Genetic variation in the hepatocyte nuclear factor-3beta gene (HNF3B) does not contribute to maturity-onset diabetes of the young in French Caucasians
Genetic variation in the hepatocyte nuclear factor-3beta gene (HNF3B) does not contribute to maturity-onset diabetes of the young in French Caucasians. A Abderrahmani , J C Chèvre , S Otabe , M Chikri , E H Hani , M Vaxillaire , Y Hinokio , Y Horikawa , G I Bell and P Froguel Unité Propre de Recherc...
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Veröffentlicht in: | Diabetes (New York, N.Y.) N.Y.), 2000-02, Vol.49 (2), p.306-308 |
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Zusammenfassung: | Genetic variation in the hepatocyte nuclear factor-3beta gene (HNF3B) does not contribute to maturity-onset diabetes of the
young in French Caucasians.
A Abderrahmani ,
J C Chèvre ,
S Otabe ,
M Chikri ,
E H Hani ,
M Vaxillaire ,
Y Hinokio ,
Y Horikawa ,
G I Bell and
P Froguel
Unité Propre de Recherche de l'Enseignement Supérieur Associée au Centre National de la Recherche Scientifique (CNRS UPRES-A)
8090, Institut de Biologie de Lille, France.
Abstract
Mutations in genes encoding hepatocyte nuclear factor (HNF) are responsible for three of the five subtypes of maturity-onset
diabetes of the young (MODY). This observation and molecular studies indicate that the HNF network is required for normal
function of pancreatic beta-cells. This suggests that transcription factors involved in this complex network are candidates
for genetic defects in MODY. Because the HNF-3beta gene is implicated in this network, we screened it for mutations in 21
probands of French ancestry with clinical diagnosis of MODY and early-onset type 2 diabetes. All of the five known MODY genes,
HNF-4alpha, glucokinase, HNF-1alpha, HNF-1beta, and IPF1, were previously excluded as being the cause of diabetes in these
families. By direct sequencing, we identified two transitions, an A-to-G at position -213 and a C-to-T at position -63 in
the promoter and exon 1, respectively, of the HNF-3beta gene. A G-to-C transversion at position +32 in the intron 1 and three
transitions, C-to-T at position 291, A-to-G at position 837, and G-to-A at position 1188 in the exon 3, resulting in noncoding
mutations Ala97Ala, Gly279Gly, and Gln396Gln, respectively, were also identified. The allele frequencies were not significantly
different between a control group and MODY probands. Familial segregation studies and linkage analysis showed that genetic
variation in the HNF-3beta gene is unlikely to be the cause of early-onset type 2 diabetes in these Caucasian families. |
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ISSN: | 0012-1797 1939-327X |
DOI: | 10.2337/diabetes.49.2.306 |