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Expression and methylation of DNA repair genes in lens epithelium cells of age-related cataract

机译:DNA修复基因在年龄相关性白内障晶状体上皮细胞中的表达和甲基化

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摘要

The development of age-related cataract (ARC) is associated with DNA damage of the lens epithelial cells (LECs). This study aimed to investigate the expression level of DNA repair genes in LECs of ARC and examine whether any altered expression observed could result from DNA methylation of the promoter region of the genes. The expression levels of DNA repair genes were evaluated by microarray analysis. The results were further confirmed by qRT-PCR. DNA methylation of genes with altered expression was determined by bisulfite-specific (BSP) PCR. The mRNA levels of 10 DNA repair genes were decreased and the level of 1 DNA repair gene was increased in LECs of ARC patients compared with controls. The promoter region of the MGMT gene was hypermethylated in ARC tissue compared to controls. The data provide evidence that altered expression of DNA repair genes is associated with pathogenesis of ARC. DNA methylation of MGMT may regulate the expression of the gene and be involved in the development of ARC.
机译:年龄相关性白内障(ARC)的发展与晶状体上皮细胞(LEC)的DNA损伤有关。这项研究旨在调查ARC LEC中DNA修复基因的表达水平,并检查观察到的任何表达变化是否可能由基因启动子区域的DNA甲基化引起。通过微阵列分析评估DNA修复基因的表达水平。通过qRT-PCR进一步证实了结果。通过亚硫酸氢盐特异性(BSP)PCR确定表达改变的基因的DNA甲基化。与对照组相比,ARC患者的LEC中10个DNA修复基因的mRNA水平降低,而1个DNA修复基因的水平升高。与对照相比,MGMT基因的启动子区域在ARC组织中被高度甲基化。数据提供了证据,证明DNA修复基因表达的改变与ARC的发病有关。 MGMT的DNA甲基化可能调节该基因的表达,并参与ARC的发展。

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