Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association

P Saisawat, S Kohl, AC Hilger, DY Hwang, HY Gee, GC Dworschak, V Tasic, T Pennimpede, S Natarajan, E Sperry, DS Matassa, N Stajic, R Bogdanovic, Ivo Blaauw, CLM Marcelis, CHW Wijers, E Bartels, E Schmiedeke, D Schmidt, S MarzheuserS Grasshoff-Derr, S Holland-Cunz, M Ludwig, MM Nothen, M Draaken, Erwin Brosens, H (Hugo Anne) van der Heij, Dick Tibboel, BG Herrmann, BD Solomon, Annelies de Klein, IALM van Rooij, F Esposito, HM Reutter, F Hildebrandt

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Congenital abnormalities of the kidney and urinary tract (CAKUT) account for approximately half of children with chronic kidney disease and they are the most frequent cause of end-stage renal disease in children in the US. However, its genetic etiology remains mostly elusive. VACTERL association is a rare disorder that involves congenital abnormalities in multiple organs including the kidney and urinary tract in up to 60% of the cases. By homozygosity mapping and whole-exome resequencing combined with high-throughput mutation analysis by array-based multiplex PCR and next-generation sequencing, we identified recessive mutations in the gene TNF receptor-associated protein 1 (TRAP1) in two families with isolated CAKUT and three families with VACTERL association. TRAP1 is a heat-shock protein 90-related mitochondrial chaperone possibly involved in antiapoptotic and endoplasmic reticulum stress signaling. Trap1 is expressed in renal epithelia of developing mouse kidney E13.5 and in the kidney of adult rats, most prominently in proximal tubules and in thick medullary ascending limbs of Henle's loop. Thus, we identified mutations in TRAP1 as highly likely causing CAKUT or VACTERL association with CAKUT.
Original languageUndefined/Unknown
Pages (from-to)1310-1317
Number of pages8
JournalKidney International
Issue number6
Publication statusPublished - 2014

Research programs

  • EMC MGC-02-53-01-A
  • EMC MGC-02-96-01

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