Scanning the HNF4A gene mutation from Chinese pedigrees with early- and/or multiple-onset diabetes.
- Author:
Rong ZHANG
1
;
Cheng HU
;
Cong-rong WANG
;
Qi-chen FANG
;
Xiao-jing MA
;
Wei-ping JIA
;
Kun-san XIANG
Author Information
- Publication Type:Journal Article
- MeSH: Adult; Age of Onset; Base Sequence; China; epidemiology; Diabetes Mellitus; epidemiology; genetics; Female; Gene Frequency; Genotype; Hepatocyte Nuclear Factor 4; genetics; Humans; Male; Mutation; Pedigree; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Sequence Analysis, DNA
- From: Chinese Journal of Medical Genetics 2006;23(4):406-409
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo screen the mutation of hepatocyte nuclear factor 4 alpha gene (HNF4A) in Chinese pedigrees with early and/or multiplex-onset diabetes in Shanghai and nearby area.
METHODSBy PCR-single strand conformation polymorphism (PCR-SSCP) and direct sequencing, the mutation screen of HNF4A gene was performed in 93 normal controls and 154 unrelated probands from early- and/or multiplex-onset diabetes. The PCR-RFLP was used to analyze the frequencies of the discovered mutations and variants.
RESULTSTwo synonymous mutations (N153N, A158A) were found in two families, of which the N153N was co-segregated with early-onset diabetes. These two synonymous mutations were not detected in the 93 normal controls. Three variants, IVS1+308(A to G)(rs2071197), IVS1+357(A to T)(rs2071198), IVS1-5(C to T)(rs745975), were also identified in this study. The genotype and allele frequencies of the three variants had no difference between the probands and normal controls.
CONCLUSIONHNF4A gene mutation is rare in Chinese pedigrees with early and/or multiplex-onset diabetes.
