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人类胰岛素基因附近的一个多态性位点与胰岛素依赖型糖尿病相关。

A polymorphic locus near the human insulin gene is associated with insulin-dependent diabetes mellitus.

作者信息

Bell G I, Horita S, Karam J H

出版信息

Diabetes. 1984 Feb;33(2):176-83. doi: 10.2337/diab.33.2.176.

Abstract

A polymorphic region flanking the human insulin gene on the short arm of chromosome 11, the insulin-gene-linked DNA polymorphism, can be described as a locus with at least three classes of alleles: a common small "class 1" allele averaging 570 base pairs, a rare intermediate "class 2" allele of about 1320 base pairs, and a large "class 3" allele averaging 2470 base pairs in size. We have determined the genotype at this locus of 393 unrelated diabetic and nondiabetic individuals. Differences were observed in the genotypic and allelic frequencies between groups of different races. Asians [17 nondiabetic, 2 with insulin-dependent diabetes mellitus (IDDM), and 8 with non-insulin-dependent diabetes mellitus (NIDDM)] exhibited the least variation in the size of this locus and 98% of the alleles in this group were class 1. A group of American blacks (32 nondiabetic, 5 with IDDM, and 40 with NIDDM) exhibited considerable variation in the size of this locus, and about 22% of the individuals examined had a genotype that included a rare class 2 allele. In neither of these two racial groups were the genotypic or allelic frequencies different between the nondiabetic and diabetic segments of these groups. However, in a group of Caucasians (83 nondiabetic, 113 with IDDM, and 76 with NIDDM), there was a significantly higher frequency of class 1 alleles and genotypes containing two class 1 alleles in the diabetic patients compared with nondiabetic controls.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

位于11号染色体短臂上的人类胰岛素基因侧翼的一个多态性区域,即胰岛素基因连锁DNA多态性,可被描述为一个至少有三类等位基因的位点:常见的小“1类”等位基因,平均长度为570个碱基对;罕见的中等“2类”等位基因,约1320个碱基对;以及大的“3类”等位基因,平均大小为2470个碱基对。我们确定了393名无亲缘关系的糖尿病患者和非糖尿病患者在该位点的基因型。不同种族群体之间在基因型和等位基因频率上存在差异。亚洲人(17名非糖尿病患者,2名胰岛素依赖型糖尿病患者和8名非胰岛素依赖型糖尿病患者)在该位点大小上表现出最小的变异,该组中98%的等位基因为1类。一组美国黑人(32名非糖尿病患者,5名胰岛素依赖型糖尿病患者和40名非胰岛素依赖型糖尿病患者)在该位点大小上表现出相当大的变异,约22%的受检个体具有包含罕见2类等位基因的基因型。在这两个种族群体中,非糖尿病组和糖尿病组之间的基因型或等位基因频率均无差异。然而,在一组白种人(83名非糖尿病患者,113名胰岛素依赖型糖尿病患者和76名非胰岛素依赖型糖尿病患者)中,与非糖尿病对照组相比,糖尿病患者中1类等位基因以及含有两个1类等位基因的基因型的频率显著更高。(摘要截短于250字)

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