Aguti Sara, Bolduc Véronique, Ala Pierpaolo, Turmaine Mark, Bönnemann Carsten G, Muntoni Francesco, Zhou Haiyan
The Dubowitz Neuromuscular Centre, Molecular Neurosciences Section, Developmental Neurosciences Research and Teaching Department, Great Ormond Street Institute of Child Health, University College London, 30 Guilford Street, London WC1N 1EH, UK.
Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland MD 20892, USA.
Mol Ther Nucleic Acids. 2020 Sep 4;21:205-216. doi: 10.1016/j.omtn.2020.05.029. Epub 2020 Jun 1.
Collagen VI-related congenital muscular dystrophies (COL6-CMDs) are the second most common form of congenital muscular dystrophy. Currently, there is no effective treatment available. COL6-CMDs are caused by recessive or dominant mutations in one of the three genes encoding for the α chains of collagen type VI (COL6A1, COL6A2, and COL6A3). One of the most common mutations in COL6-CMD patients is a de novo deep intronic c.930+189C > T mutation in COL6A1 gene. This mutation creates a cryptic donor splice site and induces incorporation of a novel in-frame pseudo-exon in the mature transcripts. In this study, we systematically evaluated the splice switching approach using antisense oligonucleotides (ASOs) to correct this mutation. Fifteen ASOs were designed using the RNA-tiling approach to target the misspliced pseudo-exon and its flanking sequences. The efficiency of ASOs was evaluated at RNA, protein, and structural levels in skin fibroblasts established from four patients carrying the c.930+189C > T mutation. We identified two additional lead ASO candidates that efficiently induce pseudo-exon exclusion from the mature transcripts, thus allowing for the restoration of a functional collagen VI microfibrillar matrix. Our findings provide further evidence for ASO exon skipping as a therapeutic approach for COL6-CMD patients carrying this common intronic mutation.
与胶原蛋白VI相关的先天性肌营养不良症(COL6-CMDs)是先天性肌营养不良症的第二常见类型。目前,尚无有效的治疗方法。COL6-CMDs是由编码VI型胶原蛋白(COL6A1、COL6A2和COL6A3)α链的三个基因之一的隐性或显性突变引起的。COL6-CMD患者最常见的突变之一是COL6A1基因中的一个新生的内含子深处c.930+189C>T突变。该突变产生一个隐蔽的供体剪接位点,并诱导在成熟转录本中掺入一个新的框内假外显子。在本研究中,我们系统地评估了使用反义寡核苷酸(ASO)来纠正该突变的剪接转换方法。使用RNA平铺方法设计了15种ASO,以靶向错配的假外显子及其侧翼序列。在从四名携带c.930+189C>T突变的患者建立的皮肤成纤维细胞中,在RNA、蛋白质和结构水平上评估了ASO的效率。我们确定了另外两个主要的ASO候选物,它们能有效地诱导成熟转录本中假外显子的排除,从而恢复功能性胶原蛋白VI微纤维基质。我们的研究结果为ASO外显子跳跃作为携带这种常见内含子突变的COL6-CMD患者的治疗方法提供了进一步的证据。