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Hypermethylation of the PRKCZ Gene in Type 2 Diabetes Mellitus
Li Zou1, Shirong Yan, Xueping Guan
1Clinical Laboratory of Renmin Hospital, The Third Affiliated Hospital of Hubei University of Medicine, 39 Chaoyang Road, Shiyan, Hubei Province 442000, China.
Abstract:
Objectives. To study the correlation between the methylation of protein kinase C epsilon zeta (PRKCZ) gene promoters and type 2 diabetes mellitus (T2DM). Methods. The case-control method was implemented in 272 unrelated to one another cases in Shiyan People's Hospital. Of those, 152 were diagnosed as T2DM cases, and the other 120 cases were healthy individuals visiting the hospital for a physical examination. The subjects were first divided into two groups: the T2DM group and the normal control (NC) group. Next, methylated DNA immunoprecipitation chip (MeDIP-chip) was used for detection. Bisulfite sequencing PCR (BSP) and gene sequencing were then performed to detect and analyze the correlation between PRKCZ gene promoter methylation and T2DM. Finally, Western blotting was applied to determine the serum level of PRKCZ. The data were then analyzed with the statistics analyzing software SPSS 17.0. Results. In contrast with cases in NC, T2DM patients showed a high level of methylation, with 7 of 9 CpG sites were shown to be methylated, whereas, in the control group, only one CpG site was found to be methylated. The methylated CpG sites for the two groups showed marked differences (P < 0.01). Additionally, the level of PRKCZ was decreased in T2DM subjects, and the difference between the two groups was statistically significant (P < 0.05). Discussion. This study suggests that the PRKCZ gene is the hypermethylated gene of T2DM and the hypermethylation PRKCZ gene may be involved in the pathogenesis of T2DM.
Insights
Type 2 diabetes mellitus (T2DM) is linked to increased methylation of the protein kinase C epsilon zeta (PRKCZ) gene. This gene hypermethylation may play a role in T2DM development, with lower PRKCZ levels observed in patients.
Area of Science:
- Epigenetics
- Molecular Biology
- Endocrinology
Background:
- Type 2 Diabetes Mellitus (T2DM) is a global health concern.
- Epigenetic modifications, such as DNA methylation, are increasingly recognized as contributing factors in T2DM pathogenesis.
- The role of specific gene promoter methylation in T2DM requires further elucidation.
Purpose of the Study:
- To investigate the correlation between the methylation status of the protein kinase C epsilon zeta (PRKCZ) gene promoter and T2DM.
- To assess the serum levels of PRKCZ in T2DM patients compared to healthy controls.
Main Methods:
- A case-control study involving 152 T2DM patients and 120 healthy controls.
- Methylated DNA immunoprecipitation chip (MeDIP-chip) for initial screening.
- Bisulfite sequencing PCR (BSP) and gene sequencing for detailed methylation analysis of PRKCZ gene promoter CpG sites.
- Western blotting to determine serum PRKCZ levels.
Main Results:
- T2DM patients exhibited significantly higher methylation levels at 7 out of 9 analyzed CpG sites in the PRKCZ gene promoter compared to controls (P < 0.01).
- Serum PRKCZ levels were significantly decreased in T2DM subjects compared to the normal control group (P < 0.05).
Conclusions:
- The PRKCZ gene promoter is significantly hypermethylated in individuals with T2DM.
- PRKCZ gene hypermethylation is suggested to be involved in the pathogenesis of T2DM.
- Reduced PRKCZ levels may serve as a potential biomarker or therapeutic target in T2DM.
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