D; Beissert, A; Mir, S; Berdeli, A; Varpizen, S; Zenker, M; Matejas, V; Santos-Ocaña, C; Navas, P; Kusakabe, T; Kispert, A; Akman, S; Soliman, NA; Krick, S; Mundel, P; Reiser, J; Nürnberg, P; Clarke, CF; Wiggins, RC; Faul, C; Hildebrandt, F

Published Date

  • May 2011

Published In

Volume / Issue

  • 121 / 5

Start / End Page

  • 2013 - 2024

PubMed ID

  • 21540551

Pubmed Central ID

  • 21540551

Electronic International Standard Serial Number (EISSN)

  • 1558-8238

International Standard Serial Number (ISSN)

  • 0021-9738

Digital Object Identifier (DOI)

  • 10.1172/JCI45693

Language

  • eng