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WI-38 senescence is associated with global and site-specific hypomethylation

机译:WI-38衰老与全身性和部位特异性低甲基化有关

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摘要

Cellular senescence plays an important role in the age-dependent functional decline of organs and organ systems, as well as in age-related pathologies, such as cancer. Therefore, a better understanding of its underlying molecular mechanisms is crucial in the search for intervening measures. In this study, we considered the role of DNA methylation in senescence. We found that senescence is associated with global DNA hypomethylation, but also involves site-specific DNA hypo- and hypermethylation. In some cases, this differential methylation may affect gene expression and thereby modulate functional processes within cells. However, the majority of the CpG sites that were differentially methylated did not correspond with altered gene expression, suggesting that DNA methylation affects senescence by other means also, such as, for instance, genome stability.
机译:细胞衰老在依赖年龄的器官和器官系统功能衰退以及与年龄相关的病理学(例如癌症)中起着重要作用。因此,更好地了解其潜在分子机制对于寻找干预措施至关重要。在这项研究中,我们考虑了DNA甲基化在衰老中的作用。我们发现衰老与总体DNA甲基化不足有关,但也涉及特定于位点的DNA甲基化和甲基化过高。在某些情况下,这种差异甲基化可能影响基因表达,从而调节细胞内的功能过程。但是,大多数甲基化的CpG位点与基因表达的改变并不对应,这表明DNA甲基化还通过其他方式(例如,基因组稳定性)影响衰老。

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