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中国北方汉族2型糖尿病家系1号染色体上易感基因位点的确认

Confirmation of susceptibility gene loci on chromosome 1 in northern China Han families with type 2 diabetes.

作者信息

Du W, Sun H, Wang H, Qiang B, Shen Y, Yao Z, Gu J, Xiong M, Huang W, Chen Z, Zuo J, Hua X, Gao W, Sun Q, Fang F

机构信息

Department of Biochemistry and Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100005, China.

出版信息

Chin Med J (Engl). 2001 Aug;114(8):876-8.

Abstract

OBJECTIVE

To confirm previous effort to identify type 2 diabetes susceptibility genes in a Northern Chinese population by conducting a new genome scan with both an increased number of type 2 diabetes families and a new set of microsatellite markers within the previously localized regions.

METHODS

A genome scan method was applied. After multiplexed PCR, electrophoreses, genescan and genotyping analysis, we obtained size information for all loci, and then a further study was done by both parametric and non-parametric linkage analysis to investigate the P values and Z values of these loci.

RESULTS

We surveyed 34 microsatellite markers which distributed within 5 regions along chromosome 1, and a total of 12,000 genotypes were screened. Evidence of linkage with diabetes was identified for 8 of the 34 loci. All P values of the 8 loci were lower than 0.05, and the highest Z value was 2.17. A very interesting finding is that all 5 markers at the p- terminal 1p36.3-1p36.23 region, spanning a long range of 16.9 cM, were identified to have a low P value of less than 0.05, which suggests that this region may contain multiple susceptibility genes. Regions 4 and 5 also confirmed the previous findings, and we narrowed these two regions to a 2.7 cM and 2.5 cM regions, respectively.

CONCLUSIONS

We further confirmed the results gained in the previous genome-wide scan using an increased number of NIDDM families and a new set of microsatellite markers lying within the initially localized regions. The fact that all 5 loci at the p- terminal region displayed a low P value of less than 0.05 suggests that more than 1 susceptibility gene may reside in this region.

摘要

目的

通过对更多的2型糖尿病家系进行新的基因组扫描,并在先前定位的区域内使用一组新的微卫星标记,来确认之前在中国北方人群中鉴定2型糖尿病易感基因的工作。

方法

应用基因组扫描方法。经过多重聚合酶链反应、电泳、基因扫描和基因分型分析,我们获得了所有位点的大小信息,然后通过参数和非参数连锁分析进一步研究这些位点的P值和Z值。

结果

我们检测了分布在1号染色体上5个区域的34个微卫星标记,共筛选了12000个基因型。在34个位点中的8个位点发现了与糖尿病连锁的证据。这8个位点的所有P值均低于0.05,最高Z值为2.17。一个非常有趣的发现是,在1p36.3 - 1p36.23区域的p末端的所有5个标记,跨度长达16.9厘摩,被鉴定为具有小于0.05的低P值,这表明该区域可能包含多个易感基因。区域4和区域5也证实了先前的发现,我们将这两个区域分别缩小到2.7厘摩和2.5厘摩的区域。

结论

我们使用更多的非胰岛素依赖型糖尿病家系和一组位于最初定位区域内的新的微卫星标记,进一步证实了先前全基因组扫描获得的结果。p末端区域的所有5个位点均显示出小于0.05的低P值,这一事实表明该区域可能存在不止1个易感基因。

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