Jenquin Jana R, O'Brien Alana P, Poukalov Kiril, Lu Yidan, Frias Jesus A, Shorrock Hannah K, Richardson Jared I, Mazdiyasni Hormoz, Yang Hongfen, Huigens Robert W, Boykin David, Ranum Laura P W, Cleary John Douglas, Wang Eric T, Berglund J Andrew
Department of Biochemistry and Molecular Biology, Center for NeuroGenetics, College of Medicine, University of Florida, Gainesville, FL 32610, USA.
RNA Institute, College of Arts and Sciences, University at Albany-SUNY, Albany, NY 12222, USA.
iScience. 2022 Apr 4;25(5):104198. doi: 10.1016/j.isci.2022.104198. eCollection 2022 May 20.
Myotonic dystrophy type 1 (DM1) and type 2 (DM2) are common forms of adult onset muscular dystrophy. Pathogenesis in both diseases is largely driven by production of toxic-expanded repeat RNAs that sequester MBNL RNA-binding proteins, causing mis-splicing. Given this shared pathogenesis, we hypothesized that diamidines, small molecules that rescue mis-splicing in DM1 models, could also rescue mis-splicing in DM2 models. While several DM1 cell models exist, few are available for DM2 limiting research and therapeutic development. Here, we characterize DM1 and DM2 patient-derived fibroblasts for use in small molecule screens and therapeutic studies. We identify mis-splicing events unique to DM2 fibroblasts and common events shared with DM1 fibroblasts. We show that diamidines can partially rescue molecular phenotypes in both DM1 and DM2 fibroblasts. This study demonstrates the potential of fibroblasts as models for DM1 and DM2, which will help meet an important need for well-characterized DM2 cell models.
1型强直性肌营养不良(DM1)和2型强直性肌营养不良(DM2)是成人起病的常见肌营养不良形式。两种疾病的发病机制很大程度上是由毒性扩增重复RNA的产生驱动的,这些RNA会隔离MBNL RNA结合蛋白,导致剪接错误。鉴于这种共同的发病机制,我们推测双脒类化合物(一种能挽救DM1模型中剪接错误的小分子)也能挽救DM2模型中的剪接错误。虽然存在几种DM1细胞模型,但可用于DM2的模型很少,这限制了研究和治疗开发。在这里,我们对来自DM1和DM2患者的成纤维细胞进行了表征,以用于小分子筛选和治疗研究。我们确定了DM2成纤维细胞特有的剪接错误事件以及与DM1成纤维细胞共有的常见事件。我们表明,双脒类化合物可以部分挽救DM1和DM2成纤维细胞中的分子表型。这项研究证明了成纤维细胞作为DM1和DM2模型的潜力,这将有助于满足对特征明确的DM2细胞模型的重要需求。