University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.
University of Groningen, University Medical Center Groningen, Department of Dermatology Center for Blistering Diseases, Groningen, The Netherlands.
Methods Mol Biol. 2022;2434:185-190. doi: 10.1007/978-1-0716-2010-6_11.
The genodermatosis dystrophic epidermolysis bullosa (DEB) is caused by mutations in the COL7A1 gene which encodes type VII collagen (C7). In the cutaneous basement membrane zone, C7 secures attachment of the epidermal basal keratinocyte to the papillary dermis by means of anchoring fibril formation. The complete absence of these anchoring fibrils leads to severe blistering of skin and mucosa upon the slightest friction and early mortality. To date, although preclinical advances toward therapy are promising, treatment for the disease is merely symptomatic. Therefore, research into novel therapeutics is warranted.Antisense oligonucleotide (ASO)-mediated exon skipping is such a therapy . Clinical examination of naturally occurring exon skipping suggested that this mechanism could most likely benefit the most severely affected patients. The severe form of DEB is caused by biallelic null mutations. Exon skipping aims to bind an ASO to the mutated exon of the pre-mRNA in the cell nucleus. Thereby, the ASO inhibits the recognition of the mutated exon by the splicing machinery, and as a result, the mutated exon is spliced out from the mRNA with its surrounding introns, i.e., it is skipped. Here, we describe in vitro methods to evaluate ASO-mediated exon skipping in a preclinical setting.
遗传性皮肤病营养不良性大疱性表皮松解症(DEB)是由编码 VII 型胶原(C7)的 COL7A1 基因突变引起的。在皮肤基底膜带,C7 通过锚定纤维形成将表皮基底层角质形成细胞固定到乳头真皮。这些锚定纤维的完全缺失导致皮肤和粘膜在受到最轻微的摩擦和早期死亡时严重起疱。迄今为止,尽管针对治疗的临床前进展很有希望,但该疾病的治疗仅是对症治疗。因此,有必要研究新的治疗方法。反义寡核苷酸(ASO)介导的外显子跳跃就是这样一种治疗方法。对自然发生的外显子跳跃的临床检查表明,这种机制最有可能使受影响最严重的患者受益。DEB 的严重形式是由双等位基因无效突变引起的。外显子跳跃旨在将 ASO 结合到细胞核中前体 mRNA 的突变外显子上。因此,ASO 抑制剪接机制对外显子突变的识别,结果是突变的外显子与其周围的内含子一起从 mRNA 中剪接出来,即被跳过。在这里,我们描述了在临床前环境中评估 ASO 介导的外显子跳跃的体外方法。