Institut de Génétique Humaine (IGH), Université de Montpellier-Centre National de la Recherche Scientifique, 34396 Montpellier, France.
Department of Biological Hematology, CHU Montpellier, 34295 Montpellier, France.
Int J Mol Sci. 2021 Jul 12;22(14):7461. doi: 10.3390/ijms22147461.
In order to tackle the study of DNA repair pathways, the physical and chemical agents creating DNA damage, the genotoxins, are frequently employed. Despite their utility, their effects are rarely restricted to DNA, and therefore simultaneously harm other cell biomolecules. Methyl methanesulfonate (MMS) is an alkylating agent that acts on DNA by preferentially methylating guanine and adenine bases. It is broadly used both in basic genome stability research and as a model for mechanistic studies to understand how alkylating agents work, such as those used in chemotherapy. Nevertheless, MMS exerts additional actions, such as oxidation and acetylation of proteins. In this work, we introduce the important notion that MMS also triggers a lipid stress that stems from and affects the inner nuclear membrane. The inner nuclear membrane plays an essential role in virtually all genome stability maintenance pathways. Thus, we want to raise awareness that the relative contribution of lipid and genotoxic stresses when using MMS may be difficult to dissect and will matter in the conclusions drawn from those studies.
为了研究 DNA 修复途径,人们经常使用物理和化学因素来制造 DNA 损伤,即遗传毒素。尽管这些方法很有用,但它们的作用很少仅限于 DNA,因此也会同时损害其他细胞生物分子。甲磺酸甲酯(MMS)是一种烷化剂,通过优先甲基化鸟嘌呤和腺嘌呤碱基来作用于 DNA。它广泛应用于基础基因组稳定性研究和作为机制研究的模型,以了解烷化剂的作用方式,如化疗中使用的烷化剂。然而,MMS 还会产生其他作用,如蛋白质的氧化和乙酰化。在这项工作中,我们提出了一个重要的观点,即 MMS 还会引发脂质应激,这种应激源于并影响核内。核内起着维持几乎所有基因组稳定性途径的关键作用。因此,我们想提醒大家,在使用 MMS 时,脂质和遗传毒性应激的相对贡献可能难以区分,并且会影响从这些研究中得出的结论。