Zhu Yingbao, Xiao Shengwei, Guan Xinxin, Deng Haitao, Ai Liqiang, Fan Kaijing, Xue Jin, Li Guangxu, Bi Xiaoxue, Xiao Qiao, Huang Yuanjiang, Jiang Lin, Huang Wen, Jin Peng, Duan Ranhui
Furong Laboratory, Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Hunan Key Laboratory of Medical Genetics, Changsha, Hunan, China.
EMBO Mol Med. 2025 May;17(5):967-992. doi: 10.1038/s44321-025-00217-3. Epub 2025 Mar 25.
Myotonic dystrophy type 2 (DM2), caused by CCTG repeat expansion, is a common adult-onset disorder characterized by myotonia and progressive muscle degeneration with no effective treatment. Here, we identified Tyrosyl-DNA phosphodiesterase 1 (TDP1) as a novel modifier for DM2 therapeutic intervention through a high-throughput chemical screening of 2160 compounds. Moreover, we detailed how both genetic and pharmacological inhibition of TDP1 translates to a cascade of beneficial effects, including improved motor functions, amelioration of progressive muscle degeneration, repair of muscle fiber damage, and normalization of aberrant molecular pathology. Remarkably, the TDP1 inhibition led to substantial CCTG repeat contractions, a mechanism that underlies the observed muscle toxicity and neurodegeneration. Our results highlighted the potential of TDP1 as a molecular target for addressing the complex interplay between repeat expansions and neuromuscular degeneration in DM2, hinting at broader applicability in a spectrum of repeat expansion disorders.
2型强直性肌营养不良症(DM2)由CCTG重复序列扩增引起,是一种常见的成人发病疾病,其特征为肌强直和进行性肌肉退化,目前尚无有效治疗方法。在此,我们通过对2160种化合物进行高通量化学筛选,鉴定出酪氨酰-DNA磷酸二酯酶1(TDP1)作为DM2治疗干预的一种新型修饰因子。此外,我们详细阐述了TDP1的基因抑制和药物抑制如何转化为一系列有益效果,包括改善运动功能、减轻进行性肌肉退化、修复肌纤维损伤以及使异常分子病理学正常化。值得注意的是,TDP1抑制导致CCTG重复序列大幅收缩,这是观察到的肌肉毒性和神经变性的潜在机制。我们的结果突出了TDP1作为解决DM2中重复序列扩增与神经肌肉变性之间复杂相互作用的分子靶点的潜力,暗示其在一系列重复序列扩增疾病中具有更广泛的适用性。