Department of Neurology, Osaka University Graduate School of Medicine, Osaka, Japan.
Program of Genetics & Genome Biology, The Hospital for Sick Children, The Peter Gilgan Centre for Research and Learning, Toronto, Ontario, Canada.
Nat Genet. 2020 Feb;52(2):146-159. doi: 10.1038/s41588-019-0575-8. Epub 2020 Feb 14.
In many repeat diseases, such as Huntington's disease (HD), ongoing repeat expansions in affected tissues contribute to disease onset, progression and severity. Inducing contractions of expanded repeats by exogenous agents is not yet possible. Traditional approaches would target proteins driving repeat mutations. Here we report a compound, naphthyridine-azaquinolone (NA), that specifically binds slipped-CAG DNA intermediates of expansion mutations, a previously unsuspected target. NA efficiently induces repeat contractions in HD patient cells as well as en masse contractions in medium spiny neurons of HD mouse striatum. Contractions are specific for the expanded allele, independently of DNA replication, require transcription across the coding CTG strand and arise by blocking repair of CAG slip-outs. NA-induced contractions depend on active expansions driven by MutSβ. NA injections in HD mouse striatum reduce mutant HTT protein aggregates, a biomarker of HD pathogenesis and severity. Repeat-structure-specific DNA ligands are a novel avenue to contract expanded repeats.
在许多重复疾病中,例如亨廷顿病(HD),受影响组织中的持续重复扩展导致疾病的发生、进展和严重程度。目前还不可能通过外源性试剂诱导扩展重复的收缩。传统的方法将针对驱动重复突变的蛋白质。在这里,我们报告了一种化合物,萘啶并氮杂喹啉(NA),它特异性地结合扩展突变的滑移 CAG DNA 中间体,这是一个以前未被怀疑的靶点。NA 可有效诱导 HD 患者细胞中的重复收缩,以及 HD 小鼠纹状体中型多棘神经元中的大规模收缩。收缩特异性针对扩展等位基因,与 DNA 复制无关,需要跨越编码 CTG 链的转录,并通过阻断 CAG 滑出的修复而产生。NA 诱导的收缩取决于 MutSβ 驱动的活性扩展。NA 在 HD 小鼠纹状体中的注射可减少突变 HTT 蛋白聚集体,这是 HD 发病机制和严重程度的生物标志物。重复结构特异性 DNA 配体是收缩扩展重复的新途径。