Department of Immunobiology, Yale University School of Medicine, New Haven, CT 06520, USA.
Department of Comparative Medicine and Yale Center for Molecular and Systems Metabolism, Yale University School of Medicine, New Haven, CT 06510, USA.
Neuron. 2022 Oct 19;110(20):3278-3287.e8. doi: 10.1016/j.neuron.2022.08.011. Epub 2022 Sep 6.
Dysregulation of long interspersed nuclear element 1 (LINE-1, L1), a dominant class of transposable elements in the human genome, has been linked to neurodegenerative diseases, but whether elevated L1 expression is sufficient to cause neurodegeneration has not been directly tested. Here, we show that the cerebellar expression of L1 is significantly elevated in ataxia telangiectasia patients and strongly anti-correlated with the expression of epigenetic silencers. To examine the role of L1 in the disease etiology, we developed an approach for direct targeting of the L1 promoter for overexpression in mice. We demonstrated that L1 activation in the cerebellum led to Purkinje cell dysfunctions and degeneration and was sufficient to cause ataxia. Treatment with a nucleoside reverse transcriptase inhibitor blunted ataxia progression by reducing DNA damage, attenuating gliosis, and reversing deficits of molecular regulators for calcium homeostasis in Purkinje cells. Our study provides the first direct evidence that L1 activation can drive neurodegeneration.
长散布核元件 1(LINE-1,L1)的失调与神经退行性疾病有关,L1 是人类基因组中占主导地位的转座元件之一,但 L1 表达水平升高是否足以导致神经退行性变尚未得到直接验证。在这里,我们发现小脑表达的 L1 在共济失调毛细血管扩张症患者中显著升高,与表观遗传沉默因子的表达呈强烈负相关。为了研究 L1 在疾病发病机制中的作用,我们开发了一种方法,可直接靶向 L1 启动子在小鼠中进行过表达。我们证明小脑 L1 的激活导致浦肯野细胞功能障碍和退化,足以引起共济失调。用核苷逆转录酶抑制剂治疗可通过减少 DNA 损伤、减轻神经胶质增生以及逆转浦肯野细胞钙稳态分子调节剂的缺陷来减轻共济失调的进展。我们的研究提供了第一个直接证据,证明 L1 的激活可以驱动神经退行性变。