Identification of seven novel nucleotide variants in the hepatocyte nuclear factor-1α (TCF1) promoter region in MODY patients

François Godart, Christine Bellanné-Chantelot, Séverine Clauin, Claudia Gragnoli, Amar Abderrahmani, Hélène Blanché, Philippe Boutin, Jean Claude Chèvre, Philippe Froguel, Bernard Bailleul

Research output: Contribution to journalArticlepeer-review

38 Scopus citations

Abstract

Maturity onset diabetes of the young (MODY) is a heterogeneous subtype of type II diabetes mellitus. To date, five MODY genes have been identified. Mutations in the hepatocyte nuclear factor-1α (HNF-1α) gene are associated with MODY3. In the present work, we implemented the HNF-1α promoter region in the screening of MODY-suspect patients and identified seven variants not detected in control subjects. The family was available for the - 119delG variant, and segregration between MODY and the variant is observed. Most of these variants are located in highly conserved regions and may alter HNF-1α expression through binding alteration of nuclear factors or other mechanisms. We demonstrate by functional studies that the transcriptional activity of the -283A> C and -218T> C variant promoters were 30% and 70% of the wild type activity, respectively. These data suggest that HNF-1α promoter variants could be diabetogenic mutations, and emphasize that the accurate HNF-1α expression is important for the maintenance of normal pancreatic β cell function. (C) 2000 Wiley-Liss, Inc.

Original languageEnglish (US)
Pages (from-to)173-180
Number of pages8
JournalHuman mutation
Volume15
Issue number2
DOIs
StatePublished - 2000
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Genetics
  • Genetics(clinical)

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