T130I mutation in HNF-4[alpha] gene is a loss-of-function mutation in hepatocytes and is associated with late-onset Type 2 diabetes mellitus in Japanese subjects

Aims/hypothesis. Mutations in hepatocyte nuclear factor (HNF)-4α gene cause a form of maturity-onset diabetes of the young (MODY1). The T130I mutation is a rare missense mutation, which affects a conserved amino acid in a DNA binding domain. This mutation can be found in the general population, so t...

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Published inDiabetologia Vol. 46; no. 4; p. 567
Main Authors Zhu, Q, Yamagata, K, Miura, A, Shihara, N, Horikawa, Y, Takeda, J, Miyagawa, J, Matsuzawa, Y
Format Journal Article
LanguageEnglish
Published Heidelberg Springer Nature B.V 01.04.2003
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ISSN0012-186X
1432-0428
DOI10.1007/s00125-003-1067-y

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Summary:Aims/hypothesis. Mutations in hepatocyte nuclear factor (HNF)-4α gene cause a form of maturity-onset diabetes of the young (MODY1). The T130I mutation is a rare missense mutation, which affects a conserved amino acid in a DNA binding domain. This mutation can be found in the general population, so this variant alone does not cause MODY. However, its significance in the development of late-onset Type 2 diabetes is not known. Methods. We screened 423 unrelated Japanese patients with late-onset Type 2 diabetes and 354 unrelated non-diabetic control subjects for the T130I mutation in the HNF-4α gene. The transactivation ability of T130I-HNF-4α was assessed using reporter gene assay. Results. The frequency of the T130I mutation was higher in Type 2 diabetic patients (p=0.015, odds ratio 4.3, 95%CI 1.24-14.98) than control subjects. The serum HDL-cholesterol concentration was lower in Type 2 diabetic patients with the T130I mutation compared with those without this mutation (p=0.006). Reporter gene analysis showed that T130I-HNF-4α transcriptional activity was not impaired compared with wild-type HNF-4α in Hela and MIN6 cells, but it was reduced in HepG2 and primary cultured mouse hepatocytes (27-78% of wild type, p<0.05). Conclusion/interpretation. Our findings suggest that T130I-HNF-4α is a loss-of-function mutation in hepatocytes and that this mutation is associated with late-onset Type 2 diabetes in Japanese subjects. The T130I mutation in the HNF-4α gene might be involved in the development of Type 2 diabetes in the Japanese population.
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ISSN:0012-186X
1432-0428
DOI:10.1007/s00125-003-1067-y