Contribution of the Akt2 gene to type 2 diabetes in the Chinese Han population

被引:2
|
作者
Sun Xiu-qin [1 ]
Luo Ying-ying [1 ]
An Ling-wang [1 ]
Chu Lin [1 ]
Huo Li-li [1 ]
Han Xue-yao [1 ]
Zhou Xiang-hai [1 ]
Ren Qian [1 ]
Ji Li-nong [1 ]
机构
[1] Peking Univ, Peoples Hosp, Dept Endocrinol & Metab, Ctr Diabet, Beijing 100044, Peoples R China
关键词
diabetes mellitus; Chinese Han; Akt2 protein kinase; insulin resistance; SEVERE INSULIN-RESISTANCE; PROTEIN-KINASE B; MICE LACKING; GLUCOSE; AKT2/PKB-BETA; ACTIVATION; MELLITUS; BETA;
D O I
10.3760/cma.j.issn.0366-6999.2011.05.017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The Akt2 protein kinase is thought to be a key mediator of the insulin signal transduction process. Akt2 is suggested to play a role in glucose metabolism and the development or maintenance of proper adipose tissue and islet mass. In order to determine whether the Akt2 gene plays a role in the pathogenesis of type 2 diabetes characterized by insulin resistance, and to further identify if variations in this gene have a relationship with type 2 diabetes, we sequenced the entire coding region and splice junctions of Akt2 and made a further case-control study to explore the association between single-nucleotide polymorphisms (SNPs) in this gene and type 2 diabetes in the Chinese Han population. Methods We selected 23 probands with a type 2 diabetic pedigree whose family members' average onset age was within 25 to 45 years old. The body mass index of all the participants was lower than 28 kg/m(2) and all of them were insulin-resistant (the fasting insulin level >100 pmol/L or 16 mu lU/ml). The entire coding region and splice junctions of Akt2 were directly sequenced in these 23 probands. SNPs with a frequency of minor allele over 20 percent were selected to be further studied in a case-control study. We chose 743 non-diabetic subjects as the control group and 742 type 2 diabetic patients as the case group. All these subjects were genotyped. A Snapshot Technology Platform (Applied Biosystems) was used for genotyping. Results The Akt2 genes from all 23 subjects were successfully sequenced. We did not identify any mutation in the type 2 diabetic pedigree. Two SNPs were identified, 13010323T>C and 13007939G>T. 13010323T>C was in intron 9, which was the location of rs2304188 reported in Genbank. Its minor allele frequency was 13.04%. 13007939G>T was in the 3'-untranslated region (UTR) of exon 14, which was the location of rs2304186 reported in Genbank. Its minor allele frequency was 34.78%. The allele frequency of rs2304188 and rs2304186 were consistent with the frequency reported in Genbank. In the case-control study with 742 patients and 743 controls, there was no significant difference between the two groups for the allele frequency of rs2304186 (odd ratio: 0.96, 95% confidence interval: 0.82-1.12, P=0.597). Conclusions The Akt2 gene is not a major cause of diabetes in a non-obese Chinese Han population characterized by insulin resistance. There is no significant relationship between rs2304186 and type 2 diabetes in the Chinese Han population. Chin Med J 2011;124(5):725-728
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页码:725 / 728
页数:4
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