Promoter variation in the liver glucokinase is a risk factor for non-insulin-dependent diabetes mellitus

被引:11
作者
Chiu, KC
McCarthy, JE
机构
[1] Div. of Endocrinology and Metabolism, School of Medicine, Univ. of California at Los Angeles, Los Angeles
关键词
D O I
10.1006/bbrc.1996.0644
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have previously reported a common variation in the liver promoter of the human glucokinase, which is regulated by insulin, in the patients with non-insulin-dependent diabetes mellitus (NIDDM). The variation occurred within a 10-bp region completely conserved between human and rat. Its basic motif was almost identical to the insulin regulatory element of the phosphoenolpyruvate carboxykinase gene. In vitro transfection experiment showed that the G-to-A variation causes a 58% reduction in the promoter activity. After oral glucose challenge, the homozygous A/A subjects had the highest stimulated insulin levels at 60 and 90 minutes and the highest insulin area under the curve as compared to the subjects with other genotypes, which suggested the homozygous A/A subjects were more insulin resistant. As insulin resistance is a risk factor of NIDDM, we concluded that this promoter variation is a risk factor for NIDDM. (C) 1996 Academic Press, Inc.
引用
收藏
页码:614 / 618
页数:5
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