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An aging and p53 related marker:

机译:衰老和P53相关标记:

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摘要

The process of aging has been associated with differential patterns of DNA methylation which relate to changes in gene expression. Hence, we aimed to identify genes with significant age-related methylation differences and to study their mRNA and protein expression profile. Genome-wide DNA methylation analysis was performed with the Illumina Infinium Methylation EPIC BeadChip Microarray on bisulfite-converted DNA prepared from monocytes derived from young (average age: 23.8 yrs) and old (average age: 81.5 yrs) volunteers that are separated by at least 50 years of age difference, n=4, respectively. Differentially methylated CpG sites were assigned to the associated genes and validated by deep sequencing analysis (n=20). Demonstrating an age-associated significant increase of methylation in the promoter region (p=1x10-8), Homeobox A5 (HOXA5), also known to activate p53, emerged as an interesting candidate for further expression analyses by Realtime PCR, ELISA and Western Blot Analysis (n=30, respectively). Consistent with its hypermethylation we observed significant HOXA5 mRNA downregulation (p=0.0053) correlating with significant p53 downregulation (p=0.0431) in the old cohort. Moreover, we observed a significant change in HOXA5 protein expression (p=3x10-5) negatively correlating with age and promoter methylation thus qualifying HOXA5 for an eligible p53-related aging marker.
机译:衰老过程与DNA甲基化的差异模式有关,其与基因表达的变化有关。因此,我们旨在鉴定具有重要年龄相关的甲基化差异的基因,并研究其mRNA和蛋白质表达谱。在亚硫酸氟镁 - 转化的DNA上用来自营养的单核(平均年龄:23​​.8yrs)和旧(平均年龄:81.5yrs)志愿者至少的单核 - 转化的DNA进行了基因组 - 转化的DNA甲基化分析。 50年龄差异,n = 4分别。将差异甲基化的CpG位点分配给相关基因并通过深度测序分析(n = 20)进行验证。证明在启动子区(P = 1×10-8)中的甲基化的年龄相关显着增加,Ojox A5(Hoxa5),也已知激活P53,作为进一步的表达分析通过RealTime PCR,ELISA和Western印迹进行进一步的表达分析分析(分别为n = 30)。与其高甲基化一致我们观察到旧队列中的显着p53下调(P = 0.0431)相关的显着HOXA5 mRNA下调(P = 0.0053)。此外,我们观察到Hoxa5蛋白表达(P = 3x10-5)的显着变化与年龄和启动子甲基化负相关,从而鉴定Hoxa5,用于符合条件的P53相关的老化标记。

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