Protection of nuclear DNA by lifespan-extending compounds in the yeast Saccharomyces cerevisiae

IF 1.5 4区 医学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Mutation Research-Fundamental and Molecular Mechanisms of Mutagenesis Pub Date : 2021-01-01 DOI:10.1016/j.mrfmmm.2021.111738
Wei-Hsuan Su, Christelle E.T. Chan, Ting Lian, Mareena Biju, Ayaka Miura, Sarah A. Alkhafaji, Kelton K. Do, Brandon Latifi, Thi T. Nguyen, Samuel E. Schriner
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引用次数: 5

Abstract

DNA damage has been hypothesized to be a driving force of the aging process. At the same time, there exists multiple compounds that can extend lifespan in model organisms, such as yeast, worms, flies, and mice. One possible mechanism of action for these compounds is a protective effect against DNA damage. We investigated whether five of these lifespan-extending compounds, dinitrophenol, metformin, rapamycin, resveratrol, and spermidine, could protect nuclear DNA in the yeast Saccharomyces cerevisiae at the same doses under which they confer lifespan extension. We found that rapamycin and spermidine were able to decrease the spontaneous mutation rate at the CAN1 locus, whereas dinitrophenol, metformin, and resveratrol were able to protect yeast against CAN1 mutations induced by ethyl methanesulfonate (EMS). We also tested whether these compounds could enhance survival against EMS, ultraviolet (UV) light, or hydrogen peroxide (H2O2) insult. All five compounds conferred a protective effect against EMS, while metformin and spermidine protected yeast against UV light. Somewhat surprisingly, none of the compounds were able to afford a significant protection against H2O2, with spermidine dramatically sensitizing cells. We also examined the ability of these compounds to increase lifespan when growth-arrested by hydroxyurea; only spermidine was found to have a positive effect. Overall, our results suggest that lifespan-extending compounds may act in part by protecting nuclear DNA.

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延长寿命化合物对酵母核DNA的保护
DNA损伤被假设为衰老过程的驱动力。同时,在酵母菌、蠕虫、苍蝇、老鼠等模式生物中,存在多种可以延长寿命的化合物。这些化合物的一种可能的作用机制是对DNA损伤的保护作用。我们研究了五种延长寿命的化合物,二硝基苯酚,二甲双胍,雷帕霉素,白藜芦醇和亚精胺,在它们延长寿命的相同剂量下,是否可以保护酵母的核DNA。我们发现雷帕霉素和亚精胺能够降低CAN1位点的自发突变率,而二硝基酚、二甲双胍和白藜芦醇能够保护酵母免受甲磺酸乙酯(EMS)诱导的CAN1突变。我们还测试了这些化合物是否可以提高抗EMS,紫外线(UV)光或过氧化氢(H2O2)损伤的存活率。所有五种化合物都具有抗EMS的保护作用,而二甲双胍和亚精胺可以保护酵母免受紫外线的伤害。有些令人惊讶的是,没有一种化合物能够提供对H2O2的显著保护,亚精胺显着使细胞敏感。我们还研究了这些化合物在被羟基脲抑制生长时延长寿命的能力;只有亚精胺被发现有积极作用。总的来说,我们的研究结果表明,延长寿命的化合物可能部分地通过保护核DNA起作用。
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来源期刊
CiteScore
4.90
自引率
0.00%
发文量
24
审稿时长
51 days
期刊介绍: Mutation Research (MR) provides a platform for publishing all aspects of DNA mutations and epimutations, from basic evolutionary aspects to translational applications in genetic and epigenetic diagnostics and therapy. Mutations are defined as all possible alterations in DNA sequence and sequence organization, from point mutations to genome structural variation, chromosomal aberrations and aneuploidy. Epimutations are defined as alterations in the epigenome, i.e., changes in DNA methylation, histone modification and small regulatory RNAs. MR publishes articles in the following areas: Of special interest are basic mechanisms through which DNA damage and mutations impact development and differentiation, stem cell biology and cell fate in general, including various forms of cell death and cellular senescence. The study of genome instability in human molecular epidemiology and in relation to complex phenotypes, such as human disease, is considered a growing area of importance. Mechanisms of (epi)mutation induction, for example, during DNA repair, replication or recombination; novel methods of (epi)mutation detection, with a focus on ultra-high-throughput sequencing. Landscape of somatic mutations and epimutations in cancer and aging. Role of de novo mutations in human disease and aging; mutations in population genomics. Interactions between mutations and epimutations. The role of epimutations in chromatin structure and function. Mitochondrial DNA mutations and their consequences in terms of human disease and aging. Novel ways to generate mutations and epimutations in cell lines and animal models.
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