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通过单核苷酸多态性分析筛查中国人群2型糖尿病的易感基因

[Screening susceptibility genes of type 2 diabetes in Chinese population by single nucleotide polymorphism analysis].

作者信息

Li Yi, Wu Guo-dong, Zuo Jin, Meng Yan, Fang Fu-de

机构信息

National Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, CAMS and PUMC, Beijing 100005, China.

出版信息

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2005 Jun;27(3):274-9.

Abstract

OBJECTIVE

To search for the susceptibility variant (s) of type 2 diabetes in the susceptible regions on chr.1 (1p36.23-36.33, 1q24.3-25.1, and 1q42.12-42.13) by genotyping SNP markers in case-control DNA samples and identifying the haplotype associated with type 2 diabetes.

METHODS

Totally 124 SNPs in 33 candidate genes in the mapped regions were chosen from public SNP data or identified by sequencing the samples that were used to search for SNP locus. Sequencing method was used to genotype the loci for 236 sporadic type 2 diabetes patients and 152 normal subjects in Northern Han Chinese population. The haplotypes with significant difference were further analyzed.

RESULTS

Of 124 SNPs successfully typed, 4 SNPs that showed association with diabetes status were found: rs203849 (P=0.005, OR=1.60) and rs203826 (P=0.016, OR=1.60) located in sAC gene, rs7535528 (P=0.028, OR=1.45) located in PANK4, rs884363 (P=0.043, OR=1.37) located in CASP9 gene. In addition, the frequencies of two combination types from these 4 SNP genotypes were significantly different between case and control groups (P < 0.001). Furthermore, four haplotypes associated with diabetes were found in haplotype analysis of sAC gene.

CONCLUSION

sAC, PANK4, and CA SP9 may be associated with type 2 diabetes in Han population in north China, and it seems that the synergetic effect of these genes is responsible for the development of type 2 diabetes.

摘要

目的

通过对病例对照DNA样本中的单核苷酸多态性(SNP)标记进行基因分型,并识别与2型糖尿病相关的单倍型,来寻找1号染色体上易感区域(1p36.23 - 36.33、1q24.3 - 25.1和1q42.12 - 42.13)中的2型糖尿病易感变异。

方法

从公共SNP数据中选取或通过对用于寻找SNP位点的样本进行测序,确定定位区域内33个候选基因中的124个SNP。采用测序方法对236例中国北方汉族散发性2型糖尿病患者和152例正常对照的这些位点进行基因分型。对有显著差异的单倍型进行进一步分析。

结果

在成功分型的124个SNP中,发现4个与糖尿病状态相关的SNP:位于sAC基因的rs203849(P = 0.005,OR = 1.60)和rs203826(P = 0.016,OR = 1.60),位于PANK4的rs7535528(P = 0.028,OR = 1.45),位于CASP9基因的rs884363(P = 0.043,OR = 1.37)。此外,这4种SNP基因型的两种组合类型在病例组和对照组之间的频率有显著差异(P < 0.001)。此外,在sAC基因的单倍型分析中发现了4种与糖尿病相关的单倍型。

结论

sAC、PANK4和CASP9可能与中国北方汉族人群的2型糖尿病相关,似乎这些基因的协同作用与2型糖尿病的发生有关。

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