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Gene expression changes in response to aging compared to heat stress oxidative stress and ionizing radiation in Drosophila melanogaster

机译:与果蝇的热应激氧化应激和电离辐射相比基因表达随老化而变化

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摘要

Gene expression changes in response to aging, heat stress, hyperoxia, hydrogen peroxide, and ionizing radiation were compared using microarrays. A set of 18 genes were up-regulated across all conditions, indicating a general stress response shared with aging, including the heat shock protein (Hsp) genes Hsp70, Hsp83 and l(2)efl, the glutathione-S-transferase gene GstD2, and the mitochondrial unfolded protein response (mUPR) gene ref(2)P. Selected gene expression changes were confirmed using quantitative PCR, Northern analysis and GstD-GFP reporter constructs. Certain genes were altered in only a subset of the conditions, for example, up-regulation of numerous developmental pathway and signaling genes in response to hydrogen peroxide. While aging shared features with each stress, aging was more similar to the stresses most associated with oxidative stress (hyperoxia, hydrogen peroxide, ionizing radiation) than to heat stress. Aging is associated with down-regulation of numerous mitochondrial genes, including electron-transport-chain (ETC) genes and mitochondrial metabolism genes, and a sub-set of these changes was also observed upon hydrogen peroxide stress and ionizing radiation stress. Aging shared the largest number of gene expression changes with hyperoxia. The extensive down-regulation of mitochondrial and ETC genes during aging is consistent with an aging-associated failure in mitochondrial maintenance, which may underlie the oxidative stress-like and proteotoxic stress-like responses observed during aging.
机译:使用微阵列比较了响应于衰老,热应激,高氧,过氧化氢和电离辐射的基因表达变化。在所有条件下,一组18个基因均上调,表明与衰老共享一般应激反应,包括热休克蛋白(Hsp)基因Hsp70,Hsp83和l(2)efl,谷胱甘肽S-转移酶基因GstD2,和线粒体展开蛋白反应(mUPR)基因ref(2)P。使用定量PCR,Northern分析和GstD-GFP报告基因构建体确认了选定的基因表达变化。某些基因仅在一部分条件下发生了变化,例如,响应于过氧化氢,许多发育途径和信号基因的上调。老化与每种应力都有共同的特征,但与热应力相比,老化与与氧化应力(高氧,过氧化氢,电离辐射)最相关的应力更相似。衰老与许多线粒体基因的下调相关,包括电子传输链(ETC)基因和线粒体代谢基因,并且在过氧化氢胁迫和电离辐射胁迫下也观察到这些变化的子集。衰老与高氧症共享最多的基因表达变化。衰老过程中线粒体和ETC基因的广泛下调与衰老相关的线粒体维持失败相一致,这可能是衰老过程中观察到的类似氧化应激和蛋白毒性应激反应的基础。

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