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肝细胞核因子-4α中的一个错义突变,导致转录激活活性降低,与人类晚发性非胰岛素依赖型糖尿病有关。

A missense mutation in hepatocyte nuclear factor-4 alpha, resulting in a reduced transactivation activity, in human late-onset non-insulin-dependent diabetes mellitus.

作者信息

Hani E H, Suaud L, Boutin P, Chèvre J C, Durand E, Philippi A, Demenais F, Vionnet N, Furuta H, Velho G, Bell G I, Laine B, Froguel P

机构信息

Centre National de la Recherche Scientifique (CNRS) EP10-Institute of Biology, Pasteur Institute of Lille & CHRU-Lille, 59019 Lille, France.

出版信息

J Clin Invest. 1998 Feb 1;101(3):521-6. doi: 10.1172/JCI1403.

Abstract

Non-insulin-dependent diabetes mellitus (NIDDM) is a heterogeneous disorder characterized by hyperglycemia resulting from defects in insulin secretion and action. Recent studies have found mutations in the hepatocyte nuclear factor-4 alpha gene (HNF-4alpha) in families with maturity-onset diabetes of the young (MODY), an autosomal dominant form of diabetes characterized by early age at onset and a defect in glucose-stimulated insulin secretion. During the course of our search for susceptibility genes contributing to the more common late-onset NIDDM forms, we observed nominal evidence for linkage between NIDDM and markers in the region of the HNF-4alpha/MODY1 locus in a subset of French families with NIDDM diagnosed before 45 yr of age. Thus, we screened these families for mutations in the HNF-4alpha gene. We found a missense mutation, resulting in a valine-to-isoleucine substitution at codon 393 in a single family. This mutation cosegregated with diabetes and impaired insulin secretion, and was not present in 119 control subjects. Expression studies showed that this conservative substitution is associated with a marked reduction of transactivation activity, a result consistent with this mutation contributing to the insulin secretory defect observed in this family.

摘要

非胰岛素依赖型糖尿病(NIDDM)是一种异质性疾病,其特征为因胰岛素分泌和作用缺陷导致的高血糖症。最近的研究发现,在青少年发病的成年型糖尿病(MODY)家族中,肝细胞核因子-4α基因(HNF-4α)存在突变,MODY是一种常染色体显性糖尿病,其特征为发病年龄早且葡萄糖刺激的胰岛素分泌存在缺陷。在我们寻找导致更常见的晚发型NIDDM形式的易感基因的过程中,我们在一部分45岁之前被诊断为NIDDM的法国家族中,观察到NIDDM与HNF-4α/MODY1基因座区域的标记之间存在名义上的连锁证据。因此,我们对这些家族的HNF-4α基因进行了突变筛查。我们在一个家族中发现了一个错义突变,该突变导致第393位密码子处缬氨酸被异亮氨酸取代。此突变与糖尿病和胰岛素分泌受损共分离,且在119名对照受试者中不存在。表达研究表明,这种保守性取代与反式激活活性的显著降低相关,这一结果与该突变导致此家族中观察到的胰岛素分泌缺陷相符。

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