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Single nucleotide polymorphisms on SHIP2 is associated with Type 2 diabetes mellitus in Chinese Han population
1Department of Endocrinology, the Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, People's Republic of China. lianfu@163.com.
Objective:
Type 2 diabetes mellitus (T2DM) is a chronic disease characterized by insulin resistance in the target tissue of insulin with insufficient insulin secretion in pancreatic β-cells. Src homology 2-containing 5'-inositol phosphatase 2 (SHIP2) is a lipid phosphatase that hydrolyzes PI3-kinase product PI(3,4,5)P3 to PI(3,4)P2, which contributes to the negative regulation of insulin signaling both in vitro and in vivo. Some polymorphisms of SHIP2 have been reported to be associated with the metabolic syndrome including T2DM and hypertension in British, French and Japanese T2DM population.
Patients And Methods:
In our present study, we investigated the relation between single nucleotide polymorphisms (SNPs) on SHIP2 gene and the pathogenesis of T2DM in Chinese Han population.
Results And Conclusions:
Our results indicated that the genotype and allele frequency of SHIP2 (+1893CC/AA) locus in T2DM patients showed significantly different from between the healthy control population. In addition, the G allele of SHIP2 (+2945A/G) seemed to increase the susceptibility to hypertension for T2DM patients.
Insights
Genetic variations in the SHIP2 gene are linked to type 2 diabetes mellitus (T2DM) and hypertension in the Chinese Han population. Specifically, SHIP2 (+1893CC/AA) showed significant differences, and the SHIP2 (+2945A/G) G allele increased hypertension susceptibility in T2DM patients.
Area of Science:
- Genetics
- Endocrinology
- Metabolic Diseases
Background:
- Type 2 diabetes mellitus (T2DM) involves insulin resistance and impaired insulin secretion.
- SHIP2 (Src homology 2-containing 5'-inositol phosphatase 2) negatively regulates insulin signaling.
- SHIP2 gene polymorphisms have been associated with metabolic syndrome and T2DM in various populations.
Purpose of the Study:
- To investigate the association between single nucleotide polymorphisms (SNPs) in the SHIP2 gene and the pathogenesis of T2DM in the Chinese Han population.
- To explore the relationship between SHIP2 SNPs and hypertension in T2DM patients.
Main Methods:
- Case-control study design.
- Genotyping of SHIP2 gene single nucleotide polymorphisms (SNPs) in T2DM patients and healthy controls.
- Statistical analysis of genotype and allele frequencies.
Main Results:
- Significant differences in genotype and allele frequencies of the SHIP2 (+1893CC/AA) locus were observed between T2DM patients and controls.
- The G allele of the SHIP2 (+2945A/G) polymorphism was associated with an increased susceptibility to hypertension in T2DM patients.
Conclusions:
- SHIP2 gene polymorphisms are associated with T2DM pathogenesis in the Chinese Han population.
- The SHIP2 (+2945A/G) G allele may be a risk factor for hypertension in T2DM patients.
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