Riedmayr Lisa M
Center for Integrated Protein Science Munich CIPSM, Ludwig-Maximilians-Universität München, Munich, Germany.
Department of Pharmacy, Center for Drug Research, Ludwig-Maximilians-Universität München, Munich, Germany.
Methods Mol Biol. 2020;2079:219-232. doi: 10.1007/978-1-4939-9904-0_17.
Spliceosome-mediated mRNA trans-splicing (SMaRT) is a promising strategy for treatment of genetic diseases which cannot be targeted via classical therapy approaches. SMaRT utilizes an exogenous pre-mRNA trans-splicing molecule (PTM) to correct a diseased target pre-mRNA. This process relies on splicing of two separate pre-mRNA molecules in trans creating a mature chimeric mRNA molecule which consists of the protein coding sequence of the PTM as well as the endogenous mRNA. For therapeutic implications, the most critical step in SMaRT is to develop PTMs resulting in a high ratio of trans-splicing to regular cis-splicing.This protocol provides guidelines on how to design PTMs and describes a fast screening assay to test their efficiencies. To elucidate the therapeutic potential of the best candidates in a more native setting, these PTMs are tested further on mini genes.
剪接体介导的mRNA反式剪接(SMaRT)是一种很有前景的治疗遗传疾病的策略,而传统治疗方法无法针对这些疾病。SMaRT利用外源性前体mRNA反式剪接分子(PTM)来校正患病的靶向前体mRNA。这个过程依赖于两个单独的前体mRNA分子的反式剪接,从而产生一个成熟的嵌合mRNA分子,该分子由PTM的蛋白质编码序列以及内源性mRNA组成。对于治疗意义而言,SMaRT中最关键的步骤是开发能使反式剪接与常规顺式剪接比例较高的PTM。本方案提供了关于如何设计PTM的指导方针,并描述了一种快速筛选测定法以测试其效率。为了在更天然的环境中阐明最佳候选物的治疗潜力,这些PTM将在微型基因上进一步测试。