NONSENSE MUTATION IN THE GLUCOKINASE GENE CAUSES EARLY-ONSET NON-INSULIN-DEPENDENT DIABETES-MELLITUS

被引:568
作者
VIONNET, N
STOFFEL, M
TAKEDA, J
YASUDA, K
BELL, GI
ZOUALI, H
LESAGE, S
VELHO, G
IRIS, F
PASSA, P
FROGUEL, P
COHEN, D
机构
[1] UNIV CHICAGO,HOWARD HUGHES MED INST,DEPT BIOCHEM,5841 S MARYLAND AVE,MC1028,CHICAGO,IL 60637
[2] HOP ST LOUIS,SERV ENDOCRINOL,F-75010 PARIS,FRANCE
[3] CTR ETUD POLYMORPHISME HUMAIN,F-91000 EVRY,FRANCE
[4] UNIV CHICAGO,DEPT MOLEC BIOL & MED,CHICAGO,IL 60637
[5] GENETHON,F-91000 EVRY,FRANCE
关键词
D O I
10.1038/356721a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MATURITY-ONSET diabetes of the young (MODY) is a form of non-insulin-dependent (type 2) diabetes mellitus (NIDDM) which is characterized by an early age at onset and an autosomal dominant mode of inheritance 1. Except for these features, the clinical characteristics of patients with MODY are similar to those with the more common late-onset form(s) of NIDDM. Previously 2 we observed tight linkage between DNA polymorphisms in the glucokinase gene on the short arm of chromosome 7 and NIDDM in a cohort of sixteen French families having MODY. Glucokinase is an enzyme that catalyses the formation of glucose-6-phosphate from glucose and may be involved in the regulation of insulin secretion and integration of hepatic intermediary metabolism 3. Because the glucokinase gene was a candidate for the site of the genetic lesion in these families, we scanned this gene for mutations. Here we report the identification of a nonsense mutation in the gene encoding glucokinase and its linkage with early-onset diabetes in one family. To our knowledge, this result is the first evidence implicating a mutation in a gene involved in glucose metabolism in the pathogenesis of NIDDM.
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页码:721 / 722
页数:2
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