Centre for Interdisciplinary Research in Biology (CIRB), Collège de France, CNRS UMR 7241/INSERM U1050, PSL Research University, Paris Cedex 05, France.
Centre for Interdisciplinary Research in Biology (CIRB), Collège de France, CNRS UMR 7241/INSERM U1050, PSL Research University, Paris Cedex 05, France
EMBO J. 2018 Aug 1;37(15). doi: 10.15252/embj.201797374. Epub 2018 Jun 25.
LINE-1 mobile genetic elements have shaped the mammalian genome during evolution. A minority of them have escaped fossilization which, when activated, can threaten genome integrity. We report that LINE-1 are expressed in substantia nigra ventral midbrain dopaminergic neurons, a class of neurons that degenerate in Parkinson's disease. In heterozygotes, these neurons show a progressive degeneration that starts at 6 weeks of age, coinciding with an increase in LINE-1 expression. Similarly, DNA damage and cell death, induced by an acute oxidative stress applied to embryonic midbrain neurons in culture or to adult midbrain dopaminergic neurons , are accompanied by enhanced LINE-1 expression. Reduction of LINE-1 activity through (i) direct transcriptional repression by Engrailed, (ii) a siRNA directed against LINE-1, (iii) the nucleoside analogue reverse transcriptase inhibitor stavudine, and (iv) viral Piwil1 expression, protects against oxidative stress and We thus propose that LINE-1 overexpression triggers oxidative stress-induced DNA strand breaks and that an Engrailed adult function is to protect mesencephalic dopaminergic neurons through the repression of LINE-1 expression.
LINE-1 移动遗传元件在进化过程中塑造了哺乳动物的基因组。它们中的一小部分逃脱了石化,当被激活时,可能会威胁到基因组的完整性。我们报告说,LINE-1 在黑质腹侧中脑多巴胺能神经元中表达,这是一类在帕金森病中退化的神经元。在杂合子中,这些神经元表现出进行性退化,从 6 周龄开始,与 LINE-1 表达的增加相吻合。同样,通过急性氧化应激应用于培养的胚胎中脑神经元或成年中脑多巴胺能神经元诱导的 DNA 损伤和细胞死亡伴随着 LINE-1 表达的增强。通过 (i) Engrailed 直接转录抑制、(ii) 针对 LINE-1 的 siRNA、(iii) 核苷类似物逆转录酶抑制剂司他夫定和 (iv) 病毒 Piwil1 表达降低 LINE-1 活性,可预防氧化应激。因此,我们提出 LINE-1 的过度表达引发氧化应激诱导的 DNA 链断裂,而 Engrailed 的成人功能是通过抑制 LINE-1 表达来保护中脑多巴胺能神经元。