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调控性单核苷酸多态性改变糖尿病视网膜病变相关分泌因子的基因表达。

Regulatory SNPs Alter the Gene Expression of Diabetic Retinopathy Associated Secretary Factors.

作者信息

Chen Chian-Feng, Liou Shiow-Wen, Wu Hsin-Han, Lin Chin-Hui, Huang Li-Shan, Woung Lin-Chung, Tsai Ching-Yao

机构信息

VYM Genome Research Center, National Yang-Ming University, Taipei, Taiwan;

Department of Ophthalmology, Taipei City Hospital, Taipei, Taiwan;; Department of Ophthalmology, Shin Kong Wu Ho-Su Memorial Hospital, Taipei, Taiwan;; Department of Ophthalmology, Taipei Medical University, Taipei, Taiwan;; Department of Ophthalmology, Taiwan University Hospital, Taipei, Taiwan;

出版信息

Int J Med Sci. 2016 Sep 12;13(9):717-23. doi: 10.7150/ijms.16345. eCollection 2016.

Abstract

OBJECTIVES

Diabetic retinopathy (DR) is a common microvascular complication in both type I and type II diabetes. Several previous reports indicated the serum centration of some secretary factors were highly associated with DR. Therefore, we hypothesis regulatory SNPs (rSNPs) genotype in secretary factors may alter these gene expression and lead to DR.

METHODS

At first, pyrosequencing were applying to screen the SNPs which present allele frequency different in DR and DNR. Then individual genotyping was processed by Taqman assays in Taiwanese DR and DNR patients. To evaluate the effect of SNP allele on transcriptional activity, we measured promoter activity using luciferase reporter constructs.

RESULTS

We found the frequencies of the CC, CG, and GG genotype of the rs2010963 polymorphism were 15.09%, 47.14%, and 37.74% in DR and 12.90%, 19.35%, and 67.74% in DNR, respectively (p = 0.0205). The prevalence of DR was higher (p = 0.00793) in patients with the CC or CG genotype (62.26% and 32.26% for DR and DNR, respectively) compared with the patients with the GG genotype. To evaluate the effect of rs2010963-C allele on transcriptional activity, we measured promoter activity using luciferase reporter constructs. The rs2010963-C reporter showed 1.6 to 2-fold higher luciferase activity than rs2010963-G in 3 cell lines.

CONCLUSION

Our data proposed rs2010963-C altered the expression level of VEGFA in different tissues. We suggested small increase but long term exposure to VEGFA may lead to DR finally.

摘要

目的

糖尿病视网膜病变(DR)是I型和II型糖尿病常见的微血管并发症。此前有多项报告指出,某些分泌因子的血清浓度与DR高度相关。因此,我们推测分泌因子中的调控单核苷酸多态性(rSNP)基因型可能会改变这些基因的表达并导致DR。

方法

首先,采用焦磷酸测序法筛选在DR和非糖尿病视网膜病变(DNR)中存在等位基因频率差异的SNP。然后,通过Taqman分析对台湾DR和DNR患者进行个体基因分型。为了评估SNP等位基因对转录活性的影响,我们使用荧光素酶报告构建体测量启动子活性。

结果

我们发现,rs2010963多态性的CC、CG和GG基因型频率在DR中分别为15.09%、47.14%和37.74%,在DNR中分别为12.90%、19.35%和67.74%(p = 0.0205)。与GG基因型患者相比,CC或CG基因型患者的DR患病率更高(p = 0.00793)(DR和DNR分别为62.26%和32.26%)。为了评估rs2010963 - C等位基因对转录活性的影响,我们使用荧光素酶报告构建体测量启动子活性。在3种细胞系中,rs2010963 - C报告基因显示出比rs2010963 - G高1.6至2倍的荧光素酶活性。

结论

我们的数据表明rs2010963 - C改变了不同组织中VEGFA的表达水平。我们认为,VEGFA的小幅增加但长期暴露最终可能导致DR。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97b1/5027191/c23f6e857626/ijmsv13p0717g001.jpg

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