Hitman G A, Kambo P K, Viswanathan M, Mohan V
Department of Medicine, London Hospital, Whitechapel.
J Med Genet. 1991 Feb;28(2):97-100. doi: 10.1136/jmg.28.2.97.
We have previously described an increased incidence of the class 3 allele of the hypervariable region (HVR) 5' to the insulin gene in south Indian non-insulin dependent diabetics; this association is absent in Punjabi Sikhs with this disorder. Using the polymerase chain reaction we have amplified parts of the insulin gene from 130 subjects to look for mutations which may be in linkage disequilibrium with the class 3 allele and hence explain its association with non-insulin dependent diabetes (NIDDM). In 23 south Indian subjects with NIDDM, using the restriction enzyme MboII, a B chain mutant (insulin Chicago) was excluded. Two patterns (alpha and beta) were found, representing a PstI polymorphism in the 3' untranslated region of the insulin gene. In subjects homozygous for the class 1 allele, the allelic frequency for alpha was 0.94 (143/152) and for beta was 0.06, in heterozygotes (1,3) alpha 0.63 (54/86) and beta 0.37, and in homozygotes for the class 3 allele alpha 0.18 (4/22) and beta 0.82 (p less than 0.001), thus establishing linkage disequilibrium between these two loci. No differences in allelic frequency were found in the south Indians or Punjabi Sikhs between controls and the different types of non-insulin requiring diabetes (NIDDM, fibrocalculous pancreatic diabetes and maturity onset diabetes of the young) when both groups were matched for insulin genotypes. Thus, although this polymorphism in the 3' untranslated region of the insulin gene is in linkage disequilibrium with the class 3 allele, it does not appear to be any better at predicting diabetes than the class 3 allele itself.
我们之前曾描述过,在印度南部非胰岛素依赖型糖尿病患者中,胰岛素基因5'端高变区(HVR)3类等位基因的发生率有所增加;而患有该疾病的旁遮普锡克教徒中不存在这种关联。我们使用聚合酶链反应从130名受试者中扩增了胰岛素基因的部分片段,以寻找可能与3类等位基因处于连锁不平衡状态的突变,从而解释其与非胰岛素依赖型糖尿病(NIDDM)的关联。在23名患有NIDDM的印度南部受试者中,使用限制性内切酶MboII排除了B链突变体(胰岛素芝加哥型)。发现了两种模式(α和β),代表胰岛素基因3'非翻译区的PstI多态性。在1类等位基因纯合子受试者中,α等位基因频率为0.94(143/152),β为0.06;在杂合子(1,3)中,α为0.63(54/86),β为0.37;在3类等位基因纯合子中,α为0.18(4/22),β为0.82(p<0.001),从而确定了这两个基因座之间的连锁不平衡。当两组胰岛素基因型匹配时,在印度南部人和旁遮普锡克教徒的对照组与不同类型的非胰岛素依赖型糖尿病(NIDDM、纤维钙化性胰腺糖尿病和青少年成年起病型糖尿病)患者之间,未发现等位基因频率有差异。因此,尽管胰岛素基因3'非翻译区的这种多态性与3类等位基因处于连锁不平衡状态,但它在预测糖尿病方面似乎并不比3类等位基因本身更好。