Mutation analysis of the Uromodulin gene in 96 individuals with urinary tract anomalies (CAKUT)

Matthias T F Wolf, Bethan E. Hoskins, Bodo B. Beck, Bernd Hoppe, Velibor Tasic, Edgar A. Otto, Friedhelm Hildebrandt

Research output: Contribution to journalArticle

11 Scopus citations

Abstract

Uromodulin (UMOD) mutations were described in patients with medullary cystic kidney disease (MCKD2), familial juvenile hyperuricemic nephropathy (FJHN), and glomerulocystic kidney disease (GCKD). UMOD transcription is activated by the transcription factor HNF1B. Mutations in HNF1B cause a phenotype similar to FJHN/GCKD but also congenital anomalies of the kidney and the urinary tract (CAKUT). Moreover, we recently detected UMOD mutations in two patients with CAKUT. As HNF1B and UMOD act in the same pathway and cause similar phenotypes, we here examined whether UMOD mutations would be found in patients with CAKUT. Mutation analysis of UMOD was performed in 96 individuals with CAKUT by direct sequencing of exons 4 and 5 and by heteroduplex analysis following CEL I digestion assay of exons 3 and 6-12. Mean patient age was 11.4 years, and in 36.4% of patients, family history was positive for CAKUT. In the CEL I assay, 12 aberrant bands were detected in 103 of 960 polymerase chain reaction (PCR) products and were sequenced. Six previously known and seven new single nucleotide polymorphisms (SNPs) were detected. As no UMOD mutations were identified in these 96 patients with CAKUT, UMOD mutations do not seem to be a significant cause of CAKUT in this cohort.

Original languageEnglish (US)
Pages (from-to)55-60
Number of pages6
JournalPediatric Nephrology
Volume24
Issue number1
DOIs
StatePublished - Jan 1 2009

Keywords

  • CAKUT
  • Mutation analysis
  • Tamm-Horsfall protein
  • Urinary tract malformation
  • Uromodulin

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Nephrology

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